Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers. - Wikidata - awgldk - TriplyDB

Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers.

Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers.

http://www.wikidata.org/entity/Q41882302

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Calcium antagonists for Duchenne muscular dystrophy Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle Diacylglycerol kinase-zeta localization in skeletal muscle is regulated by phosphorylation and interaction with syntrophins Caveolae regulation of mechanosensitive channel function in myotubes Early pathogenesis of Duchenne muscular dystrophy modelled in patient-derived human induced pluripotent stem cells.Interaction between mitsugumin 29 and TRPC3 participates in regulating Ca(2+) transients in skeletal muscle Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression Genetic evidence in the mouse solidifies the calcium hypothesis of myofiber death in muscular dystrophy Rat hypocretin/orexin neurons are maintained in a depolarized state by TRPC channels Increasing the expression of calcium-permeable TRPC3 and TRPC7 channels enhances constitutive secretion Mice lacking Homer 1 exhibit a skeletal myopathy characterized by abnormal transient receptor potential channel activity Tissue-specific expression of TRP channel genes in the mouse and its variation in three different mouse strains L-type Ca2+ channel function is linked to dystrophin expression in mammalian muscle Rapid Ca2+ flux through the transverse tubular membrane, activated by individual action potentials in mammalian skeletal muscle.Role of TRPC1 channel in skeletal muscle function.Skeletal muscle NADPH oxidase is increased and triggers stretch-induced damage in the mdx mouse.Enhanced Ca²⁺ influx from STIM1-Orai1 induces muscle pathology in mouse models of muscular dystrophy.TRPC3 cation channel plays an important role in proliferation and differentiation of skeletal muscle myoblasts.High-frequency fatigue of skeletal muscle: role of extracellular Ca(2+).Compromised store-operated Ca2+ entry in aged skeletal muscle.Impaired Orai1-mediated resting Ca2+ entry reduces the cytosolic [Ca2+] and sarcoplasmic reticulum Ca2+ loading in quiescent junctophilin 1 knock-out myotubes Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscle Orai1 mediates exacerbated Ca(2+) entry in dystrophic skeletal muscle Classical Transient Receptor Potential 1 (TRPC1): Channel or Channel Regulator?Mechanosensitive channels in striated muscle and the cardiovascular system: not quite a stretch anymore.Expression and localization of TRPC proteins in rat ventricular myocytes at various developmental stages.Ca(2+) permeation and/or binding to CaV1.1 fine-tunes skeletal muscle Ca(2+) signaling to sustain muscle function.TRPC1 expression and distribution in rat hearts Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation, and increased expression of extracellular matrix proteins in laminin α2 chain-deficient muscle.Whole body periodic acceleration is an effective therapy to ameliorate muscular dystrophy in mdx mice.TRPC3 channels confer cellular memory of recent neuromuscular activity.The dynamic complexity of the TRPC1 channelosome.Sarcoplasmic reticulum Ca2+ permeation explored from the lumen side in mdx muscle fibers under voltage control 4-IBP, a sigma1 receptor agonist, decreases the migration of human cancer cells, including glioblastoma cells, in vitro and sensitizes them in vitro and in vivo to cytotoxic insults of proapoptotic and proautophagic drugs Hypertrophy in skeletal myotubes induced by junctophilin-2 mutant, Y141H, involves an increase in store-operated Ca2+ entry via Orai1.Mutation of delta-sarcoglycan is associated with Ca(2+) -dependent vascular remodeling in the Syrian hamster.Increased resting intracellular calcium modulates NF-κB-dependent inducible nitric-oxide synthase gene expression in dystrophic mdx skeletal myotubes Pathways of Ca²⁺ entry and cytoskeletal damage following eccentric contractions in mouse skeletal muscle Mechanisms of stretch-induced muscle damage in normal and dystrophic muscle: role of ionic changes.Characterization and Functional Analysis of Extracellular Vesicles and Muscle-Abundant miRNAs (miR-1, miR-133a, and miR-206) in C2C12 Myocytes and mdx Mice

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P2860

Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers.

http://www.wikidata.org/entity/Q41882302

description

2002 nî lūn-bûn

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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2002年论文

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2002年论文

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name

Involvement of TRPC in the abn ...... mouse skeletal muscle fibers.

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type

label

Involvement of TRPC in the abn ...... mouse skeletal muscle fibers.

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prefLabel

Involvement of TRPC in the abn ...... mouse skeletal muscle fibers.

@en

P1433

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P1476

Involvement of TRPC in the abn ...... mouse skeletal muscle fibers.

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P2093

Clarisse Vandebrouck

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Dominique Martin

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Huguette Debaix

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Monique Colson-Van Schoor

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Philippe Gailly

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P2860

Direct activation of human TRPC6 and TRPC3 channels by diacylglycerol

Modulation of Ca(2+) entry by polypeptides of the inositol 1,4, 5-trisphosphate receptor (IP3R) that bind transient receptor potential (TRP): evidence for roles of TRP and IP3R in store depletion-activated Ca(2+) entry

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

trp, a novel mammalian gene family essential for agonist-activated capacitative Ca2+ entry

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

Functional interaction between InsP3 receptors and store-operated Htrp3 channels

Calcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes

Regulation of Ca2+-release-activated Ca2+ current (Icrac) by ryanodine receptors in inositol 1,4,5-trisphosphate-receptor-deficient DT40 cells

Depletion of Ca2+ in the sarcoplasmic reticulum stimulates Ca2+ entry into mouse skeletal muscle fibres

Molecular and functional characterization of a novel mouse transient receptor potential protein homologue TRP7. Ca(2+)-permeable cation channel that is constitutively activated and enhanced by stimulation of G protein-coupled receptor

P304

1089-1096

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10.1083/JCB.200203091

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6

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158

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Huguette Debaix

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2002-09-16T00:00:00Z

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11155810

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12235126

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2173225

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