Publications associated with registered cell lines

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Rajpurohit CS, Kumar V, Cheffer A, Oliveira D, Ulrich H, Okamoto OK, Zatz M, Ansari UA, Khanna VK, Pant AB

Mechanistic Insights of Astrocyte-Mediated Hyperactive Autophagy and Loss of Motor Neuron Function in SOD1^L39R Linked Amyotrophic Lateral Sclerosis
Rajpurohit CS et al. Mechanistic Insights of Astrocyte-Mediated Hyperactive Autophagy and Loss of Motor Neuron Function in SOD1^L39R Linked Amyotrophic Lateral Sclerosis. . 2020-10-00. Pubmed ID: 32676988; DOI: 10.1007/s12035-020-02006-0 HEBHMUi001-A 2020-10-00 2020-10-00
PubMed: 32676988 DOI: 10.1007/s12035-020-02006-0
Associated cell lines:
- HEBHMUi001-A
Metzler Eric, Telugu Narasimha, Diecke Sebastian, Spuler Simone, Escobar Helena

Generation of two human induced pluripotent stem cell lines derived from myoblasts (MDCi014-A) and from peripheral blood mononuclear cells (MDCi014-B) from the same donor
Metzler Eric et al. Generation of two human induced pluripotent stem cell lines derived from myoblasts (MDCi014-A) and from peripheral blood mononuclear cells (MDCi014-B) from the same donor. . 2020-10-00. DOI: 10.1016/j.scr.2020.101998 MDCi014-AMDCi014-B 2020-10-00 2020-10-00
DOI: 10.1016/j.scr.2020.101998
Associated cell lines:
- MDCi014-A
- MDCi014-B
Zhao Qingyang, Cui Yazhou, Wang Jing, Shi Liang, Qi Zijuan, Luan Jing, Zhang Yuang, Zhou Xiaoyan, Han Jinxiang

Development of a human iPSC line (SMBCi004-A) from a patient with Gaucher disease
Zhao Qingyang et al. Development of a human iPSC line (SMBCi004-A) from a patient with Gaucher disease. . 2020-10-00. DOI: 10.1016/j.scr.2020.101989 SMBCi004-A 2020-10-00 2020-10-00
DOI: 10.1016/j.scr.2020.101989
Associated cell lines:
- SMBCi004-A
Lee SJ, Kim JH, Kang KW, Park Y, Kim BS

Supporting data on enhanced reprogramming of human CD34+ hematopoietic stem cells to induced pluripotent stem cells using human placenta-derived cell conditioned medium
Lee SJ et al. Supporting data on enhanced reprogramming of human CD34+ hematopoietic stem cells to induced pluripotent stem cells using human placenta-derived cell conditioned medium. . 2020-10-00. Pubmed ID: 32904343; DOI: 10.1016/j.dib.2020.106140; PMC: PMC7452686 KUMCi001-A 2020-10-00 2020-10-00
PubMed: 32904343 DOI: 10.1016/j.dib.2020.106140
Associated cell lines:
- KUMCi001-A
Zhao Huifang, He Lang, Huang Hualin, Li Shuai, Cheng Na, Tang Feng, Han Xiaobo, Lin Zuoxian, Huang Rongqi, Zhou Peng, Deng Sihao, Huang Jufang, Li Zhiyuan

Generation of a tdTomato-GAD67 reporter human epilepsia mutation induced pluripotent stem cell line, USTCi001-A-2, using CRISPR/Cas9 editing
Zhao Huifang et al. Generation of a tdTomato-GAD67 reporter human epilepsia mutation induced pluripotent stem cell line, USTCi001-A-2, using CRISPR/Cas9 editing. . 2020-10-00. DOI: 10.1016/j.scr.2020.102003 USTCi001-A-2 2020-10-00 2020-10-00
DOI: 10.1016/j.scr.2020.102003
Associated cell lines:
- USTCi001-A-2
Tan Chengning, Dai Limeng, Yang Wuchen, Li Fengjie, Wang Li, Xiao Yanni, Wang Xiaojie, Zhang Yichi, Wang Yali, Zeng Cheng, Xiang Zheng, Zhang Xiaomei, Zhang Weiwei, Ran Qian, Chen Maoshan, Li Zhongjun, Chen Li

Generation of the human induced pluripotent stem cell line (SHAMUi001-A) carrying the heterozygous c.-128G>T mutation in the 5′-UTR of the ANKRD26 gene
Tan Chengning et al. Generation of the human induced pluripotent stem cell line (SHAMUi001-A) carrying the heterozygous c.-128G>T mutation in the 5′-UTR of the ANKRD26 gene. . 2020-10-00. DOI: 10.1016/j.scr.2020.102002 SHAMUi001-A 2020-10-00 2020-10-00
DOI: 10.1016/j.scr.2020.102002
Associated cell lines:
- SHAMUi001-A
Sripathy SR, Wang Y, Moses RL, Fatemi A, Batista DA, Maher BJ

Generation of 10 patient-specific induced pluripotent stem cells (iPSCs) to model Pitt-Hopkins Syndrome
Sripathy SR et al. Generation of 10 patient-specific induced pluripotent stem cells (iPSCs) to model Pitt-Hopkins Syndrome. . 2020-09-17. Pubmed ID: 32971458; DOI: 10.1016/j.scr.2020.102001 LIBDi010-ALIBDi011-ALIBDi012-ALIBDi013-ALIBDi014-ALIBDi015-ALIBDi016-ALIBDi017-ALIBDi018-ALIBDi019-A 2020-09-17 2020-09-17
PubMed: 32971458 DOI: 10.1016/j.scr.2020.102001
Associated cell lines:
- LIBDi010-A
- LIBDi011-A
- LIBDi012-A
- LIBDi013-A
- LIBDi014-A
- LIBDi015-A
- LIBDi016-A
- LIBDi017-A
- LIBDi018-A
- LIBDi019-A
Tang Y, Han Y, Yu H, Zhang B, Li G

Increased GABAergic development in iPSC-derived neurons from patients with sporadic Alzheimer's disease
Tang Y et al. Increased GABAergic development in iPSC-derived neurons from patients with sporadic Alzheimer's disease. . 2020-09-14. Pubmed ID: 32615251; DOI: 10.1016/j.neulet.2020.135208 TUSMi001-ATUSMi008-A 2020-09-14 2020-09-14
PubMed: 32615251 DOI: 10.1016/j.neulet.2020.135208
Associated cell lines:
- TUSMi001-A
- TUSMi008-A
Aqel YWA, Ali G, Elsayed AK, Al-Khawaga S, Hussain K, Abdelalim EM

Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene
Aqel YWA et al. Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene. . 2020-09-13. Pubmed ID: 32971462; DOI: 10.1016/j.scr.2020.101991 QBRIi010-AQBRIi011-A 2020-09-13 2020-09-13
PubMed: 32971462 DOI: 10.1016/j.scr.2020.101991
Associated cell lines:
- QBRIi010-A
- QBRIi011-A
Kim KP, Yoon J, Kim J, Röpke A, Shin B, Wook Han D, Greber B, Schöler HR

Generation of a human iPSC line (MPIi007-A) from a patient with Metachromatic leukodystrophy
Kim KP et al. Generation of a human iPSC line (MPIi007-A) from a patient with Metachromatic leukodystrophy. . 2020-09-13. Pubmed ID: 32950023; DOI: 10.1016/j.scr.2020.101993 MPIi007-A 2020-09-13 2020-09-13
PubMed: 32950023 DOI: 10.1016/j.scr.2020.101993
Associated cell lines:
- MPIi007-A
Yu Z, Dmitrieva NI, Walts AD, Jin H, Liu Y, Ping X, Ferrante EA, Qiu L, Holland SM, Freeman AF, Chen G, Boehm M

STAT3 modulates reprogramming efficiency of human somatic cells; insights from autosomal dominant Hyper IgE syndrome caused by STAT3 mutations
Yu Z et al. STAT3 modulates reprogramming efficiency of human somatic cells; insights from autosomal dominant Hyper IgE syndrome caused by STAT3 mutations. . 2020-09-10. Pubmed ID: 32580970; DOI: 10.1242/bio.052662; PMC: PMC7502598 NIHTVBi011-ANIHTVBi012-ANIHTVBi013-A 2020-09-10 2020-09-10
PubMed: 32580970 DOI: 10.1242/bio.052662
Associated cell lines:
Metzler E, Telugu N, Diecke S, Spuler S, Escobar H

Generation of three age and gender matched pairs of human induced pluripotent stem cells derived from myoblasts (MDCi011-A, MDCi012-A, MDCi013-A) and from peripheral blood mononuclear cells (MDCi011-B, MDCi012-B, MDCi013-B) from the same donor
Metzler E et al. Generation of three age and gender matched pairs of human induced pluripotent stem cells derived from myoblasts (MDCi011-A, MDCi012-A, MDCi013-A) and from peripheral blood mononuclear cells (MDCi011-B, MDCi012-B, MDCi013-B) from the same donor. . 2020-09-08. Pubmed ID: 32961449; DOI: 10.1016/j.scr.2020.101987 MDCi011-AMDCi011-BMDCi012-AMDCi012-BMDCi013-AMDCi013-B 2020-09-08 2020-09-08
PubMed: 32961449 DOI: 10.1016/j.scr.2020.101987
Associated cell lines:
- MDCi011-A
- MDCi011-B
- MDCi012-A
- MDCi012-B
- MDCi013-A
- MDCi013-B
Gao X, Qiu SW, Feng ML, Huang SS, Kang DY, Han MY, Dai P, Yuan YY

Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2
Gao X et al. Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2. . 2020-09-08. Pubmed ID: 32961450; DOI: 10.1016/j.scr.2020.101986 CPGHi002-A 2020-09-08 2020-09-08
PubMed: 32961450 DOI: 10.1016/j.scr.2020.101986
Associated cell lines:
- CPGHi002-A
Sahabian A, von Schlehdorn L, Drick N, Pink I, Dahlmann J, Haase A, Göhring G, Welte T, Martin U, Ringshausen FC, Olmer R

Generation of two hiPSC clones (MHHi019-A, MHHi019-B) from a primary ciliary dyskinesia patient carrying a homozygous deletion in the NME5 gene (c.415delA (p.Ile139Tyrfs*8))
Sahabian A et al. Generation of two hiPSC clones (MHHi019-A, MHHi019-B) from a primary ciliary dyskinesia patient carrying a homozygous deletion in the NME5 gene (c.415delA (p.Ile139Tyrfs*8)). . 2020-09-07. Pubmed ID: 32950024; DOI: 10.1016/j.scr.2020.101988 MHHi019-AMHHi019-B 2020-09-07 2020-09-07
PubMed: 32950024 DOI: 10.1016/j.scr.2020.101988
Associated cell lines:
- MHHi019-A
- MHHi019-B
Ferreira Mendes JM, de Faro Valverde L, Torres Andion Vidal M, Paredes BD, Coelho P, Allahdadi KJ, Coletta RD, Souza BSF, Rocha CAG

Effects of IGF-1 on Proliferation, Angiogenesis, Tumor Stem Cell Populations and Activation of AKT and Hedgehog Pathways in Oral Squamous Cell Carcinoma
Ferreira Mendes JM et al. Effects of IGF-1 on Proliferation, Angiogenesis, Tumor Stem Cell Populations and Activation of AKT and Hedgehog Pathways in Oral Squamous Cell Carcinoma. . 2020-09-05. Pubmed ID: 32899449; DOI: 10.3390/ijms21186487 CBTCi001-A 2020-09-05 2020-09-05
PubMed: 32899449 DOI: 10.3390/ijms21186487
Associated cell lines:
- CBTCi001-A
Strnadel J, Zahumenska R, Nosal V, Smolar M, Marcinek J, Kalman M, Juhas S, Juhasova J, Studenovska H, Dumortier H, Chromec T, Skovierova H, Mitruskova B, Kapralik I, Mersakova S, Brany D, Halasova E

Generation of ORIONi001-A induced pluripotent stem cell line for in vitro modeling of sporadic form of amyotrophic lateral sclerosis
Strnadel J et al. Generation of ORIONi001-A induced pluripotent stem cell line for in vitro modeling of sporadic form of amyotrophic lateral sclerosis. . 2020-09-04. Pubmed ID: 32919353; DOI: 10.1016/j.scr.2020.101981 ORIONi001-A 2020-09-04 2020-09-04
PubMed: 32919353 DOI: 10.1016/j.scr.2020.101981
Associated cell lines:
- ORIONi001-A
Liu H, Li S, Ren C, Liu W, Zhu B, Wang L, Xu H, Xie W, Zuo X, Zhou Y, Luo L, Jiang X

Generation of an ESRG Pr-tdTomato reporter human embryonic stem cell line, CSUe011-A, using CRISPR/Cas9 editing
Liu H et al. Generation of an ESRG Pr-tdTomato reporter human embryonic stem cell line, CSUe011-A, using CRISPR/Cas9 editing. . 2020-09-03. Pubmed ID: 32919352; DOI: 10.1016/j.scr.2020.101983 CSUe011-A 2020-09-03 2020-09-03
PubMed: 32919352 DOI: 10.1016/j.scr.2020.101983
Associated cell lines:
- CSUe011-A
Rolova T, Wu YC, Koskuvi M, Voutilainen J, Sonninen TM, Kuusisto J, Laakso M, Hämäläinen RH, Koistinaho J, Lehtonen Š

Generation of a human induced pluripotent stem cell line (UEFi003-A) carrying heterozygous A673T variant in amyloid precursor protein associated with a reduced risk of Alzheimer's disease
Rolova T et al. Generation of a human induced pluripotent stem cell line (UEFi003-A) carrying heterozygous A673T variant in amyloid precursor protein associated with a reduced risk of Alzheimer's disease. . 2020-09-02. Pubmed ID: 32911327; DOI: 10.1016/j.scr.2020.101968 UEFi003-A 2020-09-02 2020-09-02
PubMed: 32911327 DOI: 10.1016/j.scr.2020.101968
Associated cell lines:
- UEFi003-A
Das D, Li J, Liu S, Oh E, Cheng L, Lyketsos C, Mahairaki V

Generation and characterization of a novel human iPSC line from a resilient Alzheimer's disease patient
Das D et al. Generation and characterization of a novel human iPSC line from a resilient Alzheimer's disease patient. . 2020-09-02. Pubmed ID: 32916633; DOI: 10.1016/j.scr.2020.101979 JHUi002-A 2020-09-02 2020-09-02
PubMed: 32916633 DOI: 10.1016/j.scr.2020.101979
Associated cell lines:
- JHUi002-A
Xia S, Wang X, Yue P, Li Y, Zhang D

Establishment of induced pluripotent stem cell lines from a family of an ARVC patient receiving heart transplantation in infant age carrying compound heterozygous mutations in DSP gene
Xia S et al. Establishment of induced pluripotent stem cell lines from a family of an ARVC patient receiving heart transplantation in infant age carrying compound heterozygous mutations in DSP gene. . 2020-09-02. Pubmed ID: 32942234; DOI: 10.1016/j.scr.2020.101977 HUBUi001-AHUBUi002-AHUBUi003-A 2020-09-02 2020-09-02
PubMed: 32942234 DOI: 10.1016/j.scr.2020.101977
Associated cell lines:
Wu X, Zhao Y, Wang X

Generation of a human embryonic stem cell line (WAe009-A-43) carrying a Long QT syndrome related mutation in KCNH2 gene
Wu X et al. Generation of a human embryonic stem cell line (WAe009-A-43) carrying a Long QT syndrome related mutation in KCNH2 gene. . 2020-09-02. Pubmed ID: 32911324; DOI: 10.1016/j.scr.2020.101976 WAe009-AWAe009-A-43 2020-09-02 2020-09-02
PubMed: 32911324 DOI: 10.1016/j.scr.2020.101976
Associated cell lines:
- WAe009-A
- WAe009-A-43
Zlotnik D, Rabinski T, Ofir R, Hershkovitz E, Vatine GD

Generation of iPSC lines from two (BGUi002-A and BGUi003-A) homozygous p450 oxidoreductase-deficient patients and from one (BGUi001-A) heterozygous healthy family relative
Zlotnik D et al. Generation of iPSC lines from two (BGUi002-A and BGUi003-A) homozygous p450 oxidoreductase-deficient patients and from one (BGUi001-A) heterozygous healthy family relative. . 2020-09-01. Pubmed ID: 32905996; DOI: 10.1016/j.scr.2020.101975 BGUi001-ABGUi002-ABGUi003-ABGUi004-ABGUi005-A 2020-09-01 2020-09-01
PubMed: 32905996 DOI: 10.1016/j.scr.2020.101975
Associated cell lines:
- BGUi001-A
- BGUi002-A
- BGUi003-A
- BGUi004-A
- BGUi005-A
Kamand M, Ilieva M, Louise Forsberg S, Thomassen M, Meyer M, Fex Svenningsen Å, Maria Michel T

Derivation of induced pluripotent stem cells (SDUKIi003-A) from a 20-year-old male patient diagnosed with Asperger syndrome
Kamand M et al. Derivation of induced pluripotent stem cells (SDUKIi003-A) from a 20-year-old male patient diagnosed with Asperger syndrome. . 2020-09-01. Pubmed ID: 32916638; DOI: 10.1016/j.scr.2020.101974 SDUKIi002-ASDUKIi003-A 2020-09-01 2020-09-01
PubMed: 32916638 DOI: 10.1016/j.scr.2020.101974
Associated cell lines:
- SDUKIi002-A
- SDUKIi003-A
Wang Hongyang, Wu Kaiwen, Guan Jing, Wang Qiuju

Generation of a human induced pluripotent stem cell line (CPGHi001-A) from a hearing loss patient with the TMC1 p.M418K mutation
Wang Hongyang et al. Generation of a human induced pluripotent stem cell line (CPGHi001-A) from a hearing loss patient with the TMC1 p.M418K mutation. . 2020-09-00. DOI: 10.1016/j.scr.2020.101982 CPGHi001-A 2020-09-00 2020-09-00
DOI: 10.1016/j.scr.2020.101982
Associated cell lines:
- CPGHi001-A
-

56^th EASD Annual Meeting of the European Association for the Study of Diabetes : 21-25 September 2020
(unknown author). 56^th EASD Annual Meeting of the European Association for the Study of Diabetes : 21-25 September 2020. . 2020-09-00. Pubmed ID: 32840677; DOI: 10.1007/s00125-020-05221-5; PMC: PMC7445463 MHHi006-A 2020-09-00 2020-09-00
PubMed: 32840677 DOI: 10.1007/s00125-020-05221-5
Associated cell lines:
- MHHi006-A
Alowaysia Maryam, Fiaccoa Elisabetta, Astro Veronica, Adamo Antonio

Establishment of iPSC lines from a high-grade Klinefelter Syndrome patient (49-XXXXY) and two genetically matched healthy relatives (KAUSTi003-A, KAUSTi004-A, KAUSTi004-B, KAUSTi005-A, KAUSTi005-B, KAUSTi005-C)
Alowaysia Maryam et al. Establishment of iPSC lines from a high-grade Klinefelter Syndrome patient (49-XXXXY) and two genetically matched healthy relatives (KAUSTi003-A, KAUSTi004-A, KAUSTi004-B, KAUSTi005-A, KAUSTi005-B, KAUSTi005-C). . 2020-09-00. DOI: 10.1016/j.scr.2020.102008 KAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-C 2020-09-00 2020-09-00
DOI: 10.1016/j.scr.2020.102008
Associated cell lines:
Zhu Xiyu, Wang Junxia, Chong Hoshun, Wang Jiaxian, Wang Dongjin

Generation of induced pluripotent stem cells (NJDTHi001-A) from a Danon disease child with mutation of c.467 T>G in LAMP2 gene
Zhu Xiyu et al. Generation of induced pluripotent stem cells (NJDTHi001-A) from a Danon disease child with mutation of c.467 T>G in LAMP2 gene. . 2020-09-00. DOI: 10.1016/j.scr.2020.101994 NJDTHi001-A 2020-09-00 2020-09-00
DOI: 10.1016/j.scr.2020.101994
Associated cell lines:
- NJDTHi001-A
Ababneh NA, Ali D, Barham R, Al-Kurdi B, Sharar N, Al Hadidi S, Qanno' O, Ryalat AT, Salah B, Awidi A

Establishment of a human induced pluripotent stem cell line, JUCTCi012-A, from multiple symmetric lipomatosis (MSL) patient carrying a homozygous Arg707Trp (c.2119C > T) mutation in the MFN2 gene
Ababneh NA et al. Establishment of a human induced pluripotent stem cell line, JUCTCi012-A, from multiple symmetric lipomatosis (MSL) patient carrying a homozygous Arg707Trp (c.2119C > T) mutation in the MFN2 gene. . 2020-08-31. Pubmed ID: 32916636; DOI: 10.1016/j.scr.2020.101967 JUCTCi012-A 2020-08-31 2020-08-31
PubMed: 32916636 DOI: 10.1016/j.scr.2020.101967
Associated cell lines:
- JUCTCi012-A
Shrestha R, Wen YT, Tsai RK

Effective Differentiation and Biological Characterization of Retinal Pigment Epithelium Derived from Human Induced Pluripotent Stem Cells
Shrestha R et al. Effective Differentiation and Biological Characterization of Retinal Pigment Epithelium Derived from Human Induced Pluripotent Stem Cells. . 2020-09-00. Pubmed ID: 31984806; DOI: 10.1080/02713683.2020.1722180 TCIERi001-A 2020-09-00 2020-09-00
PubMed: 31984806 DOI: 10.1080/02713683.2020.1722180
Associated cell lines:
- TCIERi001-A
Calzari L, Barcella M, Alari V, Braga D, Muñoz-Viana R, Barlassina C, Finelli P, Gervasini C, Barco A, Russo S, Larizza L

Transcriptome Analysis of iPSC-Derived Neurons from Rubinstein-Taybi Patients Reveals Deficits in Neuronal Differentiation
Calzari L et al. Transcriptome Analysis of iPSC-Derived Neurons from Rubinstein-Taybi Patients Reveals Deficits in Neuronal Differentiation. . 2020-09-00. Pubmed ID: 32562237; DOI: 10.1007/s12035-020-01983-6; PMC: PMC7399686 IAIi001-AIAIi002-AIAIi003-AIAIi004-A 2020-09-00 2020-09-00
PubMed: 32562237 DOI: 10.1007/s12035-020-01983-6
Associated cell lines:
HW Kung Louise, Sampurno Lisa, Yammine Kathryn M., Graham Alison, McDonald Penny, Bateman John F., Shoulders Matthew D., Lamandé Shireen R.

CRISPR/Cas9 editing to generate a heterozygous COL2A1 p.G1170S human chondrodysplasia iPSC line, MCRIi019-A-2, in a control iPSC line, MCRIi019-A
HW Kung Louise et al. CRISPR/Cas9 editing to generate a heterozygous COL2A1 p.G1170S human chondrodysplasia iPSC line, MCRIi019-A-2, in a control iPSC line, MCRIi019-A. . 2020-09-00. DOI: 10.1016/j.scr.2020.101962 MCRIi019-AMCRIi019-A-2 2020-09-00 2020-09-00
DOI: 10.1016/j.scr.2020.101962
Associated cell lines:
- MCRIi019-A
- MCRIi019-A-2
Meynier S, Rieux-Laucat F

After 95 years, it's time to eRASe JMML
Meynier S et al. After 95 years, it's time to eRASe JMML. . 2020-09-00. Pubmed ID: 31980238; DOI: 10.1016/j.blre.2020.100652 CHOPi001-A 2020-09-00 2020-09-00
PubMed: 31980238 DOI: 10.1016/j.blre.2020.100652
Associated cell lines:
- CHOPi001-A
Ge Ning, Liu Min, Krawczyk Janusz, McInerney Veronica, Ward Deirdre, Shen Sanbing, O'Brien Timothy, Prendiville Terence

Generation and characterization of an induced pluripotent stem cell (iPSC) line (NUIGi003-A) from a Long QT Syndrome Type 2 (LQT2) patient harbouring the KCNH2 c.2464G>A pathogenic variant
Ge Ning et al. Generation and characterization of an induced pluripotent stem cell (iPSC) line (NUIGi003-A) from a Long QT Syndrome Type 2 (LQT2) patient harbouring the KCNH2 c.2464G>A pathogenic variant. . 2020-09-00. DOI: 10.1016/j.scr.2020.101997 NUIGi003-A 2020-09-00 2020-09-00
DOI: 10.1016/j.scr.2020.101997
Associated cell lines:
- NUIGi003-A
Ali Eltahir, Ferraro Rosalba Monica, Lanzi Gaetana, Masneri Stefania, Piovani Giovanna, Mazzoldi Elena Laura, Serpieri Valentina, Valente Enza Maria, Giordano Lucio, Giliani Silvia Clara

Generation of induced pluripotent stem cell (iPSC) lines from a Joubert syndrome patient with compound heterozygous mutations in C5orf42 gene
Ali Eltahir et al. Generation of induced pluripotent stem cell (iPSC) lines from a Joubert syndrome patient with compound heterozygous mutations in C5orf42 gene. . 2020-09-00. DOI: 10.1016/j.scr.2020.102007 UNIBSi011-AUNIBSi011-BUNIBSi011-C 2020-09-00 2020-09-00
DOI: 10.1016/j.scr.2020.102007
Associated cell lines:
Marchiano Silvia, Hsiang Tien-Ying, Higashi Ty, Khanna Akshita, Reinecke Hans, Yang Xiulan, Pabon Lil, Sniadecki Nathan J., Bertero Alessandro, Gale Michael, Murry Charles E.

SARS-CoV-2 infects human pluripotent stem cell-derived cardiomyocytes, impairing electrical and mechanical function
Marchiano Silvia et al. SARS-CoV-2 infects human pluripotent stem cell-derived cardiomyocytes, impairing electrical and mechanical function. . 2020-08-30. DOI: 10.1101/2020.08.30.274464 RUESe002-A 2020-08-30 2020-08-30
DOI: 10.1101/2020.08.30.274464
Associated cell lines:
- RUESe002-A
Ebrahimi V, Hashemi A

Challenges of in vitro genome editing with CRISPR/Cas9 and possible solutions: A review
Ebrahimi V et al. Challenges of in vitro genome editing with CRISPR/Cas9 and possible solutions: A review. . 2020-08-30. Pubmed ID: 32470504; DOI: 10.1016/j.gene.2020.144813 MUSIi012-AMUSIi012-A-1 2020-08-30 2020-08-30
PubMed: 32470504 DOI: 10.1016/j.gene.2020.144813
Associated cell lines:
- MUSIi012-A
- MUSIi012-A-1
Lai LL, Chen YJ, Li YL, Lin XH, Wang MW, Dong EL, Wang N, Chen WJ, Lin X

Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia
Lai LL et al. Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia. . 2020-08-29. Pubmed ID: 32860341; DOI: 10.1002/acn3.51169 FJMUi001-A 2020-08-29 2020-08-29
PubMed: 32860341 DOI: 10.1002/acn3.51169
Associated cell lines:
- FJMUi001-A
Jamwal VS, Vishnu VV, Domreddy A, Parekh Y, Kumar BK, Chandra Shekar P, Singh S

Generation of iPSC from fetal fibroblast cells obtained from an abortus with type-I tri-allelic variants
Jamwal VS et al. Generation of iPSC from fetal fibroblast cells obtained from an abortus with type-I tri-allelic variants. . 2020-08-27. Pubmed ID: 32916634; DOI: 10.1016/j.scr.2020.101963 CCMBi001-A 2020-08-27 2020-08-27
PubMed: 32916634 DOI: 10.1016/j.scr.2020.101963
Associated cell lines:
- CCMBi001-A
Stock R, Vogel S, Mau-Holzmann UA, Kriebel M, Wüst R, Fallgatter AJ, Volkmer H

Generation and characterization of human induced pluripotent stem cells lines from four patients diagnosed with schizophrenia and one healthy control
Stock R et al. Generation and characterization of human induced pluripotent stem cells lines from four patients diagnosed with schizophrenia and one healthy control. . 2020-08-27. Pubmed ID: 32911325; DOI: 10.1016/j.scr.2020.101961 NMIi001-ANMIi002-ANMIi004-ANMIi005-ANMIi006-ANMIi002-BNMIi006-B 2020-08-27 2020-08-27
PubMed: 32911325 DOI: 10.1016/j.scr.2020.101961
Associated cell lines:
- NMIi001-A
- NMIi002-A
- NMIi004-A
- NMIi005-A
- NMIi006-A
- NMIi002-B
- NMIi006-B
Liu S, Niu S, Li Y, Xiong H, Li Y, Jian L, Zhang L

Establishment of an induced pluripotent stem cell line (ZZUSAHi002-A) derived from peripheral blood mononuclear cells of a healthy individual
Liu S et al. Establishment of an induced pluripotent stem cell line (ZZUSAHi002-A) derived from peripheral blood mononuclear cells of a healthy individual. . 2020-08-27. Pubmed ID: 32911326; DOI: 10.1016/j.scr.2020.101966 ZZUSAHi002-A 2020-08-27 2020-08-27
PubMed: 32911326 DOI: 10.1016/j.scr.2020.101966
Associated cell lines:
- ZZUSAHi002-A
Zhou D, Sun Y, Shen J, Su J, Gong T, Jiang C, Liang P

Generation of an induced pluripotent stem cell line from the dermal fibroblasts of a patient with arrhythmogenic right ventricular cardiomyopathy carrying a PKP2/c.2489 + 1G > A mutation
Zhou D et al. Generation of an induced pluripotent stem cell line from the dermal fibroblasts of a patient with arrhythmogenic right ventricular cardiomyopathy carrying a PKP2/c.2489 + 1G > A mutation. . 2020-08-27. Pubmed ID: 32916635; DOI: 10.1016/j.scr.2020.101965 ZJUi004-A 2020-08-27 2020-08-27
PubMed: 32916635 DOI: 10.1016/j.scr.2020.101965
Associated cell lines:
- ZJUi004-A
Sequiera GL, Rockman-Greenberg C, Dhingra S

Induced pluripotent stem cell line UOMi002-A from a patient with Leigh syndrome with compound heterozygous mutations in the NDUFV1 gene
Sequiera GL et al. Induced pluripotent stem cell line UOMi002-A from a patient with Leigh syndrome with compound heterozygous mutations in the NDUFV1 gene. . 2020-08-27. Pubmed ID: 32871395; DOI: 10.1016/j.scr.2020.101964 UOMi002-A 2020-08-27 2020-08-27
PubMed: 32871395 DOI: 10.1016/j.scr.2020.101964
Associated cell lines:
- UOMi002-A
Yoshida S, Okura H, Suga H, Soen M, Kawaguchi Y, Kurimoto J, Miyata T, Takagi H, Arima H, Fujikawa T, Otsuka F, Matsuyama A

Generation of four induced pluripotent stem cell lines (FHUi003-A, FHUi003-B, FHUi004-A and FHUi004-B) from two affected individuals of a familial neurohypophyseal diabetes insipidus family
Yoshida S et al. Generation of four induced pluripotent stem cell lines (FHUi003-A, FHUi003-B, FHUi004-A and FHUi004-B) from two affected individuals of a familial neurohypophyseal diabetes insipidus family. . 2020-08-26. Pubmed ID: 32927425; DOI: 10.1016/j.scr.2020.101960 FHUi003-AFHUi003-BFHUi004-AFHUi004-B 2020-08-26 2020-08-26
PubMed: 32927425 DOI: 10.1016/j.scr.2020.101960
Associated cell lines:
Sanjurjo-Rodríguez C, Castro-Viñuelas R, Piñeiro-Ramil M, Rodríguez-Fernández S, Fuentes-Boquete I, Blanco FJ, Díaz-Prado S

Versatility of Induced Pluripotent Stem Cells (iPSCs) for Improving the Knowledge on Musculoskeletal Diseases
Sanjurjo-Rodríguez C et al. Versatility of Induced Pluripotent Stem Cells (iPSCs) for Improving the Knowledge on Musculoskeletal Diseases. . 2020-08-25. Pubmed ID: 32854405; DOI: 10.3390/ijms21176124 ISMMSi002-BESi080-A 2020-08-25 2020-08-25
PubMed: 32854405 DOI: 10.3390/ijms21176124
Associated cell lines:
- ISMMSi002-B
- ESi080-A
Varma R, Soleas JP, Waddell TK, Karoubi G, McGuigan AP

Current strategies and opportunities to manufacture cells for modeling human lungs
Varma R et al. Current strategies and opportunities to manufacture cells for modeling human lungs. . 2020-08-22. Pubmed ID: 32835746; DOI: 10.1016/j.addr.2020.08.005; PMC: PMC7442933 MHHi006-AMHHi006-A-4 2020-08-22 2020-08-22
PubMed: 32835746 DOI: 10.1016/j.addr.2020.08.005
Associated cell lines:
- MHHi006-A
- MHHi006-A-4
Kido J, Nakamura K, Era T

Role of induced pluripotent stem cells in lysosomal storage diseases
Kido J et al. Role of induced pluripotent stem cells in lysosomal storage diseases. . 2020-08-21. Pubmed ID: 32828964; DOI: 10.1016/j.mcn.2020.103540 TRNDi006-ATRNDi001-DUNIGEi001-A 2020-08-21 2020-08-21
PubMed: 32828964 DOI: 10.1016/j.mcn.2020.103540
Associated cell lines:
Quelennec E, Banal C, Hamlin M, Clémantine D, Michael M, Lefort N

Generation of two induced pluripotent stem cell lines IMAGINi004-A and IMAGINi005-A from healthy donors
Quelennec E et al. Generation of two induced pluripotent stem cell lines IMAGINi004-A and IMAGINi005-A from healthy donors. . 2020-08-20. Pubmed ID: 32866896; DOI: 10.1016/j.scr.2020.101959 IMAGINi004-AIMAGINi005-A 2020-08-20 2020-08-20
PubMed: 32866896 DOI: 10.1016/j.scr.2020.101959
Associated cell lines:
- IMAGINi004-A
- IMAGINi005-A
Eintracht Jonathan, Toms Maria, Moosajee Mariya

The Use of Induced Pluripotent Stem Cells as a Model for Developmental Eye Disorders
Eintracht Jonathan et al. The Use of Induced Pluripotent Stem Cells as a Model for Developmental Eye Disorders. . 2020-08-20. DOI: 10.3389/fncel.2020.00265 MCRIi001-AMCRIi001-A-1 2020-08-20 2020-08-20
DOI: 10.3389/fncel.2020.00265
Associated cell lines:
- MCRIi001-A
- MCRIi001-A-1
Kumamoto T, Maurinot F, Barry-Martinet R, Vaslin C, Vandormael-Pournin S, Le M, Lerat M, Niculescu D, Cohen-Tannoudji M, Rebsam A, Loulier K, Nedelec S, Tozer S, Livet J

Direct Readout of Neural Stem Cell Transgenesis with an Integration-Coupled Gene Expression Switch
Kumamoto T et al. Direct Readout of Neural Stem Cell Transgenesis with an Integration-Coupled Gene Expression Switch. . 2020-08-19. Pubmed ID: 32559415; DOI: 10.1016/j.neuron.2020.05.038; PMC: PMC7447981 WTSIi008-A 2020-08-19 2020-08-19
PubMed: 32559415 DOI: 10.1016/j.neuron.2020.05.038
Associated cell lines:
- WTSIi008-A
Ratnavadivel S, Szymanski de Toledo M, Rasmussen TB, Šarić T, Gummert J, Zenke M, Milting H

Human pluripotent stem cell line (HDZi001-A) derived from a patient carrying the ARVC-5 associated mutation TMEM43-p.S358L
Ratnavadivel S et al. Human pluripotent stem cell line (HDZi001-A) derived from a patient carrying the ARVC-5 associated mutation TMEM43-p.S358L. . 2020-08-19. Pubmed ID: 32858485; DOI: 10.1016/j.scr.2020.101957 HDZi001-A 2020-08-19 2020-08-19
PubMed: 32858485 DOI: 10.1016/j.scr.2020.101957
Associated cell lines:
- HDZi001-A
Kim MJ, Lee EY, You YH, Yang HK, Yoon KH, Kim JW

Generation of iPSC-derived insulin-producing cells from patients with type 1 and type 2 diabetes compared with healthy control
Kim MJ et al. Generation of iPSC-derived insulin-producing cells from patients with type 1 and type 2 diabetes compared with healthy control. . 2020-08-18. Pubmed ID: 32882526; DOI: 10.1016/j.scr.2020.101958 CMCi003-ACMCi004-ACMCi005-A 2020-08-18 2020-08-18
PubMed: 32882526 DOI: 10.1016/j.scr.2020.101958
Associated cell lines:
Kaewkhaw R, Rojanaporn D

Retinoblastoma: Etiology, Modeling, and Treatment
Kaewkhaw R et al. Retinoblastoma: Etiology, Modeling, and Treatment. . 2020-08-16. Pubmed ID: 32824373; DOI: 10.3390/cancers12082304; PMC: PMC7465685 VRFi001-A 2020-08-16 2020-08-16
PubMed: 32824373 DOI: 10.3390/cancers12082304
Associated cell lines:
- VRFi001-A
Amano G, Matsuzaki S, Mori Y, Miyoshi K, Han S, Shikada S, Takamura H, Yoshimura T, Katayama T

SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis
Amano G et al. SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis. . 2020-08-15. Pubmed ID: 32583741; DOI: 10.1091/mbc.e20-02-0100 DHMCi005-A 2020-08-15 2020-08-15
PubMed: 32583741 DOI: 10.1091/mbc.e20-02-0100
Associated cell lines:
- DHMCi005-A
Falik D, Rabinski T, Zlotnik D, Eshel R, Zorsky M, Garin-Shkolnik T, Ofir R, Adato A, Ashkenazi A, Vatine GD

Generation and characterization of iPSC lines (BGUi004-A, BGUi005-A) from two identical twins with polyalanine expansion in the paired-like homeobox 2B (PHOX2B) gene
Falik D et al. Generation and characterization of iPSC lines (BGUi004-A, BGUi005-A) from two identical twins with polyalanine expansion in the paired-like homeobox 2B (PHOX2B) gene. . 2020-08-14. Pubmed ID: 32822965; DOI: 10.1016/j.scr.2020.101955 BGUi004-ABGUi005-A 2020-08-14 2020-08-14
PubMed: 32822965 DOI: 10.1016/j.scr.2020.101955
Associated cell lines:
- BGUi004-A
- BGUi005-A
Riccetti S, Sinigaglia A, Desole G, Nowotny N, Trevisan M, Barzon L

Modelling West Nile Virus and Usutu Virus Pathogenicity in Human Neural Stem Cells
Riccetti S et al. Modelling West Nile Virus and Usutu Virus Pathogenicity in Human Neural Stem Cells. . 2020-08-12. Pubmed ID: 32806715; DOI: 10.3390/v12080882; PMC: PMC7471976 UNIPDi002-A 2020-08-12 2020-08-12
PubMed: 32806715 DOI: 10.3390/v12080882
Associated cell lines:
- UNIPDi002-A
Wang L, Li Z, Sievert D, Smith DEC, Mendes MI, Chen DY, Stanley V, Ghosh S, Wang Y, Kara M, Aslanger AD, Rosti RO, Houlden H, Salomons GS, Gleeson JG

Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly
Wang L et al. Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly. . 2020-08-12. Pubmed ID: 32788587; DOI: 10.1038/s41467-020-17454-4; PMC: PMC7424529 WAe001-A 2020-08-12 2020-08-12
PubMed: 32788587 DOI: 10.1038/s41467-020-17454-4
Associated cell lines:
- WAe001-A
Kobold S, Guhr A, Mah N, Bultjer N, Seltmann S, Seiler Wulczyn AEM, Stacey G, Jie H, Liu W, Löser P, Kurtz A

A Manually Curated Database on Clinical Studies Involving Cell Products Derived from Human Pluripotent Stem Cells
Kobold S et al. A Manually Curated Database on Clinical Studies Involving Cell Products Derived from Human Pluripotent Stem Cells. . 2020-08-11. Pubmed ID: 32679065; DOI: 10.1016/j.stemcr.2020.06.014; PMC: PMC7419703 TECHe003-AAXORe001-AACTe002-AWAe001-AWAe009-ARCe013-AVCYTe001-AHADe007-AHADe008-A 2020-08-11 2020-08-11
PubMed: 32679065 DOI: 10.1016/j.stemcr.2020.06.014
Associated cell lines:
- TECHe003-A
- AXORe001-A
- ACTe002-A
- WAe001-A
- WAe009-A
- RCe013-A
- VCYTe001-A
- HADe007-A
- HADe008-A
Pournasr B, Duncan SA

Generation of isogenic Propionyl-CoA carboxylase beta subunit (PCCB) deficient induced pluripotent stem cell lines
Pournasr B et al. Generation of isogenic Propionyl-CoA carboxylase beta subunit (PCCB) deficient induced pluripotent stem cell lines. . 2020-08-08. Pubmed ID: 32822967; DOI: 10.1016/j.scr.2020.101953 MUSCSDi001-A-1MUSCSDi001-A-2 2020-08-08 2020-08-08
PubMed: 32822967 DOI: 10.1016/j.scr.2020.101953
Associated cell lines:
- MUSCSDi001-A-1
- MUSCSDi001-A-2
Malakhova AA, Grigor'eva EV, Pavlova SV, Malankhanova TB, Valetdinova KR, Vyatkin YV, Khabarova EA, Rzaev JA, Zakian SM, Medvedev SP

