Publications associated with registered cell lines

Ergin Ahmet Doğan, Seçen Erhan, Celik Aybuke, Uner Burcu

DQAsomes as a Coenzyme Q10 Delivery Vehicle: A Step Forward Therapy in Leigh Disease

Lyu Yongkang, Cui Yonglin, Chen Xiaolin, Shen Hao, Xu He, Zhang Changzhe, Meng Qingtian

Mechanics of poly-arginine adsorption onto cell membrane by GM1 and their cluster forming: Coarse-grained molecular dynamics study

Lee Younsu, Koo Okjae, Saadeldin Islam M.

Generation of induced pluripotent stem cells from the Asian bats

Wydrych Agata, Pakuła Barbara, Janikiewicz Justyna, Dobosz Aneta M., Jakubek-Olszewska Patrycja, Skowrońska Marta, Kurkowska-Jastrzębska Iwona, Cwyl Maciej, Popielarz Mariola, Pinton Paolo, Zavan Barbara, Dobrzyń Agnieszka, Lebiedzińska-Arciszewska Magdalena, Więckowski Mariusz R.

Metabolic impairments in neurodegeneration with brain iron accumulation

Holtes Lara K., de Bruijn Suzanne E., Cremers Frans P.M., Roosing Susanne

Dual inheritance patterns: A spectrum of non-syndromic inherited retinal disease phenotypes with varying molecular mechanisms

Lv Yafeng, Cui Zhi, Li Hongbo, Wang Jing, Wei Mulan, Hu Yuanlang, Li Xun, Cao Chunyu, Zhang Ye, Wang Wei

Identification of AAV serotypes for gene therapy in Krabbe iPSCs-derived brain organoids

Lu S, Chen M, Liu X, Li J, Liu H, Li S

Generation of a BEST1 Pr-EGFP reporter human embryonic stem cell line via CRISPR/Cas9 editing

Bastrich Asya, Antonov Daniil, Podzhilkova Aleksandra, Petrova Darya A., Pylina Svetlana V., Laptev Dmitriy N., Sechko Elena A., Kuznetsov Sergey N., Vetchinkina Ekaterina A., Mokrysheva Natalia G.

Generation of an induced pluripotent stem cell line ERCi003-A derived from a patient with maturity-onset diabetes of the young type 10 caused by a heterozygousINSmutation

Bastrich Asya, Antonov Daniil, Podzhilkova Aleksandra, Petrova Darya A., Pylina Svetlana V., Laptev Dmitriy N., Sechko Elena A., Kuznetsov Sergey N., Vetchinkina Ekaterina A., Mokrysheva Natalia G.

Generation of iPSC line ERCi004-A from human dermal fibroblasts of a patient with maturity-onset diabetes of the young type 3 caused by a heterozygous mutation in theHNF1Agene

Nitaramorn N, Kobpornchai P, Tongkrajang N, Chaisri U, Imwong M, Kulkeaw K

Human liver organoids are susceptible to Plasmodium vivax infection

Nayak D, Shivakumar S, Shetty R, Prashanthi KN, Ghosh A, Jeyabalan N, Chakrabarty K

Trehalose extricates impaired mitochondrial and autophagy dysregulation in patient iPSC-derived macular corneal dystrophy disease model

Bekhite MM, Hübner S, Kretzschmar T, Backsch C, Weise A, Klein E, Bogoviku J, Westphal J, Schulze PC

Generation of a human induced pluripotent stem cell lines (UKJi003-A) from a patient with Fabry disease and healthy donor (UKJi004-A)

Zhang D, Huang D, Larcher LM, Zaw K, Chen SC, Jennings L, Lamey TM, Thompson JA, McLaren TL, Chen FK, McLenachan S

Derivation of two induced pluripotent stem cell lines from a healthy control subject

Baiocco Paola, Barolo Lorenzo, Mautone Lorenza, Gigante Ylenia, Ghirga Silvia, Mura Francesco, Farina Maria Vittoria, Tacconi Stefano, Dini Luciana, Ruocco Giancarlo, Boffi Alberto, Milanetti Edoardo, Angelantonio Silvia Di

Short-Chain Polyphosphates Induce Tau Fibrillation and Neurotoxicity in Human iPSC-Derived Retinal Neurons

Xin H, Li Y, Zhang K, Ji A, Fan M

Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation

Sun X, Mao S, Liang Y, Duan C, Cui Z, Gu J, Jiang B, Ding C, Chen J, Tang S

Introduction of an RS1 mutation causative variant consistent with identified XLRS patient using CRISPR/Cas9 technology in normal iPSC

Rha AK, Christensen CL, Kan SH, Harb JF, Andrade-Heckman P, Wang RY

Generation of an infantile GM1 gangliosidosis induced pluripotent stem cell line (CHOCi005-A) for disease modeling and therapeutic testing

Liu R, Weng G, Zheng F, Chen J, Wang K, Han J, Huang J, Yan L, Jin J

Generation of an integration-free induced pluripotent stem cell line, FJMAi001-A, from a Marfan syndrome patient with a heterozygous mutation c.2777G > A (p.Cys926Tyr) in FBN1

Rodriguez-Lopez A, Huang X, Chen C, Zou J, Zheng W, Chen G

Generation of an induced pluripotent stem cell line (TRNDi042-A) from a Mucopolysaccharidosis type IIIB patient with homozygous p. R626X (c. 1876C > T) mutation in the NAGLU gene

Liu D, Shen J, Yang Z, Fan H, Wang H, Liang P, Gong T

Generation of a lamin A/C knockout human induced pluripotent stem cell line (ZJULLi007-A) via CRISPR/Cas9

Cheng J, Zhai Y, Guo X, Wang X, Ma M, Ren X, Wang S, Cui H, Ren Q

Generation of an induced pluripotent stem cell line (HMSCATi004-A) from an early onset Parkinson's disease patient with PRKN gene mutation

Jyoti Saikia B, Bhardwaj J, Saini A, Rajan R, B K B

Generation of an induced pluripotent stem cell (iPSC) line (IGIBi026-A) derived from Wilson disease patient harboring compound heterozygous mutations [c.2165dupT (p.R723Efs31) and c.C813A (p.C271*)] in the ATP7B gene

Jiang X, Liu Q, Yang L, Zhang X, Gao J, Jiang Y

Generation of a MYH6 (c.4034T > C) mutant human embryonic stem cell line via CRISPR base editing

Tohari M, Sanjaya R, Yuliana Sari S, Tedjobagaskara B, Ibnu Faisal A, Alvin Prawira M, Oktaviani Dwi Putri A, Faza N, Murti H, Widyastuti HP

Generation of footprint-free human induced pluripotent stem cell line (SCIKFi001-B) from cGMP grade umbilical cord-derived mesenchymal stem cells (UC-MSCs) using episomal-plasmid based reprogramming approach

Woo Lim S, In Lee K, Cui S, Fang X, Jin Shin Y, Lee H, Woo Yang C, Young Lee J, Ha Chung B

Generation of a human SLC12A3 knock-in human induced pluripotent stem cell line (CMCi014-A-82) using CRISPR-Cas9 system

Mizuno-Iijima S, Kawamoto S, Asano M, Mashimo T, Wakana S, Nakamura K, Nishijima KI, Okamoto H, Saito K, Yoshina S, Miwa Y, Nakamura Y, Ohkuma M, Yoshiki A

Mammalian genome research resources available from the National BioResource Project in Japan

Sleiman Y, Reisqs JB, Bianca Tan R, Cecchin F, Chahine M, Boutjdir M

Generation of an iPSC cell line (VANYHHi001-A) from a patient with cardiac arrythmias carrying CACNA1D, SCN5A, and DSP variants

Sun T, Chen B, Zhang D, Xu X, Gao J, Sun J, Wei M

Generation of hereditary spastic paraplegia patient-derived induced pluripotent stem cell line UJSi003-A

Boen HM, Vandendriessche B, Schippers J, Rabaut L, Nijak-Paeske A, Ponsaerts P, Van Craenenbroeck EM, Loeys B, Alaerts M

Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin

Africano Chiara, Bachetti Tiziana, Uva Paolo, Pitollat Gabriel, Del Zotto Genny, Giacopelli Francesca, Recchi Giada, Lenfant Nicolas, Madani Amélia, Beckouche Nathan, Thoby-Brisson Muriel, Ceccherini Isabella

Identification of a histone deacetylase inhibitor as a therapeutic candidate for congenital central hypoventilation syndrome

Jiao K, Zhang J, Wang N, Gu X, Chang X, Xia X, Zhu B, Gao M, Cheng N, Zhao C, Xi J, Zhu W

Human induced pluripotent stem cell line (FDHSi005-A) derived from a patient with a deep intronic variant in the GNE gene

Wang Yanli, Liu Zengping, Li Yong, Nie Zhipeng, Xu Baicheng, Zhu Yiming, Duan Shihong, Chen Xingjian, Tan Huan, Dang Jiong, Guan Minxin, Guo Yufen

A Novel Mutation Located in the N‐Terminal Domain of MYO15A Caused Sensorineural Hearing Loss

Boullé M, Leleu A, Schacre S, Banal C, Boucharlat A, Renault S, Hollenstein M, Frosk P, Yates F, Lefort N, Agou F

Generation of IPi002-A/B/C human induced pluripotent stem cell lines from MARCH amniotic fluid cells

Okumura H, Hayashi Y, Arioka Y, Kushima I, Mori D, Ozaki N

Generation of induced pluripotent stem cells from a schizophrenia patient with heterozygous 1q21.1 deletion

Erliandri I, Sangotra A, Keller L, Lieberman AP, Smith GD

A spinal and bulbar muscular atrophy (SBMA) disease-specific human embryonic stem cell (hESC) line, UMICHe002-A/UM197-1

Arunachal G, Nimonkar MM, Mahadeva P, Sukrutha R, Raghavendra K, Chetan GK, Venkataswamy MM, Mehta B, Markandeya YS

Generation of induced pluripotent stem cell line, NIMHi013-A, from PBMCs of a female child with epilepsy carrying a novel SCN1A variant

Cheng Y, Sun H, Chen X, Li X, Xu Y, Wang Y

Generation of induced pluripotent stem cell line (ZZUi037-A) from a patient with spinocerebellar ataxia type 3

Li Y, Du M, Jin Z

Generation of ID1/3 knockout human embryonic stem cell lines (WAe009-A-2A and WAe009-A-2B) derived from H9 using CRISPR/Cas9

Krogulec E, Dobosz AM, Liszewska E, Majchrowicz L, Dobrzyń A

Generation of four human induced pluripotent stem cell lines derived from patients with MPAN, subtype of NBIA, carrying the c.204_214del11 mutation in the C19orf12 gene

Gubinelli Francesco, Salazar Jose M., Kaspar Janina, Ortiz Irene Santisteban, Schafer Simon T., Burbulla Lena F.

Translational View on Therapeutic Strategies and Upcoming Issues: Stem Cell and Brain Organoid Approaches for Parkinson’s Disease Therapy

Aalders J, Léger L, Hassannia B, Goossens V, Vanden Berghe T, van Hengel J

Improving cardiac differentiation of human pluripotent stem cells by targeting ferroptosis

Wang Jinling, Ye Di, Li Shuangpeng, Lu Xuan, Chi Yue, Tang Chengcheng, Zhou Xiaoqing, Chen Min, Zheng Yunwen, Ge Jianyun, Zou Qingjian

Generation of human induced pluripotent stem cells carrying albumin-sfGFP reporter

Bekhite MM, Hübner S, Kretzschmar T, Backsch C, Weise A, Klein E, Bogoviku J, Westphal J, Christian Schulze P

Generation of human induced pluripotent stem cell lines UKJi001-A and UKJi006-A from patients with heterozygous mutation in the PKP2 gene

Wongkidakarn S, Yodtup C, Jantapalaboon D, Phairoh P, Suparak S, Dhepakson P, Tubsuwan A, Bumroongthai K

Generation of human induced pluripotent stem cell (DMSCi001-A) line from hematopoietic stem cells of a healthy female donor

Léger L, Aalders J, Heymans N, Van Acker-Verberckt K, De Bleeckere L, Coucke P, Menten B, Bauce B, Vitiello L, Rampazzo A, Calore M, van Hengel J

Generation of a human induced pluripotent stem cell line UGENTi002-A from an arrhythmogenic cardiomyopathy patient carrying the c.817C>T DSP heterozygous variant and isogenic control using CRISPR/Cas9 editing

Ruotolo G, D'Anzi A, Giovenale AMG, Giacometti C, Ferrari D, Vulcano E, D'Asdia C, Lattante S, Sabatelli M, Codazzi F, Consalez G, Marano M, Di Lazzaro V, Pennuto M, Vescovi A, Rosati J

Induced pluripotent stem cell production (CSSi019-A)(14432) from an asymptomatic subject carrying a expansion of C9orf72 gene

Tanzer K, Meier B, Vulinovic F, Pawlack H, Klein C, Seibler P, Rakovic A

Generation of four human-derived iPSC TorsinA-3xFLAG reporter lines from a DYT-TOR1A patient

Hua C, Sun W, Zhang C, Tian X, Qin X, Dong J, Li X

Generation of a human induced pluripotent stem cell line ZZUNEUi030-A from a female patient carrying a heterozygous CALM2 (c.395 A > T) mutation

Giraldo-Berrio Daniela, Jimenez-Del-Rio Marlene, Velez-Pardo Carlos

Minocycline mitigates Aβ and TAU pathology, neuronal dysfunction, and death in the PSEN1 E280A cholinergic-like neurons model of familial Alzheimer’s disease

Uno Narumi, Miyamoto Hitomaru, Yamazaki Kyotaro, Egawa Masaya, Kobayashi Hiroaki, Kazuki Kanako, Osaki Mitsuhiko, Suzuki Teruhiko, Hamamichi Shusei, Oshimura Mitsuo, Tomizuka Kazuma, Kazuki Yasuhiro

Microcell-mediated chromosome transfer between non-identical human iPSCs

A Ababneh N, Barham R, Al-Kurdi B, Al Hadidi S, Ali D, Abdulelah AA, Madadha A, Masri A, Awidi A

Establishment of a human induced pluripotent stem cell (iPSC) line (JUCTCi018-A) from a patient with Charcot-Marie-Tooth disease type 2EE (CMT2EE) due to a homozygous c.122G > A p.(Arg41Gln) mutation in the MPV17 gene

Jiang M, Long Y, Liu Y, Li R, Xu J, Chi T, Sun M, Li M, Yu H, Yu L, Han X

Establishment of an induced pluripotent stem cell (iPSC) line (JNMUi002-A) from a male patient with schizophrenia

Xu X, Wang W, Liu Y, Bäckemo J, Heuchel M, Wang W, Nie Y, Iqbal I, Kratz K, Lendlein A, Ma N

Substrates mimicking the blastocyst geometry revert pluripotent stem cell to naivety

