Association of cystic fibrosis transmembrane conductance regulator with epithelial sodium channel subunits carrying Liddle's syndrome mutations.

导出 OA

翻译打印收藏纠错

第一作者： Arun K,Rooj

第一单位： Department of Cell, Developmental & Integrative Biology, The University of Alabama at Birmingham School of Medicine, Birmingham, Alabama.

作者： Arun K,Rooj ^[1] ; Estelle,Cormet-Boyaka ^[2] ; Edlira B,Clark ^[1] ; Yawar J,Qadri ^[3] ; William,Lee ^[4] ; Ravindra,Boddu ^[5] ; Anupam,Agarwal ^[5] ; Richa,Tambi ^[6] ; Mohammed,Uddin ^[6] ; Vladimir,Parpura ^[4] ; Eric J,Sorscher ^[7] ; Cathy M,Fuller ^[1] ; Bakhrom K,Berdiev ^[1]

作者单位： Department of Cell, Developmental & Integrative Biology, The University of Alabama at Birmingham School of Medicine, Birmingham, Alabama. ^[1] Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio. ^[2] Department of Anesthesiology, The Emory University School of Medicine, Atlanta, Georgia. ^[3] Department of Neurobiology, The University of Alabama at Birmingham School of Medicine, Birmingham, Alabama. ^[4] Department of Medicine, The University of Alabama at Birmingham School of Medicine, Birmingham, Alabama. ^[5] College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates. ^[6] Department of Pediatrics, The Emory University School of Medicine, Atlanta, Georgia. ^[7]

关键词 CFTR ENaC FLIM Liddle’s syndrome cystic fibrosis

主题词囊性纤维化跨膜传导调节因子(Cystic Fibrosis Transmembrane Conductance Regulator);荧光共振能量转移(Fluorescence Resonance Energy Transfer);HEK293细胞(HEK293 Cells);人类(Humans);Liddle综合征(Liddle Syndrome);突变(Mutation)

DOI 10.1152/ajplung.00298.2020

PMID 34037494

发布时间 2022-08-02

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交