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DNA repair and mutagenesis in vertebrate mitochondria: evidence for the asymmetric DNA strand inheritance

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.200501956openalex-snapshot

2‐Deoxyribonolactone Lesions in X‐ray‐Irradiated DNA: Quantitative Determination by Catalytic 5‐Methylene‐2‐furanone Release

inferredcites →https://doi.org/10.1002/bies.201800102openalex-snapshot

Known Unknowns of Mammalian Mitochondrial DNA Maintenance

inferredcites →https://doi.org/10.1002/jcp.10159openalex-snapshot

H2O2 induces translocation of APE/Ref‐1 to mitochondria in the Raji B‐cell line

inferredcites →https://doi.org/10.1002/stem.542openalex-snapshot

Mitochondrial DNA Integrity Is Essential For Mitochondrial Maturation During Differentiation of Neural Stem Cells

inferredcites →https://doi.org/10.1006/jmbi.1995.0430openalex-snapshot

Novel Mutagenic Properties of Abasic Sites inSaccharomyces cerevisiae

inferredcites →https://doi.org/10.1006/jmbi.1997.1268openalex-snapshot

DNA repair of UV photoproducts and mutagenesis in human mitochondrial DNA

inferredcites →https://doi.org/10.1007/3-540-30592-0openalex-snapshot

Free-Radical-Induced DNA Damage and Its Repair

inferredcites →https://doi.org/10.1007/978-0-387-72974-9openalex-snapshot

Oxidative Damage to Nucleic Acids

inferredcites →https://doi.org/10.1007/978-0-387-72974-9_4openalex-snapshot

Nucleotide Incision Repair: An Alternative and Ubiquitous Pathway to Handle Oxidative DNA Damage

inferredcites →https://doi.org/10.1007/978-1-4684-2898-8_26openalex-snapshot

Absence of a Pyrimidine Dimer Repair Mechanism for Mitochondrial DNA in Mouse and Human Cells

inferredcites →https://doi.org/10.1007/bf01734101openalex-snapshot

Mitochondrial DNA sequences of primates: Tempo and mode of evolution

inferredcites →https://doi.org/10.1007/s00239-001-0078-xopenalex-snapshot

Evolution of DNA Polymerase Families: Evidences for Multiple Gene Exchange Between Cellular and Viral Proteins

inferredcites →https://doi.org/10.1007/s00249-016-1114-5openalex-snapshot

Delaunay algorithm and principal component analysis for 3D visualization of mitochondrial DNA nucleoids by Biplane FPALM/dSTORM

inferredcites →https://doi.org/10.1016/0012-1606(74)90012-8openalex-snapshot

Mitochondrial DNA in Xenopus laevis oocytes

inferredcites →https://doi.org/10.1016/0014-4827(83)90114-3openalex-snapshot

Changes in D-loop frequency and superhelicity among the mitochondrial DNA molecules in relation to organelle biogenesis in oocytes of

inferredcites →https://doi.org/10.1016/0022-2836(74)90355-6openalex-snapshot

Mechanism of mitochondrial DNA replication in mouse L-cells: Asynchronous replication of strands, segregation of circular daughter molecules, aspects of topology and turnover of an initiation sequence

inferredcites →https://doi.org/10.1016/0027-5107(86)90081-3openalex-snapshot

Site-specific mutagenesis in vivo by single methylated or deaminated purine bases

inferredcites →https://doi.org/10.1016/0027-5107(90)90153-uopenalex-snapshot

Why do O6-alkylguanine and O4-alkylthymine miscode? The relationship between the structure of DNA containing O6-alkylguanine and O4-alkylthymine and the mutagenic properties of these bases

inferredcites →https://doi.org/10.1016/0092-8674(82)90049-6openalex-snapshot

Replication of animal mitochondrial DNA

inferredcites →https://doi.org/10.1016/0168-9525(93)90089-zopenalex-snapshot

Mutagenesis by 8-oxoguanine: an enemy within

inferredcites →https://doi.org/10.1016/0531-5565(80)90010-8openalex-snapshot

Mitochondrial role in cell aging

inferredcites →https://doi.org/10.1016/0925-4439(95)00024-xopenalex-snapshot

Mitochondrial decay in aging

inferredcites →https://doi.org/10.1016/b978-0-12-394625-6.00002-7openalex-snapshot