Generation of induced pluripotent stem cell lines ICGi021-A and ICGi022-A from peripheral blood mononuclear cells of two healthy individuals from Siberian population
Malakhova AA et al. Generation of induced pluripotent stem cell lines ICGi021-A and ICGi022-A from peripheral blood mononuclear cells of two healthy individuals from Siberian population. . 2020-08-08. Pubmed ID: 32805537; DOI: 10.1016/j.scr.2020.101952 ICGi015-AICGi015-BICGi021-AICGi022-A 2020-08-08 2020-08-08
PubMed: 32805537 DOI: 10.1016/j.scr.2020.101952
Associated cell lines:
Barbuti PA, Santos BFR, Dording CM, Cruciani G, Massart F, Hummel A, Krüger R

Generation of two iPS cell lines (HIHDNDi001-A and HIHDNDi001-B) from a Parkinson's disease patient carrying the heterozygous p.A30P mutation in SNCA
Barbuti PA et al. Generation of two iPS cell lines (HIHDNDi001-A and HIHDNDi001-B) from a Parkinson's disease patient carrying the heterozygous p.A30P mutation in SNCA. . 2020-08-08. Pubmed ID: 32798915; DOI: 10.1016/j.scr.2020.101951 LCSBi001-AHIHDNDi001-AHIHDNDi001-B 2020-08-08 2020-08-08
PubMed: 32798915 DOI: 10.1016/j.scr.2020.101951
Associated cell lines:
Nieuwenhuis B, Barber AC, Evans RS, Pearson CS, Fuchs J, MacQueen AR, van Erp S, Haenzi B, Hulshof LA, Osborne A, Conceicao R, Khatib TZ, Deshpande SS, Cave J, Ffrench-Constant C, Smith PD, Okkenhaug K, Eickholt BJ, Martin KR, Fawcett JW, Eva R

PI 3-kinase delta enhances axonal PIP₃ to support axon regeneration in the adult CNS
Nieuwenhuis B et al. PI 3-kinase delta enhances axonal PIP₃ to support axon regeneration in the adult CNS. . 2020-08-07. Pubmed ID: 32558386; DOI: 10.15252/emmm.201911674; PMC: PMC7411663 RCe015-A 2020-08-07 2020-08-07
PubMed: 32558386 DOI: 10.15252/emmm.201911674
Associated cell lines:
- RCe015-A
Tang BL

RAB39B's role in membrane traffic, autophagy, and associated neuropathology
Tang BL. RAB39B's role in membrane traffic, autophagy, and associated neuropathology. . 2020-08-06. Pubmed ID: 32761840; DOI: 10.1002/jcp.29962 ZZUi005-A 2020-08-06 2020-08-06
PubMed: 32761840 DOI: 10.1002/jcp.29962
Associated cell lines:
- ZZUi005-A
Lorthongpanich C, Laowtammathron C, Jiamvoraphong N, Srisook P, Chingsuwanrote P, Klaihmon P, Waeteekul S, U-Pratya Y, Issaragrisil S

Generation of a serine/threonine-protein kinase LATS1 gene-edited iPSC MUSIi012-A-3
Lorthongpanich C et al. Generation of a serine/threonine-protein kinase LATS1 gene-edited iPSC MUSIi012-A-3. . 2020-08-06. Pubmed ID: 32791482; DOI: 10.1016/j.scr.2020.101950 MUSIi012-AMUSIi012-A-3 2020-08-06 2020-08-06
PubMed: 32791482 DOI: 10.1016/j.scr.2020.101950
Associated cell lines:
- MUSIi012-A
- MUSIi012-A-3
Dai Q, Zhang W, Guo J, Di W, Zhao J, Zhang B, Wang Y

Generation of an induced pluripotent stem cell line (SIAISi003-A) from a 79-year-old patient with Alzheimer's disease having APOE3/4 genetic background
Dai Q et al. Generation of an induced pluripotent stem cell line (SIAISi003-A) from a 79-year-old patient with Alzheimer's disease having APOE3/4 genetic background. . 2020-08-05. Pubmed ID: 32822964; DOI: 10.1016/j.scr.2020.101949 SIAISi003-A 2020-08-05 2020-08-05
PubMed: 32822964 DOI: 10.1016/j.scr.2020.101949
Associated cell lines:
- SIAISi003-A
Jennings L, Zhang D, Chen SC, Moon SY, Lamey T, Thompson JA, McLaren T, De Roach JN, Chen FK, McLenachan S

Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4
Jennings L et al. Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4. . 2020-08-05. Pubmed ID: 32810830; DOI: 10.1016/j.scr.2020.101947 LEIi012-ALEIi012-B 2020-08-05 2020-08-05
PubMed: 32810830 DOI: 10.1016/j.scr.2020.101947
Associated cell lines:
- LEIi012-A
- LEIi012-B
Sung JJ, Park S, Choi SH, Kim J, Cho MS, Kim DW

Generation of a gene edited hemophilia A patient-derived iPSC cell line, YCMi001-B-1, by targeted insertion of coagulation factor FVIII using CRISPR/Cas9
Sung JJ et al. Generation of a gene edited hemophilia A patient-derived iPSC cell line, YCMi001-B-1, by targeted insertion of coagulation factor FVIII using CRISPR/Cas9. . 2020-08-05. Pubmed ID: 32798916; DOI: 10.1016/j.scr.2020.101948 YCMi001-BYCMi001-B-1 2020-08-05 2020-08-05
PubMed: 32798916 DOI: 10.1016/j.scr.2020.101948
Associated cell lines:
- YCMi001-B
- YCMi001-B-1
Yang J, Liu H, Sun H, Wang Z, Zhang R, Liu Y, Zhang Q, Zhang S, Zhang J, Shi C, Wang Y, Xu Y

Construction of induced pluripotent stem cell line (ZZUi0017-A) from the fibroblast cells of a female patient with CACNA1A mutation by unintegrated reprogramming approach
Yang J et al. Construction of induced pluripotent stem cell line (ZZUi0017-A) from the fibroblast cells of a female patient with CACNA1A mutation by unintegrated reprogramming approach. . 2020-08-04. Pubmed ID: 32791484; DOI: 10.1016/j.scr.2020.101946 ZZUi017-A 2020-08-04 2020-08-04
PubMed: 32791484 DOI: 10.1016/j.scr.2020.101946
Associated cell lines:
- ZZUi017-A
Sequiera GL, Rockman-Greenberg C, Dhingra S

Establishment of variant free-iPSC (UOMi003-A) line from patient with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes
Sequiera GL et al. Establishment of variant free-iPSC (UOMi003-A) line from patient with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes. . 2020-08-03. Pubmed ID: 32777772; DOI: 10.1016/j.scr.2020.101935 UOMi003-A 2020-08-03 2020-08-03
PubMed: 32777772 DOI: 10.1016/j.scr.2020.101935
Associated cell lines:
- UOMi003-A
Valetdinova KR, Maretina MA, Vyatkin YV, Perepelkina MP, Egorova AA, Baranov VS, Kiselev AV, Gershovich PM, Zakian SM

Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C
Valetdinova KR et al. Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C. . 2020-08-03. Pubmed ID: 32777771; DOI: 10.1016/j.scr.2020.101941 ICGi002-AICGi002-BICGi002-C 2020-08-03 2020-08-03
PubMed: 32777771 DOI: 10.1016/j.scr.2020.101941
Associated cell lines:
Sequiera GL, Rockman-Greenberg C, Dhingra S

Generation of human induced pluripotent stem cell (hiPSC) line UOMi001-A from a patient with Leigh-like syndrome harbouring compound heterozygous variants in ECHS1 gene
Sequiera GL et al. Generation of human induced pluripotent stem cell (hiPSC) line UOMi001-A from a patient with Leigh-like syndrome harbouring compound heterozygous variants in ECHS1 gene. . 2020-08-03. Pubmed ID: 32777769; DOI: 10.1016/j.scr.2020.101934 UOMi001-A 2020-08-03 2020-08-03
PubMed: 32777769 DOI: 10.1016/j.scr.2020.101934
Associated cell lines:
- UOMi001-A
Cosset E, Vannary T, Sloan-Béna F, Gimelli S, Gerstel E, Krause KH, Marteyn A

Generation of human induced pluripotent stem cell line UNIGEi003-A from skin fibroblasts of an apparently healthy male donor
Cosset E et al. Generation of human induced pluripotent stem cell line UNIGEi003-A from skin fibroblasts of an apparently healthy male donor. . 2020-08-03. Pubmed ID: 32805538; DOI: 10.1016/j.scr.2020.101928 UNIGEi003-A 2020-08-03 2020-08-03
PubMed: 32805538 DOI: 10.1016/j.scr.2020.101928
Associated cell lines:
- UNIGEi003-A
Shan H, Ye J, Hai Ping X, XinYue H, ShuYang Z

Establishment of an induced pluripotent stem cell line from a patient with hereditary transthyretin amyloidosis carrying transthyretin (TTR) mutation p.Phe53Val
Shan H et al. Establishment of an induced pluripotent stem cell line from a patient with hereditary transthyretin amyloidosis carrying transthyretin (TTR) mutation p.Phe53Val. . 2020-08-03. Pubmed ID: 32858486; DOI: 10.1016/j.scr.2020.101940 PUMCHi005-A 2020-08-03 2020-08-03
PubMed: 32858486 DOI: 10.1016/j.scr.2020.101940
Associated cell lines:
- PUMCHi005-A
Peron C, Mauceri R, Cabassi T, Segnali A, Maresca A, Iannielli A, Rizzo A, Sciacca FL, Broccoli V, Carelli V, Tiranti V

Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON)
Peron C et al. Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON). . 2020-08-03. Pubmed ID: 32771908; DOI: 10.1016/j.scr.2020.101939 FINCBi001-A 2020-08-03 2020-08-03
PubMed: 32771908 DOI: 10.1016/j.scr.2020.101939
Associated cell lines:
- FINCBi001-A
Lee M, Choi NY, Park S, Bang JS, Lee Y, Jeong D, Ham S, Lim S, Kim KH, Ko K

Generation of OCT4-EGFP, NANOG-tdTomato dual reporter human induced pluripotent stem cell line, KKUi001-A, using the CRISPR/Cas9 system
Lee M et al. Generation of OCT4-EGFP, NANOG-tdTomato dual reporter human induced pluripotent stem cell line, KKUi001-A, using the CRISPR/Cas9 system. . 2020-08-03. Pubmed ID: 32777770; DOI: 10.1016/j.scr.2020.101943 BCRTi001-AKKUi001-A 2020-08-03 2020-08-03
PubMed: 32777770 DOI: 10.1016/j.scr.2020.101943
Associated cell lines:
- BCRTi001-A
- KKUi001-A
Nur Patria Y, Stenta T, Lilianty J, Rowley L, Stanley EG, Elefanty AG, Bateman JF, Lamandé SR

CRISPR/Cas9 gene editing of a SOX9 reporter human iPSC line to produce two TRPV4 patient heterozygous missense mutant iPSC lines, MCRIi001-A-3 (TRPV4 p.F273L) and MCRIi001-A-4 (TRPV4 p.P799L)
Nur Patria Y et al. CRISPR/Cas9 gene editing of a SOX9 reporter human iPSC line to produce two TRPV4 patient heterozygous missense mutant iPSC lines, MCRIi001-A-3 (TRPV4 p.F273L) and MCRIi001-A-4 (TRPV4 p.P799L). . 2020-08-03. Pubmed ID: 32771907; DOI: 10.1016/j.scr.2020.101942 MCRIi001-AMCRIi001-A-2MCRIi001-A-3MCRIi001-A-4 2020-08-03 2020-08-03
PubMed: 32771907 DOI: 10.1016/j.scr.2020.101942
Associated cell lines:
Wu F, Li X, Bai R, Li Y, Gao J, Lan F

Generation of a Junctophilin-2 homozygous knockout human embryonic stem cell line (WAe009-A-36) by an episomal vector-based CRISPR/Cas9 system
Wu F et al. Generation of a Junctophilin-2 homozygous knockout human embryonic stem cell line (WAe009-A-36) by an episomal vector-based CRISPR/Cas9 system. . 2020-08-03. Pubmed ID: 32777767; DOI: 10.1016/j.scr.2020.101930 WAe009-AWAe009-A-36 2020-08-03 2020-08-03
PubMed: 32777767 DOI: 10.1016/j.scr.2020.101930
Associated cell lines:
- WAe009-A
- WAe009-A-36
Chen M, Maimaitili M, Habekost M, Gill KP, Mermet-Joret N, Nabavi S, Febbraro F, Denham M

Rapid generation of regionally specified CNS neurons by sequential patterning and conversion of human induced pluripotent stem cells
Chen M et al. Rapid generation of regionally specified CNS neurons by sequential patterning and conversion of human induced pluripotent stem cells. . 2020-08-03. Pubmed ID: 32791483; DOI: 10.1016/j.scr.2020.101945 DANi001-CDANi002-CDANi003-HDANi004-ADANi005-ADANi006-FDANi007-ADANi008-FDANi009-CDANi010-ADANi011-A 2020-08-03 2020-08-03
PubMed: 32791483 DOI: 10.1016/j.scr.2020.101945
Associated cell lines:
- DANi001-C
- DANi002-C
- DANi003-H
- DANi004-A
- DANi005-A
- DANi006-F
- DANi007-A
- DANi008-F
- DANi009-C
- DANi010-A
- DANi011-A
Ovechkina VS, Maretina MA, Egorova AA, Baranov VS, Kiselev AV, Zakian SM, Valetdinova KR

Generation of a spinal muscular atrophy type III patient-specific induced pluripotent stem cell line ICGi003-A
Ovechkina VS et al. Generation of a spinal muscular atrophy type III patient-specific induced pluripotent stem cell line ICGi003-A. . 2020-08-03. Pubmed ID: 32795928; DOI: 10.1016/j.scr.2020.101938 ICGi003-A 2020-08-03 2020-08-03
PubMed: 32795928 DOI: 10.1016/j.scr.2020.101938
Associated cell lines:
- ICGi003-A
Dmitrieva NI, Walts AD, Nguyen DP, Grubb A, Zhang X, Wang X, Ping X, Jin H, Yu Z, Yu ZX, Yang D, Schwartzbeck R, Dalgard CL, Kozel BA, Levin MD, Knutsen RH, Liu D, Milner JD, López DB, O'Connell MP, Lee CR, Myles IA, Hsu AP, Freeman AF, Holland SM, Chen G, Boehm M

Impaired angiogenesis and extracellular matrix metabolism in autosomal-dominant hyper-IgE syndrome
Dmitrieva NI et al. Impaired angiogenesis and extracellular matrix metabolism in autosomal-dominant hyper-IgE syndrome. . 2020-08-03. Pubmed ID: 32369445; DOI: 10.1172/jci135490; PMC: PMC7410079 NIHTVBi011-ANIHTVBi012-ANIHTVBi013-A 2020-08-03 2020-08-03
PubMed: 32369445 DOI: 10.1172/jci135490
Associated cell lines:
Banal C, Quelennec E, Bertani-Torres W, Gacem N, Amiel J, Marlin S, Petit F, Pingault V, Lefort N, Bondurand N

Generation of an iPSC line (IMAGINi022-A) from a patient carrying a SOX10 missense mutation and presenting with deafness, depigmentation and progressive neurological impairment
Banal C et al. Generation of an iPSC line (IMAGINi022-A) from a patient carrying a SOX10 missense mutation and presenting with deafness, depigmentation and progressive neurological impairment. . 2020-08-02. Pubmed ID: 32795927; DOI: 10.1016/j.scr.2020.101936 IMAGINi022-A 2020-08-02 2020-08-02
PubMed: 32795927 DOI: 10.1016/j.scr.2020.101936
Associated cell lines:
- IMAGINi022-A
Kondrateva E, Adilgereeva E, Amelina E, Tabakov V, Demchenko A, Ustinov K, Yasinovsky M, Voronina E, Lavrov A, Smirnikhina S

Generation of induced pluripotent stem cell line (RCMGi001-A) from human skin fibroblasts of a cystic fibrosis patient with p.F508del mutation
Kondrateva E et al. Generation of induced pluripotent stem cell line (RCMGi001-A) from human skin fibroblasts of a cystic fibrosis patient with p.F508del mutation. . 2020-08-02. Pubmed ID: 32777768; DOI: 10.1016/j.scr.2020.101933 RCMGi001-A 2020-08-02 2020-08-02
PubMed: 32777768 DOI: 10.1016/j.scr.2020.101933
Associated cell lines:
- RCMGi001-A
Wang W, Lv YF, Zhang YJ, Dong WJ, Zhang Y

Generation of a human induced pluripotent stem cell line PUMCi001-A from a patient with Krabbe disease
Wang W et al. Generation of a human induced pluripotent stem cell line PUMCi001-A from a patient with Krabbe disease. . 2020-08-02. Pubmed ID: 32763824; DOI: 10.1016/j.scr.2020.101937 PUMCi001-A 2020-08-02 2020-08-02
PubMed: 32763824 DOI: 10.1016/j.scr.2020.101937
Associated cell lines:
- PUMCi001-A
D'Adamo MC, Liantonio A, Conte E, Pessia M, Imbrici P

Ion Channels Involvement in Neurodevelopmental Disorders
D'Adamo MC et al. Ion Channels Involvement in Neurodevelopmental Disorders. . 2020-08-01. Pubmed ID: 32473276; DOI: 10.1016/j.neuroscience.2020.05.032 HIHDNEi002-A 2020-08-01 2020-08-01
PubMed: 32473276 DOI: 10.1016/j.neuroscience.2020.05.032
Associated cell lines:
- HIHDNEi002-A
Porta F, Ponzone A, Spada M

Phenylalanine and tyrosine metabolism in DNAJC12 deficiency: A comparison between inherited hyperphenylalaninemias and healthy subjects
Porta F et al. Phenylalanine and tyrosine metabolism in DNAJC12 deficiency: A comparison between inherited hyperphenylalaninemias and healthy subjects. . 2020-08-01. Pubmed ID: 32800687; DOI: 10.1016/j.ejpn.2020.07.011 DHMCi003-ADHMCi003-B 2020-08-01 2020-08-01
PubMed: 32800687 DOI: 10.1016/j.ejpn.2020.07.011
Associated cell lines:
- DHMCi003-A
- DHMCi003-B
Samlali K, Ahmadi F, Quach ABV, Soffer G, Shih SCC

One Cell, One Drop, One Click: Hybrid Microfluidics for Mammalian Single Cell Isolation
Samlali K et al. One Cell, One Drop, One Click: Hybrid Microfluidics for Mammalian Single Cell Isolation. . 2020-08-00. Pubmed ID: 32705796; DOI: 10.1002/smll.202002400 KICRi002-AKICRi002-A-3 2020-08-00 2020-08-00
PubMed: 32705796 DOI: 10.1002/smll.202002400
Associated cell lines:
- KICRi002-A
- KICRi002-A-3
Schoger Eric, Argyriou Loukas, Cyganek Lukas, Zelarayán Laura Cecilia

Generation of homozygous CRISPRa human induced pluripotent stem cell (hiPSC) lines for sustained endogenous gene activation
Schoger Eric et al. Generation of homozygous CRISPRa human induced pluripotent stem cell (hiPSC) lines for sustained endogenous gene activation. . 2020-08-00. DOI: 10.1016/j.scr.2020.101944 RUCDRi002-A-5 2020-08-00 2020-08-00
DOI: 10.1016/j.scr.2020.101944
Associated cell lines:
- RUCDRi002-A-5
Ababneh NA, Al-Kurdi B, Ali D, Barham R, Sharar N, Mrahleh MM, Salah B, Awidi A

Generation of a human induced pluripotent stem cell (iPSC) line (JUCTCi011-A) from skin fibroblasts of a healthy Jordanian male subject
Ababneh NA et al. Generation of a human induced pluripotent stem cell (iPSC) line (JUCTCi011-A) from skin fibroblasts of a healthy Jordanian male subject. . 2020-07-31. Pubmed ID: 32771906; DOI: 10.1016/j.scr.2020.101923 JUCTCi011-A 2020-07-31 2020-07-31
PubMed: 32771906 DOI: 10.1016/j.scr.2020.101923
Associated cell lines:
- JUCTCi011-A
Gamu D, Gibson WT

Reciprocal skeletal phenotypes of PRC2-related overgrowth and Rubinstein-Taybi syndromes: potential role of H3K27 modifications
Gamu D et al. Reciprocal skeletal phenotypes of PRC2-related overgrowth and Rubinstein-Taybi syndromes: potential role of H3K27 modifications. . 2020-08-00. Pubmed ID: 32843427; DOI: 10.1101/mcs.a005058; PMC: PMC7476411 IAIi001-A 2020-08-00 2020-08-00
PubMed: 32843427 DOI: 10.1101/mcs.a005058
Associated cell lines:
- IAIi001-A
Genova E, Cavion F, Lucafò M, Pelin M, Lanzi G, Masneri S, Ferraro RM, Fazzi EM, Orcesi S, Decorti G, Tommasini A, Giliani S, Stocco G

Biomarkers and Precision Therapy for Primary Immunodeficiencies: An In Vitro Study Based on Induced Pluripotent Stem Cells From Patients
Genova E et al. Biomarkers and Precision Therapy for Primary Immunodeficiencies: An In Vitro Study Based on Induced Pluripotent Stem Cells From Patients. . 2020-08-00. Pubmed ID: 32243572; DOI: 10.1002/cpt.1837 UNIBSi008-AUNIBSi008-BUNIBSi008-C 2020-08-00 2020-08-00
PubMed: 32243572 DOI: 10.1002/cpt.1837
Associated cell lines:
Lu JZ, Zhang L, Zhu HY, Qi YY, Bai ZH, Jia WW, Liu ZM

An induced pluripotent stem cell line (EHTJUi002-A) derived from a neonate with c.678G>A mutation in the gene FZD4 causing exudative vitreoretinopathy
Lu JZ et al. An induced pluripotent stem cell line (EHTJUi002-A) derived from a neonate with c.678G>A mutation in the gene FZD4 causing exudative vitreoretinopathy. . 2020-07-30. Pubmed ID: 32889247; DOI: 10.1016/j.scr.2020.101932 EHTJUi002-A 2020-07-30 2020-07-30
PubMed: 32889247 DOI: 10.1016/j.scr.2020.101932
Associated cell lines:
- EHTJUi002-A
Gois Beghini D, Iwao Horita S, Cascabulho CM, Anastácio Alves L, Henriques-Pons A

Induced Pluripotent Stem Cells: Hope in the Treatment of Diseases, including Muscular Dystrophies
Gois Beghini D et al. Induced Pluripotent Stem Cells: Hope in the Treatment of Diseases, including Muscular Dystrophies. . 2020-07-30. Pubmed ID: 32751747; DOI: 10.3390/ijms21155467; PMC: PMC7432218 FAMRCi006-AFAMRCi006-B 2020-07-30 2020-07-30
PubMed: 32751747 DOI: 10.3390/ijms21155467
Associated cell lines:
- FAMRCi006-A
- FAMRCi006-B
Schnichels S, Paquet-Durand F, Löscher M, Tsai T, Hurst J, Joachim SC, Klettner A

Retina in a dish: Cell cultures, retinal explants and animal models for common diseases of the retina
Schnichels S et al. Retina in a dish: Cell cultures, retinal explants and animal models for common diseases of the retina. . 2020-07-25. Pubmed ID: 32721458; DOI: 10.1016/j.preteyeres.2020.100880 CABi003-A 2020-07-25 2020-07-25
PubMed: 32721458 DOI: 10.1016/j.preteyeres.2020.100880
Associated cell lines:
- CABi003-A
Malakhova AA, Grigor'eva EV, Vasilyeva OY, Zhigalina DI, Skryabin NA, Sivtcev AA, Kolesnikov NA, Bueverov AO, Lebedev IN, Bogomolov PO, Zakian SM

Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson's disease
Malakhova AA et al. Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson's disease. . 2020-07-25. Pubmed ID: 32738633; DOI: 10.1016/j.scr.2020.101922 ICGi020-AICGi020-B 2020-07-25 2020-07-25
PubMed: 32738633 DOI: 10.1016/j.scr.2020.101922
Associated cell lines:
- ICGi020-A
- ICGi020-B
Patel A, Garcia Diaz A, Moore JC, Sirabella D, Corneo B

Establishment and characterization of two iPSC lines derived from healthy controls
Patel A et al. Establishment and characterization of two iPSC lines derived from healthy controls. . 2020-07-25. Pubmed ID: 32738631; DOI: 10.1016/j.scr.2020.101926 CUIMCi001-ACUIMCi002-A 2020-07-25 2020-07-25
PubMed: 32738631 DOI: 10.1016/j.scr.2020.101926
Associated cell lines:
- CUIMCi001-A
- CUIMCi002-A
Gusev K, Khudiakov A, Zaytseva A, Perepelina K, Makeenok S, Kaznacheyeva E, Kostareva A

Impact of the DSP-H1684R Genetic Variant on Ion Channels Activity in iPSC-Derived Cardiomyocytes
Gusev K et al. Impact of the DSP-H1684R Genetic Variant on Ion Channels Activity in iPSC-Derived Cardiomyocytes. . 2020-07-25. Pubmed ID: 32706220; DOI: 10.33594/000000249 FAMRCi004-AFAMRCi004-B 2020-07-25 2020-07-25
PubMed: 32706220 DOI: 10.33594/000000249
Associated cell lines:
- FAMRCi004-A
- FAMRCi004-B
D'Anzi A, Altieri F, Perciballi E, Ferrari D, Bernardini L, Goldoni M, Mazzini L, De Marchi F, Di Pierro A, D'Alfonso S, Gelati M, Vescovi AL, Rosati J

Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene
D'Anzi A et al. Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene. . 2020-07-25. Pubmed ID: 32739880; DOI: 10.1016/j.scr.2020.101924 CSSi011-A 2020-07-25 2020-07-25
PubMed: 32739880 DOI: 10.1016/j.scr.2020.101924
Associated cell lines:
- CSSi011-A
Shahryari A, Moya N, Siehler J, Wang X, Karolina Blöchinger A, Burtscher I, Bakhti M, Mowla SJ, Lickert H

Generation of a human iPSC line harboring a biallelic large deletion at the INK4 locus (HMGUi001-A-5)
Shahryari A et al. Generation of a human iPSC line harboring a biallelic large deletion at the INK4 locus (HMGUi001-A-5). . 2020-07-25. Pubmed ID: 32739881; DOI: 10.1016/j.scr.2020.101927 HMGUi001-AHMGUi001-A-5 2020-07-25 2020-07-25
PubMed: 32739881 DOI: 10.1016/j.scr.2020.101927
Associated cell lines:
- HMGUi001-A
- HMGUi001-A-5
Ababneh NA, Al-Kurdi B, Ali D, Abuarqoub D, Barham R, Alzibdeh AM, Khanfar AN, Altantawi AM, Ryalat AT, Sharrack B, Awidi A

Generation and characterization of induced pluripotent stem cell (iPSC) line (JUCTCi002-A) from a patient with ataxia with oculomotor apraxia type 1 (AOA1) harboring a homozygous mutation in the APTX gene
Ababneh NA et al. Generation and characterization of induced pluripotent stem cell (iPSC) line (JUCTCi002-A) from a patient with ataxia with oculomotor apraxia type 1 (AOA1) harboring a homozygous mutation in the APTX gene. . 2020-07-25. Pubmed ID: 32769066; DOI: 10.1016/j.scr.2020.101925 JUCTCi002-A 2020-07-25 2020-07-25
PubMed: 32769066 DOI: 10.1016/j.scr.2020.101925
Associated cell lines:
- JUCTCi002-A
Feyen DAM, McKeithan WL, Bruyneel AAN, Spiering S, Hörmann L, Ulmer B, Zhang H, Briganti F, Schweizer M, Hegyi B, Liao Z, Pölönen RP, Ginsburg KS, Lam CK, Serrano R, Wahlquist C, Kreymerman A, Vu M, Amatya PL, Behrens CS, Ranjbarvaziri S, Maas RGC, Greenhaw M, Bernstein D, Wu JC, Bers DM, Eschenhagen T, Metallo CM, Mercola M

Metabolic Maturation Media Improve Physiological Function of Human iPSC-Derived Cardiomyocytes
Feyen DAM et al. Metabolic Maturation Media Improve Physiological Function of Human iPSC-Derived Cardiomyocytes. . 2020-07-21. Pubmed ID: 32697997; DOI: 10.1016/j.celrep.2020.107925; PMC: PMC7437654 UKEi001-AUKEi003-AUKEi003-C 2020-07-21 2020-07-21
PubMed: 32697997 DOI: 10.1016/j.celrep.2020.107925
Associated cell lines:
Filippo Buono M, von Boehmer L, Strang J, Hoerstrup SP, Emmert MY, Nugraha B

Human Cardiac Organoids for Modeling Genetic Cardiomyopathy
Filippo Buono M et al. Human Cardiac Organoids for Modeling Genetic Cardiomyopathy. . 2020-07-20. Pubmed ID: 32698471; DOI: 10.3390/cells9071733; PMC: PMC7409052 WTSIi020-AUKKi025-A 2020-07-20 2020-07-20
PubMed: 32698471 DOI: 10.3390/cells9071733
Associated cell lines:
- WTSIi020-A
- UKKi025-A
Chen D, Li Z, Liu Y, Sampaio N, Yang D, Aksentijevich I, Boehm M, Chen G

Human induced pluripotent stem cells generated from a patient with a homozygous L272P mutation in the OTULIN gene (NIHTVBi014-A)
Chen D et al. Human induced pluripotent stem cells generated from a patient with a homozygous L272P mutation in the OTULIN gene (NIHTVBi014-A). . 2020-07-20. Pubmed ID: 32721894; DOI: 10.1016/j.scr.2020.101921 NIHTVBi014-A 2020-07-20 2020-07-20
PubMed: 32721894 DOI: 10.1016/j.scr.2020.101921
Associated cell lines:
- NIHTVBi014-A
Chen X, Yang Y, Luo L, Xu L, Liu B, Jiang G, Hu X, Zeng Y, Wang Z

An iPSC line (TYWHSTi002-A) derived from a patient with Pendred syndrome caused by compound heterozygous mutations in the SLC26A4 gene
Chen X et al. An iPSC line (TYWHSTi002-A) derived from a patient with Pendred syndrome caused by compound heterozygous mutations in the SLC26A4 gene. . 2020-07-20. Pubmed ID: 32717573; DOI: 10.1016/j.scr.2020.101919 TYWHSTi002-A 2020-07-20 2020-07-20
PubMed: 32717573 DOI: 10.1016/j.scr.2020.101919
Associated cell lines:
- TYWHSTi002-A
Vaidyanath A, Khan M, Vaishnav B, Kakrani AL, Patil S, Shiras A

Development and characterization of two independent integration free iPSC clones NCCSi010-A and NCCSi010-B from a patient with alcoholic liver cirrhosis of Indian ethnicity
Vaidyanath A et al. Development and characterization of two independent integration free iPSC clones NCCSi010-A and NCCSi010-B from a patient with alcoholic liver cirrhosis of Indian ethnicity. . 2020-07-20. Pubmed ID: 32745713; DOI: 10.1016/j.scr.2020.101911 NCCSi010-ANCCSi010-B 2020-07-20 2020-07-20
PubMed: 32745713 DOI: 10.1016/j.scr.2020.101911
Associated cell lines:
- NCCSi010-A
- NCCSi010-B
Fukunaga I, Shirai K, Oe Y, Danzaki K, Ohta S, Shiga T, Chen C, Ikeda K, Akamatsu W, Kawano A, Kamiya K

Generation of two induced pluripotent stem cell lines from PBMCs of siblings carrying c.235delC mutation in the GJB2 gene associated with sensorineural hearing loss
Fukunaga I et al. Generation of two induced pluripotent stem cell lines from PBMCs of siblings carrying c.235delC mutation in the GJB2 gene associated with sensorineural hearing loss. . 2020-07-19. Pubmed ID: 32745712; DOI: 10.1016/j.scr.2020.101910 JUFMDOi005-AJUFMDOi006-A 2020-07-19 2020-07-19
PubMed: 32745712 DOI: 10.1016/j.scr.2020.101910
Associated cell lines:
- JUFMDOi005-A
- JUFMDOi006-A
Vallejo-Diez S, Martín-Fernández JM, Sánchez-Gilabert A, Fleischer A, Gayá A, Castresana M, Bachiller D

Generation of a human iPSC line (IMEDEAi008-A) derived from natural homozygous CCR5-Δ32 PBMCs enriched in the pro-erythroblast population
Vallejo-Diez S et al. Generation of a human iPSC line (IMEDEAi008-A) derived from natural homozygous CCR5-Δ32 PBMCs enriched in the pro-erythroblast population. . 2020-07-17. Pubmed ID: 32702648; DOI: 10.1016/j.scr.2020.101918 IMEDEAi006-AIMEDEAi008-A 2020-07-17 2020-07-17
PubMed: 32702648 DOI: 10.1016/j.scr.2020.101918
Associated cell lines:
- IMEDEAi006-A
- IMEDEAi008-A
Vallejo-Diez S, Fleischer A, María Martín-Fernández J, Sánchez-Gilabert A, Gómez-Martínez C, Castresana M, Bachiller D

Generation of one iPSC line (IMEDEAi007-A) by Sendai Virus transduction of PBMCs from a Psoriasis donor
Vallejo-Diez S et al. Generation of one iPSC line (IMEDEAi007-A) by Sendai Virus transduction of PBMCs from a Psoriasis donor. . 2020-07-17. Pubmed ID: 32707489; DOI: 10.1016/j.scr.2020.101917 IMEDEAi007-A 2020-07-17 2020-07-17
PubMed: 32707489 DOI: 10.1016/j.scr.2020.101917
Associated cell lines:
- IMEDEAi007-A
Xian Y, Xie Y, Song B, Ou Z, Ouyang S, Xie Y, Yang Y, Xiong Z, Li H, Sun X

The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice
Xian Y et al. The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice. . 2020-07-16. Pubmed ID: 32678022; DOI: 10.1186/s13287-020-01765-w; PMC: PMC7367314 GZHMUi001-A 2020-07-16 2020-07-16
PubMed: 32678022 DOI: 10.1186/s13287-020-01765-w
Associated cell lines:
- GZHMUi001-A
Niu S, Xiong H, Li Y, Zhang L

Generation of patient-specific induced pluripotent stem cells (ZZUSAHi001-A) derived from a familial atrial fibrillation patient carrying KCNA5 c.775G>A mutation
Niu S et al. Generation of patient-specific induced pluripotent stem cells (ZZUSAHi001-A) derived from a familial atrial fibrillation patient carrying KCNA5 c.775G>A mutation. . 2020-07-15. Pubmed ID: 32721895; DOI: 10.1016/j.scr.2020.101915 ZZUSAHi001-A 2020-07-15 2020-07-15
PubMed: 32721895 DOI: 10.1016/j.scr.2020.101915
Associated cell lines:
- ZZUSAHi001-A
Wei L, Zhang J, Chen D, Feng L, Wu C, Wang R, Li X

Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi005-A) from a Wilson's disease patient harboring a homozygous Pro992Leu mutation in ATP7B gene
Wei L et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi005-A) from a Wilson's disease patient harboring a homozygous Pro992Leu mutation in ATP7B gene. . 2020-07-15. Pubmed ID: 32745714; DOI: 10.1016/j.scr.2020.101909 ZZUNEUi005-A 2020-07-15 2020-07-15
PubMed: 32745714 DOI: 10.1016/j.scr.2020.101909
Associated cell lines:
- ZZUNEUi005-A
Naumovska E, Aalderink G, Wong Valencia C, Kosim K, Nicolas A, Brown S, Vulto P, Erdmann KS, Kurek D

Direct On-Chip Differentiation of Intestinal Tubules from Induced Pluripotent Stem Cells
Naumovska E et al. Direct On-Chip Differentiation of Intestinal Tubules from Induced Pluripotent Stem Cells. . 2020-07-14. Pubmed ID: 32674311; DOI: 10.3390/ijms21144964; PMC: PMC7404294 UOSi001-A 2020-07-14 2020-07-14
PubMed: 32674311 DOI: 10.3390/ijms21144964
Associated cell lines:
- UOSi001-A
Lee SJ, Kang KW, Kim JH, Park Y, Kim BS

Generation of an induced pluripotent stem cell line KUMCi001-A from CD34+ bone marrow cells of a patient with acute lymphoblastic leukemia using human placenta-derived cell conditioned medium
Lee SJ et al. Generation of an induced pluripotent stem cell line KUMCi001-A from CD34+ bone marrow cells of a patient with acute lymphoblastic leukemia using human placenta-derived cell conditioned medium. . 2020-07-13. Pubmed ID: 32707488; DOI: 10.1016/j.scr.2020.101913 KUMCi001-A 2020-07-13 2020-07-13
PubMed: 32707488 DOI: 10.1016/j.scr.2020.101913
Associated cell lines:
- KUMCi001-A
Yi T, Bai R, Sun H, Lan F, Zhang H, He Y

Generation of a NONO homozygous knockout human induced pluripotent stem cell line by CRISPR/Cas9 editing
Yi T et al. Generation of a NONO homozygous knockout human induced pluripotent stem cell line by CRISPR/Cas9 editing. . 2020-07-08. Pubmed ID: 32717574; DOI: 10.1016/j.scr.2020.101893 CMUi002-ACMUi002-A-1 2020-07-08 2020-07-08
PubMed: 32717574 DOI: 10.1016/j.scr.2020.101893
Associated cell lines:
- CMUi002-A
- CMUi002-A-1
Gutbier S, Wanke F, Dahm N, Rümmelin A, Zimmermann S, Christensen K, Köchl F, Rautanen A, Hatje K, Geering B, Zhang JD, Britschgi M, Cowley SA, Patsch C

Large-Scale Production of Human iPSC-Derived Macrophages for Drug Screening
Gutbier S et al. Large-Scale Production of Human iPSC-Derived Macrophages for Drug Screening. . 2020-07-07. Pubmed ID: 32645954; DOI: 10.3390/ijms21134808; PMC: PMC7370446 STBCi024-BSTBCi026-B 2020-07-07 2020-07-07
PubMed: 32645954 DOI: 10.3390/ijms21134808
Associated cell lines:
- STBCi024-B
- STBCi026-B
Iismaa SE, Hesselson S, McGrath-Cadell L, Muller DW, Fatkin D, Giannoulatou E, Kovacic J, Graham RM

Spontaneous Coronary Artery Dissection and Fibromuscular Dysplasia: Vasculopathies With a Predilection for Women
Iismaa SE et al. Spontaneous Coronary Artery Dissection and Fibromuscular Dysplasia: Vasculopathies With a Predilection for Women. . 2020-07-06. Pubmed ID: 32713767; DOI: 10.1016/j.hlc.2020.05.110 VCCRIi001-A 2020-07-06 2020-07-06
PubMed: 32713767 DOI: 10.1016/j.hlc.2020.05.110
Associated cell lines:
- VCCRIi001-A
Zheng Z, Lu W, Pei Z, Chen J, Yang T, Luo F

Generation of an induced pluripotent stem cell line (CHFUi001-A) from an osteogenesis imperfecta patient with COL1A2 mutation
Zheng Z et al. Generation of an induced pluripotent stem cell line (CHFUi001-A) from an osteogenesis imperfecta patient with COL1A2 mutation. . 2020-07-05. Pubmed ID: 32659730; DOI: 10.1016/j.scr.2020.101907 FDCHi004-A 2020-07-05 2020-07-05
PubMed: 32659730 DOI: 10.1016/j.scr.2020.101907
Associated cell lines:
- FDCHi004-A
Nengqing L, Dian L, Yingjun X, Yi C, Lina H, Diyu C, Yinghong Y, Bing S, Xiaofang S

Generation of induced pluripotent stem cell GZHMCi001-A and GZHMCi001-B derived from peripheral blood mononuclear cells of epileptic patients with KCNC1 mutation
Nengqing L et al. Generation of induced pluripotent stem cell GZHMCi001-A and GZHMCi001-B derived from peripheral blood mononuclear cells of epileptic patients with KCNC1 mutation. . 2020-07-05. Pubmed ID: 32712483; DOI: 10.1016/j.scr.2020.101897 GZHMCi001-AGZHMCi001-B 2020-07-05 2020-07-05
PubMed: 32712483 DOI: 10.1016/j.scr.2020.101897
Associated cell lines:
- GZHMCi001-A
- GZHMCi001-B
Yan Y, Wu S, Jiang L, Yang B, Chen X, Liu Y, Yu B, Fu J, Yu J, Ning H, Chu M, Yang J

Generation of a human iPSC line CIBi007-A from a patient with young-onset Parkinson's disease carrying variants in PRKN and HTRA2
Yan Y et al. Generation of a human iPSC line CIBi007-A from a patient with young-onset Parkinson's disease carrying variants in PRKN and HTRA2. . 2020-07-03. Pubmed ID: 32688332; DOI: 10.1016/j.scr.2020.101905 CIBi007-A 2020-07-03 2020-07-03
PubMed: 32688332 DOI: 10.1016/j.scr.2020.101905
Associated cell lines:
- CIBi007-A
Ababneh NA, Al-Kurdi B, Ali D, Abuarqoub D, Barham R, Ryalat AT, Awidi A

Establishment of (JUCTCi007-A) iPSC line from a patient with congenital myasthenic syndrome (CMS) carrying a homozygous mutation p.Arg331Trp (c.991C > T) in the CHRNE gene
Ababneh NA et al. Establishment of (JUCTCi007-A) iPSC line from a patient with congenital myasthenic syndrome (CMS) carrying a homozygous mutation p.Arg331Trp (c.991C > T) in the CHRNE gene. . 2020-07-03. Pubmed ID: 32645605; DOI: 10.1016/j.scr.2020.101906 JUCTCi007-A 2020-07-03 2020-07-03
PubMed: 32645605 DOI: 10.1016/j.scr.2020.101906
Associated cell lines:
- JUCTCi007-A
Rebs S, Sedaghat-Hamedani F, Kayvanpour E, Meder B, Streckfuss-Bömeke K

