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American Journal of Physiology. Lung Cellular and Molecular Physiology
|
September 8, 2025
TGF-β induces excessive pulmonary IL-6 secretion in cystic fibrosis via PI3K
Grace Scharf, Cynthia R Davidson, Vladimir Ustiyan, et al.
Biochemistry
|
November 12, 2003
Activation of chloride secretion in cystic fibrosis cells and tissues by the substituted imidazole SRI 2931
Julie R Jones, Erik M Schwiebert, Michael D DuVall, et al.
Neuromuscular Disorders : NMD
|
January 26, 2015
Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease
Laura E Case, Carl Bjartmar, Claire Morgan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 25, 2019
Utilizing centralized biorepository samples for biomarkers of cystic fibrosis lung disease severity
Scott D Sagel, Brandie D Wagner, Assem Ziady, et al.
JCI Insight
|
October 6, 2017
Guanylate cyclase 2C agonism corrects CFTR mutants
Kavisha Arora, Yunjie Huang, Kyushik Mun, et al.
Pediatric Pulmonology
|
October 11, 2023
A personalized medicine approach to optimize care for a pediatric cystic fibrosis patient with atypical clinical symptoms
Jesun Lee, Ammar Husami, Kavisha Arora, et al.
Environmental Advances
|
December 14, 2023
Social-environmental phenotypes of rapid cystic fibrosis lung disease progression in adolescents and young adults living in the United States
Anushka K Palipana, Andrew Vancil, Emrah Gecili, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 7, 2004
Assessment of CFTR localisation in native airway epithelial cells obtained by nasal brushing
Ceinwen M Harris, Filipa Mendes, Anca Dragomir, et al.
The Journal of Clinical Investigation
|
March 28, 2023
Pharmacologic improvement of CFTR function rapidly decreases sputum pathogen density, but lung infections generally persist
David P Nichols, Sarah J Morgan, Michelle Skalland, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 14, 2017
Home Monitoring of Patients with Cystic Fibrosis to Identify and Treat Acute Pulmonary Exacerbations. eICE Study Results
Noah Lechtzin, Nicole Mayer-Hamblett, Natalie E West, et al.
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of 13
Search research articles
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Showing results (91-100 of 121) with videos related to
Sort By:
Page
of 13
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
September 8, 2025
TGF-β induces excessive pulmonary IL-6 secretion in cystic fibrosis via PI3K
Grace Scharf, Cynthia R Davidson, Vladimir Ustiyan, et al.
Biochemistry
|
November 12, 2003
Activation of chloride secretion in cystic fibrosis cells and tissues by the substituted imidazole SRI 2931
Julie R Jones, Erik M Schwiebert, Michael D DuVall, et al.
Neuromuscular Disorders : NMD
|
January 26, 2015
Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease
Laura E Case, Carl Bjartmar, Claire Morgan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 25, 2019
Utilizing centralized biorepository samples for biomarkers of cystic fibrosis lung disease severity
Scott D Sagel, Brandie D Wagner, Assem Ziady, et al.
JCI Insight
|
October 6, 2017
Guanylate cyclase 2C agonism corrects CFTR mutants
Kavisha Arora, Yunjie Huang, Kyushik Mun, et al.
Pediatric Pulmonology
|
October 11, 2023
A personalized medicine approach to optimize care for a pediatric cystic fibrosis patient with atypical clinical symptoms
Jesun Lee, Ammar Husami, Kavisha Arora, et al.
Environmental Advances
|
December 14, 2023
Social-environmental phenotypes of rapid cystic fibrosis lung disease progression in adolescents and young adults living in the United States
Anushka K Palipana, Andrew Vancil, Emrah Gecili, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 7, 2004
Assessment of CFTR localisation in native airway epithelial cells obtained by nasal brushing
Ceinwen M Harris, Filipa Mendes, Anca Dragomir, et al.
The Journal of Clinical Investigation
|
March 28, 2023
Pharmacologic improvement of CFTR function rapidly decreases sputum pathogen density, but lung infections generally persist
David P Nichols, Sarah J Morgan, Michelle Skalland, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 14, 2017
Home Monitoring of Patients with Cystic Fibrosis to Identify and Treat Acute Pulmonary Exacerbations. eICE Study Results
Noah Lechtzin, Nicole Mayer-Hamblett, Natalie E West, et al.
Page
of 13