Mitochondrial DNA mutations in human disease - Wikidata - awgldk - TriplyDB

Mitochondrial DNA mutations in human disease

Mitochondrial DNA mutations in human disease

http://www.wikidata.org/entity/Q24676881

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Keeping mtDNA in shape between generations Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies Mitochondrial DNA haplogroup analysis reveals no association between the common genetic lineages and prostate cancer in the Korean population Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits Increased life span due to calorie restriction in respiratory-deficient yeast Mitochondrial modulators for bipolar disorder: A pathophysiologically informed paradigm for new drug development Overexpression of DNA ligase III in mitochondria protects cells against oxidative stress and improves mitochondrial DNA base excision repair Structural analysis and DNA binding of the HMG domains of the human mitochondrial transcription factor A Alterations of the mitochondrial proteome caused by the absence of mitochondrial DNA: A proteomic view Pentatricopeptide repeat domain protein 1 lowers the levels of mitochondrial leucine tRNAs in cells Genome-wide RNAi screen identifies ATPase inhibitory factor 1 (ATPIF1) as essential for PARK2 recruitment and mitophagy Phytochemical modulators of mitochondria: the search for chemopreventive agents and supportive therapeutics A "Copernican" reassessment of the human mitochondrial DNA tree from its root Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease Mitochondrial gene replacement in primate offspring and embryonic stem cells.Polymorphisms in mitochondrial genes and prostate cancer risk Mitochondrial defects in acute multiple sclerosis lesions Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs The rise of mitochondria in medicine Genetic manipulation for inherited neurodegenerative diseases: myth or reality?Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease Breast Cancer Metabolism and Mitochondrial Activity: The Possibility of Chemoprevention with Metformin Resources, challenges and way forward in rare mitochondrial diseases research Mitochondria-Targeted Protective Compounds in Parkinson's and Alzheimer's Diseases Mitophagy in hematopoietic stem cells: the case for exploration Mitochondrial disorders: challenges in diagnosis & treatment Mitochondrial DNA disease-molecular insights and potential routes to a cure Evolutionary defined role of the mitochondrial DNA in fertility, disease and ageing Detection of heteroplasmic mitochondrial DNA in single mitochondria Strong purifying selection in transmission of mammalian mitochondrial DNA Solution structure and siRNA-mediated knockdown analysis of the mitochondrial disease-related protein C12orf65 Double-stranded DNA-dependent ATPase Irc3p is directly involved in mitochondrial genome maintenance The conserved translocase Tim17 prevents mitochondrial DNA loss Coa3 and Cox14 are essential for negative feedback regulation of COX1 translation in mitochondria.Mitochondrial transfer: Implications for assisted reproductive technologies Function of the SIRT3 mitochondrial deacetylase in cellular physiology, cancer, and neurodegenerative disease An Overview of Genetic Changes and Risk of Pancreatic Ductal Adenocarcinoma A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation Epileptic syndromes: From clinic to genetic The Red Queen in mitochondria: cyto-nuclear co-evolution, hybrid breakdown and human disease

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Mitochondrial DNA mutations in human disease

http://www.wikidata.org/entity/Q24676881

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2005 nî lūn-bûn

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2005年の論文

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2005年論文

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Mitochondrial DNA mutations in human disease

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Mitochondrial DNA mutations in human disease

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Mitochondrial DNA mutations in human disease

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Mitochondrial DNA mutations in human disease

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Mitochondrial DNA mutations in human disease

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Mitochondrial DNA mutations in human disease

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Mitochondrial DNA mutations in human disease

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Nature Reviews Genetics

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Mitochondrial DNA mutations in human disease

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Doug M Turnbull

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Robert W Taylor

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Mitochondrial Genome Evolution and the Origin of Eukaryotes

Premature ageing in mice expressing defective mitochondrial DNA polymerase

Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA

Classification of European mtDNAs from an analysis of three European populations

Maternal inheritance of mouse mtDNA in interspecific hybrids: segregation of the leaked paternal mtDNA followed by the prevention of subsequent paternal leakage

The mitochondrial RNA polymerase contributes critically to promoter specificity in mammalian cells

Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups.

Reconstitution of a minimal mtDNA replisome in vitro

Maternal inheritance of human mitochondrial DNA

The epidemiology of Leber hereditary optic neuropathy in the North East of England

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10.1038/NRG1606

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mitochondrial DNA

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1762815

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