Esteves F, Brito D, Rajado AT, Silva N, Apolónio J, Roberto VP, ALFA Score Consortium, Andrade RP, Calado S, Faleiro ML, Matos C, Marques N, Marreiros A, Nzwalo H, Pais S, Palmeirim I, Simãoa S, Joaquim N, Miranda R, Pêgas A, Raposo DM, Sardo A, Araújo I, Nóbrega C, Castelo-Branco P, Bragança J

Establishment of an induced pluripotent cell line (ABCRIi001-A) from an elderly female for ageing research

Su S, Ren Y, Zhang H, Liu Y, Liu Y, Li Z, Zhang T, Fang F

Establishment of a transgene-free iPS cell line (SDCHi002-A) from a young patient bearing a NPRL3 mutation and suffering from Epilepsy

Li Z, Li Z, Lv Y, Gao M, Liu N, Gai Z, Liu Q

Establishment of a non-integrated iPS cell line (SDQLCHi072-A) from a patient suffered from AUTS2 syndrome

Verma S, Dalabehera S, Maurya R, Singh D, Prasher B, Pandey R, Bapat S, Ramalingam S, Sachidanandan C

Corrigendum to "Generation of an induced pluripotent stem cell line IGIBi18-A from an Indian patient with rubinstein taybi syndrome" [Stem Cell Res. 78 (2024) 103456]

Li Y, Du M, Jin Z

Corrigendum to "Generation of ID1/3 knockout human embryonic stem cell lines (WAe009-A-2A and WAe009-A-2B) derived from H9 using CRISPR/Cas9" [Stem Cell Research 81 (2024) 103569]

Mun D, Kang JY, Park M, Yoo G, Kim H, Yun N, Mi Hwang Y, Joung B

Establishment of a human-induced pluripotent stem cell line from a long QT syndrome type 2 patient harboring a KCNH2 mutation

Zhang S, Li J, Pan W, Ren Q, Zhou Y, Chen M, Qu J, Li S

Establishment of a CPAMD8-GFP reporter human embryonic stem cell line, IBBDe001-B, using CRISPR/Cas9 editing

Wang S, Zeng Q, Chen M, Zhang H, Lv X

Establishment of an induced pluripotent stem cell line (SDCHi011-A) from a healthy Chinese female donor

Shao J, Shao C, Yang G, Jin Y

Establishing an induced pluripotent stem cell line (SDPHi006-A) from a healthy Chinese female donor represents an accomplishment

Fekadu-Siebald Julia, Fuchs Nina V, Zahn Stella, Rommel Marcel G E, Schenk Franziska, Huenecke Sabine, Bremm Melanie, Kreyenberg Hermann, Kuci Zyrafete, Jacobsen Eva-Maria, Hoenig Manfred, Schwarz Klaus, Bader Peter, Modlich Ute, König Renate, Bakhtiar Shahrzad

Eight induced pluripotent stem cell lines (iPSCs) derived from two patients with Leukocyte adhesion deficiency Type I (LAD I) with mutations in the ITGB2 gene

Liang Yuqin, Sun Xihao, Chen Hang, Cui Zekai, Gu Jianing, Duan Chunwen, Mao Shengru, Chen Yuexi, Li Xiaoxue, Xiong Siqi, Chen Jiansu

CRISPR/Cas9-mediated generation of a human induced pluripotent stem cell line with PRPF6 c.2699 G > A mutation to model retinitis pigmentosa

Guo X, Zhang M, Xu Z, Yu Y, Shen Z

CRISPR/Cas9-mediated generation of AP-1 activity reporter cell line in human embryonic stem cell (WAe007-A-5)

Kim AH, Lee HM, Kim HS, Jeong SW, Jun JK, Jang J

CRISPR/Cas9-mediated knock-in of a fluorescent reporter into the target locus of interest in human pluripotent stem cells

Treschow AF, Vinggaard AM, Valente MJ

Standardization and optimization of the hiPSC-based PluriLum assay for detection of embryonic and developmental toxicants

Hu B, Wang Z, Ma T, Fan P, Li L

Research progress on the pathogenesis of multiple symmetrical lipomatosis

Dwojak E, O'Mard D, Zou J, Wassif CA, Burkett S, Eckhaus M, Rueda Faucz F, Padilla C, Villasmil R, Zheng W, Dang Do AN

Six induced pluripotent stem cell lines from fibroblasts of individuals with CLN3-related conditions

Hou X, Wang Z, Guo R, Zhou Z, Zhang J, Li Y, Yao Akogo H, Ma J, Chen W, Sun D, Ma J, Guo Q, Cui H

Derivation of induced pluripotent stem cell from a Baraitser-Winter Cerebrofrontofacial syndrome with ACTB mutation

Wu Y, Meng XY, Sun HF, Zhang YJ, Liu XH, Wang DD, Liu DH, Li SM, Li JK, Li WX, Li SA, Liu PP, Kang JS

Construction of induced pluripotent stem cell line (CSBZZUi002-A) from the fibroblast cells of a healthy female

Zhang C, Li J, Sai Y, Su H, Jiang Y, Zhang L, Jian L, Zhang H, Guo G, Li E, Li X, Sun L

Establishment of heterozygous LMOD2 knockout human embryonic stem cell line (ZZUNEUi022-A-1) using CRISPR/Cas9 system

Ruan J, Wu M, Xiang J, Hui X, Yang L, Lin R, Xu W, Shu Q

Generation of a human induced pluripotent stem cell line from a female patient carrying LZTR1 gene mutation

Leavens Karla F., Osorio-Quintero Catherine, Yeuteuh Elisabeth Ashlyne, Perez-Profeta Francesca T., Dattoli Anna Ada, Cardenas-Diaz Fabian L., French Deborah L., Gadue Paul

Generation of a fluorescent mNeonGreen insulin reporter line in the H1 (WA01) hESC background

Xi S, Xue B, Wang Y, Shan Z, Song T, Sun J, Qin S

Generation of patient-derived induced pluripotent stem cell line UJSi004-A from ultra-treatment-resistant schizophrenia

Lee Y, Park HJ, Kim YO, Kim BY

Generation of a human induced pluripotent stem cell line (KSCBi016-A) from a CPVT patient with an RYR2 mutation

Mengnan W, Yan C, Qiong X, Man X

Generation of a human induced pluripotent stem cell line (FDIBSi001-A) from a patient with ADNP syndrome carrying ADNP mutation (c. 2059 T>C)

Weng Shiwen, Liu Xiang, Wang Dayan, Wang Jiaxuan, Ren Qian, Wang Qun, Shan Wei

Generation of a human induced pluripotent stem cell (iPSC) line from a patient with a CDKL5 gene mutation

Srisantitham J, Suwanpitak S, Thongsin N, Wattanapanitch M

Generation of a homozygous TIGIT gene knockout (TIGIT(-/-)) human iPSC line (MUSIi001-A-3) using CRISPR/Cas9 system

Kang Y, Liang S, Gao S, Chen J

Generation of a hiPSC line (TONGJIi001-A) from a 46,XX,ins(1;15)(p13.3; q22.31q26.1),inv(2)(p22.1p16.3),t(2;14)(q34;q12) infertility patient

Syed Ali G, Rebs S, Eberl H, Zinke C, Hübscher D, Maurer W, Busley A, Cyganek L, Streckfuss-Bömeke K

Generation of a heterozygous Calsequestrin 2 F189L iPSC line (UMGi158-B) by CRISPR/Cas9 genome editing to investigate the cardiac pathophysiology of Takotsubo Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia

Sun X, Liang Y, Duan C, Liu X, Zhou Y, Mao S, Cui Z, Gu J, Ding C, Chen J, Tang S

Generation of a gene-corrected isogenic human iPSC line (CSUASOi006-A-1) from a retinitis pigmentosa patient with heterozygous c.5792C > T mutation in the PRPF8 gene

De Serres-Bérard T, Pouliot V, Puymirat J, Chahine M

Generation of a control induced pluripotent stem cell line (CBRCULi014-A) derived from the lymphoblastoid cells of a pediatric individual

Jager Joanna, Ribeiro Marta, Furtado Marta, Carvalho Teresa, Syrris Petros, Lopes Luis R., Elliott Perry M., Cabral Joaquim M.S., Carmo-Fonseca Maria, da Rocha Simão Teixeira, Martins Sandra

Patient-derived induced pluripotent stem cells to study non-canonical splicing variants associated with Hypertrophic Cardiomyopathy

Pachis ST, Ramovs V, Freund C, Has C, Raymond K

Generation and genetic repair of two human induced pluripotent stem cell lines from patients with Epidermolysis Bullosa simplex associated with a heterozygous mutation in the translation initiation codon of KLHL24

Ferreira A, Calado SM, Jorge X, de Lange J, Carvalhal S

Generation and characterization of two isogenic induced pluripotent stem cell lines from a young female with microcephaly carrying a compound heterozygous mutation in BUB1 gene

Naidoo J, Hurrell T, Scholefield J

The generation of human induced pluripotent stem cell lines from individuals of Black African ancestry in South Africa

Davidenko Alina, Bogomazova Alexandra, Illarioshkin Sergey, Lagarkova Maria

Molecular Mechanisms of Spinocerebellar Ataxia Type 17

Zhang Hao, Thai Phung N., Shivnaraine Rabindra V., Ren Lu, Wu Xuekun, Siepe Dirk H., Liu Yu, Tu Chengyi, Shin Hye Sook, Caudal Arianne, Mukherjee Souhrid, Leitz Jeremy, Wen Wilson Tan Lek, Liu Wenqiang, Zhu Wenjuan, Chiamvimonvat Nipavan, Wu Joseph C.

Multiscale drug screening for cardiac fibrosis identifies MD2 as a therapeutic target

Song Xiao-Yan, Fan Cun-xiu, Atta-ur-Rahman, Choudhary Muhammad Iqbal, Wang Xiao-Ping

Neuro-regeneration or Repair: Cell Therapy of Neurological Disorders as A Way Forward

Mun D, Yoo G, Park M, Kang JY, Yun N, Joung B

Establishment of two human induced pluripotent stem cell lines from familial long QT syndrome type 1 patients carrying KCNQ1 mutation

Fetisoa Monia Ravelonandrasana, Acheampong Adolf, Bondzie-Quaye Precious, Bashir Mona Alrasheed, Huang Qing

Synergistic strategies for optimizing microalgae-based wastewater treatment: a comprehensive review

Guan J, Duan C, Lv Y, Zhang H, Liu G, Liu Y

Establishment of iPS cell line (SDQLCHi080-A) from a patient with GM1 gangliosidosis due to GLB1 mutation

Pavlova S, Shulgina A, Minina J, Zakian S, Dementyeva E.

Generation of Isogenic iPSC Lines for Studying the Effect of the p.N515del (c.1543_1545delAAC) Variant on MYBPC3 Function and Hypertrophic Cardiomyopathy Pathogenesis

Sharaf A, Frimat JP, Accardo A

Mechanical confinement matters: Unveiling the effect of two-photon polymerized 2.5D and 3D microarchitectures on neuronal YAP expression and neurite outgrowth

Sun H, Li Q, Xu T, Zhang W, Sun J, Liu H

Generation of SFTPC-mCherry knock-in reporter human embryonic stem cell line, WAe001-A-2H, using CRISPR/Cas9-based gene targeting

Haferkamp U, Telugu N, Krieg K, Schaefer W, Lam D, Binkle-Ladisch L, Friese MA, Diecke S, Pless O

Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4

Devito LG, Lim ES, O'Toole SM, Shepherd STC, Deng D, Feng H, Barber T, Drake WM, Turajlic S, Healy L

Generation of TWO iPSC lines (CRICKi009-A; CRICKi010-A) from patients with type 1 von Hippel-Lindau (VHL) and histopathologically confirmed renal cell carcinoma (RCC)

Sun J, Ren L, Canel Rivero G, Xu L, Ladabaum U, C Wu J

Generation of two induced pluripotent stem cell lines from patients with Li-Fraumeni Syndrome carrying TP53 mutation

Naigles Beverly, Soroczynski Jan, Hao Nan

Genetic Knock-Ins of Endogenous Fluorescent Tags in RAW 264.7 Murine Macrophages Using CRISPR/Cas9 Genome Editing

Giovenale AMG, Turco EM, Mazzoni M, Ferrone I, Torres B, Bernardini L, Vulcano E, Ferrari D, Onesimo R, D'Arrigo S, Zampino G, Pennuto M, De Luca A, Vescovi AL, Rosati J

Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome region

Widyastuti HP, van der Vaart B, Pachis ST, Freund C, Gidrol X, Raymond K

Generation of XPA p.Arg228T mutant LUMCi004-A cell line for modeling Xeroderma pigmentosum group A

Chen W, Wang H, Zhu K, Wang T, Yu W, Wu Q

Generation of the TSHSUi002-A induced pluripotent stem cell line from a patient with Peutz-Jeghers syndrome carring STK11 gene mutation

Guo Fuying, Xu Ping, Zheng Dandan, Zhong Xiufeng

Generation of two hiPSC lines carrying compound heterozygous RDH12 mutations in a LCA patient

Lee SE, Park S, Kang R, Lee T, Yu WJ, Chang S, Park JC

Hippocampal tau-induced GRIN3A deficiency in Alzheimer's disease

Vincent Ambily, Krishnakumar Subramanian, Parameswaran Sowmya

Heterozygous RB1 mutation enhanced ATP production in human iPSC-derived retinal organoids

Sundstrom J, Vanderleeden E, Barton N, Redick S, Dawes P, Murray L, Olson M, Tran K, Chigas S, Orszulak A, Church G, Readhead B, Oh H, Harlan D, Knipe D, Wang J, Chan Y, Lim E.

