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SDQLCHi032-A
Registration Summary
:
A
P
E
C
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
SDQLCHi032-A
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
SDQLCHi032-A (RRID:CVCL_A4XP)
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
11th September 2020
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Provider
Generator
Children’s Hospital affiliated to Shandong University (SDQLCH)
External Databases
Cellosaurus
CVCL_A4XP
Wikidata
Q107116887
General Information
Publications
Li Y et al. Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation. Stem cell research. 2021 Apr;52:102217.
Charoenngam N et al. Hereditary Metabolic Bone Diseases: A Review of Pathogenesis, Diagnosis and Management. Genes. 2022 Oct 17;13(10).
Zhou Y et al. Generation of one human induced pluripotent stem cell line (XACHi004-A) with heterozygous mutation of RYR2 gene from an atrial fibrillation patient. Stem cell research. 2022 Dec;65:102955.
Ai D et al. Generation of an induced pluripotent stem cell line SDPHi002-A from a patient with lung cancer. Stem cell research. 2023 Jun;69:103096.
hIPSC Derivation
General
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