Targeted deletion of Kcne3 impairs skeletal muscle function in mice-Reference-Cited by-同舟云学术

Targeted deletion of Kcne3 impairs skeletal muscle function in mice

Published:2017-03-29 Issue:7 Volume:31 Page:2937-2947
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

King Elizabeth C.¹,Patel Vishal²,Anand Marie³⁴,Zhao Xiaoli²⁵,Crump Shawn M.³⁴,Hu Zhaoyang³⁴,Weisleder Noah²⁶,Abbott Geoffrey W.³⁴

Affiliation:

1. Department of PharmacologyWeill Medical College of Cornell UniversityNew York New York USA

2. Department of Physiology and BiophysicsUniversity of Medicine and Dentistry of New Jersey–Robert Wood Johnson Medical SchoolPiscataway New Jersey USA

3. Department of PharmacologySchool of MedicineUniversity of CaliforniaIrvine California USA

4. Department of Physiology and BiophysicsSchool of MedicineUniversity of CaliforniaIrvine California USA

5. Department of Physiological SciencesEastern Virginia Medical SchoolNorfolk VA USA

6. Department of Physiology and Cell BiologyDavis Heart and Lung Research InstituteOhio State UniversityColumbus OH USA

Funder

National Institutes of Health

National Heart, Lung, and Blood Institute

University of California

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.201600965RR

Reference43 articles.

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

2. A constitutively open potassium channel formed by KCNQ1 and KCNE3

3. MiRP2 Forms Potassium Channels in Skeletal Muscle with Kv3.4 and Is Associated with Periodic Paralysis

4. Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis

5. Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation

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