Generation of pluripotent stem cell lines and CRISPR/Cas9 modified isogenic controls from a patient with dilated cardiomyopathy harboring a RBM20 p.R634W mutation
Rebs S et al. Generation of pluripotent stem cell lines and CRISPR/Cas9 modified isogenic controls from a patient with dilated cardiomyopathy harboring a RBM20 p.R634W mutation. . 2020-07-02. Pubmed ID: 32674065; DOI: 10.1016/j.scr.2020.101901 UMGi144-AUMGi144-A-1 2020-07-02 2020-07-02
PubMed: 32674065 DOI: 10.1016/j.scr.2020.101901
Associated cell lines:
- UMGi144-A
- UMGi144-A-1
Lemme M, Braren I, Prondzynski M, Aksehirlioglu B, Ulmer BM, Schulze ML, Ismaili D, Meyer C, Hansen A, Christ T, Lemoine MD, Eschenhagen T

Chronic intermittent tachypacing by an optogenetic approach induces arrhythmia vulnerability in human engineered heart tissue
Lemme M et al. Chronic intermittent tachypacing by an optogenetic approach induces arrhythmia vulnerability in human engineered heart tissue. . 2020-07-01. Pubmed ID: 31598634; DOI: 10.1093/cvr/cvz245; PMC: PMC7314638 UKEi001-A 2020-07-01 2020-07-01
PubMed: 31598634 DOI: 10.1093/cvr/cvz245
Associated cell lines:
- UKEi001-A
Yoshida S, Okura H, Suga H, Nishitomi T, Sakurai A, Arima H, Matsuyama A

Generation of three induced pluripotent stem cell (iPSC) lines from a multiple endocrine neoplasia type 1 (MEN1) patient and three iPSC lines from an unaffected relative of the patient
Yoshida S et al. Generation of three induced pluripotent stem cell (iPSC) lines from a multiple endocrine neoplasia type 1 (MEN1) patient and three iPSC lines from an unaffected relative of the patient. . 2020-07-00. Pubmed ID: 32460232; DOI: 10.1016/j.scr.2020.101846 FHUi001-AFHUi002-AFHUi001-BFHUi001-CFHUi002-BFHUi002-C 2020-07-00 2020-07-00
PubMed: 32460232 DOI: 10.1016/j.scr.2020.101846
Associated cell lines:
- FHUi001-A
- FHUi002-A
- FHUi001-B
- FHUi001-C
- FHUi002-B
- FHUi002-C
Sawada T, Benjamin KJM, Brandtjen AC, Tietze E, Allen SJ, Paquola ACM, Kleinman JE, Hyde TM, Erwin JA

Generation of four postmortem dura-derived iPS cell lines from four control individuals with genotypic and brain-region-specific transcriptomic data available through the BrainSEQ consortium
Sawada T et al. Generation of four postmortem dura-derived iPS cell lines from four control individuals with genotypic and brain-region-specific transcriptomic data available through the BrainSEQ consortium. . 2020-07-00. Pubmed ID: 32446240; DOI: 10.1016/j.scr.2020.101806 LIBDi002-ALIBDi006-ALIBDi007-ALIBDi009-A 2020-07-00 2020-07-00
PubMed: 32446240 DOI: 10.1016/j.scr.2020.101806
Associated cell lines:
Zhao H, He L, Li S, Huang H, Tang F, Han X, Lin Z, Tian C, Huang R, Zhou P, Huang J, Deng S, Li Z

Generation of corrected-hiPSC (USTCi001-A-1) from epilepsy patient iPSCs using TALEN-mediated editing of the SCN1A gene
Zhao H et al. Generation of corrected-hiPSC (USTCi001-A-1) from epilepsy patient iPSCs using TALEN-mediated editing of the SCN1A gene. . 2020-07-00. Pubmed ID: 32544858; DOI: 10.1016/j.scr.2020.101864 USTCi001-AUSTCi001-A-1 2020-07-00 2020-07-00
PubMed: 32544858 DOI: 10.1016/j.scr.2020.101864
Associated cell lines:
- USTCi001-A
- USTCi001-A-1
Chen J, Yang X, Fu B, Zhu P, Zhu Y, Guo X, Sha J, Yuan Y

Generation of human induced pluripotent stem cell (SKLRMi001-A) from a patient with partial androgen insensitivity syndrome (PAIS)
Chen J et al. Generation of human induced pluripotent stem cell (SKLRMi001-A) from a patient with partial androgen insensitivity syndrome (PAIS). . 2020-07-00. Pubmed ID: 32505105; DOI: 10.1016/j.scr.2020.101863 SKLRMi001-A 2020-07-00 2020-07-00
PubMed: 32505105 DOI: 10.1016/j.scr.2020.101863
Associated cell lines:
- SKLRMi001-A
Mui BWH, Arora D, Mallon BS, Martinez AF, Lee JS, Muenke M, Kruszka P, Kidwai FK, Robey PG

Generation of human induced pluripotent stem cell line (NIDCRi001-A) from a Muenke syndrome patient with an FGFR3 p.Pro250Arg mutation
Mui BWH et al. Generation of human induced pluripotent stem cell line (NIDCRi001-A) from a Muenke syndrome patient with an FGFR3 p.Pro250Arg mutation. . 2020-07-00. Pubmed ID: 32505898; DOI: 10.1016/j.scr.2020.101823 NIDCRi001-A 2020-07-00 2020-07-00
PubMed: 32505898 DOI: 10.1016/j.scr.2020.101823
Associated cell lines:
- NIDCRi001-A
Buers I, Schöning L, Tomas Loges N, Nitschke Y, Höben IM, Röpke A, Crisponi L, Omran H, Rutsch F

Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line
Buers I et al. Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line. . 2020-07-00. Pubmed ID: 32512309; DOI: 10.1016/j.scr.2020.101855 UKMi002-A 2020-07-00 2020-07-00
PubMed: 32512309 DOI: 10.1016/j.scr.2020.101855
Associated cell lines:
- UKMi002-A
Meraviglia V, Arendzen CH, Tok M, Freund C, Maione AS, Sommariva E, Bellin M

Generation of human induced pluripotent stem cell line LUMCi027-A and its isogenic gene-corrected line from a patient affected by arrhythmogenic cardiomyopathy and carrying the c.2013delC PKP2 mutation
Meraviglia V et al. Generation of human induced pluripotent stem cell line LUMCi027-A and its isogenic gene-corrected line from a patient affected by arrhythmogenic cardiomyopathy and carrying the c.2013delC PKP2 mutation. . 2020-07-00. Pubmed ID: 32485643; DOI: 10.1016/j.scr.2020.101835 LUMCi027-ALUMCi027-A-1 2020-07-00 2020-07-00
PubMed: 32485643 DOI: 10.1016/j.scr.2020.101835
Associated cell lines:
- LUMCi027-A
- LUMCi027-A-1
Drick N, Dahlmann J, Sahabian A, Haase A, Göhring G, Lachmann N, Ringshausen FC, Welte T, Martin U, Olmer R

Generation of two human induced pluripotent stem cell lines (MHHi017-A, MHHi017-B) from a patient with primary ciliary dyskinesia carrying a homozygous mutation (c.7915C > T [p.Arg2639*]) in the DNAH5 gene
Drick N et al. Generation of two human induced pluripotent stem cell lines (MHHi017-A, MHHi017-B) from a patient with primary ciliary dyskinesia carrying a homozygous mutation (c.7915C > T [p.Arg2639*]) in the DNAH5 gene. . 2020-07-00. Pubmed ID: 32470793; DOI: 10.1016/j.scr.2020.101848 MHHi017-AMHHi017-B 2020-07-00 2020-07-00
PubMed: 32470793 DOI: 10.1016/j.scr.2020.101848
Associated cell lines:
- MHHi017-A
- MHHi017-B
Toombs J, Panther L, Ornelas L, Liu C, Gomez E, Martín-Ibáñez R, Cox SR, Ritchie SJ, Harris SE, Taylor A, Redmond P, Russ TC, Murphy L, Cooper JD, Burr K, Selvaraj BT, Browne C, Svendsen CN, Cowley SA, Deary IJ, Chandran S, Spires-Jones TL, Sareen D

Generation of twenty four induced pluripotent stem cell lines from twenty four members of the Lothian Birth Cohort 1936
Toombs J et al. Generation of twenty four induced pluripotent stem cell lines from twenty four members of the Lothian Birth Cohort 1936. . 2020-07-00. Pubmed ID: 32450543; DOI: 10.1016/j.scr.2020.101851; PMC: PMC7347008 EDi021-AEDi022-AEDi023-AEDi024-AEDi025-AEDi026-AEDi027-AEDi028-AEDi029-AEDi030-AEDi031-AEDi032-AEDi033-AEDi034-AEDi035-AEDi036-AEDi037-AEDi038-AEDi039-AEDi040-AEDi041-AEDi042-AEDi043-AEDi044-AEDi045-A 2020-07-00 2020-07-00
PubMed: 32450543 DOI: 10.1016/j.scr.2020.101851
Associated cell lines:
- EDi021-A
- EDi022-A
- EDi023-A
- EDi024-A
- EDi025-A
- EDi026-A
- EDi027-A
- EDi028-A
- EDi029-A
- EDi030-A
- EDi031-A
- EDi032-A
- EDi033-A
- EDi034-A
- EDi035-A
- EDi036-A
- EDi037-A
- EDi038-A
- EDi039-A
- EDi040-A
- More
Hu J, Lu C, Zhu W, Jiang Q, Du W, Wu N

Establishment of an induced pluripotent stem cell line (SHFDi001-A) from a patient with ankylosing spondylitis
Hu J et al. Establishment of an induced pluripotent stem cell line (SHFDi001-A) from a patient with ankylosing spondylitis. . 2020-07-00. Pubmed ID: 32570173; DOI: 10.1016/j.scr.2020.101879 SHFDi001-A 2020-07-00 2020-07-00
PubMed: 32570173 DOI: 10.1016/j.scr.2020.101879
Associated cell lines:
- SHFDi001-A
Arbini A, Gilmore J, King MD, Gorman KM, Krawczyk J, McInerney V, O'Brien T, Shen S, Allen NM

Generation of three induced pluripotent stem cell (iPSC) lines from a patient with developmental epileptic encephalopathy due to the pathogenic KCNA2 variant c.869T>G; p.Leu290Arg (NUIGi052-A, NUIGi052-B, NUIGi052-C)
Arbini A et al. Generation of three induced pluripotent stem cell (iPSC) lines from a patient with developmental epileptic encephalopathy due to the pathogenic KCNA2 variant c.869T>G; p.Leu290Arg (NUIGi052-A, NUIGi052-B, NUIGi052-C). . 2020-07-00. Pubmed ID: 32540721; DOI: 10.1016/j.scr.2020.101853 NUIGi052-ANUIGi052-BNUIGi052-C 2020-07-00 2020-07-00
PubMed: 32540721 DOI: 10.1016/j.scr.2020.101853
Associated cell lines:
Han MJ, Annunziata I, Weesner J, Campos Y, Salie M, O'Reilly C, d'Azzo A

Generation of human induced pluripotent stem cells (hIPSCs) from sialidosis types I and II patients with pathogenic neuraminidase 1 mutations
Han MJ et al. Generation of human induced pluripotent stem cells (hIPSCs) from sialidosis types I and II patients with pathogenic neuraminidase 1 mutations. . 2020-07-00. Pubmed ID: 32485644; DOI: 10.1016/j.scr.2020.101836; PMC: PMC7446138 STJUDEi001-ASTJUDEi002-ASTJUDEi003-A 2020-07-00 2020-07-00
PubMed: 32485644 DOI: 10.1016/j.scr.2020.101836
Associated cell lines:
Kamand M, Ilieva M, Forsberg SL, Thomassen M, Fex Svenningsen Å, Holst B, Meyer M, Michel TM

Generation of human induced pluripotent stem cells (SDUKIi002-A) from a 22-year-old male diagnosed with autism spectrum disorder
Kamand M et al. Generation of human induced pluripotent stem cells (SDUKIi002-A) from a 22-year-old male diagnosed with autism spectrum disorder. . 2020-07-00. Pubmed ID: 32447258; DOI: 10.1016/j.scr.2020.101834 SDUKIi002-A 2020-07-00 2020-07-00
PubMed: 32447258 DOI: 10.1016/j.scr.2020.101834
Associated cell lines:
- SDUKIi002-A
Schöning L, Loges NT, Nitschke Y, Höben IM, Röpke A, Crisponi L, Omran H, Rutsch F, Buers I

Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual
Schöning L et al. Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual. . 2020-07-00. Pubmed ID: 32492556; DOI: 10.1016/j.scr.2020.101820 UKMi001-AUKMi001-BUKMi001-C 2020-07-00 2020-07-00
PubMed: 32492556 DOI: 10.1016/j.scr.2020.101820
Associated cell lines:
Na DH, Lim SW, Kim BM, Kim KW, Shin YJ, Chae H, Ko EJ, Yang CW, Kim M, Chung BH

Generation of a human induced pluripotent stem cell line (CMCi001-A) from a patient with karyomegalic interstitial nephritis with homozygous frameshift deletion mutation c.1985_1994del10 of the FANCD2/FANCI-Associated Nuclease 1 gene
Na DH et al. Generation of a human induced pluripotent stem cell line (CMCi001-A) from a patient with karyomegalic interstitial nephritis with homozygous frameshift deletion mutation c.1985_1994del10 of the FANCD2/FANCI-Associated Nuclease 1 gene. . 2020-07-00. Pubmed ID: 32563974; DOI: 10.1016/j.scr.2020.101876 CMCi001-A 2020-07-00 2020-07-00
PubMed: 32563974 DOI: 10.1016/j.scr.2020.101876
Associated cell lines:
- CMCi001-A
Zhang SJ, Lian TY, Zhu XJ, Lu D, Xu XQ, Jiang X, Jing ZC

Derivation of an induced pluripotent stem cell line (PUMCHi003-A) from a patient with pulmonary arterial hypertension carrying heterozygous mutation in PTGIS gene
Zhang SJ et al. Derivation of an induced pluripotent stem cell line (PUMCHi003-A) from a patient with pulmonary arterial hypertension carrying heterozygous mutation in PTGIS gene. . 2020-07-00. Pubmed ID: 32559633; DOI: 10.1016/j.scr.2020.101875 PUMCHi003-A 2020-07-00 2020-07-00
PubMed: 32559633 DOI: 10.1016/j.scr.2020.101875
Associated cell lines:
- PUMCHi003-A
Li Y, Ibañez DP, Fan W, Zhao P, Chen S, Md Abdul M, Jiang Y, Fu L, Luo Z, Liu Z, Yang Y, Guo J, Volpe G, Kanwal S, Wang D, Tang B, Li W

Generation of an induced pluripotent stem cell line (GIBHi004-A) from a Parkinson's disease patient with mutant DJ-1/PARK7 (p.L10P)
Li Y et al. Generation of an induced pluripotent stem cell line (GIBHi004-A) from a Parkinson's disease patient with mutant DJ-1/PARK7 (p.L10P). . 2020-07-00. Pubmed ID: 32534165; DOI: 10.1016/j.scr.2020.101845 GIBHi004-A 2020-07-00 2020-07-00
PubMed: 32534165 DOI: 10.1016/j.scr.2020.101845
Associated cell lines:
- GIBHi004-A
Menara G, Lefort N, Antignac C, Mollet G

Generation of an induced pluripotent stem cell (iPSC) line (IMAGINi007) from a patient with steroid-resistant nephrotic syndrome carrying the homozygous p.R138Q mutation in the podocin-encoding NPHS2 gene
Menara G et al. Generation of an induced pluripotent stem cell (iPSC) line (IMAGINi007) from a patient with steroid-resistant nephrotic syndrome carrying the homozygous p.R138Q mutation in the podocin-encoding NPHS2 gene. . 2020-07-00. Pubmed ID: 32585588; DOI: 10.1016/j.scr.2020.101878 IMAGINi007-A 2020-07-00 2020-07-00
PubMed: 32585588 DOI: 10.1016/j.scr.2020.101878
Associated cell lines:
- IMAGINi007-A
Bouma MJ, Orlova V, van den Hil FE, Mager HJ, Baas F, de Knijff P, Mummery CL, Mikkers H, Freund C

Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2
Bouma MJ et al. Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2. . 2020-07-00. Pubmed ID: 32485642; DOI: 10.1016/j.scr.2020.101786 LUMCi030-ALUMCi030-BLUMCi030-A-1LUMCi030-B-1 2020-07-00 2020-07-00
PubMed: 32485642 DOI: 10.1016/j.scr.2020.101786
Associated cell lines:
Moya N, Shahryari A, Burtscher I, Beckenbauer J, Bakhti M, Lickert H

Generation of a homozygous ARX nuclear CFP (ARX^nCFP/nCFP) reporter human iPSC line (HMGUi001-A-4)
Moya N et al. Generation of a homozygous ARX nuclear CFP (ARX^nCFP/nCFP) reporter human iPSC line (HMGUi001-A-4). . 2020-07-00. Pubmed ID: 32544857; DOI: 10.1016/j.scr.2020.101874 HMGUi001-AHMGUi001-A-4 2020-07-00 2020-07-00
PubMed: 32544857 DOI: 10.1016/j.scr.2020.101874
Associated cell lines:
- HMGUi001-A
- HMGUi001-A-4
Wang Y, Yuan F, Wang A, Wang C, Lin L, Wang S, Wang C, Luo X, Xu Q, Yin R, Cheng H, Zhang Y, Sun X, Xi J, Yan J, Zeng F, Chen Y

Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome
Wang Y et al. Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome. . 2020-07-00. Pubmed ID: 32505899; DOI: 10.1016/j.scr.2020.101838 SHCDNi002-A 2020-07-00 2020-07-00
PubMed: 32505899 DOI: 10.1016/j.scr.2020.101838
Associated cell lines:
- SHCDNi002-A
Kim BY, Lee JS, Kim YO, Koo SK, Park MH

Generation of induced pluripotent stem cells (KSCBi009-A) from a patient with Prader-Willi syndrome (PWS) featuring deletion of the paternal chromosome region 15q11.2-q13
Kim BY et al. Generation of induced pluripotent stem cells (KSCBi009-A) from a patient with Prader-Willi syndrome (PWS) featuring deletion of the paternal chromosome region 15q11.2-q13. . 2020-07-00. Pubmed ID: 32474395; DOI: 10.1016/j.scr.2020.101847 KSCBi009-A 2020-07-00 2020-07-00
PubMed: 32474395 DOI: 10.1016/j.scr.2020.101847
Associated cell lines:
- KSCBi009-A
Shi L, Cui Y, Qi Z, Zhou X, Luan J, Han J

Generation of two non-integrated induced pluripotent stem cell lines from urine-derived cells of a Chinese patient carrying NF1 gene mutation
Shi L et al. Generation of two non-integrated induced pluripotent stem cell lines from urine-derived cells of a Chinese patient carrying NF1 gene mutation. . 2020-07-00. Pubmed ID: 32554297; DOI: 10.1016/j.scr.2020.101842 SMBCi003-ASMBCi003-B 2020-07-00 2020-07-00
PubMed: 32554297 DOI: 10.1016/j.scr.2020.101842
Associated cell lines:
- SMBCi003-A
- SMBCi003-B
Janz A, Chen R, Regensburger M, Ueda Y, Rost S, Klopocki E, Günther K, Edenhofer F, Duff HJ, Ergün S, Gerull B

Generation of two patient-derived iPSC lines from siblings (LIBUCi001-A and LIBUCi002-A) and a genetically modified iPSC line (JMUi001-A-1) to mimic dilated cardiomyopathy with ataxia (DCMA) caused by a homozygous DNAJC19 mutation
Janz A et al. Generation of two patient-derived iPSC lines from siblings (LIBUCi001-A and LIBUCi002-A) and a genetically modified iPSC line (JMUi001-A-1) to mimic dilated cardiomyopathy with ataxia (DCMA) caused by a homozygous DNAJC19 mutation. . 2020-07-00. Pubmed ID: 32521499; DOI: 10.1016/j.scr.2020.101856 LIBUCi001-ALIBUCi002-AJMUi001-AJMUi001-A-1 2020-07-00 2020-07-00
PubMed: 32521499 DOI: 10.1016/j.scr.2020.101856
Associated cell lines:
Kim KP, Yoon J, Shin B, Röpke A, Han DW, Schöler HR

Generation of a human iPSC line (MPIi006-A) from a patient with Pelizaeus-Merzbacher disease
Kim KP et al. Generation of a human iPSC line (MPIi006-A) from a patient with Pelizaeus-Merzbacher disease. . 2020-07-00. Pubmed ID: 32446239; DOI: 10.1016/j.scr.2020.101839 MPIi006-A 2020-07-00 2020-07-00
PubMed: 32446239 DOI: 10.1016/j.scr.2020.101839
Associated cell lines:
- MPIi006-A
Dementyeva EV, Kovalenko VR, Zhiven MK, Ustyantseva EI, Kretov EI, Vyatkin YV, Zakian SM

Generation of two clonal iPSC lines, ICGi019-A and ICGi019-B, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.M659I mutation in MYH7
Dementyeva EV et al. Generation of two clonal iPSC lines, ICGi019-A and ICGi019-B, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.M659I mutation in MYH7. . 2020-07-00. Pubmed ID: 32422568; DOI: 10.1016/j.scr.2020.101840 ICGi019-AICGi019-B 2020-07-00 2020-07-00
PubMed: 32422568 DOI: 10.1016/j.scr.2020.101840
Associated cell lines:
- ICGi019-A
- ICGi019-B
Wang J, Su J, Gong T, Li T, Shen J, Wang H, Xie H, Zhou L, Zheng S, Liang P

Generation of ZJUi003-A, an induced pluripotent stem cell line from a Wilson's disease patient carrying a c.180_181del mutation in ATP7B gene
Wang J et al. Generation of ZJUi003-A, an induced pluripotent stem cell line from a Wilson's disease patient carrying a c.180_181del mutation in ATP7B gene. . 2020-07-00. Pubmed ID: 32534167; DOI: 10.1016/j.scr.2020.101873 ZJUi003-A 2020-07-00 2020-07-00
PubMed: 32534167 DOI: 10.1016/j.scr.2020.101873
Associated cell lines:
- ZJUi003-A
Wang A, Xi J, Yuan F, Wang Y, Wang S, Wang C, Wang C, Lin L, Luo X, Xu Q, Yin R, Cheng H, Zhang Y, Sun X, Yang J, Yan J, Zeng F, Chen Y

Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan-Herndon-Dudley syndrome
Wang A et al. Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan-Herndon-Dudley syndrome. . 2020-07-00. Pubmed ID: 32603881; DOI: 10.1016/j.scr.2020.101872 SHCDNi003-A 2020-07-00 2020-07-00
PubMed: 32603881 DOI: 10.1016/j.scr.2020.101872
Associated cell lines:
- SHCDNi003-A
Dahlmann J, Sahabian A, Drick N, Haase A, Göhring G, Lachmann N, Ringshausen FC, Welte T, Martin U, Olmer R

Generation of two hiPSC lines (MHHi016-A, MHHi016-B) from a primary ciliary dyskinesia patient carrying a homozygous 5 bp duplication (c.248_252dup (p.Gly85Cysfs*11)) in exon 1 of the CCNO gene
Dahlmann J et al. Generation of two hiPSC lines (MHHi016-A, MHHi016-B) from a primary ciliary dyskinesia patient carrying a homozygous 5 bp duplication (c.248_252dup (p.Gly85Cysfs*11)) in exon 1 of the CCNO gene. . 2020-07-00. Pubmed ID: 32464346; DOI: 10.1016/j.scr.2020.101850 MHHi016-AMHHi016-B 2020-07-00 2020-07-00
PubMed: 32464346 DOI: 10.1016/j.scr.2020.101850
Associated cell lines:
- MHHi016-A
- MHHi016-B
Hepburn AC, Curry EL, Moad M, Steele RE, Franco OE, Wilson L, Singh P, Buskin A, Crawford SE, Gaughan L, Mills IG, Hayward SW, Robson CN, Heer R

Propagation of human prostate tissue from induced pluripotent stem cells
Hepburn AC et al. Propagation of human prostate tissue from induced pluripotent stem cells. . 2020-07-00. Pubmed ID: 32170918; DOI: 10.1002/sctm.19-0286; PMC: PMC7308643 IBPi002-A 2020-07-00 2020-07-00
PubMed: 32170918 DOI: 10.1002/sctm.19-0286
Associated cell lines:
- IBPi002-A
Fan C, Shah Z, Ullah H, Philonenko ES, Zhang B, Tan Y, Wang C, Zhang J, Samokhvalov IM

TALEN-mediated biallelic inactivation of MYB in human embryonic stem cell lines WAe001-A-45 and WAe001-A-46
Fan C et al. TALEN-mediated biallelic inactivation of MYB in human embryonic stem cell lines WAe001-A-45 and WAe001-A-46. . 2020-07-00. Pubmed ID: 32526676; DOI: 10.1016/j.scr.2020.101854 WAe001-AWAe001-A-45WAe001-A-46 2020-07-00 2020-07-00
PubMed: 32526676 DOI: 10.1016/j.scr.2020.101854
Associated cell lines:
Zulueta A, Mingione A, Signorelli P, Caretti A, Ghidoni R, Trinchera M

Simple and Complex Sugars in Parkinson's Disease: a Bittersweet Taste
Zulueta A et al. Simple and Complex Sugars in Parkinson's Disease: a Bittersweet Taste. . 2020-07-00. Pubmed ID: 32430844; DOI: 10.1007/s12035-020-01931-4 ICCSICi005-A 2020-07-00 2020-07-00
PubMed: 32430844 DOI: 10.1007/s12035-020-01931-4
Associated cell lines:
- ICCSICi005-A
Lacassie Y, Johnson B, Lay-Son G, Quintana R, King A, Cortes F, Alvarez C, Gomez R, Vargas A, Chalew S, King A, Guardia S, Sorensen RU, Aradhya S

Severe SOPH syndrome due to a novel NBAS mutation in a 27-year-old woman-Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades
Lacassie Y et al. Severe SOPH syndrome due to a novel NBAS mutation in a 27-year-old woman-Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades. . 2020-07-00. Pubmed ID: 32297715; DOI: 10.1002/ajmg.a.61597 DHMCi004-A 2020-07-00 2020-07-00
PubMed: 32297715 DOI: 10.1002/ajmg.a.61597
Associated cell lines:
- DHMCi004-A
Grzela DP, Marciniak B, Pulaski L

Characterization of an induced pluripotent stem cell line (IMBPASi001-A) derived from fibroblasts of a patient affected by Wolfram Syndrome
Grzela DP et al. Characterization of an induced pluripotent stem cell line (IMBPASi001-A) derived from fibroblasts of a patient affected by Wolfram Syndrome. . 2020-07-00. Pubmed ID: 32521500; DOI: 10.1016/j.scr.2020.101858 IMBPASi001-A 2020-07-00 2020-07-00
PubMed: 32521500 DOI: 10.1016/j.scr.2020.101858
Associated cell lines:
- IMBPASi001-A
Deng X, Iwagawa T, Fukushima M, Watanabe S

Characterization of human-induced pluripotent stem cells carrying homozygous RB1 gene deletion
Deng X et al. Characterization of human-induced pluripotent stem cells carrying homozygous RB1 gene deletion. . 2020-07-00. Pubmed ID: 32277725; DOI: 10.1111/gtc.12771 VRFi001-A 2020-07-00 2020-07-00
PubMed: 32277725 DOI: 10.1111/gtc.12771
Associated cell lines:
- VRFi001-A
Collado MS, Armstrong AJ, Olson M, Hoang SA, Day N, Summar M, Chapman KA, Reardon J, Figler RA, Wamhoff BR

Biochemical and anaplerotic applications of in vitro models of propionic acidemia and methylmalonic acidemia using patient-derived primary hepatocytes
Collado MS et al. Biochemical and anaplerotic applications of in vitro models of propionic acidemia and methylmalonic acidemia using patient-derived primary hepatocytes. . 2020-07-00. Pubmed ID: 32451238; DOI: 10.1016/j.ymgme.2020.05.003; PMC: PMC7337260 UAMi004-A 2020-07-00 2020-07-00
PubMed: 32451238 DOI: 10.1016/j.ymgme.2020.05.003
Associated cell lines:
- UAMi004-A
Gauthier-Fisher A, Kauffman A, Librach CL

Potential use of stem cells for fertility preservation
Gauthier-Fisher A et al. Potential use of stem cells for fertility preservation. . 2020-07-00. Pubmed ID: 31560823; DOI: 10.1111/andr.12713 MUSIi006-A 2020-07-00 2020-07-00
PubMed: 31560823 DOI: 10.1111/andr.12713
Associated cell lines:
- MUSIi006-A
Wei L, Zhang J, Chen D, Feng L, Wu C, Wang R, Li X

Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi002-A) from a patient with spinocerebellar ataxia type 3
Wei L et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi002-A) from a patient with spinocerebellar ataxia type 3. . 2020-06-29. Pubmed ID: 32650241; DOI: 10.1016/j.scr.2020.101898 ZZUNEUi002-A 2020-06-29 2020-06-29
PubMed: 32650241 DOI: 10.1016/j.scr.2020.101898
Associated cell lines:
- ZZUNEUi002-A
Perepelina K, Kostina A, Klauzen P, Khudiakov A, Rabino M, Crasto S, Zlotina A, Fomicheva Y, Sergushichev A, Oganesian M, Dmitriev A, Kostareva A, Di Pasquale E, Malashicheva A

Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln
Perepelina K et al. Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln. . 2020-06-29. Pubmed ID: 32659731; DOI: 10.1016/j.scr.2020.101895 FAMRCi007-AFAMRCi007-B 2020-06-29 2020-06-29
PubMed: 32659731 DOI: 10.1016/j.scr.2020.101895
Associated cell lines:
- FAMRCi007-A
- FAMRCi007-B
Boerstler T, Wend H, Krumbiegel M, Kavyanifar A, Reis A, Lie DC, Winner B, Turan S

CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome
Boerstler T et al. CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome. . 2020-06-29. Pubmed ID: 32682288; DOI: 10.1016/j.scr.2020.101889 HVRDe006-A-1HVRDe006-A-4HVRDe006-A-6UKERe006-BUKERe006-CUKERe006-D 2020-06-29 2020-06-29
PubMed: 32682288 DOI: 10.1016/j.scr.2020.101889
Associated cell lines:
Leventoux N, Morimoto S, Hara K, Nakamura S, Ozawa F, Mitsuzawa S, Akiyama T, Nishiyama A, Suzuki N, Warita H, Aoki M, Okano H

Generation of an ALS human iPSC line KEIOi001-A from peripheral blood of a Charcot disease-affected patient carrying TARDBP p.N345K heterozygous SNP mutation
Leventoux N et al. Generation of an ALS human iPSC line KEIOi001-A from peripheral blood of a Charcot disease-affected patient carrying TARDBP p.N345K heterozygous SNP mutation. . 2020-06-28. Pubmed ID: 32659732; DOI: 10.1016/j.scr.2020.101896 KEIOi001-A 2020-06-28 2020-06-28
PubMed: 32659732 DOI: 10.1016/j.scr.2020.101896
Associated cell lines:
- KEIOi001-A
De Masi C, Spitalieri P, Murdocca M, Novelli G, Sangiuolo F

Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery
De Masi C et al. Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery. . 2020-06-26. Pubmed ID: 32591003; DOI: 10.1186/s40246-020-00276-2; PMC: PMC7318728 IRFMNi003-AIRFMNi003-A-1IRFMNi003-A-2 2020-06-26 2020-06-26
PubMed: 32591003 DOI: 10.1186/s40246-020-00276-2
Associated cell lines:
Guo X, Wang L, Chen K, Song S, Wang X, Gu X, Niu C, Chu M

Generation of urine-derived iPS cell line via a non-integrative method from a Barth syndrome patient with TAZ gene mutation
Guo X et al. Generation of urine-derived iPS cell line via a non-integrative method from a Barth syndrome patient with TAZ gene mutation. . 2020-06-24. Pubmed ID: 32619718; DOI: 10.1016/j.scr.2020.101886 WMUi002-A 2020-06-24 2020-06-24
PubMed: 32619718 DOI: 10.1016/j.scr.2020.101886
Associated cell lines:
- WMUi002-A
Ababneh NA, Al-Kurdi B, Ali D, Abuarqoub D, Barham R, Salah B, Awidi A

Establishment of a human induced pluripotent stem cell (iPSC) line (JUCTCi010-A) from a healthy Jordanian female skin dermal fibroblasts
Ababneh NA et al. Establishment of a human induced pluripotent stem cell (iPSC) line (JUCTCi010-A) from a healthy Jordanian female skin dermal fibroblasts. . 2020-06-24. Pubmed ID: 32622344; DOI: 10.1016/j.scr.2020.101891 JUCTCi010-A 2020-06-24 2020-06-24
PubMed: 32622344 DOI: 10.1016/j.scr.2020.101891
Associated cell lines:
- JUCTCi010-A
Li X, Lu Y, Wang J, Liu M, Wang M, Hu L, Du W, Wang L, Jiang Z, Gu X, Ding Z, Feng D, Li L, Dong J, Zhao X

An integration-free iPSC line ZZUNEUi008-A derived from dermal fibroblasts of a child with cardiac valvular dysplasia carrying a mutation in FLNA gene
Li X et al. An integration-free iPSC line ZZUNEUi008-A derived from dermal fibroblasts of a child with cardiac valvular dysplasia carrying a mutation in FLNA gene. . 2020-06-22. Pubmed ID: 32592953; DOI: 10.1016/j.scr.2020.101882 ZZUNEUi008-A 2020-06-22 2020-06-22
PubMed: 32592953 DOI: 10.1016/j.scr.2020.101882
Associated cell lines:
- ZZUNEUi008-A
Romano E, Trionfini P, Ciampi O, Benigni A, Tomasoni S

Generation of PKD1 mono-allelic and bi-allelic knockout iPS cell lines using CRISPR-Cas9 system
Romano E et al. Generation of PKD1 mono-allelic and bi-allelic knockout iPS cell lines using CRISPR-Cas9 system. . 2020-06-19. Pubmed ID: 32592954; DOI: 10.1016/j.scr.2020.101881 IRFMNi001-B 2020-06-19 2020-06-19
PubMed: 32592954 DOI: 10.1016/j.scr.2020.101881
Associated cell lines:
- IRFMNi001-B
Sanjurjo-Soriano C, Erkilic N, Baux D, Mamaeva D, Hamel CP, Meunier I, Roux AF, Kalatzis V

Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles
Sanjurjo-Soriano C et al. Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles. . 2020-06-12. Pubmed ID: 31909088; DOI: 10.1016/j.omtm.2019.11.016; PMC: PMC6938853 INMi001-AINMi002-A 2020-06-12 2020-06-12
PubMed: 31909088 DOI: 10.1016/j.omtm.2019.11.016
Associated cell lines:
- INMi001-A
- INMi002-A
Fleischer A, Vallejo-Díez S, Martín-Fernández JM, Sánchez-Gilabert A, Castresana M, Del Pozo A, Esquisabel A, Ávila S, Castrillo JL, Gaínza E, Pedraz JL, Viñas M, Bachiller D

iPSC-Derived Intestinal Organoids from Cystic Fibrosis Patients Acquire CFTR Activity upon TALEN-Mediated Repair of the p.F508del Mutation
Fleischer A et al. iPSC-Derived Intestinal Organoids from Cystic Fibrosis Patients Acquire CFTR Activity upon TALEN-Mediated Repair of the p.F508del Mutation. . 2020-06-12. Pubmed ID: 32373648; DOI: 10.1016/j.omtm.2020.04.005; PMC: PMC7195499 IMEDEAi001-F 2020-06-12 2020-06-12
PubMed: 32373648 DOI: 10.1016/j.omtm.2020.04.005
Associated cell lines:
- IMEDEAi001-F
Cai Y, Lin J, Ma K, He M, Li B

Generation of a human induced pluripotent stem cell line (SHUPLi001-A) from PBMCs of a healthy male donor
Cai Y et al. Generation of a human induced pluripotent stem cell line (SHUPLi001-A) from PBMCs of a healthy male donor. . 2020-06-10. Pubmed ID: 32592952; DOI: 10.1016/j.scr.2020.101871 SHUPLi001-A 2020-06-10 2020-06-10
PubMed: 32592952 DOI: 10.1016/j.scr.2020.101871
Associated cell lines:
- SHUPLi001-A
Grubman A, Vandekolk TH, Schröder J, Sun G, Hatwell-Humble J, Chan J, Oksanen M, Lehtonen S, Hunt C, Koistinaho JE, Nilsson SK, Haynes JM, Pouton CW, Polo JM

A CX3CR1 Reporter hESC Line Facilitates Integrative Analysis of In-Vitro-Derived Microglia and Improved Microglia Identity upon Neuron-Glia Co-culture
Grubman A et al. A CX3CR1 Reporter hESC Line Facilitates Integrative Analysis of In-Vitro-Derived Microglia and Improved Microglia Identity upon Neuron-Glia Co-culture. . 2020-06-09. Pubmed ID: 32442534; DOI: 10.1016/j.stemcr.2020.04.007; PMC: PMC7355140 WAe009-AWAe009-A-24 2020-06-09 2020-06-09
PubMed: 32442534 DOI: 10.1016/j.stemcr.2020.04.007
Associated cell lines:
- WAe009-A
- WAe009-A-24
Grigor'eva EV, Malankhanova TB, Surumbayeva A, Pavlova SV, Minina JM, Kizilova EA, Suldina LA, Morozova KN, Kiseleva E, Sorokoumov ED, Lebedev IN, Zakian SM, Malakhova AA

Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells
Grigor'eva EV et al. Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells. . 2020-06-09. Pubmed ID: 32519278; DOI: 10.1007/s10616-020-00406-7 ICGi007-A 2020-06-09 2020-06-09
PubMed: 32519278 DOI: 10.1007/s10616-020-00406-7
Associated cell lines:
- ICGi007-A
Halliwell JA, Frith TJR, Laing O, Price CJ, Bower OJ, Stavish D, Gokhale PJ, Hewitt Z, El-Khamisy SF, Barbaric I, Andrews PW

Nucleosides Rescue Replication-Mediated Genome Instability of Human Pluripotent Stem Cells
Halliwell JA et al. Nucleosides Rescue Replication-Mediated Genome Instability of Human Pluripotent Stem Cells. . 2020-06-09. Pubmed ID: 32413278; DOI: 10.1016/j.stemcr.2020.04.004; PMC: PMC7355123 UOSi001-AUOSe015-ARUCDRi002-A 2020-06-09 2020-06-09
PubMed: 32413278 DOI: 10.1016/j.stemcr.2020.04.004
Associated cell lines:
Bose B

Induced Pluripotent Stem Cells (iPSCs) Derived 3D Human Lung Organoids from Different Ethnicities to Understand the SARS-CoV2 Severity/Infectivity Percentage
Bose B. Induced Pluripotent Stem Cells (iPSCs) Derived 3D Human Lung Organoids from Different Ethnicities to Understand the SARS-CoV2 Severity/Infectivity Percentage. . 2020-06-04. Pubmed ID: 32500482; DOI: 10.1007/s12015-020-09989-2; PMC: PMC7272136 CSSi001-A 2020-06-04 2020-06-04
PubMed: 32500482 DOI: 10.1007/s12015-020-09989-2
Associated cell lines:
- CSSi001-A
Giacomelli E, Meraviglia V, Campostrini G, Cochrane A, Cao X, van Helden RWJ, Krotenberg Garcia A, Mircea M, Kostidis S, Davis RP, van Meer BJ, Jost CR, Koster AJ, Mei H, Míguez DG, Mulder AA, Ledesma-Terrón M, Pompilio G, Sala L, Salvatori DCF, Slieker RC, Sommariva E, de Vries AAF, Giera M, Semrau S, Tertoolen LGJ, Orlova VV, Bellin M, Mummery CL

Human-iPSC-Derived Cardiac Stromal Cells Enhance Maturation in 3D Cardiac Microtissues and Reveal Non-cardiomyocyte Contributions to Heart Disease
Giacomelli E et al. Human-iPSC-Derived Cardiac Stromal Cells Enhance Maturation in 3D Cardiac Microtissues and Reveal Non-cardiomyocyte Contributions to Heart Disease. . 2020-06-04. Pubmed ID: 32459996; DOI: 10.1016/j.stem.2020.05.004; PMC: PMC7284308 LUMCi004-ALUMCi028-A 2020-06-04 2020-06-04
PubMed: 32459996 DOI: 10.1016/j.stem.2020.05.004
Associated cell lines:
- LUMCi004-A
- LUMCi028-A
Wang X, Wei C, Zhang Z, Liu D, Guo Y, Sun G, Wang Y, Li H, Tian Y, Kang X, Han R, Li Z

Association of growth traits with a structural variation downstream of the KCNJ11 gene: a large population-based study in chickens
Wang X et al. Association of growth traits with a structural variation downstream of the KCNJ11 gene: a large population-based study in chickens. . 2020-06-00. Pubmed ID: 32008360; DOI: 10.1080/00071668.2020.1724878 WAe001-AWAe001-A-12 2020-06-00 2020-06-00
PubMed: 32008360 DOI: 10.1080/00071668.2020.1724878
Associated cell lines:
- WAe001-A
- WAe001-A-12
Heck AM, Russo J, Wilusz J, Nishimura EO, Wilusz CJ

YTHDF2 destabilizes m⁶A-modified neural-specific RNAs to restrain differentiation in induced pluripotent stem cells
Heck AM et al. YTHDF2 destabilizes m⁶A-modified neural-specific RNAs to restrain differentiation in induced pluripotent stem cells. . 2020-06-00. Pubmed ID: 32169943; DOI: 10.1261/rna.073502.119; PMC: PMC7266156 ICGi007-A 2020-06-00 2020-06-00
PubMed: 32169943 DOI: 10.1261/rna.073502.119
Associated cell lines:
- ICGi007-A
Comella-Bolla A, Orlandi JG, Miguez A, Straccia M, García-Bravo M, Bombau G, Galofré M, Sanders P, Carrere J, Segovia JC, Blasi J, Allen ND, Alberch J, Soriano J, Canals JM

Human Pluripotent Stem Cell-Derived Neurons Are Functionally Mature In Vitro and Integrate into the Mouse Striatum Following Transplantation
Comella-Bolla A et al. Human Pluripotent Stem Cell-Derived Neurons Are Functionally Mature In Vitro and Integrate into the Mouse Striatum Following Transplantation. . 2020-06-00. Pubmed ID: 32356172; DOI: 10.1007/s12035-020-01907-4; PMC: PMC7253531 GENEAe020-A 2020-06-00 2020-06-00
PubMed: 32356172 DOI: 10.1007/s12035-020-01907-4
Associated cell lines:
- GENEAe020-A
Liu WS, Wang RR, Li WY, Rong M, Liu CL, Ma Y, Wang RL

Investigating the reason for loss-of-function of Src homology 2 domain-containing protein tyrosine phosphatase 2 (SHP2) caused by Y279C mutation through molecular dynamics simulation
Liu WS et al. Investigating the reason for loss-of-function of Src homology 2 domain-containing protein tyrosine phosphatase 2 (SHP2) caused by Y279C mutation through molecular dynamics simulation. . 2020-06-00. Pubmed ID: 31258001; DOI: 10.1080/07391102.2019.1634641 TRNDi003-A 2020-06-00 2020-06-00
PubMed: 31258001 DOI: 10.1080/07391102.2019.1634641
Associated cell lines:
- TRNDi003-A
Hassoun D., Djukanovic R., Bedel A., de Vos J.

