Published in Mitochondrion on November 10, 2009
Inherited mitochondrial DNA variants can affect complement, inflammation and apoptosis pathways: insights into mitochondrial-nuclear interactions. Hum Mol Genet (2014) 1.23
Mitochondria and cell bioenergetics: increasingly recognized components and a possible etiologic cause of Alzheimer's disease. Antioxid Redox Signal (2011) 1.21
Advances in exercise, fitness, and performance genomics in 2010. Med Sci Sports Exerc (2011) 1.12
The mitochondrial paradigm for cardiovascular disease susceptibility and cellular function: a complementary concept to Mendelian genetics. Lab Invest (2011) 0.99
MtDNA haplogroups M7 and B in southwestern Han Chinese at risk for acute mountain sickness. Mitochondrion (2011) 0.97
Mitochondrial DNA variants mediate energy production and expression levels for CFH, C3 and EFEMP1 genes: implications for age-related macular degeneration. PLoS One (2013) 0.96
Functional differences between mitochondrial haplogroup T and haplogroup H in HEK293 cybrid cells. PLoS One (2012) 0.95
Association of mitochondrial DNA variations with lung cancer risk in a Han Chinese population from southwestern China. PLoS One (2012) 0.91
The role of the mitochondrial genome in ageing and carcinogenesis. J Aging Res (2011) 0.90
Mitochondrial-nuclear epistasis: implications for human aging and longevity. Ageing Res Rev (2010) 0.89
Mitochondrial DNA (mtDNA) haplogroups and serum levels of anti-oxidant enzymes in patients with osteoarthritis. BMC Musculoskelet Disord (2011) 0.87
Mitochondrial DNA variation in human metabolic rate and energy expenditure. Mitochondrion (2011) 0.87
Mitochondrial haplogroups define two phenotypes of osteoarthritis. Front Physiol (2012) 0.86
mtDNA haplogroup J modulates telomere length and nitric oxide production. BMC Musculoskelet Disord (2011) 0.85
May "mitochondrial eve" and mitochondrial haplogroups play a role in neurodegeneration and Alzheimer's disease? Int J Alzheimers Dis (2011) 0.83
Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population. PLoS One (2013) 0.82
Mitochondrial haplogroups H and J: risk and protective factors for ischemic cardiomyopathy. PLoS One (2012) 0.81
Epidermal nerve fiber density, oxidative stress, and mitochondrial haplogroups in HIV-infected Thais initiating therapy. AIDS (2014) 0.80
Mitochondrial J haplogroup is associated with lower blood pressure and anti-oxidant status: findings in octo/nonagenarians from the BELFAST Study. Age (Dordr) (2012) 0.79
Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy. PLoS One (2015) 0.77
Relationship between mitochondrial haplogroup and physiological responses to hypobaric hypoxia. J Physiol Anthropol (2016) 0.77
The mitochondrial DNA Northeast Asia CZD haplogroup is associated with good disease-free survival among male oral squamous cell carcinoma patients. PLoS One (2012) 0.77
Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia. J Neurol (2011) 0.77
Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt-Jakob disease. Eur J Hum Genet (2014) 0.76
Mitochondrial and genomic ancestry are associated with etiology of heart failure in Brazilian patients. J Hum Hypertens (2015) 0.76
Mitochondrial DNA haplogroups modulate the radiographic progression of Spanish patients with osteoarthritis. Rheumatol Int (2014) 0.76
Mitochondrial Haplogroups and Risk of Pulmonary Arterial Hypertension. PLoS One (2016) 0.75
DNA Methyltransferase Gene Polymorphisms for Prediction of Radiation-Induced Skin Fibrosis after Treatment of Breast Cancer: A Multifactorial Genetic Approach. Cancer Res Treat (2016) 0.75
Relationship between European mitochondrial haplogroups and chronic renal allograft rejection in patients with kidney transplant. Int J Med Sci (2014) 0.75
Association between mitochondrial DNA haplogroup and myelodysplastic syndromes. Genes Chromosomes Cancer (2016) 0.75
