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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 18, 2022
Mucus aberrant properties in CF: Insights from cells and animal models
Camille Ehre, Gunnar C Hansson, David J Thornton, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 3, 2012
Human-mouse cystic fibrosis transmembrane conductance regulator (CFTR) chimeras identify regions that partially rescue CFTR-ΔF508 processing and alter its gating defect
Qian Dong, Lynda S Ostedgaard, Christopher Rogers, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 13, 2003
Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia
Lynda S Ostedgaard, Christoph Randak, Tatiana Rokhlina, et al.
The Journal of Biological Chemistry
|
December 8, 2004
Curcumin stimulates cystic fibrosis transmembrane conductance regulator Cl- channel activity
Allan L Berger, Christoph O Randak, Lynda S Ostedgaard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 3, 2011
Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice
Lynda S Ostedgaard, David K Meyerholz, Daniel W Vermeer, et al.
The Journal of Biological Chemistry
|
April 19, 2015
Mutating the Conserved Q-loop Glutamine 1291 Selectively Disrupts Adenylate Kinase-dependent Channel Gating of the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Reduces Channel Function in Primary Human Airway Epithelia
Qian Dong, Sarah E Ernst, Lynda S Ostedgaard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 27, 2016
Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies
Viral S Shah, Sarah Ernst, Xiao Xiao Tang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 21, 2002
CFTR with a partially deleted R domain corrects the cystic fibrosis chloride transport defect in human airway epithelia in vitro and in mouse nasal mucosa in vivo
Lynda S Ostedgaard, Joseph Zabner, Daniel W Vermeer, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 7, 2004
Methods to study CFTR protein in vitro
Dale J Benos, Bakhrom K Berdiev, Iskander I Ismailov, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 18, 2007
Processing and function of CFTR-DeltaF508 are species-dependent
Lynda S Ostedgaard, Christopher S Rogers, Qian Dong, et al.
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of 4
Search research articles
Search
Showing results (1-10 of 32) with videos related to
Sort By:
Page
of 4
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 18, 2022
Mucus aberrant properties in CF: Insights from cells and animal models
Camille Ehre, Gunnar C Hansson, David J Thornton, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 3, 2012
Human-mouse cystic fibrosis transmembrane conductance regulator (CFTR) chimeras identify regions that partially rescue CFTR-ΔF508 processing and alter its gating defect
Qian Dong, Lynda S Ostedgaard, Christopher Rogers, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 13, 2003
Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia
Lynda S Ostedgaard, Christoph Randak, Tatiana Rokhlina, et al.
The Journal of Biological Chemistry
|
December 8, 2004
Curcumin stimulates cystic fibrosis transmembrane conductance regulator Cl- channel activity
Allan L Berger, Christoph O Randak, Lynda S Ostedgaard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 3, 2011
Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice
Lynda S Ostedgaard, David K Meyerholz, Daniel W Vermeer, et al.
The Journal of Biological Chemistry
|
April 19, 2015
Mutating the Conserved Q-loop Glutamine 1291 Selectively Disrupts Adenylate Kinase-dependent Channel Gating of the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Reduces Channel Function in Primary Human Airway Epithelia
Qian Dong, Sarah E Ernst, Lynda S Ostedgaard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 27, 2016
Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies
Viral S Shah, Sarah Ernst, Xiao Xiao Tang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 21, 2002
CFTR with a partially deleted R domain corrects the cystic fibrosis chloride transport defect in human airway epithelia in vitro and in mouse nasal mucosa in vivo
Lynda S Ostedgaard, Joseph Zabner, Daniel W Vermeer, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 7, 2004
Methods to study CFTR protein in vitro
Dale J Benos, Bakhrom K Berdiev, Iskander I Ismailov, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 18, 2007
Processing and function of CFTR-DeltaF508 are species-dependent
Lynda S Ostedgaard, Christopher S Rogers, Qian Dong, et al.
Page
of 4