Les révolutions technologiques : de la prédiction au ciblage thérapeutique
Hassoun D. et al. Les révolutions technologiques : de la prédiction au ciblage thérapeutique. . 2020-06-00. DOI: 10.1016/s1877-1203(20)30016-1 UHOMi001-A 2020-06-00 2020-06-00
DOI: 10.1016/s1877-1203(20)30016-1
Associated cell lines:
- UHOMi001-A
Varderidou-Minasian S, Hinz L, Hagemans D, Posthuma D, Altelaar M, Heine VM

Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors
Varderidou-Minasian S et al. Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors. . 2020-05-27. Pubmed ID: 32460858; DOI: 10.1186/s13229-020-00344-3; PMC: PMC7251722 TRNDi001-D 2020-05-27 2020-05-27
PubMed: 32460858 DOI: 10.1186/s13229-020-00344-3
Associated cell lines:
- TRNDi001-D
Yousefi N, Abdollahii S, Kouhbanani MAJ, Hassanzadeh A

Induced pluripotent stem cells (iPSCs) as game-changing tools in the treatment of neurodegenerative disease: Mirage or reality?
Yousefi N et al. Induced pluripotent stem cells (iPSCs) as game-changing tools in the treatment of neurodegenerative disease: Mirage or reality?. . 2020-05-21. Pubmed ID: 32437029; DOI: 10.1002/jcp.29800 IRMBi001-AZZUi003-AZZUi007-AZZUi010-ACSSi002-ACSSi004-AICGi007-ANUIGi043-ANUIGi043-BNUIGi043-CNUIGi044-ANUIGi044-BNUIGi044-CICGi014-A 2020-05-21 2020-05-21
PubMed: 32437029 DOI: 10.1002/jcp.29800
Associated cell lines:
- IRMBi001-A
- ZZUi003-A
- ZZUi007-A
- ZZUi010-A
- CSSi002-A
- CSSi004-A
- ICGi007-A
- NUIGi043-A
- NUIGi043-B
- NUIGi043-C
- NUIGi044-A
- NUIGi044-B
- NUIGi044-C
- ICGi014-A
Tiklová K, Nolbrant S, Fiorenzano A, Björklund ÅK, Sharma Y, Heuer A, Gillberg L, Hoban DB, Cardoso T, Adler AF, Birtele M, Lundén-Miguel H, Volakakis N, Kirkeby A, Perlmann T, Parmar M

Single cell transcriptomics identifies stem cell-derived graft composition in a model of Parkinson's disease
Tiklová K et al. Single cell transcriptomics identifies stem cell-derived graft composition in a model of Parkinson's disease. . 2020-05-15. Pubmed ID: 32415072; DOI: 10.1038/s41467-020-16225-5; PMC: PMC7229159 WAe009-ARCe021-AKIe033-A 2020-05-15 2020-05-15
PubMed: 32415072 DOI: 10.1038/s41467-020-16225-5
Associated cell lines:
Ścieżyńska A, Soszyńska M, Komorowski M, Podgórska A, Krześniak N, Nogowska A, Smolińska M, Szulborski K, Szaflik JP, Noszczyk B, Ołdak M, Malejczyk J

Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
Ścieżyńska A et al. Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles. . 2020-05-13. Pubmed ID: 32413971; DOI: 10.3390/ijms21103430; PMC: PMC7279462 FRIMOi003-AFRIMOi004-A 2020-05-13 2020-05-13
PubMed: 32413971 DOI: 10.3390/ijms21103430
Associated cell lines:
- FRIMOi003-A
- FRIMOi004-A
Martin-Fernandez M, Bravo García-Morato M, Gruber C, Murias Loza S, Malik MNH, Alsohime F, Alakeel A, Valdez R, Buta S, Buda G, Marti MA, Larralde M, Boisson B, Feito Rodriguez M, Qiu X, Chrabieh M, Al Ayed M, Al Muhsen S, Desai JV, Ferre EMN, Rosenzweig SD, Amador-Borrero B, Bravo-Gallego LY, Olmer R, Merkert S, Bret M, Sood AK, Al-Rabiaah A, Temsah MH, Halwani R, Hernandez M, Pessler F, Casanova JL, Bustamante J, Lionakis MS, Bogunovic D

Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin Lesions
Martin-Fernandez M et al. Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin Lesions. . 2020-05-12. Pubmed ID: 32402279; DOI: 10.1016/j.celrep.2020.107633; PMC: PMC7331931 MHHi001-A 2020-05-12 2020-05-12
PubMed: 32402279 DOI: 10.1016/j.celrep.2020.107633
Associated cell lines:
- MHHi001-A
Lee H, Flynn R, Sharma I, Haberman E, Carling PJ, Nicholls FJ, Stegmann M, Vowles J, Haenseler W, Wade-Martins R, James WS, Cowley SA

LRRK2 Is Recruited to Phagosomes and Co-recruits RAB8 and RAB10 in Human Pluripotent Stem Cell-Derived Macrophages
Lee H et al. LRRK2 Is Recruited to Phagosomes and Co-recruits RAB8 and RAB10 in Human Pluripotent Stem Cell-Derived Macrophages. . 2020-05-12. Pubmed ID: 32359446; DOI: 10.1016/j.stemcr.2020.04.001; PMC: PMC7221108 STBCi004-B-1STBCi026-A-1STBCi026-A-2 2020-05-12 2020-05-12
PubMed: 32359446 DOI: 10.1016/j.stemcr.2020.04.001
Associated cell lines:
McNeill RV, Ziegler GC, Radtke F, Nieberler M, Lesch KP, Kittel-Schneider S

Mental health dished up-the use of iPSC models in neuropsychiatric research
McNeill RV et al. Mental health dished up-the use of iPSC models in neuropsychiatric research. . 2020-05-07. Pubmed ID: 32377792; DOI: 10.1007/s00702-020-02197-9 TUSMi004-ATUSMi005-A 2020-05-07 2020-05-07
PubMed: 32377792 DOI: 10.1007/s00702-020-02197-9
Associated cell lines:
- TUSMi004-A
- TUSMi005-A
Sürün D, Schneider A, Mircetic J, Neumann K, Lansing F, Paszkowski-Rogacz M, Hänchen V, Lee-Kirsch MA, Buchholz F

Efficient Generation and Correction of Mutations in Human iPS Cells Utilizing mRNAs of CRISPR Base Editors and Prime Editors
Sürün D et al. Efficient Generation and Correction of Mutations in Human iPS Cells Utilizing mRNAs of CRISPR Base Editors and Prime Editors. . 2020-05-06. Pubmed ID: 32384610; DOI: 10.3390/genes11050511; PMC: PMC7288465 BIHi001-ABIHi001-A-2 2020-05-06 2020-05-06
PubMed: 32384610 DOI: 10.3390/genes11050511
Associated cell lines:
- BIHi001-A
- BIHi001-A-2
Yan Y, Qiu Y, Zhao A, Zhao J, Wang Y, Deng Y

Establishment of SIAISi002-A, an induced pluripotent stem cell (iPSC) line from 39-year old healthy female donor with a family history of Alzheimer's disease (AD) and two copies of APOE4 gene
Yan Y et al. Establishment of SIAISi002-A, an induced pluripotent stem cell (iPSC) line from 39-year old healthy female donor with a family history of Alzheimer's disease (AD) and two copies of APOE4 gene. . 2020-05-00. Pubmed ID: 32339902; DOI: 10.1016/j.scr.2020.101792 SIAISi002-A 2020-05-00 2020-05-00
PubMed: 32339902 DOI: 10.1016/j.scr.2020.101792
Associated cell lines:
- SIAISi002-A
Lilianty J, Nur Patria Y, Stanley EG, Elefanty AG, Bateman JF, Lamandé SR

Generation of a heterozygous COL2A1 (p.R989C) spondyloepiphyseal dysplasia congenita mutation iPSC line, MCRIi001-B, using CRISPR/Cas9 gene editing
Lilianty J et al. Generation of a heterozygous COL2A1 (p.R989C) spondyloepiphyseal dysplasia congenita mutation iPSC line, MCRIi001-B, using CRISPR/Cas9 gene editing. . 2020-05-00. Pubmed ID: 32446218; DOI: 10.1016/j.scr.2020.101843 MCRIi001-AMCRIi001-A-2MCRIi001-B 2020-05-00 2020-05-00
PubMed: 32446218 DOI: 10.1016/j.scr.2020.101843
Associated cell lines:
Tariq M, Liu H, Ibañez DP, Li Y, Chen S, Jiang M, Fan W, Zhao P, Luo Z, Wang D, Kanwal S

Generation of three induced pluripotent stem cell lines from a Parkinson's disease patient with mutant PARKIN (p. C253Y)
Tariq M et al. Generation of three induced pluripotent stem cell lines from a Parkinson's disease patient with mutant PARKIN (p. C253Y). . 2020-05-00. Pubmed ID: 32387897; DOI: 10.1016/j.scr.2020.101822 GIBHi006-AGIBHi006-BGIBHi006-C 2020-05-00 2020-05-00
PubMed: 32387897 DOI: 10.1016/j.scr.2020.101822
Associated cell lines:
Chen G, Li Z, Liu Y, Chen D, Beers J, Cudrici C, Ferrante EA, Schwartzbeck R, Dmitrieva N, Yang D, Zou J, Iruela-Arispe ML, Boehm M

Generation of human induced pluripotent stem cells (NIHTVBi004-A, NIHTVBi005-A, NIHTVBi006-A, NIHTVBi007-A, NIHTVBi008-A) from 5 CADASIL patients with NOTCH3 mutation
Chen G et al. Generation of human induced pluripotent stem cells (NIHTVBi004-A, NIHTVBi005-A, NIHTVBi006-A, NIHTVBi007-A, NIHTVBi008-A) from 5 CADASIL patients with NOTCH3 mutation. . 2020-05-00. Pubmed ID: 32344328; DOI: 10.1016/j.scr.2020.101821; PMC: PMC7309701 NIHTVBi004-ANIHTVBi005-ANIHTVBi006-ANIHTVBi007-ANIHTVBi008-A 2020-05-00 2020-05-00
PubMed: 32344328 DOI: 10.1016/j.scr.2020.101821
Associated cell lines:
Seo HH, Han HW, Kim JH

Generation of a TLR7 heterozygous knockout line (WAe009-A-18) from human embryonic stem cells using CRISPR/Cas9
Seo HH et al. Generation of a TLR7 heterozygous knockout line (WAe009-A-18) from human embryonic stem cells using CRISPR/Cas9. . 2020-05-00. Pubmed ID: 32268246; DOI: 10.1016/j.scr.2020.101735 WAe009-AWAe009-A-18 2020-05-00 2020-05-00
PubMed: 32268246 DOI: 10.1016/j.scr.2020.101735
Associated cell lines:
- WAe009-A
- WAe009-A-18
Gatinois V, Desprat R, Pichard L, Becker F, Goldenberg A, Balguerie X, Pellestor F, Lemaitre JM

iPSC reprogramming of fibroblasts from a patient with a Rothmund-Thomson syndrome RTS
Gatinois V et al. iPSC reprogramming of fibroblasts from a patient with a Rothmund-Thomson syndrome RTS. . 2020-05-00. Pubmed ID: 32416578; DOI: 10.1016/j.scr.2020.101807 REGUi003-AREGUi005-A 2020-05-00 2020-05-00
PubMed: 32416578 DOI: 10.1016/j.scr.2020.101807
Associated cell lines:
- REGUi003-A
- REGUi005-A
Main H, Hedenskog M, Acharya G, Hovatta O, Lanner F

Karolinska Institutet Human Embryonic Stem Cell Bank
Main H et al. Karolinska Institutet Human Embryonic Stem Cell Bank. . 2020-05-00. Pubmed ID: 32339905; DOI: 10.1016/j.scr.2020.101810 KIe001-AKIe002-AKIe003-AKIe004-AKIe005-AKIe006-AKIe007-AKIe008-AKIe009-AKIe010-AKIe011-AKIe012-AKIe013-AKIe014-AKIe015-AKIe016-AKIe017-AKIe018-AKIe019-AKIe020-AKIe021-AKIe022-AKIe023-AKIe024-AKIe025-AKIe026-AKIe027-AKIe028-AKIe029-AKIe030-AKIe031-AKIe001-A-1KIe032-AKIe033-AKIe034-AKIe035-AKIe036-AKIe037-AKIe038-AKIe039-AKIe040-AKIe041-AKIe042-AKIe043-AKIe044-AKIe045-AKIe046-AKIe047-AKIe048-AKIe049-AKIe050-AKIe051-AKIe052-AKIe053-AKIe054-AKIe055-AKIe056-AKIe057-AKIe058-AKIe059-AKIe060-AKIe061-A 2020-05-00 2020-05-00
PubMed: 32339905 DOI: 10.1016/j.scr.2020.101810
Associated cell lines:
- KIe001-A
- KIe002-A
- KIe003-A
- KIe004-A
- KIe005-A
- KIe006-A
- KIe007-A
- KIe008-A
- KIe009-A
- KIe010-A
- KIe011-A
- KIe012-A
- KIe013-A
- KIe014-A
- KIe015-A
- KIe016-A
- KIe017-A
- KIe018-A
- KIe019-A
- KIe020-A
- More
Long P, Liu Z, Wu B, Chen J, Sun C, Wang F, Huang Y, Chen H, Li Q, Ma Y

Generation of an induced pluripotent stem cell line from chorionic villi of a Patau syndrome spontaneous abortion
Long P et al. Generation of an induced pluripotent stem cell line from chorionic villi of a Patau syndrome spontaneous abortion. . 2020-05-00. Pubmed ID: 32361311; DOI: 10.1016/j.scr.2020.101789 HNMUi001-A 2020-05-00 2020-05-00
PubMed: 32361311 DOI: 10.1016/j.scr.2020.101789
Associated cell lines:
- HNMUi001-A
Kamata K, Otsuka Y, Imamura K, Oishi A, Kondo T, Suga M, Shibukawa R, Okanishi Y, Sagara Y, Tsukita K, Yasukawa T, Usui H, Muguruma K, Tsujikawa A, Inoue H

Generation of a human induced pluripotent stem cell line, BRCi004-A, derived from a patient with age-related macular degeneration
Kamata K et al. Generation of a human induced pluripotent stem cell line, BRCi004-A, derived from a patient with age-related macular degeneration. . 2020-05-00. Pubmed ID: 32416577; DOI: 10.1016/j.scr.2020.101787 BRCi004-A 2020-05-00 2020-05-00
PubMed: 32416577 DOI: 10.1016/j.scr.2020.101787
Associated cell lines:
- BRCi004-A
Huang CY, Tsai YH, Tsai YC, Lu YC, Chan YH, Hsu CJ, Chiou SH, Wu CC, Cheng YF

Establishment of an induced pluripotent stem cell (iPSC) line from a 7-year-old male patient with profound hearing loss carrying c.235delC in GJB2 gene
Huang CY et al. Establishment of an induced pluripotent stem cell (iPSC) line from a 7-year-old male patient with profound hearing loss carrying c.235delC in GJB2 gene. . 2020-05-00. Pubmed ID: 32388442; DOI: 10.1016/j.scr.2020.101795 TVGHi007-A 2020-05-00 2020-05-00
PubMed: 32388442 DOI: 10.1016/j.scr.2020.101795
Associated cell lines:
- TVGHi007-A
He S, Hu J, Zheng Z, Wang J, Chen J, Zhang C, Li L, Wang J, Chen Z, Shi H, Wang J

Establishment of an induced pluripotent stem cell line from a patient with CHARGE syndrome carrying a CHD7 (p.L1151Gfs*17) mutation
He S et al. Establishment of an induced pluripotent stem cell line from a patient with CHARGE syndrome carrying a CHD7 (p.L1151Gfs*17) mutation. . 2020-05-00. Pubmed ID: 32247258; DOI: 10.1016/j.scr.2020.101774 JTUi001-A 2020-05-00 2020-05-00
PubMed: 32247258 DOI: 10.1016/j.scr.2020.101774
Associated cell lines:
- JTUi001-A
Meraviglia V, Arendzen CH, Freund C, Atsma DE, Mummery CL, Bellin M

Generation of two human induced pluripotent stem cell lines, LUMCi020-A and LUMCi021-A, from two patients with Catecholaminergic Polymorphic Ventricular Tachycardia carrying heterozygous mutations in the RYR2 gene
Meraviglia V et al. Generation of two human induced pluripotent stem cell lines, LUMCi020-A and LUMCi021-A, from two patients with Catecholaminergic Polymorphic Ventricular Tachycardia carrying heterozygous mutations in the RYR2 gene. . 2020-05-00. Pubmed ID: 32315959; DOI: 10.1016/j.scr.2020.101764 LUMCi020-ALUMCi021-A 2020-05-00 2020-05-00
PubMed: 32315959 DOI: 10.1016/j.scr.2020.101764
Associated cell lines:
- LUMCi020-A
- LUMCi021-A
Kamata K, Otsuka Y, Imamura K, Oishi A, Kondo T, Suga M, Shibukawa R, Okanishi Y, Sagara Y, Tsukita K, Yasukawa T, Usui H, Muguruma K, Tsujikawa A, Inoue H

Generation of a human induced pluripotent stem cell line, BRCi005-A, derived from a Best disease patient with BEST1 mutations
Kamata K et al. Generation of a human induced pluripotent stem cell line, BRCi005-A, derived from a Best disease patient with BEST1 mutations. . 2020-05-00. Pubmed ID: 32416576; DOI: 10.1016/j.scr.2020.101782 BRCi005-A 2020-05-00 2020-05-00
PubMed: 32416576 DOI: 10.1016/j.scr.2020.101782
Associated cell lines:
- BRCi005-A
Döpper H, Horstmann M, Menges J, Bozet M, Kanber D, Steenpass L

Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines
Döpper H et al. Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines. . 2020-05-00. Pubmed ID: 32268247; DOI: 10.1016/j.scr.2020.101779 WAe009-A-30WAe009-A-31WAe009-A-32WAe009-A-33WAe009-A-34WAe009-A-35 2020-05-00 2020-05-00
PubMed: 32268247 DOI: 10.1016/j.scr.2020.101779
Associated cell lines:
Chen Z, Peng F, Liu J, Xie B, Xu P, Gan Z, Li M, Xu L, Zhong X

Generation of an iPSC line (SKLOi001-A) from a patient with CLCN2-related leukoencephalopathy
Chen Z et al. Generation of an iPSC line (SKLOi001-A) from a patient with CLCN2-related leukoencephalopathy. . 2020-05-00. Pubmed ID: 32278302; DOI: 10.1016/j.scr.2020.101769 SKLOi001-A 2020-05-00 2020-05-00
PubMed: 32278302 DOI: 10.1016/j.scr.2020.101769
Associated cell lines:
- SKLOi001-A
Suzuki H, Egawa N, Kondo T, Imamura K, Enami T, Tsukita K, Suga M, Shibukawa R, Okanishi Y, Uchiyama T, Inoue H, Takahashi R

Generation of a human induced pluripotent stem cell line derived from a Parkinson's disease patient carrying SNCA duplication
Suzuki H et al. Generation of a human induced pluripotent stem cell line derived from a Parkinson's disease patient carrying SNCA duplication. . 2020-05-00. Pubmed ID: 32413791; DOI: 10.1016/j.scr.2020.101828 BRCi008-A 2020-05-00 2020-05-00
PubMed: 32413791 DOI: 10.1016/j.scr.2020.101828
Associated cell lines:
- BRCi008-A
Konala VBR, Nandakumar S, Battu R, Pal R

Derivation of three induced pluripotent stem cell lines under feeder-free culture conditions from peripheral blood mononuclear cells (PBMC) of Indian patients suffering from inherited retinal diseases carrying different mutations
Konala VBR et al. Derivation of three induced pluripotent stem cell lines under feeder-free culture conditions from peripheral blood mononuclear cells (PBMC) of Indian patients suffering from inherited retinal diseases carrying different mutations. . 2020-05-00. Pubmed ID: 32278301; DOI: 10.1016/j.scr.2020.101757 ERPLi001-AERPLi002-AERPLi003-A 2020-05-00 2020-05-00
PubMed: 32278301 DOI: 10.1016/j.scr.2020.101757
Associated cell lines:
Wan R, Zhang Q, Li H, Xu X, Tang S

Generation of an iPSC line (CHWi001-A) from peripheral blood mononuclear cells in a patient with intellectual disability and haploinsufficiency of PLPPR4
Wan R et al. Generation of an iPSC line (CHWi001-A) from peripheral blood mononuclear cells in a patient with intellectual disability and haploinsufficiency of PLPPR4. . 2020-05-00. Pubmed ID: 32388443; DOI: 10.1016/j.scr.2020.101811 PUMCHi001-ACHWi001-A 2020-05-00 2020-05-00
PubMed: 32388443 DOI: 10.1016/j.scr.2020.101811
Associated cell lines:
- PUMCHi001-A
- CHWi001-A
Arai Y, Takami M, An Y, Matsuo-Takasaki M, Hemmi Y, Wakabayashi T, Inoue J, Noguchi M, Nakamura Y, Sugimoto K, Takemura T, Okita K, Osafune K, Takasato M, Hayata T, Hayashi Y

Generation of two human induced pluripotent stem cell lines derived from two juvenile nephronophthisis patients with NPHP1 deletion
Arai Y et al. Generation of two human induced pluripotent stem cell lines derived from two juvenile nephronophthisis patients with NPHP1 deletion. . 2020-05-00. Pubmed ID: 32361464; DOI: 10.1016/j.scr.2020.101815 BRCi010-ABRCi011-A 2020-05-00 2020-05-00
PubMed: 32361464 DOI: 10.1016/j.scr.2020.101815
Associated cell lines:
- BRCi010-A
- BRCi011-A
Hu J, Ren W, Qiu W, Lv J, Zhang C, Xu C, DU W, Wu M, Wang J, Quan R

Generation of induced pluripotent stem cell line (XDCMHi001-A) from an Ankylosing spondylitis patient with JAK2 mutation
Hu J et al. Generation of induced pluripotent stem cell line (XDCMHi001-A) from an Ankylosing spondylitis patient with JAK2 mutation. . 2020-05-00. Pubmed ID: 32388440; DOI: 10.1016/j.scr.2020.101788 XDCMHi001-A 2020-05-00 2020-05-00
PubMed: 32388440 DOI: 10.1016/j.scr.2020.101788
Associated cell lines:
- XDCMHi001-A
Vaidyanath A, Khan M, Shiras A

Generation of two control iPSC clones NCCSi008-A and NCCSi008-B from an individual of Indian ethnicity
Vaidyanath A et al. Generation of two control iPSC clones NCCSi008-A and NCCSi008-B from an individual of Indian ethnicity. . 2020-05-00. Pubmed ID: 32315960; DOI: 10.1016/j.scr.2020.101765 NCCSi008-ANCCSi008-B 2020-05-00 2020-05-00
PubMed: 32315960 DOI: 10.1016/j.scr.2020.101765
Associated cell lines:
- NCCSi008-A
- NCCSi008-B
Zhang Y, Li H, Wang J, Wang G, Tan X, Lei M

Generation of three iPSC lines (XACHi007-A, XACHi008-A, XACHi009-A) from a Chinese family with long QT syndrome type 5 with heterozygous c.226G>A (p.D76N) mutation in KCNE1gene
Zhang Y et al. Generation of three iPSC lines (XACHi007-A, XACHi008-A, XACHi009-A) from a Chinese family with long QT syndrome type 5 with heterozygous c.226G>A (p.D76N) mutation in KCNE1gene. . 2020-05-00. Pubmed ID: 32344329; DOI: 10.1016/j.scr.2020.101798 XACHi007-AXACHi008-AXACHi009-A 2020-05-00 2020-05-00
PubMed: 32344329 DOI: 10.1016/j.scr.2020.101798
Associated cell lines:
Duarte AJ, Ribeiro D, Santos R, Moreira L, Bragança J, Amaral O

Induced pluripotent stem cell line (INSAi002-A) from a Fabry Disease patient hemizygote for the rare p.W287X mutation
Duarte AJ et al. Induced pluripotent stem cell line (INSAi002-A) from a Fabry Disease patient hemizygote for the rare p.W287X mutation. . 2020-05-00. Pubmed ID: 32388441; DOI: 10.1016/j.scr.2020.101794 INSAi002-A 2020-05-00 2020-05-00
PubMed: 32388441 DOI: 10.1016/j.scr.2020.101794
Associated cell lines:
- INSAi002-A
Larsen SB, Hanss Z, Cruciani G, Massart F, Barbuti PA, Mellick G, Krüger R

Induced pluripotent stem cell line (LCSBi001-A) derived from a patient with Parkinson's disease carrying the p.D620N mutation in VPS35
Larsen SB et al. Induced pluripotent stem cell line (LCSBi001-A) derived from a patient with Parkinson's disease carrying the p.D620N mutation in VPS35. . 2020-05-00. Pubmed ID: 32387898; DOI: 10.1016/j.scr.2020.101776 LCSBi001-A 2020-05-00 2020-05-00
PubMed: 32387898 DOI: 10.1016/j.scr.2020.101776
Associated cell lines:
- LCSBi001-A
Feng B, Ma J, Amponsah AE, Guo R, Kong D, He J, Jiang Y, Zhang W, Zhang Z, Song Y, Shen S, O'Brien T, Cui H

Induced pluripotent stem cell line derived from a sporadic amyotrophic lateral sclerosis patient
Feng B et al. Induced pluripotent stem cell line derived from a sporadic amyotrophic lateral sclerosis patient. . 2020-05-00. Pubmed ID: 32434130; DOI: 10.1016/j.scr.2020.101841 HEBHMUi004-A 2020-05-00 2020-05-00
PubMed: 32434130 DOI: 10.1016/j.scr.2020.101841
Associated cell lines:
- HEBHMUi004-A
Zhang H, Ma Y, Lv Y, Wan Y, Zhao Q, Gai Z, Liu Y

An integration-free iPSC line SDQLCHi025-A from a girl with multiminicore disease carrying compound heterozygote mutations in RYR1 gene
Zhang H et al. An integration-free iPSC line SDQLCHi025-A from a girl with multiminicore disease carrying compound heterozygote mutations in RYR1 gene. . 2020-05-00. Pubmed ID: 32272370; DOI: 10.1016/j.scr.2020.101775 SDQLCHi025-A 2020-05-00 2020-05-00
PubMed: 32272370 DOI: 10.1016/j.scr.2020.101775
Associated cell lines:
- SDQLCHi025-A
Sun X, Zhou X, Xiao X, Chi J, Dong B, Wang Y

Generation of the induced pluripotent stem cell(iPSC) line (AHQUi001-A) from a patient with familial hypertriglyceridemia (FHTG) carrying a heterozygous p.C310R (c.928 T > C) mutation in LPL gene
Sun X et al. Generation of the induced pluripotent stem cell(iPSC) line (AHQUi001-A) from a patient with familial hypertriglyceridemia (FHTG) carrying a heterozygous p.C310R (c.928 T > C) mutation in LPL gene. . 2020-05-00. Pubmed ID: 32353702; DOI: 10.1016/j.scr.2020.101802 AHQUi001-A 2020-05-00 2020-05-00
PubMed: 32353702 DOI: 10.1016/j.scr.2020.101802
Associated cell lines:
- AHQUi001-A
Zhou Y, Jing Y, Mao S, Liu J, Cui Z, Wang Y, Chen J, Chan HF, Tang S, Chen J

Establishment of induced pluripotent stem cell line CSUASOi004-A by reprogramming peripheral blood mononuclear cells of a PRPF6-related dominant retinitis pigmentosa patient
Zhou Y et al. Establishment of induced pluripotent stem cell line CSUASOi004-A by reprogramming peripheral blood mononuclear cells of a PRPF6-related dominant retinitis pigmentosa patient. . 2020-05-00. Pubmed ID: 32335390; DOI: 10.1016/j.scr.2020.101793 CSUASOi004-A 2020-05-00 2020-05-00
PubMed: 32335390 DOI: 10.1016/j.scr.2020.101793
Associated cell lines:
- CSUASOi004-A
Liu CL, Huang CY, Chen HC, Lu HE, Hsieh PCH, Lee JJ

Generation of a gene corrected human isogenic IBMS-iPSC-014-C from polycystic-kidney-disease induced pluripotent stem cell line using CRISPR/Cas9
Liu CL et al. Generation of a gene corrected human isogenic IBMS-iPSC-014-C from polycystic-kidney-disease induced pluripotent stem cell line using CRISPR/Cas9. . 2020-05-00. Pubmed ID: 32361310; DOI: 10.1016/j.scr.2020.101784 IBMSi003-A-1 2020-05-00 2020-05-00
PubMed: 32361310 DOI: 10.1016/j.scr.2020.101784
Associated cell lines:
- IBMSi003-A-1
Raman S, Brookhouser N, Brafman DA

Using human induced pluripotent stem cells (hiPSCs) to investigate the mechanisms by which Apolipoprotein E (APOE) contributes to Alzheimer's disease (AD) risk
Raman S et al. Using human induced pluripotent stem cells (hiPSCs) to investigate the mechanisms by which Apolipoprotein E (APOE) contributes to Alzheimer's disease (AD) risk. . 2020-05-00. Pubmed ID: 32032733; DOI: 10.1016/j.nbd.2020.104788; PMC: PMC7098264 UKBi011-AASUi001-AASUi002-AASUi003-AASUi004-ATUSMi003-AASUi005-AASUi006-A 2020-05-00 2020-05-00
PubMed: 32032733 DOI: 10.1016/j.nbd.2020.104788
Associated cell lines:
- UKBi011-A
- ASUi001-A
- ASUi002-A
- ASUi003-A
- ASUi004-A
- TUSMi003-A
- ASUi005-A
- ASUi006-A
Zhao H, Li S, He L, Han X, Huang H, Tang F, Lin Z, Deng S, Tian C, Huang R, Li Z

Generation of iPSC line (USTCi001-A) from human skin fibroblasts of a patient with epilepsy
Zhao H et al. Generation of iPSC line (USTCi001-A) from human skin fibroblasts of a patient with epilepsy. . 2020-05-00. Pubmed ID: 32335389; DOI: 10.1016/j.scr.2020.101785 USTCi001-A 2020-05-00 2020-05-00
PubMed: 32335389 DOI: 10.1016/j.scr.2020.101785
Associated cell lines:
- USTCi001-A
Sun C, Zhou P, Yuan S, Guo R, Zhang Z, Xu Q, Han D, He L, Tang H, Xu K, Hu H, Li N

Generation of an induced pluripotent stem cell line SYSUi-004-A from a child of microcephaly with TYW1 mutations
Sun C et al. Generation of an induced pluripotent stem cell line SYSUi-004-A from a child of microcephaly with TYW1 mutations. . 2020-05-00. Pubmed ID: 32279010; DOI: 10.1016/j.scr.2020.101783 SYSUi004-A 2020-05-00 2020-05-00
PubMed: 32279010 DOI: 10.1016/j.scr.2020.101783
Associated cell lines:
- SYSUi004-A
Khurana P, Kolundzic N, Rogar M, Hobbs C, Wong XFCC, Common JEA, Ilic D, Liovic M

Stem Cell Research Lab Resource: Stem Cell LineInduced pluripotent stem cell (iPSC) line MLi-003A derived from an individual with the maximum number of filaggrin (FLG) tandem repeats
Khurana P et al. Stem Cell Research Lab Resource: Stem Cell LineInduced pluripotent stem cell (iPSC) line MLi-003A derived from an individual with the maximum number of filaggrin (FLG) tandem repeats. . 2020-05-00. Pubmed ID: 32361315; DOI: 10.1016/j.scr.2020.101827 MLi003-AKCLi003-A 2020-05-00 2020-05-00
PubMed: 32361315 DOI: 10.1016/j.scr.2020.101827
Associated cell lines:
- MLi003-A
- KCLi003-A
Tang X, Liu X, Chen Z, Luo L, Liu X, Deng J, Li DW, Liu Y

Using inducible lentiviral vectors to generate induced pluripotent stem cell line ZOCi001-A from peripheral blood cells of a patient with CRB1^-/- retinitis pigmentosa
Tang X et al. Using inducible lentiviral vectors to generate induced pluripotent stem cell line ZOCi001-A from peripheral blood cells of a patient with CRB1^-/- retinitis pigmentosa. . 2020-05-00. Pubmed ID: 32387899; DOI: 10.1016/j.scr.2020.101817 ZOCi001-A 2020-05-00 2020-05-00
PubMed: 32387899 DOI: 10.1016/j.scr.2020.101817
Associated cell lines:
- ZOCi001-A
Blöchinger AK, Siehler J, Wißmiller K, Shahryari A, Burtscher I, Lickert H

Generation of an INSULIN-H2B-Cherry reporter human iPSC line
Blöchinger AK et al. Generation of an INSULIN-H2B-Cherry reporter human iPSC line. . 2020-05-00. Pubmed ID: 32361463; DOI: 10.1016/j.scr.2020.101797 HMGUi001-AHMGUi001-A-1 2020-05-00 2020-05-00
PubMed: 32361463 DOI: 10.1016/j.scr.2020.101797
Associated cell lines:
- HMGUi001-A
- HMGUi001-A-1
Laidou S, Alanis-Lobato G, Pribyl J, Raskó T, Tichy B, Mikulasek K, Tsagiopoulou M, Oppelt J, Kastrinaki G, Lefaki M, Singh M, Zink A, Chondrogianni N, Psomopoulos F, Prigione A, Ivics Z, Pospisilova S, Skladal P, Izsvák Z, Andrade-Navarro MA, Petrakis S

Nuclear inclusions of pathogenic ataxin-1 induce oxidative stress and perturb the protein synthesis machinery
Laidou S et al. Nuclear inclusions of pathogenic ataxin-1 induce oxidative stress and perturb the protein synthesis machinery. . 2020-05-00. Pubmed ID: 32145456; DOI: 10.1016/j.redox.2020.101458; PMC: PMC7058924 LUMCi002-ALUMCi003-A 2020-05-00 2020-05-00
PubMed: 32145456 DOI: 10.1016/j.redox.2020.101458
Associated cell lines:
- LUMCi002-A
- LUMCi003-A
Zhang J, Wei L, Wang R, Li X, Liu Z

Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi001-A) from a healthy male individual
Zhang J et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi001-A) from a healthy male individual. . 2020-05-00. Pubmed ID: 32361313; DOI: 10.1016/j.scr.2020.101809 SYSUi001-AZZUNEUi001-AZZUNEUi003-A 2020-05-00 2020-05-00
PubMed: 32361313 DOI: 10.1016/j.scr.2020.101809
Associated cell lines:
Chen M, Maimaitili M, Buchholdt SH, Jensen UB, Febbraro F, Denham M

Generation of an induced pluripotent stem cell line (DANi-011A) from a Parkinson's disease patient with a LRRK2 p.G2019S mutation
Chen M et al. Generation of an induced pluripotent stem cell line (DANi-011A) from a Parkinson's disease patient with a LRRK2 p.G2019S mutation. . 2020-05-00. Pubmed ID: 32305865; DOI: 10.1016/j.scr.2020.101781 DANi011-A 2020-05-00 2020-05-00
PubMed: 32305865 DOI: 10.1016/j.scr.2020.101781
Associated cell lines:
- DANi011-A
He L, Zhao H, Li S, Han X, Chen Z, Wang C, Tian C, Tang F, Huang R, Lin Z, Li Z, Tang B, Jiang H

Generation of induced pluripotent stem cell line (CSUXHi002-A) from a patient with spinocerebellar ataxia type 1
He L et al. Generation of induced pluripotent stem cell line (CSUXHi002-A) from a patient with spinocerebellar ataxia type 1. . 2020-05-00. Pubmed ID: 32335388; DOI: 10.1016/j.scr.2020.101816 CSUXHi002-A 2020-05-00 2020-05-00
PubMed: 32335388 DOI: 10.1016/j.scr.2020.101816
Associated cell lines:
- CSUXHi002-A
Ciolak A, Krzyzosiak WJ, Kozlowska E, Fiszer A

Generation of human iPS cell line IBCHi002-A from spinocerebellar ataxia type 3/Machado-Joseph disease patient's fibroblasts
Ciolak A et al. Generation of human iPS cell line IBCHi002-A from spinocerebellar ataxia type 3/Machado-Joseph disease patient's fibroblasts. . 2020-05-00. Pubmed ID: 32361312; DOI: 10.1016/j.scr.2020.101796 IBCHi001-AIBCHi002-A 2020-05-00 2020-05-00
PubMed: 32361312 DOI: 10.1016/j.scr.2020.101796
Associated cell lines:
- IBCHi001-A
- IBCHi002-A
Yuan F, Wang C, Xi J, Wang S, Lin L, Wang Y, Wang A, Wang C, Luo X, Xu Q, Yin R, Cheng H, Zhang Y, Sun X, Chen Y

Generation of an induced pluripotent stem cell line SHCDNi001-A from a one-year-old Chinese girl with mitochondrial DNA depletion syndrome 13
Yuan F et al. Generation of an induced pluripotent stem cell line SHCDNi001-A from a one-year-old Chinese girl with mitochondrial DNA depletion syndrome 13. . 2020-05-00. Pubmed ID: 32416579; DOI: 10.1016/j.scr.2020.101832 SHCDNi001-A 2020-05-00 2020-05-00
PubMed: 32416579 DOI: 10.1016/j.scr.2020.101832
Associated cell lines:
- SHCDNi001-A
Ullah H, You H, Shah Z, Fan C, Zhang B, Liu H, Zhang J, Abbas N, Filonenko ES, Samokhvalov IM

Generation of RUNX1-null reporter human embryonic stem cell line GIBHe008-A
Ullah H et al. Generation of RUNX1-null reporter human embryonic stem cell line GIBHe008-A. . 2020-05-00. Pubmed ID: 32371361; DOI: 10.1016/j.scr.2020.101800 WAe001-A-44 2020-05-00 2020-05-00
PubMed: 32371361 DOI: 10.1016/j.scr.2020.101800
Associated cell lines:
- WAe001-A-44
Sun L, Zhang J, Kuang XY, Kang YL, Wu Y, Huang WY

Generation of an induced pluripotent stem cell line (SHCDNRi001-A) from a patient with X-linked Alport syndrome carrying a heterozygous p.G409S (c. 1225 G > A) mutation in the COL4A5 gene
Sun L et al. Generation of an induced pluripotent stem cell line (SHCDNRi001-A) from a patient with X-linked Alport syndrome carrying a heterozygous p.G409S (c. 1225 G > A) mutation in the COL4A5 gene. . 2020-05-00. Pubmed ID: 32416580; DOI: 10.1016/j.scr.2020.101833 SHCDNRi001-A 2020-05-00 2020-05-00
PubMed: 32416580 DOI: 10.1016/j.scr.2020.101833
Associated cell lines:
- SHCDNRi001-A
Rovina D, Castiglioni E, Niro F, Farini A, Belicchi M, Di Fede E, Gervasini C, Paganini S, Di Segni M, Torrente Y, Santoro R, Pompilio G, Gowran A

Generation of the Becker muscular dystrophy patient derived induced pluripotent stem cell line carrying the DMD splicing mutation c.1705-8 T>C
Rovina D et al. Generation of the Becker muscular dystrophy patient derived induced pluripotent stem cell line carrying the DMD splicing mutation c.1705-8 T>C. . 2020-05-00. Pubmed ID: 32348941; DOI: 10.1016/j.scr.2020.101819; PMC: PMC7264707 CCMi004-A 2020-05-00 2020-05-00
PubMed: 32348941 DOI: 10.1016/j.scr.2020.101819
Associated cell lines:
- CCMi004-A
Chen S, Luo Z, Ward C, Ibañez DP, Liu H, Zhong X, Sharma NK, Qin B, Fan W, Wang D