Herpes Simplex Virus 1 Infection of Human Brain Organoids and Pancreatic Stem Cell-Islets Drives Organoid-Specific Transcripts Associated with Alzheimer’s Disease and Autoimmune Diseases

Sundstrom J, Vanderleeden E, Barton NJ, Redick SD, Dawes P, Murray LF, Olson MN, Tran K, Chigas SM, Orszulak AR, Church GM, Readhead B, Oh HS, Harlan DM, Knipe DM, Wang JP, Chan Y, Lim ET

Herpes Simplex Virus 1 Infection of Human Brain Organoids and Pancreatic Stem Cell-Islets Drives Organoid-Specific Transcripts Associated with Alzheimer's Disease and Autoimmune Diseases

Maione Angela Serena, Iengo Lara, Sala Luca, Massaiu Ilaria, Chiesa Mattia, Lippi Melania, Ghilardi Stefania, Florindi Chiara, Lodola Francesco, Zaza Antonio, Tondo Claudio, Schiavone Marco, Banfi Cristina, Pompilio Giulio, Poggio Paolo, Sommariva Elena

Cardiomyocyte and stromal cell cross-talk influences the pathogenesis of arrhythmogenic cardiomyopathy: a multi-level analysis uncovers DLK1-NOTCH pathway role in fibro-adipose remodelling

Chao Clifford, Martinez Isabella G., Wagenblast Elvin

Models to study myelodysplastic syndrome and acute myeloid leukaemia

Akerman Emily, Capel Rebecca A, Read Matthew, Song Qianqian, Bose Samuel J, Calamaio Serena, Aston Daniel, Koschinski Andreas, Lloyd Scott, Bell Laura, Rashbrook Victoria S, Keller Marco, Bracher Franz, Potter Barry VL, Rivolta Ilaria, Galione Antony, Sparrow Duncan B, Conti Alana, Terrar Derek A, Zaccolo Manuela, Burton Rebecca AB

Lysosomal calcium signalling contributes to the acute α-adrenergic response via calcium-stimulated adenylyl cyclase 1 and 8

Matsuyama Makoto, Iwamiya Takahiro

Novel and effective plasmid transfection protocols for functional analysis of genetic elements in human cardiac fibroblasts

Costa A, Hunkler HJ, Chatterjee S, Cushman S, Hilbold E, Xiao K, Lu D, Leonardy J, Juchem M, Sansonetti M, Hoepfner J, Thum T, Bär C

A reporter system for live cell tracking of human cardiomyocyte proliferation

Siehler Johanna, Bilekova Sara, Chapouton Prisca, Dema Alessandro, Albanese Pascal, Tamara Sem, Jain Chirag, Sterr Michael, Enos Stephen J., Chen Chunguang, Malhotra Chetna, Villalba Adrian, Schomann Leopold, Bhattacharya Sreya, Feng Jin, Akgün Canan Melis, Ribaudo Federico, Ansarullah, Burtscher Ingo, Ahlbrecht Christin, Plettenburg Oliver, Kurth Thomas, Scharfmann Raphael, Speier Stephan, Scheltema Richard A., Lickert Heiko

Inceptor binds to and directs insulin towards lysosomal degradation in β cells

Marcella BM, Hockey BL, Braun JL, Whitley KC, Geromella MS, Baranowski RW, Watson CJF, Silvera S, Hamstra SI, Wasilewicz LJ, Crozier RWE, Marais AAT, Kim KH, Lee G, Vandenboom R, Roy BD, MacNeil AJ, MacPherson REK, Fajardo VA

GSK3 inhibition improves skeletal muscle function and whole-body metabolism in male mouse models of Duchenne muscular dystrophy

Dionne Olivier, Sabatié Salomé, Fortin Fléchère, Corbin François, Laurent Benoit

Efficient generation of human induced pluripotent stem cells from urine samples of patients with Fragile X syndrome

Sheveleva O, Protasova E, Grigor'eva E, Butorina N, Kuziaeva V, Antonov D, Melnikova V, Medvedev S, Lyadova I

The Generation of Genetically Engineered Human Induced Pluripotent Stem Cells Overexpressing IFN-β for Future Experimental and Clinically Oriented Studies

El-Banna Ahmed H., Abo El-Ela Fatma I., Abdel-Wahab Ahmed, Gamal Amr, Abdel-Razik Abdel-Razik H., El-Banna Hossny A., Elsamannoudy Salma.I., Ibrahim Marwa A., Abdelghany Asmaa K.

Therapeutic efficacy of amygdaline and amygdaline-loaded niosomes in a rat model of Alzheimer’s disease via oxidative stress, brain neurotransmitters, and apoptotic pathway

Karimpour Sedigheh, De Costa Peter, Nazari Mostafa

Emotions in switching the code: contributions for English language teachers’ identity construction

Tumdam Roshan, Hussein Yara, Garin-Shkolnik Tali, Stern Shani

NMDA Receptors in Neurodevelopmental Disorders: Pathophysiology and Disease Models

Peltonen S, Sonninen TM, Niskanen J, Koistinaho J, Ruponen M, Lehtonen Š

Mutated LRRK2 induces a reactive phenotype and alters migration in human iPSC-derived pericyte-like cells

Arber C, Casey JM, Crawford S, Rambarack N, Yaman U, Wiethoff S, Augustin E, Piers TM, Price M, Rostagno A, Ghiso J, Lewis PA, Revesz T, Hardy J, Pocock JM, Houlden H, Schott JM, Salih DA, Lashley T, Wray S

Microglia contribute to the production of the amyloidogenic ABri peptide in familial British dementia

Mothes T, Konstantinidis E, Eltom K, Dakhel A, Rostami J, Erlandsson A

Tau processing and tau-mediated inflammation differ in human APOEε2 and APOEε4 astrocytes

Iyer DP, Khoei HH, van der Weijden VA, Kagawa H, Pradhan SJ, Novatchkova M, McCarthy A, Rayon T, Simon CS, Dunkel I, Wamaitha SE, Elder K, Snell P, Christie L, Schulz EG, Niakan KK, Rivron N, Bulut-Karslioğlu A

mTOR activity paces human blastocyst stage developmental progression

Thongsin N, Suwanpitak S, Augsornworawat P, Srisantitham J, Saiprayong K, Jenjaroenpun P, Wattanapanitch M

Phenotypic and transcriptomic profiling of induced pluripotent stem cell (iPSC)-derived NK cells and their cytotoxicity against cancers

Ge N, Suzuki K, Sato I, Noguchi M, Nakamura Y, Matsuo-Takasaki M, Fujishiro J, Hayashi Y

Generation of human induced pluripotent stem cell lines derived from patients of cystic biliary atresia

Yang Wenke, Wang Shuyue, Yang Ke, Li Yanjun, Guo Zhenglong, Huang Jianmei, Wang Jinming, Liao Shixiu

Transcriptome analyses reveal molecular mechanisms of novel compound heterozygous ACO2 variants causing infantile cerebellar retinal degeneration

Scuto Maria, Majzúnová Miroslava, Torcitto Gessica, Antonuzzo Silvia, Rampulla Francesco, Di Fatta Eleonora, Trovato Salinaro Angela

Functional Food Nutrients, Redox Resilience Signaling and Neurosteroids for Brain Health

Yammine Kathryn M., Abularach Sophia Mirda, Xiong Michael, Kim Seo-yeon, Bikovtseva Agata A., Butty Vincent L., Schiavoni Richard P., Bateman John F., Lamandé Shireen R., Shoulders Matthew D.

Human cartilage model of the precocious osteoarthritis-inducingCOL2A1p.Arg719Cys reveals pathology-driving matrix defects and a failure of the ER proteostasis network to recognize the defective procollagen-II

Huang C, Qiu L, Zhou W, Shao C, Wang X, Zhang Q, Chen W, Xiong M, Huang M, Tang M, Zou L, Xu X

A human-induced pluripotent stem cell (iPSC) line (SMUSHi006-A) from an ALS patient carrying a mutation c.1126C > T in the FUS gene

Begovic Merima, Schneider Luca, Zhou Xiaobo, Hamdani Nazha, Akin Ibrahim, El-Battrawy Ibrahim

The Role of Human-Induced Pluripotent Stem Cells in Studying Cardiac Channelopathies

Silvestri B, Mochi M, Mawrie D, de Turris V, Colantoni A, Borhy B, Medici M, Anderson EN, Garone MG, Zammerilla CP, Simula M, Ballarino M, Pandey UB, Rosa A

HuD impairs neuromuscular junctions and induces apoptosis in human iPSC and Drosophila ALS models

Li J, Wiesinger A, Fokkert L, Bakker P, de Vries DK, Tijsen AJ, Pinto YM, Verkerk AO, Christoffels VM, Boink GJJ, Devalla HD

Modeling the atrioventricular conduction axis using human pluripotent stem cell-derived cardiac assembloids

Mao YQ, Jahanshahi S, Malty R, Van Ommen DAJ, Wan Y, Morey TM, Chuang SHW, Pavlova V, Ahmed C, Dahal S, Lin F, Mangos M, Nurtanto J, Song Y, Been T, Christie-Holmes N, Gray-Owen SD, Babu M, Wong AP, Batey RA, Attisano L, Cochrane A, Houry WA

Targeting protein homeostasis with small molecules as a strategy for the development of pan-coronavirus antiviral therapies

Rahimov F, Nieminen P, Kumari P, Juuri E, Nikopensius T, Paraiso K, German J, Karvanen A, Kals M, Elnahas AG, Karjalainen J, Kurki M, Palotie A, FinnGen, Estonian Biobank Research Team, Heliövaara A, Esko T, Jukarainen S, Palta P, Ganna A, Patni AP, Mar D, Bomsztyk K, Mathieu J, Ruohola-Baker H, Visel A, Fakhouri WD, Schutte BC, Cornell RA, Rice DP

High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene

Kania Evan E., Fenix Aidan, Marciniak Daphnée M., Lin Qiaoyi, Bianchi Sara, Hristov Borislav, Li Shuai, Camplisson Conor K., Fields Rose, Beliveau Brian J., Schweppe Devin K., Noble William S., Ong Shao-En, Bertero Alessandro, Murry Charles E., Shechner David M.

Nascent transcript O-MAP reveals the molecular architecture of a single-locus subnuclear compartment built by RBM20 and theTTNRNA

McKinnon Jayden C., Balez Rachelle, Young Reuben S.E., Brown Mikayla L., Lum Jeremy S., Robinson Liam, Belov Mikhail E., Ooi Lezanne, Tortorella Sara, Mitchell Todd W., Ellis Shane R.

MALDI-2-Enabled Oversampling for the Mass Spectrometry Imaging of Metabolites at Single-Cell Resolution

De La Cruz B, Mitra S, He B, Çelik M, Kaminski D, Smedler E, Sterky F.

Efficient Gene-Editing in Human Pluripotent Stem Cells Through Simplified Assembly of Adeno-Associated Viral (AAV) Donor Templates

Javed Sundas, Fersini Marco, Bernardini Giulia

Unleashing the Power of Induced Pluripotent stem Cells in in vitro Modelling of Lesch-Nyhan Disease

Chen Chaoxian, Zhang Houan, Qiao Dongxu, Xia Peng, Zhang Yunhao, Dang Wei, Gu Siyong, Yang Yihang

Microstructure and mechanical properties of (Ti, W, Mo, Nb, Ta) (C0.78, N0.22) high entropy cermets with 5–25 wt% Co–Ni binders

Nuermaimaiti Maierdanjiang, Ishikawa Kei-ichi, Oyama Genko, Nonaka Risa, Shiga Takahiro, Jo Takayuki, Tsunemi Taiji, Nakamura Ryota, Krüger Rejko, Akamatsu Wado, Hattori Nobutaka

Human induced pluripotent stem cell-derived dopaminergic neurons release alpha-synuclein through neuronal activity

Kim D, Lim H, Youn J, Park TE, Kim DS

Scalable production of uniform and mature organoids in a 3D geometrically-engineered permeable membrane

Henke Marie‐Thérèse, Prigione Alessandro, Schuelke Markus

Disease models of Leigh syndrome: From yeast to organoids

Zhuang Mengjie, Zhu Sensen, Su Liping, Liu Li, Ji Min, Xiao Jinling, Guan Yaling, Dai Chenlu, Liu Jingyu, Yang Long, Pu Hongwei

SNTA1 inhibits the PI3K/AKT signaling pathway leading to increased mitochondrial dysfunction and arrhythmia caused by diacetylmorphine

AlAbdi Lama, Maddirevula Sateesh, Aljamal Bayan, Hamid Halima, Almulhim Aisha, Hashem Mais O., Algoos Yusra, Alqahtani Mashael, Albaloshi Shahad, Alghamdi Mohammed, Alduaylij Mohammed, Shamseldin Hanan E., Nadeef Seba, Patel Nisha, Abdulwahab Firdous, Abouyousef Omar, Alshidi Tarfa, Jaafar Amal, Abouelhoda Mohamed, Alhazzani Adel, Alfares Ahmed, Qudair Ahmad, Alsulaiman Ahood, Alhashem Amal, Khan Arif O., Chedrawi Aziza, Alebdi Basel, AlAjlan Fahad, Alotaibi Fawaz, Alzaidan Hamad, Banjar Hanaa, Abdelraouf Hanem, Alkuraya Hisham, Abumansour Iman, Alfayez Khowlah, Tulbah Maha, Alowain Mohammed, Alqahtani Mohammed, El-Kalioby Mohammed, Shboul Mohammad, Sulaiman Raashda, Al Tala Saed, Khan Sameena, Coskun Serdar, Mrouge Sobaihi, Alenazi Walaa, Rahbeeni Zuhair, Alkuraya Fowzan S.

Arab founder variants: Contributions to clinical genomics and precision medicine

Peters Marijn C., Zaldumbide Arnaud, Groeneveld Esmee J., Rabelink Martijn J.W.E., Peerlings Janneke H., van den Bogaerdt Antoon, Bouten Carlijn V.C., Hoeben Rob C., Goumans Marie-Jose, van Wijk Abraham

Immune Shielding of Human Heart Valves

Kuroda Yukiko, Uehara Takeshi, Enomoto Yumi, Naruto Takuya, Matsumura Nozomi, Kurosawa Kenji

GPC4 truncating variant associated with Keipert syndrome and lacrimal punctal agenesis

Xie Changning, Kessi Miriam, Yin Fei, Peng Jing

Roles of KCNA2 in Neurological Diseases: from Physiology to Pathology

Pandit A, Indurkar A, Locs J, Haugen HJ, Loca D

Calcium Phosphates: A Key to Next-Generation In Vitro Bone Modeling

Raabe J, Wittig I, Laurette P, Stathopoulou K, Brand T, Schulze T, Klampe B, Orthey E, Cabrera-Orefice A, Meisterknecht J, Thiemann E, Laufer SD, Shibamiya A, Reinsch M, Fuchs S, Kaiser J, Yang J, Zehr S, Wrona KM, Lorenz K, Lukowski R, Hansen A, Gilsbach R, Brandes RP, Ulmer BM, Eschenhagen T, Cuello F

Physioxia rewires mitochondrial complex composition to protect stem cell viability

Liu W. Q., Zhu L. F., Zhang T., Zeng S. X., Hu L.

Bioinformatic Analysis of the Molecular Pathways of ATRX and XIST in X Chromosome Inactivation

Dya German A., Lebedeva Olga S., Gushchevarov Daniil A., Volovikov Egor A., Belikova Lilia D., Kopylova Irina V., Postnikov Alexander B., Artemieva Marina M., Medvedeva Natalia A., Lagarkova Maria A., Katrukha Alexey G., Serebryanaya Daria V.

