-
Subject Areas on Research
-
A colony color method identifies the vulnerability of mitochondria to oxidative damage.
-
A comparative study of asymmetric migration events across a marine biogeographic boundary.
-
A haplotype map of the human genome.
-
A hot-vent gastropod with iron sulfide dermal sclerites.
-
A multi-locus assessment of connectivity and historical demography in the bluehead wrasse (Thalassoma bifasciatum).
-
A multi-locus molecular phylogeny of the Lepidoziaceae: laying the foundations for a stable classification.
-
A new activating role for CO in cardiac mitochondrial biogenesis.
-
A phase I trial of low-dose inhaled carbon monoxide in sepsis-induced ARDS.
-
A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.
-
ATM inhibition enhances cancer immunotherapy by promoting mtDNA leakage and cGAS/STING activation.
-
Absence of mitochondrial progesterone receptor polymorphisms in women with spontaneous preterm birth.
-
Acute pancreatitis in an infant with lactic acidosis and a mutation at nucleotide 3243 in the mitochondrial DNA tRNALeu(UUR) gene.
-
Adipose-specific deletion of TFAM increases mitochondrial oxidation and protects mice against obesity and insulin resistance.
-
Age-related declines in α-Klotho drive progenitor cell mitochondrial dysfunction and impaired muscle regeneration.
-
An allele of HRAS1 3'variable number of tandem repeats is a frailty allele: implication for an evolutionarily-conserved pathway involved in longevity.
-
Analysis of DNA damage and repair in nuclear and mitochondrial DNA of animal cells using quantitative PCR.
-
Analysis of European mitochondrial haplogroups with Alzheimer disease risk.
-
Analysis of microsatellite mutations in the mitochondrial DNA of Saccharomyces cerevisiae.
-
Ancient X chromosomes reveal contrasting sex bias in Neolithic and Bronze Age Eurasian migrations.
-
Ancient co-speciation of simian foamy viruses and primates.
-
Another surprise from the mitochondrial genome.
-
Association of mtDNA haplogroup F with healthy longevity in the female Chuang population, China.
-
Autophagy protects against aminochrome-induced cell death in substantia nigra-derived cell line.
-
CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease.
-
Can three incongruence tests predict when data should be combined?
-
Canaries in the coal mine: mitochondrial DNA and vascular injury from reactive oxygen species.
-
Cancer-associated isocitrate dehydrogenase mutations induce mitochondrial DNA instability.
-
Carbon monoxide, skeletal muscle oxidative stress, and mitochondrial biogenesis in humans.
-
Cardiac involvement in mitochondrial diseases, and vice versa.
-
Chronic cigarette smoke extract treatment selects for apoptotic dysfunction and mitochondrial mutations in minimally transformed oral keratinocytes.
-
Circulating mitochondria in deceased organ donors are associated with immune activation and early allograft dysfunction.
-
Class-level relationships in the phylum Cnidaria: evidence from mitochondrial genome structure.
-
Class-level relationships in the phylum Cnidaria: molecular and morphological evidence.
-
Co-regulation of nuclear respiratory factor-1 by NFkappaB and CREB links LPS-induced inflammation to mitochondrial biogenesis.
-
Comparative toxicity of silver nanoparticles on oxidative stress and DNA damage in the nematode, Caenorhabditis elegans.
-
Contrasting quaternary histories in an ecologically divergent sister pair of low-dispersing intertidal fish (Xiphister) revealed by multilocus DNA analysis.
-
Cryptic Patterns of Speciation in Cryptic Primates: Microendemic Mouse Lemurs and the Multispecies Coalescent.
-
Cryptococcus neoformans mitochondrial genomes from serotype A and D strains do not influence virulence.
-
Deciding among green plants for whole genome studies.
-
Defining spatial and temporal patterns of phylogeographic structure in Madagascar's iguanid lizards (genus Oplurus).
-
Delayed cytotoxicity and selective loss of mitochondrial DNA in cells treated with the anti-human immunodeficiency virus compound 2',3'-dideoxycytidine.
-
Delimiting species without nuclear monophyly in Madagascar's mouse lemurs.
-
Differential expression of mitochondrial DNA replication factors in mammalian tissues.
