Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-Targeted Therapeutics for Cystic Fibrosis
Diana‐Florentina Veselu(University of Bristol), David N. Sheppard(University of Edinburgh), Jacob D. Bradbury(University of Bristol), A. Sofia F. Oliveira(University of Bristol), Yanira Manzanares Fornies(University of Bristol), Hongyu Li(University of Bristol), Tzyh‐Chang Hwang(National Yang Ming Chiao Tung University), Han‐I Yeh(National Yang Ming Chiao Tung University), Deborah K. Shoemark(Southmead Hospital), Mayuree Rodrat(Mahidol University)
Cited by 2
Related Papers
Structure and Function of the CFTR Chloride Channel
|Physiological Reviews|1999|999
The Microbiome and Disease: Reviewing the Links between the Oral Microbiome, Aging, and Alzheimer's Disease
|Journal of Alzheimer s Disease|2014|250
The protein kinase A-regulated cardiac CI− channel resembles the cystic fibrosis transmembrane conductance regulator
|Nature|1992|173
Modulation of CFTR chloride channels by calyculin A and genistein
|American Journal of Physiology-Cell Physiology|1997|151
Deletion of phenylalanine 508 causes attenuated phosphorylation‐dependent activation of CFTR chloride channels
|The Journal of Physiology|2000|102