JSPHi001-A

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iPSC Line
hPSCreg name	JSPHi001-A
Cite as:	JSPHi001-A (RRID:CVCL_A7JD)
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	23rd April 2021
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Provider
Generator	Division of Cardiology, The First Affiliated Hospital of Nanjing Medical University (Jiangsu Province Hospital) (JSPH)
External iPSC Databases
Cellosaurus	CVCL_A7JD
Wikidata	Q107115509
General iPSC Information
Publications	Zhang Y et al. Establishment of an iPSC line (JSPHi001-A) from a patient with familial dilated cardiomyopathy and atrial fibrillation caused by LMNA missense mutation (c.1003C > T). Stem cell research. 2021 May;53:102349. Iop L et al. Inherited and Acquired Rhythm Disturbances in Sick Sinus Syndrome, Brugada Syndrome, and Atrial Fibrillation: Lessons from Preclinical Modeling. Cells. 2021 Nov 15;10(11). Zhang Y et al. Familial atrial myopathy in a large multigenerational heart-hand syndrome pedigree carrying an LMNA missense variant in rod 2B domain (p.R335W). Heart rhythm. 2022 Mar;19(3):466-475. Siikjärvi Aura et al. Cardiac Phenotype Associated with Two Heterozygous LMNA Variants. Cardiogenetics. 2025-05-01. Gerritse Merel et al. Characteristics and pharmacological responsiveness in hiPSC models of inherited cardiomyopathy. Pharmacology & Therapeutics. 2025-08-00.