-
Differential patterns of male and female mtDNA exchange across the Atlantic Ocean in the blue mussel, Mytilus edulis.
-
Disentangling the Collema-Leptogium complex through a molecular phylogenetic study of the Collemataceae (Peltigerales, lichen-forming Ascomycota).
-
Divergence dates for Malagasy lemurs estimated from multiple gene loci: geological and evolutionary context.
-
Divergent mitochondrial biogenesis responses in human cardiomyopathy.
-
Diversification before the most recent glaciation in Balanus glandula.
-
Diversity in the weapons of sexual selection: horn evolution in the beetle genus Onthophagus (Coleoptera: Scarabaeidae).
-
Dramatic mitochondrial gene rearrangements in the hermit crab Pagurus longicarpus (Crustacea, anomura).
-
Early-life mitochondrial DNA damage results in lifelong deficits in energy production mediated by redox signaling in Caenorhabditis elegans.
-
Ecological significance of mitochondrial toxicants.
-
Editor's Highlight: Base Excision Repair Variants and Pesticide Exposure Increase Parkinson's Disease Risk.
-
Effect of anti-human immunodeficiency virus nucleoside analogs on mitochondrial DNA and its implication for delayed toxicity.
-
Effects of 5'-fluoro-2-deoxyuridine on mitochondrial biology in Caenorhabditis elegans.
-
Effects of air pollution on mitochondrial function, mitochondrial DNA methylation, and mitochondrial peptide expression.
-
Effects of benzo[a]pyrene on mitochondrial and nuclear DNA damage in Atlantic killifish (Fundulus heteroclitus) from a creosote-contaminated and reference site.
-
Effects of early life exposure to ultraviolet C radiation on mitochondrial DNA content, transcription, ATP production, and oxygen consumption in developing Caenorhabditis elegans.
-
Effects of reduced mitochondrial DNA content on secondary mitochondrial toxicant exposure in Caenorhabditis elegans.
-
Effects of selection and mutation on mitochondrial variation and inferences of historical population expansion in a Caribbean reef fish.
-
Epigenome-wide association study of mitochondrial genome copy number.
-
Erythropoietin activates mitochondrial biogenesis and couples red cell mass to mitochondrial mass in the heart.
-
Evidence against equimolarity of large repeat arrangements and a predominant master circle structure of the mitochondrial genome from a monkeyflower (Mimulus guttatus) lineage with cryptic CMS.
-
Evidence for Compartmentalized Axonal Mitochondrial Biogenesis: Mitochondrial DNA Replication Increases in Distal Axons As an Early Response to Parkinson's Disease-Relevant Stress.
-
Evidence for selection at multiple allozyme loci across a mussel hybrid zone.
-
Exposure to mitochondrial genotoxins and dopaminergic neurodegeneration in Caenorhabditis elegans.
-
Expression, purification, and in vitro assays of mitochondrial single-stranded DNA-binding protein.
-
Extracellular Mitochondrial DNA and N-Formyl Peptides in Trauma and Critical Illness: A Systematic Review.
-
Failure of the ILD to determine data combinability for slow loris phylogeny.
-
Flow cytometric analysis of DNA content in budding yeast.
-
Frequency and phenotypic implications of mitochondrial DNA mutations in human squamous cell cancers of the head and neck.
-
Genes and longevity: lessons from studies of centenarians.
-
Genes, demography, and life span: the contribution of demographic data in genetic studies on aging and longevity.
-
Genetic and 'cultural' similarity in wild chimpanzees.
-
Genetic structure in a dynamic baboon hybrid zone corroborates behavioural observations in a hybrid population.
-
Genetic variation in the spread of Drosophila subobscura from a nonequilibrium population.
-
Genetic variation within and among populations of the threatened lichen Lobaria pulmonaria in Switzerland and implications for its conservation.
-
Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra.
-
Geogenetic patterns in mouse lemurs (genus Microcebus) reveal the ghosts of Madagascar's forests past.
-
Glutathione regulates susceptibility to oxidant-induced mitochondrial DNA damage in human lymphocytes.
-
Heme Oxygenase-1/Carbon Monoxide System and Embryonic Stem Cell Differentiation and Maturation into Cardiomyocytes.