Mitochondrial DNA Mutations in Aging

inferredcites →https://doi.org/10.1016/j.ajhg.2008.07.004openalex-snapshot

Pathogenic Mitochondrial DNA Mutations Are Common in the General Population

inferredcites →https://doi.org/10.1016/j.bbabio.2009.09.005openalex-snapshot

Mitochondrial DNA mutations and human disease

inferredcites →https://doi.org/10.1016/j.bbagen.2009.07.007openalex-snapshot

Functional complementation of mitochondrial DNAs: Mobilizing mitochondrial genetics against dysfunction

inferredcites →https://doi.org/10.1016/j.bbagrm.2011.11.005openalex-snapshot

Mitochondrial DNA nucleoid structure

inferredcites →https://doi.org/10.1016/j.canlet.2012.01.016openalex-snapshot

Oxidatively induced DNA damage: Mechanisms, repair and disease

inferredcites →https://doi.org/10.1016/j.cell.2006.07.003openalex-snapshot

MutLα: At the Cutting Edge of Mismatch Repair

inferredcites →https://doi.org/10.1016/j.celrep.2014.05.046openalex-snapshot

In Vitro-Reconstituted Nucleoids Can Block Mitochondrial DNA Replication and Transcription

inferredcites →https://doi.org/10.1016/j.dnarep.2005.08.004openalex-snapshot

Monoclonal B-cell hyperplasia and leukocyte imbalance precede development of B-cell malignancies in uracil-DNA glycosylase deficient mice

inferredcites →https://doi.org/10.1016/j.dnarep.2006.08.001openalex-snapshot

Major oxidative products of cytosine are substrates for the nucleotide incision repair pathway

inferredcites →https://doi.org/10.1016/j.dnarep.2006.10.010openalex-snapshot

Intracellular trafficking and regulation of mammalian AP-endonuclease 1 (APE1), an essential DNA repair protein

inferredcites →https://doi.org/10.1016/j.dnarep.2009.01.021openalex-snapshot

Novel DNA mismatch-repair activity involving YB-1 in human mitochondria

inferredcites →https://doi.org/10.1016/j.dnarep.2009.03.001openalex-snapshot

Targeted deletion of the genes encoding NTH1 and NEIL1 DNA N-glycosylases reveals the existence of novel carcinogenic oxidative damage to DNA

inferredcites →https://doi.org/10.1016/j.dnarep.2009.07.008openalex-snapshot

Evidence for a role of FEN1 in maintaining mitochondrial DNA integrity

inferredcites →https://doi.org/10.1016/j.dnarep.2011.12.001openalex-snapshot

Lack of the DNA glycosylases MYH and OGG1 in the cancer prone double mutant mouse does not increase mitochondrial DNA mutagenesis

inferredcites →https://doi.org/10.1016/j.dnarep.2012.06.002openalex-snapshot

Oxidants and not alkylating agents induce rapid mtDNA loss and mitochondrial dysfunction

inferredcites →https://doi.org/10.1016/j.dnarep.2015.01.003openalex-snapshot

Suppression of oxidative phosphorylation in mouse embryonic fibroblast cells deficient in apurinic/apyrimidinic endonuclease

inferredcites →https://doi.org/10.1016/j.exger.2014.03.027openalex-snapshot

In D-loop: 40years of mitochondrial 7S DNA

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2010.03.025openalex-snapshot

Oxidatively generated base damage to cellular DNA

inferredcites →https://doi.org/10.1016/j.gde.2016.03.005openalex-snapshot

Human mitochondrial DNA replication machinery and disease

inferredcites →https://doi.org/10.1016/j.jmb.2006.02.073openalex-snapshot

A Novel Processive Mechanism for DNA Synthesis Revealed by Structure, Modeling and Mutagenesis of the Accessory Subunit of Human Mitochondrial DNA Polymerase

inferredcites →https://doi.org/10.1016/j.jmb.2008.01.035openalex-snapshot

Structure–Function Defects of the TWINKLE Linker Region in Progressive External Ophthalmoplegia

inferredcites →https://doi.org/10.1016/j.jmb.2010.09.015openalex-snapshot

Translesion Synthesis across Abasic Lesions by Human B-Family and Y-Family DNA Polymerases α, δ, η, ι, κ, and REV1

