Generation of two iPSC lines from patients with Aicardi-Goutières syndrome carrying either biallelic ADAR1 mutations (PC138) or a heterozygous IFIH1 mutation (PC139).
第一作者:
Lisa,Zerad
第一单位:
Université Paris Cité, Imagine Institute, Laboratory of Neurogenetics and Neuroinflammation, F-75015 Paris, France; Université Paris Cité, Imagine Institute, Laboratory of Embryology and Genetics of Human Malformation, F-75015 Paris, France. Electronic address: lisa.zerad@hotmail.fr.
作者:
医学主题词
人类(Humans);腺苷脱氨酶(Adenosine Deaminase);神经系统自身免疫疾病(Autoimmune Diseases of the Nervous System);神经系统畸形(Nervous System Malformations);诱导多能干细胞(Induced Pluripotent Stem Cells);RNA结合蛋白质类(RNA-Binding Proteins);突变(Mutation);杂合子(Heterozygote);男(雄)性(Male);等位基因(Alleles);细胞系(Cell Line);女(雌)性(Female)
DOI
10.1016/j.scr.2025.103873
PMID
41351966
发布时间
2026-01-08
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Stem cell research
103873页
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