Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene
about
Molecular cloning and characterization of a human brain ryanodine receptorIn situ modulation of the human cardiac ryanodine receptor (hRyR2) by FKBP12.6Requirement for the ryanodine receptor type 3 for efficient contraction in neonatal skeletal muscles.Multiple regions of RyR1 mediate functional and structural interactions with alpha(1S)-dihydropyridine receptors in skeletal muscleAbsence of the beta subunit (cchb1) of the skeletal muscle dihydropyridine receptor alters expression of the alpha 1 subunit and eliminates excitation-contraction couplingFunctional analysis of a frame-shift mutant of the dihydropyridine receptor pore subunit (alpha1S) expressing two complementary protein fragmentsSingle-Particle Cryo-EM of the Ryanodine Receptor Channel in an Aqueous EnvironmentFrog alpha- and beta-ryanodine receptors provide distinct intracellular Ca2+ signals in a myogenic cell linePharmGKB summary: very important pharmacogene information for RYR1Calcium waves induced by hypertonic solutions in intact frog skeletal muscle fibresProperties of Ca(2+) release induced by clofibric acid from the sarcoplasmic reticulum of mouse skeletal muscle fibresEffects of dantrolene and its derivatives on Ca(2+) release from the sarcoplasmic reticulum of mouse skeletal muscle fibresThe properties of ryanodine-sensitive Ca(2+) release in mouse gastric smooth muscle cellsMinding the calcium store: Ryanodine receptor activation as a convergent mechanism of PCB toxicityStac3 is a novel regulator of skeletal muscle development in miceDisturbance of cerebellar synaptic maturation in mutant mice lacking BSRPs, a novel brain-specific receptor-like protein familyMG53 nucleates assembly of cell membrane repair machinery.Embryonic lethality and abnormal cardiac myocytes in mice lacking ryanodine receptor type 2.Ca(2+)-induced Ca2+ release in myocytes from dyspedic mice lacking the type-1 ryanodine receptorType 3 and type 1 ryanodine receptors are localized in triads of the same mammalian skeletal muscle fibersAn Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse lineSkeletal muscle-specific T-tubule protein STAC3 mediates voltage-induced Ca2+ release and contractilityFunctional uncoupling between Ca2+ release and afterhyperpolarization in mutant hippocampal neurons lacking junctophilinsCardiac defects and altered ryanodine receptor function in mice lacking FKBP12Isolation and partial cloning of ryanodine-sensitive Ca2+ release channel protein isoforms from human myometrial smooth muscle.STAC3 stably interacts through its C1 domain with CaV1.1 in skeletal muscle triadsStac3 has a direct role in skeletal muscle-type excitation-contraction coupling that is disrupted by a myopathy-causing mutation.Mitsugumin29, a novel synaptophysin family member from the triad junction in skeletal muscle.Comprehensive behavioral phenotyping of ryanodine receptor type 3 (RyR3) knockout mice: decreased social contact duration in two social interaction tests.Unrestrained nociceptive response and disregulation of hearing ability in mice lacking the nociceptin/orphaninFQ receptor.Structural and functional properties of ryanodine receptor type 3 in zebrafish tail muscle.Type 3 ryanodine receptors of skeletal muscle are segregated in a parajunctional position.Contribution of ryanodine receptor subtype 3 to ca2+ responses in Ca2+-overloaded cultured rat portal vein myocytes.Mechanical tension and spontaneous muscle twitching precede the formation of cross-striated muscle in vivo.Genetics and pathogenesis of malignant hyperthermia.The Cavβ1a subunit regulates gene expression and suppresses myogenin in muscle progenitor cells.Functional expression of transgenic 1sDHPR channels in adult mammalian skeletal muscle fibres.Dantrolene mitigates caerulein-induced pancreatitis in vivo in mice.Ryanodine receptors, a family of intracellular calcium ion channels, are expressed throughout early vertebrate development.Contribution of ryanodine receptor type 3 to Ca(2+) sparks in embryonic mouse skeletal muscle
P2860
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P2860
Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene
description
1994 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի հունիսին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Nature
@fr
artículu científicu espublizáu en 1994
@ast
scientific journal article
@en
vedecký článok (publikovaný 1994/06/16)
@sk
vědecký článek publikovaný v roce 1994
@cs
wetenschappelijk artikel (gepubliceerd op 1994/06/16)
@nl
наукова стаття, опублікована в червні 1994
@uk
مقالة علمية (نشرت في 16-6-1994)
@ar
name
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@ast
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@en
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@nl
type
label
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@ast
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@en
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@nl
prefLabel
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@ast
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@en
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@nl
P2093
P3181
P356
P1433
P1476
Excitation-contraction uncoupl ...... muscle ryanodine-receptor gene
@en
P2093
Takekura H
P2888
P304
P3181
P356
10.1038/369556A0
P407
P577
1994-06-01T00:00:00Z
P6179
1011082718