Specific cleavage of IGFBP-4 by papp-a in nervous tissue

Yang M, You D, Liu G, Lu Y, Yang G, O'Brien T, Henshall DC, Hardiman O, Cai L, Liu M, Shen S

Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons

Wolnik Jan, Adamska Patrycja, Oleksy Aleksandra, Sanetra Anna Magdalena, Palus-Chramiec Katarzyna, Lewandowski Marian Henryk, Dulak Józef, Biniecka Monika

A novel 3D cardiac microtissue model for investigation of cardiovascular complications in rheumatoid arthritis

Langlois J, Lange S, Ebeling M, Macnair W, Schmucki R, Li C, DeGeer J, Sudharshan TJJ, Yong VW, Shen YA, Harp C, Collin L, Keaney J

Fenebrutinib, a Bruton's tyrosine kinase inhibitor, blocks distinct human microglial signaling pathways

Li Lei, Zhao Zijuan, Liu Zihao, Tang Yuquan, Yang Tan, Gong Nailin, Liao Bing, Long Yang, Nie Yongmei, Yu Fengxu

Identification of the optimal reference genes for atrial fibrillation model established by iPSC-derived atrial myocytes

Tong X, Poramba-Liyanage DW, van Hoolwerff M, Riemers FM, Montilla-Rojo J, Warin J, Salvatori D, Camus A, Meulenbelt I, Ramos YFM, Geijsen N, Tryfonidou MA, Shang P

Isolation and tracing of matrix-producing notochordal and chondrocyte cells using ACAN-2A-mScarlet reporter human iPSC lines

Wang Brian Xiangzhi

Investigating Inherited Heart Diseases Using Human Induced Pluripotent Stem Cell-Based Models

Semenova P. I., Panova A. V., Sopova J. V., Krasnova O. A., Turilova V. I., Yakovleva T. K., Kulikova K. S., Petrova D. A., Kiselev S. L., Neganova I. E.

Generation of CRISPR/Cas9 modified human iPSC line with correction of heterozygous mutation in exon 6 of the CaSR gene

Borisch Carla, Thum Thomas, Bär Christian, Hoepfner Jeannine

Human in vitro models for Fabry disease: new paths for unravelling disease mechanisms and therapies

Ging K, Frick L, Schlachetzki J, Armani A, Zhu Y, Gilormini PA, Dhingra A, Böck D, Marques A, Deen M, Chen X, Serdiuk T, Trevisan C, Sellitto S, Pisano C, Glass CK, Heutink P, Yin JA, Vocadlo DJ, Aguzzi A

Direct and indirect regulation of β-glucocerebrosidase by the transcription factors USF2 and ONECUT2

Liu S, Yang N, Yan Y, Wang S, Chen J, Wang Y, Gan X, Zhou J, Xie G, Wang H, Huang T, Ji W, Wang Z, Si W

An accelerated Parkinson's disease monkey model using AAV-α-synuclein plus poly(ADP-ribose)

Rosochowicz MA, Lach MS, Richter M, Jagiełło I, Suchorska WM, Trzeciak T

The iPSC secretome is beneficial for in vitro propagation of primary osteoarthritic chondrocytes cell lines

Vicente Pedro, Almeida Joana I., Crespo Inês E., Virgolini Nikolaus, Isidro Inês A., Calleja-Cervantes Maria Eréndira, Rodriguez-Madoz Juan R., Prosper Felipe, Alves Paula M., Serra Margarida

Oxygen control in bioreactor drives high yield production of functional hiPSC-like hepatocytes for advanced liver disease modelling

Trinh J, Schaake S, Gabbert C, Lüth T, Cowley SA, Fienemann A, Ullrich KK, Klein C, Seibler P

Optical genome mapping of structural variants in Parkinson's disease-related induced pluripotent stem cells

Ewoldt JK, Wang MC, McLellan MA, Cloonan PE, Chopra A, Gorham J, Li L, DeLaughter DM, Gao X, Lee JH, Willcox JAL, Layton O, Luu RJ, Toepfer CN, Eyckmans J, Seidman CE, Seidman JG, Chen CS

Hypertrophic cardiomyopathy-associated mutations drive stromal activation via EGFR-mediated paracrine signaling

Yang HS, Zheng YX, Bai X, He XY, Wang TH

Application prospects of urine-derived stem cells in neurological and musculoskeletal diseases

Lee Yoo Jin, Jo Dong Hyun

Retinal Organoids from Induced Pluripotent Stem Cells of Patients with Inherited Retinal Diseases: A Systematic Review

Ge Ning, Li Rui, Liu Min, Xia Wenxin, O'Brien Stephen T., McInerney Veronica, Galvin Joseph, Ward Deirdre, McGorrian Catherine, O'Brien Timothy, Shen Sanbing, Prendiville Terence W.

Defining Cardiomyocyte Repolarization Response to Pharmacotherapy in Long‐QT Syndrome Type 3

Cotta GC, Teixeira Dos Santos RC, Costa GMJ, Lacerda SMDSN

Reporter Alleles in hiPSCs: Visual Cues on Development and Disease

Fischer Inbar, Shohat Sophie, Leichtmann-Bardoogo Yael, Nayak Ritu, Wiener Gal, Rosh Idan, Shemen Aviram, Tripathi Utkarsh, Rokach May, Bar Ela, Hussein Yara, Castro Ana Carolina, Chen Gal, Soffer Adi, Schokoroy-Trangle Sari, Elad-Sfadia Galit, Assaf Yaniv, Schroeder Avi, Monteiro Patricia, Stern Shani, Maoz Ben M., Barak Boaz

Shank3 mutation impairs glutamate signaling and myelination in ASD mouse model and human iPSC-derived OPCs

Pietsch N, Chen CY, Kupsch S, Bacmeister L, Geertz B, Herrera-Rivero M, Siebels B, Voß H, Krämer E, Braren I, Westermann D, Schlüter H, Mearini G, Schlossarek S, van der Velden J, Caporizzo MA, Lindner D, Prosser BL, Carrier L

Chronic Activation of Tubulin Tyrosination Improves Heart Function

Sugie Kazuma, Nishino Ichizo

History and Perspective of LAMP-2 Deficiency (Danon Disease)

Villafranco Javier, Martínez-Ramírez Gabriela, Magaña-Maldonado Roxana, González-Ruvalcaba Anna Paola, López-Ornelas Adolfo, Velasco Iván, Becerril-Villanueva Enrique, Pavón Lenin, Estudillo Enrique, Pérez-Sánchez Gilberto

The use of induced pluripotent stem cells as a platform for the study of depression

Chang Y, Bai R, Zhang Y, Lu WJ, Ma S, Zhu M, Lan F, Jiang Y

SMYD1 modulates the proliferation of multipotent cardiac progenitor cells derived from human pluripotent stem cells during myocardial differentiation through GSK3β/β-catenin&ERK signaling

Wells CA, Guhr A, Bairoch A, Chen Y, Hu M, Löser P, Ludwig TE, Mah N, Mueller SC, Seiler Wulczyn AEM, Seltmann S, Rossbach B, Kurtz A

Guidelines for managing and using the digital phenotypes of pluripotent stem cell lines

Tang Fan, Dong Tao, Zhou Chengqian, Deng Leon, Liu Hans B., Wang Wenshen, Liu Guanshu, Ying Mingyao, Li Pan P.

Genetically engineered human induced pluripotent stem cells for the production of brain-targeting extracellular vesicles

Zheng Yiting, Chen Jing

Voltage-gated potassium channels and genetic epilepsy

Baldé H, Geurts B, Fischer HT, Menelik-Obbarius S, Kaba I, Merhi V, Stein K, Diaconu V, Bahr T, Weishaar H, Delamou A, Mbawah AK, El-Bcheraoui C

Responding to fluctuations in public and community trust and health seeking behaviour during the COVID-19 pandemic: a qualitative study of national decision-makers' perspectives in Guinea and Sierra Leone

Janpipatkul K, Sutjarit N, Tangprasittipap A, Chaiamarit T, Innachai P, Suksen K, Chokpanuwat T, Tim-Aroon T, Anurathapan U, Jearawiriyapaisarn N, Tubsuwan A, Bowornpinyo S, Asavapanumas N, Chairoungdua A, Bhukhai K, Hongeng S

Therapeutic delivery of recombinant glucocerebrosidase enzyme-containing extracellular vesicles to human cells from Gaucher disease patients

Baggiani Matteo, Damiani Devid, Privitera Flavia, Della Vecchia Stefania, Tessa Alessandra, Santorelli Filippo Maria

Generation and Characterization of hiPS Lines from Three Patients Affected by Different Forms of HPDL-Related Neurological Disorders

Almeida Zaida L., Vaz Daniela C., Brito Rui M. M.

Transthyretin mutagenesis: impact on amyloidogenesis and disease

van de Weijer ML, Samanta K, Sergejevs N, Jiang L, Dueñas ME, Heunis T, Huang TY, Kaufman RJ, Trost M, Sanyal S, Cowley SA, Carvalho P

Tapasin assembly surveillance by the RNF185/Membralin ubiquitin ligase complex regulates MHC-I surface expression

Vasilyeva Tatyana, Kadyshev Vitaly, Khalanskaya Olga, Kuznetsova Svetlana, Ionova Sofya, Marakhonov Andrey, Zinchenko Rena

Clinical and Molecular Findings in Patients with Knobloch Syndrome 1: Case Series Report

Peng J.

Update of generation and application of skin organoids

Bai L.

Update of the treatment for primary cutanious amyloidosis

Chi H, Qu B, Prawira A, Richardt T, Maurer L, Hu J, Fu RM, Lempp FA, Zhang Z, Grimm D, Wu X, Urban S, Dao Thi VL

An hepatitis B and D virus infection model using human pluripotent stem cell-derived hepatocytes

Sareen N, Srivastava A, Mittal I, Shah AH, Dhingra S

Establishment of a new human iPSC cell line (UOMi012-A) from a patient with congenital heart defect who has undergone Fontan procedure

Shishkova Daria K., Frolov Alexey V., Markova Victoria E., Markova Yulia O., Lazebnaya Anastasia I., Kutikhin Anton G.

IMPROVING METHODOLOGY OF ENDOTHELIAL CELL RESEARCH: SYNOPSIS AND PROSPECTS

Alwohoush Enas, Ismail Mohammad A., Al-Kurdi Ban, Barham Raghda, Al Hadidi Sabal, Awidi Abdalla, Ababneh Nidaa A.

Effect of hypoxia on proliferation and differentiation of induced pluripotent stem cell-derived mesenchymal stem cells

Oh JY, Yoo DH, Im YS, Kim YO

Generation and characterization of a human iPSC line expressing EGFP-tagged CDH1, KSCBi002-A-3

Hanley M, Alonzo M, Ye S, Yu Y, Contreras J, Hayden J, Garg V, Zhao MT

Characterization of an induced pluripotent stem cell line (NCHi013-A) from a 5-year-old male with pulmonary atresia with intact ventricular septum and a biventricular repair

Ahmad I, Kapoor H, Kumar Srivastava A, Faruq M

Generation and characterization of human-derived induced pluripotent stem cell line (IGIBi010-A) from a patient with neurodegenerative disease phenotype carrying mutation in SQSTM1/p62 gene

Joseph B, Varea I, Emmerich K, Manohar-Sindhu S, Zou J, Friend K, Sipwoli C, Tang X, Yang D, de Jesus Rasheed AA, Goldbach-Mansky R, Boehm M

Establishment of a human induced pluripotent stem cell line (NIHTVBi031-A) derived from a COPA syndrome patient with a heterozygous p.Ala239Pro mutation

Alsalloum A, Shefer K, Bogdanov P, Mingaleva N, Kim A, Feoktistova S, Mityaeva O, Volchkov P

Establishment of a human induced pluripotent stem cell line (ABi004-A) carrying a compound heterozygous mutation in the KCNV2 gene

Jiang C, Huang W, Zhou Y, Wang J, Lei H, Niu Y, Zhou R, Zhang Y

Generating a human induced pluripotent stem cell line (XACHi018-A) from a Timothy syndrome infant carrying heterozygous CACNA1C c.1216G>A (p.G406R) mutation

Bianchini L, Sieber L, Hammad R, Schäfer R, Kutscher LM

Generation of two isogenic patient-derived human-induced pluripotent stem cell clones with 6q27 deletion

Varea I, Joseph B, Emmerich K, Manohar-Sindhu S, Zou J, Friend K, Tang X, Yang D, de Jesus Rasheed AA, Goldbach-Mansky R, Boehm M

Human induced pluripotent stem cells (NIHTVBi029-A and NIHTVBi030-A) generated from two patients with a heterozygous mutation in the CDC42 gene

Lim SW, Lee KI, Cui S, Fang X, Shin YJ, Lee H, Lee JY, Chung BH, Yang CW

Generation of green fluorescent protein reporter knock-in iPSC line at the 3'UTR region of the KLOTHO locus

Kelters Ilse R., Verbueken Devin, Beekink Tess, Van Laake Linda W., Sluijter Joost P.G., Maas Renee G.C., Buikema Jan W.

Generation of human induced pluripotent stem cell (hiPSC) lines derived from three patients carrying the pathogenic CRYAB (A527G) mutation and one non-carrier family member

Shin Yoo Jin, Chae Seung Yun, Lee Hanbi, Fang Xianying, Cui Sheng, Lim Sun Woo, Lee Kang In, Lee Jae Young, Li Can, Yang Chul Woo, Chung Byung Ha

CRISPR/Cas9-mediated suppression of A4GALT rescues endothelial cell dysfunction in a fabry disease vasculopathy model derived from human induced pluripotent stem cells

Wang X, Zhuang H, Tan Y, Lei F, Li C, Zhang C, Yu X, Sang H

Generation of a human induced pluripotent stem cell (iPSC, DVSi001-A) with a heterozygous mutation in KRAS (A209T)

Bai Ruiqi, Hao Lixia, Zhou Guiwen, Fu Qiang, Zhang Peixuan, Lin Pianpian, Chen Minliang

The mechanism of TGF-β mediating BRD4/STAT3 signaling pathway to promote fibroblast proliferation and thus promote keloid progression

Tang P, Keshi E, Wilken S, Wutsdorff L, Mougnekabol J, Pratschke J, Sauer IM, Haep N

Generation of an induced pluripotent stem cell (iPSC) line (EXSURGi001-A) from a patient homozygous for the p.Ala165Thr mutation in the MTARC1 gene

Wang B, Yang L, Gao M, Zhang H, Ji A, Liu G, Liu Y

Establishment of a human induced pluripotent stem cell line (SDQLCHi079-A) from a patient with Johanson-Blizzard syndrome carrying heterozygous mutation in UBR1 gene

Pornratananont G, Tangprasittipap A, Hongeng S, Anurathapan U

Generation of integration-free human induced pluripotent stem cell line MURAi003-A derived from the peripheral blood mononuclear cells of a donor with homozygous Class I and Class II HLAs (A*11:01, B*46:01; C*01:02; DRB1*09:01; DQB1*03:03)

Fatima N, Dillen L, Hommersom MP, Çepni E, Fatima F, van Beusekom E, Albert S, Ali Khan A, de Brouwer APM, van Bokhoven H

Generation of induced pluripotent stem cell line (UCSFi001-A-77) carrying a biallelic frameshift variant in exon 4 of SGIP1 through CRISPR/Cas9

Heider Johanna, González Emilio Pardo, Hartmann Sophia-Marie, Kannaiyan Nirmal, Vogel Sabrina, Wüst Richard, Fallgatter Andreas J., Rossner Moritz J., Kraushaar Udo, Volkmer Hansjürgen

Aberrant neuronal connectivity and network activity of neurons derived from patients with idiopathic schizophrenia

Vacante F, Venkateshappa R, Htet M, Yan C, Wu JC

Generation of Marfan syndrome-specific induced pluripotent stem cells harboring FBN1 mutations

Qin H, Yu Y, Ye S, Alonzo M, Garg V, Zhao MT

Generation of an induced pluripotent stem cell line (NCHi016-A) from a 5-year-old female with pulmonary atresia with intact ventricular septum and one-and-half ventricle palliation

Jin Meng, Zhang Guowei, Wang Shouqi, Zhao Rou, Zhang Haitao

ISL1 and AQP5 complement each other to enhance gastric cancer cell stemness by regulating CD44 expression

Wang L, Guo R, Zhang X, Zhou Z, Yao Akogo H, Fu Z, Song Y, Li M, Ma J

An integration-free induced pluripotent stem cell line from a 42-year-old female donor with the APOE-ε2/ε2 allele

Zhang Denglu, Li KaiLin, Yang XianZhen, Wang Haitao, Yu Xin

Establishment of an induced pluripotent stem cell line from a patient with X-linked Alport syndrome carrying a hemizygous splicing variant (NM_033380; c.929[exon 16]delG) in the collagen type IV alpha 5 chain gene

Jiang S, Dai T, Li Q, Xu T, Zhang W, Sun J, Liu H

Generation of ASCL1-mCherry knock-in reporter in human embryonic stem cell line, WAe001-A-2E, using CRISPR/Cas9-based gene targeting

Dexheimer R, Manhas A, Wu D, Tripathi D, Yu Chan S, Li J, Yu R, Sayed N, Wu JC, Sallam K

Generation of two iPSC lines from dilated cardiomyopathy patients with pathogenic variants in the SCN5A gene

Ma Shi-chao, Xie Yi-lin, Wang Qian, Fu Shan-gui, Wu Hong-ze

Application of eye organoids in the study of eye diseases

Clayton Joshua S., Vo Christina, Crane Jordan, Scriba Carolin K., Saker Safaa, Larmonier Thierry, Malfatti Edoardo, Romero Norma B., Ravenscroft Gianina, Laing Nigel G., Taylor Rhonda L.

