KCNJ11 Gene - GeneCards | KCJ11 Protein | KCJ11 Antibody
2024年12月25日 · KCNJ11 (Potassium Inwardly Rectifying Channel Subfamily J Member 11) is a Protein Coding gene. Diseases associated with KCNJ11 include Hyperinsulinemic …
KCNJ11 gene - MedlinePlus
KCNJ11 gene mutations that cause permanent neonatal diabetes mellitus change single amino acids in the protein sequence. These mutations result in K-ATP channels that do not close, …
Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a
2022年12月1日 · Due to the central role in insulin secretion, the potassium inwardly-rectifying channel subfamily J member 11 (KCNJ11) gene is one of the essential genes for type 2 …
KCNJ11 potassium inwardly rectifying channel subfamily J …
KCNJ11 mutations are rare in patients diagnosed with type 1 diabetes, the identification of a KCNJ11 mutation may have important treatment implications. mutations in KCNJ11 are the …
KCNJ11基因突变导致的不同类型糖代谢异常 - 中华糖尿病杂志
KCNJ11基因编码ATP敏感性钾通道（K ATP）的Kir6.2亚基，是调节胰岛β细胞胰岛素分泌的重要基因。 KCNJ11基因不同突变位点可导致一系列连续的、不同轻重的糖代谢异常，包括新生儿 …
钾内向整流通道亚家族 J 成员 11（KCNJ11）基因 | MCE
该基因编码的蛋白是一种完整的膜蛋白和内向整流型钾通道。 编码的蛋白质更倾向于让钾流入细胞而不是流出细胞，它受 G 蛋白控制，并被发现与磺酰脲受体 SUR 相关。 该基因的突变是导 …
KCNJ11: Genetic Polymorphisms and Risk of Diabetes Mellitus
Numerous studies have reported the involvement of single nucleotide polymorphisms of the KCNJ11 gene and their interactions in the susceptibility to DM. This review discusses the …
KCNJ11突变的年轻成年发病型糖尿病13型家系临床分析
对2个伴有整流性钾离子通道j家族11因子（kcnj11）突变的mody13家系进行遗传病因分析。应用全外显子组测序分析发现,两个家系为kcnj11突变,但突变位点不同。本报告首次报道有关kcnj11 …
KCNJ11 potassium inwardly rectifying channel subfamily J …
2025年1月11日 · Mutations in KCNJ11 are associated with the development of autosomal dominant, early-onset type 2 diabetes. Functional characterization of a novel KCNJ11 in frame …
KCNJ11 potassium inwardly rectifying channel subfamily J …
2020年12月13日 · Title: Potassium inwardly-rectifying channel subfamily J member 11 (KCNJ11) gene polymorphism in Egyptian type 2 diabetic patients: a single-center study. Molecular …