-
Heme oxygenase-1 regulates cardiac mitochondrial biogenesis via Nrf2-mediated transcriptional control of nuclear respiratory factor-1.
-
Heteroplasmic mitochondrial DNA mutations in normal and tumour cells.
-
Host-symbiont stability and fast evolutionary rates in an ant-bacterium association: cospeciation of camponotus species and their endosymbionts, candidatus blochmannia.
-
Hybrid male sterility in Mimulus (Phrymaceae) is associated with a geographically restricted mitochondrial rearrangement.
-
Ice-age survival of Atlantic cod: agreement between palaeoecology models and genetics.
-
Identification of asteroid genera with species capable of larval cloning.
-
Increased mtDNA levels without change in mitochondrial enzymes in peripheral blood mononuclear cells of infants born to HIV-infected mothers on antiretroviral therapy.
-
Induction of mitochondrial biogenesis protects against acetaminophen hepatotoxicity.
-
Inherited variants in mitochondrial biogenesis genes may influence epithelial ovarian cancer risk.
-
Inter-genomic cross talk between mitochondria and the nucleus plays an important role in tumorigenesis.
-
Interference of nuclear mitochondrial DNA segments in mitochondrial DNA testing resembles biparental transmission of mitochondrial DNA in humans.
-
Intraspecific phylogenetic congruence among multiple symbiont genomes.
-
Involvement of autophagy and mitochondrial dynamics in determining the fate and effects of irreparable mitochondrial DNA damage.
-
Is congruence between data partitions a reliable predictor of phylogenetic accuracy? Empirically testing an iterative procedure for choosing among phylogenetic methods.
-
Klotho, an antiaging molecule, attenuates oxidant-induced alveolar epithelial cell mtDNA damage and apoptosis.
-
LRRK2 G2019S-induced mitochondrial DNA damage is LRRK2 kinase dependent and inhibition restores mtDNA integrity in Parkinson's disease.
-
LRRK2 mutations cause mitochondrial DNA damage in iPSC-derived neural cells from Parkinson's disease patients: reversal by gene correction.
-
Lipopolysaccharide induces oxidative cardiac mitochondrial damage and biogenesis.
-
Lipopolysaccharide stimulates mitochondrial biogenesis via activation of nuclear respiratory factor-1.
-
Manganese superoxide dismutase is a mitochondrial fidelity protein that protects Polγ against UV-induced inactivation.
-
Maternal lineages and Alzheimer disease risk in the Old Order Amish.
-
Metabolic capacity regulates iron homeostasis in endothelial cells.
-
Method for the structural analysis of Twinkle mitochondrial DNA helicase by cryo-EM.
-
Mitochondria as a target of environmental toxicants
-
Mitochondria in Ovarian Aging and Reproductive Longevity.
-
Mitochondria in lung biology and pathology: more than just a powerhouse.
-
Mitochondria in sporadic amyotrophic lateral sclerosis.
-
Mitochondria, energetics, epigenetics, and cellular responses to stress.
-
Mitochondrial C-tract alteration in premalignant lesions of the head and neck: a marker for progression and clonal proliferation.
-
Mitochondrial DNA Mutagenesis: Feature of and Biomarker for Environmental Exposures and Aging.
-
Mitochondrial DNA Sequence Variation Associated With Peripheral Nerve Function in the Elderly.
-
Mitochondrial DNA alterations in thyroid cancer.
-
Mitochondrial DNA damage as a peripheral biomarker for mitochondrial toxin exposure in rats.
-
Mitochondrial DNA damage induced autophagy, cell death, and disease.
-
Mitochondrial DNA damage: molecular marker of vulnerable nigral neurons in Parkinson's disease.
-
Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease.
-
Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration.
-
Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans.
-
Mitochondrial DNA sequence variation associated with dementia and cognitive function in the elderly.
-
Mitochondrial DNA structure and expression in specialized subtypes of mammalian striated muscle.
-
Mitochondrial DNA variant in COX1 subunit significantly alters energy metabolism of geographically divergent wild isolates in Caenorhabditis elegans.
-
Mitochondrial DNA variation in human metabolic rate and energy expenditure.
-
Mitochondrial DNA, oxidants, and innate immunity.
-
Mitochondrial DNA-depleted A549 cells are resistant to bleomycin.
