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Canadian Journal of Microbiology|September 10, 2013
Impact of D-amino acid dehydrogenase on virulence factor production by a Pseudomonas aeruginosaKathryn E Oliver, Laura Silo-Suh
Expert Opinion on Pharmacotherapy|June 28, 2023
The revolution of personalized pharmacotherapies for cystic fibrosis: what does the future hold?Kathryn E Oliver, Marianne S Carlon, Nicoletta Pedemonte, et al.
Current Opinion in Pharmacology|October 17, 2017
Transformative therapies for rare CFTR missense allelesKathryn E Oliver, Sangwoo T Han, Eric J Sorscher, et al.
Journal of Clinical & Translational Endocrinology|May 20, 2024
Racial inequities and rare <i>CFTR</i> variants: Impact on cystic fibrosis diagnosis and treatmentMalinda Wu, Jacob D Davis, Conan Zhao, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
Benchmarking AlphaMissense Pathogenicity Predictions Against Cystic Fibrosis VariantsEli Fritz McDonald, Kathryn E Oliver, Jonathan P Schlebach, et al.
Frontiers in Genetics|May 11, 2023
Features of CFTR mRNA and implications for therapeutics developmentJaNise J Jackson, Yiyang Mao, Tyshawn R White, et al.
Plos One|January 25, 2024
Benchmarking AlphaMissense pathogenicity predictions against cystic fibrosis variantsEli Fritz McDonald, Kathryn E Oliver, Jonathan P Schlebach, et al.
International Journal of Neonatal Screening|October 24, 2025
<i>CFTR</i> Variant Frequencies and Newborn Screening Panel Performance in the Diverse CF Population Receiving Care in the State of GeorgiaEileen Barr, Brittany Truitt, Andrew Jergel, et al.
International Journal of Neonatal Screening|October 24, 2025
Evaluating Georgia's Cystic Fibrosis Newborn Screening Algorithm to Inform Improvement RecommendationsBrittany Truitt, Eileen Barr, Angela Wittenauer, et al.
BMC Genomics|July 17, 2019
Assessing cell-specific effects of genetic variations using tRNA microarraysChristine Polte, Daniel Wedemeyer, Kathryn E Oliver, et al.
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