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Cell
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March 1, 2024
A cryptic plasmid is among the most numerous genetic elements in the human gut
Emily C Fogarty, Matthew S Schechter, Karen Lolans, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
April 30, 2023
Inhaled mRNA therapy for treatment of cystic fibrosis: Interim results of a randomized, double-blind, placebo-controlled phase 1/2 clinical study
S M Rowe, J B Zuckerman, D Dorgan, et al.
Annals of the American Thoracic Society
|
September 8, 2025
Evaluating Long-Term Effectiveness of Cystic Fibrosis Modulator Therapies After Rapid Adoption: A Dual-Approach Study
Pedro Miranda Afonso, Grace C Zhou, Weiji Su, et al.
Nature Microbiology
|
May 16, 2025
Author Correction: Dietary- and host-derived metabolites are used by diverse gut bacteria for anaerobic respiration
Alexander S Little, Isaac T Younker, Matthew S Schechter, et al.
Nature Microbiology
|
January 4, 2024
Dietary- and host-derived metabolites are used by diverse gut bacteria for anaerobic respiration
Alexander S Little, Isaac T Younker, Matthew S Schechter, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 2, 2015
Official American Thoracic Society technical standards: flexible airway endoscopy in children
Albert Faro, Robert E Wood, Michael S Schechter, et al.
Annals of the American Thoracic Society
|
March 8, 2023
Lung Function Decline in Cystic Fibrosis: Impact of Data Availability and Modeling Strategies on Clinical Interpretations
Rhonda Szczesniak, Eleni-Rosalina Andrinopoulou, Weiji Su, et al.
The Journal of Urology
|
August 1, 2016
Design and Methodological Considerations of the Centers for Disease Control and Prevention Urologic and Renal Protocol for the Newborn and Young Child with Spina Bifida
Jonathan C Routh, Earl Y Cheng, J Christopher Austin, et al.
Thorax
|
August 10, 2011
Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation
J P Clancy, Steven M Rowe, Frank J Accurso, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 24, 2024
Standards for the care of people with cystic fibrosis (CF); Planning for a longer life
Andrea Gramegna, Charlotte Addy, Lorna Allen, et al.
Page
of 36
Search research articles
Search
Showing results (341-350 of 354) with videos related to
Sort By:
Page
of 36
Cell
|
March 1, 2024
A cryptic plasmid is among the most numerous genetic elements in the human gut
Emily C Fogarty, Matthew S Schechter, Karen Lolans, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
April 30, 2023
Inhaled mRNA therapy for treatment of cystic fibrosis: Interim results of a randomized, double-blind, placebo-controlled phase 1/2 clinical study
S M Rowe, J B Zuckerman, D Dorgan, et al.
Annals of the American Thoracic Society
|
September 8, 2025
Evaluating Long-Term Effectiveness of Cystic Fibrosis Modulator Therapies After Rapid Adoption: A Dual-Approach Study
Pedro Miranda Afonso, Grace C Zhou, Weiji Su, et al.
Nature Microbiology
|
May 16, 2025
Author Correction: Dietary- and host-derived metabolites are used by diverse gut bacteria for anaerobic respiration
Alexander S Little, Isaac T Younker, Matthew S Schechter, et al.
Nature Microbiology
|
January 4, 2024
Dietary- and host-derived metabolites are used by diverse gut bacteria for anaerobic respiration
Alexander S Little, Isaac T Younker, Matthew S Schechter, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 2, 2015
Official American Thoracic Society technical standards: flexible airway endoscopy in children
Albert Faro, Robert E Wood, Michael S Schechter, et al.
Annals of the American Thoracic Society
|
March 8, 2023
Lung Function Decline in Cystic Fibrosis: Impact of Data Availability and Modeling Strategies on Clinical Interpretations
Rhonda Szczesniak, Eleni-Rosalina Andrinopoulou, Weiji Su, et al.
The Journal of Urology
|
August 1, 2016
Design and Methodological Considerations of the Centers for Disease Control and Prevention Urologic and Renal Protocol for the Newborn and Young Child with Spina Bifida
Jonathan C Routh, Earl Y Cheng, J Christopher Austin, et al.
Thorax
|
August 10, 2011
Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation
J P Clancy, Steven M Rowe, Frank J Accurso, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 24, 2024
Standards for the care of people with cystic fibrosis (CF); Planning for a longer life
Andrea Gramegna, Charlotte Addy, Lorna Allen, et al.
Page
of 36