Mitochondrial DNA variation in human evolution and disease
about
The peopling of Korea revealed by analyses of mitochondrial DNA and Y-chromosomal markersMitochondrial DNA polymorphism A4917G is independently associated with age-related macular degenerationWhole-mtDNA Genome Sequence Analysis of Ancient African LineagesWhere west meets east: the complex mtDNA landscape of the southwest and Central Asian corridor.Natural selection shaped regional mtDNA variation in humansReduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups.Ancient DNA reveals prehistoric gene-flow from siberia in the complex human population history of North East EuropeRole of Redox Status in Development of GlioblastomaPharmacogenetics as a tool to tailor antiretroviral therapy: A reviewThe Red Queen in mitochondria: cyto-nuclear co-evolution, hybrid breakdown and human diseaseGenetic evidence supports demic diffusion of Han cultureMitochondrial DNA subhaplogroups L0a2 and L2a modify susceptibility to peripheral neuropathy in malawian adults on stavudine containing highly active antiretroviral therapyA cytochrome c fusion protein domain for convenient detection, quantification, and enhanced production of membrane proteins in Escherichia coli--expression and characterization of cytochrome-tagged Complex I subunitsGenetic variation and adaptation in Africa: implications for human evolution and diseaseMitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson DiseaseA mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicinePaxillin mutations affect focal adhesions and lead to altered mitochondrial dynamics: relevance to lung cancerBioenergetics in human evolution and disease: implications for the origins of biological complexity and the missing genetic variation of common diseases.On the origin of Iberomaurusians: new data based on ancient mitochondrial DNA and phylogenetic analysis of Afalou and Taforalt populations.HmtDB, a human mitochondrial genomic resource based on variability studies supporting population genetics and biomedical research.Minisequencing mitochondrial DNA pathogenic mutations.New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation.Mitochondrial DNA evidence for a diversified origin of workers building First Emperor of ChinaLimited clinical relevance of mitochondrial DNA mutation and gene expression analyses in ovarian cancer.Mitochondrial haplogroups and control region polymorphisms are not associated with prostate cancer in Middle European Caucasians.Mitochondria, bioenergetics, and the epigenome in eukaryotic and human evolutionMultiplex analysis of mitochondrial DNA pathogenic and polymorphic sequence variants.The episode of genetic drift defining the migration of humans out of Africa is derived from a large east African population sizeMitochondrial DNA variants in the pathogenesis of type 2 diabetes - relevance of asian population studies.Disease-related versus polymorphic mutations in human mitochondrial tRNAs. Where is the difference?Mitochondrial DNA variant in COX1 subunit significantly alters energy metabolism of geographically divergent wild isolates in Caenorhabditis elegansIrritable bowel syndrome may be associated with maternal inheritance and mitochondrial DNA control region sequence variantsEvolutionary toxicology: contaminant-induced genetic mutations in mosquitofish from Sumgayit, Azerbaijan.Cattle phenotypes can disguise their maternal ancestryMitochondriome and cholangiocellular carcinomaThe heritage of pathogen pressures and ancient demography in the human innate-immunity CD209/CD209L regionThe peopling of Europe from the maternal and paternal perspectives.TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?Zidovudine exposure in HIV-1 infected Tanzanian women increases mitochondrial DNA levels in placenta and umbilical cordsMitochondrial DNA mutations in human disease.
P2860
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P2860
Mitochondrial DNA variation in human evolution and disease
description
1999 nî lūn-bûn
@nan
1999 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Mitochondrial DNA variation in human evolution and disease
@ast
Mitochondrial DNA variation in human evolution and disease
@en
Mitochondrial DNA variation in human evolution and disease
@nl
type
label
Mitochondrial DNA variation in human evolution and disease
@ast
Mitochondrial DNA variation in human evolution and disease
@en
Mitochondrial DNA variation in human evolution and disease
@nl
prefLabel
Mitochondrial DNA variation in human evolution and disease
@ast
Mitochondrial DNA variation in human evolution and disease
@en
Mitochondrial DNA variation in human evolution and disease
@nl
P2093
P3181
P1433
P1476
Mitochondrial DNA variation in human evolution and disease
@en
P2093
P304
P3181
P356
10.1016/S0378-1119(99)00295-4
P407
P577
1999-09-30T00:00:00Z