Generation of iPSC lines from three Laing distal myopathy patients with a recurrent MYH7 p.Lys1617del variant

Claeys Kristl G., Savarese Marco, Jonson Per Harald, Goosens Veerle, Topf Ana, Vihola Anna, Straub Volker, Udd Bjarne

A Titin Truncating Variant Causing a Dominant Myopathy With Cardiac Involvement in a Large Family

Zhang H, Zhang Q, Chen X, Wang M, Li L, Yu C

Establishment of a transgene-free iPS cell line (SDCHi008-A) from a young patient bearing a KCNQ2 mutation and suffering from Epilepsy

Muhammad Z, Brown PW, Babazau L, Alkhamis AI, Goni BW, Nggada HA, Mbaya KM, Wray S, Marte IH, Karch CM, Serpell LC, Maina MB

Generation of an induced pluripotent stem cell line (BIORTCi001-A) from a healthy adult indigenous Nigerian participant

Lin Chensheng, Liu Shiyu, Huang Minjun, Zhang Yanding, Hu Xuefeng

Induction of human stem cells into ameloblasts by reaggregation strategy

Ahmed H. Shafeeq

The Multifaceted Role of L-Type Amino Acid Transporter 1 at the Blood–Brain Barrier: Structural Implications and Therapeutic Potential

E S K, A K Z, M Yu S, K I P, N L R, E G N, K S S, A A K, T L V, A S M, E N M, T M P, E S V, A A K

Distinct molecular features of FLNC mutations, associated with different clinical phenotypes

Sheveleva O. N., Nenasheva T. A., Lyadova I. V.

Early markers of induced pluripotent stem cell hematopoietic development

Remmert C, Otgonbayar M, Perschel JA, Marder M, Meier M

Protocol to generate a microfluidic vessels-on-chip platform using human pluripotent stem cell-derived endothelial cells

Petersilie L, Kafitz KW, Neu LA, Heiduschka S, Le S, Prigione A, Rose CR

Protocol for the generation of cultured cortical brain organoid slices

Bozhokin Mikhail S., Marchenko Daria M., Mikhaylova Elena R., Rakhimov Bulat R., Bozhkova Svetlana A., Korneva Yulia S., Aleksandrova Svetlana A., Khotin Mikhail G.

Evaluation of chondrogenic potential of human dermal fibroblasts after modification with differentiation media and cytokine TGF-β3

Fasano C, Cavaliere A, Tiranti V, Peron C

Protocol for evaluating mitochondrial respiration in iPSC-derived neurons by the Seahorse XF analyzer

Yan Hao, Zang Ruge, Cui Tiantian, Liu Yiming, Zhang Biao, Zhao Lingpin, Li Hongyu, Zhou Juannian, Wang Haiyang, Zeng Quan, Xu Lei, Zhou Yuqi, Pei Xuetao, Xi Jiafei, Yue Wen

PROTAC-mediated vimentin degradation promotes terminal erythroid differentiation of pluripotent stem cells

Giacomoni J, Bruzelius A, Habekost M, Kajtez J, Ottosson DR, Fiorenzano A, Storm P, Parmar M

3D model for human glia conversion into subtype-specific neurons, including dopamine neurons

Graceffo E, Opitz R, Megges M, Krude H, Schuelke M

RNA Sequencing Reveals a Strong Predominance of THRA Splicing Isoform 2 in the Developing and Adult Human Brain

Retter Ida, Behm Laura, Grohmann Lisa, Schmelz Karin, Rosowski Jennifer, Hippenstiel Stefan

3R centres contributions to change animal experimentation

Rezaeiani S, Rezaee M, Shafaghi M, Karami M, Hamidi R, Khodayari H, Vahdat S, Pahlavan S, Baharvand H

Expandable hESC-derived cardiovascular progenitor cells generate functional cardiac lineage cells for microtissue construction

Qi L, Groeger M, Sharma A, Goswami I, Chen E, Zhong F, Ram A, Healy K, Hsiao EC, Willenbring H, Stahl A

Adipocyte inflammation is the primary driver of hepatic insulin resistance in a human iPSC-based microphysiological system

Joshi Jyotsna, Albers Cora, Smole Nathan, Guo Shuliang, Smith Sakima A.

Human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) for modeling cardiac arrhythmias: strengths, challenges and potential solutions

Micolonghi Caterina, Perrone Federica, Fabiani Marco, Caroselli Silvia, Savio Camilla, Pizzuti Antonio, Germani Aldo, Visco Vincenzo, Petrucci Simona, Rubattu Speranza, Piane Maria

Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review

Sun Wenxian, Chen Yufei, Yang Yuting, Wang Pin, Gong Jin, Han Xiaodong, Xu Chang, Luan Heya, Li Shaoqi, Li Ruina, Wen Boye, Lv Sirong, Wei Cuibai

Characteristics and Transcriptomic Analysis of Cholinergic Neurons Derived from Induced Pluripotent Stem Cells with APP Mutation in Alzheimer’s Disease

Clark Branden J, Lelos Mariah J, Loring Jeanne F

Advancing Parkinson’s disease treatment: cell replacement therapy with neurons derived from pluripotent stem cells

Yi R, Chen S, Guan M, Liao C, Zhu Y, Ip JPK, Ye T, Chen Y

A single-cell transcriptomic dataset of pluripotent stem cell-derived astrocytes via NFIB/SOX9 overexpression

Niu Wenkang, Li Guifang, Zhang Tingting, Ma Lei

Prostate cancer subtyping and differential methylation analysis based on the ETS family of transcription factors fusion genes

Thamarai P, Karishma S, Kamalesh R, Shaji A, Saravanan A, Bibi S, Vickram AS, Chopra H, Saleem RA, Alsharif KF, Theyab A, Kamel M, Alamoudi MK, Kumer A, Chopra S, Abdel-Daim MM

Current advancements in nanotechnology for stem cells

Gerasimova Tatiana, Poberezhniy Daniil, Nenasheva Valentina, Stepanenko Ekaterina, Arsenyeva Elena, Novosadova Lyudmila, Grivennikov Igor, Illarioshkin Sergey, Lagarkova Maria, Tarantul Vyacheslav, Novosadova Ekaterina

Inflammatory Intracellular Signaling in Neurons Is Influenced by Glial Soluble Factors in iPSC-Based Cell Model of PARK2-Associated Parkinson’s Disease

Hutschalik T, Özgül O, Casini M, Szabó B, Peyronnet R, Bártulos Ó, Argenziano M, Schotten U, Matsa E

Immune response caused by M1 macrophages elicits atrial fibrillation-like phenotypes in coculture model with isogenic hiPSC-derived cardiomyocytes

Díaz Alicia González, Possenti Andrea, Urrutia Gustavo Antonio, Bian Yuqi, Kedia Shekhar, Boeken Dorothea, Lim Christine M., Licastro Danilo, Mannini Benedetta, Klenerman David, Vendruscolo Michele

A human neuronal model of sporadic Alzheimer’s disease induced byFBXO2downregulation shows Aβ aggregation, tau hyperphosphorylation and functional network impairment

Stepanov AI, Shuvaeva AA, Putlyaeva LV, Lukyanov DK, Galiakberova AA, Gorbachev DA, Maltsev DI, Pronina V, Dylov DV, Terskikh AV, Lukyanov KA, Gurskaya NG

Tracking induced pluripotent stem cell differentiation with a fluorescent genetically encoded epigenetic probe

Law Christine, Pattathil Niveditha, Simpson Hailey, Ward Michael J., Lampen Shaun, Kamath Binita, Aleman Tomas S.

Intraretinal hemorrhages and detailed retinal phenotype of three patients with Alagille syndrome

Baggiani M, Santorelli FM, Mero S, Privitera F, Damiani D, Tessa A

Generation of a human induced pluripotent stem cell line (FSMi001-A) from fibroblasts of a patient carrying heterozygous mutation in the REEP1 gene

Ning J, Zhou T, Luo X, Ma J, Zhang Z, Gao L, Zhu Y

Establishment of an iPSC line from a NDD patient with a heterozygous mutation in the CTNNB1 gene

Qin Y, Godoy-Parejo C, Skowronska M, Verma A, Dejosez M, Zwaka TP

Generation of human pluripotent stem cell lines (WAe009-A) with THAP11(F80L) cobalamin disorder-associated mutation

Alowaysi M, Baadhaim M, Al-Shehri M, Alzahrani H, Badkok A, Attas H, Zakri S, Alameer S, Malibari D, Hosawi M, Daghestani M, Al-Ghamdi K, Muharraq M, Zia A, Tegne J, Alfadhel M, Aboalola D, Alsayegh K

Derivation of two iPSC lines (KAIMRCi004-A, KAIMRCi004-B) from a Saudi patient with Biotin-Thiamine-responsive Basal Ganglia Disease (BTBGD) carrying homozygous pathogenic missense variant in the SCL19A3 gene

Pierre Marion, Djemai Mohammed, Pouliot Valérie, Poulin Hugo, Gollob Michael H., Chahine Mohamed

Exploring SCN5A variants associated with atrial fibrillation in atrial cardiomyocytes derived from human induced pluripotent stem cells: A characterization study

Takagi D, Tsukamoto S, Nakade K, Shimizu T, Arai Y, Matsuo-Takasaki M, Noguchi M, Nakamura Y, Yumoto N, Kawada J, Hayata T, Hayashi Y

Generation of MBP-tdTomato reporter human induced pluripotent stem cell line for live myelin visualization

Arai D, Takahashi-Shibata M, Ukaji T, Tsutsumi H, Tajima S, Nishio SY, Ishikawa KI, Akamatsu W, Matsumoto F, Ikeda K, Usami SI, Kamiya K

Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH23

Ltaief SM, Elsayed AK, Al-Shammari AR

Generation of nine induced pluripotent stem cell lines from six young children with autism spectrum disorder and three matched control subjects from the Qatari population

Wang X, Gao J, Liu C, Sun J

Establishment of human embryonic stem cell lines carrying LQT1 mutations by CRISPR base editing

Hall FD 3rd, Miller CN, Gerecht S, Boheler KR

Generation of an induced pluripotent stem cell line, JHUi005-A, from a Marfan Syndrome patient harboring a pathogenic c.3338-2A>C intronic splicing variant

Volke L, Daya NM, Döring K, Rohm M, Athamneh M, Zaehres H, Roos A, Güttsches AK, Mavrommatis L, Vorgerd M

Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onset

Zanetti Alessandra, Tomanin Rosella

Targeting Neurological Aspects of Mucopolysaccharidosis Type II: Enzyme Replacement Therapy and Beyond

Tangprasittipap A, Innachai P, Chumchuen S, Chiangjong W, Jinawath N, Sirachainan N, Hongeng S

Establishment of human induced pluripotent stem cell line MURAi001-A from skin fibroblasts of a patient carrying a c.4404A > G mutation in the TET1 gene

Wong EYM, Khoh XE, Chen SC, Lye J, Leith FK, Zhang D, Lamey TM, Thompson JA, McLaren TL, Atlas MD, Chen FK, McLenachan S

Generation of two induced pluripotent stem cell lines from an Usher syndrome type 1B patient with the homozygous c.496del MYO7A variant

Zhang H, Zhang T, Wang Y, Shi J, Meng Y, Zhang Q, Guo Q, Duan C

Establishment of a transgene-free iPS cell line (SDCHi007-A) from a young patient bearing a ATP1A2 mutation and suffering from Epilepsy

Meng XY, Sun HF, Zhang YJ, Li WX, Wang DD, Liu DH, Li SM, Wu Y, Li JK, Liu XH, Liu PP, Yang RZ, Li SA, Kang JS

Generation of an induced pluripotent stem cell line (CSBZZUi001-A) from a female Alzheimer's patient carrying the PSEN1 709 T > C heterozygous mutation

Iqbal Muhammad Khalid, Ambreen Alia, Mujahid Muhammad, Zarlashat Yusra, Abid Muhammad, Yasin Ayesha, Ullah Muhammad Naeem, Shahzad Raheel, Harlina Putri Widyanti, Khan Shahid Ullah, Alissa Mohammed, Algopishi Uthman Balgith, Almubarak Hassan Ali

Cardiomegaly: Navigating the uncharted territories of heart failure - A multimodal radiological journey through advanced imaging, pathophysiological landscapes, and innovative therapeutic frontiers

Schuurmans IME, van Karnebeek CDM, Hoogendoorn ADM, Nadif Kasri N, Garanto A

Generation of hiPSC lines from four pyridoxine-dependent epilepsy (PDE) patients carrying the variant c.1279G>C in ALDH7A1 in homozygosis

Oliva MK, Bourke J., Kornienko D., Mattei C., Mao M., Kuanyshbek A., Ovchinnikov D., Bryson A., Karle TJ, Maljevic S., Petrou S.

