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Frontiers in Molecular Biosciences|April 3, 2023
Personalized medicine: Function of CFTR variant p.Arg334Trp is rescued by currently available CFTR modulatorsVioleta Railean, Cláudia S Rodrigues, Sofia S Ramalho, et al.Respiratory Medicine|July 11, 2025
N1303K (p.Asn1303Lys) variant: Expanding frontiers in the treatment of cystic fibrosisJoana Pacheco, Leonor Almeida, Rita Boaventura, et al.Cell Death & Disease|October 27, 2020
Mutant CFTR Drives TWIST1 mediated epithelial-mesenchymal transitionMargarida C Quaresma, Ines Pankonien, Luka A Clarke, et al.Progress in Retinal and Eye Research|September 8, 2024
The role of CFTR in the eye, and the effect of early highly effective modulator treatment for cystic fibrosis on eye healthElena K Schneider-Futschik, Yimin Zhu, Danni Li, et al.Pediatric Pulmonology|March 15, 2005
Processing of CFTR: traversing the cellular maze--how much CFTR needs to go through to avoid cystic fibrosis?Margarida D AmaralJournal of Inherited Metabolic Disease|June 10, 2006
Therapy through chaperones: sense or antisense? Cystic fibrosis as a model diseaseMargarida D AmaralEuropean Journal of Medicinal Chemistry|November 16, 2020
How to determine the mechanism of action of CFTR modulator compounds: A gateway to theranosticsMargarida D AmaralMethods in Molecular Biology (Clifton, N.J.)|May 7, 2011
Introduction to section III: resources for CFTR researchMargarida D AmaralCurrent Drug Targets|November 3, 2010
Targeting CFTR: how to treat cystic fibrosis by CFTR-repairing therapiesMargarida D AmaralJournal of Molecular Neuroscience : MN|May 6, 2004
CFTR and chaperones: processing and degradationMargarida D AmaralPageof 17