inferredcites →https://doi.org/10.1016/j.mad.2004.07.009openalex-snapshot

The role of oxidative damage and stress in aging

inferredcites →https://doi.org/10.1016/j.mito.2007.06.004openalex-snapshot

Mammalian mitochondrial nucleoids: Organizing an independently minded genome

inferredcites →https://doi.org/10.1016/j.mito.2017.09.002openalex-snapshot

Metabolism and DNA repair shape a specific modification pattern in mitochondrial DNA

inferredcites →https://doi.org/10.1016/j.molcel.2005.05.002openalex-snapshot

A Bidirectional Origin of Replication Maps to the Major Noncoding Region of Human Mitochondrial DNA

inferredcites →https://doi.org/10.1016/j.molcel.2008.09.024openalex-snapshot

Human DNA2 Is a Mitochondrial Nuclease/Helicase for Efficient Processing of DNA Replication and Repair Intermediates

inferredcites →https://doi.org/10.1016/j.molcel.2008.11.007openalex-snapshot

DNA2 Resolves Expanding Flap in Mitochondrial Base Excision Repair

inferredcites →https://doi.org/10.1016/j.molcel.2009.12.021openalex-snapshot

Mitochondrial RNA Polymerase Is Needed for Activation of the Origin of Light-Strand DNA Replication

inferredcites →https://doi.org/10.1016/j.molcel.2016.01.028openalex-snapshot

The Mitochondrial Basis of Aging

inferredcites →https://doi.org/10.1016/j.molcel.2017.11.033openalex-snapshot

Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA

inferredcites →https://doi.org/10.1016/j.mrfmmm.2003.07.002openalex-snapshot

Mutagenicity, toxicity and repair of DNA base damage induced by oxidation

inferredcites →https://doi.org/10.1016/j.mrfmmm.2003.09.001openalex-snapshot

Oxidative damage to DNA: formation, measurement and biochemical features

inferredcites →https://doi.org/10.1016/j.mrfmmm.2005.12.012openalex-snapshot

Origins of human mitochondrial point mutations as DNA polymerase γ-mediated errors

inferredcites →https://doi.org/10.1016/j.tcb.2018.11.004openalex-snapshot

The Cellular Mitochondrial Genome Landscape in Disease

inferredcites →https://doi.org/10.1016/j.tig.2005.11.007openalex-snapshot

Bacteriophage origins of mitochondrial replication and transcription proteins

inferredcites →https://doi.org/10.1016/j.tim.2005.08.012openalex-snapshot

Viral proteins functioning in organelles: a cryptic origin?

inferredcites →https://doi.org/10.1016/s0006-3495(98)77988-3openalex-snapshot

Geometry and Physics of Catenanes Applied to the Study of DNA Replication

inferredcites →https://doi.org/10.1016/s0021-9258(18)37787-1openalex-snapshot

Mitochondrial endonuclease activities specific for apurinic/apyrimidinic sites in DNA from mouse cells.

inferredcites →https://doi.org/10.1016/s0021-9258(18)42629-4openalex-snapshot

Purification and identification of subunit structure of the human mitochondrial DNA polymerase.

inferredcites →https://doi.org/10.1016/s0021-9258(20)30047-8openalex-snapshot

Unified catalytic mechanism for DNA glycosylases

inferredcites →https://doi.org/10.1016/s0027-5107(00)00022-1openalex-snapshot

p53 mutational spectra and the role of methylated CpG sequences

inferredcites →https://doi.org/10.1016/s0079-6603(08)60800-4openalex-snapshot

DNA Glycosylases, Endonucleases for Apurinic/Apyrimidinic Sites, and Base Excision-Repair

inferredcites →https://doi.org/10.1016/s0092-8674(00)80688-1openalex-snapshot

Coupled Leading- and Lagging-Strand Synthesis of Mammalian Mitochondrial DNA

inferredcites →https://doi.org/10.1016/s0300-483x(00)00307-3openalex-snapshot

Ultrasensitive and specific detection methods for exocylic DNA adducts: Markers for lipid peroxidation and oxidative stress

inferredcites →https://doi.org/10.1016/s0891-5849(99)00239-7openalex-snapshot

Polynucleotide degradation during early stage response to oxidative stress is specific to mitochondria

