Orphan Missense Mutations in the Cystic Fibrosis Transmembrane Conductance Regulator-Reference-Cited by-同舟云学术

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Orphan Missense Mutations in the Cystic Fibrosis Transmembrane Conductance Regulator

Published:2011-09 Issue:5 Volume:13 Page:520-527
ISSN:1525-1578
Container-title:The Journal of Molecular Diagnostics
language:en
Short-container-title:The Journal of Molecular Diagnostics

Author:

Fresquet Fleur,Clement Romain,Norez Caroline,Sterlin Adélaïde,Melin Patricia,Becq Frédéric,Kitzis Alain,Thoreau Vincent,Bilan Frédéric

Publisher

Elsevier BV

Subject

Molecular Medicine,Pathology and Forensic Medicine

Reference24 articles.

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

2. Identification of the cystic fibrosis gene: chromosome walking and jumping;Rommens;Science,1989

3. CFTR function and prospects for therapy;Riordan;Annu Rev Biochem,2008

4. Genetics of cystic fibrosis;Lommatzsch;Semin Respir Crit Care Med,2009

5. Structure of ABC transporters;Linton,2003

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

2. How to determine the mechanism of action of CFTR modulator compounds: A gateway to theranostics;European Journal of Medicinal Chemistry;2021-01

3. Modulating the cystic fibrosis transmembrane regulator and the development of new precision drugs;Expert Review of Precision Medicine and Drug Development;2018-11-02

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