Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency.

Sheppard, D N

Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency. [electronic resource] - The EMBO journal Mar 1995 - 876-83 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

0261-4189

10.1002/j.1460-2075.1995.tb07069.x doi


Adenosine Triphosphate--metabolism
Animals
Chloride Channels--metabolism
Cyclic AMP--agonists
Cystic Fibrosis--genetics
Cystic Fibrosis Transmembrane Conductance Regulator
Epithelial Cells
Epithelium--metabolism
HeLa Cells
Humans
Ion Channel Gating
Membrane Proteins--genetics
Mutation--physiology
Pancreas--metabolism
Patch-Clamp Techniques
Phosphorylation
Rats
Rats, Inbred F344
Thyroid Gland--physiology