Published in Mamm Genome on June 01, 2004
DNA polymerase gamma and mitochondrial disease: understanding the consequence of POLG mutations. Biochim Biophys Acta (2008) 1.43
CAG-encoded polyglutamine length polymorphism in the human genome. BMC Genomics (2007) 1.36
POLG1 polyglutamine tract variants associated with Parkinson's disease. Neurosci Lett (2010) 0.96
CAG-repeat variant in the polymerase γ gene and male infertility in the Chinese population: a meta-analysis. Asian J Androl (2010) 0.82
Mitochondrial DNA polymerase gamma gene polymorphism is not associated with male infertility. J Assist Reprod Genet (2013) 0.76
The POLG Polyglutamine Tract Variants in Iranian Patients with Multiple Sclerosis. Iran J Child Neurol (2015) 0.75
The sequence and de novo assembly of the giant panda genome. Nature (2009) 15.76
Premature ageing in mice expressing defective mitochondrial DNA polymerase. Nature (2004) 11.59
Impacts of the Cretaceous Terrestrial Revolution and KPg extinction on mammal diversification. Science (2011) 8.23
Intra- and interspecific variation in primate gene expression patterns. Science (2002) 7.92
Comparison of fine-scale recombination rates in humans and chimpanzees. Science (2005) 7.86
Drive against hotspot motifs in primates implicates the PRDM9 gene in meiotic recombination. Science (2009) 7.35
Comparison of cytochrome P450 (CYP) genes from the mouse and human genomes, including nomenclature recommendations for genes, pseudogenes and alternative-splice variants. Pharmacogenetics (2004) 5.12
Correlation between genetic and geographic structure in Europe. Curr Biol (2008) 5.02
Insights into hominid evolution from the gorilla genome sequence. Nature (2012) 4.12
Comparative and demographic analysis of orang-utan genomes. Nature (2011) 3.83
The dawn of human matrilineal diversity. Am J Hum Genet (2008) 3.60
Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production. Proc Natl Acad Sci U S A (2005) 3.42
The derived FOXP2 variant of modern humans was shared with Neandertals. Curr Biol (2007) 3.39
Quantification of plasma Epstein-Barr virus DNA in patients with advanced nasopharyngeal carcinoma. N Engl J Med (2004) 3.19
Immunomodulatory effect of human adipose tissue-derived adult stem cells: comparison with bone marrow mesenchymal stem cells. Br J Haematol (2005) 3.12
The origin of European cattle: evidence from modern and ancient DNA. Proc Natl Acad Sci U S A (2006) 3.09
Great ape genetic diversity and population history. Nature (2013) 2.95
Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress. Int J Biochem Cell Biol (2005) 2.91
Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency. Nat Genet (2010) 2.81
Oxidative stress-related alteration of the copy number of mitochondrial DNA in human leukocytes. Free Radic Res (2003) 2.70
Genomic affinities of two 7,000-year-old Iberian hunter-gatherers. Curr Biol (2012) 2.67
A global perspective on genetic variation at the ADH genes reveals unusual patterns of linkage disequilibrium and diversity. Am J Hum Genet (2002) 2.60
Genomic ancestry of North Africans supports back-to-Africa migrations. PLoS Genet (2012) 2.51
Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients. EMBO J (2010) 2.43
Unparalleled complexity of the MHC class I region in rhesus macaques. Proc Natl Acad Sci U S A (2005) 2.41
Coordinated changes of mitochondrial biogenesis and antioxidant enzymes during osteogenic differentiation of human mesenchymal stem cells. Stem Cells (2008) 2.34
Biased incorporation of ribonucleotides on the mitochondrial L-strand accounts for apparent strand-asymmetric DNA replication. Cell (2002) 2.32
In vitro-differentiated embryonic stem cells give rise to male gametes that can generate offspring mice. Dev Cell (2006) 2.30
Evidence for a genetic discontinuity between Neandertals and 24,000-year-old anatomically modern Europeans. Proc Natl Acad Sci U S A (2003) 2.25
Attenuation of oxidative stress after varicocelectomy in subfertile patients with varicocele. J Urol (2007) 2.20
Mouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPase. PLoS Genet (2009) 2.15
A melanocortin 1 receptor allele suggests varying pigmentation among Neanderthals. Science (2007) 2.15
Lightening up the UV response by identification of the arylhydrocarbon receptor as a cytoplasmatic target for ultraviolet B radiation. Proc Natl Acad Sci U S A (2007) 2.08
Comparative biology of mammalian telomeres: hypotheses on ancestral states and the roles of telomeres in longevity determination. Aging Cell (2011) 2.07
Somatic mutations in the D-loop and decrease in the copy number of mitochondrial DNA in human hepatocellular carcinoma. Mutat Res (2004) 2.01
Loss of urate oxidase activity in hominoids and its evolutionary implications. Mol Biol Evol (2002) 2.00
Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number. Hum Mol Genet (2004) 2.00
The portability of tagSNPs across populations: a worldwide survey. Genome Res (2006) 1.99
Mitochondrial DNA mutations and mitochondrial DNA depletion in gastric cancer. Genes Chromosomes Cancer (2005) 1.99
Mitochondrial genome instability and mtDNA depletion in human cancers. Ann N Y Acad Sci (2005) 1.97
Perampanel: a novel, orally active, noncompetitive AMPA-receptor antagonist that reduces seizure activity in rodent models of epilepsy. Epilepsia (2011) 1.94
Replication of vertebrate mitochondrial DNA entails transient ribonucleotide incorporation throughout the lagging strand. EMBO J (2006) 1.93
Comparative analysis of gene-expression patterns in human and African great ape cultured fibroblasts. Genome Res (2003) 1.92