inferredcites →https://doi.org/10.1016/s0921-8777(00)00068-9openalex-snapshot

Mitochondrial localization of APE/Ref-1 in thyroid cells

inferredcites →https://doi.org/10.1016/s0921-8777(97)00008-6openalex-snapshot

DNA glycosylases

inferredcites →https://doi.org/10.1016/s1097-2765(03)00088-1openalex-snapshot

Failure to Produce Mitochondrial DNA Results in Embryonic Lethality in Rnaseh1 Null Mice

inferredcites →https://doi.org/10.1021/ar700245eopenalex-snapshot

Oxidatively Generated Damage to the Guanine Moiety of DNA: Mechanistic Aspects and Formation in Cells

inferredcites →https://doi.org/10.1021/bi00210a031openalex-snapshot

Mutagenic and genotoxic effects of three vinyl chloride-induced DNA lesions: 1,N6-ethenoadenine, 3,N4-ethenocytosine, and 4-amino-5-(imidazol-2-yl)imidazole

inferredcites →https://doi.org/10.1021/bi00713a035openalex-snapshot

Heat-induced deamination of cytosine residues in deoxyribonucleic acid

inferredcites →https://doi.org/10.1021/bi00749a020openalex-snapshot

Heat-induced depyrimidination of deoxyribonucleic acid in neutral solution

inferredcites →https://doi.org/10.1021/bi00769a019openalex-snapshot

Rate of chain breakage at apurinic sites in double-stranded deoxyribonucleic acid

inferredcites →https://doi.org/10.1021/bi960001xopenalex-snapshot

Accelerated Deamination of Cytosine Residues in UV-Induced Cyclobutane Pyrimidine Dimers Leads to CC→TT Transitions

inferredcites →https://doi.org/10.1021/bi960170hopenalex-snapshot

1,N6-Ethenodeoxyadenosine, a DNA Adduct Highly Mutagenic in Mammalian Cells

inferredcites →https://doi.org/10.1021/bi9811922openalex-snapshot

Fragmented Mitochondrial DNA Is the Predominant Carrier of Oxidized DNA Bases

inferredcites →https://doi.org/10.1021/tx00036a005openalex-snapshot

Endogenous DNA adducts: Potential and paradox

inferredcites →https://doi.org/10.1038/264333a0openalex-snapshot

All oxygens in nucleic acids react with carcinogenic ethylating agents

inferredcites →https://doi.org/10.1038/362709a0openalex-snapshot

Instability and decay of the primary structure of DNA

inferredcites →https://doi.org/10.1038/415183aopenalex-snapshot

Alternative nucleotide incision repair pathway for oxidative DNA damage

inferredcites →https://doi.org/10.1038/90058openalex-snapshot

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

inferredcites →https://doi.org/10.1038/ng.2501openalex-snapshot

Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease

inferredcites →https://doi.org/10.1038/ng1778openalex-snapshot

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons

inferredcites →https://doi.org/10.1038/nrc3365openalex-snapshot

Mitochondria and cancer

inferredcites →https://doi.org/10.1038/nrm3822openalex-snapshot

Understanding nucleotide excision repair and its roles in cancer and ageing

inferredcites →https://doi.org/10.1038/nrm3877openalex-snapshot

Mitochondrial dynamics and inheritance during cell division, development and disease

inferredcites →https://doi.org/10.1038/s41598-017-10843-8openalex-snapshot

Live imaging reveals the dynamics and regulation of mitochondrial nucleoids during the cell cycle in Fucci2-HeLa cells

inferredcites →https://doi.org/10.1038/sj.emboj.7600257openalex-snapshot

Reconstitution of a minimal mtDNA replisome in vitro

inferredcites →https://doi.org/10.1038/sj.emboj.7601392openalex-snapshot

Replication of vertebrate mitochondrial DNA entails transient ribonucleotide incorporation throughout the lagging strand

inferredcites →https://doi.org/10.1038/sj.onc.1206178openalex-snapshot

Dynamics and diversions in base excision DNA repair of oxidized abasic lesions

inferredcites →https://doi.org/10.1042/bj20081386openalex-snapshot

How mitochondria produce reactive oxygen species

inferredcites →https://doi.org/10.1042/ebc20170100openalex-snapshot

Mitochondrial DNA replication in mammalian cells: overview of the pathway

inferredcites →https://doi.org/10.1046/j.1365-2559.1998.00541.xopenalex-snapshot

Expression and subcellular localization of human AP endonuclease 1 (HAP1/Ref‐1) protein: a basis for its role in human disease

