Zhiwei W. Cai
AuthID: R-00F-XC6
1
TITLE: Partial rescue of F508del-cystic fibrosis transmembrane conductance regulator channel gating with modest improvement of protein processing, but not stability, by a dual-acting small molecule Full Text
AUTHORS: Jia Liu; Hermann Bihler; Carlos M Farinha; Nikhil T Awatade; Ana M Romao; Dayna Mercadante; Yi Cheng; Isaac Musisi; Walailak Jantarajit; Yiting T Wang; Zhiwei W Cai; Margarida D Amaral; Martin Mense; David N Sheppard;
PUBLISHED: 2018, SOURCE: BRITISH JOURNAL OF PHARMACOLOGY, VOLUME: 175, ISSUE: 7
AUTHORS: Jia Liu; Hermann Bihler; Carlos M Farinha; Nikhil T Awatade; Ana M Romao; Dayna Mercadante; Yi Cheng; Isaac Musisi; Walailak Jantarajit; Yiting T Wang; Zhiwei W Cai; Margarida D Amaral; Martin Mense; David N Sheppard;
PUBLISHED: 2018, SOURCE: BRITISH JOURNAL OF PHARMACOLOGY, VOLUME: 175, ISSUE: 7
INDEXED IN: 
Scopus 
WOS
Scopus WOS2
TITLE: Revertant mutants modify, but do not rescue, the gating defect of the cystic fibrosis mutant G551D-CFTR. Impact of revertant mutants on G551D-CFTR Full Text
AUTHORS: Zhe Xu; Luisa S Pissarra; Carlos M Farinha; Jia Liu; Zhiwei W Cai; Patrick H Thibodeau; Margarida D Amaral; David N Sheppard;
PUBLISHED: 2014, SOURCE: JOURNAL OF PHYSIOLOGY-LONDON, VOLUME: 592, ISSUE: 9
AUTHORS: Zhe Xu; Luisa S Pissarra; Carlos M Farinha; Jia Liu; Zhiwei W Cai; Patrick H Thibodeau; Margarida D Amaral; David N Sheppard;
PUBLISHED: 2014, SOURCE: JOURNAL OF PHYSIOLOGY-LONDON, VOLUME: 592, ISSUE: 9
3
TITLE: Prolonged treatment of cells with genistein modulates the expression and function of the cystic fibrosis transmembrane conductance regulator. Long-term effects of genistein on CFTR Full Text
AUTHORS: Schmidt, A; Hughes, LK; Cai, Z; Mendes, F ; Li, H; Sheppard, DN; Amaral, MD ;
PUBLISHED: 2008, SOURCE: BRITISH JOURNAL OF PHARMACOLOGY, VOLUME: 153, ISSUE: 6
AUTHORS: Schmidt, A; Hughes, LK; Cai, Z; Mendes, F ; Li, H; Sheppard, DN; Amaral, MD ;
PUBLISHED: 2008, SOURCE: BRITISH JOURNAL OF PHARMACOLOGY, VOLUME: 153, ISSUE: 6
4
TITLE: Solubilizing mutations used to crystallize one CFTR domain attenuate the trafficking and channel defects caused by the major cystic fibrosis mutation
AUTHORS: Luisa S Pissarra; Carlos M Farinha ; Zhe Xu; Andre Schmidt; Patrick H Thibodeau; Zhiwei W Cai; Philip J Thomas; David N Sheppard; Margaricla D Amaral ;
PUBLISHED: 2008, SOURCE: CHEMISTRY & BIOLOGY, VOLUME: 15, ISSUE: 1
AUTHORS: Luisa S Pissarra; Carlos M Farinha ; Zhe Xu; Andre Schmidt; Patrick H Thibodeau; Zhiwei W Cai; Philip J Thomas; David N Sheppard; Margaricla D Amaral ;
PUBLISHED: 2008, SOURCE: CHEMISTRY & BIOLOGY, VOLUME: 15, ISSUE: 1
5
TITLE: Strategies to investigate the mechanism of action of CFTR modulators Full Text
AUTHORS: Cai, Z; Scott Ward, TS; Li, H; Schmidt, A; Sheppard, DN;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
AUTHORS: Cai, Z; Scott Ward, TS; Li, H; Schmidt, A; Sheppard, DN;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
INDEXED IN: Scopus 
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