Generation of two LRRK2 homozygous knockout human induced pluripotent stem cell lines using CRISPR/Cas9
Chen S et al. Generation of two LRRK2 homozygous knockout human induced pluripotent stem cell lines using CRISPR/Cas9. . 2020-05-00. Pubmed ID: 32339904; DOI: 10.1016/j.scr.2020.101804 GIBHi002-AGIBHi002-A-3GIBHi002-A-4 2020-05-00 2020-05-00
PubMed: 32339904 DOI: 10.1016/j.scr.2020.101804
Associated cell lines:
Alexeeva V, Aydin IT, Schaniel C, Stranahan AW, D'Souza SL, Bieker JJ

A human H1-HBB11-GFP reporter embryonic stem cell line (WAe001-A-2) generated using TALEN-based genome editing
Alexeeva V et al. A human H1-HBB11-GFP reporter embryonic stem cell line (WAe001-A-2) generated using TALEN-based genome editing. . 2020-05-00. Pubmed ID: 32413789; DOI: 10.1016/j.scr.2020.101837; PMC: PMC7297435 WAe001-AWAe001-A-2 2020-05-00 2020-05-00
PubMed: 32413789 DOI: 10.1016/j.scr.2020.101837
Associated cell lines:
- WAe001-A
- WAe001-A-2
Liu B, Chen L, Sun J, Zhang L, Chen M, Qian Y, Wang Y, Yan K, Hou L, Huang Y, Zhang D, Xu Y, Yu J, Zhang J, Dong M

Generation of the human induced pluripotent stem cell line (ZJUi005-A) from a patient with Pelizaeus-Merzbacher disease (PMD) carrying a novel hemizygous mutation in PLP1 gene
Liu B et al. Generation of the human induced pluripotent stem cell line (ZJUi005-A) from a patient with Pelizaeus-Merzbacher disease (PMD) carrying a novel hemizygous mutation in PLP1 gene. . 2020-05-00. Pubmed ID: 32402715; DOI: 10.1016/j.scr.2020.101791 ZJUi005-A 2020-05-00 2020-05-00
PubMed: 32402715 DOI: 10.1016/j.scr.2020.101791
Associated cell lines:
- ZJUi005-A
Zhang L, Ren Q, Liu G, Wu R, Meng S, Xiahou K, Jiang N, Zhang Y, Zhou W

Establishment of two induced pluripotent stem cell line from healthy elderly (IPTi005-A and IPTi007-A)
Zhang L et al. Establishment of two induced pluripotent stem cell line from healthy elderly (IPTi005-A and IPTi007-A). . 2020-05-00. Pubmed ID: 32402716; DOI: 10.1016/j.scr.2020.101808 IPTi005-AIPTi007-A 2020-05-00 2020-05-00
PubMed: 32402716 DOI: 10.1016/j.scr.2020.101808
Associated cell lines:
- IPTi005-A
- IPTi007-A
Grosch M, Ittermann S, Rusha E, Greisle T, Ori C, Truong DJ, O'Neill AC, Pertek A, Westmeyer GG, Drukker M

Nucleus size and DNA accessibility are linked to the regulation of paraspeckle formation in cellular differentiation
Grosch M et al. Nucleus size and DNA accessibility are linked to the regulation of paraspeckle formation in cellular differentiation. . 2020-04-22. Pubmed ID: 32321486; DOI: 10.1186/s12915-020-00770-y; PMC: PMC7178590 MHHi006-AMHHi006-A-2 2020-04-22 2020-04-22
PubMed: 32321486 DOI: 10.1186/s12915-020-00770-y
Associated cell lines:
- MHHi006-A
- MHHi006-A-2
Page S, Patel R, Raut S, Al-Ahmad A

Neurological diseases at the blood-brain barrier: Stemming new scientific paradigms using patient-derived induced pluripotent cells
Page S et al. Neurological diseases at the blood-brain barrier: Stemming new scientific paradigms using patient-derived induced pluripotent cells. . 2020-04-01. Pubmed ID: 30593893; DOI: 10.1016/j.bbadis.2018.12.009 FUi002-A 2020-04-01 2020-04-01
PubMed: 30593893 DOI: 10.1016/j.bbadis.2018.12.009
Associated cell lines:
- FUi002-A
Ali G, Elsayed AK, Nandakumar M, Bashir M, Younis I, Abu Aqel Y, Memon B, Temanni R, Abubaker F, Taheri S, Abdelalim EM

Keratinocytes Derived from Patient-Specific Induced Pluripotent Stem Cells Recapitulate the Genetic Signature of Psoriasis Disease
Ali G et al. Keratinocytes Derived from Patient-Specific Induced Pluripotent Stem Cells Recapitulate the Genetic Signature of Psoriasis Disease. . 2020-04-01. Pubmed ID: 31996098; DOI: 10.1089/scd.2019.0150; PMC: PMC7153648 QBRIi001-AQBRIi002-AQBRIi001-BQBRIi001-CQBRIi002-BQBRIi002-CQBRIi005-AQBRIi005-BQBRIi005-CQBRIi006-AQBRIi006-BQBRIi006-C 2020-04-01 2020-04-01
PubMed: 31996098 DOI: 10.1089/scd.2019.0150
Associated cell lines:
- QBRIi001-A
- QBRIi002-A
- QBRIi001-B
- QBRIi001-C
- QBRIi002-B
- QBRIi002-C
- QBRIi005-A
- QBRIi005-B
- QBRIi005-C
- QBRIi006-A
- QBRIi006-B
- QBRIi006-C
Zumwalt M, Reddy AP

Stem Cells for Treatment of Musculoskeletal Conditions - Orthopaedic/Sports Medicine Applications
Zumwalt M et al. Stem Cells for Treatment of Musculoskeletal Conditions - Orthopaedic/Sports Medicine Applications. . 2020-04-01. Pubmed ID: 31794866; DOI: 10.1016/j.bbadis.2019.165624 SDQLCHi004-A 2020-04-01 2020-04-01
PubMed: 31794866 DOI: 10.1016/j.bbadis.2019.165624
Associated cell lines:
- SDQLCHi004-A
Rehakova D, Souralova T, Koutna I

Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy
Rehakova D et al. Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy. . 2020-03-31. Pubmed ID: 32244538; DOI: 10.3390/ijms21072435; PMC: PMC7177280 RCe013-ARCe015-A 2020-03-31 2020-03-31
PubMed: 32244538 DOI: 10.3390/ijms21072435
Associated cell lines:
- RCe013-A
- RCe015-A
Xiao C, Yu M, Liu J, Wu H, Deng M, Zhang Q, Xiao X

Generation of an isogenic gene-corrected iPSC line (PUMCHi001-A-1) from a familial partial lipodystrophy type 2 (FPLD2) patient with a heterozygous R349W mutation in the LMNA gene
Xiao C et al. Generation of an isogenic gene-corrected iPSC line (PUMCHi001-A-1) from a familial partial lipodystrophy type 2 (FPLD2) patient with a heterozygous R349W mutation in the LMNA gene. . 2020-04-00. Pubmed ID: 32213461; DOI: 10.1016/j.scr.2020.101753 PUMCHi001-APUMCHi001-A-1 2020-04-00 2020-04-00
PubMed: 32213461 DOI: 10.1016/j.scr.2020.101753
Associated cell lines:
- PUMCHi001-A
- PUMCHi001-A-1
Elsayed AK, Aghadi M, Al-Khawaga S, Hussain K, Abdelalim EM

Derivation of a human induced pluripotent stem cell line (QBRIi007-A) from a patient carrying a homozygous intronic mutation (c.613-7T>G) in the SLC2A2 gene
Elsayed AK et al. Derivation of a human induced pluripotent stem cell line (QBRIi007-A) from a patient carrying a homozygous intronic mutation (c.613-7T>G) in the SLC2A2 gene. . 2020-04-00. Pubmed ID: 32146263; DOI: 10.1016/j.scr.2020.101736 QBRIi007-A 2020-04-00 2020-04-00
PubMed: 32146263 DOI: 10.1016/j.scr.2020.101736
Associated cell lines:
- QBRIi007-A
Datta I, Sowmithra, Jagtap S, Potdar C, Yadav R, Pal P

Generation of induced pluripotent stem cells (NIMHi001-A) from a Parkinson's disease patient of East Indian ethnicity carrying LRRK2 I1371V variant
Datta I et al. Generation of induced pluripotent stem cells (NIMHi001-A) from a Parkinson's disease patient of East Indian ethnicity carrying LRRK2 I1371V variant. . 2020-04-00. Pubmed ID: 32244201; DOI: 10.1016/j.scr.2020.101768 NIMHi001-A 2020-04-00 2020-04-00
PubMed: 32244201 DOI: 10.1016/j.scr.2020.101768
Associated cell lines:
- NIMHi001-A
Fatima A, Schuster J, Akram T, González CM, Sobol M, Hoeber J, Dahl N

Incontinentia pigmenti: Generation of an IKBKG deficient human iPSC line (KICRi002-A-1) on a 46,XY background using CRISPR/Cas9
Fatima A et al. Incontinentia pigmenti: Generation of an IKBKG deficient human iPSC line (KICRi002-A-1) on a 46,XY background using CRISPR/Cas9. . 2020-04-00. Pubmed ID: 32126327; DOI: 10.1016/j.scr.2020.101739 KICRi002-AKICRi002-A-1 2020-04-00 2020-04-00
PubMed: 32126327 DOI: 10.1016/j.scr.2020.101739
Associated cell lines:
- KICRi002-A
- KICRi002-A-1
Lin HY, Tsai LK, Cheng YC, Lu HE, Huang CY, Hsieh PCH, Lin CH

Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-048-05) from a patient with ALS and parkinsonism having a hexanucleotide repeat expansion mutation in C9orf72 gene
Lin HY et al. Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-048-05) from a patient with ALS and parkinsonism having a hexanucleotide repeat expansion mutation in C9orf72 gene. . 2020-04-00. Pubmed ID: 32151952; DOI: 10.1016/j.scr.2020.101734 IBMSi019-A 2020-04-00 2020-04-00
PubMed: 32151952 DOI: 10.1016/j.scr.2020.101734
Associated cell lines:
- IBMSi019-A
Zhou Y, Ding C, Xia S, Jing Y, Mao S, Liu J, Chen J, Chan HF, Tang S, Chen J

Establishment of induced pluripotent stem cell line CSUASOi003- A from an autosomal recessive retinitis pigmentosa patient carrying compound heterozygous mutations in CRB1 gene
Zhou Y et al. Establishment of induced pluripotent stem cell line CSUASOi003- A from an autosomal recessive retinitis pigmentosa patient carrying compound heterozygous mutations in CRB1 gene. . 2020-04-00. Pubmed ID: 32244200; DOI: 10.1016/j.scr.2020.101742 CSUASOi003-A 2020-04-00 2020-04-00
PubMed: 32244200 DOI: 10.1016/j.scr.2020.101742
Associated cell lines:
- CSUASOi003-A
Merkert S, Schubert M, Haase A, Janssens HM, Scholte B, Lachmann N, Göhring G, Martin U

Generation of an induced pluripotent stem cell line (MHHi018-A) from a patient with Cystic Fibrosis carrying p.Asn1303Lys (N1303K) mutation
Merkert S et al. Generation of an induced pluripotent stem cell line (MHHi018-A) from a patient with Cystic Fibrosis carrying p.Asn1303Lys (N1303K) mutation. . 2020-04-00. Pubmed ID: 32220772; DOI: 10.1016/j.scr.2020.101744 MHHi018-A 2020-04-00 2020-04-00
PubMed: 32220772 DOI: 10.1016/j.scr.2020.101744
Associated cell lines:
- MHHi018-A
Shuvalova LD, Eremeev AV, Bogomazova AN, Novosadova EV, Zerkalenkova EA, Olshanskaya YV, Fedotova EY, Glagoleva ES, Illarioshkin SN, Lebedeva OS, Lagarkova MA

Generation of induced pluripotent stem cell line RCPCMi004-A derived from patient with Parkinson's disease with deletion of the exon 2 in PARK2 gene
Shuvalova LD et al. Generation of induced pluripotent stem cell line RCPCMi004-A derived from patient with Parkinson's disease with deletion of the exon 2 in PARK2 gene. . 2020-04-00. Pubmed ID: 32151951; DOI: 10.1016/j.scr.2020.101733 RCPCMi004-A 2020-04-00 2020-04-00
PubMed: 32151951 DOI: 10.1016/j.scr.2020.101733
Associated cell lines:
- RCPCMi004-A
Malakhova AA, Grigor'eva EV, Malankhanova TB, Pavlova SV, Valetdinova KR, Abramycheva NY, Vetchinova AS, Illarioshkin SN, Zakian SM

Generation of induced pluripotent stem cell line ICGi018-A from peripheral blood mononuclear cells of a patient with Huntington's disease
Malakhova AA et al. Generation of induced pluripotent stem cell line ICGi018-A from peripheral blood mononuclear cells of a patient with Huntington's disease. . 2020-04-00. Pubmed ID: 32179492; DOI: 10.1016/j.scr.2020.101743 ICGi018-A 2020-04-00 2020-04-00
PubMed: 32179492 DOI: 10.1016/j.scr.2020.101743
Associated cell lines:
- ICGi018-A
Bchetnia M, Martineau L, Racine V, Powell J, McCuaig C, Puymirat J, Laprise C

Generation of a human induced pluripotent stem cell line (UQACi001-A) from a severe epidermolysis bullosa simplex patient with the heterozygous mutation p.R125S in the KRT14 gene
Bchetnia M et al. Generation of a human induced pluripotent stem cell line (UQACi001-A) from a severe epidermolysis bullosa simplex patient with the heterozygous mutation p.R125S in the KRT14 gene. . 2020-04-00. Pubmed ID: 32179493; DOI: 10.1016/j.scr.2020.101748 UQACi001-A 2020-04-00 2020-04-00
PubMed: 32179493 DOI: 10.1016/j.scr.2020.101748
Associated cell lines:
- UQACi001-A
Zhang B, Wang Y, Peng J, Hao Y, Guan Y

Generation of a human induced pluripotent stem cell line from an epilepsy patient carrying mutations in the PIK3R2 gene
Zhang B et al. Generation of a human induced pluripotent stem cell line from an epilepsy patient carrying mutations in the PIK3R2 gene. . 2020-04-00. Pubmed ID: 32155459; DOI: 10.1016/j.scr.2020.101711 SJTUi001-A 2020-04-00 2020-04-00
PubMed: 32155459 DOI: 10.1016/j.scr.2020.101711
Associated cell lines:
- SJTUi001-A
de la Cruz BM, Ding Y, McInerney V, Krawczyk J, Lu Y, Yang G, Qian X, Li W, Howard L, Allen NM, O'Brien T, Gallagher L, Shen S

Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A)
de la Cruz BM et al. Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A). . 2020-04-00. Pubmed ID: 32097875; DOI: 10.1016/j.scr.2020.101722 NUIGi033-ANUIGi034-A 2020-04-00 2020-04-00
PubMed: 32097875 DOI: 10.1016/j.scr.2020.101722
Associated cell lines:
- NUIGi033-A
- NUIGi034-A
Slot E, de Klein A, Rottier RJ

Generation of three iPSC lines from two patients with heterozygous FOXF1 mutations associated to Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins
Slot E et al. Generation of three iPSC lines from two patients with heterozygous FOXF1 mutations associated to Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins. . 2020-04-00. Pubmed ID: 32169823; DOI: 10.1016/j.scr.2020.101745 EMCi127-AEMCi127-BEMCi128-A 2020-04-00 2020-04-00
PubMed: 32169823 DOI: 10.1016/j.scr.2020.101745
Associated cell lines:
Hübscher D, Rebs S, Maurer W, Ghadri JR, Dressel R, Templin C, Streckfuss-Bömeke K

Generation of iPSC-lines from two independent Takotsubo syndrome patients with recurrent Takotsubo events
Hübscher D et al. Generation of iPSC-lines from two independent Takotsubo syndrome patients with recurrent Takotsubo events. . 2020-04-00. Pubmed ID: 32302918; DOI: 10.1016/j.scr.2020.101746 UMGi145-AUMGi146-A 2020-04-00 2020-04-00
PubMed: 32302918 DOI: 10.1016/j.scr.2020.101746
Associated cell lines:
- UMGi145-A
- UMGi146-A
Fatima A, Schuster J, Akram T, Sobol M, Hoeber J, Dahl N

Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9
Fatima A et al. Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9. . 2020-04-00. Pubmed ID: 32203915; DOI: 10.1016/j.scr.2020.101758 KICRi002-AKICRi002-A-3 2020-04-00 2020-04-00
PubMed: 32203915 DOI: 10.1016/j.scr.2020.101758
Associated cell lines:
- KICRi002-A
- KICRi002-A-3
Yang T, Qin J, Zhang Q, Sun H, Wang Z, Yang J, Liu H, Zhang C, Zhang S, Zhang J, Wang Y, Xu Y

Generation of induced pluripotent stem cell line (ZZUi0018-A ) from a patient with spinocerebellar ataxia type 6
Yang T et al. Generation of induced pluripotent stem cell line (ZZUi0018-A ) from a patient with spinocerebellar ataxia type 6. . 2020-04-00. Pubmed ID: 32229428; DOI: 10.1016/j.scr.2020.101777 ZZUi018-A 2020-04-00 2020-04-00
PubMed: 32229428 DOI: 10.1016/j.scr.2020.101777
Associated cell lines:
- ZZUi018-A
Yang M, Liu M, Ding Y, Vajda A, Ma J, Cui H, O'Brien T, Henshall D, Hardiman O, Shen S

Generation of twelve induced pluripotent stem cell lines from two healthy controls and two patients with sporadic amyotrophic lateral sclerosis
Yang M et al. Generation of twelve induced pluripotent stem cell lines from two healthy controls and two patients with sporadic amyotrophic lateral sclerosis. . 2020-04-00. Pubmed ID: 32208303; DOI: 10.1016/j.scr.2020.101752 NUIGi048-ANUIGi048-BNUIGi048-CNUIGi049-ANUIGi049-BNUIGi049-CNUIGi050-ANUIGi050-BNUIGi050-CNUIGi051-ANUIGi051-BNUIGi051-C 2020-04-00 2020-04-00
PubMed: 32208303 DOI: 10.1016/j.scr.2020.101752
Associated cell lines:
- NUIGi048-A
- NUIGi048-B
- NUIGi048-C
- NUIGi049-A
- NUIGi049-B
- NUIGi049-C
- NUIGi050-A
- NUIGi050-B
- NUIGi050-C
- NUIGi051-A
- NUIGi051-B
- NUIGi051-C
Zhou W, Ma D, Tan EK

Mitochondrial CHCHD2 and CHCHD10: Roles in Neurological Diseases and Therapeutic Implications
Zhou W et al. Mitochondrial CHCHD2 and CHCHD10: Roles in Neurological Diseases and Therapeutic Implications. . 2020-04-00. Pubmed ID: 31526091; DOI: 10.1177/1073858419871214 ZZUi007-A 2020-04-00 2020-04-00
PubMed: 31526091 DOI: 10.1177/1073858419871214
Associated cell lines:
- ZZUi007-A
Li R, Pradhan M, Xu M, Roeder A, Beers J, Zou J, Liu C, Porter FD, Zheng W

An induced pluripotent stem cell line (TRNDi001-D) from a Niemann-Pick disease type C1 (NPC1) patient carrying a homozygous p. I1061T (c. 3182T>C) mutation in the NPC1 gene
Li R et al. An induced pluripotent stem cell line (TRNDi001-D) from a Niemann-Pick disease type C1 (NPC1) patient carrying a homozygous p. I1061T (c. 3182T>C) mutation in the NPC1 gene. . 2020-04-00. Pubmed ID: 32114296; DOI: 10.1016/j.scr.2020.101737; PMC: PMC7218921 TRNDi001-D 2020-04-00 2020-04-00
PubMed: 32114296 DOI: 10.1016/j.scr.2020.101737
Associated cell lines:
- TRNDi001-D
Vasconcelos E Sá J, Simão D, Terrasso AP, Silva MM, Brito C, Isidro IA, Alves PM, Carrondo MJT

Unveiling dynamic metabolic signatures in human induced pluripotent and neural stem cells
Vasconcelos E Sá J et al. Unveiling dynamic metabolic signatures in human induced pluripotent and neural stem cells. . 2020-04-00. Pubmed ID: 32298259; DOI: 10.1371/journal.pcbi.1007780; PMC: PMC7188302 RIi001-A 2020-04-00 2020-04-00
PubMed: 32298259 DOI: 10.1371/journal.pcbi.1007780
Associated cell lines:
- RIi001-A
Wang P, Wang J, Xing Y, Wang H, Yu D, Feng Y, Wu H, Wu Y, Chen Z, Wang J, Shi H

Establishment of an iPSC line (JTUi002-A) from a patient with Waardenburg syndrome caused by a SOX10 mutation and carrying a GJB2 mutation
Wang P et al. Establishment of an iPSC line (JTUi002-A) from a patient with Waardenburg syndrome caused by a SOX10 mutation and carrying a GJB2 mutation. . 2020-04-00. Pubmed ID: 32199281; DOI: 10.1016/j.scr.2020.101756 JTUi002-A 2020-04-00 2020-04-00
PubMed: 32199281 DOI: 10.1016/j.scr.2020.101756
Associated cell lines:
- JTUi002-A
Huo Y, Wang J, He J, Kong D, Ma J

Establishment of human induced pluripotent stem cell line from dermal fibroblasts of a healthy individual
Huo Y et al. Establishment of human induced pluripotent stem cell line from dermal fibroblasts of a healthy individual. . 2020-04-00. Pubmed ID: 32224419; DOI: 10.1016/j.scr.2020.101762 DHMCi005-AHEBHMUi002-AHEBHMUi005-A 2020-04-00 2020-04-00
PubMed: 32224419 DOI: 10.1016/j.scr.2020.101762
Associated cell lines:
Tembe S, Fernandes S, Khan N, Melinkeri S, Kale V, Limaye L

Establishment of human iPSC line from patient of Indian ethnicity carrying homozygous CD8/9 (+G) beta thalassemia mutation
Tembe S et al. Establishment of human iPSC line from patient of Indian ethnicity carrying homozygous CD8/9 (+G) beta thalassemia mutation. . 2020-04-00. Pubmed ID: 32278313; DOI: 10.1016/j.scr.2020.101772 NCCSi009-A 2020-04-00 2020-04-00
PubMed: 32278313 DOI: 10.1016/j.scr.2020.101772
Associated cell lines:
- NCCSi009-A
Pichard L, Brondelo JM, Becker F, Desprat R, De Ceuninck F, Pastoureau P, Noel D, Jorgensen C, Lemaitre JM

Generation of human pluripotent stem cell lines (iPSCs) from mesenchymal stem cells (MSCs) from three elderly patients with osteoarthritis
Pichard L et al. Generation of human pluripotent stem cell lines (iPSCs) from mesenchymal stem cells (MSCs) from three elderly patients with osteoarthritis. . 2020-04-00. Pubmed ID: 32200258; DOI: 10.1016/j.scr.2020.101721 REGUi003-AREGUi006-AREGUi007-AREGUi008-A 2020-04-00 2020-04-00
PubMed: 32200258 DOI: 10.1016/j.scr.2020.101721
Associated cell lines:
Secardin L, Limia CEG, di Stefano A, Bonamino MH, Saliba J, Kataoka K, Rehen SK, Raslova H, Marty C, Ogawa S, Vainchenker W, Monte-Mor BDCR, Plo I

TET2 haploinsufficiency alters reprogramming into induced pluripotent stem cells
Secardin L et al. TET2 haploinsufficiency alters reprogramming into induced pluripotent stem cells. . 2020-04-00. Pubmed ID: 32193150; DOI: 10.1016/j.scr.2020.101755 INCABRi002-A 2020-04-00 2020-04-00
PubMed: 32193150 DOI: 10.1016/j.scr.2020.101755
Associated cell lines:
- INCABRi002-A
Zhang J, Wei L, Chen D, Feng L, Wu C, Wang R, Li X, Liu H

Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi004-A) from a Wilson's disease patient harboring a homozygous Pro992Leu mutation in ATP7B gene
Zhang J et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi004-A) from a Wilson's disease patient harboring a homozygous Pro992Leu mutation in ATP7B gene. . 2020-04-00. Pubmed ID: 32113134; DOI: 10.1016/j.scr.2020.101741 ZZUNEUi004-A 2020-04-00 2020-04-00
PubMed: 32113134 DOI: 10.1016/j.scr.2020.101741
Associated cell lines:
- ZZUNEUi004-A
Ma J, Feng B, Kong D, He J, Guo R, Amponsah AE, Zhang W, Zhang S, Lv F, Song Y, Liu A, Cui H

Production and validation of human induced pluripotent stem cell line from sporadic amyotrophic lateral sclerosis (SALS)
Ma J et al. Production and validation of human induced pluripotent stem cell line from sporadic amyotrophic lateral sclerosis (SALS). . 2020-04-00. Pubmed ID: 32203916; DOI: 10.1016/j.scr.2020.101760 HEBHMUi002-AHEBHMUi003-A 2020-04-00 2020-04-00
PubMed: 32203916 DOI: 10.1016/j.scr.2020.101760
Associated cell lines:
- HEBHMUi002-A
- HEBHMUi003-A
van Riet S, Ninaber DK, Mikkers HMM, Tetley TD, Jost CR, Mulder AA, Pasman T, Baptista D, Poot AA, Truckenmüller R, Mummery CL, Freund C, Rottier RJ, Hiemstra PS

In vitro modelling of alveolar repair at the air-liquid interface using alveolar epithelial cells derived from human induced pluripotent stem cells
van Riet S et al. In vitro modelling of alveolar repair at the air-liquid interface using alveolar epithelial cells derived from human induced pluripotent stem cells. . 2020-03-26. Pubmed ID: 32218519; DOI: 10.1038/s41598-020-62226-1; PMC: PMC7099095 LUMCi031-A 2020-03-26 2020-03-26
PubMed: 32218519 DOI: 10.1038/s41598-020-62226-1
Associated cell lines:
- LUMCi031-A
Frew J, Baradaran-Heravi A, Balgi AD, Wu X, Yan TD, Arns S, Shidmoossavee FS, Tan J, Jaquith JB, Jansen-West KR, Lynn FC, Gao FB, Petrucelli L, Feldman HH, Mackenzie IR, Roberge M, Nygaard HB

Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiency
Frew J et al. Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiency. . 2020-03-16. Pubmed ID: 32178712; DOI: 10.1186/s13024-020-00369-5; PMC: PMC7075020 UBCi001-A 2020-03-16 2020-03-16
PubMed: 32178712 DOI: 10.1186/s13024-020-00369-5
Associated cell lines:
- UBCi001-A
Okubo T, Hayashi R, Shibata S, Kudo Y, Ishikawa Y, Inoue S, Kobayashi Y, Honda A, Honma Y, Kawasaki S, Nishida K

Generation and validation of a PITX2-EGFP reporter line of human induced pluripotent stem cells enables isolation of periocular mesenchymal cells
Okubo T et al. Generation and validation of a PITX2-EGFP reporter line of human induced pluripotent stem cells enables isolation of periocular mesenchymal cells. . 2020-03-13. Pubmed ID: 32034090; DOI: 10.1074/jbc.ra119.010713; PMC: PMC7076207 KUIFMSi004-C 2020-03-13 2020-03-13
PubMed: 32034090 DOI: 10.1074/jbc.ra119.010713
Associated cell lines:
- KUIFMSi004-C
Xu H, Jia Z, Ma K, Zhang J, Dai C, Yao Z, Deng W, Su J, Wang R, Chen X

Protective effect of BMSCs-derived exosomes mediated by BDNF on TBI via miR-216a-5p
Xu H et al. Protective effect of BMSCs-derived exosomes mediated by BDNF on TBI via miR-216a-5p. . 2020-03-09. Pubmed ID: 32150531; DOI: 10.12659/msm.920855; PMC: PMC7081927 NYGCe001-A 2020-03-09 2020-03-09
PubMed: 32150531 DOI: 10.12659/msm.920855
Associated cell lines:
- NYGCe001-A
Casamassa A, Ferrari D, Gelati M, Carella M, Vescovi AL, Rosati J

A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15
Casamassa A et al. A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15. . 2020-03-09. Pubmed ID: 32182809; DOI: 10.3390/ijms21051860; PMC: PMC7084702 EURACi001-AEURACi002-AEURACi003-ACSSi005-AIITi001-AVRFi001-ACCMi003-AEURACi005-AUNIBSi008-AUNIBSi008-BUNIBSi008-CSDQLCHi008-ASDQLCHi014-AQBRIi009-A 2020-03-09 2020-03-09
PubMed: 32182809 DOI: 10.3390/ijms21051860
Associated cell lines:
- EURACi001-A
- EURACi002-A
- EURACi003-A
- CSSi005-A
- IITi001-A
- VRFi001-A
- CCMi003-A
- EURACi005-A
- UNIBSi008-A
- UNIBSi008-B
- UNIBSi008-C
- SDQLCHi008-A
- SDQLCHi014-A
- QBRIi009-A
Khadjeh S, Hindmarsh V, Weber F, Cyganek L, Vidal RO, Torkieh S, Streckfuss-Bömeke K, Lbik D, Tiburcy M, Mohamed BA, Bonn S, Toischer K, Hasenfuss G

CRISPLD1: a novel conserved target in the transition to human heart failure
Khadjeh S et al. CRISPLD1: a novel conserved target in the transition to human heart failure. . 2020-03-07. Pubmed ID: 32146539; DOI: 10.1007/s00395-020-0784-4; PMC: PMC7060963 UMGi014-BUMGi014-B-3 2020-03-07 2020-03-07
PubMed: 32146539 DOI: 10.1007/s00395-020-0784-4
Associated cell lines:
- UMGi014-B
- UMGi014-B-3
Castro-Viñuelas R, Sanjurjo-Rodríguez C, Piñeiro-Ramil M, Hermida-Gómez T, Rodríguez-Fernández S, Oreiro N, de Toro J, Fuentes I, Blanco FJ, Díaz-Prado S

Generation and characterization of human induced pluripotent stem cells (iPSCs) from hand osteoarthritis patient-derived fibroblasts
Castro-Viñuelas R et al. Generation and characterization of human induced pluripotent stem cells (iPSCs) from hand osteoarthritis patient-derived fibroblasts. . 2020-03-06. Pubmed ID: 32144293; DOI: 10.1038/s41598-020-61071-6; PMC: PMC7060311 ESi080-A 2020-03-06 2020-03-06
PubMed: 32144293 DOI: 10.1038/s41598-020-61071-6
Associated cell lines:
- ESi080-A
Fang F, Li Z, Zhao Q, Xiong C, Ni K

Analysis of multi-lineage gene expression dynamics during primordial germ cell induction from human induced pluripotent stem cells
Fang F et al. Analysis of multi-lineage gene expression dynamics during primordial germ cell induction from human induced pluripotent stem cells. . 2020-03-04. Pubmed ID: 32127035; DOI: 10.1186/s13287-020-01620-y; PMC: PMC7055065 HUSTi001-A 2020-03-04 2020-03-04
PubMed: 32127035 DOI: 10.1186/s13287-020-01620-y
Associated cell lines:
- HUSTi001-A
Yan YI, Qiu Y, Zhao A, Zhao J, Wang Y, Deng Y

Establishment of SIAISi001-A, an induced pluripotent stem cell (iPSC) line from 66-year old mild cognitive impairment (MCI) with two copies of APOE4 gene
Yan YI et al. Establishment of SIAISi001-A, an induced pluripotent stem cell (iPSC) line from 66-year old mild cognitive impairment (MCI) with two copies of APOE4 gene. . 2020-03-00. Pubmed ID: 32007762; DOI: 10.1016/j.scr.2020.101702 SIAISi001-A 2020-03-00 2020-03-00
PubMed: 32007762 DOI: 10.1016/j.scr.2020.101702
Associated cell lines:
- SIAISi001-A
Puentes-Tellez MA, Lerma-Barbosa PA, Garzón-Jaramillo RG, Suarez DA, Espejo-Mojica AJ, Guevara JM, Echeverri OY, Solano-Galarza D, Uribe-Ardila A, Alméciga-Díaz CJ

A perspective on research, diagnosis, and management of lysosomal storage disorders in Colombia
Puentes-Tellez MA et al. A perspective on research, diagnosis, and management of lysosomal storage disorders in Colombia. . 2020-03-00. Pubmed ID: 32258481; DOI: 10.1016/j.heliyon.2020.e03635; PMC: PMC7113438 TRNDi005-A 2020-03-00 2020-03-00
PubMed: 32258481 DOI: 10.1016/j.heliyon.2020.e03635
Associated cell lines:
- TRNDi005-A
Gripp KW, Schill L, Schoyer L, Stronach B, Bennett AM, Blaser S, Brown A, Burdine R, Burkitt-Wright E, Castel P, Darilek S, Dias A, Dyer T, Ellis M, Erickson G, Gelb BD, Green T, Gross A, Ho A, Holder JL Jr, Inoue SI, Jelin AC, Kennedy A, Klein R, Kontaridis MI, Magoulas P, McConnell DB, McCormick F, Neel BG, Prada CE, Rauen KA, Roberts A, Rodriguez-Viciana P, Rosen N, Rumbaugh G, Sablina A, Solman M, Tartaglia M, Thomas A, Timmer WC, Venkatachalam K, Walsh KS, Wolters PL, Yi JS, Zenker M, Ratner N

The sixth international RASopathies symposium: Precision medicine-From promise to practice
Gripp KW et al. The sixth international RASopathies symposium: Precision medicine-From promise to practice. . 2020-03-00. Pubmed ID: 31825160; DOI: 10.1002/ajmg.a.61434; PMC: PMC7021559 TRNDi003-A 2020-03-00 2020-03-00
PubMed: 31825160 DOI: 10.1002/ajmg.a.61434
Associated cell lines:
- TRNDi003-A
Ding Y, Carvalho E, Murphy C, McInerney V, Krawczyk J, O'Brien T, Howard L, Cai L, Shen S

Derivation of familial iPSC lines from three patients with retinitis pigmentosa carrying an autosomal dominant RPE65 mutation (NUIGi027-A, NUIGi028-A, NUIGi029-A)
Ding Y et al. Derivation of familial iPSC lines from three patients with retinitis pigmentosa carrying an autosomal dominant RPE65 mutation (NUIGi027-A, NUIGi028-A, NUIGi029-A). . 2020-03-00. Pubmed ID: 31954326; DOI: 10.1016/j.scr.2019.101665 NUIGi027-ANUIGi028-ANUIGi029-A 2020-03-00 2020-03-00
PubMed: 31954326 DOI: 10.1016/j.scr.2019.101665
Associated cell lines:
Ullah I, Busch JF, Rabien A, Ergün B, Stamm C, Knosalla C, Hippenstiel S, Reinke P, Kurtz A

Adult Tissue Extracellular Matrix Determines Tissue Specification of Human iPSC-Derived Embryonic Stage Mesodermal Precursor Cells
Ullah I et al. Adult Tissue Extracellular Matrix Determines Tissue Specification of Human iPSC-Derived Embryonic Stage Mesodermal Precursor Cells. . 2020-03-00. Pubmed ID: 32154066; DOI: 10.1002/advs.201901198; PMC: PMC7055561 WISCi004-ABCRTi005-ABIHi004-A 2020-03-00 2020-03-00
PubMed: 32154066 DOI: 10.1002/advs.201901198
Associated cell lines:
Gatinois V, Desprat R, Becker F, Pichard L, Bernex F, Isidor B, Pellestor F, Lemaitre JM

iPSC line derived from a Bloom syndrome patient retains an increased disease-specific sister-chromatid exchange activity
Gatinois V et al. iPSC line derived from a Bloom syndrome patient retains an increased disease-specific sister-chromatid exchange activity. . 2020-03-00. Pubmed ID: 31918214; DOI: 10.1016/j.scr.2019.101696 REGUi003-AREGUi004-A 2020-03-00 2020-03-00
PubMed: 31918214 DOI: 10.1016/j.scr.2019.101696
Associated cell lines:
- REGUi003-A
- REGUi004-A
Park H, Han J, Lee Y, Kwak S, Koo SK

Generation of a human induced pluripotent stem cell line from a patient with Leber congenital amaurosis
Park H et al. Generation of a human induced pluripotent stem cell line from a patient with Leber congenital amaurosis. . 2020-03-00. Pubmed ID: 32036247; DOI: 10.1016/j.scr.2020.101725 KSCBi011-A 2020-03-00 2020-03-00
PubMed: 32036247 DOI: 10.1016/j.scr.2020.101725
Associated cell lines:
- KSCBi011-A
Petters J, Cimmaruta C, Iwanov K, Chang ML, Völkner C, Knuebel G, Murua Escobar H, Frech MJ, Hermann A, Rolfs A, Lukas J

Generation of induced pluripotent stem cell lines AKOSi002-A and AKOSi003-A from symptomatic female adults with Wilson disease
Petters J et al. Generation of induced pluripotent stem cell lines AKOSi002-A and AKOSi003-A from symptomatic female adults with Wilson disease. . 2020-03-00. Pubmed ID: 32028086; DOI: 10.1016/j.scr.2020.101708 AKOSi002-AAKOSi003-A 2020-03-00 2020-03-00
PubMed: 32028086 DOI: 10.1016/j.scr.2020.101708
Associated cell lines:
- AKOSi002-A
- AKOSi003-A
Laowtammathron C, Chingsuwanrote P, Choavaratana R, Phornwilardsiri S, Sitthirit K, Kaewjunun C, Makemaharn O, Terbto P, Waeteekul S, Lorthongpanich C, U-Pratya Y, Srisook P, Kheolamai P, Issaragrisil S

Derivation of human embryonic stem cell line MUSIe001-A from an embryo with homozygous α⁰-thalassemia (SEA deletion)
Laowtammathron C et al. Derivation of human embryonic stem cell line MUSIe001-A from an embryo with homozygous α⁰-thalassemia (SEA deletion). . 2020-03-00. Pubmed ID: 31945613; DOI: 10.1016/j.scr.2019.101695 MUSIe001-A 2020-03-00 2020-03-00
PubMed: 31945613 DOI: 10.1016/j.scr.2019.101695
Associated cell lines:
- MUSIe001-A
Guan J, Li Z, Zhang H, Yang X, Ma Y, Li Y, Dong R, Gai Z, Liu Y

Generation of a Human iPSC line (SDQLCHi021-A) from a patient with methylmalonic acidemia cblC type carrying compound heterozygous mutations in MMAHC gene
Guan J et al. Generation of a Human iPSC line (SDQLCHi021-A) from a patient with methylmalonic acidemia cblC type carrying compound heterozygous mutations in MMAHC gene. . 2020-03-00. Pubmed ID: 32058304; DOI: 10.1016/j.scr.2020.101709 SDQLCHi021-A 2020-03-00 2020-03-00
PubMed: 32058304 DOI: 10.1016/j.scr.2020.101709
Associated cell lines:
- SDQLCHi021-A
Fukunaga I, Shiga T, Chen C, Oe Y, Danzaki K, Ohta S, Matsuoka R, Anzai T, Hibiya-Motegi R, Tajima S, Ikeda K, Akamatsu W, Kamiya K

Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutation
Fukunaga I et al. Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutation. . 2020-03-00. Pubmed ID: 31926383; DOI: 10.1016/j.scr.2019.101674 JUFMDOi004-A 2020-03-00 2020-03-00
PubMed: 31926383 DOI: 10.1016/j.scr.2019.101674
Associated cell lines:
- JUFMDOi004-A
Perepelina K, Klauzen P, Khudiakov A, Zlotina A, Fomicheva Y, Rudenko D, Gordeev M, Sergushichev A, Malashicheva A, Kostareva A

Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro
Perepelina K et al. Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro. . 2020-03-00. Pubmed ID: 32059175; DOI: 10.1016/j.scr.2020.101714 FAMRCi006-AFAMRCi006-B 2020-03-00 2020-03-00
PubMed: 32059175 DOI: 10.1016/j.scr.2020.101714
Associated cell lines:
- FAMRCi006-A
- FAMRCi006-B
Fuchs NV, Schieck M, Neuenkirch M, Tondera C, Schmitz H, Wendeburg L, Steinemann D, Elpers C, Rutsch F, König R

Generation of three induced pluripotent cell lines (iPSCs) from an Aicardi-Goutières syndrome (AGS) patient harboring a deletion in the genomic locus of the sterile alpha motif and HD domain containing protein 1 (SAMHD1)
Fuchs NV et al. Generation of three induced pluripotent cell lines (iPSCs) from an Aicardi-Goutières syndrome (AGS) patient harboring a deletion in the genomic locus of the sterile alpha motif and HD domain containing protein 1 (SAMHD1). . 2020-03-00. Pubmed ID: 32062129; DOI: 10.1016/j.scr.2019.101697 PEIi002-APEIi002-BPEIi002-C 2020-03-00 2020-03-00
PubMed: 32062129 DOI: 10.1016/j.scr.2019.101697
Associated cell lines:
Khudiakov A, Perepelina K, Klauzen P, Zlotina A, Gusev K, Kaznacheyeva E, Malashicheva A, Kostareva A