inferredcites →https://doi.org/10.1073/pnas.0805399105openalex-snapshot

Human mitochondrial RNA polymerase primes lagging-strand DNA synthesis in vitro

inferredcites →https://doi.org/10.1073/pnas.1109263108openalex-snapshot

Super-resolution microscopy reveals that mammalian mitochondrial nucleoids have a uniform size and frequently contain a single copy of mtDNA

inferredcites →https://doi.org/10.1073/pnas.1119738109openalex-snapshot

Mammalian transcription factor A is a core component of the mitochondrial transcription machinery

inferredcites →https://doi.org/10.1073/pnas.1121558109openalex-snapshot

Correlative 3D superresolution fluorescence and electron microscopy reveal the relationship of mitochondrial nucleoids to membranes

inferredcites →https://doi.org/10.1073/pnas.1301951110openalex-snapshot

Dynamics of nucleoid structure regulated by mitochondrial fission contributes to cristae reformation and release of cytochrome c

inferredcites →https://doi.org/10.1073/pnas.1305624110openalex-snapshot

Uracil in duplex DNA is a substrate for the nucleotide incision repair pathway in human cells

inferredcites →https://doi.org/10.1073/pnas.1314970111openalex-snapshot

Transcription could be the key to the selection advantage of mitochondrial deletion mutants in aging

inferredcites →https://doi.org/10.1073/pnas.1419651112openalex-snapshot

Extensive tissue-related and allele-related mtDNA heteroplasmy suggests positive selection for somatic mutations

inferredcites →https://doi.org/10.1073/pnas.1503653112openalex-snapshot

Primer retention owing to the absence of RNase H1 is catastrophic for mitochondrial DNA replication

inferredcites →https://doi.org/10.1073/pnas.1512131112openalex-snapshot

Cross-strand binding of TFAM to a single mtDNA molecule forms the mitochondrial nucleoid

inferredcites →https://doi.org/10.1073/pnas.1600537113openalex-snapshot

Pathological ribonuclease H1 causes R-loop depletion and aberrant DNA segregation in mitochondria

inferredcites →https://doi.org/10.1073/pnas.69.12.3810openalex-snapshot

Replication of Mitochondrial DNA in Mouse L Cells and Their Thymidine Kinase - Derivatives: Displacement Replication on a Covalently-Closed Circular Template

inferredcites →https://doi.org/10.1073/pnas.75.2.735openalex-snapshot

Human mitochondrial DNA: analysis of 7S DNA from the origin of replication.

inferredcites →https://doi.org/10.1073/pnas.85.17.6465openalex-snapshot

Normal oxidative damage to mitochondrial and nuclear DNA is extensive.

inferredcites →https://doi.org/10.1073/pnas.89.8.3380openalex-snapshot

Endogenous oxidative damage of deoxycytidine in DNA.

inferredcites →https://doi.org/10.1073/pnas.91.25.11899openalex-snapshot

Mutagenic potency of exocyclic DNA adducts: marked differences between Escherichia coli and simian kidney cells.

inferredcites →https://doi.org/10.1073/pnas.94.2.514openalex-snapshot

Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress

inferredcites →https://doi.org/10.1073/pnas.95.21.12244openalex-snapshot

Identification of 5′-deoxyribose phosphate lyase activity in human DNA polymerase γ and its role in mitochondrial base excision repair in vitro

inferredcites →https://doi.org/10.1073/pnas.95.7.3578openalex-snapshot

Oxidized, deaminated cytosines are a source of C → T transitions in vivo

inferredcites →https://doi.org/10.1074/jbc.274.21.14779openalex-snapshot

Functional Interactions of Mitochondrial DNA Polymerase and Single-stranded DNA-binding Protein

inferredcites →https://doi.org/10.1074/jbc.275.16.11678openalex-snapshot

Formation of the Main UV-induced Thymine Dimeric Lesions within Isolated and Cellular DNA as Measured by High Performance Liquid Chromatography-Tandem Mass Spectrometry

