Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation

Neuron. 1992 May;8(5):821-9. doi: 10.1016/0896-6273(92)90196-k.

Authors

M J Welsh¹, M P Anderson, D P Rich, H A Berger, G M Denning, L S Ostedgaard, D N Sheppard, S H Cheng, R J Gregory, A E Smith

Affiliation

¹ Howard Hughes Medical Institute, Department of Internal Medicine, University of Iowa College of Medicine, Iowa City 52242.

PMID: 1375035
DOI: 10.1016/0896-6273(92)90196-k

No abstract available

Publication types

Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Review

MeSH terms

Adenosine Triphosphate / metabolism
Adenosine Triphosphate / pharmacology
Cell Membrane / chemistry
Chloride Channels
Cystic Fibrosis / physiopathology*
Cystic Fibrosis Transmembrane Conductance Regulator
Humans
Membrane Proteins / genetics
Membrane Proteins / physiology*
Mutation
Phosphorylation

Substances

CFTR protein, human
Chloride Channels
Membrane Proteins
Cystic Fibrosis Transmembrane Conductance Regulator
Adenosine Triphosphate