生物
肥厚性心肌病
诱导多能干细胞
错义突变
突变
外周血单个核细胞
仙台病毒
MYH7
心肌病
肌肉肥大
癌症研究
心肌细胞
干细胞
心源性猝死
分子生物学
细胞生物学
基因
基因突变
细胞培养
肌球蛋白
左心室肥大
心力衰竭
猝死
点突变
细胞分化
遗传学
细胞
表型
病理
内科学
肌节
HEK 293细胞
作者
Dongping Liu,Ming‐Yu Yang,Shasha Fan,Manyu Gong,Ying Zhang,Yanan Jiang,Siyu Wang,Hao Wang,Maomao Zhang,Ying Zhang
标识
DOI:10.1016/j.scr.2025.103841
摘要
Hypertrophic cardiomyopathy (HCM) is an inherited cardiovascular disorder characterized by left ventricular hypertrophy and an elevated risk of sudden cardiac death. Cardiac myosin binding protein C (MYBPC3) is the most frequently mutated gene leading to HCM. In this study, peripheral blood mononuclear cells isolated from an HCM patient harboring a heterozygous MYBPC3 missense mutation (c.3072C > A; p.S1024R) were reprogrammed via Sendai virus vectors to generate a patient-specific induced pluripotent stem cell (iPSC) line. The iPSC line exhibits normal morphology and karyotype, alongside definitive hallmarks of pluripotency, including trilineage differentiation potential.
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