Standardizing a method for functional assessment of neural networks in brain organoids

Pachernegg S, Robevska G, G A Ferreira L, van den Bergen JA, Vlahos K, Howden SE, Sinclair AH, Ayers KL

Generation of heterozygous (MCRIi031-A-1) and homozygous (MCRIi031-A-2) SOX9 knockout human iPSC lines

Gong J, Li S, Sun W, Wang P, Han X, Xu C, Chen Y, Yang Y, Luan H, Li R, Wen B, Lv S, Chen R, Guo J, Wei C

Generation of induced pluripotent stem cell line (XWHNi003-A) from a female with APOE gene mutation

Juchem M, Lehmann N, Behrens YL, Bär C, Thum T, Hoepfner J

CRISPR/Cas9-based GLA knockout to generate the female Fabry disease human induced pluripotent stem cell line MHHi001-A-15

Hernández D, Morgan Schlicht S, Elli Clarke J, Daniszewski M, Karch CM, Dominantly Inherited Alzheimer Network (DIAN), Goate AM, Pébay A

Generation of a gene-corrected human isogenic iPSC line from an Alzheimer's disease iPSC line carrying the PSEN1 H163R mutation

Wang T, Li Y, Yang C, Yuan H, Na W, Yu S

Generation of iPSC line (FMCPGHi003-A) from human PBMCs of a patient with Familial hemiplegic migraine type 3

Manhas A, Tripathi D, Noishiki C, Wu D, Liu L, Sallam K, Lee JT, Fukaya E, Sayed N

Generation of two iPSC lines from vascular Ehlers-Danlos Syndrome (vEDS) patients carrying a missense mutation in COL3A1 gene

Yammine KM, Mirda Abularach S, Kim SY, Bikovtseva AA, Lilianty J, Butty VL, Schiavoni RP, Bateman JF, Lamandé SR, Shoulders MD

ER procollagen storage defect without coupled unfolded protein response drives precocious arthritis

Gopurappilly R, Musthafa T, Sukumaran S, Viswanath B, Hasan G

Corrigendum to "Generation of feeder-independent transgene-free iPSC lines from a young-onset Parkinson's disease (YOPD) patient with a homozygous PLA2G6: c.2222G>A (p. Arg741Gln) mutation (NCBSi003-A) and unaffected heterozygous parent (NCBSi004-A)" [Stem Cell Res. 67 (2023) 103033]

Saegusa C, Mutai H, Saeki T, Matsuzaki S, Mizukoshi A, Kitajiri SI, Matsunaga T, Hosoya M, Okano H, Fujioka M

Generation of four induced pluripotent stem cell lines (KEIUi004-A, KEIUi005-A, KEIUi006-A, and KEIUi007-A) from patients with sensorineural hearing loss with mutation in EYA4 gene

Djemai Mohammed, Jalouli Maroua, Chahine Mohamed

Impacts of DCM-linked gating pore currents on the electrophysiological characteristics of hiPSC-CM monolayers

Pachernegg S, Robevska G, Ferreira LGA, van den Bergen JA, Vlahos K, Howden SE, Sinclair AH, Ayers KL

Generation of a homozygous (MCRIi031-A-3) WT1 knockout human iPSC line

Berrocal-Rubio MA, Pawer YDJ, Dinevska M, De Paoli-Iseppi R, Widodo SS, Gleeson J, Rajab N, De Nardo W, Hallab J, Li A, Mantamadiotis T, Clark MB, Wells CA

Discovery of NRG1-VII: the myeloid-derived class of NRG1

Thimm Chantelle, Adjaye James

Untangling the Uncertain Role of Overactivation of the Renin–Angiotensin–Aldosterone System with the Aging Process Based on Sodium Wasting Human Models

Zanfrini Elisa, Bandral Manuj, Jarc Luka, Ramirez-Torres Maria Alejandra, Pezzolla Daniela, Kufrin Vida, Rodriguez-Aznar Eva, Avila Ana Karen Mojica, Cohrs Christian, Speier Stephan, Neumann Katrin, Gavalas Anthony

Generation and application of novel hES cell reporter lines for the differentiation and maturation of hPS cell-derived islet-like clusters

McCulloch Mary Kate, Mehryab Fatemeh, Rashnonejad Afrooz

Navigating the Landscape of CMT1B: Understanding Genetic Pathways, Disease Models, and Potential Therapeutic Approaches

Conteduca Giuseppina, Cangelosi Davide, Baldo Chiara, Arado Alessia, Testa Barbara, Wagner Ryan T., Robertson Keith D., Dequiedt Franck, Fitzsimmons Lane, Malacarne Michela, Filaci Gilberto, Coviello Domenico A.

Impact of NSD1 Alternative Transcripts in Actin Filament Formation and Cellular Division Pathways in Fibroblasts

Sleiman Yvonne, Reisqs Jean-Baptiste, Boutjdir Mohamed

Differentiation of Sinoatrial-like Cardiomyocytes as a Biological Pacemaker Model

Farboud SP, Fathi E, Valipour B, Farahzadi R

Toward the latest advancements in cardiac regeneration using induced pluripotent stem cells (iPSCs) technology: approaches and challenges

Lisowski P, Lickfett S, Rybak-Wolf A, Menacho C, Le S, Pentimalli TM, Notopoulou S, Dykstra W, Oehler D, López-Calcerrada S, Mlody B, Otto M, Wu H, Richter Y, Roth P, Anand R, Kulka LAM, Meierhofer D, Glazar P, Legnini I, Telugu NS, Hahn T, Neuendorf N, Miller DC, Böddrich A, Polzin A, Mayatepek E, Diecke S, Olzscha H, Kirstein J, Ugalde C, Petrakis S, Cambridge S, Rajewsky N, Kühn R, Wanker EE, Priller J, Metzger JJ, Prigione A

Mutant huntingtin impairs neurodevelopment in human brain organoids through CHCHD2-mediated neurometabolic failure

-

Enhanced Maturity and Functionality of Vascularized Human Liver Organoids through 3D Bioprinting and Pillar Plate Culture

Iuso Arcangela, Zhang Fangfang, Dorn Tatjana, Gnutti Barbara, Anikster Yair, Kuebler Sarah, Ahrens-Nicklas Rebecca, Gosselin Rachel, Rahman Shamima, Durst Ronen, Zanuttigh Enrica, Güra Miriam, Poch Christine, Meier Anna, Laugwitz Karl-Ludwig, Schüller Hans-Joachim, Messias Ana, Sibon Ody, Finazzi Dario, Rippert Alyssa, Li Dong, Truxal Kristen, Nandi Deipanjan, Lampert Brent, Yeo Mildrid, Gardham Alice, Nissan Batel, Cederboim Smadar Horowitz, Moretti Alessandra

Pantethine ameliorates dilated cardiomyopathy features in PPCS deficiency disorder: evidence from patients and models of the disease

Shan Y, Zhang Y, Wei Y, Zhang C, Lin H, He J, Wang J, Guo W, Li H, Chen Q, Zhou T, Xing Q, Liu Y, Chen J, Pan G

METTL3/METTL14 maintain human nucleoli integrity by mediating SUV39H1/H2 degradation

Zhou Wei, Li Huizhong, Song Jinxiu, Suo Feng, Gu Maosheng, Qi Suhua

Healthy Plasma Exosomes Exert Potential Neuroprotective Effects against Methylmalonic Acid-Induced Hippocampal Neuron Injury

Grass T, Dokuzluoglu Z, Buchner F, Rosignol I, Thomas J, Caldarelli A, Dalinskaya A, Becker J, Rost F, Marass M, Wirth B, Beyer M, Bonaguro L, Rodriguez-Muela N

Isogenic patient-derived organoids reveal early neurodevelopmental defects in spinal muscular atrophy initiation

Li Yuening, Gray Elizabeth H., Ross Rosie, Zebochin Irene, Lock Amy, Fedele Laura, Kamajaya Louisa Janice, Marrow Rebecca J., Ryan Sarah, Röderer Pascal, Brüstle Oliver, John Susan, Denk Franziska, Taams Leonie S.

Blockade of rheumatoid arthritis synovial fluid-induced sensory neuron activation by JAK inhibitors

Matsuo Kinya, Nagamatsu Jun, Nagata Kazuhiro, Umeda Ryusei, Shiota Takaya, Morimoto Satoru, Suzuki Naoki, Aoki Masashi, Okano Hideyuki, Nakamori Masayuki, Nishihara Hideaki

Establishment of a novel amyotrophic lateral sclerosis patient (TARDBPN345K/+)-derived brain microvascular endothelial cell model reveals defective Wnt/β-catenin signaling: investigating diffusion barrier dysfunction and immune cell interaction

Johnson Omar D., Paul Sayan, Gutierrez Jose A., Russell William K., Ward Michelle C.

DNA damage-associated protein co-expression network in cardiomyocytes informs on tolerance to genetic variation and disease

Stüdemann T, Schwarzová B, Schneidewind T, Geertz B, von Bibra C, Nehring M, Rössinger J, Wiegert JS, Eschenhagen T, Weinberger F

Impulse initiation in engrafted pluripotent stem cell-derived cardiomyocytes can stimulate the recipient heart

Li Yuening, Lock Amy, Fedele Laura, Zebochin Irene, Sabate Alba, Siddle Matthew, Cainarca Silvia, Röderer Pascal, Montag Katharina, Tarroni Paola, Brüstle Oliver, Shaw Tanya, Taams Leonie, Denk Franziska

Modelling inflammation-induced peripheral sensitization in a dish - more complex than expected?

Pavlova SV, Shulgina AE, Zakian SM, Dementyeva EV

Studying Pathogenetic Contribution of a Variant of Unknown Significance, p.M659I (c.1977G > A) in MYH7, to the Development of Hypertrophic Cardiomyopathy Using CRISPR/Cas9-Engineered Isogenic Induced Pluripotent Stem Cells

Stallmeyer Birgit, Bühlmann Clara, Stakaitis Rytis, Dicke Ann-Kristin, Ghieh Farah, Meier Luisa, Zoch Ansgar, MacKenzie MacLeod David, Steingröver Johanna, Okutman Özlem, Fietz Daniela, Pilatz Adrian, Riera-Escamilla Antoni, Xavier Miguel J., Ruckert Christian, Di Persio Sara, Neuhaus Nina, Gurbuz Ali Sami, Şalvarci Ahmet, Le May Nicolas, McEleny Kevin, Friedrich Corinna, van der Heijden Godfried, Wyrwoll Margot J., Kliesch Sabine, Veltman Joris A., Krausz Csilla, Viville Stéphane, Conrad Donald F., O’Carroll Dónal, Tüttelmann Frank

Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility

Zhao Yang, Li Citing, Zhou Xiaozhou (Emily)

Chinese learners’ Swahili learning motivational trajectories

Alsalloum Almaqdad, Mosin Ilya, Shefer Kristina, Mingaleva Natalia, Kim Alexander, Feoktistova Sofya, Malyugin Boris, Boiko Ernest, Sultanov Shamil, Mityaeva Olga, Volchkov Pavel

Novel and Previously Known Mutations of the KCNV2 Gene Cause Various Variants of the Clinical Course of Cone Dystrophy with Supernormal Rod Response in Children

Wu Xin-Yi, Lee Yee-Ki, Lau Yee-Man, Au Ka-Wing, Tse Yiu-Lam, Ng Kwong-Man, Wong Chun-Ka, Tse Hung-Fat

The Pathogenic Mechanisms of and Novel Therapies for Lamin A/C-Related Dilated Cardiomyopathy Based on Patient-Specific Pluripotent Stem Cell Platforms and Animal Models

Liu Zhonglin, Wang Chunyan, Ni Feng, Li Tingshu, Yang Fenglian, Wei Han, Li Tengyan, Huang Changhui, Wang Junli, Wang Binbin

Identification of a Homozygous Mutation of CCDC40 in a Chinese Infertile Man with MMAF and PCD-like Phenotypes

Masano Y, Saegusa C, Ishikawa M, Matsunaga T, Okano H, Fujioka M

Generation of an induced pluripotent stem cell line (KEIUi008-A) from a hearing loss patient with an A1555G mutation in mitochondrial DNA

Gao Jingjing, Gunasekar Swetharajan, Xia Ziting, Shalin Kiruba, Jiang Christopher, Chen Hao, Lee Dongtak, Lee Sohyung, Pisal Nishkal D., Luo James N., Griciuc Ana, Karp Jeffrey M., Tanzi Rudolph, Joshi Nitin

Gene therapy for CNS disorders: modalities, delivery and translational challenges

Casamassa A, Rotundo G, Ceresoni C, Turco EM, Torrente I, Candido O, Nicita F, Tonduti D, Bertini E, Marano M, Ferrari D, Cereda C, Pennuto M, Vescovi AL, Carelli S, Rosati J

Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A)

Russell Grace C., Hamzaoui Yassin, Rho Daniel, Sutrave Gaurav, Choi Joseph S., Missan Dara S., Reckard Gabrielle A., Gustafson Michael P., Kim Gloria B.

Synthetic biology approaches for enhancing safety and specificity of CAR-T cell therapies for solid cancers

Gurwitz David, Steeg Rachel

Enriching iPSC research diversity: Harnessing human biobank collections for improved ethnic representation

Zaki-Dizaji Majid, Abazari Mohammad Foad, Razzaghi Hossein, Shkolnikov Irene, Christie Brian R.