-
Mitochondrial biogenesis in striated muscles: rapid induction of citrate synthase mRNA by nerve stimulation.
-
Mitochondrial dynamics and autophagy aid in removal of persistent mitochondrial DNA damage in Caenorhabditis elegans
-
Mitochondrial dysfunction and insulin resistance: a matter of lifestyle?
-
Mitochondrial fusion, fission, and mitochondrial toxicity.
-
Mitochondrial gene expression in mammalian striated muscle. Evidence that variation in gene dosage is the major regulatory event.
-
Mitochondrial gene rearrangements confirm the parallel evolution of the crab-like form.
-
Mitochondrial genetic background in Ghanaian patients with primary open-angle glaucoma.
-
Mitochondrial hTERT exacerbates free-radical-mediated mtDNA damage.
-
Mitochondrial localization of telomerase as a determinant for hydrogen peroxide-induced mitochondrial DNA damage and apoptosis.
-
Mitochondrial mutations are a late event in the progression of head and neck squamous cell cancer.
-
Mitochondrial mutations in adenoid cystic carcinoma of the salivary glands.
-
Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.
-
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.
-
Mitochondrial resequencing arrays detect tumor-specific mutations in salivary rinses of patients with head and neck cancer.
-
Mitochondrial toxicity in hearts of CD-1 mice following perinatal exposure to AZT, 3TC, or AZT/3TC in combination.
-
Mitochondrial transcription factor A induction by redox activation of nuclear respiratory factor 1.
-
Mobile elements and mitochondrial genome expansion in the soil fungus and potato pathogen Rhizoctonia solani AG-3.
-
Modelling the effects of age-related mtDNA mutation accumulation; complex I deficiency, superoxide and cell death.
-
Molecular ecology and natural history of simian foamy virus infection in wild-living chimpanzees.
-
Molecular evolutionary dynamics of cytochrome b in strepsirrhine primates: the phylogenetic significance of third-position transversions.
-
Molecular phylogenetic analysis of the Papionina using concatenation and species tree methods.
-
Molecular phylogeny of the Entomophthoromycota:
-
Multiple colonisations of the western Indian Ocean by Pteropus fruit bats (Megachiroptera: Pteropodidae): the furthest islands were colonised first.
-
Multiple nuclear loci reveal patterns of incomplete lineage sorting and complex species history within western mouse lemurs (Microcebus).
-
Muscle oxidative capacity during IL-6-dependent cancer cachexia.
-
Mutations in TFAM, encoding mitochondrial transcription factor A, cause neonatal liver failure associated with mtDNA depletion.
-
Nearshore fish (Pholis gunnellus) persists across the North Atlantic through multiple glacial episodes.
-
New insights into classification and evolution of the Lecanoromycetes (Pezizomycotina, Ascomycota) from phylogenetic analyses of three ribosomal RNA- and two protein-coding genes.
-
Newly Revised Quantitative PCR-Based Assay for Mitochondrial and Nuclear DNA Damage.
-
Nitric oxide synthase-2 induction optimizes cardiac mitochondrial biogenesis after endotoxemia.
-
Nitric oxide synthase-2 regulates mitochondrial Hsp60 chaperone function during bacterial peritonitis in mice.
-
Nonselective autophagy reduces mitochondrial content during starvation in Caenorhabditis elegans.
-
Nonsynonymous somatic mitochondrial mutations occur in the majority of cutaneous melanomas.
-
Nrf2 promotes alveolar mitochondrial biogenesis and resolution of lung injury in Staphylococcus aureus pneumonia in mice.
-
Nuclear responses to depletion of mitochondrial DNA in human cells.
-
Obtaining mtDNA genomes from next-generation transcriptome sequencing: a case study on the basal Passerida (Aves: Passeriformes) phylogeny.
-
Optimizing the dose of glutamine dipeptides and antioxidants in critically ill patients: a phase I dose-finding study.
-
Origin of HIV-1 in the chimpanzee Pan troglodytes troglodytes.
-
Oxygen-induced mitochondrial biogenesis in the rat hippocampus.
-
PCR based determination of mitochondrial DNA copy number in multiple species.
-
PCR-Based Analysis of Mitochondrial DNA Copy Number, Mitochondrial DNA Damage, and Nuclear DNA Damage.
