Neuronal degeneration and mitochondrial dysfunction. - Wikidata - awgldk - TriplyDB

Neuronal degeneration and mitochondrial dysfunction.

Neuronal degeneration and mitochondrial dysfunction.

http://www.wikidata.org/entity/Q35060350

about

A mitochondrial protein compendium elucidates complex I disease biology Truncated product of the bifunctional DLST gene involved in biogenesis of the respiratory chain Cardiomyopathy in Friedreich ataxia: clinical findings and research Mitochondrial genome changes and neurodegenerative diseases Pathogenesis of ataxia-telangiectasia: the next generation of ATM functions Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction The G336S variant in the human neurofilament-M gene does not affect its assembly or distribution: importance of the functional analysis of neurofilament variants Transgenic control of mitochondrial fission induces mitochondrial uncoupling and relieves diabetic oxidative stress.A Drosophila model of mitochondrial disease caused by a complex I mutation that uncouples proton pumping from electron transfer.Validation of microarray data in human lymphoblasts shows a role of the ubiquitin-proteasome system and NF-kB in the pathogenesis of Down syndrome.Neuroprotection by a mitochondria-targeted drug in a Parkinson's disease model Silybum marianum oil attenuates oxidative stress and ameliorates mitochondrial dysfunction in mice treated with D-galactose.Mitochondrial dysfunction in the striatum of aged chronic mouse model of Parkinson's disease.Mitochondrial dysfunction links ceramide activated HRK expression and cell death.The metabolic enhancer piracetam ameliorates the impairment of mitochondrial function and neurite outgrowth induced by beta-amyloid peptide The neurodegenerative mitochondriopathies.Oxidative stress, mitochondrial damage and neurodegenerative diseases Complex I deficiency primes Bax-dependent neuronal apoptosis through mitochondrial oxidative damage Impaired mitochondrial respiration and protein nitration in the rat hippocampus after acute inhalation of combustion smoke.Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31.Neuronal inactivation of peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) protects mice from diet-induced obesity and leads to degenerative lesions In vivo quantification reveals extensive natural variation in mitochondrial form and function in Caenorhabditis briggsae.Modeling mitochondrial function and its role in disease.Disruption of adaptive energy metabolism and elevated ribosomal p-S6K1 levels contribute to INCL pathogenesis: partial rescue by resveratrol Are maternal mitochondria the selfish entities that are masters of the cells of eukaryotic multicellular organisms?Effects of astaxanthin-rich Haematococcus pluvialis extract on cognitive function: a randomised, double-blind, placebo-controlled study.Parkin ubiquitinates Drp1 for proteasome-dependent degradation: implication of dysregulated mitochondrial dynamics in Parkinson disease Medication-induced mitochondrial damage and disease.Neurodegeneration: what is it and where are we?Genetic and cellular studies of oxidative stress in methylmalonic aciduria (MMA) cobalamin deficiency type C (cblC) with homocystinuria (MMACHC).Genetics and mitochondrial abnormalities in autism spectrum disorders: a review.The striatum is highly susceptible to mitochondrial oxidative phosphorylation dysfunctions IRS2 increases mitochondrial dysfunction and oxidative stress in a mouse model of Huntington disease Roles of oxidative stress, apoptosis, PGC-1α and mitochondrial biogenesis in cerebral ischemia.Mitochondrial encephalomyopathies: therapeutic approach.Sustained expression of PGC-1α in the rat nigrostriatal system selectively impairs dopaminergic function.Time-Dependent Progression of Demyelination and Axonal Pathology in MP4-Induced Experimental Autoimmune Encephalomyelitis.Proteomic Profiling in the Brain of CLN1 Disease Model Reveals Affected Functional Modules.Assessment and treatment in autism spectrum disorders: a focus on genetics and psychiatry Mitochondrial DNA and disease.

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Neuronal degeneration and mitochondrial dysfunction.

http://www.wikidata.org/entity/Q35060350

description

2003 nî lūn-bûn

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2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2003 թվականի փետրվարին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Neuronal degeneration and mitochondrial dysfunction.

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Neuronal degeneration and mitochondrial dysfunction.

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Neuronal degeneration and mitochondrial dysfunction.

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Neuronal degeneration and mitochondrial dysfunction.

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Neuronal degeneration and mitochondrial dysfunction.

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Journal of Clinical Investigation

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Neuronal degeneration and mitochondrial dysfunction.

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Eric A Schon

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Giovanni Manfredi

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P2860

Recruitment and activation of caspase-8 by the Huntingtin-interacting protein Hip-1 and a novel partner Hippi

Mutant and wild-type alpha-synuclein interact with mitochondrial cytochrome C oxidase

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

ARC, an inhibitor of apoptosis expressed in skeletal muscle and heart that interacts selectively with caspases

A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness

Apaf-1, a human protein homologous to C. elegans CED-4, participates in cytochrome c-dependent activation of caspase-3

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

Sequence and organization of the human mitochondrial genome

Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex

Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase

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