Drastic reduction of calsequestrin-like proteins and impaired calcium binding in dystrophic mdx muscle.
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Calsequestrin content and SERCA determine normal and maximal Ca2+ storage levels in sarcoplasmic reticulum of fast- and slow-twitch fibres of ratProteomic profiling of antisense-induced exon skipping reveals reversal of pathobiochemical abnormalities in dystrophic mdx diaphragm.Application of fluorescence two-dimensional difference in-gel electrophoresis as a proteomic biomarker discovery tool in muscular dystrophy researchSkeletal muscle homeostasis in duchenne muscular dystrophy: modulating autophagy as a promising therapeutic strategy.Comparison of Atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (CMS)Low-Level Laser Therapy (LLLT) in Dystrophin-Deficient Muscle Cells: Effects on Regeneration Capacity, Inflammation Response and Oxidative StressIncreased resting intracellular calcium modulates NF-κB-dependent inducible nitric-oxide synthase gene expression in dystrophic mdx skeletal myotubesProfiling of age-related changes in the tibialis anterior muscle proteome of the mdx mouse model of dystrophinopathyAltered calcium pump and secondary deficiency of gamma-sarcoglycan and microspan in sarcoplasmic reticulum membranes isolated from delta-sarcoglycan knockout mice.Animal models of muscular dystrophyDystrophic skeletal muscle fibers display alterations at the level of calcium microdomains.Control of muscle ryanodine receptor calcium release channels by proteins in the sarcoplasmic reticulum lumen.Proteomic profiling of x-linked muscular dystrophy.Proteomic profiling of animal models mimicking skeletal muscle disorders.Cardiac and respiratory dysfunction in Duchenne muscular dystrophy and the role of second messengers.The physiological response of protease inhibition in dystrophic muscle.Chaperoning heat shock proteins: proteomic analysis and relevance for normal and dystrophin-deficient muscle.Dysregulation of calcium homeostasis in muscular dystrophies.Overexpression of SERCA1a in the mdx diaphragm reduces susceptibility to contraction-induced damage.Second-generation compound for the modulation of utrophin in the therapy of DMD.Drastic reduction of sarcalumenin in Dp427 (dystrophin of 427 kDa)-deficient fibres indicates that abnormal calcium handling plays a key role in muscular dystrophy.Autophagy as a new therapeutic target in Duchenne muscular dystrophyUpregulation of the creatine synthetic pathway in skeletal muscles of mature mdx mice.Supramolecular calsequestrin complex.Depolarization-induced contraction and SR function in mechanically skinned muscle fibers from dystrophic mdx mice.The action potential-evoked sarcoplasmic reticulum calcium release is impaired in mdx mouse muscle fibres.Subproteomics analysis of Ca+-binding proteins demonstrates decreased calsequestrin expression in dystrophic mouse skeletal muscle.Diltiazem and verapamil protect dystrophin-deficient muscle fibers of MDX mice from degeneration: a potential role in calcium buffering and sarcolemmal stability.Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres of mdx and normal mice.Effect of cyclopiazonic acid, an inhibitor of the sarcoplasmic reticulum Ca-ATPase, on skeletal muscles from normal and mdx mice.Propagation in the transverse tubular system and voltage dependence of calcium release in normal and mdx mouse muscle fibres.Opposite pathobiochemical fate of pyruvate kinase and adenylate kinase in aged rat skeletal muscle as revealed by proteomic DIGE analysis.Muscle-specific overexpression of IGF-I improves E-C coupling in skeletal muscle fibers from dystrophic mdx mice.Benefits of Prenatal Taurine Supplementation in Preventing the Onset of Acute Damage in the Mdx Mouse.Changes in contractile and metabolic parameters of skeletal muscle as rats age from 3 to 12 months.Proteomic profiling of the dystrophin complex and membrane fraction from dystrophic mdx muscle reveals decreases in the cytolinker desmoglein and increases in the extracellular matrix stabilizers biglycan and fibronectin.The effect of taurine and β-alanine supplementation on taurine transporter protein and fatigue resistance in skeletal muscle from mdx mice.Sarcoplasmic-endoplasmic-reticulum Ca2+-ATPase and calsequestrin are overexpressed in spared intrinsic laryngeal muscles of dystrophin-deficient mdx mice.Comparative Label-Free Mass Spectrometric Analysis of Mildly versus Severely Affected mdx Mouse Skeletal Muscles Identifies Annexin, Lamin, and Vimentin as Universal Dystrophic Markers.
P2860
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P2860
Drastic reduction of calsequestrin-like proteins and impaired calcium binding in dystrophic mdx muscle.
description
2002 nî lūn-bûn
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2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
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2002年學術文章
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2002年學術文章
@zh-hant
name
Drastic reduction of calseques ...... ding in dystrophic mdx muscle.
@en
Drastic reduction of calseques ...... ding in dystrophic mdx muscle.
@nl
type
label
Drastic reduction of calseques ...... ding in dystrophic mdx muscle.
@en
Drastic reduction of calseques ...... ding in dystrophic mdx muscle.
@nl
prefLabel
Drastic reduction of calseques ...... ding in dystrophic mdx muscle.
@en
Drastic reduction of calseques ...... ding in dystrophic mdx muscle.
@nl
P2093
P1476
Drastic reduction of calseques ...... ding in dystrophic mdx muscle.
@en
P2093
Kay Ohlendieck
Kevin Culligan
Niamh Banville
P304
P356
10.1152/JAPPLPHYSIOL.00903.2001
P407
P50
P577
2002-02-01T00:00:00Z