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Showing results (841-850 of 950) with videos related to

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American Journal of Respiratory and Critical Care Medicine|June 4, 2016
Sources of Variation in Sweat Chloride Measurements in Cystic FibrosisJoseph M Collaco, Scott M Blackman, Karen S Raraigh, et al.
Pediatric Pulmonology|April 24, 2023
First reports of primary ciliary dyskinesia caused by a shared DNAH11 allele in Canadian InuitJulia Hunter-Schouela, Michael T Geraghty, Robert A Hegele, et al.
Biology of Reproduction|August 19, 2007
A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axonemeZhibing Zhang, Maimoona A Zariwala, Maha M Mahadevan, et al.
Trials|September 11, 2016
The Stroke and Carer Optimal Health Program (SCOHP) to enhance psychosocial health: study protocol for a randomized controlled trialCatherine Brasier, Chantal F Ski, David R Thompson, et al.
The Journal of Physical Chemistry. C, Nanomaterials and Interfaces|February 25, 2026
Leveraging Multiproton-Coupled Electron Transfer to Improve Ir(III) Photocatalyst EfficiencyEris Villalona, Rodrigo E Domínguez, Edwin J Gonzalez Lopez, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 16, 2021
Complete CFTR gene sequencing in 5,058 individuals with cystic fibrosis informs variant-specific treatmentKaren S Raraigh, Melis A Aksit, Kurt Hetrick, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 10, 2000
Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosisP G Noone, K W Hohneker, Z Zhou, et al.
The Journal of Pediatrics|March 13, 2013
Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communitiesThomas W Ferkol, Erik G Puffenberger, Hauw Lie, et al.
American Journal of Human Genetics|September 11, 2024
Genetic modifiers of body mass index in individuals with cystic fibrosisHua Ling, Karen S Raraigh, Elizabeth W Pugh, et al.
Plos Genetics|August 19, 2015
Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic FibrosisMary J Emond, Tin Louie, Julia Emerson, et al.
Pageof 95

Showing results (841-850 of 950) with videos related to

Sort By:
Pageof 95
American Journal of Respiratory and Critical Care Medicine|June 4, 2016
Sources of Variation in Sweat Chloride Measurements in Cystic FibrosisJoseph M Collaco, Scott M Blackman, Karen S Raraigh, et al.
Pediatric Pulmonology|April 24, 2023
First reports of primary ciliary dyskinesia caused by a shared DNAH11 allele in Canadian InuitJulia Hunter-Schouela, Michael T Geraghty, Robert A Hegele, et al.
Biology of Reproduction|August 19, 2007
A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axonemeZhibing Zhang, Maimoona A Zariwala, Maha M Mahadevan, et al.
Trials|September 11, 2016
The Stroke and Carer Optimal Health Program (SCOHP) to enhance psychosocial health: study protocol for a randomized controlled trialCatherine Brasier, Chantal F Ski, David R Thompson, et al.
The Journal of Physical Chemistry. C, Nanomaterials and Interfaces|February 25, 2026
Leveraging Multiproton-Coupled Electron Transfer to Improve Ir(III) Photocatalyst EfficiencyEris Villalona, Rodrigo E Domínguez, Edwin J Gonzalez Lopez, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 16, 2021
Complete CFTR gene sequencing in 5,058 individuals with cystic fibrosis informs variant-specific treatmentKaren S Raraigh, Melis A Aksit, Kurt Hetrick, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 10, 2000
Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosisP G Noone, K W Hohneker, Z Zhou, et al.
The Journal of Pediatrics|March 13, 2013
Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communitiesThomas W Ferkol, Erik G Puffenberger, Hauw Lie, et al.
American Journal of Human Genetics|September 11, 2024
Genetic modifiers of body mass index in individuals with cystic fibrosisHua Ling, Karen S Raraigh, Elizabeth W Pugh, et al.
Plos Genetics|August 19, 2015
Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic FibrosisMary J Emond, Tin Louie, Julia Emerson, et al.
Pageof 95