Annotation of functional impact of voltage-gated sodium channel mutations-Reference-Cited by-同舟云学术

Annotation of functional impact of voltage-gated sodium channel mutations

Published:2017-02-28 Issue:5 Volume:38 Page:485-493
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Hinard Valérie¹,Britan Aurore¹,Schaeffer Mathieu¹,Zahn-Zabal Monique¹,Thomet Urs²,Rougier Jean-Sébastien²,Bairoch Amos³,Abriel Hugues²,Gaudet Pascale¹³

Affiliation:

1. CALIPHO Group; SIB Swiss Institute of Bioinformatics; Geneva Switzerland

2. Institute of Biochemistry and Molecular Medicine; Bern Switzerland

3. Department of Human Protein Science, Faculty of Medicine; University of Geneva; Geneva Switzerland

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.23191/fullpdf

Reference17 articles.

1. Regulation of the voltage-gated cardiac sodium channel Nav1.5 by interacting proteins;Abriel;Trends in Cardiovascular Medicine,2005

2. The hitchhiker's guide to the voltage-gated sodium channel galaxy;Ahern;The Journal of General Physiology,2016

3. From molecule to malady;Ashcroft;Nature,2006

4. Molecular mechanism for an inherited cardiac arrhythmia;Bennett;Nature,1995

5. A unique role for the S4 segment of domain 4 in the inactivation of sodium channels;Chen;The Journal of General Physiology,1996

Cited by 10 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

1. Congenital insensitivity to pain;Pain;2021-11-15

2. Functional cross-talk between phosphorylation and disease-causing mutations in the cardiac sodium channel Nav1.5;Proceedings of the National Academy of Sciences;2021-08-09

3. Structural basis of cytoplasmic NaV1.5 and NaV1.4 regulation;Journal of General Physiology;2020-12-11

4. Functional crosstalk between phosphorylation and disease-causing mutations in the cardiac sodium channel Nav1.5;2020-12-11

5. Predicting novel disease mutations in the cardiac sodium channel;Biochemical and Biophysical Research Communications;2020-01