| scholarly article | Q13442814 |
| P2093 | author name string | Campbell C | |
| Thyagarajan B | |||
| Padua RA | |||
| P2860 | cites work | A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 |
| Sequence and organization of the human mitochondrial genome | Q27860659 | ||
| The double-strand-break repair model for recombination | Q28267259 | ||
| Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations | Q28283523 | ||
| Retention of both parental mitochondrial DNA species in mouse-Chinese hamster somatic cell hybrids. | Q54482196 | ||
| KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION | Q56568036 | ||
| MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROME | Q56864006 | ||
| Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy | Q28292821 | ||
| Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer | Q28294774 | ||
| Sequence and gene organization of mouse mitochondrial DNA | Q29618227 | ||
| A homolog of Escherichia coli RecA protein in plastids of higher plants | Q31076611 | ||
| DNA Strand-Transfer Activity in Pea (Pisum sativum L.) Chloroplasts | Q34149565 | ||
| Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by a kinetic PCR analysis | Q34196561 | ||
| Treatment of pea (Pisum sativum L.) protoplasts with DNA-damaging agents induces a 39-kilodalton chloroplast protein immunologically related to Escherichia coli RecA. | Q34335774 | ||
| Homologous recombination intermediates between two duplex DNA catalysed by human cell extracts | Q34692824 | ||
| An update on the mitochondrial-DNA mutation hypothesis of cell aging | Q35340996 | ||
| Mitochondrial DNA damage by anticancer agents | Q35531430 | ||
| Mitochondrial DNA mutation associated with aging and degenerative disease | Q35659526 | ||
| Inhibition of chloroplast DNA recombination and repair by dominant negative mutants of Escherichia coli RecA. | Q36551272 | ||
| Repair of deletions and double-strand gaps by homologous recombination in a mammalian in vitro system | Q36681196 | ||
| Test of the double-strand-break repair model of recombination in Xenopus laevis oocytes | Q36807903 | ||
| Hyperactive recombination in the mitochondrial DNA of the natural death nuclear mutant of Neurospora crassa | Q36825116 | ||
| Efficient repair of HO-induced chromosomal breaks in Saccharomyces cerevisiae by recombination between flanking homologous sequences | Q36845568 | ||
| Homologous recombination catalyzed by human cell extracts | Q36887489 | ||
| Characterization of an ATP-dependent DNA strand transferase from human cells | Q36920812 | ||
| Intermolecular homologous recombination between transfected sequences in mammalian cells is primarily nonconservative | Q36922440 | ||
| Neurological disorders due to mutations of the mitochondrial genome | Q37070280 | ||
| Transfection and homologous recombination involving single-stranded DNA substrates in mammalian cells and nuclear extracts | Q37392520 | ||
| The absence of a pyrimidine dimer repair mechanism in mammalian mitochondria | Q37452565 | ||
| Topography and kinetics of genetic recombination in Escherichia coli treated with psoralen and light | Q37586660 | ||
| Evidence for increased in vitro recombination with insertion of human hepatitis B virus DNA | Q37608976 | ||
| Stable DNA heteroduplex formation catalyzed by the Escherichia coli RecA protein in the absence of ATP hydrolysis | Q37655391 | ||
| Energetics of RecA-mediated recombination reactions. Without ATP hydrolysis RecA can mediate polar strand exchange but is unable to recycle | Q38338289 | ||
| Organelle transformation | Q39337418 | ||
| Replication of animal mitochondrial DNA. | Q40103664 | ||
| Analysis of DNA damage and repair in murine leukemia L1210 cells using a quantitative polymerase chain reaction assay | Q40423060 | ||
| Mitochondrial DNA mutations in human degenerative diseases and aging | Q40437251 | ||
| Two alternative pathways of double-strand break repair that are kinetically separable and independently modulated | Q40678286 | ||
| Why does RecA protein hydrolyse ATP? | Q40682056 | ||
| Repair of N-methylpurines in the mitochondrial DNA of xeroderma pigmentosum complementation group D cells | Q41554888 | ||