Mammalian mitochondrial DNA replicates bidirectionally from an initiation zone. J Biol Chem (2003) 1.83
No influence of Indy on lifespan in Drosophila after correction for genetic and cytoplasmic background effects. PLoS Genet (2007) 1.82
The DAZL family proteins are PABP-binding proteins that regulate translation in germ cells. EMBO J (2005) 1.82
Prognostic variables in thoracic esophageal squamous cell carcinoma. Ann Thorac Surg (2009) 1.81
Response: The mitochondrial DNA replication bubble has not burst. Trends Biochem Sci (2003) 1.80
A bidirectional origin of replication maps to the major noncoding region of human mitochondrial DNA. Mol Cell (2005) 1.79
Nuclear gene indicates coat-color polymorphism in mammoths. Science (2006) 1.77
Gene flow from North Africa contributes to differential human genetic diversity in southern Europe. Proc Natl Acad Sci U S A (2013) 1.77
Mitochondrial DNA mutations and mitochondrial DNA depletion in breast cancer. Genes Chromosomes Cancer (2006) 1.77
Polybrominated diphenyl ethers induce developmental neurotoxicity in a human in vitro model: evidence for endocrine disruption. Environ Health Perspect (2010) 1.75
Y-chromosomal diversity in Lebanon is structured by recent historical events. Am J Hum Genet (2008) 1.75
Detection of mitochondrial DNA depletion in living human cells using PicoGreen staining. Exp Cell Res (2004) 1.74
Dazl binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells. Hum Mol Genet (2005) 1.72
Mitochondrial DNA of an Iberian Neandertal suggests a population affinity with other European Neandertals. Curr Biol (2006) 1.69
Microsatellite typing of the rhesus macaque MHC region. Immunogenetics (2005) 1.69
A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies. PLoS Genet (2012) 1.66
The value of avian genomics to the conservation of wildlife. BMC Genomics (2009) 1.63
Balancing selection is the main force shaping the evolution of innate immunity genes. J Immunol (2008) 1.63
MHC class I A region diversity and polymorphism in macaque species. Immunogenetics (2007) 1.63
Mitochondrial medicine: a metabolic perspective on the pathology of oxidative phosphorylation disorders. Cell Metab (2006) 1.62
Two novel proteins recruited by synaptonemal complex protein 1 (SYCP1) are at the centre of meiosis. J Cell Sci (2005) 1.62
Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice. Genes Dev (2009) 1.61
Tracking down human contamination in ancient human teeth. Mol Biol Evol (2006) 1.61
A massively parallel sequencing approach uncovers ancient origins and high genetic variability of endangered Przewalski's horses. Genome Biol Evol (2011) 1.60
A highly divergent mtDNA sequence in a Neandertal individual from Italy. Curr Biol (2006) 1.59
Organization and evolution of the Cyp2 gene cluster on mouse chromosome 7, and comparison with the syntenic human cluster. Environ Health Perspect (2003) 1.58
The RNA helicase p68 is a novel androgen receptor coactivator involved in splicing and is overexpressed in prostate cancer. Cancer Res (2008) 1.58
Admixture, migrations, and dispersals in Central Asia: evidence from maternal DNA lineages. Eur J Hum Genet (2004) 1.55
Sotrastaurin (AEB071) alone and in combination with cyclosporine A prolongs survival times of non-human primate recipients of life-supporting kidney allografts. Transplantation (2012) 1.54
Genome wide identification of promoter binding sites for H4K12ac in human sperm and its relevance for early embryonic development. Epigenetics (2012) 1.53
Molecular decay of the tooth gene Enamelin (ENAM) mirrors the loss of enamel in the fossil record of placental mammals. PLoS Genet (2009) 1.52
Macroevolutionary dynamics and historical biogeography of primate diversification inferred from a species supermatrix. PLoS One (2012) 1.52
ISAG/IUIS-VIC Comparative MHC Nomenclature Committee report, 2005. Immunogenetics (2006) 1.52
Mouse MAELSTROM: the link between meiotic silencing of unsynapsed chromatin and microRNA pathway? Hum Mol Genet (2006) 1.52
Evolutionary dynamics of the human ABO gene. Hum Genet (2008) 1.51
Alterations to the expression level of mitochondrial transcription factor A, TFAM, modify the mode of mitochondrial DNA replication in cultured human cells. Nucleic Acids Res (2006) 1.51
Human mitochondrial transcription factor A induces a U-turn structure in the light strand promoter. Nat Struct Mol Biol (2011) 1.51
Mammalian mitochondrial DNA replication intermediates are essentially duplex but contain extensive tracts of RNA/DNA hybrid. J Mol Biol (2010) 1.50
Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean. Am J Hum Genet (2008) 1.50
Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans. Nat Commun (2013) 1.50
A natural history of FUT2 polymorphism in humans. Mol Biol Evol (2009) 1.49
Alu insertion loci and platyrrhine primate phylogeny. Mol Phylogenet Evol (2005) 1.49
Anti-human leukocyte antigen immunization after early allograft nephrectomy. Transplantation (2012) 1.47
Donor-specific antibodies after ceasing immunosuppressive therapy, with or without an allograft nephrectomy. Clin J Am Soc Nephrol (2012) 1.46
Genetic analysis in Leber's hereditary optic neuropathy using the comparative genomic hybridization technique. Clin Experiment Ophthalmol (2003) 1.45
Oxidative stress, mitochondrial DNA mutation, and apoptosis in aging. Exp Biol Med (Maywood) (2007) 1.45
Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repair. PLoS Genet (2009) 1.44
SYCE2 is required for synaptonemal complex assembly, double strand break repair, and homologous recombination. J Cell Biol (2007) 1.43