RyR1-mediated Ca2+ leak and Ca2+ entry determine resting intracellular Ca2+ in skeletal myotubes.
about
Calcium homeostasis in myogenic differentiation factor 1 (MyoD)-transformed, virally-transduced, skin-derived equine myotubesCongenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3.Myoplasmic resting Ca2+ regulation by ryanodine receptors is under the control of a novel Ca2+-binding region of the receptor.Electrical coupling between the human serotonin transporter and voltage-gated Ca(2+) channels.IL-1α reversibly inhibits skeletal muscle ryanodine receptor. a novel mechanism for critical illness myopathy?Malignant hyperthermia susceptibility arising from altered resting coupling between the skeletal muscle L-type Ca2+ channel and the type 1 ryanodine receptorAblation of skeletal muscle triadin impairs FKBP12/RyR1 channel interactions essential for maintaining resting cytoplasmic Ca2+Impaired Orai1-mediated resting Ca2+ entry reduces the cytosolic [Ca2+] and sarcoplasmic reticulum Ca2+ loading in quiescent junctophilin 1 knock-out myotubesFunctional and biochemical properties of ryanodine receptor type 1 channels from heterozygous R163C malignant hyperthermia-susceptible mice.Orthograde dihydropyridine receptor signal regulates ryanodine receptor passive leakThe couplonopathies: A comparative approach to a class of diseases of skeletal and cardiac muscle.Mice expressing T4826I-RYR1 are viable but exhibit sex- and genotype-dependent susceptibility to malignant hyperthermia and muscle damageRole of Ryanodine and NMDA Receptors in Tetrabromobisphenol A-Induced Calcium Imbalance and Cytotoxicity in Primary Cultures of Rat Cerebellar Granule Cells.Increased resting intracellular calcium modulates NF-κB-dependent inducible nitric-oxide synthase gene expression in dystrophic mdx skeletal myotubesGene profiling of embryonic skeletal muscle lacking type I ryanodine receptor Ca(2+) release channel.Nonspecific sarcolemmal cation channels are critical for the pathogenesis of malignant hyperthermia.Skeletal Muscle Microalterations in Patients Carrying Malignant Hyperthermia-Related Mutations of the e-c Coupling Machinery.Na+ dysregulation coupled with Ca2+ entry through NCX1 promotes muscular dystrophy in mice.Associations of biochemical changes and maternal traits with mutation 1843 (C>T) in the RYR1 gene as a common cause for porcine stress syndrome.RyR1 expression and the cell boundary theoremReply to Ríos: Cell Boundary Theorem and Ca2+ Fluxes in Skeletal Muscle.RyR1 deficiency in congenital myopathies disrupts excitation-contraction coupling.Distinct transcriptomic changes in E14.5 mouse skeletal muscle lacking RYR1 or Cav1.1 converge at E18.5.
P2860
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P2860
RyR1-mediated Ca2+ leak and Ca2+ entry determine resting intracellular Ca2+ in skeletal myotubes.
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
RyR1-mediated Ca2+ leak and Ca ...... lar Ca2+ in skeletal myotubes.
@ast
RyR1-mediated Ca2+ leak and Ca ...... lar Ca2+ in skeletal myotubes.
@en
type
label
RyR1-mediated Ca2+ leak and Ca ...... lar Ca2+ in skeletal myotubes.
@ast
RyR1-mediated Ca2+ leak and Ca ...... lar Ca2+ in skeletal myotubes.
@en
prefLabel
RyR1-mediated Ca2+ leak and Ca ...... lar Ca2+ in skeletal myotubes.
@ast
RyR1-mediated Ca2+ leak and Ca ...... lar Ca2+ in skeletal myotubes.
@en
P2093
P2860
P356
P1476
RyR1-mediated Ca2+ leak and Ca ...... lar Ca2+ in skeletal myotubes.
@en
P2093
Isaac N Pessah
José M Eltit
José R Lopez
Paul D Allen
Tadeusz F Molinski
Tianzhong Yang
P2860
P304
13781-13787
P356
10.1074/JBC.M110.107300
P407
P577
2010-03-05T00:00:00Z