-
PCR-Based Determination of Mitochondrial DNA Copy Number in Multiple Species.
-
Peripheral Blood Mononuclear Cells Demonstrate Mitochondrial Damage Clearance During Sepsis.
-
Peroxisome proliferator-activated receptor-gamma coactivator-1alpha overexpression increases lipid oxidation in myocytes from extremely obese individuals.
-
Phylogenetic affiliations of members of the heterogeneous lichen-forming fungi of the genus Lecidea sensu Zahlbruckner (Lecanoromycetes, Ascomycota).
-
Phylogeny and evolution of Malagasy plated lizards.
-
Phylogeography of a Morphologically Cryptic Golden Mole Assemblage from South-Eastern Africa.
-
Phylogeography of the arid-adapted Malagasy bullfrog, Laliostoma labrosum, influenced by past connectivity and habitat stability.
-
Population genetics of a trochid gastropod broadens picture of Caribbean Sea connectivity.
-
Post-Austronesian migrational wave of West Polynesians to Micronesia.
-
Postlipopolysaccharide oxidative damage of mitochondrial DNA.
-
Predictors of mitochondrial DNA copy number and damage in a mercury-exposed rural Peruvian population near artisanal and small-scale gold mining: An exploratory study.
-
Preferential synthesis of yeast mitochondrial DNA in alpha factor-arrested cells.
-
Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.
-
Prophylaxis for second eye involvement in leber hereditary optic neuropathy: an open-labeled, nonrandomized multicenter trial of topical brimonidine purite.
-
Purifying selection, sequence composition, and context-specific indel mutations shape intraspecific variation in a bacterial endosymbiont.
-
QPCR: a tool for analysis of mitochondrial and nuclear DNA damage in ecotoxicology.
-
Quantitative PCR-based measurement of nuclear and mitochondrial DNA damage and repair in mammalian cells.
-
Quantitative PCR-based measurement of nuclear and mitochondrial DNA damage and repair in mammalian cells.
-
RNA subunit of mitochondrial RNA-processing enzyme is induced by contractile activity in striated muscle.
-
Rapid mtDNA deletion by oxidants in rat liver mitochondria after hemin exposure.
-
Reducing mitochondrial reads in ATAC-seq using CRISPR/Cas9.
-
Regulation of cytochrome c oxidase subunit 1 (COX1) expression in Cryptococcus neoformans by temperature and host environment.
-
Regulation of mitochondrial biogenesis in skeletal muscle by CaMK.
-
Regulation of nuclear and mitochondrial gene expression by contractile activity in skeletal muscle.
-
Remarkable species diversity in Malagasy mouse lemurs (primates, Microcebus).
-
Replication and preferential inheritance of hypersuppressive petite mitochondrial DNA.
-
Reply to Lazaridis and Reich: Robust model-based inference of male-biased admixture during Bronze Age migration from the Pontic-Caspian Steppe.
-
Resistance of mitochondrial DNA to cadmium and Aflatoxin B1 damage-induced germline mutation accumulation in C. elegans.
-
Role of mitochondrial DNA damage and dysfunction in veterans with Gulf War Illness.
-
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder.
-
SXI1alpha controls uniparental mitochondrial inheritance in Cryptococcus neoformans.
-
Saccharomyces cerevisiae Ntg1p and Ntg2p: broad specificity N-glycosylases for the repair of oxidative DNA damage in the nucleus and mitochondria.
-
Severe Leber Hereditary Optic Neuropathy Plus Disease in a Middle-Aged Man.
-
Single origin and subsequent diversification of central Andean endemic Umbilicaria species.
-
Size and structure of yeast chromosomal DNA.
-
Skeletal muscle Nur77 expression enhances oxidative metabolism and substrate utilization.
-
Social affiliation predicts mitochondrial DNA copy number in female rhesus macaques.
-
Sources, mechanisms, and consequences of chemical-induced mitochondrial toxicity.
-
Species delimitation in lemurs: multiple genetic loci reveal low levels of species diversity in the genus Cheirogaleus.
-
Species discovery and validation in a cryptic radiation of endangered primates: coalescent-based species delimitation in Madagascar's mouse lemurs.
