Mice with R2509C-RYR1 mutation exhibit dysfunctional Ca2+ dynamics in primary skeletal myocytes
Author(s) -
Yoshitaka Tsuboi,
Kotaro Oyama,
Fuyu Kobirumaki-Shimozawa,
Takashi Murayama,
Nagomi Kurebayashi,
Toshiaki Tachibana,
Yoshinobu Manome,
Emi Kikuchi,
S. Noguchi,
Takayoshi Inoue,
Yukiko Inoue,
Ichizo Nishino,
Shuichi Mori,
Ryosuke Ishida,
Hiroyuki Kagechika,
Madoka Suzuki,
Norio Fukuda,
Toshiko Yamazawa
Publication year - 2022
Publication title -
the journal of general physiology
Language(s) - English
Resource type - Journals
eISSN - 1540-7748
pISSN - 0022-1295
DOI - 10.1085/jgp.202213136
Subject(s) - ryr1 , myocyte , ryanodine receptor , skeletal muscle , malignant hyperthermia , sarcomere , endoplasmic reticulum , endocrinology , medicine , biology , intracellular , chemistry , microbiology and biotechnology , pathology
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