Lv0
0 积分 2023-11-25 加入
Abstract 13159: SCN5A and Nedd4.2 S-Nitrosylation by nNOS Decreases SCN5A Ubiquitinization: A Mechanism for Increased Peak and Late Sodium Current
3天前
求助中
Familial atrial myopathy in a large multigenerational heart-hand syndrome pedigree carrying an LMNA missense variant in rod 2B domain (p.R335W)
14天前
已完结
Complex genotypes in family with metachromatic leukodystrophy: Effect of trans and cis mutations distribution on the phenotype variability
1个月前
已完结
A heterozygous missense SCN5A mutation associated with early repolarization syndrome
1个月前
已完结
Cardiac-specific overexpression of CREM-IbΔC-X via CRISPR/Cas9 in mice presents a new model of atrial cardiomyopathy with spontaneous atrial fibrillation
1个月前
已完结
p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient
2个月前
已完结
Familial atrial myopathy in a large multigenerational heart-hand syndrome pedigree carrying an LMNA missense variant in rod 2B domain (p.R335W)
2个月前
已完结
Familial atrial myopathy in a large multigenerational heart-hand syndrome pedigree carrying an LMNA missense variant in rod 2B domain (p.R335W)
2个月前
已完结
Familial atrial myopathy in a large multigenerational heart-hand syndrome pedigree carrying an LMNA missense variant in rod 2B domain (p.R335W)
2个月前
已完结
Subcellular diversity of Nav1.5 in cardiomyocytes: distinct functions, mechanisms and targets
3个月前
已完结
皖公网安备34019202002308
