Functional recurrent mutations in the human mitochondrial phylogeny: dual roles in evolution and disease
about
Mitochondrial cytochrome c oxidase deficiencyMitochondrial variations in the MT-ND4 and MT-TL1 genes are associated with male infertility.Underlying Data for Sequencing the Mitochondrial Genome with the Massively Parallel Sequencing Platform Ion Torrent™ PGM™Disease-associated mitochondrial mutations and the evolution of primate mitogenomes.Mitochondrial DNA variant in COX1 subunit significantly alters energy metabolism of geographically divergent wild isolates in Caenorhabditis elegansDNA barcoding works in practice but not in (neutral) theory.Late-onset Mitochondrial Cardiomyopathy Triggered by Anticancer TreatmentMito-nuclear co-evolution: the positive and negative sides of functional ancient mutationsOrigins and functional consequences of somatic mitochondrial DNA mutations in human cancerAre mutagenic non D-loop direct repeat motifs in mitochondrial DNA under a negative selection pressure?Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry.Ancient Out-of-Africa Mitochondrial DNA Variants Associate with Distinct Mitochondrial Gene Expression Patterns.Mitochondrial Involvement in Vertebrate Speciation? The Case of Mito-nuclear Genetic Divergence in Chameleons.The Mitonuclear Dimension of Neanderthal and Denisovan Ancestry in Modern Human Genomes.Heteroplasmic shifts in tumor mitochondrial genomes reveal tissue-specific signals of relaxed and positive selection.Transcription factors bind negatively selected sites within human mtDNA genes.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.Codon based co-occurrence network motifs in human mitochondria.A common pattern of DNase I footprinting throughout the human mtDNA unveils clues for a chromatin-like organization
P2860
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P2860
Functional recurrent mutations in the human mitochondrial phylogeny: dual roles in evolution and disease
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Functional recurrent mutations ...... roles in evolution and disease
@en
type
label
Functional recurrent mutations ...... roles in evolution and disease
@en
prefLabel
Functional recurrent mutations ...... roles in evolution and disease
@en
P2093
P2860
P356
P1476
Functional recurrent mutations ...... roles in evolution and disease
@en
P2093
Dan Mishmar
Hadas Hawlena
Ilia Zhidkov
Liron Levin
Yotam Gurman
P2860
P304
P356
10.1093/GBE/EVT058
P577
2013-01-01T00:00:00Z