ABCC8相关论文
A novel compound heterozygous mutation of ABCC8 gene causing a diazoxide-unresponsive congenital hyp
Congenital hyperinsulinism (CHI) is a severe heterogeneous disorder due to dysregulation of insulin secretion from the p......
Effect of genetic variants in KCNJ11, ABCC8, PPARG and HNF4A loci on the susceptibility of type 2 di
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A novel compound heterozygous mutation of ABCC8 gene causing a diazoxide-unresponsive congenital hyp
Congenital hyperinsulinism (CHI) is a severe heterogeneous disorder due to dysregulation of insulin secretion from t......
目的:寻找与乳腺癌细胞株间药物敏感性差异相关的基因启动子CpG岛甲基化异常,为DNA甲基化异常作为临床化疗敏感性预测手段提供依据......
Effect of genetic variants in KCNJ11, ABCC8, PPARG and HNF4A loci on the susceptibility of type 2 di
Background KCNJ11, ABCC8, PPARG, and HNF4A have been found to be associated with type 2 diabetes in populations with dif......
目的比较早发糖尿病(诊断年龄小于等于40岁)中经典1型糖尿病(T1DM)、成人隐匿性自身免疫糖尿病(latent autoimmune diabetes in ad......
由ABCC8基因编码的磺脲类受体1（SUR1）广泛存在于胰岛β细胞、脑和肌肉组织中,它是腺苷三磷酸（ATP）敏感性钾离子通道的组成亚基之一。在......
目的 ABCC8是ATP-敏感性K+(KATP)通道的调节亚基(又称SUR1),本研究拟对ABCC8基因15th内含子与16th外显子剪切处C1799854T(NCBI数据......
ABCC8是ATP敏感性K＋通道的调节亚基（又名SUR1），最大摄氧量关联基因定位技术显示，其所在区域与有氧耐力表型高度相关。鉴于此，目前该基因......