| Sequence analysis of mitochondrial chloramphenicol resistance mutations in Chinese hamster cells | Q41579495 | ||
| Repair of double-stranded DNA breaks by homologous DNA fragments during transfer of DNA into mouse L cells | Q41750735 | ||
| Intermolecular recombination between DNAs introduced into mouse L cells is mediated by a nonconservative pathway that leads to crossover products | Q41750743 | ||
| Mitochondrial DNA damage by bleomycin | Q41771739 | ||
| Elevated levels of homologous DNA recombination activity in the regenerating rat liver | Q42518209 | ||
| Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies | Q43484805 | ||
| Isolation of highly purified rat liver mitochondria for the study of the biotransformation of drugs (author's transl) | Q45213442 | ||
| Repair of mitochondrial DNA after various types of DNA damage in Chinese hamster ovary cells | Q46434994 | ||
| The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants | Q50192890 | ||
| P433 | issue | 44 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | mitochondrion | Q39572 |
| P304 | page(s) | 27536-27543 | |
| P577 | publication date | 1996-11-01 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Mammalian mitochondria possess homologous DNA recombination activity | |
| P478 | volume | 271 |
| Q46030185 | "Patchy-tachy" leads to false positives for recombination. |
| Q36643808 | 'To repair or not to repair - no longer a question': repair of mitochondrial DNA shielding against age and cancer |
| Q46535835 | A century of mitochondrial research: achievements and perspectives |
| Q42558198 | A multipartite mitochondrial genome in the potato cyst nematode Globodera pallida. |
| Q28661305 | Afrobatrachian mitochondrial genomes: genome reorganization, gene rearrangement mechanisms, and evolutionary trends of duplicated and rearranged genes |
| Q73439545 | An Arabidopsis homologue of bacterial RecA that complements an E. coli recA deletion is targeted to plant mitochondria |
| Q77922003 | An alcoholic binge causes massive degradation of hepatic mitochondrial DNA in mice |
| Q34586803 | Analysis of repeat-mediated deletions in the mitochondrial genome of Saccharomyces cerevisiae |
| Q35873907 | Animal models of mitochondrial DNA transactions in disease and ageing |
| Q44041085 | Base composition at mtDNA boundaries suggests a DNA triple helix model for human mitochondrial DNA large-scale rearrangements. |
| Q73702426 | Can paternal mtDNA be inherited? |
| Q40023798 | Characterization of a Holliday junction-resolving enzyme from Schizosaccharomyces pombe |
| Q34625273 | Chimeric mitochondrial minichromosomes of the human body louse, Pediculus humanus: Evidence for homologous and non-homologous recombination |
| Q51971435 | Chlamydomonas chloroplasts can use short dispersed repeats and multiple pathways to repair a double-strand break in the genome. |
| Q60585044 | Comparison of Oxidative Base Damage in Mitochondrial and Nuclear DNA |
| Q46961729 | Complete mitochondrial DNA sequence of the scallop Placopecten magellanicus: evidence of transposition leading to an uncharacteristically large mitochondrial genome |
| Q34235748 | Cytoplasmic inheritance and its implications for animal biotechnology |
| Q33740063 | DNA damage related crosstalk between the nucleus and mitochondria |
| Q34183328 | DNA repair deficiency in neurodegeneration. |
| Q37764794 | DNA repair in mammalian mitochondria: Much more than we thought? |
| Q37800526 | DNA repair in organelles: Pathways, organization, regulation, relevance in disease and aging |
| Q24547711 | Departure from neutrality at the mitochondrial NADH dehydrogenase subunit 2 gene in humans, but not in chimpanzees |
| Q33952475 | Direct evidence for homologous recombination in mussel (Mytilus galloprovincialis) mitochondrial DNA. |
| Q24307674 | Discovery of a novel function for human Rad51: maintenance of the mitochondrial genome |
| Q77830355 | Do animal mitochondrial genomes recombine? |
| Q34111837 | Do mitochondria recombine in humans? |
| Q24535778 | Dual localization of human DNA topoisomerase IIIalpha to mitochondria and nucleus |
| Q73674707 | Elevated homologous recombination activity in fanconi anemia fibroblasts |
