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Tzyh-Chang Hwang

Showing results (21-30 of 71) with videos related to

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The Journal of Physiology|February 6, 2016
On the mechanism of gating defects caused by the R117H mutation in cystic fibrosis transmembrane conductance regulatorYing-Chun Yu, Yoshiro Sohma, Tzyh-Chang Hwang
The Journal of General Physiology|September 12, 2012
Nonintegral stoichiometry in CFTR gating revealed by a pore-lining mutationKang-Yang Jih, Yoshiro Sohma, Tzyh-Chang Hwang
Current Pharmaceutical Design|January 22, 2013
Curcumin and genistein: the combined effects on disease-associated CFTR mutants and their clinical implicationsYoshiro Sohma, Ying-Chun Yu, Tzyh-Chang Hwang
Frontiers in Molecular Biosciences|July 11, 2022
Pharmacological Responses of the G542X-CFTR to CFTR ModulatorsXinxiu Fang, Jiunn-Tyng Yeh, Tzyh-Chang Hwang
Biochemistry|November 19, 2003
Genistein can modulate channel function by a phosphorylation-independent mechanism: importance of hydrophobic mismatch and bilayer mechanicsTzyh-Chang Hwang, Roger E Koeppe, Olaf S Andersen
The Journal of General Physiology|November 17, 2010
On the mechanism of CFTR inhibition by a thiazolidinone derivativeZoia Kopeikin, Yoshiro Sohma, Min Li, et al.
The Journal of General Physiology|December 17, 2014
Modulation of CFTR gating by permeant ionsHan-I Yeh, Jiunn-Tyng Yeh, Tzyh-Chang Hwang
The Journal of General Physiology|September 17, 2014
A single amino acid substitution in CFTR converts ATP to an inhibitory ligandWen-Ying Lin, Kang-Yang Jih, Tzyh-Chang Hwang
The Journal of Physiology|November 9, 2018
Structural mechanisms for defective CFTR gating caused by the Q1412X mutation, a severe Class VI pathogenic mutation in cystic fibrosisJiunn-Tyng Yeh, Ying-Chun Yu, Tzyh-Chang Hwang
The Journal of General Physiology|December 31, 2008
Mutations at the signature sequence of CFTR create a Cd(2+)-gated chloride channelXiaohui Wang, Silvia G Bompadre, Min Li, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
The Journal of Physiology|February 6, 2016
On the mechanism of gating defects caused by the R117H mutation in cystic fibrosis transmembrane conductance regulatorYing-Chun Yu, Yoshiro Sohma, Tzyh-Chang Hwang
The Journal of General Physiology|September 12, 2012
Nonintegral stoichiometry in CFTR gating revealed by a pore-lining mutationKang-Yang Jih, Yoshiro Sohma, Tzyh-Chang Hwang
Current Pharmaceutical Design|January 22, 2013
Curcumin and genistein: the combined effects on disease-associated CFTR mutants and their clinical implicationsYoshiro Sohma, Ying-Chun Yu, Tzyh-Chang Hwang
Frontiers in Molecular Biosciences|July 11, 2022
Pharmacological Responses of the G542X-CFTR to CFTR ModulatorsXinxiu Fang, Jiunn-Tyng Yeh, Tzyh-Chang Hwang
Biochemistry|November 19, 2003
Genistein can modulate channel function by a phosphorylation-independent mechanism: importance of hydrophobic mismatch and bilayer mechanicsTzyh-Chang Hwang, Roger E Koeppe, Olaf S Andersen
The Journal of General Physiology|November 17, 2010
On the mechanism of CFTR inhibition by a thiazolidinone derivativeZoia Kopeikin, Yoshiro Sohma, Min Li, et al.
The Journal of General Physiology|December 17, 2014
Modulation of CFTR gating by permeant ionsHan-I Yeh, Jiunn-Tyng Yeh, Tzyh-Chang Hwang
The Journal of General Physiology|September 17, 2014
A single amino acid substitution in CFTR converts ATP to an inhibitory ligandWen-Ying Lin, Kang-Yang Jih, Tzyh-Chang Hwang
The Journal of Physiology|November 9, 2018
Structural mechanisms for defective CFTR gating caused by the Q1412X mutation, a severe Class VI pathogenic mutation in cystic fibrosisJiunn-Tyng Yeh, Ying-Chun Yu, Tzyh-Chang Hwang
The Journal of General Physiology|December 31, 2008
Mutations at the signature sequence of CFTR create a Cd(2+)-gated chloride channelXiaohui Wang, Silvia G Bompadre, Min Li, et al.
Pageof 8