Characterization of the novel mutant A78T-HERG from a long QT syndrome type 2 patient: Instability of the mutant protein and stabilization by heat shock factor 1

BACKGROUND: The human ether-a-go-go-related gene (HERG) encodes the α-subunit of rapidly activating delayed-rectifier potassium channels. Mutations in this gene cause long QT syndrome type 2 (LQT2). In most cases, mutations reduce the stability of the channel protein, which can be restored by heat s...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:J Arrhythm
Main Authors: Kondo, Takehito, Hisatome, Ichiro, Yoshimura, Shouichi, Mahati, Endang, Notsu, Tomomi, Li, Peili, Iitsuka, Kazuhiko, Kato, Masaru, Ogura, Kazuyoshi, Miake, Junichiro, Aiba, Takeshi, Shimizu, Wataru, Kurata, Yasutaka, Sakata, Shinji, Nakasone, Naoe, Ninomiya, Haruaki, Nakai, Akira, Higaki, Katsumi, Kawata, Yasushi, Shirayoshi, Yasuaki, Yoshida, Akio, Yamamoto, Kazuhiro
Formato: Artigo
Idioma:Inglês
Publicado: Elsevier 2016
Assuntos:
Original Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5063263/
https://ncbi.nlm.nih.gov/pubmed/27761169
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.joa.2015.10.005
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares