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American Journal of Physiology. Lung Cellular and Molecular Physiology
|
September 3, 2020
G551D mutation impairs PKA-dependent activation of CFTR channel that can be restored by novel GOF mutations
Wei Wang, Lianwu Fu, Zhiyong Liu, et al.
Journal of Molecular and Cellular Cardiology
|
January 26, 2016
Increased fibroblast chymase production mediates procollagen autophagic digestion in volume overload
Lianwu Fu, Chih-Chang Wei, Pamela C Powell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 27, 2025
Identity, functional consequences, and context effects of amino acids inserted during suppression of CFTR nonsense mutations
Kari Thrasher, Jianguo Chen, Lianwu Fu, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
April 4, 2023
The synthetic aminoglycoside ELX-02 induces readthrough of G550X-CFTR producing superfunctional protein that can be further enhanced by CFTR modulators
Jianguo Chen, Kari Thrasher, Lianwu Fu, et al.
American Journal of Respiratory and Critical Care Medicine
|
August 15, 2025
Ionocyte CFTR Coordinates Chloride Absorption and Secretion to Balance Airway Fluid
Feng Yuan, Javahir Hajibabazade, Yaling Yi, et al.
Cellular & Molecular Biology Letters
|
May 25, 2017
Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator
Rafal Bartoszewski, Jaroslaw Króliczewski, Arkadiusz Piotrowski, et al.
JCI Insight
|
September 24, 2016
Analysis of cystic fibrosis-associated P67L CFTR illustrates barriers to personalized therapeutics for orphan diseases
Carleen M Sabusap, Wei Wang, Carmel M McNicholas, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 3, 2013
The silent codon change I507-ATC->ATT contributes to the severity of the ΔF508 CFTR channel dysfunction
Ahmed Lazrak, Lianwu Fu, Vedrana Bali, et al.
Nature Cell Biology
|
April 19, 2011
ARFGAP1 promotes AP-2-dependent endocytosis
Ming Bai, Helge Gad, Gabriele Turacchio, et al.
Plos One
|
November 29, 2023
Prime editing-mediated correction of the CFTR W1282X mutation in iPSCs and derived airway epithelial cells
Chao Li, Zhong Liu, Justin Anderson, et al.
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Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
September 3, 2020
G551D mutation impairs PKA-dependent activation of CFTR channel that can be restored by novel GOF mutations
Wei Wang, Lianwu Fu, Zhiyong Liu, et al.
Journal of Molecular and Cellular Cardiology
|
January 26, 2016
Increased fibroblast chymase production mediates procollagen autophagic digestion in volume overload
Lianwu Fu, Chih-Chang Wei, Pamela C Powell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 27, 2025
Identity, functional consequences, and context effects of amino acids inserted during suppression of CFTR nonsense mutations
Kari Thrasher, Jianguo Chen, Lianwu Fu, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
April 4, 2023
The synthetic aminoglycoside ELX-02 induces readthrough of G550X-CFTR producing superfunctional protein that can be further enhanced by CFTR modulators
Jianguo Chen, Kari Thrasher, Lianwu Fu, et al.
American Journal of Respiratory and Critical Care Medicine
|
August 15, 2025
Ionocyte CFTR Coordinates Chloride Absorption and Secretion to Balance Airway Fluid
Feng Yuan, Javahir Hajibabazade, Yaling Yi, et al.
Cellular & Molecular Biology Letters
|
May 25, 2017
Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator
Rafal Bartoszewski, Jaroslaw Króliczewski, Arkadiusz Piotrowski, et al.
JCI Insight
|
September 24, 2016
Analysis of cystic fibrosis-associated P67L CFTR illustrates barriers to personalized therapeutics for orphan diseases
Carleen M Sabusap, Wei Wang, Carmel M McNicholas, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 3, 2013
The silent codon change I507-ATC->ATT contributes to the severity of the ΔF508 CFTR channel dysfunction
Ahmed Lazrak, Lianwu Fu, Vedrana Bali, et al.
Nature Cell Biology
|
April 19, 2011
ARFGAP1 promotes AP-2-dependent endocytosis
Ming Bai, Helge Gad, Gabriele Turacchio, et al.
Plos One
|
November 29, 2023
Prime editing-mediated correction of the CFTR W1282X mutation in iPSCs and derived airway epithelial cells
Chao Li, Zhong Liu, Justin Anderson, et al.
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of 4