Recurrent tissue-specific mtDNA mutations are common in humans. - Wikidata - wikimedia - TriplyDB

Recurrent tissue-specific mtDNA mutations are common in humans.

Recurrent tissue-specific mtDNA mutations are common in humans.

http://www.wikidata.org/entity/Q37288998

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Keeping mtDNA in shape between generations The rise of mitochondria in medicine Mitochondrial DNA heteroplasmy in the emerging field of massively parallel sequencing Mitochondrial DNA disease and developmental implications for reproductive strategies Segregation of Naturally Occurring Mitochondrial DNA Variants in a Mini-Pig Model Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma.Mitochondria sequence mapping strategies and practicability of mitochondria variant detection from exome and RNA sequencing data.MitoRS, a method for high throughput, sensitive, and accurate detection of mitochondrial DNA heteroplasmy.The road to rack and ruin: selecting deleterious mitochondrial DNA variants Transmission from centenarians to their offspring of mtDNA heteroplasmy revealed by ultra-deep sequencing.Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing.MtDNA segregation in heteroplasmic tissues is common in vivo and modulated by haplotype differences and developmental stage.Maternal age effect and severe germ-line bottleneck in the inheritance of human mitochondrial DNA.Insights from space: potential role of diet in the spatial organization of chromosomes.Extensive tissue-related and allele-related mtDNA heteroplasmy suggests positive selection for somatic mutations.Can paternal leakage maintain sexually antagonistic polymorphism in the cytoplasm?Investigation of Toll-Like Receptor-2 (2258G/A) and Interferon Gamma (+874T/A) Gene Polymorphisms among Infertile Women with Female Genital Tuberculosis First complete mitochondrial genome of the South American annual fish Austrolebias charrua (Cyprinodontiformes: Rivulidae): peculiar features among cyprinodontiforms mitogenomes.Age-Related and Heteroplasmy-Related Variation in Human mtDNA Copy Number Mitochondrial heteroplasmy in vertebrates using ChIP-sequencing data Explaining additional genetic variation in complex traits Mitochondrial DNA copy number variation across human cancers A Mitochondrial DNA A8701G Mutation Associated with Maternally Inherited Hypertension and Dilated Cardiomyopathy in a Chinese Pedigree of a Consanguineous Marriage Selfish drive can trump function when animal mitochondrial genomes compete.Sensing risk, fearing uncertainty: systems science approach to change Cancer: Mitochondrial Origins Mitochondrial DNA heteroplasmy in human health and disease.Heteroplasmic shifts in tumor mitochondrial genomes reveal tissue-specific signals of relaxed and positive selection.Identical mitochondrial somatic mutations unique to chronic periodontitis and coronary artery disease.Mitochondria single nucleotide variation across six blood cell types.Mitochondrial quality control: Cell-type-dependent responses to pathological mutant mitochondrial DNA Mitochondrial mutations drive prostate cancer aggression.The molecular characterization of porcine egg precursor cells.Genomics: Organ roles for mitochondrial mutations?Mitochondrial Abnormality Facilitates Cyst Formation in Autosomal Dominant Polycystic Kidney Disease.Sensitive detection of mitochondrial DNA variants for analysis of mitochondrial DNA-enriched extracts from frozen tumor tissue.A Population Phylogenetic View of Mitochondrial Heteroplasmy.The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease.Influence of Electron-Holes on DNA Sequence-Specific Mutation Rates.Tumor-Specific Mitochondrial DNA Variants Are Rarely Detected in Cell-Free DNA.

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Recurrent tissue-specific mtDNA mutations are common in humans.

http://www.wikidata.org/entity/Q37288998

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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2013年學術文章

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name

Recurrent tissue-specific mtDNA mutations are common in humans.

@en

Recurrent tissue-specific mtDNA mutations are common in humans.

@nl

type

label

Recurrent tissue-specific mtDNA mutations are common in humans.

@en

Recurrent tissue-specific mtDNA mutations are common in humans.

@nl

prefLabel

Recurrent tissue-specific mtDNA mutations are common in humans.

@en

Recurrent tissue-specific mtDNA mutations are common in humans.

@nl

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Recurrent tissue-specific mtDNA mutations are common in humans.

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Bingshan Li

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Chun Li

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Deborah G Murdock

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Douglas P Mortlock

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Eric Torstenson

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Hayley Boyd Clay

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Robert D Hoffman

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Scott M Williams

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Tia M Hughes

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Tricia A Thornton-Wells

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P2860

Fast and accurate short read alignment with Burrows-Wheeler transform

Strong purifying selection in transmission of mammalian mitochondrial DNA

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene

Novel mitochondrial DNA length variants and genetic instability in a family with diabetes and deafness

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

Characterization of human control region sequences of the African American SWGDAM forensic mtDNA data set.

Evaluation of variation in control region sequences for Hispanic individuals in the SWGDAM mtDNA data set.

The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method.

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9

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David C. Samuels

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2013-11-07T00:00:00Z

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258639428

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