Generation of two iPSC lines (FAMRCi004-A and FAMRCi004-B) from patient with familial progressive cardiac conduction disorder carrying genetic variant DSP p.His1684Arg
Khudiakov A et al. Generation of two iPSC lines (FAMRCi004-A and FAMRCi004-B) from patient with familial progressive cardiac conduction disorder carrying genetic variant DSP p.His1684Arg. . 2020-03-00. Pubmed ID: 32062131; DOI: 10.1016/j.scr.2020.101720 FAMRCi004-AFAMRCi004-B 2020-03-00 2020-03-00
PubMed: 32062131 DOI: 10.1016/j.scr.2020.101720
Associated cell lines:
- FAMRCi004-A
- FAMRCi004-B
Li X, Liu Y, Liu F, Wang X, Liu M, Du W, Zhao J, Wang M, Hu L, Wang C, Fu W, Dong J, Zhao X

Generation of a hiPSC line ZZUNEUi007-A from a patient with hypertrophic cardiomyopathy caused by mutation in MYH7
Li X et al. Generation of a hiPSC line ZZUNEUi007-A from a patient with hypertrophic cardiomyopathy caused by mutation in MYH7. . 2020-03-00. Pubmed ID: 31931472; DOI: 10.1016/j.scr.2020.101699 ZZUNEUi007-A 2020-03-00 2020-03-00
PubMed: 31931472 DOI: 10.1016/j.scr.2020.101699
Associated cell lines:
- ZZUNEUi007-A
Pongpamorn P, Dahlmann J, Haase A, Ebeling CT, Merkert S, Göhring G, Lachmann N, Martens A, Haverich A, Martin U, Olmer R

Generation of three induced pluripotent stem cell lines (MHHi012-A, MHHi013-A, MHHi014-A) from a family with Loeys-Dietz syndrome carrying a heterozygous p.M253I (c.759G>A) mutation in the TGFBR1 gene
Pongpamorn P et al. Generation of three induced pluripotent stem cell lines (MHHi012-A, MHHi013-A, MHHi014-A) from a family with Loeys-Dietz syndrome carrying a heterozygous p.M253I (c.759G>A) mutation in the TGFBR1 gene. . 2020-03-00. Pubmed ID: 32062130; DOI: 10.1016/j.scr.2020.101707 MHHi012-AMHHi013-AMHHi014-A 2020-03-00 2020-03-00
PubMed: 32062130 DOI: 10.1016/j.scr.2020.101707
Associated cell lines:
Panda A, Gurusamy N, Rajasingh S, Carter HK, Thomas EL, Rajasingh J

Non-viral reprogramming and induced pluripotent stem cells for cardiovascular therapy
Panda A et al. Non-viral reprogramming and induced pluripotent stem cells for cardiovascular therapy. . 2020-03-00. Pubmed ID: 31954271; DOI: 10.1016/j.diff.2019.12.001; PMC: PMC7138699 TRNDi003-A 2020-03-00 2020-03-00
PubMed: 31954271 DOI: 10.1016/j.diff.2019.12.001
Associated cell lines:
- TRNDi003-A
Liu X, Yang X, Li Y, Wang X, Ma J, Jiang W, Liu Y, Sun W, Gong Y

Generation of patient-specific pluripotent induced stem cell line SDUBMSI002-A from a patient with X-linked mental retardation syndrome
Liu X et al. Generation of patient-specific pluripotent induced stem cell line SDUBMSI002-A from a patient with X-linked mental retardation syndrome. . 2020-03-00. Pubmed ID: 32078988; DOI: 10.1016/j.scr.2020.101724 SDUBMSi002-A 2020-03-00 2020-03-00
PubMed: 32078988 DOI: 10.1016/j.scr.2020.101724
Associated cell lines:
- SDUBMSi002-A
Castro-Viñuelas R, Sanjurjo-Rodríguez C, Piñeiro-Ramil M, Rodríguez-Fernández S, Fuentes-Boquete IM, Blanco FJ, Díaz-Prado SM

Generation of a human control iPS cell line (ESi080-A) from a donor with no rheumatic diseases
Castro-Viñuelas R et al. Generation of a human control iPS cell line (ESi080-A) from a donor with no rheumatic diseases. . 2020-03-00. Pubmed ID: 31962233; DOI: 10.1016/j.scr.2019.101683 ESi080-A 2020-03-00 2020-03-00
PubMed: 31962233 DOI: 10.1016/j.scr.2019.101683
Associated cell lines:
- ESi080-A
Mao S, Ding C, Zhou Y, Jing Y, Chen J, Guo Y, Liu J, Cui Z, Yan X, Gu J, Wang Y, Chen J, Tang S

Establishment of a human induced pluripotent stem cell line (CSUASOi005-A), from peripheral blood mononuclear cells of a patient with X-linked juvenile retinoschisis carrying a novel mutation in RS1 gene
Mao S et al. Establishment of a human induced pluripotent stem cell line (CSUASOi005-A), from peripheral blood mononuclear cells of a patient with X-linked juvenile retinoschisis carrying a novel mutation in RS1 gene. . 2020-03-00. Pubmed ID: 32050117; DOI: 10.1016/j.scr.2020.101718 CSUASOi005-A 2020-03-00 2020-03-00
PubMed: 32050117 DOI: 10.1016/j.scr.2020.101718
Associated cell lines:
- CSUASOi005-A
Azevedo C, Chumarina M, Serafimova E, Goldwurm S, Collin A, Roybon L, Savchenko E, Pomeshchik Y

Generation of an induced pluripotent stem cell line (CSC-32) from a patient with Parkinson's disease carrying a heterozygous variation p.A53T in the SNCA gene
Azevedo C et al. Generation of an induced pluripotent stem cell line (CSC-32) from a patient with Parkinson's disease carrying a heterozygous variation p.A53T in the SNCA gene. . 2020-03-00. Pubmed ID: 31954327; DOI: 10.1016/j.scr.2019.101694 ULUNDi008-A 2020-03-00 2020-03-00
PubMed: 31954327 DOI: 10.1016/j.scr.2019.101694
Associated cell lines:
- ULUNDi008-A
Ferrari G, Muntoni F, Tedesco FS

Generation of two genomic-integration-free DMD iPSC lines with mutations affecting all dystrophin isoforms and potentially amenable to exon-skipping
Ferrari G et al. Generation of two genomic-integration-free DMD iPSC lines with mutations affecting all dystrophin isoforms and potentially amenable to exon-skipping. . 2020-03-00. Pubmed ID: 32087527; DOI: 10.1016/j.scr.2019.101688; PMC: PMC7057262 UCLi011-AUCLi012-A 2020-03-00 2020-03-00
PubMed: 32087527 DOI: 10.1016/j.scr.2019.101688
Associated cell lines:
- UCLi011-A
- UCLi012-A
Zhou HM, Zhou XQ, Lu JZ, Jia WW, Kang JH

An induced pluripotent stem cell line (SHEHi002-A (5426))from a patient of long QT syndrome type 8 with c.2573G>A mutation in the gene CACNA1C
Zhou HM et al. An induced pluripotent stem cell line (SHEHi002-A (5426))from a patient of long QT syndrome type 8 with c.2573G>A mutation in the gene CACNA1C. . 2020-03-00. Pubmed ID: 32062134; DOI: 10.1016/j.scr.2020.101731 SHEHi002-A 2020-03-00 2020-03-00
PubMed: 32062134 DOI: 10.1016/j.scr.2020.101731
Associated cell lines:
- SHEHi002-A
Wang J, Cui Y, Xing K, Luan J, Han J

Generation and characterization of a human iPSC line derived from congenital clubfoot amniotic fluid cells
Wang J et al. Generation and characterization of a human iPSC line derived from congenital clubfoot amniotic fluid cells. . 2020-03-00. Pubmed ID: 31986484; DOI: 10.1016/j.scr.2020.101712 SMBCi002-A 2020-03-00 2020-03-00
PubMed: 31986484 DOI: 10.1016/j.scr.2020.101712
Associated cell lines:
- SMBCi002-A
Xu C, Zhou Z, Liu C, Kang X, Zhong X, Zhang Q, Xu Y

Generation of a DAPK1 knockout first (conditional ready) human embryonic stem cell line (ZSSYe001-A) by CRISPR-Cas9 technology
Xu C et al. Generation of a DAPK1 knockout first (conditional ready) human embryonic stem cell line (ZSSYe001-A) by CRISPR-Cas9 technology. . 2020-03-00. Pubmed ID: 31978714; DOI: 10.1016/j.scr.2019.101693 ZSSYe001-A 2020-03-00 2020-03-00
PubMed: 31978714 DOI: 10.1016/j.scr.2019.101693
Associated cell lines:
- ZSSYe001-A
Haake K, Wüstefeld T, Merkert S, Lüttge D, Göhring G, Auber B, Baumann U, Lachmann N

Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis
Haake K et al. Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis. . 2020-03-00. Pubmed ID: 32000109; DOI: 10.1016/j.scr.2020.101713 MHHi010-A 2020-03-00 2020-03-00
PubMed: 32000109 DOI: 10.1016/j.scr.2020.101713
Associated cell lines:
- MHHi010-A
Gao Y, Wang Y, Wang Z, Sun H, Zhang R, Yang J, Liu Y, Liu H, Zhang Q, Zhang S, Shi C, Xu Y, Song B

Generation of induced pluripotent stem cell line (ZZUi0016-A) from dermal fibroblasts of a normal human
Gao Y et al. Generation of induced pluripotent stem cell line (ZZUi0016-A) from dermal fibroblasts of a normal human. . 2020-03-00. Pubmed ID: 32007761; DOI: 10.1016/j.scr.2020.101717 ZZUi016-A 2020-03-00 2020-03-00
PubMed: 32007761 DOI: 10.1016/j.scr.2020.101717
Associated cell lines:
- ZZUi016-A
Cao X, van den Hil FE, Mummery CL, Orlova VV

Generation and Functional Characterization of Monocytes and Macrophages Derived from Human Induced Pluripotent Stem Cells
Cao X et al. Generation and Functional Characterization of Monocytes and Macrophages Derived from Human Induced Pluripotent Stem Cells. . 2020-03-00. Pubmed ID: 32159928; DOI: 10.1002/cpsc.108; PMC: PMC7154707 LUMCi001-A 2020-03-00 2020-03-00
PubMed: 32159928 DOI: 10.1002/cpsc.108
Associated cell lines:
- LUMCi001-A
Lorthongpanich C, Laowtammathron C, Jiamvoraphong N, Srisook P, Chingsuwanrote P, Klaihmon P, Damkham N, Terbto P, Waeteekul S, U-Pratya Y, Issaragrisil S

YAP-depleted iPSC MUSIi012-A-2 maintained all normal stem cell characteristics
Lorthongpanich C et al. YAP-depleted iPSC MUSIi012-A-2 maintained all normal stem cell characteristics. . 2020-03-00. Pubmed ID: 32018207; DOI: 10.1016/j.scr.2020.101723 MUSIi012-AMUSIi012-A-2 2020-03-00 2020-03-00
PubMed: 32018207 DOI: 10.1016/j.scr.2020.101723
Associated cell lines:
- MUSIi012-A
- MUSIi012-A-2
Klauzen P, Perepelina K, Khudiakov A, Zlotina A, Fomicheva Y, Pervunina T, Vershinina T, Kostareva A, Malashicheva A

Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val
Klauzen P et al. Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val. . 2020-03-00. Pubmed ID: 32062135; DOI: 10.1016/j.scr.2020.101719 FAMRCi005-AFAMRCi005-B 2020-03-00 2020-03-00
PubMed: 32062135 DOI: 10.1016/j.scr.2020.101719
Associated cell lines:
- FAMRCi005-A
- FAMRCi005-B
Jin P, Wang S, Jiang X, Shan X, Jiang S, Quan Y, Zhang T, Yang J, Zhang H, Ma J, Dong M, Fan J, Fan X, Gong Y, Wang Y

Generation of human induced pluripotent stem cell line (WMUi001-A) from a patient with aortic dissection
Jin P et al. Generation of human induced pluripotent stem cell line (WMUi001-A) from a patient with aortic dissection. . 2020-03-00. Pubmed ID: 32062133; DOI: 10.1016/j.scr.2020.101730 WMUi001-A 2020-03-00 2020-03-00
PubMed: 32062133 DOI: 10.1016/j.scr.2020.101730
Associated cell lines:
- WMUi001-A
Xiaojing W, Yanyan M, Ruonan D, Xiaolin L, Haiyan Z, Jian M, Yi L, Wenjie S, Qiji L

Generation of a human induced pluripotent stem cell line (SDUBMSi001-A) from a hereditary spastic paraplegia patient carrying kif1a c.773C>T missense mutation
Xiaojing W et al. Generation of a human induced pluripotent stem cell line (SDUBMSi001-A) from a hereditary spastic paraplegia patient carrying kif1a c.773C>T missense mutation. . 2020-03-00. Pubmed ID: 32045731; DOI: 10.1016/j.scr.2020.101727 SDUBMSi001-A 2020-03-00 2020-03-00
PubMed: 32045731 DOI: 10.1016/j.scr.2020.101727
Associated cell lines:
- SDUBMSi001-A
Ma Y, Zhang H, Li X, Yang X, Li Y, Guan J, Lv Y, Gai Z, Liu Y

An integration-free iPSC line (SDQLCHi017-A) derived from a patient with nemaline myopathy-2 disease carrying compound heterozygote mutations in NEB gene
Ma Y et al. An integration-free iPSC line (SDQLCHi017-A) derived from a patient with nemaline myopathy-2 disease carrying compound heterozygote mutations in NEB gene. . 2020-03-00. Pubmed ID: 32062132; DOI: 10.1016/j.scr.2020.101729 SDQLCHi017-A 2020-03-00 2020-03-00
PubMed: 32062132 DOI: 10.1016/j.scr.2020.101729
Associated cell lines:
- SDQLCHi017-A
Yang X, Yan B, Zhang H, Ma Y, Zhou Q, Li Y, Guan J, Wang D, Liu Y, Gai Z

Generation of an induced pluripotent stem cell line (SDQLCHi009-A) from a patient with 47,XXY and ornithine transcarbamylase deficiency carrying a hemizygote mutation in OTC
Yang X et al. Generation of an induced pluripotent stem cell line (SDQLCHi009-A) from a patient with 47,XXY and ornithine transcarbamylase deficiency carrying a hemizygote mutation in OTC. . 2020-03-00. Pubmed ID: 32014801; DOI: 10.1016/j.scr.2020.101704 SDQLCHi009-A 2020-03-00 2020-03-00
PubMed: 32014801 DOI: 10.1016/j.scr.2020.101704
Associated cell lines:
- SDQLCHi009-A
van den Brink L, Brandão KO, Yiangou L, Mol MPH, Grandela C, Mummery CL, Verkerk AO, Davis RP

Cryopreservation of human pluripotent stem cell-derived cardiomyocytes is not detrimental to their molecular and functional properties
van den Brink L et al. Cryopreservation of human pluripotent stem cell-derived cardiomyocytes is not detrimental to their molecular and functional properties. . 2020-03-00. Pubmed ID: 31945612; DOI: 10.1016/j.scr.2019.101698 LUMCi004-A 2020-03-00 2020-03-00
PubMed: 31945612 DOI: 10.1016/j.scr.2019.101698
Associated cell lines:
- LUMCi004-A
Sun C, Yang M, Qin F, Guo R, Liang S, Hu H

Generation of an induced pluripotent stem cell line SYSUi-003-A from a child with epilepsy carrying GRIN2A mutation
Sun C et al. Generation of an induced pluripotent stem cell line SYSUi-003-A from a child with epilepsy carrying GRIN2A mutation. . 2020-03-00. Pubmed ID: 32036246; DOI: 10.1016/j.scr.2020.101706 SYSUi003-A 2020-03-00 2020-03-00
PubMed: 32036246 DOI: 10.1016/j.scr.2020.101706
Associated cell lines:
- SYSUi003-A
Korshunova I, Rhein S, García-González D, Stölting I, Pfisterer U, Barta A, Dmytriyeva O, Kirkeby A, Schwaninger M, Khodosevich K

Genetic modification increases the survival and the neuroregenerative properties of transplanted neural stem cells
Korshunova I et al. Genetic modification increases the survival and the neuroregenerative properties of transplanted neural stem cells. . 2020-02-27. Pubmed ID: 31999645; DOI: 10.1172/jci.insight.126268; PMC: PMC7101138 WAe009-ARCe021-A 2020-02-27 2020-02-27
PubMed: 31999645 DOI: 10.1172/jci.insight.126268
Associated cell lines:
- WAe009-A
- RCe021-A
Claus C, Jung M, Hübschen JM

Pluripotent Stem Cell-Based Models: A Peephole into Virus Infections during Early Pregnancy
Claus C et al. Pluripotent Stem Cell-Based Models: A Peephole into Virus Infections during Early Pregnancy. . 2020-02-26. Pubmed ID: 32110999; DOI: 10.3390/cells9030542; PMC: PMC7140399 WISCi004-B 2020-02-26 2020-02-26
PubMed: 32110999 DOI: 10.3390/cells9030542
Associated cell lines:
- WISCi004-B
Ke M, Chong CM, Zeng H, Huang M, Huang Z, Zhang K, Cen X, Lu JH, Yao X, Qin D, Su H

Azoramide protects iPSC-derived dopaminergic neurons with PLA2G6 D331Y mutation through restoring ER function and CREB signaling
Ke M et al. Azoramide protects iPSC-derived dopaminergic neurons with PLA2G6 D331Y mutation through restoring ER function and CREB signaling. . 2020-02-18. Pubmed ID: 32071291; DOI: 10.1038/s41419-020-2312-8; PMC: PMC7028918 IBMSi012-A 2020-02-18 2020-02-18
PubMed: 32071291 DOI: 10.1038/s41419-020-2312-8
Associated cell lines:
- IBMSi012-A
D'Avanzo F, Rigon L, Zanetti A, Tomanin R

Mucopolysaccharidosis Type II: One Hundred Years of Research, Diagnosis, and Treatment
D'Avanzo F et al. Mucopolysaccharidosis Type II: One Hundred Years of Research, Diagnosis, and Treatment. . 2020-02-13. Pubmed ID: 32070051; DOI: 10.3390/ijms21041258; PMC: PMC7072947 TRNDi008-A 2020-02-13 2020-02-13
PubMed: 32070051 DOI: 10.3390/ijms21041258
Associated cell lines:
- TRNDi008-A
Saleem U, Mannhardt I, Braren I, Denning C, Eschenhagen T, Hansen A

Force and Calcium Transients Analysis in Human Engineered Heart Tissues Reveals Positive Force-Frequency Relation at Physiological Frequency
Saleem U et al. Force and Calcium Transients Analysis in Human Engineered Heart Tissues Reveals Positive Force-Frequency Relation at Physiological Frequency. . 2020-02-11. Pubmed ID: 31956082; DOI: 10.1016/j.stemcr.2019.12.011; PMC: PMC7013237 UKEi001-AUKEi003-C 2020-02-11 2020-02-11
PubMed: 31956082 DOI: 10.1016/j.stemcr.2019.12.011
Associated cell lines:
- UKEi001-A
- UKEi003-C
Choi IY, Lim H, Cho HJ, Oh Y, Chou BK, Bai H, Cheng L, Kim YJ, Hyun S, Kim H, Shin JH, Lee G

Transcriptional landscape of myogenesis from human pluripotent stem cells reveals a key role of TWIST1 in maintenance of skeletal muscle progenitors
Choi IY et al. Transcriptional landscape of myogenesis from human pluripotent stem cells reveals a key role of TWIST1 in maintenance of skeletal muscle progenitors. . 2020-02-03. Pubmed ID: 32011235; DOI: 10.7554/elife.46981; PMC: PMC6996923 WAe009-A 2020-02-03 2020-02-03
PubMed: 32011235 DOI: 10.7554/elife.46981
Associated cell lines:
- WAe009-A
McLoughlin HS, Moore LR, Paulson HL

Pathogenesis of SCA3 and implications for other polyglutamine diseases
McLoughlin HS et al. Pathogenesis of SCA3 and implications for other polyglutamine diseases. . 2020-02-00. Pubmed ID: 31669734; DOI: 10.1016/j.nbd.2019.104635; PMC: PMC6980715 MUSIi004-A 2020-02-00 2020-02-00
PubMed: 31669734 DOI: 10.1016/j.nbd.2019.104635
Associated cell lines:
- MUSIi004-A
Ben M'Barek K, Bertin S, Brazhnikova E, Jaillard C, Habeler W, Plancheron A, Fovet CM, Demilly J, Jarraya M, Bejanariu A, Sahel JA, Peschanski M, Goureau O, Monville C

Clinical-grade production and safe delivery of human ESC derived RPE sheets in primates and rodents
Ben M'Barek K et al. Clinical-grade production and safe delivery of human ESC derived RPE sheets in primates and rodents. . 2020-02-00. Pubmed ID: 31732225; DOI: 10.1016/j.biomaterials.2019.119603 RCe013-A 2020-02-00 2020-02-00
PubMed: 31732225 DOI: 10.1016/j.biomaterials.2019.119603
Associated cell lines:
- RCe013-A
Hu T, Yao B, Huang S, Fu X

Insight into cellular dedifferentiation in regenerative medicine
Hu T et al. Insight into cellular dedifferentiation in regenerative medicine. . 2020-02-00. Pubmed ID: 31187305; DOI: 10.1007/s11427-019-9571-y ISMMSi002-BZZUi003-AIISHDOi001-A 2020-02-00 2020-02-00
PubMed: 31187305 DOI: 10.1007/s11427-019-9571-y
Associated cell lines:
Sung TC, Li HF, Higuchi A, Kumar SS, Ling QD, Wu YW, Burnouf T, Nasu M, Umezawa A, Lee KF, Wang HC, Chang Y, Hsu ST

Effect of cell culture biomaterials for completely xeno-free generation of human induced pluripotent stem cells
Sung TC et al. Effect of cell culture biomaterials for completely xeno-free generation of human induced pluripotent stem cells. . 2020-02-00. Pubmed ID: 31810728; DOI: 10.1016/j.biomaterials.2019.119638 GPCCi001-A 2020-02-00 2020-02-00
PubMed: 31810728 DOI: 10.1016/j.biomaterials.2019.119638
Associated cell lines:
- GPCCi001-A
Vélez JI, Lopera F, Silva CT, Villegas A, Espinosa LG, Vidal OM, Mastronardi CA, Arcos-Burgos M

Familial Alzheimer's Disease and Recessive Modifiers
Vélez JI et al. Familial Alzheimer's Disease and Recessive Modifiers. . 2020-02-00. Pubmed ID: 31664702; DOI: 10.1007/s12035-019-01798-0; PMC: PMC7031188 IMEDEAi006-A 2020-02-00 2020-02-00
PubMed: 31664702 DOI: 10.1007/s12035-019-01798-0
Associated cell lines:
- IMEDEAi006-A
Liu G, David BT, Trawczynski M, Fessler RG

Advances in Pluripotent Stem Cells: History, Mechanisms, Technologies, and Applications
Liu G et al. Advances in Pluripotent Stem Cells: History, Mechanisms, Technologies, and Applications. . 2020-02-00. Pubmed ID: 31760627; DOI: 10.1007/s12015-019-09935-x; PMC: PMC6987053 ZZUi004-AZZUi011-A 2020-02-00 2020-02-00
PubMed: 31760627 DOI: 10.1007/s12015-019-09935-x
Associated cell lines:
- ZZUi004-A
- ZZUi011-A
Pölönen RP, Swan H, Aalto-Setälä K

Mutation-specific differences in arrhythmias and drug responses in CPVT patients: simultaneous patch clamp and video imaging of iPSC derived cardiomyocytes
Pölönen RP et al. Mutation-specific differences in arrhythmias and drug responses in CPVT patients: simultaneous patch clamp and video imaging of iPSC derived cardiomyocytes. . 2020-02-00. Pubmed ID: 31786768; DOI: 10.1007/s11033-019-05201-y TAUi002-A 2020-02-00 2020-02-00
PubMed: 31786768 DOI: 10.1007/s11033-019-05201-y
Associated cell lines:
- TAUi002-A
Piers TM, Cosker K, Mallach A, Johnson GT, Guerreiro R, Hardy J, Pocock JM

A locked immunometabolic switch underlies TREM2 R47H loss of function in human iPSC-derived microglia
Piers TM et al. A locked immunometabolic switch underlies TREM2 R47H loss of function in human iPSC-derived microglia. . 2020-02-00. Pubmed ID: 31907987; DOI: 10.1096/fj.201902447r; PMC: PMC7027848 BIONi010-C 2020-02-00 2020-02-00
PubMed: 31907987 DOI: 10.1096/fj.201902447r
Associated cell lines:
- BIONi010-C
Ast J, Arvaniti A, Fine NHF, Nasteska D, Ashford FB, Stamataki Z, Koszegi Z, Bacon A, Jones BJ, Lucey MA, Sasaki S, Brierley DI, Hastoy B, Tomas A, D'Agostino G, Reimann F, Lynn FC, Reissaus CA, Linnemann AK, D'Este E, Calebiro D, Trapp S, Johnsson K, Podewin T, Broichhagen J, Hodson DJ

Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
Ast J et al. Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics. . 2020-01-24. Pubmed ID: 31980626; DOI: 10.1038/s41467-020-14309-w; PMC: PMC6981144 WAe001-A 2020-01-24 2020-01-24
PubMed: 31980626 DOI: 10.1038/s41467-020-14309-w
Associated cell lines:
- WAe001-A
Satir TM, Nazir FH, Vizlin-Hodzic D, Hardselius E, Blennow K, Wray S, Zetterberg H, Agholme L, Bergström P

Accelerated neuronal and synaptic maturation by BrainPhys medium increases Aβ secretion and alters Aβ peptide ratios from iPSC-derived cortical neurons
Satir TM et al. Accelerated neuronal and synaptic maturation by BrainPhys medium increases Aβ secretion and alters Aβ peptide ratios from iPSC-derived cortical neurons. . 2020-01-17. Pubmed ID: 31953468; DOI: 10.1038/s41598-020-57516-7; PMC: PMC6969066 WTSIi015-A 2020-01-17 2020-01-17
PubMed: 31953468 DOI: 10.1038/s41598-020-57516-7
Associated cell lines:
- WTSIi015-A
Assou S, Girault N, Plinet M, Bouckenheimer J, Sansac C, Combe M, Mianné J, Bourguignon C, Fieldes M, Ahmed E, Commes T, Boureux A, Lemaître JM, De Vos J

Recurrent Genetic Abnormalities in Human Pluripotent Stem Cells: Definition and Routine Detection in Culture Supernatant by Targeted Droplet Digital PCR
Assou S et al. Recurrent Genetic Abnormalities in Human Pluripotent Stem Cells: Definition and Routine Detection in Culture Supernatant by Targeted Droplet Digital PCR. . 2020-01-14. Pubmed ID: 31902703; DOI: 10.1016/j.stemcr.2019.12.004; PMC: PMC6962701 UHOMi001-A 2020-01-14 2020-01-14
PubMed: 31902703 DOI: 10.1016/j.stemcr.2019.12.004
Associated cell lines:
- UHOMi001-A
Vázquez-Vélez GE, Gonzales KA, Revelli JP, Adamski CJ, Alavi Naini F, Bajić A, Craigen E, Richman R, Heman-Ackah SM, Wood MJA, Rousseaux MWC, Zoghbi HY

Doublecortin-like Kinase 1 Regulates α-Synuclein Levels and Toxicity
Vázquez-Vélez GE et al. Doublecortin-like Kinase 1 Regulates α-Synuclein Levels and Toxicity. . 2020-01-08. Pubmed ID: 31748376; DOI: 10.1523/jneurosci.1076-19.2019; PMC: PMC6948939 WAe009-A 2020-01-08 2020-01-08
PubMed: 31748376 DOI: 10.1523/jneurosci.1076-19.2019
Associated cell lines:
- WAe009-A
Wang X, Xie S, Li Z, Ye Z, Gu X, Zhou L, Li H

Generation of an iPSC line (HUSTi002-A) from fibroblasts of a patient with Sertoli cell-only syndrome carrying c.731_732delAT in PIWIL2 gene
Wang X et al. Generation of an iPSC line (HUSTi002-A) from fibroblasts of a patient with Sertoli cell-only syndrome carrying c.731_732delAT in PIWIL2 gene. . 2020-01-00. Pubmed ID: 32006804; DOI: 10.1016/j.scr.2020.101703 HUSTi002-A 2020-01-00 2020-01-00
PubMed: 32006804 DOI: 10.1016/j.scr.2020.101703
Associated cell lines:
- HUSTi002-A
Ma B, Luo M, Yang H, Li T, Liu W, Xu F, Shu C, Chen G, Zhou Z

Generation of a human induced pluripotent stem cell line (NCCDFWi001-A) from a Marfan syndrome patient carrying two FBN1 variants (c.2613A > C and c.684_736 + 4del)
Ma B et al. Generation of a human induced pluripotent stem cell line (NCCDFWi001-A) from a Marfan syndrome patient carrying two FBN1 variants (c.2613A > C and c.684_736 + 4del). . 2020-01-00. Pubmed ID: 31901832; DOI: 10.1016/j.scr.2019.101690 NCCDFWi001-A 2020-01-00 2020-01-00
PubMed: 31901832 DOI: 10.1016/j.scr.2019.101690
Associated cell lines:
- NCCDFWi001-A
Elsayed AK, Aghadi M, Ali G, Al-Khawaga S, Hussain K, Abdelalim EM

Generation of a human induced pluripotent stem cell line (QBRIi009-A) from a patient with a heterozygous deletion of FOXA2
Elsayed AK et al. Generation of a human induced pluripotent stem cell line (QBRIi009-A) from a patient with a heterozygous deletion of FOXA2. . 2020-01-00. Pubmed ID: 31991389; DOI: 10.1016/j.scr.2020.101705 QBRIi009-A 2020-01-00 2020-01-00
PubMed: 31991389 DOI: 10.1016/j.scr.2020.101705
Associated cell lines:
- QBRIi009-A
Drick N, Sahabian A, Pongpamorn P, Merkert S, Göhring G, Welte T, Martin U, Olmer R

Generation of a NKX2.1 - p63 double transgenic knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-4)
Drick N et al. Generation of a NKX2.1 - p63 double transgenic knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-4). . 2020-01-00. Pubmed ID: 31791010; DOI: 10.1016/j.scr.2019.101659 MHHi006-AMHHi006-A-2MHHi006-A-4 2020-01-00 2020-01-00
PubMed: 31791010 DOI: 10.1016/j.scr.2019.101659
Associated cell lines:
Ma J, Zhang J, He J, Zhang Z, Li W, Feng B, Guo R, Amponsah AE, Kong D, Liu A, Song Y, Wei L, Cui H

Induced pluripotent stem cell (iPSC) line (HEBHMUi002-A) from a healthy female individual and neural differentiation
Ma J et al. Induced pluripotent stem cell (iPSC) line (HEBHMUi002-A) from a healthy female individual and neural differentiation. . 2020-01-00. Pubmed ID: 31791011; DOI: 10.1016/j.scr.2019.101669 DHMCi005-AHEBHMUi002-A 2020-01-00 2020-01-00
PubMed: 31791011 DOI: 10.1016/j.scr.2019.101669
Associated cell lines:
- DHMCi005-A
- HEBHMUi002-A
Fuchs NV, Schieck M, Neuenkirch M, Tondera C, Schmitz H, Steinemann D, Göhring G, König R

Induced pluripotent stem cell line (PEIi003-A) derived from an apparently healthy male individual
Fuchs NV et al. Induced pluripotent stem cell line (PEIi003-A) derived from an apparently healthy male individual. . 2020-01-00. Pubmed ID: 31837633; DOI: 10.1016/j.scr.2019.101679 PEIi001-APEIi003-A 2020-01-00 2020-01-00
PubMed: 31837633 DOI: 10.1016/j.scr.2019.101679
Associated cell lines:
- PEIi001-A
- PEIi003-A
Nur Patria Y, Lilianty J, Elefanty AG, Stanley EG, Labonne T, Bateman JF, Lamandé SR

Generation of a SOX9-tdTomato reporter human iPSC line, MCRIi001-A-2, using CRISPR/Cas9 editing
Nur Patria Y et al. Generation of a SOX9-tdTomato reporter human iPSC line, MCRIi001-A-2, using CRISPR/Cas9 editing. . 2020-01-00. Pubmed ID: 31884373; DOI: 10.1016/j.scr.2019.101689 MCRIi001-AMCRIi001-A-2 2020-01-00 2020-01-00
PubMed: 31884373 DOI: 10.1016/j.scr.2019.101689
Associated cell lines:
- MCRIi001-A
- MCRIi001-A-2
Benetó N, Cozar M, Gort L, Pacheco L, Vilageliu L, Grinberg D, Canals I

Generation of two NAGLU-mutated homozygous cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo B syndrome
Benetó N et al. Generation of two NAGLU-mutated homozygous cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo B syndrome. . 2020-01-00. Pubmed ID: 31825816; DOI: 10.1016/j.scr.2019.101668 UBi001-AUBi001-A-3UBi001-A-4 2020-01-00 2020-01-00
PubMed: 31825816 DOI: 10.1016/j.scr.2019.101668
Associated cell lines:
Chen M, Maimaitili M, Buchholdt SH, Jensen UB, Febbraro F, Denham M

Generation of eight human induced pluripotent stem cell lines from Parkinson's disease patients carrying familial mutations
Chen M et al. Generation of eight human induced pluripotent stem cell lines from Parkinson's disease patients carrying familial mutations. . 2020-01-00. Pubmed ID: 31786474; DOI: 10.1016/j.scr.2019.101657 DANi002-CDANi003-HDANi004-ADANi005-ADANi006-FDANi007-ADANi008-FDANi009-C 2020-01-00 2020-01-00
PubMed: 31786474 DOI: 10.1016/j.scr.2019.101657
Associated cell lines:
- DANi002-C
- DANi003-H
- DANi004-A
- DANi005-A
- DANi006-F
- DANi007-A
- DANi008-F
- DANi009-C
Kim YK, Yu JH, Min SH, Park SW

Generation of a GLA knock-out human-induced pluripotent stem cell line, KSBCi002-A-1, using CRISPR/Cas9
Kim YK et al. Generation of a GLA knock-out human-induced pluripotent stem cell line, KSBCi002-A-1, using CRISPR/Cas9. . 2020-01-00. Pubmed ID: 31841972; DOI: 10.1016/j.scr.2019.101676 KSCBi002-AKSCBi002-A-1 2020-01-00 2020-01-00
PubMed: 31841972 DOI: 10.1016/j.scr.2019.101676
Associated cell lines:
- KSCBi002-A
- KSCBi002-A-1
Xiao C, Yu M, Liu J, Wu H, Deng M, Zhang Q, Xiao X

Generation of an integration-free induced pluripotent stem cell line (PUMCHi001-A) from a patient with familial partial lipodystrophy type 2 (FPLD2) carrying a heterozygous p.R349W (c.1045C > T) mutation in the LMNA gene
Xiao C et al. Generation of an integration-free induced pluripotent stem cell line (PUMCHi001-A) from a patient with familial partial lipodystrophy type 2 (FPLD2) carrying a heterozygous p.R349W (c.1045C > T) mutation in the LMNA gene. . 2020-01-00. Pubmed ID: 31794942; DOI: 10.1016/j.scr.2019.101651 PUMCHi001-A 2020-01-00 2020-01-00
PubMed: 31794942 DOI: 10.1016/j.scr.2019.101651
Associated cell lines:
- PUMCHi001-A
Guan J, Liu X, Zhang H, Yang X, Ma Y, Li Y, Gai Z, Liu Y

Reprogramming of human Peripheral Blood Mononuclear Cell (PBMC) from a Chinese patient suffering Duchenne muscular dystrophy to iPSC line (SDQLCHi007-A) carrying deletion of 49-50 exons in the DMD gene
Guan J et al. Reprogramming of human Peripheral Blood Mononuclear Cell (PBMC) from a Chinese patient suffering Duchenne muscular dystrophy to iPSC line (SDQLCHi007-A) carrying deletion of 49-50 exons in the DMD gene. . 2020-01-00. Pubmed ID: 31812072; DOI: 10.1016/j.scr.2019.101666 SDQLCHi007-A 2020-01-00 2020-01-00
PubMed: 31812072 DOI: 10.1016/j.scr.2019.101666
Associated cell lines:
- SDQLCHi007-A
Lu HE, Tsai CL, Chiu IM, Pan YL, Lin YF, Lin HC, Hsu YC

Generation of induced pluripotent stem cells MMCi001-A from a Taiwanese hearing loss patient carrying GJB2 pV37I mutation
Lu HE et al. Generation of induced pluripotent stem cells MMCi001-A from a Taiwanese hearing loss patient carrying GJB2 pV37I mutation. . 2020-01-00. Pubmed ID: 31896484; DOI: 10.1016/j.scr.2019.101692 MMCi001-A 2020-01-00 2020-01-00
PubMed: 31896484 DOI: 10.1016/j.scr.2019.101692
Associated cell lines:
- MMCi001-A
Mura M, Bastaroli F, Corli M, Ginevrino M, Calabrò F, Boni M, Crotti L, Valente EM, Schwartz PJ, Gnecchi M

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1
Mura M et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1. . 2020-01-00. Pubmed ID: 31785541; DOI: 10.1016/j.scr.2019.101658 PSMi006-A 2020-01-00 2020-01-00
PubMed: 31785541 DOI: 10.1016/j.scr.2019.101658
Associated cell lines:
- PSMi006-A
Han S, Zhang YY, Meng MY, Hou ZL, Meng P, Zhao YY, Gao H, Tang J, Liu Z, Yang LL, Jiang LH, Li YX

Generation of human iPSC line from a patient with Tetralogy of Fallot, YAHKMUi001-A, carrying a mutation in TBX1 gene
Han S et al. Generation of human iPSC line from a patient with Tetralogy of Fallot, YAHKMUi001-A, carrying a mutation in TBX1 gene. . 2020-01-00. Pubmed ID: 31869684; DOI: 10.1016/j.scr.2019.101687 YAHKMUi001-A 2020-01-00 2020-01-00
PubMed: 31869684 DOI: 10.1016/j.scr.2019.101687
Associated cell lines:
- YAHKMUi001-A
Lanzi G, Ferraro RM, Masneri S, Piovani G, Barisani C, Sobacchi C, Villa A, Vezzoni P, Giliani S

Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene
Lanzi G et al. Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene. . 2020-01-00. Pubmed ID: 31794943; DOI: 10.1016/j.scr.2019.101660 UNIBSi010-AUNIBSi010-BUNIBSi010-C 2020-01-00 2020-01-00
PubMed: 31794943 DOI: 10.1016/j.scr.2019.101660
Associated cell lines:
Ustyantseva EI, Medvedev SP, Vetchinova AS, Illarioshkin SN, Leonov SV, Zakian SM

Generation of an induced pluripotent stem cell line, ICGi014-A, by reprogramming peripheral blood mononuclear cells from a patient with homozygous D90A mutation in SOD1 causing Amyotrophic lateral sclerosis
Ustyantseva EI et al. Generation of an induced pluripotent stem cell line, ICGi014-A, by reprogramming peripheral blood mononuclear cells from a patient with homozygous D90A mutation in SOD1 causing Amyotrophic lateral sclerosis. . 2020-01-00. Pubmed ID: 31830646; DOI: 10.1016/j.scr.2019.101675 ICGi014-A 2020-01-00 2020-01-00
PubMed: 31830646 DOI: 10.1016/j.scr.2019.101675
Associated cell lines:
- ICGi014-A
Rodríguez-Traver E, Díaz-Guerra E, Rodríguez C, Arenas F, Orera M, Kulisevsky J, Moratalla R, Vicario C

A collection of three integration-free iPSCs derived from old male and female healthy subjects
Rodríguez-Traver E et al. A collection of three integration-free iPSCs derived from old male and female healthy subjects. . 2020-01-00. Pubmed ID: 31794941; DOI: 10.1016/j.scr.2019.101663 ICCSICi012-AICCSICi013-AICCSICi014-A 2020-01-00 2020-01-00
PubMed: 31794941 DOI: 10.1016/j.scr.2019.101663
Associated cell lines:
Khan M, Vaidyanath A, Suresh D, Vaishnav B, Kakrani AL, Patil S, Shiras A

Generation and characterization of three clones (NCCSi007A, NCCSi007B and NCCSi007C) of an integration free induced Pluripotent Stem Cell line from a patient with alcoholic liver cirrhosis of Indian ethnicity
Khan M et al. Generation and characterization of three clones (NCCSi007A, NCCSi007B and NCCSi007C) of an integration free induced Pluripotent Stem Cell line from a patient with alcoholic liver cirrhosis of Indian ethnicity. . 2020-01-00. Pubmed ID: 31862609; DOI: 10.1016/j.scr.2019.101678 NCCSi007-ANCCSi007-BNCCSi007-C 2020-01-00 2020-01-00
PubMed: 31862609 DOI: 10.1016/j.scr.2019.101678
Associated cell lines:
Balez R, Berg T, Bax M, Muñoz SS, Cabral-da-Silva MC, Engel M, Do-Ha D, Stevens CH, Rowe D, Yang S, Blair IP, Ooi L

The mRNA-based reprogramming of fibroblasts from a SOD1^E101G familial amyotrophic lateral sclerosis patient to induced pluripotent stem cell line UOWi007
Balez R et al. The mRNA-based reprogramming of fibroblasts from a SOD1^E101G familial amyotrophic lateral sclerosis patient to induced pluripotent stem cell line UOWi007. . 2020-01-00. Pubmed ID: 32006803; DOI: 10.1016/j.scr.2020.101701 UOWi007-A 2020-01-00 2020-01-00
PubMed: 32006803 DOI: 10.1016/j.scr.2020.101701
Associated cell lines:
- UOWi007-A
Trionfini P, Ciampi O, Romano E, Benigni A, Tomasoni S

