Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health. - Wikidata - awgldk - TriplyDB

Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health.

Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health.

http://www.wikidata.org/entity/Q34472544

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Mitochondrial DNA variation in human radiation and disease Resources, challenges and way forward in rare mitochondrial diseases research Mitochondrial Dysfunction Contributes to Hypertensive Target Organ Damage: Lessons from an Animal Model of Human Disease Ndufc2 Gene Inhibition Is Associated With Mitochondrial Dysfunction and Increased Stroke Susceptibility in an Animal Model of Complex Human Disease Mito-nuclear co-evolution: the positive and negative sides of functional ancient mutations The influence of gender on inheritance of exceptional longevity.Structure of subcomplex Iβ of mammalian respiratory complex I leads to new supernumerary subunit assignments The evolution of sex: A new hypothesis based on mitochondrial mutational erosion: Mitochondrial mutational erosion in ancestral eukaryotes would favor the evolution of sex, harnessing nuclear recombination to optimize compensatory nuclear coadaptati Compatibility between mitochondrial and nuclear genomes correlates with the quantitative trait of lifespan in Caenorhabditis elegans.Testing for the Occurrence of Selective Episodes During the Divergence of Otophysan Fishes: Insights from Mitogenomics.Mitochondrial Involvement in Vertebrate Speciation? The Case of Mito-nuclear Genetic Divergence in Chameleons.Mitochondrial-Nuclear Epistasis Impacts Fitness and Mitochondrial Physiology of Interpopulation Caenorhabditis briggsae Hybrids Integrative Approaches for Studying Mitochondrial and Nuclear Genome Co-evolution in Oxidative Phosphorylation.The on-again, off-again relationship between mitochondrial genomes and species boundaries.Genome-wide methylation profile following prenatal and postnatal dietary omega-3 fatty acid supplementation in pigs.Initiation of mtDNA transcription is followed by pausing, and diverges across human cell types and during evolution.MtDNA meta-analysis reveals both phenotype specificity and allele heterogeneity: a model for differential association.Risks inherent to mitochondrial replacement Breast cancer-associated mitochondrial DNA haplogroup promotes neoplastic growth via ROS-mediated AKT activation.In vitro characterization of mitochondrial function and structure in rat and human cells with a deficiency of the NADH: ubiquinone oxidoreductase Ndufc2 subunit.Divergent Patterns of Mitochondrial and Nuclear Ancestry Are Associated with the Risk for Preterm Birth.Mitonuclear linkage disequilibrium in human populations.

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P2860

Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health.

http://www.wikidata.org/entity/Q34472544

description

2014 nî lūn-bûn

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2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Genome Biology and Evolution

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Anat Tsur

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Aviv Bergman

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Gil Atzmon

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Julio Wainstein

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Leo Nijtmans

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Liron Levin

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Naama Shani

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Nir Barzilai

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Ofer Ovadia

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Sara Dadon

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P2860

Mitochondrial DNA backgrounds might modulate diabetes complications rather than T2DM as a whole

NDUFA4 is a subunit of complex IV of the mammalian electron transport chain

Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder

Statistical significance for genomewide studies

Structure of the membrane domain of respiratory complex I

Mitochondrial disorders

Subtle alterations in PCNA-partner interactions severely impair DNA replication and repair

Supercomplex assembly determines electron flux in the mitochondrial electron transport chain

Genetic and epigenetic factors are associated with expression of respiratory chain component NDUFB6 in human skeletal muscle

Parental diabetes status reveals association of mitochondrial DNA haplogroup J1 with type 2 diabetes.

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2665-2680

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10.1093/GBE/EVU208

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10

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6

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Benjamin Glaser

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2014-09-22T00:00:00Z

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266026835

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25245408

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