about
YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferationDNA damage signaling and p53-dependent senescence after prolonged beta-interferon stimulationMitochondrial disorders of DNA polymerase γ dysfunction: from anatomic to molecular pathology diagnosisMetabolic control analysis in a cellular model of elevated MAO-B: relevance to Parkinson's diseaseThe Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure.Mitochondrial dysfunction in psychiatric morbidity: current evidence and therapeutic prospectsMitochondrial geneticsMitochondrial genome changes and neurodegenerative diseasesSelection against heteroplasmy explains the evolution of uniparental inheritance of mitochondriaRelationship between mitochondrial electron transport chain dysfunction, development, and life extension in Caenorhabditis elegansMaternal smoking is associated with mitochondrial DNA depletion and respiratory chain complex III deficiency in placentaCurrent versus future reproduction and longevity: a re-evaluation of predictions and mechanismsNoninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometryRedox biology and the interface between bioenergetics, autophagy and circadian control of metabolismThe Role of Exercise in Cardiac Aging: From Physiology to Molecular MechanismsModeling of mitochondria bioenergetics using a composable chemiosmotic energy transduction rate law: theory and experimental validationGenetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum DisorderThe Trojan female technique: a novel, effective and humane approach for pest population controlComplex I-associated hydrogen peroxide production is decreased and electron transport chain enzyme activities are altered in n-3 enriched fat-1 miceA Systems Approach to Elucidate Heterosis of Protein Abundances in YeastDiverse cytopathologies in mitochondrial disease are caused by AMP-activated protein kinase signaling.Adapted Boolean network models for extracellular matrix formation.Extraction and annotation of human mitochondrial genomes from 1000 Genomes Whole Exome Sequencing dataMitochondrial respiratory dysfunction disturbs neuronal and cardiac lineage commitment of human iPSCs.Stochastic drift in mitochondrial DNA point mutations: a novel perspective ex silicoHmtDB 2016: data update, a better performing query system and human mitochondrial DNA haplogroup predictorAccumulation of mitochondrial DNA deletion mutations in aged muscle fibers: evidence for a causal role in muscle fiber lossEstablishment of a new method for precisely determining the functions of individual mitochondrial genes, using Dictyostelium cells.Silencing of PINK1 expression affects mitochondrial DNA and oxidative phosphorylation in dopaminergic cells.Mitochondrial DNA depletion and respiratory chain activity in primary human subcutaneous adipocytes treated with nucleoside analogue reverse transcriptase inhibitorsMitochondrial complex III defects contribute to inefficient respiration and ATP synthesis in the myocardium of Trypanosoma cruzi-infected miceAge-related changes in mitochondrial respiration and oxidative damage in the cerebral cortex of the Fischer 344 rat.Natural variation in life history and aging phenotypes is associated with mitochondrial DNA deletion frequency in Caenorhabditis briggsaeMitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations.Mitochondrial protease AtFtsH4 protects ageing Arabidopsis rosettes against oxidative damage under short-day photoperiodThe strength and timing of the mitochondrial bottleneck in salmon suggests a conserved mechanism in vertebrates.Oxazolidinones inhibit cellular proliferation via inhibition of mitochondrial protein synthesisA yeast-based assay identifies drugs active against human mitochondrial disordersMechanisms of pathogenesis in drug hepatotoxicity putting the stress on mitochondria.Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
name
Mitochondrial threshold effects.
@ast
Mitochondrial threshold effects.
@en
type
label
Mitochondrial threshold effects.
@ast
Mitochondrial threshold effects.
@en
prefLabel
Mitochondrial threshold effects.
@ast
Mitochondrial threshold effects.
@en
P2093
P2860
P356
P1433
P1476
Mitochondrial threshold effects
@en
P2093
Benjamin Faustin
Jean-Pierre Mazat
Monique Malgat
Rodrigue Rossignol
Thierry Letellier
P2860
P304
P356
10.1042/BJ20021594
P407
P577
2003-03-01T00:00:00Z