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Nature Communications|April 26, 2020
Conditional deletion of Nedd4-2 in lung epithelial cells causes progressive pulmonary fibrosis in adult miceJulia Duerr, Dominik H W Leitz, Magdalena Szczygiel, et al.
American Journal of Respiratory and Critical Care Medicine|March 18, 2021
A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del AlleleEdith T Zemanick, Jennifer L Taylor-Cousar, Jane Davies, et al.
Science Translational Medicine|December 8, 2022
Loss of endothelial CFTR drives barrier failure and edema formation in lung infection and can be targeted by CFTR potentiationLasti Erfinanda, Lin Zou, Birgitt Gutbier, et al.
The New England Journal of Medicine|August 26, 2021
Triple Therapy for Cystic Fibrosis Phe508del-Gating and -Residual Function GenotypesPeter J Barry, Marcus A Mall, Antonio Álvarez, et al.
The Lancet. Respiratory Medicine|February 26, 2023
Safety and efficacy of vanzacaftor-tezacaftor-deutivacaftor in adults with cystic fibrosis: randomised, double-blind, controlled, phase 2 trialsAhmet Z Uluer, Gordon MacGregor, Pilar Azevedo, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 2, 2026
Effects of Elexacaftor/Tezacaftor/Ivacaftor on cough frequency, physical activity patterns, and sleep quality in adolescents and adults with cystic fibrosisEva Van Braeckel, Andrew T Braun, Nicholas J Simmonds, et al.
Science Translational Medicine|December 18, 2024
Dextromethorphan inhibits collagen and collagen-like cargo secretion to ameliorate lung fibrosisMuzamil M Khan, George Galea, Juan Jung, et al.
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