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Journal of Immunology (Baltimore, Md. : 1950)|March 18, 2011
Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cellsValentino Bezzerri, Pio d'Adamo, Alessandro Rimessi, et al.
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.
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.
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