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The Journal of General Physiology
|
March 14, 2007
G551D and G1349D, two CF-associated mutations in the signature sequences of CFTR, exhibit distinct gating defects
Silvia G Bompadre, Yoshiro Sohma, Min Li, et al.
The Journal of General Physiology
|
April 18, 2012
Identification of a novel post-hydrolytic state in CFTR gating
Kang-Yang Jih, Yoshiro Sohma, Min Li, et al.
The Journal of General Physiology
|
October 29, 2017
A common mechanism for CFTR potentiators
Han-I Yeh, Yoshiro Sohma, Katja Conrath, et al.
Plos One
|
January 1, 2019
Functional characterization reveals that zebrafish CFTR prefers to occupy closed channel conformations
Jingyao Zhang, Ying-Chun Yu, Jiunn-Tyng Yeh, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
November 6, 2017
Ion channels as targets to treat cystic fibrosis lung disease
S Lorraine Martin, Vinciane Saint-Criq, Tzyh-Chang Hwang, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 10, 2022
Structure basis of CFTR folding, function and pharmacology
Tzyh-Chang Hwang, Ineke Braakman, Peter van der Sluijs, et al.
Current Opinion in Pharmacology
|
October 27, 2017
CFTR potentiators: from bench to bedside
Kang-Yang Jih, Wen-Ying Lin, Yoshiro Sohma, et al.
The Journal of Physiology
|
April 14, 2011
The most common cystic fibrosis-associated mutation destabilizes the dimeric state of the nucleotide-binding domains of CFTR
Kang-Yang Jih, Min Li, Tzyh-Chang Hwang, et al.
The Journal of Physiology
|
March 8, 2002
Mutation of Walker-A lysine 464 in cystic fibrosis transmembrane conductance regulator reveals functional interaction between its nucleotide-binding domains
Allan C Powe, Layla Al-Nakkash, Min Li, et al.
Handbook of Experimental Pharmacology
|
August 16, 2022
CFTR Modulators: From Mechanism to Targeted Therapeutics
Han-I Yeh, Katy J Sutcliffe, David N Sheppard, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 71) with videos related to
Sort By:
Page
of 8
The Journal of General Physiology
|
March 14, 2007
G551D and G1349D, two CF-associated mutations in the signature sequences of CFTR, exhibit distinct gating defects
Silvia G Bompadre, Yoshiro Sohma, Min Li, et al.
The Journal of General Physiology
|
April 18, 2012
Identification of a novel post-hydrolytic state in CFTR gating
Kang-Yang Jih, Yoshiro Sohma, Min Li, et al.
The Journal of General Physiology
|
October 29, 2017
A common mechanism for CFTR potentiators
Han-I Yeh, Yoshiro Sohma, Katja Conrath, et al.
Plos One
|
January 1, 2019
Functional characterization reveals that zebrafish CFTR prefers to occupy closed channel conformations
Jingyao Zhang, Ying-Chun Yu, Jiunn-Tyng Yeh, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
November 6, 2017
Ion channels as targets to treat cystic fibrosis lung disease
S Lorraine Martin, Vinciane Saint-Criq, Tzyh-Chang Hwang, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 10, 2022
Structure basis of CFTR folding, function and pharmacology
Tzyh-Chang Hwang, Ineke Braakman, Peter van der Sluijs, et al.
Current Opinion in Pharmacology
|
October 27, 2017
CFTR potentiators: from bench to bedside
Kang-Yang Jih, Wen-Ying Lin, Yoshiro Sohma, et al.
The Journal of Physiology
|
April 14, 2011
The most common cystic fibrosis-associated mutation destabilizes the dimeric state of the nucleotide-binding domains of CFTR
Kang-Yang Jih, Min Li, Tzyh-Chang Hwang, et al.
The Journal of Physiology
|
March 8, 2002
Mutation of Walker-A lysine 464 in cystic fibrosis transmembrane conductance regulator reveals functional interaction between its nucleotide-binding domains
Allan C Powe, Layla Al-Nakkash, Min Li, et al.
Handbook of Experimental Pharmacology
|
August 16, 2022
CFTR Modulators: From Mechanism to Targeted Therapeutics
Han-I Yeh, Katy J Sutcliffe, David N Sheppard, et al.
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of 8