Therapeutic approaches to CFTR dysfunction: From discovery to drug development-Reference-Cited by-同舟云学术

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Therapeutic approaches to CFTR dysfunction: From discovery to drug development

Published:2018-03 Issue:2 Volume:17 Page:S14-S21
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Li Hongyu,Pesce Emanuela,Sheppard David N.,Singh Ashvani K.,Pedemonte Nicoletta

Funder

Engineering and Physical Sciences Research Council

Italian Cystic Fibrosis Foundation

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference55 articles.

1. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA;Riordan;Science,1989

2. Gating of the CFTR Cl− channel by ATP-driven nucleotide-binding domain dimerisation;Hwang;J. Physiol.,2009

3. Cystic fibrosis genetics: from molecular understanding to clinical application;Cutting;Nat. Rev. Genet.,2015

4. CFTR: folding, misfolding and correcting the ΔF508 conformational defect;Lukacs;Trends Mol. Med.,2012

5. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis;Cheng;Cell,1990

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