SDQLCHi036-A

A P E C

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iPSC Line
hPSCreg name	SDQLCHi036-A
Cite as:	SDQLCHi036-A (RRID:CVCL_A4XS)
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	8th February 2021
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Provider
Generator	Children’s Hospital affiliated to Shandong University (SDQLCH)
External iPSC Databases
Cellosaurus	CVCL_A4XS
Wikidata	Q107116890
General iPSC Information
Publications	Guan J et al. Generation of a human induced pluripotent stem cell line (SDQLCHi036-A) from a patient with ornithine transcarbamylase deficiency carrying a deletion involving 3-9 exons of OTC gene. Stem cell research. 2021 Apr;52:102220. Laemmle A et al. Reply. Hepatology (Baltimore, Md.). 2022 Apr;75(4):1059-1060. Zhang JW et al. Letter to the editor: The role of aquaporin 9 in modeling of ornithine transcarbamylase deficiency. Hepatology (Baltimore, Md.). 2022 Apr;75(4):1058-1059. Ghasemzad M et al. Novel Gene-Correction-Based Therapeutic Modalities for Monogenic Liver Disorders. Bioengineering (Basel, Switzerland). 2022 Aug 15;9(8). Duff C et al. Modelling urea cycle disorders using iPSCs. NPJ Regenerative medicine. 2022 Sep 26;7(1):56. Andriianov Vladimir et al. Application of Induced Pluripotent Stem Cells (iPSCs) in Hereditary and Viral Diseases of the Liver: Modeling and Treatment. International Journal of Molecular Sciences. 2025-09-26.