Phosphorylation and protonation of neighboring MiRP2 sites: function and pathophysiology of MiRP2‐Kv3.4 potassium channels in periodic paralysis-Reference-Cited by-同舟云学术

Phosphorylation and protonation of neighboring MiRP2 sites: function and pathophysiology of MiRP2‐Kv3.4 potassium channels in periodic paralysis

Published:2006-02 Issue:2 Volume:20 Page:293-301
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Abbott Geoffrey W.¹,Butler Margaret H.²,Goldstein Steve A. N.²

Affiliation:

1. Greenberg Division of Cardiology, Department of Medicine and Department of PharmacologyCornell University, Weill Medical College New York New York USA

2. Department of Pediatrics and The Institute of Molecular Pediatric SciencesUniversity of Chicago, Pritzker School of Medicine Chicago Illinois USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.05-5070com

Reference52 articles.

1. A superfamily of small potassium channel subunits: form and function of the MinK-related peptides (MiRPs)

2. The MinK-related peptides

3. KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium current

4. Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel

5. MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac Arrhythmia

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