| Q57765717 | Evidence for recombination in scorpion mitochondrial DNA (Scorpiones: Buthidae) |
| Q34588110 | Evidence for recombination of mitochondrial DNA in triploid crucian carp |
| Q37615504 | Evolution and inheritance of animal mitochondrial DNA: rules and exceptions |
| Q81731046 | Evolution of the mitochondrial genome in cephalochordata as inferred from complete nucleotide sequences from two epigonichthys species |
| Q28278871 | Evolutionary genetics: direct evidence of recombination in human mitochondrial DNA |
| Q28609384 | Expression of E. coli RecA targeted to mitochondria of human cells |
| Q36860559 | Extensive paternal mtDNA leakage in natural populations of Drosophila melanogaster |
| Q30387818 | Extreme variation in patterns of tandem repeats in mitochondrial control region of yellow-browed tits (Sylviparus modestus, Paridae) |
| Q35550624 | Forensics and Mitochondrial DNA: Applications, Debates, and Foundations |
| Q41543245 | Formation, prevention, and repair of DNA damage by iron/hydrogen peroxide |
| Q33793500 | Full mitochondrial genome sequences of two endemic Philippine hornbill species (Aves: Bucerotidae) provide evidence for pervasive mitochondrial DNA recombination |
| Q40866710 | Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell lines |
| Q36688667 | Gene therapy of the other genome: the challenges of treating mitochondrial DNA defects |
| Q34654570 | Homogenous repair of singlet oxygen-induced DNA damage in differentially transcribed regions and strands of human mitochondrial DNA. |
| Q24672162 | How clonal are human mitochondria? |
| Q34715943 | How good are indirect tests at detecting recombination in human mtDNA? |
| Q24316108 | Human Dna2 is a nuclear and mitochondrial DNA maintenance protein |
| Q37372049 | Human heart mitochondrial DNA is organized in complex catenated networks containing abundant four-way junctions and replication forks |
| Q77403432 | Human mitochondrial diseases: answering questions and questioning answers |
| Q37273617 | Intra- and inter-molecular recombination of mitochondrial DNA after in vivo induction of multiple double-strand breaks |
| Q35250582 | Intracellular mitochondrial triplasmy in a patient with two heteroplasmic base changes |
| Q34733032 | Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines |
| Q39728728 | Mammalian mitochondrial extracts possess DNA end-binding activity. |
| Q41653872 | Mammalian mitochondrial genetics: heredity, heteroplasmy and disease |
| Q27012566 | Mechanism of homologous recombination and implications for aging-related deletions in mitochondrial DNA |
| Q35833520 | Members of the RAD52 Epistasis Group Contribute to Mitochondrial Homologous Recombination and Double-Strand Break Repair in Saccharomyces cerevisiae |
| Q34786492 | Mhr1p-dependent Concatemeric Mitochondrial DNA Formation for Generating Yeast Mitochondrial Homoplasmic Cells |
| Q38044810 | Minimizing the damage: repair pathways keep mitochondrial DNA intact |
| Q36269768 | Mitochondria, oxidative DNA damage, and aging |
| Q27001150 | Mitochondrial DNA damage and its consequences for mitochondrial gene expression |
| Q36647425 | Mitochondrial DNA damage and the aging process: facts and imaginations. |
| Q47734660 | Mitochondrial DNA mutations as a fundamental mechanism in physiological declines associated with aging |
| Q37140173 | Mitochondrial DNA repair in aging and disease |
| Q33732604 | Mitochondrial DNA repair pathways. |
| Q46585553 | Mitochondrial DNA repair: a novel therapeutic target for heart failure |
| Q91715716 | Mitochondrial Homeostasis and Cellular Senescence |
| Q34044161 | Mitochondrial base excision repair assays |
| Q34282032 | Mitochondrial dysfunction due to oxidative mitochondrial DNA damage is reduced through cooperative actions of diverse proteins |
| Q28834072 | Mitochondrial genetic diversity, selection and recombination in a canine transmissible cancer |
| Q41857295 | Mitochondrial genome haplotype hypervariation within the isopod parasitic nematode Thaumamermis cosgrovei |
| Q27929976 | Mitochondrial genome maintenance: roles for nuclear nonhomologous end-joining proteins in Saccharomyces cerevisiae |
| Q33732618 | Mitochondrial mutagenesis in human cells and tissues |