Triad of Risk for Late Onset Alzheimer's: Mitochondrial Haplotype, APOE Genotype and Chromosomal Sex. Front Aging Neurosci (2016) 0.75
Mitochondrial DNA mutations and cardiovascular disease. Curr Opin Cardiol (2017) 0.75
Natural selection shaped regional mtDNA variation in humans. Proc Natl Acad Sci U S A (2002) 6.95
mtDNA mutations increase tumorigenicity in prostate cancer. Proc Natl Acad Sci U S A (2005) 4.66
Role of muscle mass on sprint performance: gender differences? Eur J Appl Physiol (2007) 2.43
Platelet cytochrome c oxidase activity and quantity in septic patients. Crit Care Med (2011) 2.23
Replication and transcription of mammalian mitochondrial DNA. Exp Physiol (2003) 1.99
Elevated male European and female African contributions to the genomes of African American individuals. Hum Genet (2006) 1.97
Isolation of biogenetically competent mitochondria from mammalian tissues and cultured cells. Methods (2002) 1.97
Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups. Hum Mol Genet (2010) 1.79
Control region mtDNA variants: longevity, climatic adaptation, and a forensic conundrum. Proc Natl Acad Sci U S A (2003) 1.57
Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease. Hum Mol Genet (2008) 1.56
Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups. Ann Hum Genet (2005) 1.54
Transient overexpression of mitochondrial transcription factor A (TFAM) is sufficient to stimulate mitochondrial DNA transcription, but not sufficient to increase mtDNA copy number in cultured cells. Nucleic Acids Res (2004) 1.53
Human mitochondrial transcription factor A induces a U-turn structure in the light strand promoter. Nat Struct Mol Biol (2011) 1.51
A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease. Mol Genet Metab (2009) 1.47
A 21-week bone deposition promoting exercise programme increases bone mass in young people with Down syndrome. Dev Med Child Neurol (2012) 1.46
An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNA. Hum Mol Genet (2003) 1.44
Mitochondrial DNA-like sequences in the nucleus (NUMTs): insights into our African origins and the mechanism of foreign DNA integration. Hum Mutat (2004) 1.39
Physical activity, sedentary index, and mental disorders in the SUN cohort study. Med Sci Sports Exerc (2008) 1.39
Adaptive selection of mitochondrial complex I subunits during primate radiation. Gene (2006) 1.31
Mitochondrial DNA haplogroups influence AIDS progression. AIDS (2008) 1.29
A randomised controlled trial of motivational interviewing for smoking cessation. Br J Gen Pract (2006) 1.27
Mitochondrial DNA haplogroups influence lipoatrophy after highly active antiretroviral therapy. J Acquir Immune Defic Syndr (2009) 1.24
A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease. Ann N Y Acad Sci (2008) 1.22
Differences of sperm motility in mitochondrial DNA haplogroup U sublineages. Gene (2005) 1.21
Adiposity, physical activity, and physical fitness among children from Aragón, Spain. Obesity (Silver Spring) (2007) 1.20
Tissue-specific differences in mitochondrial activity and biogenesis. Mitochondrion (2010) 1.17
Import of mitochondrial transcription factor A (TFAM) into rat liver mitochondria stimulates transcription of mitochondrial DNA. Nucleic Acids Res (2003) 1.12
Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion. Ann Neurol (2006) 1.12
Human mitochondrial mTERF wraps around DNA through a left-handed superhelical tandem repeat. Nat Struct Mol Biol (2010) 1.12
Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy. Biochim Biophys Acta (2012) 1.11
MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequences. Hum Mutat (2009) 1.10
Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene. Ann Neurol (2003) 1.10
Muscle mitochondrial capacity exceeds maximal oxygen delivery in humans. Mitochondrion (2010) 1.06
Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies. BMC Genomics (2014) 1.04
Human mitochondrial variants influence on oxygen consumption. Mitochondrion (2008) 1.01