GRM7 deficiency, from excitotoxicity and neuroinflammation to neurodegeneration: Systematic review of GRM7 deficient patients

Ye L, Ni B, Wu H, Han X, Li H, Liu J, Hu S, Lei W

Establishment of a human induced pluripotent stem cell line from a patient with dilated cardiomyopathy

Yu Pengfei, Bosholm Carol Christine, Zhu Hainan, Duan Zhongping, Atala Anthony, Zhang Yuanyuan

Beyond waste: understanding urine’s potential in precision medicine

Dai Y, Zhu W, Flores Banuelos AG, Li J, Mukherjee S, Algaze C, Wu JC

Generation of two induced pluripotent stem cell lines from patients with Williams syndrome

Ren L, Jahng JWS, Belbachir N, Cook Z, Rivero GC, Perez MV, Wu JC

Generation of induced pluripotent stem cell lines from patients with LQT1 caused by heterozygous mutations in the KCNQ1 gene

Teng Teng, Yang Yuting, Li Huihong, Liu Feng

Toxic effect of fluorene on Perinereis aibuhitensis body wall and its corresponding defense mechanisms: A metabolomics perspective

Neufeldt D, Schmidt A, Mohr E, Lu D, Chatterjee S, Fuchs M, Xiao K, Pan W, Cushman S, Jahn C, Juchem M, Hunkler HJ, Cipriano G, Jürgens B, Schmidt K, Groß S, Jung M, Hoepfner J, Weber N, Foo R, Pich A, Zweigerdt R, Kraft T, Thum T, Bär C

Circular RNA circZFPM2 regulates cardiomyocyte hypertrophy and survival

Chen J, Dai T, Li Q, Xu T, Zhang W, Sun J, Liu H

Generation of FOXJ1-EGFP knock-in reporter human embryonic stem cell line, WAe001-A-2D, using CRISPR/Cas9-based gene targeting

Pongpaksupasin P, Tong-Ngam P, Jearawiriyapaisarn N, Paiboonsukwong K, Sangkitporn S, Trinavarat A, Tubsuwan A, Atchaneeyasakul LO

Generation of an EYS-associated retinitis pigmentosa patient-derived human pluripotent stem cell line (MUi038-A)

Jiamvoraphong N, Lorthongpanich C, Klaihmon P, Kheolamai P, Issaragrisil S

Generation of a human iPSC cell line (MUSIi017-A) from a donor with O negative blood type

Zhang D, Jennings L, Chen SC, Zaw K, Lamey TM, Thompson JA, McLaren TL, Chen FK, McLenachan S

Establishment of an induced pluripotent stem cell line LEIi019-A from an early-onset retinal dystrophy patient with the autosomal dominant OTX2 c.259G>A variant

Brychka D, Ayala-Nunez NV, Dupas A, Bare Y, Partiot E, Mittelheisser V, Lucansky V, Goetz JG, Osmani N, Gaudin R

Targeting monocytic Occludin impairs transendothelial migration and HIV neuroinvasion

Kayser A, Dittmann S, Hamidi J, Laufer SD, Krampe R, Mearini G, Hansen A, Schulze-Bahr E

Generation of a patient-specific hiPS cell line with heterozygous GNB2 mutation (UKMi003-A) causative for human sinus node dysfunction and a corresponding CRISPR/Cas9-corrected isogenic control (UKMi004-A)

Xu Yingxi, Liu Xianbo, Ahmad Muhammad Arslan, Ao Qiang, Yu Yang, Shao Dan, Yu Tianhao

Engineering cell-derived extracellular matrix for peripheral nerve regeneration

Liu J, Du J, Ma X, Jin Y, Yang Q, Zhai Y, Cheng J, Luan F, Ma M, Zhang Z, Ren Q, Cui H

Generation of an iPSC line from a 79-year-old female patient diagnosed with sporadic Parkinson's disease

Zhong Wei, Li Dan, Fei Yue, Hong Pan

A review of type 3 Gaucher disease: unique neurological manifestations and advances in treatment

Wang G, Mao X, Wang W, Wang X, Li S, Wang Z

Bioprinted research models of urological malignancy

Kudriavskii Viacheslav V., Goncharov Anton O., Eremeev Artem V., Ruchko Evgenii S., Veselovsky Vladimir A., Klimina Ksenia M., Bogomazova Alexandra N., Lagarkova Maria A., Moshkovskii Sergei A., Kliuchnikova Anna A.

RNA Editing by ADAR Adenosine Deaminases in the Cell Models of CAG Repeat Expansion Diseases: Significant Effect of Differentiation from Stem Cells into Brain Organoids in the Absence of Substantial Influence of CAG Repeats on the Level of Editing

Yanick C, Maciel R, Jacobs E, Schatzman J, Shy M, Zuchner S, Saporta M

Generation of 3 patient induced Pluripotent stem cell lines containing SORD mutations linked to a recessive neuropathy

Zeng Y, Tan X, Xu S, Wang K, Li X, Jiang Y

Generation of an integration-free induced pluripotent stem cell (iPSC) line (SDHI001-A) from a 65-year old adult mitral valve prolapse (MVP) patient

Bouwman LF, Joosen MEM, Buijsen RAM, van der Graaf LM, Pepers BA, Voesenek BJB, Brosens E, van de Warrenburg BPC, van Roon-Mom WMC

Generation of human induced pluripotent stem cell lines (LUMCi051-A,B and LUMCi052-A,B,C) of two patients with Spinocerebellar ataxia type 7

Gao J, Li J, Xu L, Yan CD, Knowles JW, Wu JC

Generation of two familial hypercholesterolemia patient-specific induced pluripotent stem cell lines harboring heterozygous mutations in the LDLR gene

Yazdani Mazyar

Cellular and Molecular Responses to Mitochondrial DNA Deletions in Kearns-Sayre Syndrome: Some Underlying Mechanisms

Yin T, Liao Y, Li X, Wang H, Wu B, Dong X

Characterization of a human induced pluripotent stem cell line (FDCHi015-A) derived from PBMCs of a patient harbouring ALDOB mutation

Verma S, Dalabehera S, Maurya R, Singh D, Prasher B, Pandey R, Bapat S, Ramalingam S, Sachidanandan C

Generation of an induced pluripotent stem cell line IGIBi18-A from an Indian patient with Rubinstein Taybi Syndrome

Wang J, Bering J, Alonzo M, Ye S, Texter K, Garg V, Zhao MT

Generation of iPSC line NCHi015-A from a patient with truncus arteriosus carrying heterozygous variants in KMT2D and NOTCH1

Brandt Nicola, Köper Franziska, Hausmann Jens, Bräuer Anja U.

Spotlight on plasticity-related genes: Current insights in health and disease

Lee SH, Lim G, Kim H, Suh D, Choi HK, Kim HP, Yoon HG, Park SW, Kang SM, Kwon C, Oh J, Lee SH

Generation of an induced pluripotent stem cell line from a patient with arrhythmogenic right ventricular cardiomyopathy harboring a TMEM43 splice-site variant

Pidishetty D, Maddileti S, Mahato S, Agrawal T, Naik M, Kannabiran C, Jalali S, Mariappan I

Generation and characterization of a Stargardt's disease-specific induced pluripotent stem cell line (LVPEIi008-A) with a homozygous nonsense mutation in exon 44 of ABCA4

Querio G, Antoniotti S, Levi R, Fleischmann BK, Gallo MP, Malan D

Insulin-Activated Signaling Pathway and GLUT4 Membrane Translocation in hiPSC-Derived Cardiomyocytes

Risato Giovanni, Brañas Casas Raquel, Cason Marco, Bueno Marinas Maria, Pinci Serena, De Gaspari Monica, Visentin Silvia, Rizzo Stefania, Thiene Gaetano, Basso Cristina, Pilichou Kalliopi, Tiso Natascia, Celeghin Rudy

In Vivo Approaches to Understand Arrhythmogenic Cardiomyopathy: Perspectives on Animal Models

Zhao Yating, Cai Limeng, Huang Bo, Yin Xiangang, Pan Dan, Dong Jie, Zheng Lei, Chen Hao, Lin Jun, Shou Huafeng, Zhao Zhigang, Jin Lanying, Zhu Xiaoxu, Cai Luya, Zhang Xiaofei, Qian Jianhua

Reappraisal and refined diagnosis of ultrasonography and histological findings for hydatidiform moles: a multicentre retrospective study of 821 patients

Kogler S, Pedersen GM, Martínez-Ramírez F, Aizenshtadt A, Busek M, Krauss SJK, Wilson SR, Røberg-Larsen H

An FDA-Validated, Self-Cleaning Liquid Chromatography-Mass Spectrometry System for Determining Small-Molecule Drugs and Metabolites in Organoid/Organ-on-Chip Medium

Janssen J, Chirico N, Ainsworth MJ, Cedillo-Servin G, Viola M, Dokter I, Vermonden T, Doevendans PA, Serra M, Voets IK, Malda J, Castilho M, van Laake LW, Sluijter JPG, Sampaio-Pinto V, van Mil A

Hypothermic and cryogenic preservation of cardiac tissue-engineered constructs

Wilhelmsen I, Combriat T, Dalmao-Fernandez A, Stokowiec J, Wang C, Olsen PA, Wik JA, Boichuk Y, Aizenshtadt A, Krauss S

The effects of TGF-β-induced activation and starvation of vitamin A and palmitic acid on human stem cell-derived hepatic stellate cells

Zhou Heng, Ye Peng, Xiong Wei, Duan Xingxiang, Jing Shuili, He Yan, Zeng Zhi, Wei Yen, Ye Qingsong

Genome-scale CRISPR-Cas9 screening in stem cells: theories, applications and challenges

Kriedemann N, Manstein F, Hernandez-Bautista CA, Ullmann K, Triebert W, Franke A, Mertens M, Stein ICAP, Leffler A, Witte M, Askurava T, Fricke V, Gruh I, Piep B, Kowalski K, Kraft T, Zweigerdt R

Protein-free media for cardiac differentiation of hPSCs in 2000 mL suspension culture

Budny V, Knöpfli Y, Meier D, Zürcher K, Bodenmann C, Peter SL, Müller T, Tardy M, Cortijo C, Tackenberg C

APOE4 Increases Energy Metabolism in APOE-Isogenic iPSC-Derived Neurons

Na Do Hyun, Cui Sheng, Fang Xianying, Lee Hanbi, Eum Sang Hun, Shin Yoo Jin, Lim Sun Woo, Yang Chul Woo, Chung Byung Ha

Advancements in Research on Genetic Kidney Diseases Using Human-Induced Pluripotent Stem Cell-Derived Kidney Organoids

Neumayer G, Torkelson JL, Li S, McCarthy K, Zhen HH, Vangipuram M, Mader MM, Gebeyehu G, Jaouni TM, Jacków-Malinowska J, Rami A, Hansen C, Guo Z, Gaddam S, Tate KM, Pappalardo A, Li L, Chow GM, Roy KR, Nguyen TM, Tanabe K, McGrath PS, Cramer A, Bruckner A, Bilousova G, Roop D, Tang JY, Christiano A, Steinmetz LM, Wernig M, Oro AE

A scalable and cGMP-compatible autologous organotypic cell therapy for Dystrophic Epidermolysis Bullosa

Karayol R, Borroto MC, Haghshenas S, Namasivayam A, Reilly J, Levy MA, Relator R, Kerkhof J, McConkey H, Shvedunova M, Petersen AK, Magnussen K, Zweier C, Vasileiou G, Reis A, Savatt JM, Mulligan MR, Bicknell LS, Poke G, Abu-El-Haija A, Duis J, Hannig V, Srivastava S, Barkoudah E, Hauser NS, van den Born M, Hamiel U, Henig N, Baris Feldman H, McKee S, Krapels IPC, Lei Y, Todorova A, Yordanova R, Atemin S, Rogac M, McConnell V, Chassevent A, Barañano KW, Shashi V, Sullivan JA, Peron A, Iascone M, Canevini MP, Friedman J, Reyes IA, Kierstein J, Shen JJ, Ahmed FN, Mao X, Almoguera B, Blanco-Kelly F, Platzer K, Treu AB, Quilichini J, Bourgois A, Chatron N, Januel L, Rougeot C, Carere DA, Monaghan KG, Rousseau J, Myers KA, Sadikovic B, Akhtar A, Campeau PM

MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature

Zhao Song, Wang Lili, Ouyang Mingyue, Xing Sining, Liu Shuo, Sun Lingyan, Yu Huiying

Polyploid giant cancer cells induced by Docetaxel exhibit a senescence phenotype with the expression of stem cell markers in ovarian cancer cells

Jothi D., Kulka Linda Anna Michelle

Strategies for modeling aging and age-related diseases

Khampang S, Lorthongpanich C, Laowtammathron C, Klaihmon P, Meesa S, Suksomboon W, Jiamvoraphong N, Kheolamai P, Luanpitpong S, Easley CA, Mahyari E, Issaragrisil S

The dynamic expression of YAP is essential for the development of male germ cells derived from human embryonic stem cells

Zhang Huan, Hansen Marten, Di Summa Franca, Von Lindern Marieke, Gillemans Nynke, Van IJcken Wilfred F.J., Svendsen Arthur Flohr, Philipsen Sjaak, Van der Reijden Bert, Varga Eszter, Van den Akker Emile

LSD1/KDM1A and GFI1B repress endothelial fate and induce hematopoietic fate in induced pluripotent stem cell-derived hemogenic endotheliums

Feringa Femke M., Koppes-den Hertog Sascha J., Wang Lian, Derks Rico J.E., Kruijff Iris, Erlebach Lena, Heijneman Jorin, Miramontes Ricardo, Pömpner Nadine, Blomberg Niek, Olivier-Jimenez Damien, Johansen Lill Eva, Cammack Alexander J., Giblin Ashling, Toomey Christina E, Rose Indigo V.L., Yuan Hebao, Ward Michael, Isaacs Adrian M., Kampmann Martin, Kronenberg-Versteeg Deborah, Lashley Tammaryn, Thompson Leslie M., Ori Alessandro, Mohammed Yassene, Giera Martin, van der Kant Rik

The Neurolipid Atlas: a lipidomics resource for neurodegenerative diseases uncovers cholesterol as a regulator of astrocyte reactivity impaired by ApoE4

Stanojević D, Li Z, Bakić S, Foo R, Šikić M

Rockfish: A transformer-based model for accurate 5-methylcytosine prediction from nanopore sequencing

Puertas-Neyra K, Coco-Martin RM, Hernandez-Rodriguez LA, Gobelli D, Garcia-Ferrer Y, Palma-Vecino R, Tellería JJ, Simarro M, de la Fuente MA, Fernandez-Bueno I

Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

Benoit Matthieu P. M. H., Rao Lu, Asenjo Ana B., Gennerich Arne, Sosa Hernando

Cryo-EM unveils kinesin KIF1A’s processivity mechanism and the impact of its pathogenic variant P305L

Fedorenko Alisa V., Khomyakova Ekaterina A., Surdina Anastasia V., Sekretova Elizaveta K., Limanskaya Tatiana V., Belikova Lilia D., Volovikov Egor A., Gridina Maria M., Khabarova Anna A., Kashevarova Anna A., Fedotov Dmitry A., Zerkalenkova Elena A., Lagarkova Maria A., Lebedev Igor N., Bogomazova Alexandra N.

