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Annals of the American Thoracic Society
|
December 23, 2016
Digitoxin for Airway Inflammation in Cystic Fibrosis: Preliminary Assessment of Safety, Pharmacokinetics, and Dose Finding
Pamela L Zeitlin, Marie Diener-West, Karen A Callahan, et al.
American Journal of Respiratory Cell and Molecular Biology
|
April 15, 2006
Respiratory epithelial gene expression in patients with mild and severe cystic fibrosis lung disease
Jerry M Wright, Christian A Merlo, Jeffrey B Reynolds, et al.
Annals of the American Thoracic Society
|
November 30, 2016
Lumacaftor/Ivacaftor Treatment of Patients with Cystic Fibrosis Heterozygous for F508del-CFTR
Steven M Rowe, Susanna A McColley, Ernst Rietschel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 2015
Highly compacted biodegradable DNA nanoparticles capable of overcoming the mucus barrier for inhaled lung gene therapy
Panagiotis Mastorakos, Adriana L da Silva, Jane Chisholm, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 27, 2007
Patients with mutations in Gsalpha have reduced activation of a downstream target in epithelial tissues due to haploinsufficiency
Stephanie C Hsu, Joshua D Groman, Christian A Merlo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 11, 2009
Biodegradable polymer nanoparticles that rapidly penetrate the human mucus barrier
Benjamin C Tang, Michelle Dawson, Samuel K Lai, et al.
The Lancet. Respiratory Medicine
|
June 29, 2014
A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: a phase 2 randomised controlled trial
Michael P Boyle, Scott C Bell, Michael W Konstan, et al.
Chest
|
March 12, 2011
Appropriate goal level for 25-hydroxyvitamin D in cystic fibrosis
Natalie E West, Noah Lechtzin, Christian A Merlo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 30, 2014
Overcoming the cystic fibrosis sputum barrier to leading adeno-associated virus gene therapy vectors
Benjamin S Schuster, Anthony J Kim, Joshua C Kays, et al.
American Journal of Speech-Language Pathology
|
September 13, 2021
Consensus Guidelines for the Assessments of Individuals Who Stutter Across the Lifespan
Shelley B Brundage, Nan Bernstein Ratner, Michael P Boyle, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 91) with videos related to
Sort By:
Page
of 10
Annals of the American Thoracic Society
|
December 23, 2016
Digitoxin for Airway Inflammation in Cystic Fibrosis: Preliminary Assessment of Safety, Pharmacokinetics, and Dose Finding
Pamela L Zeitlin, Marie Diener-West, Karen A Callahan, et al.
American Journal of Respiratory Cell and Molecular Biology
|
April 15, 2006
Respiratory epithelial gene expression in patients with mild and severe cystic fibrosis lung disease
Jerry M Wright, Christian A Merlo, Jeffrey B Reynolds, et al.
Annals of the American Thoracic Society
|
November 30, 2016
Lumacaftor/Ivacaftor Treatment of Patients with Cystic Fibrosis Heterozygous for F508del-CFTR
Steven M Rowe, Susanna A McColley, Ernst Rietschel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 2015
Highly compacted biodegradable DNA nanoparticles capable of overcoming the mucus barrier for inhaled lung gene therapy
Panagiotis Mastorakos, Adriana L da Silva, Jane Chisholm, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 27, 2007
Patients with mutations in Gsalpha have reduced activation of a downstream target in epithelial tissues due to haploinsufficiency
Stephanie C Hsu, Joshua D Groman, Christian A Merlo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 11, 2009
Biodegradable polymer nanoparticles that rapidly penetrate the human mucus barrier
Benjamin C Tang, Michelle Dawson, Samuel K Lai, et al.
The Lancet. Respiratory Medicine
|
June 29, 2014
A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: a phase 2 randomised controlled trial
Michael P Boyle, Scott C Bell, Michael W Konstan, et al.
Chest
|
March 12, 2011
Appropriate goal level for 25-hydroxyvitamin D in cystic fibrosis
Natalie E West, Noah Lechtzin, Christian A Merlo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 30, 2014
Overcoming the cystic fibrosis sputum barrier to leading adeno-associated virus gene therapy vectors
Benjamin S Schuster, Anthony J Kim, Joshua C Kays, et al.
American Journal of Speech-Language Pathology
|
September 13, 2021
Consensus Guidelines for the Assessments of Individuals Who Stutter Across the Lifespan
Shelley B Brundage, Nan Bernstein Ratner, Michael P Boyle, et al.
Page
of 10