Generation of two isogenic knockout PKD2 iPS cell lines, IRFMNi003-A-1 and IRFMNi003-A-2, using CRISPR/Cas9 technology
Trionfini P et al. Generation of two isogenic knockout PKD2 iPS cell lines, IRFMNi003-A-1 and IRFMNi003-A-2, using CRISPR/Cas9 technology. . 2020-01-00. Pubmed ID: 31830647; DOI: 10.1016/j.scr.2019.101667 IRFMNi003-AIRFMNi003-A-1IRFMNi003-A-2IRFMNi001-B 2020-01-00 2020-01-00
PubMed: 31830647 DOI: 10.1016/j.scr.2019.101667
Associated cell lines:
Tannenbaum SE, Singer O, Gil Y, Berman-Zaken Y, Ilouz N, Khaner H, Haimov M, Reubinoff BE

Hadassah, provider of "Regulatory-Ready" pluripotent clinical-grade stem cell banks
Tannenbaum SE et al. Hadassah, provider of "Regulatory-Ready" pluripotent clinical-grade stem cell banks. . 2020-01-00. Pubmed ID: 31838378; DOI: 10.1016/j.scr.2019.101670 HADe008-AHADe009-AHADe010-AHADe011-AHADe012-AHADe013-AHADe007-BHADe008-BHADe009-B 2020-01-00 2020-01-00
PubMed: 31838378 DOI: 10.1016/j.scr.2019.101670
Associated cell lines:
- HADe008-A
- HADe009-A
- HADe010-A
- HADe011-A
- HADe012-A
- HADe013-A
- HADe007-B
- HADe008-B
- HADe009-B
Patterson K, Linask KL, Beers J, Zou J

Generation of two tdTomato reporter induced pluripotent stem cell lines (NHLBIi003-A-1 and NHLBIi003-A-2) by AAVS1 safe harbor gene-editing
Patterson K et al. Generation of two tdTomato reporter induced pluripotent stem cell lines (NHLBIi003-A-1 and NHLBIi003-A-2) by AAVS1 safe harbor gene-editing. . 2020-01-00. Pubmed ID: 31869686; DOI: 10.1016/j.scr.2019.101673; PMC: PMC7046126 TRNDi008-ANHLBIi003-ANHLBIi003-A-1NHLBIi003-A-2 2020-01-00 2020-01-00
PubMed: 31869686 DOI: 10.1016/j.scr.2019.101673
Associated cell lines:
Thayer JA, Awad O, Hegdekar N, Sarkar C, Tesfay H, Burt C, Zeng X, Feldman RA, Lipinski MM

The PARK10 gene USP24 is a negative regulator of autophagy and ULK1 protein stability
Thayer JA et al. The PARK10 gene USP24 is a negative regulator of autophagy and ULK1 protein stability. . 2020-01-00. Pubmed ID: 30957634; DOI: 10.1080/15548627.2019.1598754; PMC: PMC6984603 CRMi003-A-1 2020-01-00 2020-01-00
PubMed: 30957634 DOI: 10.1080/15548627.2019.1598754
Associated cell lines:
- CRMi003-A-1
Prestori F, Moccia F, D'Angelo E

Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA)
Prestori F et al. Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA). . 2019-12-27. Pubmed ID: 31892274; DOI: 10.3390/ijms21010216; PMC: PMC6981692 LUMCi002-ALUMCi003-A 2019-12-27 2019-12-27
PubMed: 31892274 DOI: 10.3390/ijms21010216
Associated cell lines:
- LUMCi002-A
- LUMCi003-A
Neves KB, Harvey AP, Moreton F, Montezano AC, Rios FJ, Alves-Lopes R, Nguyen Dinh Cat A, Rocchicciolli P, Delles C, Joutel A, Muir K, Touyz RM

ER stress and Rho kinase activation underlie the vasculopathy of CADASIL
Neves KB et al. ER stress and Rho kinase activation underlie the vasculopathy of CADASIL. . 2019-12-05. Pubmed ID: 31647781; DOI: 10.1172/jci.insight.131344; PMC: PMC6962020 IDISi001-A 2019-12-05 2019-12-05
PubMed: 31647781 DOI: 10.1172/jci.insight.131344
Associated cell lines:
- IDISi001-A
Sahabian A, Sgodda M, Naujok O, Dettmer R, Dahlmann J, Manstein F, Cantz T, Zweigerdt R, Martin U, Olmer R

Chemically-Defined, Xeno-Free, Scalable Production of hPSC-Derived Definitive Endoderm Aggregates with Multi-Lineage Differentiation Potential
Sahabian A et al. Chemically-Defined, Xeno-Free, Scalable Production of hPSC-Derived Definitive Endoderm Aggregates with Multi-Lineage Differentiation Potential. . 2019-12-04. Pubmed ID: 31817235; DOI: 10.3390/cells8121571; PMC: PMC6953099 MHHi001-AMHHi006-A 2019-12-04 2019-12-04
PubMed: 31817235 DOI: 10.3390/cells8121571
Associated cell lines:
- MHHi001-A
- MHHi006-A
Bendriem RM, Singh S, Aleem AA, Antonetti DA, Ross ME

Tight junction protein occludin regulates progenitor Self-Renewal and survival in developing cortex
Bendriem RM et al. Tight junction protein occludin regulates progenitor Self-Renewal and survival in developing cortex. . 2019-12-03. Pubmed ID: 31794381; DOI: 10.7554/elife.49376; PMC: PMC6890460 WAe009-A 2019-12-03 2019-12-03
PubMed: 31794381 DOI: 10.7554/elife.49376
Associated cell lines:
- WAe009-A
Papapetrou EP

Modeling Leukemia with Human Induced Pluripotent Stem Cells
Papapetrou EP. Modeling Leukemia with Human Induced Pluripotent Stem Cells. . 2019-12-02. Pubmed ID: 31451537; DOI: 10.1101/cshperspect.a034868; PMC: PMC6886454 CHOPi001-A 2019-12-02 2019-12-02
PubMed: 31451537 DOI: 10.1101/cshperspect.a034868
Associated cell lines:
- CHOPi001-A
Pettingill P, Weir GA, Wei T, Wu Y, Flower G, Lalic T, Handel A, Duggal G, Chintawar S, Cheung J, Arunasalam K, Couper E, Haupt LM, Griffiths LR, Bassett A, Cowley SA, Cader MZ

A causal role for TRESK loss of function in migraine mechanisms
Pettingill P et al. A causal role for TRESK loss of function in migraine mechanisms. . 2019-12-01. Pubmed ID: 31742594; DOI: 10.1093/brain/awz342; PMC: PMC6906598 RCi002-A 2019-12-01 2019-12-01
PubMed: 31742594 DOI: 10.1093/brain/awz342
Associated cell lines:
- RCi002-A
Mishra K, Junday K, Wong CMY, Chan AY, Hesselson S, Muller DW, Iismaa SE, Mehta A, Graham RM

Generation of VCCRIi001-A, a human induced pluripotent stem cell line, from a patient with spontaneous coronary artery dissection
Mishra K et al. Generation of VCCRIi001-A, a human induced pluripotent stem cell line, from a patient with spontaneous coronary artery dissection. . 2019-12-00. Pubmed ID: 31707208; DOI: 10.1016/j.scr.2019.101584 VCCRIi001-A 2019-12-00 2019-12-00
PubMed: 31707208 DOI: 10.1016/j.scr.2019.101584
Associated cell lines:
- VCCRIi001-A
Lu L, Jin W, Wang LL

RECQ DNA Helicases and Osteosarcoma
Lu L et al. RECQ DNA Helicases and Osteosarcoma. . 2020-00-00. Pubmed ID: 32767233; DOI: 10.1007/978-3-030-43085-6_3 REGUi003-A 2020-00-00 2020-00-00
PubMed: 32767233 DOI: 10.1007/978-3-030-43085-6_3
Associated cell lines:
- REGUi003-A
Xie L, Huang J, Li X, Dai L, Lin X, Zhang J, Luo J, Zhang W

Generation of a homozygous HDAC6 knockout human embryonic stem cell line by CRISPR/Cas9 editing
Xie L et al. Generation of a homozygous HDAC6 knockout human embryonic stem cell line by CRISPR/Cas9 editing. . 2019-12-00. Pubmed ID: 31775087; DOI: 10.1016/j.scr.2019.101610 WAe009-AWAe009-A-21 2019-12-00 2019-12-00
PubMed: 31775087 DOI: 10.1016/j.scr.2019.101610
Associated cell lines:
- WAe009-A
- WAe009-A-21
Fuchs NV, Schieck M, Neuenkirch M, Tondera C, Schmitz H, des Portes V, Germanaud D, Steinemann D, Göhring G, König R

Induced pluripotent stem cells (iPSCs) derived from a renpenning syndrome patient with c.459_462delAGAG mutation in PQBP1 (PEIi001-A)
Fuchs NV et al. Induced pluripotent stem cells (iPSCs) derived from a renpenning syndrome patient with c.459_462delAGAG mutation in PQBP1 (PEIi001-A). . 2019-12-00. Pubmed ID: 31698189; DOI: 10.1016/j.scr.2019.101592 PEIi001-A 2019-12-00 2019-12-00
PubMed: 31698189 DOI: 10.1016/j.scr.2019.101592
Associated cell lines:
- PEIi001-A
Hayashi Y, Takami M, Matsuo-Takasaki M

Studying Abnormal Chromosomal Diseases Using Patient-Derived Induced Pluripotent Stem Cells
Hayashi Y et al. Studying Abnormal Chromosomal Diseases Using Patient-Derived Induced Pluripotent Stem Cells. . 2020-00-00. Pubmed ID: 32922264; DOI: 10.3389/fncel.2020.00224; PMC: PMC7456929 NTUHi001-A 2020-00-00 2020-00-00
PubMed: 32922264 DOI: 10.3389/fncel.2020.00224
Associated cell lines:
- NTUHi001-A
Lorthongpanich C, Jiamvoraphong N, Supakun P, Damkham N, Terbto P, Waeteekul S, U-Pratya Y, Laowtammathron C, Issaragrisil S

Generation of a WWTR1 mutation induced pluripotent stem cell line, MUSIi012-A-1, using CRISPR/Cas9
Lorthongpanich C et al. Generation of a WWTR1 mutation induced pluripotent stem cell line, MUSIi012-A-1, using CRISPR/Cas9. . 2019-12-00. Pubmed ID: 31677525; DOI: 10.1016/j.scr.2019.101634 MUSIi012-AMUSIi012-A-1 2019-12-00 2019-12-00
PubMed: 31677525 DOI: 10.1016/j.scr.2019.101634
Associated cell lines:
- MUSIi012-A
- MUSIi012-A-1
Völkner C, Peter F, Liedtke M, Krohn S, Lindner I, Murua Escobar H, Cimmaruta C, Lukas J, Hermann A, Frech MJ

Generation of the Niemann-Pick type C2 patient-derived iPSC line AKOSi001-A
Völkner C et al. Generation of the Niemann-Pick type C2 patient-derived iPSC line AKOSi001-A. . 2019-12-00. Pubmed ID: 31669975; DOI: 10.1016/j.scr.2019.101606 AKOSi001-A 2019-12-00 2019-12-00
PubMed: 31669975 DOI: 10.1016/j.scr.2019.101606
Associated cell lines:
- AKOSi001-A
Ferraro RM, Masneri S, Lanzi G, Barisani C, Piovani G, Savio G, Cattalini M, Galli J, Cereda C, Muzi-Falconi M, Orcesi S, Fazzi E, Giliani S

Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B
Ferraro RM et al. Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B. . 2019-12-00. Pubmed ID: 31678772; DOI: 10.1016/j.scr.2019.101620 UNIBSi007-AUNIBSi007-BUNIBSi007-C 2019-12-00 2019-12-00
PubMed: 31678772 DOI: 10.1016/j.scr.2019.101620
Associated cell lines:
Wen MH, Xie X, Tu J, Lee DF, Chen TY

Generation of a genetically modified human embryonic stem cells expressing fluorescence tagged ATOX1
Wen MH et al. Generation of a genetically modified human embryonic stem cells expressing fluorescence tagged ATOX1. . 2019-12-00. Pubmed ID: 31704540; DOI: 10.1016/j.scr.2019.101631; PMC: PMC6939864 WAe001-AWAe001-A-29 2019-12-00 2019-12-00
PubMed: 31704540 DOI: 10.1016/j.scr.2019.101631
Associated cell lines:
- WAe001-A
- WAe001-A-29
Zhang L, Xu M, Liu G, Wu R, Meng S, Xiahou K, Jiang N, Zhang Y, Zhou W

Generation of induced pluripotent stem cell line (IPTi001-A) from a 62-year old sporadic Alzheimer's disease patient with APOE3 (ε3/ε3) genotype
Zhang L et al. Generation of induced pluripotent stem cell line (IPTi001-A) from a 62-year old sporadic Alzheimer's disease patient with APOE3 (ε3/ε3) genotype. . 2019-12-00. Pubmed ID: 31689594; DOI: 10.1016/j.scr.2019.101589 IPTi001-A 2019-12-00 2019-12-00
PubMed: 31689594 DOI: 10.1016/j.scr.2019.101589
Associated cell lines:
- IPTi001-A
Yang X, Liu Y, Zhou T, Zhang H, Dong R, Li Y, Liu N, Liu Y, Gai Z

An induced pluripotent stem cells line (SDQLCHi014-A) derived from urine cells of a patient with ASD and hyperactivity carrying a 303 kb de novo deletion at chr3p26.1 implicating GRM7 gene
Yang X et al. An induced pluripotent stem cells line (SDQLCHi014-A) derived from urine cells of a patient with ASD and hyperactivity carrying a 303 kb de novo deletion at chr3p26.1 implicating GRM7 gene. . 2019-12-00. Pubmed ID: 31707215; DOI: 10.1016/j.scr.2019.101635 SDQLCHi014-A 2019-12-00 2019-12-00
PubMed: 31707215 DOI: 10.1016/j.scr.2019.101635
Associated cell lines:
- SDQLCHi014-A
Frew J, Wu X, Hsiung GY, Feldman HH, Mackenzie IR, Nygaard HB

Generation of an induced pluripotent stem cell line (UBCi001-A) from a presymptomatic individual carrying the R418X progranulin gene mutation
Frew J et al. Generation of an induced pluripotent stem cell line (UBCi001-A) from a presymptomatic individual carrying the R418X progranulin gene mutation. . 2019-12-00. Pubmed ID: 31707213; DOI: 10.1016/j.scr.2019.101582 UBCi001-A 2019-12-00 2019-12-00
PubMed: 31707213 DOI: 10.1016/j.scr.2019.101582
Associated cell lines:
- UBCi001-A
Park H, Han J, Lee Y, Kwak S, Koo SK

Generation of human induced pluripotent stem cells from peripheral blood mononuclear cells of a Senior-Loken syndrome patient
Park H et al. Generation of human induced pluripotent stem cells from peripheral blood mononuclear cells of a Senior-Loken syndrome patient. . 2019-12-00. Pubmed ID: 31734643; DOI: 10.1016/j.scr.2019.101648 KSCBi010-A 2019-12-00 2019-12-00
PubMed: 31734643 DOI: 10.1016/j.scr.2019.101648
Associated cell lines:
- KSCBi010-A
Laowtammathron C, Srisook P, Chingsuwanrote P, Jiamvoraphong N, Waeteekul S, Terbto P, U-Pratya Y, Lorthongpanich C, Issaragrisil S

Derivation of a MUSIi012-A iPSCs from mobilized peripheral blood stem cells
Laowtammathron C et al. Derivation of a MUSIi012-A iPSCs from mobilized peripheral blood stem cells. . 2019-12-00. Pubmed ID: 31669974; DOI: 10.1016/j.scr.2019.101597 MUSIi012-A 2019-12-00 2019-12-00
PubMed: 31669974 DOI: 10.1016/j.scr.2019.101597
Associated cell lines:
- MUSIi012-A
Zhang H, Ma Y, Li X, Yang X, Li Y, Guan J, Dong R, Gai Z, Liu Y

An integration-free iPSC line (SDQLCHi013-A) derived from a patient with maple syrup urine disease carrying compound heterozygote mutations in BCKDHA gene
Zhang H et al. An integration-free iPSC line (SDQLCHi013-A) derived from a patient with maple syrup urine disease carrying compound heterozygote mutations in BCKDHA gene. . 2019-12-00. Pubmed ID: 31775088; DOI: 10.1016/j.scr.2019.101585 SDQLCHi013-A 2019-12-00 2019-12-00
PubMed: 31775088 DOI: 10.1016/j.scr.2019.101585
Associated cell lines:
- SDQLCHi013-A
Bouma MJ, Freund C, IJzerman AP, Boomsma DI, Mummery CL, Raymond K

Lymphoblast-derived hiPS cell lines generated from four individuals of a family of genetically unrelated parents and their female monozygotic twins
Bouma MJ et al. Lymphoblast-derived hiPS cell lines generated from four individuals of a family of genetically unrelated parents and their female monozygotic twins. . 2019-12-00. Pubmed ID: 31734644; DOI: 10.1016/j.scr.2019.101654 LUMCi013-ALUMCi014-ALUMCi015-ALUMCi016-A 2019-12-00 2019-12-00
PubMed: 31734644 DOI: 10.1016/j.scr.2019.101654
Associated cell lines:
Ding Y, Marcó de la Cruz B, Xia Y, Liu M, Lu Y, McInerney V, Krawczyk J, Lynch SA, Howard L, O'Brien T, Gallagher L, Shen S

Derivation of familial iPSC lines from three ASD patients carrying NRXN1α^+/- and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B)
Ding Y et al. Derivation of familial iPSC lines from three ASD patients carrying NRXN1α^+/- and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B). . 2019-12-00. Pubmed ID: 31759289; DOI: 10.1016/j.scr.2019.101653 NUIGi022-ANUIGi023-ANUIGi024-ANUIGi025-ANUIGi026-ANUIGi022-BNUIGi024-BNUIGi025-BNUIGi026-BNUIGi023-B 2019-12-00 2019-12-00
PubMed: 31759289 DOI: 10.1016/j.scr.2019.101653
Associated cell lines:
- NUIGi022-A
- NUIGi023-A
- NUIGi024-A
- NUIGi025-A
- NUIGi026-A
- NUIGi022-B
- NUIGi024-B
- NUIGi025-B
- NUIGi026-B
- NUIGi023-B
Ma Y, Zhang H, Zhang S, Dong R, Yang X, Li Y, Guan J, Gai Z, Liu Y

An integration-free iPSC line (SDQLCHi012-A) derived from a patient with inflammatory bowel disease- 28 carrying compound heterozygote mutations in IL10RA gene
Ma Y et al. An integration-free iPSC line (SDQLCHi012-A) derived from a patient with inflammatory bowel disease- 28 carrying compound heterozygote mutations in IL10RA gene. . 2019-12-00. Pubmed ID: 31648101; DOI: 10.1016/j.scr.2019.101577 SDQLCHi012-A 2019-12-00 2019-12-00
PubMed: 31648101 DOI: 10.1016/j.scr.2019.101577
Associated cell lines:
- SDQLCHi012-A
Fang F, Li Z, Zhao Q, Ye Z, Gu X, Pan F, Li H, Xiang W, Xiong C

Induced Pluripotent Stem Cells Derived From Two Idiopathic Azoospermia Patients Display Compromised Differentiation Potential for Primordial Germ Cell Fate
Fang F et al. Induced Pluripotent Stem Cells Derived From Two Idiopathic Azoospermia Patients Display Compromised Differentiation Potential for Primordial Germ Cell Fate. . 2020-00-00. Pubmed ID: 32671061; DOI: 10.3389/fcell.2020.00432; PMC: PMC7331483 HUSTi001-A 2020-00-00 2020-00-00
PubMed: 32671061 DOI: 10.3389/fcell.2020.00432
Associated cell lines:
- HUSTi001-A
Zhou H, Gong Y, Wu Q, Ye X, Yu B, Lu C, Jiang W, Ye J, Fu Z

Rare Diseases Related with Lipoprotein Metabolism
Zhou H et al. Rare Diseases Related with Lipoprotein Metabolism. . 2020-00-00. Pubmed ID: 32705600; DOI: 10.1007/978-981-15-6082-8_11 TRNDi009-C 2020-00-00 2020-00-00
PubMed: 32705600 DOI: 10.1007/978-981-15-6082-8_11
Associated cell lines:
- TRNDi009-C
Gao X, Gao X, Zhao H, Cui W, Tan M, Deng H

Establishment of induced pluripotent stem cell line (GSPHi001-A) from a 6-year old female with nephrotic syndrome
Gao X et al. Establishment of induced pluripotent stem cell line (GSPHi001-A) from a 6-year old female with nephrotic syndrome. . 2019-12-00. Pubmed ID: 31759290; DOI: 10.1016/j.scr.2019.101661 GSPHi001-A 2019-12-00 2019-12-00
PubMed: 31759290 DOI: 10.1016/j.scr.2019.101661
Associated cell lines:
- GSPHi001-A
Wohlschlegel J, Letellier C, Liu B, Méjécase C, Slembrouck-Brec A, Condroyer C, Michiels C, Sahel JA, Reichman S, Zeitz C, Goureau O, Audo I

Generation of human induced pluripotent stem cell lines from a patient with ITM2B-related retinal dystrophy and a non mutated brother
Wohlschlegel J et al. Generation of human induced pluripotent stem cell lines from a patient with ITM2B-related retinal dystrophy and a non mutated brother. . 2019-12-00. Pubmed ID: 31731182; DOI: 10.1016/j.scr.2019.101625 IDVi003-AIDVi004-AIDVi003-BIDVi003-CIDVi004-B 2019-12-00 2019-12-00
PubMed: 31731182 DOI: 10.1016/j.scr.2019.101625
Associated cell lines:
- IDVi003-A
- IDVi004-A
- IDVi003-B
- IDVi003-C
- IDVi004-B
Angsutararux P, Luanpitpong S, Chingsuwanrote P, Supraditaporn K, Waeteekul S, Terbto P, Lorthongpanich C, Laowtammathron C, U-Pratya Y, Issaragrisil S

Generation of human induced pluripotent stem cell line carrying SCN5AC2204>T Brugada mutation (MUSli009-A-1) introduced by CRISPR/Cas9-mediated genome editing
Angsutararux P et al. Generation of human induced pluripotent stem cell line carrying SCN5AC2204>T Brugada mutation (MUSli009-A-1) introduced by CRISPR/Cas9-mediated genome editing. . 2019-12-00. Pubmed ID: 31677524; DOI: 10.1016/j.scr.2019.101618 MUSIi009-A-1 2019-12-00 2019-12-00
PubMed: 31677524 DOI: 10.1016/j.scr.2019.101618
Associated cell lines:
- MUSIi009-A-1
Sharipova DV, Kovalenko VR, Bairamova EM, Vartanova VA, Grigor'eva EV, Vyatkin YV, Khabarova EA, Rzaev DA, Zakian SM, Medvedev SP

Generation of two iPSC lines, (ICGi015-A and ICGi015-B), by reprogramming peripheral blood mononuclear cells from a patient with Parkinson's disease
Sharipova DV et al. Generation of two iPSC lines, (ICGi015-A and ICGi015-B), by reprogramming peripheral blood mononuclear cells from a patient with Parkinson's disease. . 2019-12-00. Pubmed ID: 31733442; DOI: 10.1016/j.scr.2019.101652 ICGi008-AICGi008-BICGi015-AICGi015-B 2019-12-00 2019-12-00
PubMed: 31733442 DOI: 10.1016/j.scr.2019.101652
Associated cell lines:
Shrestha R, Wen YT, Tsai RK

Generation of hiPSC line TCIERi001-A from normal human epidermal keratinocytes
Shrestha R et al. Generation of hiPSC line TCIERi001-A from normal human epidermal keratinocytes. . 2019-12-00. Pubmed ID: 31683100; DOI: 10.1016/j.scr.2019.101590 TCIERi001-A 2019-12-00 2019-12-00
PubMed: 31683100 DOI: 10.1016/j.scr.2019.101590
Associated cell lines:
- TCIERi001-A
Zanon A, Riekschnitz D, von Troyer M, Volpato C, Picard A, Cantaloni C, Di Segni M, Silipigni R, Pramstaller PP, Hicks AA, Pichler I

Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKNgene
Zanon A et al. Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKNgene. . 2019-12-00. Pubmed ID: 31715428; DOI: 10.1016/j.scr.2019.101624 EURACi005-A 2019-12-00 2019-12-00
PubMed: 31715428 DOI: 10.1016/j.scr.2019.101624
Associated cell lines:
- EURACi005-A
Shindo A, Ishikawa H, Ii Y, Niwa A, Tomimoto H

Clinical Features and Experimental Models of Cerebral Small Vessel Disease
Shindo A et al. Clinical Features and Experimental Models of Cerebral Small Vessel Disease. . 2020-00-00. Pubmed ID: 32431603; DOI: 10.3389/fnagi.2020.00109; PMC: PMC7214616 LUMCi005-A 2020-00-00 2020-00-00
PubMed: 32431603 DOI: 10.3389/fnagi.2020.00109
Associated cell lines:
- LUMCi005-A
Dorszewska J, Kowalska M, Grzegorski T, Dziewulska D, Karmelita-Katulska K, Barciszewska AM, Prendecki M, Gorczyński W, Kozubski W

Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL
Dorszewska J et al. Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL. . 2020-00-00. Pubmed ID: 32337960; DOI: 10.5114/fn.2020.94009 IDISi001-A 2020-00-00 2020-00-00
PubMed: 32337960 DOI: 10.5114/fn.2020.94009
Associated cell lines:
- IDISi001-A
Ge N, Liu M, Ding Y, Krawczyk J, McInerney V, Galvin J, Shen S, Prendiville T, O'Brien T

Generation and characterization of twelve human induced pluripotent stem cell (iPSC) lines from four familial long QT syndrome type 1 (LQT1) patients carrying KCNQ1 c.1201dupC mutation
Ge N et al. Generation and characterization of twelve human induced pluripotent stem cell (iPSC) lines from four familial long QT syndrome type 1 (LQT1) patients carrying KCNQ1 c.1201dupC mutation. . 2019-12-00. Pubmed ID: 31765965; DOI: 10.1016/j.scr.2019.101650 NUIGi008-ANUIGi008-BNUIGi008-CNUIGi009-ANUIGi009-BNUIGi009-CNUIGi010-ANUIGi010-BNUIGi010-CNUIGi011-ANUIGi011-BNUIGi011-C 2019-12-00 2019-12-00
PubMed: 31765965 DOI: 10.1016/j.scr.2019.101650
Associated cell lines:
- NUIGi008-A
- NUIGi008-B
- NUIGi008-C
- NUIGi009-A
- NUIGi009-B
- NUIGi009-C
- NUIGi010-A
- NUIGi010-B
- NUIGi010-C
- NUIGi011-A
- NUIGi011-B
- NUIGi011-C
Yang Y, Wang J, Liang Q, Wang Y, Chen X, Zhang Q, Na S, Liu Y, Yan T, Hang C, Zhu Y

PHACTR1 is associated with disease progression in Chinese Moyamoya disease
Yang Y et al. PHACTR1 is associated with disease progression in Chinese Moyamoya disease. . 2020-00-00. Pubmed ID: 32411507; DOI: 10.7717/peerj.8841; PMC: PMC7207206 CSCRMi001-A 2020-00-00 2020-00-00
PubMed: 32411507 DOI: 10.7717/peerj.8841
Associated cell lines:
- CSCRMi001-A
Dulovic-Mahlow M, Lukomska A, Diaw SH, Balck A, Borsche M, Grütz K, Lenz I, Rudolph F, Lohmann K, Klein C, Seibler P

Generation and characterization of human-derived iPSC lines from three pairs of monozygotic twins discordant for Parkinson's disease
Dulovic-Mahlow M et al. Generation and characterization of human-derived iPSC lines from three pairs of monozygotic twins discordant for Parkinson's disease. . 2019-12-00. Pubmed ID: 31706098; DOI: 10.1016/j.scr.2019.101629 LUEi006-ALUEi007-ALUEi008-ALUEi009-ALUEi010-ALUEi011-A 2019-12-00 2019-12-00
PubMed: 31706098 DOI: 10.1016/j.scr.2019.101629
Associated cell lines:
- LUEi006-A
- LUEi007-A
- LUEi008-A
- LUEi009-A
- LUEi010-A
- LUEi011-A
Schuster J, Laan L, Klar J, Jin Z, Huss M, Korol S, Noraddin FH, Sobol M, Birnir B, Dahl N

Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulated pathways for chromatin remodeling and neurodevelopment
Schuster J et al. Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulated pathways for chromatin remodeling and neurodevelopment. . 2019-12-00. Pubmed ID: 31445158; DOI: 10.1016/j.nbd.2019.104583 UUIGPi006-AUUIGPi007-AUUIGPi008-A 2019-12-00 2019-12-00
PubMed: 31445158 DOI: 10.1016/j.nbd.2019.104583
Associated cell lines:
Wu SS, Li QC, Yin CQ, Xue W, Song CQ

Advances in CRISPR/Cas-based Gene Therapy in Human Genetic Diseases
Wu SS et al. Advances in CRISPR/Cas-based Gene Therapy in Human Genetic Diseases. . 2020-00-00. Pubmed ID: 32292501; DOI: 10.7150/thno.43360; PMC: PMC7150498 MCRIi001-AMCRIi001-A-1 2020-00-00 2020-00-00
PubMed: 32292501 DOI: 10.7150/thno.43360
Associated cell lines:
- MCRIi001-A
- MCRIi001-A-1
Abdul MM, Ibañez DP, Zhao P, Liu H, Zhong X, Li Y, Zhang M, Li W, Li Y, Ward C, Chen S, Wang D, Qin B, Esteban MA, Wang X, Fan W, Luo Z

Generation of an induced pluripotent stem cell line (GIBHi003-A) from a Parkinson's disease patient with mutant PINK1 (p. I368N)
Abdul MM et al. Generation of an induced pluripotent stem cell line (GIBHi003-A) from a Parkinson's disease patient with mutant PINK1 (p. I368N). . 2019-12-00. Pubmed ID: 31778937; DOI: 10.1016/j.scr.2019.101607 GIBHi003-A 2019-12-00 2019-12-00
PubMed: 31778937 DOI: 10.1016/j.scr.2019.101607
Associated cell lines:
- GIBHi003-A
Shnaider TA, Pristyazhnyuk IE, Menzorov AG, Matveeva NM, Nikitina TV, Khabarova AA, Skryabin NA, Kashevarova AA, Lopatkina ME, Nazarenko LP, Lebedev IN, Serov OL

Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability
Shnaider TA et al. Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability. . 2019-12-00. Pubmed ID: 31678775; DOI: 10.1016/j.scr.2019.101591 ICGi009-AICGi013-AICGi013-BICGi009-B 2019-12-00 2019-12-00
PubMed: 31678775 DOI: 10.1016/j.scr.2019.101591
Associated cell lines:
Lito S, Burda P, Baumgartner M, Sloan-Béna F, Táncos Z, Kobolák J, Dinnyés A, Krause KH, Marteyn A

Generation of human induced pluripotent stem cell line UNIGEi001-A from a 2-years old patient with Mucopolysaccharidosis type IH disease
Lito S et al. Generation of human induced pluripotent stem cell line UNIGEi001-A from a 2-years old patient with Mucopolysaccharidosis type IH disease. . 2019-12-00. Pubmed ID: 31678774; DOI: 10.1016/j.scr.2019.101604 UNIGEi001-A 2019-12-00 2019-12-00
PubMed: 31678774 DOI: 10.1016/j.scr.2019.101604
Associated cell lines:
- UNIGEi001-A
Ramme AP, Faust D, Koenig L, Marx U

Generation of four integration-free iPSC lines from related human donors
Ramme AP et al. Generation of four integration-free iPSC lines from related human donors. . 2019-12-00. Pubmed ID: 31704539; DOI: 10.1016/j.scr.2019.101615 TISSUi001-ATISSUi002-ATISSUi003-ATISSUi005-A 2019-12-00 2019-12-00
PubMed: 31704539 DOI: 10.1016/j.scr.2019.101615
Associated cell lines:
Arias-Fuenzalida J, Yu J, Du L, Custodio J, Notarangelo LD, Hammarström L, Pan-Hammarström Q

Generation of human induced pluripotent stem cell lines from patients with selective IgA deficiency
Arias-Fuenzalida J et al. Generation of human induced pluripotent stem cell lines from patients with selective IgA deficiency. . 2019-12-00. Pubmed ID: 31689593; DOI: 10.1016/j.scr.2019.101613 PHAi001-APHAi002-APHAi001-BPHAi002-B 2019-12-00 2019-12-00
PubMed: 31689593 DOI: 10.1016/j.scr.2019.101613
Associated cell lines:
Kim BY, Lee JS, Kim YO, Park MH, Koo SK

Generation of patient-specific induced pluripotent stem cells (KSCBi007-A) derived from a patient with Prader-Willi syndrome retain maternal uniparental disomy (UPD)
Kim BY et al. Generation of patient-specific induced pluripotent stem cells (KSCBi007-A) derived from a patient with Prader-Willi syndrome retain maternal uniparental disomy (UPD). . 2019-12-00. Pubmed ID: 31756696; DOI: 10.1016/j.scr.2019.101647 KSCBi007-A 2019-12-00 2019-12-00
PubMed: 31756696 DOI: 10.1016/j.scr.2019.101647
Associated cell lines:
- KSCBi007-A
Zhang Q, Li Z, Sun H, Zhang S, Zhang J, Wang Y, Fang H, Xu Y

Corrigendum to 'Generation of induced pluripotent stem cell line (ZZUi0012-a) from a patient with Fahr's disease caused by a novel mutation in SLC20A2 gene' [stem cell research volume 35, March 2019, 101,395]
Zhang Q et al. Corrigendum to 'Generation of induced pluripotent stem cell line (ZZUi0012-a) from a patient with Fahr's disease caused by a novel mutation in SLC20A2 gene' [stem cell research volume 35, March 2019, 101,395]. . 2019-12-00. Pubmed ID: 31439445; DOI: 10.1016/j.scr.2019.101507 ZZUi012-A 2019-12-00 2019-12-00
PubMed: 31439445 DOI: 10.1016/j.scr.2019.101507
Associated cell lines:
- ZZUi012-A
Martinez-Turrillas R, Rodriguez-Diaz S, Rodriguez-Marquez P, Martin-Mallo A, Salido E, Beck BB, Prosper F, Rodriguez-Madoz JR

Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene
Martinez-Turrillas R et al. Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene. . 2019-12-00. Pubmed ID: 31715429; DOI: 10.1016/j.scr.2019.101626 CIMAi001-A 2019-12-00 2019-12-00
PubMed: 31715429 DOI: 10.1016/j.scr.2019.101626
Associated cell lines:
- CIMAi001-A
Liu Z, Yao M, Yao H, Hu G, Qin B

Generation of Rybp homozygous knockout murine ES cell line GIBHe001-A-1 by using CRISPR/Cas9 technology
Liu Z et al. Generation of Rybp homozygous knockout murine ES cell line GIBHe001-A-1 by using CRISPR/Cas9 technology. . 2019-12-00. Pubmed ID: 31794887; DOI: 10.1016/j.scr.2019.101638 GIBHe001-A 2019-12-00 2019-12-00
PubMed: 31794887 DOI: 10.1016/j.scr.2019.101638
Associated cell lines:
- GIBHe001-A
Jelinkova S, Vilotic A, Pribyl J, Aimond F, Salykin A, Acimovic I, Pesl M, Caluori G, Klimovic S, Urban T, Dobrovolna H, Soska V, Skladal P, Lacampagne A, Dvorak P, Meli AC, Rotrekl V

DMD Pluripotent Stem Cell Derived Cardiac Cells Recapitulate in vitro Human Cardiac Pathophysiology
Jelinkova S et al. DMD Pluripotent Stem Cell Derived Cardiac Cells Recapitulate in vitro Human Cardiac Pathophysiology. . 2020-00-00. Pubmed ID: 32656189; DOI: 10.3389/fbioe.2020.00535; PMC: PMC7325914 MUNIe005-AMUNIe007-AMUNIi001-AMUNIi003-A 2020-00-00 2020-00-00
PubMed: 32656189 DOI: 10.3389/fbioe.2020.00535
Associated cell lines:
Zhang J, Wei L, Chen D, Feng L, Wu C, Wang R, Li X

Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi003-A) from a Wilson's disease patient harboring a homozygous R778L mutation in ATP7B gene
Zhang J et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi003-A) from a Wilson's disease patient harboring a homozygous R778L mutation in ATP7B gene. . 2019-12-00. Pubmed ID: 31783295; DOI: 10.1016/j.scr.2019.101664 ZZUNEUi003-A 2019-12-00 2019-12-00
PubMed: 31783295 DOI: 10.1016/j.scr.2019.101664
Associated cell lines:
- ZZUNEUi003-A
Tofoli FA, Chien HF, Barbosa ER, Pereira LV

Generation of 5 hiPSC lines derived from three unrelated idiopathic Parkinson disease patients and two unrelated healthy control individuals
Tofoli FA et al. Generation of 5 hiPSC lines derived from three unrelated idiopathic Parkinson disease patients and two unrelated healthy control individuals. . 2019-12-00. Pubmed ID: 31710912; DOI: 10.1016/j.scr.2019.101640 LANCEi014-ALANCEi015-ALANCEi016-ALANCEi017-ALANCEi018-A 2019-12-00 2019-12-00
PubMed: 31710912 DOI: 10.1016/j.scr.2019.101640
Associated cell lines:
Yamasaki AE, King NE, Matsui H, Jepsen K, Panopoulos AD

Two iPSC lines generated from the bone marrow of a relapsed/refractory AML patient display normal karyotypes and myeloid differentiation potential
Yamasaki AE et al. Two iPSC lines generated from the bone marrow of a relapsed/refractory AML patient display normal karyotypes and myeloid differentiation potential. . 2019-12-00. Pubmed ID: 31739201; DOI: 10.1016/j.scr.2019.101587 NDi002-ANDi002-B 2019-12-00 2019-12-00
PubMed: 31739201 DOI: 10.1016/j.scr.2019.101587
Associated cell lines:
- NDi002-A
- NDi002-B
Masneri S, Ferraro RM, Lanzi G, Piovani G, Mori L, Barisani C, Moratto D, Plebani A, Badolato R, Soresina A, Giliani S

Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene
Masneri S et al. Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene. . 2019-12-00. Pubmed ID: 31669783; DOI: 10.1016/j.scr.2019.101596 UNIBSi008-AUNIBSi008-BUNIBSi008-C 2019-12-00 2019-12-00
PubMed: 31669783 DOI: 10.1016/j.scr.2019.101596
Associated cell lines:
Hey CAB, Larsen LJ, Tümer Z, Brøndum-Nielsen K, Grønskov K, Hjortshøj TD, Møller LB

Generation and characterization of three isogenic induced pluripotent stem cell lines from a patient with Bardet-Biedl syndrome and homozygous for the BBS5 variant
Hey CAB et al. Generation and characterization of three isogenic induced pluripotent stem cell lines from a patient with Bardet-Biedl syndrome and homozygous for the BBS5 variant. . 2019-12-00. Pubmed ID: 31760295; DOI: 10.1016/j.scr.2019.101594 KCi003-AKCi003-BKCi003-C 2019-12-00 2019-12-00
PubMed: 31760295 DOI: 10.1016/j.scr.2019.101594
Associated cell lines:
Sanchez-Duffhues G, Mikkers H, de Jong D, Szuhai K, de Vries TJ, Freund C, Bravenboer N, van Es RJJ, Netelenbos JC, Goumans MJ, Eekhoff EMW, Ten Dijke P

Generation of Fibrodysplasia ossificans progressiva and control integration free iPSC lines from periodontal ligament fibroblasts
Sanchez-Duffhues G et al. Generation of Fibrodysplasia ossificans progressiva and control integration free iPSC lines from periodontal ligament fibroblasts. . 2019-12-00. Pubmed ID: 31733439; DOI: 10.1016/j.scr.2019.101639 LUMCi009-ALUMCi010-A 2019-12-00 2019-12-00
PubMed: 31733439 DOI: 10.1016/j.scr.2019.101639
Associated cell lines:
- LUMCi009-A
- LUMCi010-A
Zhao M, Chen YJ, Wang MW, Lin XH, Dong EL, Chen WJ, Wang N, Lin X

Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia
Zhao M et al. Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia. . 2019-12-00. Pubmed ID: 31630374; DOI: 10.1007/s40291-019-00426-w FJMUi001-A 2019-12-00 2019-12-00
PubMed: 31630374 DOI: 10.1007/s40291-019-00426-w
Associated cell lines:
- FJMUi001-A
Martins GLS, Paredes BD, Sampaio GLA, Nonaka CKV, da Silva KN, Allahdadi KJ, França LSA, Soares MBP, Dos Santos RR, Souza BSF

Generation of human iPS cell line CBTCi001-A from dermal fibroblasts obtained from a healthy donor
Martins GLS et al. Generation of human iPS cell line CBTCi001-A from dermal fibroblasts obtained from a healthy donor. . 2019-12-00. Pubmed ID: 31706097; DOI: 10.1016/j.scr.2019.101630 CBTCi001-A 2019-12-00 2019-12-00
PubMed: 31706097 DOI: 10.1016/j.scr.2019.101630
Associated cell lines:
- CBTCi001-A
Hilderink S, Devalla HD, Bosch L, Wilders R, Verkerk AO

