Molecular genetic aspects of human mitochondrial disorders.
about
Human mtDNA haplogroups associated with high or reduced spermatozoa motilityAutomating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genomeThe innate immune system in host mice targets cells with allogenic mitochondrial DNAAge-associated mosaic respiratory chain deficiency causes trans-neuronal degenerationMitochondrial disorders: challenges in diagnosis & treatmentAtg32 is a mitochondrial protein that confers selectivity during mitophagyA genomic screen for yeast mutants defective in selective mitochondria autophagy.Mitochondrial transfer: Implications for assisted reproductive technologiesAge-associated mitochondrial DNA mutations lead to small but significant changes in cell proliferation and apoptosis in human colonic cryptsDown-regulation of mitochondrial transcription factor A during spermatogenesis in humansMutational hot spots in the mitochondrial microcosmStochastic drift in mitochondrial DNA point mutations: a novel perspective ex silicoDifferential mitochondrial distribution in human pronuclear embryos leads to disproportionate inheritance between blastomeres: relationship to microtubular organization, ATP content and competence.Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).Using 454 technology for long-PCR based sequencing of the complete mitochondrial genome from single Haemonchus contortus (Nematoda).Maintenance and integrity of the mitochondrial genome: a plethora of nuclear genes in the budding yeastRevolution in mitochondrial medicine.Yeast as a model for human mtDNA replication.Mitochondrial respiratory chain disorders and the liver.Efficient repair of abasic sites in DNA by mitochondrial enzymes.Mitochondrial genome maintenance in health and disease.Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetesIdentification of multiple rate-limiting steps during the human mitochondrial transcription cycle in vitroClinical mitochondrial genetics.Mitochondrial DNA mutations regulate metastasis of human breast cancer cells.Random genetic drift determines the level of mutant mtDNA in human primary oocytesTherapies in inborn errors of oxidative metabolism.Gene therapy for progeny of mito-mice carrying pathogenic mtDNA by nuclear transplantationMitochondrial myopathies and the role of the pathologist in the molecular era.Mitochondrial dysfunction due to oxidative mitochondrial DNA damage is reduced through cooperative actions of diverse proteinstRNA and cytochrome c in cell death and beyond.Search for characteristic structural features of mammalian mitochondrial tRNAs.Aminoacylation properties of pathology-related human mitochondrial tRNA(Lys) variants.Increased mitochondrial mass in mitochondrial myopathy miceDevelopment of lipophilic cations as therapies for disorders due to mitochondrial dysfunction.Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations.Overexpression of peroxisome proliferator-activated receptor gamma co-activator-1alpha leads to muscle atrophy with depletion of ATPGermline bottlenecks, biparental inheritance and selection on mitochondrial variants: a two-level selection modelComplete repopulation of mouse mitochondrial DNA-less cells with rat mitochondrial DNA restores mitochondrial translation but not mitochondrial respiratory function.Effect of a mutation in the anticodon of human mitochondrial tRNAPro on its post-transcriptional modification pattern.
P2860
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P2860
Molecular genetic aspects of human mitochondrial disorders.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Molecular genetic aspects of human mitochondrial disorders.
@en
type
label
Molecular genetic aspects of human mitochondrial disorders.
@en
prefLabel
Molecular genetic aspects of human mitochondrial disorders.
@en
P1476
Molecular genetic aspects of human mitochondrial disorders.
@en
P2093
Clayton DA
Larsson NG
P304
P356
10.1146/ANNUREV.GE.29.120195.001055
P577
1995-01-01T00:00:00Z