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The Journal of Membrane Biology|August 13, 2002
CFTR is a monomer: biochemical and functional evidenceJ-H Chen, X-B Chang, A A Aleksandrov, et al.
Glycoconjugate Journal|July 10, 2001
A novel CFTR disease-associated mutation causes addition of an extra N-linked oligosaccharideM M Hämmerle, A A Aleksandrov, X B Chang, et al.
Nature|August 15, 1991
Phosphorylation-regulated Cl- channel in CHO cells stably expressing the cystic fibrosis geneJ A Tabcharani, X B Chang, J R Riordan, et al.
The Journal of Biological Chemistry|July 15, 1994
Mapping of cystic fibrosis transmembrane conductance regulator membrane topology by glycosylation site insertionX B Chang, Y X Hou, T J Jensen, et al.
The Journal of Biological Chemistry|July 5, 1996
cAMP- and Ca2+-independent activation of cystic fibrosis transmembrane conductance regulator channels by phenylimidazothiazole drugsF Becq, B Verrier, X B Chang, et al.
The American Journal of Physiology|August 1, 1992
Right-angle light scattering to assay basal and regulated plasma membrane Cl- conductancesS Dho, S Chou, X B Chang, et al.
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.
The Journal of Physiology|February 18, 2003
Phosphorylation of protein kinase C sites in NBD1 and the R domain control CFTR channel activation by PKAV Chappe, D A Hinkson, T Zhu, et al.
The EMBO Journal|December 8, 1998
Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasomeM A Loo, T J Jensen, L Cui, 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.
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