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Tanja Gonska

Showing results (51-60 of 100) with videos related to

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Chest|March 17, 2012
Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary diseaseTanja Gonska, Perry Choi, Anne Stephenson, et al.
Molecular Therapy. Methods & Clinical Development|January 6, 2016
Testing gene therapy vectors in human primary nasal epithelial culturesHuibi 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 trainingSarah 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 fibrosisChee 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 FibrosisSaumel 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 fibrosisSteven 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 fibrosisLiron 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 fibrosisStephanie Hirtz, Tanja Gonska, Hans H Seydewitz, et al.
Pageof 10

Showing results (51-60 of 100) with videos related to

Sort By:
Pageof 10
Chest|March 17, 2012
Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary diseaseTanja Gonska, Perry Choi, Anne Stephenson, et al.
Molecular Therapy. Methods & Clinical Development|January 6, 2016
Testing gene therapy vectors in human primary nasal epithelial culturesHuibi 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 trainingSarah 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 fibrosisChee 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 FibrosisSaumel 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 fibrosisSteven 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 fibrosisLiron 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 fibrosisStephanie Hirtz, Tanja Gonska, Hans H Seydewitz, et al.
Pageof 10