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March 17, 2012
Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary disease
Tanja Gonska, Perry Choi, Anne Stephenson, et al.
Molecular Therapy. Methods & Clinical Development
|
January 6, 2016
Testing gene therapy vectors in human primary nasal epithelial cultures
Huibi Cao, Hong Ouyang, Wan Ip, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 2, 2020
DIGEST: Developing innovative gastroenterology specialty training
Sarah Shrager Lusman, Drucy Borowitz, Bruce C Marshall, et al.
Gastroenterology
|
October 7, 2010
Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis
Chee Y Ooi, Ruslan Dorfman, Marco Cipolli, et al.
American Journal of Respiratory Cell and Molecular Biology
|
June 13, 2019
Augmentation of Cystic Fibrosis Transmembrane Conductance Regulator Function in Human Bronchial Epithelial Cells via SLC6A14-Dependent Amino Acid Uptake. Implications for Treatment of Cystic Fibrosis
Saumel Ahmadi, Yu-Sheng Wu, Mingyuan Li, et al.
Annals of the American Thoracic Society
|
April 5, 2014
Does integration of various ion channel measurements improve diagnostic performance in cystic fibrosis?
Chee Y Ooi, Annie Dupuis, Tanja Gonska, et al.
Thorax
|
October 24, 2013
Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?
Chee Y Ooi, Annie Dupuis, Lynda Ellis, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 14, 2014
Clinical mechanism of the cystic fibrosis transmembrane conductance regulator potentiator ivacaftor in G551D-mediated cystic fibrosis
Steven M Rowe, Sonya L Heltshe, Tanja Gonska, et al.
Life Science Alliance
|
April 6, 2023
Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis
Liron Birimberg-Schwartz, Wan Ip, Claire Bartlett, et al.
Gastroenterology
|
October 14, 2004
CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis
Stephanie Hirtz, Tanja Gonska, Hans H Seydewitz, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 100) with videos related to
Sort By:
Page
of 10
Chest
|
March 17, 2012
Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary disease
Tanja Gonska, Perry Choi, Anne Stephenson, et al.
Molecular Therapy. Methods & Clinical Development
|
January 6, 2016
Testing gene therapy vectors in human primary nasal epithelial cultures
Huibi Cao, Hong Ouyang, Wan Ip, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 2, 2020
DIGEST: Developing innovative gastroenterology specialty training
Sarah Shrager Lusman, Drucy Borowitz, Bruce C Marshall, et al.
Gastroenterology
|
October 7, 2010
Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis
Chee Y Ooi, Ruslan Dorfman, Marco Cipolli, et al.
American Journal of Respiratory Cell and Molecular Biology
|
June 13, 2019
Augmentation of Cystic Fibrosis Transmembrane Conductance Regulator Function in Human Bronchial Epithelial Cells via SLC6A14-Dependent Amino Acid Uptake. Implications for Treatment of Cystic Fibrosis
Saumel Ahmadi, Yu-Sheng Wu, Mingyuan Li, et al.
Annals of the American Thoracic Society
|
April 5, 2014
Does integration of various ion channel measurements improve diagnostic performance in cystic fibrosis?
Chee Y Ooi, Annie Dupuis, Tanja Gonska, et al.
Thorax
|
October 24, 2013
Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?
Chee Y Ooi, Annie Dupuis, Lynda Ellis, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 14, 2014
Clinical mechanism of the cystic fibrosis transmembrane conductance regulator potentiator ivacaftor in G551D-mediated cystic fibrosis
Steven M Rowe, Sonya L Heltshe, Tanja Gonska, et al.
Life Science Alliance
|
April 6, 2023
Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis
Liron Birimberg-Schwartz, Wan Ip, Claire Bartlett, et al.
Gastroenterology
|
October 14, 2004
CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis
Stephanie Hirtz, Tanja Gonska, Hans H Seydewitz, et al.
Page
of 10