Depletion of Ca2+ in the sarcoplasmic reticulum stimulates Ca2+ entry into mouse skeletal muscle fibres
N Kurebayashi, Y Ogawa - The Journal of physiology, 2001 - Wiley Online Library
To examine whether a capacitative Ca 2+ entry pathway is present in skeletal muscle, thin
muscle fibre bundles were isolated from extensor digitorum longus (EDL) muscle of adult mice…
muscle fibre bundles were isolated from extensor digitorum longus (EDL) muscle of adult mice…
[HTML][HTML] Regulatory mechanisms of ryanodine receptor/Ca2+ release channel revealed by recent advancements in structural studies
H Ogawa, N Kurebayashi, T Yamazawa… - Journal of Muscle …, 2021 - Springer
Ryanodine receptors (RyRs) are huge homotetrameric Ca 2+ release channels localized to
the sarcoplasmic reticulum. RyRs are responsible for the release of Ca 2+ from the SR …
the sarcoplasmic reticulum. RyRs are responsible for the release of Ca 2+ from the SR …
Ryanodine receptor isoforms in excitation-contraction coupling
Y Ogawa, N Kurebayashi, T Murayama - Advances in biophysics, 1999 - Elsevier
Three genomically distinct isoforms of RyR are now known. RyR1 homologue is the primary
isoform in skeletal muscles, whereas in cardiac muscles it is RyR2 homologue. RyR3 …
isoform in skeletal muscles, whereas in cardiac muscles it is RyR2 homologue. RyR3 …
Two ryanodine receptor isoforms in nonmammalian vertebrate skeletal muscle: Possible roles in excitation–contraction coupling and other processes
T Murayama, N Kurebayashi - Progress in Biophysics and Molecular …, 2011 - Elsevier
The ryanodine receptor (RyR) is a Ca 2+ release channel in the sarcoplasmic reticulum in
vertebrate skeletal muscle and plays an important role in excitation–contraction (E–C) …
vertebrate skeletal muscle and plays an important role in excitation–contraction (E–C) …
Nitric oxide‐induced calcium release via ryanodine receptors regulates neuronal function
Mobilization of intracellular Ca 2+ stores regulates a multitude of cellular functions, but the
role of intracellular Ca 2+ release via the ryanodine receptor (RyR) in the brain remains …
role of intracellular Ca 2+ release via the ryanodine receptor (RyR) in the brain remains …
Long‐term, but not short‐term high‐fat diet induces fiber composition changes and impaired contractile force in mouse fast‐twitch skeletal muscle
…, Y Tamura, S Kakehi, N Kurebayashi… - Physiological …, 2017 - Wiley Online Library
In this study, we investigated the effects of a short‐term and long‐term high‐fat diet ( HFD ) on
morphological and functional features of fast‐twitch skeletal muscle. Male C57 BL /6J mice …
morphological and functional features of fast‐twitch skeletal muscle. Male C57 BL /6J mice …
Use of fura red as an intracellular calcium indicator in frog skeletal muscle fibers
N Kurebayashi, AB Harkins, SM Baylor - Biophysical journal, 1993 - cell.com
Fura red, a fluorescent Ca2+ indicator with absorbance bands at visible wavelengths, was
injected into intact single muscle fibers that had been stretched to a long sarcomere length (…
injected into intact single muscle fibers that had been stretched to a long sarcomere length (…
[HTML][HTML] A type 2 ryanodine receptor variant associated with reduced Ca2+ release and short-coupled torsades de pointes ventricular arrhythmia
Y Fujii, H Itoh, S Ohno, T Murayama, N Kurebayashi… - Heart Rhythm, 2017 - Elsevier
Background Ventricular fibrillation may be caused by premature ventricular contractions (PVCs)
whose coupling intervals are <300 ms, a characteristic of the short-coupled variant of …
whose coupling intervals are <300 ms, a characteristic of the short-coupled variant of …
Structural mechanism of two gain-of-function cardiac and skeletal RyR mutations at an equivalent site by cryo-EM
Mutations in ryanodine receptors (RyRs), intracellular Ca 2+ channels, are associated with
deadly disorders. Despite abundant functional studies, the molecular mechanism of RyR …
deadly disorders. Despite abundant functional studies, the molecular mechanism of RyR …
[HTML][HTML] Assembly of the cochlear gap junction macromolecular complex requires connexin 26
K Kamiya, SW Yum, N Kurebayashi… - The Journal of …, 2014 - Am Soc Clin Investig
Hereditary deafness affects approximately 1 in 2,000 children. Mutations in the gene encoding
the cochlear gap junction protein connexin 26 (CX26) cause prelingual, nonsyndromic …
the cochlear gap junction protein connexin 26 (CX26) cause prelingual, nonsyndromic …