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The Biochemical Journal|March 10, 2001
Multiple endocytic signals in the C-terminal tail of the cystic fibrosis transmembrane conductance regulatorW Hu, M Howard, G L Lukacs
Nature Structural Biology|March 21, 1998
Limited proteolysis as a probe for arrested conformational maturation of delta F508 CFTRF Zhang, N Kartner, G L Lukacs
The Journal of Biological Chemistry|December 25, 1991
Determinants of the phagosomal pH in macrophages. In situ assessment of vacuolar H(+)-ATPase activity, counterion conductance, and H+ "leak"G L Lukacs, O D Rotstein, S Grinstein
The Journal of Biological Chemistry|December 5, 1990
Phagosomal acidification is mediated by a vacuolar-type H(+)-ATPase in murine macrophagesG L Lukacs, O D Rotstein, S Grinstein
The Journal of Cell Biology|May 31, 2001
COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartmentsM Benharouga, M Haardt, N Kartner, et al.
The Journal of Biological Chemistry|January 2, 2001
Conformational and temperature-sensitive stability defects of the delta F508 cystic fibrosis transmembrane conductance regulator in post-endoplasmic reticulum compartmentsM Sharma, M Benharouga, W Hu, et al.
The Journal of Biological Chemistry|April 15, 2000
Cystic fibrosis mutations lead to carboxyl-terminal fragments that highlight an early biogenesis step of the cystic fibrosis transmembrane conductance regulatorM Van Oene, G L Lukacs, J M Rommens
FEBS Letters|August 19, 1991
The chloride channel blocker 5-nitro-2-(3-phenylpropyl-amino) benzoic acid (NPPB) uncouples mitochondria and increases the proton permeability of the plasma membrane in phagocytic cellsG L Lukacs, A Nanda, O D Rotstein, et al.
The Biochemical Journal|January 24, 1998
Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylationG L Lukacs, G Segal, N Kartner, et al.
The Journal of Biological Chemistry|July 27, 1999
C-terminal truncations destabilize the cystic fibrosis transmembrane conductance regulator without impairing its biogenesis. A novel class of mutationM Haardt, M Benharouga, D Lechardeur, et al.
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