Mitochondrial DNA transcription and diseases: past, present and future. Biochim Biophys Acta (2006) 0.99
20 years of human mtDNA pathologic point mutations: carefully reading the pathogenicity criteria. Biochim Biophys Acta (2008) 0.98
Kearns-Sayre syndrome: cerebral folate deficiency, MRI findings and new cerebrospinal fluid biochemical features. Mitochondrion (2010) 0.97
High femoral bone mineral density accretion in prepubertal soccer players. Med Sci Sports Exerc (2004) 0.96
Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populations. Biogerontology (2008) 0.95
Liver failure caused by herpes simplex virus thymidine kinase plus ganciclovir therapy is associated with mitochondrial dysfunction and mitochondrial DNA depletion. Hum Gene Ther (2003) 0.94
The role of the mitochondrion in sperm function: is there a place for oxidative phosphorylation or is this a purely glycolytic process? Curr Top Dev Biol (2007) 0.91
Cisplatin-mediated impairment of mitochondrial DNA metabolism inversely correlates with glutathione levels. Biochem J (2008) 0.91
Physical activity during leisure time and quality of life in a Spanish cohort: SUN (Seguimiento Universidad de Navarra) project. Br J Sports Med (2011) 0.90
CPEO and KSS differ in the percentage and location of the mtDNA deletion. Mitochondrion (2009) 0.90
Genetic causes of cerebral folate deficiency: clinical, biochemical and therapeutic aspects. Drug Discov Today (2012) 0.89
Mitochondrial gene expression is regulated at multiple levels and differentially in the heart and liver by thyroid hormones. Curr Genet (2008) 0.89
Effects of weight lifting training combined with plyometric exercises on physical fitness, body composition, and knee extension velocity during kicking in football. Appl Physiol Nutr Metab (2008) 0.88
Mitochondrial diseases mimicking neurotransmitter defects. Mitochondrion (2008) 0.88
Autism associated to a deficiency of complexes III and IV of the mitochondrial respiratory chain. Invest Clin (2010) 0.88
Sitting time increases the overweight and obesity risk independently of walking time in elderly people from Spain. Maturitas (2012) 0.87
Is bone tissue really affected by swimming? A systematic review. PLoS One (2013) 0.87
A combined training intervention programme increases lean mass in youths with Down syndrome. Res Dev Disabil (2011) 0.86
Validity of hip-mounted uniaxial accelerometry with heart-rate monitoring vs. triaxial accelerometry in the assessment of free-living energy expenditure in young children: the IDEFICS Validation Study. J Appl Physiol (1985) (2012) 0.86
Mitochondrial DNA depletion syndrome: new descriptions and the use of citrate synthase as a helpful tool to better characterise the patients. Mol Genet Metab (2012) 0.86
Survival and mitochondrial function in septic patients according to mitochondrial DNA haplogroup. Crit Care (2012) 0.86
Physical fitness effect on bone mass is mediated by the independent association between lean mass and bone mass through adolescence: a cross-sectional study. J Bone Miner Metab (2008) 0.86
In vitro transcription termination activity of the Drosophila mitochondrial DNA-binding protein DmTTF. Biochem Biophys Res Commun (2005) 0.86
Mitochondrial DNA content of human spermatozoa. Biol Reprod (2003) 0.86
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction. Acta Neuropathol (2002) 0.85
New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset. Neurogenetics (2012) 0.85
Bone related health status in adolescent cyclists. PLoS One (2011) 0.85
Steady exercise removes VO(2max) difference between mitochondrial genomic variants. Mitochondrion (2009) 0.84
Mitochondrial antibiograms in personalized medicine. Hum Mol Genet (2012) 0.84
Altered expression of master regulatory genes of adipogenesis in lipomas from patients bearing tRNA(Lys) point mutations in mitochondrial DNA. Mol Genet Metab (2006) 0.84