Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases.
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The rise of mitochondria in medicinePrivate mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.Mitochondrial mutations in subjects with psychiatric disordersAltered Mitochondrial Function, Mitochondrial DNA and Reduced Metabolic Flexibility in Patients With Diabetic Nephropathy.The role of mitochondrial genomics in patients with non-alcoholic steatohepatitis (NASH).Evidence of Mitochondrial Dysfunction within the Complex Genetic Etiology of Schizophrenia.Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneckReduced mitochondrial DNA copy number is a biomarker of Parkinson's disease.Somatic mtDNA variation is an important component of Parkinson's disease.Mitochondrial content is central to nuclear gene expression: Profound implications for human health.Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains.No effect of mitochondrial genotype on reproductive plasticity following exposure to a non-infectious pathogen challenge in female or male DrosophilaMitochondria in health, aging and diseases: the epigenetic perspective.Role of the mitochondrial DNA replication machinery in mitochondrial DNA mutagenesis, aging and age-related diseases.Ulcerative Colitis Is Under Dual (Mitochondrial and Nuclear) Genetic Control.Y Chromosome, Mitochondrial DNA and Childhood Behavioural Traits.Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK women.Increased Copy Number Variation of mtDNA in an Array-based Digital PCR Assay Predicts Ulcerative Colitis-associated Colorectal Cancer.Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015.Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's disease.Generation and Bioenergetic Profiles of Cybrids with East Asian mtDNA Haplogroups.Long Oskar Controls Mitochondrial Inheritance in Drosophila melanogaster.The Emerging Role of MitomiRs in the Pathophysiology of Human Disease.The aetiology of cardiovascular disease: a role for mitochondrial DNA?Mitochondrial haplogroups in patients with rheumatoid arthritis: No association with disease and disease manifestations.Examining the role of common and rare mitochondrial variants in schizophrenia.Mitochondrial DNA Double-Strand Breaks in Oligodendrocytes Cause Demyelination, Axonal Injury, and CNS Inflammation.Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson disease.The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease.Hi-MC: a novel method for high-throughput mitochondrial haplogroup classification.mtDNA Population Variants and Neurodegenerative Diseases
P2860
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P2860
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Recent mitochondrial DNA mutat ...... mon late-onset human diseases.
@ast
Recent mitochondrial DNA mutat ...... mon late-onset human diseases.
@en
type
label
Recent mitochondrial DNA mutat ...... mon late-onset human diseases.
@ast
Recent mitochondrial DNA mutat ...... mon late-onset human diseases.
@en
prefLabel
Recent mitochondrial DNA mutat ...... mon late-onset human diseases.
@ast
Recent mitochondrial DNA mutat ...... mon late-onset human diseases.
@en
P2860
P1433
P1476
Recent mitochondrial DNA mutat ...... mon late-onset human diseases.
@en
P2093
Aurora Gomez-Duran
Gavin Hudson
P2860
P304
P356
10.1371/JOURNAL.PGEN.1004369
P577
2014-05-22T00:00:00Z