Mitochondrial alterations and oxidative stress in an acute transient mouse model of muscle degeneration: implications for muscular dystrophy and related muscle pathologies.
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Role of asymmetric cell division in lifespan control in Saccharomyces cerevisiaeMetformin protects skeletal muscle from cardiotoxin induced degenerationUlk1-mediated autophagy plays an essential role in mitochondrial remodeling and functional regeneration of skeletal muscle.Quantitative analysis of proteins of metabolism by reverse phase protein microarrays identifies potential biomarkers of rare neuromuscular diseases.Disruption of nuclear factor (erythroid-derived-2)-like 2 antioxidant signaling: a mechanism for impaired activation of stem cells and delayed regeneration of skeletal muscleCirculating Biomarkers for Duchenne Muscular Dystrophy.The transcriptional repressor Sum1p counteracts Sir2p in regulation of the actin cytoskeleton, mitochondrial quality control and replicative lifespan in Saccharomyces cerevisiae.Chaperoning heat shock proteins: proteomic analysis and relevance for normal and dystrophin-deficient muscle.Curcumin Monoglucoside Shows Improved Bioavailability and Mitigates Rotenone Induced Neurotoxicity in Cell and Drosophila Models of Parkinson's Disease.Muscle biopsies from human muscle diseases with myopathic pathology reveal common alterations in mitochondrial function.Cerebrospinal Fluid from Sporadic Amyotrophic Lateral Sclerosis Patients Induces Mitochondrial and Lysosomal Dysfunction.Dysferlinopathy: mitochondrial abnormalities in human skeletal muscle.Co-expression Network Approach Reveals Functional Similarities among Diseases Affecting Human Skeletal Muscle.Manganese- and 1-methyl-4-phenylpyridinium-induced neurotoxicity display differences in morphological, electrophysiological and genome-wide alterations: implications for idiopathic Parkinson's disease.Characterization of traumatic brain injury in human brains reveals distinct cellular and molecular changes in contusion and pericontusion.Zc3h10 is a novel mitochondrial regulator.A Futile Battle? Protein Quality Control and the Stress of Aging.Changes in Muscle Metabolism are Associated with Phenotypic Variability in Golden Retriever Muscular Dystrophy.Drug Repurposing for Duchenne Muscular Dystrophy: The Monoamine Oxidase B Inhibitor Safinamide Ameliorates the Pathological Phenotype in Mice and in Myogenic Cultures From DMD Patients
P2860
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P2860
Mitochondrial alterations and oxidative stress in an acute transient mouse model of muscle degeneration: implications for muscular dystrophy and related muscle pathologies.
description
2013 nî lūn-bûn
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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name
Mitochondrial alterations and ...... nd related muscle pathologies.
@en
Mitochondrial alterations and ...... nd related muscle pathologies.
@nl
type
label
Mitochondrial alterations and ...... nd related muscle pathologies.
@en
Mitochondrial alterations and ...... nd related muscle pathologies.
@nl
prefLabel
Mitochondrial alterations and ...... nd related muscle pathologies.
@en
Mitochondrial alterations and ...... nd related muscle pathologies.
@nl
P2093
P2860
P356
P1476
Mitochondrial alterations and ...... and related muscle pathologies
@en
P2093
Atchayaram Nalini
Balaraju Sunitha
Hindalahalli Chandregowda Harsha
Muchukunte Mukunda Srinivas Bharath
Narayanappa Gayathri
Rajeswara Babu Mythri
Renjini Ramadasan-Nair
Sudha Mishra
Ullas Kolthur-Seetharam
P2860
P304
P356
10.1074/JBC.M113.493270
P407
P577
2013-11-12T00:00:00Z