| Q37369860 | Mitochondrial-associated metabolic disorders: foundations, pathologies and recent progress |
| Q45886386 | Modification of hepatic genomic DNA using RNA/DNA oligonucleotides |
| Q34617724 | Molecular evolution and recombination in gender-associated mitochondrial DNAs of the Manila clam Tapes philippinarum |
| Q35884861 | Molecular mechanisms for age-associated mitochondrial deficiency in skeletal muscle. |
| Q54708613 | Molecular phylogeny of Acanthochitonina (Mollusca: Polyplacophora: Chitonida): three new mitochondrial genomes, rearranged gene orders and systematics |
| Q35217458 | Mre11 is expressed in mammalian mitochondria where it binds to mitochondrial DNA. |
| Q45735853 | Near neutrality, rate heterogeneity, and linkage govern mitochondrial genome evolution in Atlantic cod (Gadus morhua) and other gadine fish |
| Q29394936 | New patterns of inheritance in mitochondrial disease |
| Q37219476 | Novel DNA mismatch-repair activity involving YB-1 in human mitochondria |
| Q42660873 | Novel repetitive structures, deviant protein-encoding sequences and unidentified ORFs in the mitochondrial genome of the brachiopod Lingula anatina. |
| Q33601092 | Oxidative DNA damage processing in nuclear and mitochondrial DNA. |
| Q41574624 | Principal Aspects Regarding the Maintenance of Mammalian Mitochondrial Genome Integrity. |
| Q33757916 | Prominent mitochondrial DNA recombination intermediates in human heart muscle. |
| Q46011603 | Quantitation of age-related mitochondrial DNA deletions in rat tissues shows that their pattern of accumulation differs from that of humans. |
| Q41532624 | RNA editing in metazoan mitochondria: staying fit without sex. |
| Q51709065 | Rapid concerted evolution in animal mitochondrial DNA. |
| Q36675812 | Rare and fleeting: an example of interspecific recombination in animal mitochondrial DNA. |
| Q33770958 | Rare creation of recombinant mtDNA haplotypes in mammalian tissues |
| Q54340472 | RecA-dependent DNA repair results in increased heteroplasmy of the Arabidopsis mitochondrial genome. |
| Q34613408 | Recombination in human mitochondrial DNA? |
| Q46356998 | Recombination or mutation rate heterogeneity? Implications for Mitochondrial Eve. |
| Q36845992 | Removal of oxidative DNA damage via FEN1-dependent long-patch base excision repair in human cell mitochondria |
| Q36390323 | Repair of mitochondrial DNA in aging and carcinogenesis |
| Q27026352 | Repair of persistent strand breaks in the mitochondrial genome |
| Q34609738 | Replicative advantage and tissue-specific segregation of RR mitochondrial DNA between C57BL/6 and RR heteroplasmic mice |
| Q33735624 | Role of tyrosyl-DNA phosphodiesterase (TDP1) in mitochondria |
| Q47652155 | Saccharomyces cerevisiae Mhr1 can bind Xho I-induced mitochondrial DNA double-strand breaks in vivo |
| Q80413970 | Segregation and recombination of a multipartite mitochondrial DNA in populations of the potato cyst nematode Globodera pallida |
| Q28767985 | The complete nucleotide sequence of a snake (Dinodon semicarinatus) mitochondrial genome with two identical control regions |
| Q22009425 | The human DNA ligase III gene encodes nuclear and mitochondrial proteins |
| Q29616111 | The incomplete natural history of mitochondria |
| Q30390916 | The mitochondrial genome of Paragyrodactylus variegatus (Platyhelminthes: Monogenea): differences in major non-coding region and gene order compared to Gyrodactylus |
| Q34420786 | The mitochondrial genome: mutation, selection and recombination. |
| Q43887789 | The nuclear genome is involved in heteroplasmy control in a mitochondrial mutant strain of Drosophila subobscura |
| Q38155694 | The role of TDP1 and APTX in mitochondrial DNA repair |
| Q34570691 | What do patterns of genetic variability reveal about mitochondrial recombination? |
| Q36497430 | Yeast mitochondrial HMG proteins: DNA-binding properties of the most evolutionarily divergent component of mitochondrial nucleoids |
| Q35059486 | mtDNA Mutations and Their Role in Aging, Diseases and Forensic Sciences |
| Q35807484 | mtDNA recombination in a natural population |
| Q43105116 | mtDNA recombination: what do in vitro data mean? |
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