-
Staphylococcus aureus sepsis and mitochondrial accrual of the 8-oxoguanine DNA glycosylase DNA repair enzyme in mice.
-
Staphylococcus aureus sepsis induces early renal mitochondrial DNA repair and mitochondrial biogenesis in mice.
-
Stat3 binds to mtDNA and regulates mitochondrial gene expression in keratinocytes.
-
Structural insight and characterization of human Twinkle helicase in mitochondrial disease.
-
Support for a monophyletic Lemuriformes: Overcoming incongruence between data partitions
-
Temporal Stability of Molecular Diversity Measures in Natural Populations of Drosophila pseudoobscura and Drosophila persimilis.
-
Testing for contributions of mitochondrial DNA mutations to complex diseases.
-
The CO/HO system reverses inhibition of mitochondrial biogenesis and prevents murine doxorubicin cardiomyopathy.
-
The HO-1/CO system regulates mitochondrial-capillary density relationships in human skeletal muscle.
-
The Pleistocene history of the sheepshead minnow (Cyprinodon variegatus): Non-equilibrium evolutionary dynamics within a diversifying species complex.
-
The QPCR assay for analysis of mitochondrial DNA damage, repair, and relative copy number.
-
The cantharelloid clade: dealing with incongruent gene trees and phylogenetic reconstruction methods.
-
The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.
-
The ecology and epidemiology of malaria parasitism in wild chimpanzee reservoirs.
-
The effects of Cenozoic global change on squirrel phylogeny.
-
The effects of nucleotide substitution model assumptions on estimates of nonparametric bootstrap support.
-
The high mobility group protein Abf2p influences the level of yeast mitochondrial DNA recombination intermediates in vivo.
-
The long amplicon quantitative PCR for DNA damage assay as a sensitive method of assessing DNA damage in the environmental model, Atlantic killifish (Fundulus heteroclitus).
-
The mating type-specific homeodomain genes SXI1 alpha and SXI2a coordinately control uniparental mitochondrial inheritance in Cryptococcus neoformans.
-
The numbers of individual mitochondrial DNA molecules and mitochondrial DNA nucleoids in yeast are co-regulated by the general amino acid control pathway.
-
The quick and the dead: microbial demography at the yeast thermal limit.
-
The rate of mitochondrial mutagenesis is faster in mice than humans.
-
The role of cytoplasmic deoxycytidine kinase in the mitochondrial effects of the anti-human immunodeficiency virus compound, 2',3'-dideoxycytidine.
-
The socio-genetics of a complex society: female gelada relatedness patterns mirror association patterns in a multilevel society.
-
The spatial scale of genetic subdivision in populations of Ifremeria nautilei, a hydrothermal-vent gastropod from the southwest Pacific.
-
The ties that bind: genetic relatedness predicts the fission and fusion of social groups in wild African elephants.
-
The tobacco-specific nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) induces mitochondrial and nuclear DNA damage in Caenorhabditis elegans.
-
There is substantial agreement among interspecies estimates of DNA repair activity.
-
Toll-like receptor 4 mediates mitochondrial DNA damage and biogenic responses after heat-inactivated E. coli.
-
Transformation of Saccharomyces cerevisiae with nonhomologous DNA: illegitimate integration of transforming DNA into yeast chromosomes and in vivo ligation of transforming DNA to mitochondrial DNA sequences.
-
Transient hypoxia stimulates mitochondrial biogenesis in brain subcortex by a neuronal nitric oxide synthase-dependent mechanism.
-
UVC-induced mitochondrial degradation via autophagy correlates with mtDNA damage removal in primary human fibroblasts.
-
Unexpected link between mitochondrial DNA and T cell help in systemic lupus erythematosus.
-
Uniparental mitochondrial transmission in sexual crosses in Cryptococcus neoformans.
-
Unusual presentation of Kearns-Sayre syndrome in early childhood.
-
Using secondary structure to identify ribosomal numts: cautionary examples from the human genome.
-
Variation in modes and rates of evolution in nuclear and mitochondrial ribosomal DNA in the mushroom genus Amanita (Agaricales, Basidiomycota): phylogenetic implications.
-
Yeast RPO41 gene product is required for transcription and maintenance of the mitochondrial genome.
-
Keywords of People