Ultrarapid Delayed Rectifier K⁺ Channelopathies in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Hilderink S et al. Ultrarapid Delayed Rectifier K⁺ Channelopathies in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. . 2020-00-00. Pubmed ID: 32850774; DOI: 10.3389/fcell.2020.00536; PMC: PMC7399090 LUMCi004-A 2020-00-00 2020-00-00
PubMed: 32850774 DOI: 10.3389/fcell.2020.00536
Associated cell lines:
- LUMCi004-A
Benetó N, Cozar M, García-Morant M, Creus-Bachiller E, Vilageliu L, Grinberg D, Canals I

Generation of two compound heterozygous HGSNAT-mutated lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo C syndrome
Benetó N et al. Generation of two compound heterozygous HGSNAT-mutated lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo C syndrome. . 2019-12-00. Pubmed ID: 31731183; DOI: 10.1016/j.scr.2019.101616 UBi001-AUBi001-A-1UBi001-A-2 2019-12-00 2019-12-00
PubMed: 31731183 DOI: 10.1016/j.scr.2019.101616
Associated cell lines:
Si L, Yang R, Liu J, Dong Y, Zhang H, Xu X

Generation of two ERF gene knockout human embryonic stem cell lines using CRISPR/Cas9 system
Si L et al. Generation of two ERF gene knockout human embryonic stem cell lines using CRISPR/Cas9 system. . 2019-12-00. Pubmed ID: 31743839; DOI: 10.1016/j.scr.2019.101644 WAe001-A-33WAe001-A-34 2019-12-00 2019-12-00
PubMed: 31743839 DOI: 10.1016/j.scr.2019.101644
Associated cell lines:
- WAe001-A-33
- WAe001-A-34
Bakhti M, Scheibner K, Tritschler S, Bastidas-Ponce A, Tarquis-Medina M, Theis FJ, Lickert H

Establishment of a high-resolution 3D modeling system for studying pancreatic epithelial cell biology in vitro
Bakhti M et al. Establishment of a high-resolution 3D modeling system for studying pancreatic epithelial cell biology in vitro. . 2019-12-00. Pubmed ID: 31767167; DOI: 10.1016/j.molmet.2019.09.005; PMC: PMC6812400 HMGUi001-A 2019-12-00 2019-12-00
PubMed: 31767167 DOI: 10.1016/j.molmet.2019.09.005
Associated cell lines:
- HMGUi001-A
Guan J, Liu X, Zhang H, Lv Y, Wang X, Yang X, Ma Y, Liu Q, Liu Y, Sun W

Generation of an iPSC line (SDQLCHi015-A) from peripheral blood mononuclear cells of a patient with mental retardation type 15 carrying c.1007_1011del, p.(Ile336fs) in CUL4B gene
Guan J et al. Generation of an iPSC line (SDQLCHi015-A) from peripheral blood mononuclear cells of a patient with mental retardation type 15 carrying c.1007_1011del, p.(Ile336fs) in CUL4B gene. . 2019-12-00. Pubmed ID: 31678776; DOI: 10.1016/j.scr.2019.101628 SDQLCHi015-A 2019-12-00 2019-12-00
PubMed: 31678776 DOI: 10.1016/j.scr.2019.101628
Associated cell lines:
- SDQLCHi015-A
Zhang M, Ibañez DP, Fan W, Liu H, Zhong X, Wang X, Li Y, Md Abdul M, Li W, Li Y, Ward C, Chen S, Wang D, Qin B, Esteban MA, Zhao P, Luo Z

Generation of a PARK2 homozygous knockout induced pluripotent stem cell line (GIBHi002-A-1) with two common isoforms abolished
Zhang M et al. Generation of a PARK2 homozygous knockout induced pluripotent stem cell line (GIBHi002-A-1) with two common isoforms abolished. . 2019-12-00. Pubmed ID: 31698191; DOI: 10.1016/j.scr.2019.101602 GIBHi002-AGIBHi002-A-1 2019-12-00 2019-12-00
PubMed: 31698191 DOI: 10.1016/j.scr.2019.101602
Associated cell lines:
- GIBHi002-A
- GIBHi002-A-1
Kim BY, Ko JM, Park MH, Koo SK

Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation
Kim BY et al. Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation. . 2019-12-00. Pubmed ID: 31715426; DOI: 10.1016/j.scr.2019.101622 KSCBi006-A 2019-12-00 2019-12-00
PubMed: 31715426 DOI: 10.1016/j.scr.2019.101622
Associated cell lines:
- KSCBi006-A
Lee Y, Choi HY, Kwon A, Park H, Park MH, Kim JW, Kim MJ, Kim YO, Kwak S, Koo SK

Generation of a PDX1-EGFP reporter human induced pluripotent stem cell line, KSCBi005-A-3, using the CRISPR/Cas9 system
Lee Y et al. Generation of a PDX1-EGFP reporter human induced pluripotent stem cell line, KSCBi005-A-3, using the CRISPR/Cas9 system. . 2019-12-00. Pubmed ID: 31683099; DOI: 10.1016/j.scr.2019.101632 KSCBi005-AKSCBi005-A-3 2019-12-00 2019-12-00
PubMed: 31683099 DOI: 10.1016/j.scr.2019.101632
Associated cell lines:
- KSCBi005-A
- KSCBi005-A-3
Leitner D, Ramamoorthy M, Dejosez M, Zwaka TP

Immature mDA neurons ameliorate motor deficits in a 6-OHDA Parkinson's disease mouse model and are functional after cryopreservation
Leitner D et al. Immature mDA neurons ameliorate motor deficits in a 6-OHDA Parkinson's disease mouse model and are functional after cryopreservation. . 2019-12-00. Pubmed ID: 31731178; DOI: 10.1016/j.scr.2019.101617 ISMMSi003-A 2019-12-00 2019-12-00
PubMed: 31731178 DOI: 10.1016/j.scr.2019.101617
Associated cell lines:
- ISMMSi003-A
Zhang Y, Li A, Wang J, Wang G, Wang D

Generation of induced pluripotent stem cells (iPSCs) from an infant with Pompe disease carrying with compound mutations of R608X and E888X in GAA gene
Zhang Y et al. Generation of induced pluripotent stem cells (iPSCs) from an infant with Pompe disease carrying with compound mutations of R608X and E888X in GAA gene. . 2019-12-00. Pubmed ID: 31743840; DOI: 10.1016/j.scr.2019.101621 XACHi002-A 2019-12-00 2019-12-00
PubMed: 31743840 DOI: 10.1016/j.scr.2019.101621
Associated cell lines:
- XACHi002-A
Díaz-Guerra E, Rodríguez-Traver E, Moreno-Jiménez EP, de Rojas I, Rodríguez C, Orera M, Hernández I, Ruiz A, Vicario C

An integration-free iPSC line, ICCSICi007-A, derived from a female Alzheimer's disease patient with the APOE-ε4/ε4 alleles
Díaz-Guerra E et al. An integration-free iPSC line, ICCSICi007-A, derived from a female Alzheimer's disease patient with the APOE-ε4/ε4 alleles. . 2019-12-00. Pubmed ID: 31698192; DOI: 10.1016/j.scr.2019.101588 ICCSICi007-A 2019-12-00 2019-12-00
PubMed: 31698192 DOI: 10.1016/j.scr.2019.101588
Associated cell lines:
- ICCSICi007-A
Lamolda M, Montes R, Simón I, Perales S, Martínez-Navajas G, Lopez-Onieva L, Ríos-Pelegrina R, Del Moral RG, Griñan-Lison C, Marchal JA, Lozano ML, Ramos-Mejia V, Rivera J, Bastida JM, Real PJ

GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant
Lamolda M et al. GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant. . 2019-12-00. Pubmed ID: 31698193; DOI: 10.1016/j.scr.2019.101603 GENYOi004-AGENYOi005-A 2019-12-00 2019-12-00
PubMed: 31698193 DOI: 10.1016/j.scr.2019.101603
Associated cell lines:
- GENYOi004-A
- GENYOi005-A
Kolagar TA, Farzaneh M, Nikkar N, Khoshnam SE

Human Pluripotent Stem Cells in Neurodegenerative Diseases: Potentials, Advances and Limitations
Kolagar TA et al. Human Pluripotent Stem Cells in Neurodegenerative Diseases: Potentials, Advances and Limitations. . 2020-00-00. Pubmed ID: 31441732; DOI: 10.2174/1574888x14666190823142911 CSSi004-A 2020-00-00 2020-00-00
PubMed: 31441732 DOI: 10.2174/1574888x14666190823142911
Associated cell lines:
- CSSi004-A
Arias-Fuenzalida J, Yu J, Abolhassani H, Du L, Custodio J, Pan-Hammarström Q

Generation of a human induced pluripotent stem cell line (PHAi003) from a primary immunodeficient patient with CD70 mutation
Arias-Fuenzalida J et al. Generation of a human induced pluripotent stem cell line (PHAi003) from a primary immunodeficient patient with CD70 mutation. . 2019-12-00. Pubmed ID: 31678777; DOI: 10.1016/j.scr.2019.101612 PHAi003-B 2019-12-00 2019-12-00
PubMed: 31678777 DOI: 10.1016/j.scr.2019.101612
Associated cell lines:
- PHAi003-B
Masneri S, Lanzi G, Ferraro RM, Barisani C, Piovani G, Savio G, Cattalini M, Galli J, Cereda C, Muzi-Falconi M, Orcesi S, Fazzi E, Giliani S

Generation of three isogenic induced Pluripotent Stem Cell lines (iPSCs) from fibroblasts of a patient with Aicardi Goutières Syndrome carrying a c.2471G>A dominant mutation in IFIH1 gene
Masneri S et al. Generation of three isogenic induced Pluripotent Stem Cell lines (iPSCs) from fibroblasts of a patient with Aicardi Goutières Syndrome carrying a c.2471G>A dominant mutation in IFIH1 gene. . 2019-12-00. Pubmed ID: 31698194; DOI: 10.1016/j.scr.2019.101623 UNIBSi009-AUNIBSi009-BUNIBSi009-C 2019-12-00 2019-12-00
PubMed: 31698194 DOI: 10.1016/j.scr.2019.101623
Associated cell lines:
Ruiz JP, Chen G, Haro Mora JJ, Keyvanfar K, Liu C, Zou J, Beers J, Bloomer H, Qanash H, Uchida N, Tisdale JF, Boehm M, Larochelle A

Robust generation of erythroid and multilineage hematopoietic progenitors from human iPSCs using a scalable monolayer culture system
Ruiz JP et al. Robust generation of erythroid and multilineage hematopoietic progenitors from human iPSCs using a scalable monolayer culture system. . 2019-12-00. Pubmed ID: 31710911; DOI: 10.1016/j.scr.2019.101600; PMC: PMC6953424 TRNDi009-CRTIBDi001-A 2019-12-00 2019-12-00
PubMed: 31710911 DOI: 10.1016/j.scr.2019.101600
Associated cell lines:
- TRNDi009-C
- RTIBDi001-A
Wang AYL, Loh CYY

Episomal Induced Pluripotent Stem Cells: Functional and Potential Therapeutic Applications
Wang AYL et al. Episomal Induced Pluripotent Stem Cells: Functional and Potential Therapeutic Applications. . 2019-12-00. Pubmed ID: 31722555; DOI: 10.1177/0963689719886534; PMC: PMC7016470 UNIPDi001-ATUSMi001-ANCCSi002-ATUSMi003-AUNIPDi003-ATUSMi004-ATUSMi005-AMUSIi004-AHIHCNi002-AHIHCNi003-AFUi002-AIBPi002-AIMEDEAi004-AIMEDEAi004-BCSi001-ANCCSi004-ATUSMi007-ATUSMi008-A 2019-12-00 2019-12-00
PubMed: 31722555 DOI: 10.1177/0963689719886534
Associated cell lines:
- UNIPDi001-A
- TUSMi001-A
- NCCSi002-A
- TUSMi003-A
- UNIPDi003-A
- TUSMi004-A
- TUSMi005-A
- MUSIi004-A
- HIHCNi002-A
- HIHCNi003-A
- FUi002-A
- IBPi002-A
- IMEDEAi004-A
- IMEDEAi004-B
- CSi001-A
- NCCSi004-A
- TUSMi007-A
- TUSMi008-A
So S, Lee Y, Choi J, Kang S, Lee JY, Hwang J, Shin J, Dutton JR, Seo EJ, Lee BH, Kim CJ, Mitalipov S, Oh SJ, Kang E

The Rho-associated kinase inhibitor fasudil can replace Y-27632 for use in human pluripotent stem cell research
So S et al. The Rho-associated kinase inhibitor fasudil can replace Y-27632 for use in human pluripotent stem cell research. . 2020-00-00. Pubmed ID: 32396545; DOI: 10.1371/journal.pone.0233057; PMC: PMC7217428 VRFi001-A 2020-00-00 2020-00-00
PubMed: 32396545 DOI: 10.1371/journal.pone.0233057
Associated cell lines:
- VRFi001-A
Patterson K, Beers J, Linask KL, Lin Y, Hassanzadeh S, Sack MN, Zou J

Generation of two induced pluripotent stem cell lines (NHLBIi001-A and NHLBIi001-B) from a healthy Caucasian female volunteer with normal cardiac function
Patterson K et al. Generation of two induced pluripotent stem cell lines (NHLBIi001-A and NHLBIi001-B) from a healthy Caucasian female volunteer with normal cardiac function. . 2019-12-00. Pubmed ID: 31733441; DOI: 10.1016/j.scr.2019.101627; PMC: PMC6938693 TRNDi008-ANHLBIi001-ANHLBIi001-B 2019-12-00 2019-12-00
PubMed: 31733441 DOI: 10.1016/j.scr.2019.101627
Associated cell lines:
Wang Y, Sun H, Wang Z, Yue Y, Zhang R, Yang J, Liu Y, Liu H, Zhang Q, Zhang S, Zhang J, Xu Y, Shi C

Generation of induced pluripotent stem cell line (ZZUi0014-A) from a patient with spinocerebellar ataxia type 3
Wang Y et al. Generation of induced pluripotent stem cell line (ZZUi0014-A) from a patient with spinocerebellar ataxia type 3. . 2019-12-00. Pubmed ID: 31639609; DOI: 10.1016/j.scr.2019.101564 ZZUi014-A 2019-12-00 2019-12-00
PubMed: 31639609 DOI: 10.1016/j.scr.2019.101564
Associated cell lines:
- ZZUi014-A
Ferraro RM, Lanzi G, Masneri S, Barisani C, Piovani G, Savio G, Cattalini M, Galli J, Cereda C, Muzi-Falconi M, Orcesi S, Fazzi E, Giliani S

Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1
Ferraro RM et al. Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1. . 2019-12-00. Pubmed ID: 31644995; DOI: 10.1016/j.scr.2019.101580 UNIBSi006-AUNIBSi006-BUNIBSi006-CUNIBSi007-BUNIBSi007-C 2019-12-00 2019-12-00
PubMed: 31644995 DOI: 10.1016/j.scr.2019.101580
Associated cell lines:
Jing Y, Zhou Y, Wang C, Liu J, Guo Y, Mao S, Chan HF, Tang S, Chen J

Establishment of a non-integrate iPS cell line CSUASOi002-A, from urine-derived cells of a female patient with macular corneal dystrophy carrying compound heterozygous CHST6 mutations
Jing Y et al. Establishment of a non-integrate iPS cell line CSUASOi002-A, from urine-derived cells of a female patient with macular corneal dystrophy carrying compound heterozygous CHST6 mutations. . 2019-12-00. Pubmed ID: 31669782; DOI: 10.1016/j.scr.2019.101598 CSUASOi002-A 2019-12-00 2019-12-00
PubMed: 31669782 DOI: 10.1016/j.scr.2019.101598
Associated cell lines:
- CSUASOi002-A
Jin H, Yu Z, Navarengom K, Liu Y, Dmitrieva N, Hsu AP, Schwartzbeck R, Cudrici C, Ferrante EA, Yang D, Holland SM, Freeman AF, Boehm M, Chen G

Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutation
Jin H et al. Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutation. . 2019-12-00. Pubmed ID: 31707214; DOI: 10.1016/j.scr.2019.101586; PMC: PMC6957122 NIHTVBi011-ANIHTVBi012-ANIHTVBi013-A 2019-12-00 2019-12-00
PubMed: 31707214 DOI: 10.1016/j.scr.2019.101586
Associated cell lines:
Duarte AJ, Ribeiro D, Santos R, Moreira L, Bragança J, Amaral O

Induced pluripotent stem cell line (INSAi001-A) from a Gaucher disease type 3 patient compound heterozygote for mutations in the GBA1 gene
Duarte AJ et al. Induced pluripotent stem cell line (INSAi001-A) from a Gaucher disease type 3 patient compound heterozygote for mutations in the GBA1 gene. . 2019-12-00. Pubmed ID: 31678773; DOI: 10.1016/j.scr.2019.101595 INSAi001-A 2019-12-00 2019-12-00
PubMed: 31678773 DOI: 10.1016/j.scr.2019.101595
Associated cell lines:
- INSAi001-A
Sharma R, Smits IPM, De La Vega L, Lee C, Willerth SM

3D Bioprinting Pluripotent Stem Cell Derived Neural Tissues Using a Novel Fibrin Bioink Containing Drug Releasing Microspheres
Sharma R et al. 3D Bioprinting Pluripotent Stem Cell Derived Neural Tissues Using a Novel Fibrin Bioink Containing Drug Releasing Microspheres. . 2020-00-00. Pubmed ID: 32117936; DOI: 10.3389/fbioe.2020.00057; PMC: PMC7026266 IBMSi012-A 2020-00-00 2020-00-00
PubMed: 32117936 DOI: 10.3389/fbioe.2020.00057
Associated cell lines:
- IBMSi012-A
Slanzi A, Iannoto G, Rossi B, Zenaro E, Constantin G

In vitro Models of Neurodegenerative Diseases
Slanzi A et al. In vitro Models of Neurodegenerative Diseases. . 2020-00-00. Pubmed ID: 32528949; DOI: 10.3389/fcell.2020.00328; PMC: PMC7247860 CSSi004-ACHOPi002-ACHOPi003-ANUIGi043-ANUIGi043-BNUIGi043-CNUIGi044-ANUIGi044-BNUIGi044-C 2020-00-00 2020-00-00
PubMed: 32528949 DOI: 10.3389/fcell.2020.00328
Associated cell lines:
- CSSi004-A
- CHOPi002-A
- CHOPi003-A
- NUIGi043-A
- NUIGi043-B
- NUIGi043-C
- NUIGi044-A
- NUIGi044-B
- NUIGi044-C
Seshagiri PB, Vani V

Research on early mammalian development in India
Seshagiri PB et al. Research on early mammalian development in India. . 2020-00-00. Pubmed ID: 32658999; DOI: 10.1387/ijdb.190189ps CSCRi005-A 2020-00-00 2020-00-00
PubMed: 32658999 DOI: 10.1387/ijdb.190189ps
Associated cell lines:
- CSCRi005-A
Zhang H, Ma Y, Yu S, Yang X, Li Y, Guan J, Dong R, Gai Z, Liu Y

Establishment of a human iPSC line (SDQLCHi010-A) from a patient with optic nerve malformation carrying a heterozygous mutation in PAX6 gene
Zhang H et al. Establishment of a human iPSC line (SDQLCHi010-A) from a patient with optic nerve malformation carrying a heterozygous mutation in PAX6 gene. . 2019-12-00. Pubmed ID: 31707209; DOI: 10.1016/j.scr.2019.101611 SDQLCHi003-ASDQLCHi010-A 2019-12-00 2019-12-00
PubMed: 31707209 DOI: 10.1016/j.scr.2019.101611
Associated cell lines:
- SDQLCHi003-A
- SDQLCHi010-A
Lu C, Sanjana NE

Generation of a knock-in MAP2-tdTomato reporter human embryonic stem cell line with inducible expression of NEUROG2/1 (NYGCe001-A)
Lu C et al. Generation of a knock-in MAP2-tdTomato reporter human embryonic stem cell line with inducible expression of NEUROG2/1 (NYGCe001-A). . 2019-12-00. Pubmed ID: 31707212; DOI: 10.1016/j.scr.2019.101643; PMC: PMC6919562 NYGCe001-A 2019-12-00 2019-12-00
PubMed: 31707212 DOI: 10.1016/j.scr.2019.101643
Associated cell lines:
- NYGCe001-A
Überbacher C, Obergasteiger J, Volta M, Venezia S, Müller S, Pesce I, Pizzi S, Lamonaca G, Picard A, Cattelan G, Malpeli G, Zoli M, Beccano-Kelly D, Flynn R, Wade-Martins R, Pramstaller PP, Hicks AA, Cowley SA, Corti C

Application of CRISPR/Cas9 editing and digital droplet PCR in human iPSCs to generate novel knock-in reporter lines to visualize dopaminergic neurons
Überbacher C et al. Application of CRISPR/Cas9 editing and digital droplet PCR in human iPSCs to generate novel knock-in reporter lines to visualize dopaminergic neurons. . 2019-12-00. Pubmed ID: 31733438; DOI: 10.1016/j.scr.2019.101656; PMC: PMC7322529 STBCi026-CSTBCi063-A 2019-12-00 2019-12-00
PubMed: 31733438 DOI: 10.1016/j.scr.2019.101656
Associated cell lines:
- STBCi026-C
- STBCi063-A
Goversen B, Jonsson MK, van den Heuvel NH, Rijken R, Vos MA, van Veen TA, de Boer TP

The influence of hERG1a and hERG1b isoforms on drug safety screening in iPSC-CMs
Goversen B et al. The influence of hERG1a and hERG1b isoforms on drug safety screening in iPSC-CMs. . 2019-12-00. Pubmed ID: 30826123; DOI: 10.1016/j.pbiomolbio.2019.02.003 PSMi003-A 2019-12-00 2019-12-00
PubMed: 30826123 DOI: 10.1016/j.pbiomolbio.2019.02.003
Associated cell lines:
- PSMi003-A
Lai X, Jiang B, Liu J, Wang Y, Wu G

Generation of an induced pluripotent stem cell line (SYSUi002-A) from a patient with coronary slow flow phenomenon
Lai X et al. Generation of an induced pluripotent stem cell line (SYSUi002-A) from a patient with coronary slow flow phenomenon. . 2019-12-00. Pubmed ID: 31783296; DOI: 10.1016/j.scr.2019.101646 SYSUi002-A 2019-12-00 2019-12-00
PubMed: 31783296 DOI: 10.1016/j.scr.2019.101646
Associated cell lines:
- SYSUi002-A
Valenti MT, Serena M, Carbonare LD, Zipeto D

CRISPR/Cas system: An emerging technology in stem cell research
Valenti MT et al. CRISPR/Cas system: An emerging technology in stem cell research. . 2019-11-26. Pubmed ID: 31768221; DOI: 10.4252/wjsc.v11.i11.937; PMC: PMC6851009 CSSi002-A 2019-11-26 2019-11-26
PubMed: 31768221 DOI: 10.4252/wjsc.v11.i11.937
Associated cell lines:
- CSSi002-A
Heshusius S, Heideveld E, Burger P, Thiel-Valkhof M, Sellink E, Varga E, Ovchynnikova E, Visser A, Martens JHA, von Lindern M, van den Akker E

Large-scale in vitro production of red blood cells from human peripheral blood mononuclear cells
Heshusius S et al. Large-scale in vitro production of red blood cells from human peripheral blood mononuclear cells. . 2019-11-12. Pubmed ID: 31698463; DOI: 10.1182/bloodadvances.2019000689; PMC: PMC6855111 SANi005-A 2019-11-12 2019-11-12
PubMed: 31698463 DOI: 10.1182/bloodadvances.2019000689
Associated cell lines:
- SANi005-A
Brodehl A, Pour Hakimi SA, Stanasiuk C, Ratnavadivel S, Hendig D, Gaertner A, Gerull B, Gummert J, Paluszkiewicz L, Milting H

Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect
Brodehl A et al. Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect. . 2019-11-11. Pubmed ID: 31718026; DOI: 10.3390/genes10110918; PMC: PMC6896098 UKKi011-A 2019-11-11 2019-11-11
PubMed: 31718026 DOI: 10.3390/genes10110918
Associated cell lines:
- UKKi011-A
El-Battrawy I, Müller J, Zhao Z, Cyganek L, Zhong R, Zhang F, Kleinsorge M, Lan H, Li X, Xu Q, Huang M, Liao Z, Moscu-Gregor A, Albers S, Dinkel H, Lang S, Diecke S, Zimmermann W, Utikal J, Wieland T, Borggrefe M, Zhou X, Akin I.

Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
El-Battrawy I et al. Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes. . 2019-11-01. UMGi124-AUMGi128-AUMGi014-B 2019-11-01 2019-11-01
Associated cell lines:
Huang CY, Liu CL, Ting CY, Chiu YT, Cheng YC, Nicholson MW, Hsieh PCH

Human iPSC banking: barriers and opportunities
Huang CY et al. Human iPSC banking: barriers and opportunities. . 2019-10-28. Pubmed ID: 31660969; DOI: 10.1186/s12929-019-0578-x; PMC: PMC6819403 KSCBi003-A 2019-10-28 2019-10-28
PubMed: 31660969 DOI: 10.1186/s12929-019-0578-x
Associated cell lines:
- KSCBi003-A
Miklas JW, Clark E, Levy S, Detraux D, Leonard A, Beussman K, Showalter MR, Smith AT, Hofsteen P, Yang X, Macadangdang J, Manninen T, Raftery D, Madan A, Suomalainen A, Kim DH, Murry CE, Fiehn O, Sniadecki NJ, Wang Y, Ruohola-Baker H

TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes
Miklas JW et al. TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes. . 2019-10-11. Pubmed ID: 31604922; DOI: 10.1038/s41467-019-12482-1; PMC: PMC6789043 RUESe002-A 2019-10-11 2019-10-11
PubMed: 31604922 DOI: 10.1038/s41467-019-12482-1
Associated cell lines:
- RUESe002-A
Alari V, Russo S, Rovina D, Garzo M, Crippa M, Calzari L, Scalera C, Concolino D, Castiglioni E, Giardino D, Prosperi E, Finelli P, Gervasini C, Gowran A, Larizza L

Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c.4435G>T, p.(Gly1479*) and c.3474G>A, p.(Trp1158*) and missense c.4627G>T, p.(Asp1543Tyr) mutations
Alari V et al. Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c.4435G>T, p.(Gly1479*) and c.3474G>A, p.(Trp1158*) and missense c.4627G>T, p.(Asp1543Tyr) mutations. . 2019-10-00. Pubmed ID: 31491690; DOI: 10.1016/j.scr.2019.101553 IAIi002-AIAIi003-AIAIi004-A 2019-10-00 2019-10-00
PubMed: 31491690 DOI: 10.1016/j.scr.2019.101553
Associated cell lines:
Domingo-Prim J, Abad-Morales V, Riera M, Navarro R, Corcostegui B, Pomares E

Generation of an induced pluripotent stem cell line (FRIMOi007-A) derived from an incomplete achromatopsia patient carrying a novel homozygous mutation in PDE6C gene
Domingo-Prim J et al. Generation of an induced pluripotent stem cell line (FRIMOi007-A) derived from an incomplete achromatopsia patient carrying a novel homozygous mutation in PDE6C gene. . 2019-10-00. Pubmed ID: 31520890; DOI: 10.1016/j.scr.2019.101569 FRIMOi007-A 2019-10-00 2019-10-00
PubMed: 31520890 DOI: 10.1016/j.scr.2019.101569
Associated cell lines:
- FRIMOi007-A
Li Y, Zhang H, Yan B, Ma Y, Yang X, Guan J, Lv Y, Gao M, Ma J, Gai Z, Liu Y

An induced pluripotent stem cell line (SDQLCHi006-A) derived from a patient with maple syrup urine disease type Ib carrying compound heterozygous mutations of p.R168C and p.T322I in BCKDHB gene
Li Y et al. An induced pluripotent stem cell line (SDQLCHi006-A) derived from a patient with maple syrup urine disease type Ib carrying compound heterozygous mutations of p.R168C and p.T322I in BCKDHB gene. . 2019-10-00. Pubmed ID: 31610500; DOI: 10.1016/j.scr.2019.101579 SDQLCHi006-A 2019-10-00 2019-10-00
PubMed: 31610500 DOI: 10.1016/j.scr.2019.101579
Associated cell lines:
- SDQLCHi006-A
Zhang H, Ma Y, Yan B, Yang X, Li Y, Guan J, Dong R, Liu Y, Gai Z

Establishment of a human induced pluripotent stem cell line (SDQLCHi005-A) from a patient with mastocytosis carrying heterozygous mutation in KIT gene
Zhang H et al. Establishment of a human induced pluripotent stem cell line (SDQLCHi005-A) from a patient with mastocytosis carrying heterozygous mutation in KIT gene. . 2019-10-00. Pubmed ID: 31522012; DOI: 10.1016/j.scr.2019.101565 SDQLCHi005-A 2019-10-00 2019-10-00
PubMed: 31522012 DOI: 10.1016/j.scr.2019.101565
Associated cell lines:
- SDQLCHi005-A
Rovina D, Castiglioni E, Farini A, Bellichi M, Gervasini C, Paganini S, Di Segni M, Santoro R, Torrente Y, Pompilio G, Gowran A

Establishment of a Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line carrying a deletion of exons 51-53 of the dystrophin gene (CCMi003-A)
Rovina D et al. Establishment of a Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line carrying a deletion of exons 51-53 of the dystrophin gene (CCMi003-A). . 2019-10-00. Pubmed ID: 31465894; DOI: 10.1016/j.scr.2019.101544 CCMi003-A 2019-10-00 2019-10-00
PubMed: 31465894 DOI: 10.1016/j.scr.2019.101544
Associated cell lines:
- CCMi003-A
He L, Ye W, Chen Z, Wang C, Zhao H, Li S, Peng L, Han X, Zhou T, Li Z, Tang B, Jiang H

Generation of an induced pluripotent stem cell line (XHCSUi001-A) from urine cells of a patient with spinocerebellar ataxia type 3
He L et al. Generation of an induced pluripotent stem cell line (XHCSUi001-A) from urine cells of a patient with spinocerebellar ataxia type 3. . 2019-10-00. Pubmed ID: 31491691; DOI: 10.1016/j.scr.2019.101555 CSUXHi001-A 2019-10-00 2019-10-00
PubMed: 31491691 DOI: 10.1016/j.scr.2019.101555
Associated cell lines:
- CSUXHi001-A
Bax M, Balez R, Muñoz SS, Do-Ha D, Stevens CH, Berg T, Cabral-da-Silva MC, Engel M, Nicholson G, Yang S, Blair IP, Ooi L

Generation and characterization of a human induced pluripotent stem cell line UOWi005-A from dermal fibroblasts derived from a CCNF^S621G familial amyotrophic lateral sclerosis patient using mRNA reprogramming
Bax M et al. Generation and characterization of a human induced pluripotent stem cell line UOWi005-A from dermal fibroblasts derived from a CCNF^S621G familial amyotrophic lateral sclerosis patient using mRNA reprogramming. . 2019-10-00. Pubmed ID: 31445393; DOI: 10.1016/j.scr.2019.101530 UOWi005-A 2019-10-00 2019-10-00
PubMed: 31445393 DOI: 10.1016/j.scr.2019.101530
Associated cell lines:
- UOWi005-A
Shivaraj A, Parveen S

Generation of integration free human iPSC line SORMi002-A from neonatal foreskin fibroblasts
Shivaraj A et al. Generation of integration free human iPSC line SORMi002-A from neonatal foreskin fibroblasts. . 2019-10-00. Pubmed ID: 31454679; DOI: 10.1016/j.scr.2019.101534 SORMi002-A 2019-10-00 2019-10-00
PubMed: 31454679 DOI: 10.1016/j.scr.2019.101534
Associated cell lines:
- SORMi002-A
Cerrada V, García-López M, Moreno-Izquierdo A, Villaverde C, Zurita O, Martin-Merida MI, Arenas J, Ayuso C, Gallardo ME

Derivation of a human DOA iPSC line, IISHDOi006-A, with a mutation in the ACO2 gene: c.1999G>A; p.Glu667Lys
Cerrada V et al. Derivation of a human DOA iPSC line, IISHDOi006-A, with a mutation in the ACO2 gene: c.1999G>A; p.Glu667Lys. . 2019-10-00. Pubmed ID: 31509793; DOI: 10.1016/j.scr.2019.101566 IISHDOi006-A 2019-10-00 2019-10-00
PubMed: 31509793 DOI: 10.1016/j.scr.2019.101566
Associated cell lines:
- IISHDOi006-A
Han HJ, Han HW, Seo HH, Kim JH

Generation of a KSCBi005-A-5(TLR8KO-A10) homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9
Han HJ et al. Generation of a KSCBi005-A-5(TLR8KO-A10) homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9. . 2019-10-00. Pubmed ID: 31526944; DOI: 10.1016/j.scr.2019.101561 KSCBi005-AKSCBi005-A-5 2019-10-00 2019-10-00
PubMed: 31526944 DOI: 10.1016/j.scr.2019.101561
Associated cell lines:
- KSCBi005-A
- KSCBi005-A-5
Han HJ, Seo HH, Han HW, Kim JH

Generation of a TLR7 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9
Han HJ et al. Generation of a TLR7 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9. . 2019-10-00. Pubmed ID: 31445394; DOI: 10.1016/j.scr.2019.101520 KSCBi005-AKSCBi005-A-4 2019-10-00 2019-10-00
PubMed: 31445394 DOI: 10.1016/j.scr.2019.101520
Associated cell lines:
- KSCBi005-A
- KSCBi005-A-4
Pandolfi EC, Rojas EJ, Sosa E, Gell JJ, Hunt TJ, Goldsmith S, Fan Y, Silber SJ, Clark AT

Generation of three human induced pluripotent stem cell sublines (MZT04D, MZT04J, MZT04C) for reproductive science research
Pandolfi EC et al. Generation of three human induced pluripotent stem cell sublines (MZT04D, MZT04J, MZT04C) for reproductive science research. . 2019-10-00. Pubmed ID: 31622877; DOI: 10.1016/j.scr.2019.101576 UCLAi001-AUCLAi001-BUCLAi001-C 2019-10-00 2019-10-00
PubMed: 31622877 DOI: 10.1016/j.scr.2019.101576
Associated cell lines:
Takahashi M, Yamazaki S

Generation of a human induced pluripotent stem cell line, IMSUTi002-A-1, harboring the leukemia-specific fusion gene ETV6-RUNX1
Takahashi M et al. Generation of a human induced pluripotent stem cell line, IMSUTi002-A-1, harboring the leukemia-specific fusion gene ETV6-RUNX1. . 2019-10-00. Pubmed ID: 31476588; DOI: 10.1016/j.scr.2019.101546 IMSUTi002-A 2019-10-00 2019-10-00
PubMed: 31476588 DOI: 10.1016/j.scr.2019.101546
Associated cell lines:
- IMSUTi002-A
Díaz-Guerra E, Oria-Muriel MA, Moreno-Jiménez EP, de Rojasb I, Rodríguez C, Rodríguez-Traver E, Orera M, Hernándezb I, Ruizb A, Vicario C

Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutation
Díaz-Guerra E et al. Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutation. . 2019-10-00. Pubmed ID: 31627126; DOI: 10.1016/j.scr.2019.101574 ICCSICi006-A 2019-10-00 2019-10-00
PubMed: 31627126

Publications associated with registered cell lines

Rajpurohit CS, Kumar V, Cheffer A, Oliveira D, Ulrich H, Okamoto OK, Zatz M, Ansari UA, Khanna VK, Pant AB

Associated cell lines:

Metzler Eric, Telugu Narasimha, Diecke Sebastian, Spuler Simone, Escobar Helena

Associated cell lines:

Zhao Qingyang, Cui Yazhou, Wang Jing, Shi Liang, Qi Zijuan, Luan Jing, Zhang Yuang, Zhou Xiaoyan, Han Jinxiang

Associated cell lines:

Lee SJ, Kim JH, Kang KW, Park Y, Kim BS

Associated cell lines:

Zhao Huifang, He Lang, Huang Hualin, Li Shuai, Cheng Na, Tang Feng, Han Xiaobo, Lin Zuoxian, Huang Rongqi, Zhou Peng, Deng Sihao, Huang Jufang, Li Zhiyuan

Associated cell lines:

Tan Chengning, Dai Limeng, Yang Wuchen, Li Fengjie, Wang Li, Xiao Yanni, Wang Xiaojie, Zhang Yichi, Wang Yali, Zeng Cheng, Xiang Zheng, Zhang Xiaomei, Zhang Weiwei, Ran Qian, Chen Maoshan, Li Zhongjun, Chen Li

Associated cell lines:

Sripathy SR, Wang Y, Moses RL, Fatemi A, Batista DA, Maher BJ

Associated cell lines:

Tang Y, Han Y, Yu H, Zhang B, Li G

Associated cell lines:

Aqel YWA, Ali G, Elsayed AK, Al-Khawaga S, Hussain K, Abdelalim EM

Associated cell lines:

Kim KP, Yoon J, Kim J, Röpke A, Shin B, Wook Han D, Greber B, Schöler HR

Associated cell lines:

Yu Z, Dmitrieva NI, Walts AD, Jin H, Liu Y, Ping X, Ferrante EA, Qiu L, Holland SM, Freeman AF, Chen G, Boehm M

Associated cell lines:

Metzler E, Telugu N, Diecke S, Spuler S, Escobar H

Associated cell lines:

Gao X, Qiu SW, Feng ML, Huang SS, Kang DY, Han MY, Dai P, Yuan YY

Associated cell lines:

Sahabian A, von Schlehdorn L, Drick N, Pink I, Dahlmann J, Haase A, Göhring G, Welte T, Martin U, Ringshausen FC, Olmer R

Associated cell lines:

Ferreira Mendes JM, de Faro Valverde L, Torres Andion Vidal M, Paredes BD, Coelho P, Allahdadi KJ, Coletta RD, Souza BSF, Rocha CAG

Associated cell lines:

Strnadel J, Zahumenska R, Nosal V, Smolar M, Marcinek J, Kalman M, Juhas S, Juhasova J, Studenovska H, Dumortier H, Chromec T, Skovierova H, Mitruskova B, Kapralik I, Mersakova S, Brany D, Halasova E

Associated cell lines:

Liu H, Li S, Ren C, Liu W, Zhu B, Wang L, Xu H, Xie W, Zuo X, Zhou Y, Luo L, Jiang X

Associated cell lines:

Rolova T, Wu YC, Koskuvi M, Voutilainen J, Sonninen TM, Kuusisto J, Laakso M, Hämäläinen RH, Koistinaho J, Lehtonen Š

Associated cell lines:

Das D, Li J, Liu S, Oh E, Cheng L, Lyketsos C, Mahairaki V

Associated cell lines:

Xia S, Wang X, Yue P, Li Y, Zhang D

Associated cell lines:

Wu X, Zhao Y, Wang X

Associated cell lines:

Zlotnik D, Rabinski T, Ofir R, Hershkovitz E, Vatine GD

Associated cell lines:

Kamand M, Ilieva M, Louise Forsberg S, Thomassen M, Meyer M, Fex Svenningsen Å, Maria Michel T

Associated cell lines:

Wang Hongyang, Wu Kaiwen, Guan Jing, Wang Qiuju

Associated cell lines:

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Associated cell lines:

Alowaysia Maryam, Fiaccoa Elisabetta, Astro Veronica, Adamo Antonio

Associated cell lines:

Zhu Xiyu, Wang Junxia, Chong Hoshun, Wang Jiaxian, Wang Dongjin

Associated cell lines:

Ababneh NA, Ali D, Barham R, Al-Kurdi B, Sharar N, Al Hadidi S, Qanno' O, Ryalat AT, Salah B, Awidi A

Associated cell lines:

Shrestha R, Wen YT, Tsai RK

Associated cell lines:

Calzari L, Barcella M, Alari V, Braga D, Muñoz-Viana R, Barlassina C, Finelli P, Gervasini C, Barco A, Russo S, Larizza L

Associated cell lines:

HW Kung Louise, Sampurno Lisa, Yammine Kathryn M., Graham Alison, McDonald Penny, Bateman John F., Shoulders Matthew D., Lamandé Shireen R.

Associated cell lines:

Meynier S, Rieux-Laucat F

Associated cell lines:

Ge Ning, Liu Min, Krawczyk Janusz, McInerney Veronica, Ward Deirdre, Shen Sanbing, O'Brien Timothy, Prendiville Terence

Associated cell lines:

Ali Eltahir, Ferraro Rosalba Monica, Lanzi Gaetana, Masneri Stefania, Piovani Giovanna, Mazzoldi Elena Laura, Serpieri Valentina, Valente Enza Maria, Giordano Lucio, Giliani Silvia Clara

Associated cell lines:

Marchiano Silvia, Hsiang Tien-Ying, Higashi Ty, Khanna Akshita, Reinecke Hans, Yang Xiulan, Pabon Lil, Sniadecki Nathan J., Bertero Alessandro, Gale Michael, Murry Charles E.

Associated cell lines:

Ebrahimi V, Hashemi A

Associated cell lines:

Lai LL, Chen YJ, Li YL, Lin XH, Wang MW, Dong EL, Wang N, Chen WJ, Lin X

Associated cell lines:

Jamwal VS, Vishnu VV, Domreddy A, Parekh Y, Kumar BK, Chandra Shekar P, Singh S

Associated cell lines:

Stock R, Vogel S, Mau-Holzmann UA, Kriebel M, Wüst R, Fallgatter AJ, Volkmer H

Associated cell lines:

Liu S, Niu S, Li Y, Xiong H, Li Y, Jian L, Zhang L