Lv4
790 积分 2025-06-10 加入
A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel
1天前
已完结
SYNE1-ataxia: Novel genotypic and phenotypic findings
1天前
已完结
The regulation of FOXO1 and its role in disease progression
3天前
已完结
Cellular and pathological functions of tau
17天前
已完结
Copy number variations of SCN5A in Brugada syndrome
17天前
已完结
Gene therapy targeting protein trafficking regulator MOG1 in mouse models of Brugada syndrome, arrhythmias, and mild cardiomyopathy
22天前
已完结
Mutation profile of APP, PSEN1, and PSEN2 in Chinese familial Alzheimer's disease
1个月前
已完结
Breaking BAG: The Co-Chaperone BAG3 in Health and Disease
1个月前
已完结
Tau Clearance Mechanisms
1个月前
已完结
Advancements in autophagy perturbations in Alzheimer’s disease: Molecular aspects and therapeutics
1个月前
已完结
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