Work

Cftr Channel Gating

Year: 1999

Type: article

Abstract: Two papers, one in this issue ([Weinreich et al. 1999][1]) and the other in the April issue of The Journal ([Zeltwanger et al. 1999][2]), help clarify the gating mechanisms of cystic fibrosis transmembrane conductance regulator (CFTR) Cl− channels, the products of the gene found mutated in cystic

Source: The Journal of General Physiology

DOI: 10.1085/jgp.114.1.49

Authors: László Csanády, David C. Gadsby

Institution: Rockefeller University

Language: English

Topic: Cystic Fibrosis Research Advances

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

Open Access status: green

Funders: National Heart, Lung, and Blood Institute, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: Mechanisms of Current Modulation in Cardiac Myocytes, Mechanisms, Structure, and Regulation of CFTRs NBDs, G3560379654, G900912332