上皮钠通道
选择性拼接
钠通道
阿米洛利
蛋白质亚单位
生物
病态的
细胞生物学
蛋白质组学
神经科学
遗传学
生物信息学
钠
医学
化学
基因
基因亚型
病理
有机化学
作者
Hong Ji,Runzhen Zhao,Zai Xing Chen,Sreerama Shetty,Steven Idell,Sadis Matalon
出处
期刊:American Journal of Physiology-lung Cellular and Molecular Physiology
[American Physiological Society]
日期:2012-12-15
卷期号:303 (12): L1013-L1026
被引量:90
标识
DOI:10.1152/ajplung.00206.2012
摘要
The fourth subunit of the epithelial sodium channel, termed delta subunit (δ ENaC), was cloned in human and monkey. Increasing evidence shows that this unique subunit and its splice variants exhibit biophysical and pharmacological properties that are divergent from those of α ENaC channels. The widespread distribution of epithelial sodium channels in both epithelial and nonepithelial tissues implies a range of physiological functions. The altered expression of SCNN1D is associated with numerous pathological conditions. Genetic studies link SCNN1D deficiency with rare genetic diseases with developmental and functional disorders in the brain, heart, and respiratory systems. Here, we review the progress of research on δ ENaC in genomics, biophysics, proteomics, physiology, pharmacology, and clinical medicine.
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