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The EMBO Journal|December 15, 1994
Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATPG L Lukacs, A Mohamed, N Kartner, et al.Nature Genetics|August 1, 1992
Mislocalization of delta F508 CFTR in cystic fibrosis sweat glandN Kartner, O Augustinas, T J Jensen, et al.The Journal of Biological Chemistry|July 5, 1993
Protein kinase C mediates down-regulation of cystic fibrosis transmembrane conductance regulator levels in epithelial cellsW Breuer, H Glickstein, N Kartner, et al.The Journal of Biological Chemistry|July 25, 1992
The cystic fibrosis transmembrane regulator is present and functional in endosomes. Role as a determinant of endosomal pHG L Lukacs, X B Chang, N Kartner, et al.The Journal of Biological Chemistry|October 15, 1993
The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cellsG L Lukacs, X B Chang, C Bear, et al.The Journal of Biological Chemistry|October 15, 1991
Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis geneC E Bear, F Duguay, A L Naismith, et al.The EMBO Journal|July 1, 1992
Regulation of CFTR expression and function during differentiation of intestinal epithelial cellsR Sood, C Bear, W Auerbach, et al.Cell|February 21, 1992
Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)C E Bear, C H Li, N Kartner, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1991
cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulatorJ M Rommens, S Dho, C E Bear, et al.Cancer Chemotherapy and Pharmacology|January 1, 1997
Multidrug resistance: molecular mechanisms and clinical relevanceV LingPageof 29