TARDBP公司
生物
突变
无症状携带者
肌萎缩侧索硬化
无症状的
遗传学
基因
诱导多能干细胞
突变体
分子生物学
疾病
病理
SOD1
医学
胚胎干细胞
作者
Angela D’Anzi,Elisa Perciballi,Giorgia Ruotolo,Daniela Ferrari,Antonietta Notaro,Ivan Lombardi,Maurizio Gelati,Katia Frezza,Laura Bernardini,Isabella Torrente,Alessandro De Luca,Vincenzo La Bella,Angelo L. Vescovi,Jessica Rosati
标识
DOI:10.1016/j.scr.2022.102835
摘要
Amyotrophic Lateral Sclerosis (ALS) is a fatal disease affecting both upper and lower motoneurons. The transactive response DNA binding protein (TARDBP) gene, encoding for TDP-43, is one of the most commonly mutated gene associated with familial cases of ALS (10%). We generated a human induced pluripotent stem cell (hiPSC) line from the fibroblasts of an asymptomatic subject carrying the TARDBP p.G376D mutation. This mutation is very rare and was described in a large Apulian family, in which all ALS affected members are carriers of the mutation. The subject here described is the first identified asymptomatic carrier of the mutation.
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