Design of iPSC-based cell model to study the functions of the <i>UBE2A</i> gene

Michalska JM, Lyudchik J, Velicky P, Štefaničková H, Watson JF, Cenameri A, Sommer C, Amberg N, Venturino A, Roessler K, Czech T, Höftberger R, Siegert S, Novarino G, Jonas P, Danzl JG

Imaging brain tissue architecture across millimeter to nanometer scales

Klein Alexandra, Klug Katharina, Breyer Maximilian, Grüner Julia, Medala Vijay Krishna, Nordbeck Peter, Wanner Christoph, Klopocki Eva, Üçeyler Nurcan

Genetic variants of unknown significance in alpha‐galactosidase A: Cellular delineation from Fabry disease

Akter M, Sepehrimanesh M, Xu W, Ding B

Assembling a Coculture System to Prepare Highly Pure Induced Pluripotent Stem Cell-Derived Neurons at Late Maturation Stages

Kwartler Callie S., Esparza Pinelo Jose Emiliano

Use of iPSC-Derived Smooth Muscle Cells to Model Physiology and Pathology

Ribeiro M, Jager J, Furtado M, Carvalho T, Cabral JMS, Brito D, Carmo-Fonseca M, Martins S, da Rocha ST

Generation of induced pluripotent stem cells from an individual with early onset and severe hypertrophic cardiomyopathy linked to MYBPC3: c.772G > A mutation

Roudaut M, Caillaud A, Souguir Z, Bray L, Girardeau A, Rimbert A, Croyal M, Lambert G, Patitucci M, Delpouve G, Vandenhaute É, Le May C, Maubon N, Cariou B, Si-Tayeb K

Human induced pluripotent stem cells-derived liver organoids grown on a Biomimesys® hyaluronic acid-based hydroscaffold as a new model for studying human lipoprotein metabolism

Martinez‐Montoya Valentina, Sánchez‐Sánchez Luz María, Sandoval‐Pacheco Roberto, Castro Diana Mónica Anaya, Arellano‐Valdez Carmen Araceli, Ávila‐Rejón Carmen Amor, Aguilar‐Juárez Pedro Alejandro, Espino‐Pluma Martín, González‐Santillanes Cruz Antonio, Martínez‐Segovia Rosa Isela, Olmos‐Morfin Dorian, la Torre Ofelia Padilla‐De, Solís‐Sánchez Ishar, Espinosa Mónica Vázquez‐Del Mercado, Villarroel‐Cortés Camilo Ernesto, Velarde‐Félix Jesús Salvador, López‐Valdez Jaime, Olaiz‐Urbina Julio, Ricárdez‐Marcial Edgar, Vergara‐Sánchez Imelda, Radillo‐Díaz Pablo, Kazakova Ekaterina, De la Fuente‐Cortez Beatriz, del Carmen Marquez‐Quiróz Luz, Torres‐Octavo Benjamín, Diaz‐Martinez Rubicel

Mutational spectrum and genotype–phenotype correlation in Mexican patients with infantile‐onset and late‐onset Pompe disease

Herardot Elise, Liboz Maxime, Lamour Guillaume, Malo Michel, Plancheron Alexandra, Habeler Walter, Geiger Camille, Frank Elie, Campillo Clément, Monville Christelle, Ben M’Barek Karim

Biomechanical Characterization of Retinal Pigment Epitheliums Derived from hPSCs Using Atomic Force Microscopy

Kriedemann Nils, Triebert Wiebke, Teske Jana, Mertens Mira, Franke Annika, Ullmann Kevin, Manstein Felix, Drakhlis Lika, Haase Alexandra, Halloin Caroline, Martin Ulrich, Zweigerdt Robert

Standardized production of hPSC-derived cardiomyocyte aggregates in stirred spinner flasks

García-López Marta, Jiménez-Vicente Lydia, González-Jabardo Raquel, Dorado Helena, Gómez-Manjón Irene, Martín Miguel Ángel, Ayuso Carmen, Arenas Joaquín, Gallardo María Esther

Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene

Olijnik Aude-Anais, Rodriguez-Romera Antonio, Wong Zoë C., Shen Yuqi, Reyat Jasmeet S., Jooss Natalie J., Rayes Julie, Psaila Bethan, Khan Abdullah O.

Generating human bone marrow organoids for disease modeling and drug discovery

Goanta Emilia-Violeta, Vacarescu Cristina, Tartea Georgica, Ungureanu Adrian, Militaru Sebastian, Muraretu Alexandra, Faur-Grigori Adelina-Andreea, Petrescu Lucian, Vătăsescu Radu, Cozma Dragos

Unexpected Genetic Twists in Patients with Cardiac Devices

Acharya S, Ansari AH, Kumar Das P, Hirano S, Aich M, Rauthan R, Mahato S, Maddileti S, Sarkar S, Kumar M, Phutela R, Gulati S, Rahman A, Goel A, Afzal C, Paul D, Agrawal T, Pulimamidi VK, Jalali S, Nishimasu H, Mariappan I, Nureki O, Maiti S, Chakraborty D

PAM-flexible Engineered FnCas9 variants for robust and ultra-precise genome editing and diagnostics

Gariballa Nesrin, Mohamed Feda, Badawi Sally, Ali Bassam R.

The double whammy of ER-retention and dominant-negative effects in numerous autosomal dominant diseases: significance in disease mechanisms and therapy

Ali Eltahir Abdelrazig Mohamed, Smaida Rana, Meyer Morgane, Ou Wenxin, Li Zongjin, Han Zhongchao, Benkirane-Jessel Nadia, Gottenberg Jacques Eric, Hua Guoqiang

iPSCs chondrogenic differentiation for personalized regenerative medicine: a literature review

Arai Yutaka, Ito Hidenori, Shimizu Tomoya, Shimoda Yuzuno, Song Dan, Matsuo-Takasaki Mami, Hayata Tadayoshi, Hayashi Yohei

Patient-derived and gene-edited pluripotent stem cells lacking NPHP1 recapitulate juvenile nephronophthisis in abnormalities of primary cilia and renal cyst formation

Albuquerque-Wendt Andreia, McCoy Ciaran, Neish Rachel, Dobramysl Ulrich, Beneke Tom, Cowley Sally A., Crouch Kathryn, Wheeler Richard J., Mottram Jeremy C., Gluenz Eva

TransLeish: Identification of membrane transporters essential for survival of intracellularLeishmaniaparasites in a systematic gene deletion screen

Nebuloni F, Do QB, Cook PR, Walsh EJ, Wade-Martins R

A fluid-walled microfluidic platform for human neuron microcircuits and directed axotomy

Akgün Canan Melis, Cozzitorto Corinna, Sterr Michael, Saber Lama, Setyono Eunike S.A., Wang Xianming, Merl-Pham Juliane, Greisle Tobias, Burtscher Ingo, Lickert Heiko

Resolving human αversusβ cell fate allocation for the generation of stem cell-derived islets

Wu HF, Art J, Saini T, Zeltner N

Protocol for generating postganglionic sympathetic neurons using human pluripotent stem cells for electrophysiological and functional assessments

İş Özkan, Wang Xue, Reddy Joseph S., Min Yuhao, Yilmaz Elanur, Bhattarai Prabesh, Patel Tulsi, Bergman Jeremiah, Quicksall Zachary, Heckman Michael G., Tutor-New Frederick Q., Can Demirdogen Birsen, White Launia, Koga Shunsuke, Krause Vincent, Inoue Yasuteru, Kanekiyo Takahisa, Cosacak Mehmet Ilyas, Nelson Nastasia, Lee Annie J., Vardarajan Badri, Mayeux Richard, Kouri Naomi, Deniz Kaancan, Carnwath Troy, Oatman Stephanie R., Lewis-Tuffin Laura J., Nguyen Thuy, Carrasquillo Minerva M., Graff-Radford Jonathan, Petersen Ronald C., Jr Jack Clifford R., Kantarci Kejal, Murray Melissa E., Nho Kwangsik, Saykin Andrew J., Dickson Dennis W., Kizil Caghan, Allen Mariet, Ertekin-Taner Nilüfer

Gliovascular transcriptional perturbations in Alzheimer’s disease reveal molecular mechanisms of blood brain barrier dysfunction

Tongkrajang Nongnat, Kobpornchai Porntida, Dubey Pratima, Chaisri Urai, Kulkeaw Kasem

Modelling amoebic brain infection caused by Balamuthia mandrillaris using a human cerebral organoid

Burton REBECCA, Capel Rebecca, Akerman Emily, Rog-Zielinska Eva, Winbo Annika, Aston Daniel, Mu-u-min Razik, Read Matthew, Bose Samuel, Swietach Pawel, Wang Jingyu, Corbett Alexander, Koschinski Andreas, Montgomery Johanna, Falter Florian, Calamaio Serena, Melgari Dario, Prevostini Rachelle, Rivolta Ilaria, Ayagama Thamali, Jenkin Idan, Simon Jillian, Fakuade Funsho, Pronto Julius, Sharma Parveen, Song Qianqian, Booth Martin, Platt Frances, Lei Ming, Hester Svenja, Fischer Roman, Voigt Niels, Schotten Ulrich, Verheule Sander, Galione Antony, Keller Marco, Bracher Franz, Zaccolo Manuela, Terrar Derek

Lysosomal signalling pathways influence heart rhythm, and regulate atrial function

Walsh C, Jin S

Induced Pluripotent Stem Cells and CRISPR-Cas9 Innovations for Treating Alpha-1 Antitrypsin Deficiency and Glycogen Storage Diseases

Ackermann M, Saleh F, Abdin SM, Rafiei Hashtchin A, Gensch I, Golgath J, Carvalho Oliveira M, Nguyen AHH, Gaedcke S, Fenske A, Jang MS, Jirmo AC, Abeln M, Hansen G, Lachmann N

Standardized generation of human iPSC-derived hematopoietic organoids and macrophages utilizing a benchtop bioreactor platform under fully defined conditions

Li Yang, Ma Ke, Dong Zhujun, Gao Shijuan, Zhang Jing, Huang Shan, Yang Jie, Fang Guangming, Li Yujie, Li Xiaowei, Welch Carrie, Griffin Emily L., Ramaswamy Prema, Valivullah Zaheer, Liu Xiuying, Dong Jianzeng, Wang Dao Wen, Du, Chung Wendy K., Li Yulin

Frameshift variants in C10orf71 cause dilated cardiomyopathy in human, mouse, and organoid models

Zhou Bingna, Gao Peng, Hu Jing, Lin Xiaoyun, Sun Lei, Zhang Qian, Jiang Yan, Wang Ou, Xia Weibo, Xing Xiaoping, Li Mei

Genetic Analysis, Phenotypic Spectrum and Functional Study of Rare Osteogenesis Imperfecta Caused by CRTAP Variants

Dobner J, Nguyen T, Pavez-Giani MG, Cyganek L, Distelmaier F, Krutmann J, Prigione A, Rossi A

mtDNA analysis using Mitopore

Altmaier S, Meiser I, Stracke F, Zimmermann H

Diffusion kinetics and perfusion times in tissue models obtained by bioorthogonal Raman μ-spectroscopy

Wang Chencheng, Abadpour Shadab, Aizenshtadt Aleksandra, Dalmao-Fernandez Andrea, Høyem Merete, Wilhelmsen Ingrid, Stokowiec Justyna, Olsen Petter Angell, Krauss Stefan, Chera Simona, Ghila Luiza, Ræder Helge, Scholz Hanne

Cell identity dynamics and insight into insulin secretagogues when employing stem cell-derived islets for disease modeling

Bantounas I, Rooney KM, Lopes FM, Tengku F, Woods S, Zeef LAH, Lin IH, Kuba SY, Bates N, Hummelgaard S, Hillman KA, Cereghini S, Woolf AS, Kimber SJ

Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations

Capel Rebecca A., Akerman Emily, Rog-Zielinska Eva A., Winbo Annika, Aston Daniel, Mu-u-min Razik Bin Abdul, Read Matthew J., Bose Samuel J., Swietach Pawel, Wang Jingyu, Corbett Alexander D., Koschinski Andreas, Falter Florian, Calamaio Serena, Melgari Dario, Prevostini Rachele, Rivolta Ilaria, Ayagama Thamali, Jenkin Ifan, Simon Jillian N., Fakuade Funsho E., Pronto Julius R., Sharma Parveen, Song Qianqian, Booth Martin J, Platt Frances M., Lei Ming, Hester Svenja, Fischer Roman, Voigt Niels, Schotten Ulrich, Verheule Sander, Galione Antony, Keller Marco, Bracher Franz, Zaccolo Manuela, Terrar Derek A., Burton Rebecca A. B.

Lysosomal signalling pathways influence heart rhythm, and regulate atrial function

Tuimebayeva Gulimzhan, Shagrayeva Bibigul, Kerimbayeva Kulyash, Shertayeva Naila, Bitemirova Aliya, Abdurazova Perizat

Developing Multilingual Competence in Future Educators: Approaches, Challenges, and Best Practices

Goncu Beyza, Duzenli Omer Faruk, Yucesan Emrah

Alteration of housekeeping genes and proteins through senescence of human skin fibroblast cells

Xu W, Cao Y, Stephens SB, Arredondo MJ, Chen Y, Perez W, Sun L, Yu AC, Kim JJ, Lalani SR, Li N, Horrigan FT, Altamirano F, Wehrens XH, Miyake CY, Zhang L

Folate as a potential treatment for lethal ventricular arrhythmias in TANGO2-deficiency disorder

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Systematic optimization of culture media for maintenance of human induced pluripotent stem cells using the response surface methodology

Andrée Birgit, Voß Nils, Kriedemann Nils, Triebert Wiebke, Teske Jana, Mertens Mira, Witte Merlin, Szádocka Sára, Hilfiker Andres, Aper Thomas, Gruh Ina, Zweigerdt Robert

Fabrication of heart tubes from iPSC derived cardiomyocytes and human fibrinogen by rotating mold technology

Martins-Costa C, Wiegers A, Pham VA, Sidhaye J, Doleschall B, Novatchkova M, Lendl T, Piber M, Peer A, Möseneder P, Stuempflen M, Chow SYA, Seidl R, Prayer D, Höftberger R, Kasprian G, Ikeuchi Y, Corsini NS, Knoblich JA

ARID1B controls transcriptional programs of axon projection in an organoid model of the human corpus callosum

Iwoń Zuzanna, Krogulec Ewelina, Kierlańczyk Aleksandra, Wojasiński Michał, Jastrzębska Elżbieta

Hypoxia and re-oxygenation effects on human cardiomyocytes cultured on polycaprolactone and polyurethane nanofibrous mats

Zaytseva A. K., Perepelina K. I., Kostareva A. A.

Analysis of the role of Na_v1.5 slow inactivation in the development of inherited cardiac pathology

Wu Zixuan, Li Ling, Xu Tingting, Hu Yi, Peng Xin, Zhang Zheyuan, Yao Xiaolei, Peng Qinghua

Elucidating the multifaceted roles of GPR146 in non-specific orbital inflammation: a concerted analytical approach through the prisms of bioinformatics and machine learning

Iwoń Z, Krogulec E, Tarnowska I, Łopianiak I, Wojasiński M, Dobrzyń A, Jastrzębska E

Maturation of human cardiomyocytes derived from induced pluripotent stem cells (iPSC-CMs) on polycaprolactone and polyurethane nanofibrous mats

de Wagenaar Nathalie P, van den Bersselaar Lisa M, Odijk Hanny J H M, Stefens Sanne J M, Reinhardt Dieter P, Roos-Hesselink Jolien W, Kanaar Roland, Verhagen Judith M A, Brüggenwirth Hennie T, van de Laar Ingrid M B H, van der Pluijm Ingrid, Essers Jeroen

Functional analysis of cell lines derived from SMAD3-related Loeys-Dietz syndrome patients provides insights into genotype-phenotype relation

Ura Hiroki, Niida Yo

Comparison of RNA-Sequencing Methods for Degraded RNA

Jung YH, Ku YA, Moon J, Kim S, Ryu JS, Yoon CH, Chung MH, Kim YH, Kim MK, Kim DH

Efficacy of RCI001 as a therapeutic candidate of dry eye disease in a modified mixed dry eye model

Potdar Chandrakanta, Jagtap Soham, Singh Khushboo, Yadav Ravi, Pal Pramod Kumar, Datta Indrani