Genetics of Cystic Fibrosis
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,General Medicine
Reference54 articles.
1. Progress in therapies for cystic fibrosis;De Boeck;Lancet Respir Med,2016
2. Capitalizing on the heterogeneous effects of CFTR nonsense and frameshift variants to inform therapeutic strategy for cystic fibrosis;Sharma;PLoS Genet,2018
3. Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations - evaluated in a cohort of 639 non-vasectomized azoospermic men;Fedder;Andrology,2021
4. Functional assays are essential for interpretation of missense variants associated with variable expressivity;Raraigh;Am J Hum Genet,2018
5. Residual function of cystic fibrosis mutants predicts response to small molecule CFTR modulators;Han;JCI Insight,2018
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1. Improving health literacy of antibiotic use in people with cystic fibrosis (CF)—comparison of the readability of patient information leaflets (PILs) from the EU, USA and UK of 23 CF-related antibiotics used in the treatment of CF respiratory infections;JAC-Antimicrobial Resistance;2023-11-01
2. Lung Inflammatory Genes in Cystic Fibrosis and Their Relevance to Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapies;Genes;2023-10-20
3. L1077P CFTR pathogenic variant function rescue by Elexacaftor–Tezacaftor–Ivacaftor in cystic fibrosis patient-derived air–liquid interface (ALI) cultures and organoids: in vitro guided personalized therapy of non-F508del patients;Respiratory Research;2023-09-06
4. Proliferative activity of antigen-specific CD154+ T cells against bacterial and fungal respiratory pathogens in cystic fibrosis decreases after initiation of highly effective CFTR modulator therapy;Frontiers in Pharmacology;2023-06-20
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