Lv1
48 积分 2026-06-16 加入
Comparative analysis of SEC61A1 mutant R236C in two patient-derived cellular platforms
29天前
已完结
Hypoaldosteronism due to a novel SEC61A1 variant successfully treated with fludrocortisone
29天前
已完结
Phenylbutyrate rescues the transport defect of the Sec61α mutations V67G and T185A for renin
1个月前
已完结
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia
1个月前
已完结
Autosomal dominant tubulointerstitial kidney disease: more than just HNF1β
1个月前
已完结
Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease
1个月前
已完结
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia
1个月前
已完结
Phenotype and genotype of autosomal dominant tubulointerstitial kidney disease in a Japanese cohort
1个月前
已完结
A SEC61A1 variant is associated with autosomal dominant polycystic liver disease
2个月前
已完结
Exploring the ER channel protein Sec61: recent advances in pathophysiological significance and novel pharmacological inhibitors
2个月前
已完结
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