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Proceedings of the National Academy of Sciences of the United States of America|May 3, 2000
A functional R domain from cystic fibrosis transmembrane conductance regulator is predominantly unstructured in solutionL S Ostedgaard, O Baldursson, D W Vermeer, et al.The Journal of Biological Chemistry|December 25, 1992
Partial purification of the cystic fibrosis transmembrane conductance regulatorL S Ostedgaard, M J WelshJournal of Cell Science|June 11, 1999
Processing of CFTR bearing the P574H mutation differs from wild-type and deltaF508-CFTRL S Ostedgaard, B Zeiher, M J WelshThe American Journal of Physiology|July 1, 1992
Staphylococcus aureus alpha-toxin permeabilizes the basolateral membrane of a Cl(-)-secreting epitheliumL S Ostedgaard, D M Shasby, M J WelshThe Journal of Cell Biology|August 1, 1992
Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epitheliaG M Denning, L S Ostedgaard, M J WelshThe Journal of Biological Chemistry|August 30, 1996
Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulatorJ F Cotten, L S Ostedgaard, M R Carson, et al.The EMBO Journal|March 1, 1995
Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiencyD N Sheppard, L S Ostedgaard, M C Winter, et al.Journal of Cell Science. Supplement|January 1, 1993
Dysfunction of CFTR bearing the delta F508 mutationM J Welsh, G M Denning, L S Ostedgaard, et al.Cell|March 25, 1994
The amino-terminal portion of CFTR forms a regulated Cl- channelD N Sheppard, L S Ostedgaard, D P Rich, et al.Biochemistry|February 11, 1997
Association of domains within the cystic fibrosis transmembrane conductance regulatorL S Ostedgaard, D P Rich, L G DeBerg, et al.Pageof 37