Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
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Solution structure and siRNA-mediated knockdown analysis of the mitochondrial disease-related protein C12orf65Skeletal muscle differentiation evokes endogenous XIAP to restrict the apoptotic pathway.Morphofunctional and Biochemical Approaches for Studying Mitochondrial Changes during Myoblasts Differentiation.OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules.Immune response and mitochondrial metabolism are commonly deregulated in DMD and aging skeletal muscle.Mitochondrial dysfunction in Parkinson's disease: pathogenesis and neuroprotection.Normal levels of wild-type mitochondrial DNA maintain cytochrome c oxidase activity for two pathogenic mitochondrial DNA mutations but not for m.3243A-->G.Integrated analysis of the involvement of nitric oxide synthesis in mitochondrial proliferation, mitochondrial deficiency and apoptosis in skeletal muscle fibresMitochondrial DNA content, an inaccurate biomarker of mitochondrial alteration in human immunodeficiency virus-related lipodystrophy.Mitochondrial morphology transitions and functions: implications for retrograde signaling?NDUFS4: creation of a mouse model mimicking a Complex I disorder.Mitochondrial co-chaperone protein Tid1 is required for energy homeostasis during skeletal myogenesis.Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies.Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes.Crosstalk between mitochondrial (dys)function and mitochondrial abundance.Hypersensitivity of mtDNA-depleted cells to staurosporine-induced apoptosis: roles of Bcl-2 downregulation and cathepsin B.OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy.MFN2 mutations cause compensatory mitochondrial DNA proliferation.High cytochrome c oxidase expression links to severe skeletal energy failure by (31)P-MRS spectroscopy in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.Anatomic & metabolic brain markers of the m.3243A>G mutation: A multi-parametric 7T MRI study.Analysis of Mitochondrial Network Morphology in Cultured Myoblasts from Patients with Mitochondrial Disorders
P2860
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P2860
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
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2006年學術文章
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name
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
@en
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
@nl
type
label
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
@en
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
@nl
prefLabel
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
@en
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
@nl
P2093
P2860
P356
P1433
P1476
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
@en
P2093
Anne Lombès
Emmanuelle Lacène
Guillemette Fayet
Jean Paul Leroy
Karine Auré
Norma Beatriz Romero
P2860
P304
P356
10.1093/BRAIN/AWL061
P407
P577
2006-03-14T00:00:00Z