inferredcites →https://doi.org/10.1074/jbc.m109.069591openalex-snapshot

Identification and Characterization of Mitochondrial Targeting Sequence of Human Apurinic/Apyrimidinic Endonuclease 1

inferredcites →https://doi.org/10.1074/jbc.m112146200openalex-snapshot

Yeast Rev1 Protein Is a G Template-specific DNA Polymerase

inferredcites →https://doi.org/10.1074/jbc.m301617200openalex-snapshot

Compromised Incision of Oxidized Pyrimidines in Liver Mitochondria of Mice Deficient in NTH1 and OGG1 Glycosylases

inferredcites →https://doi.org/10.1074/jbc.m306981200openalex-snapshot

TWINKLE Has 5′ → 3′ DNA Helicase Activity and Is Specifically Stimulated by Mitochondrial Single-stranded DNA-binding Protein

inferredcites →https://doi.org/10.1074/jbc.m509730200openalex-snapshot

Functional Human Mitochondrial DNA Polymerase γ Forms a Heterotrimer

inferredcites →https://doi.org/10.1074/jbc.m803491200openalex-snapshot

Long Patch Base Excision Repair in Mammalian Mitochondrial Genomes

inferredcites →https://doi.org/10.1080/09553007714551241openalex-snapshot

Isolation of 2-deoxy- d -erythro-pentonic Acid from an Alkali-labile Site in γ-irradiated DNA

inferredcites →https://doi.org/10.1080/09553008414551341openalex-snapshot

Site of OH Radical Attack on Dihydrouracil and Some of Its Methyl Derivatives

inferredcites →https://doi.org/10.1080/10715769800300611openalex-snapshot

Age-associated change in mitochondrial DNA damage

inferredcites →https://doi.org/10.1083/jcb.200609158openalex-snapshot

The AAA+ protein ATAD3 has displacement loop binding properties and is involved in mitochondrial nucleoid organization

inferredcites →https://doi.org/10.1083/jcb.200712101openalex-snapshot

Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation

inferredcites →https://doi.org/10.1089/ars.2005.7.367openalex-snapshot

The Intracellular Localization of APE1/Ref-1: More than a Passive Phenomenon?

inferredcites →https://doi.org/10.1091/mbc.e02-07-0399openalex-snapshot

Composition and Dynamics of Human Mitochondrial Nucleoids

inferredcites →https://doi.org/10.1091/mbc.e11-05-0391openalex-snapshot

Knock-in reconstitution studies reveal an unexpected role of Cys-65 in regulating APE1/Ref-1 subcellular trafficking and function

inferredcites →https://doi.org/10.1091/mbc.e15-06-0390openalex-snapshot

Low doses of ultraviolet radiation and oxidative damage induce dramatic accumulation of mitochondrial DNA replication intermediates, fork regression, and replication initiation shift

inferredcites →https://doi.org/10.1093/carcin/13.11.1967openalex-snapshot

Repair of mitochondrial DNA after various types of DNA damage in Chinese hamster ovary cells

inferredcites →https://doi.org/10.1093/carcin/16.3.613openalex-snapshot

1,N6-Ethenodeoxyadenosine and 3,N4-ethenodeoxycytidine in liver DNA from humans and untreated rodents detected by immunoaffinity/32P-postlabelling

inferredcites →https://doi.org/10.1093/carcin/bgi330openalex-snapshot

Polymorphisms in nucleotide excision repair genes, smoking and breast cancer in African Americans and whites: a population-based case–control study

inferredcites →https://doi.org/10.1093/hmg/ddp327openalex-snapshot

Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair

inferredcites →https://doi.org/10.1093/hmg/ddr209openalex-snapshot

Biochemical analysis of human POLG2 variants associated with mitochondrial disease

inferredcites →https://doi.org/10.1093/hmg/dds435openalex-snapshot

Universal heteroplasmy of human mitochondrial DNA

inferredcites →https://doi.org/10.1093/jrr/rru059openalex-snapshot

Significant disparity in base and sugar damage in DNA resulting from neutron and electron irradiation

inferredcites →https://doi.org/10.1093/molbev/msn050openalex-snapshot

Inverted Replication of Vertebrate Mitochondria

inferredcites →https://doi.org/10.1093/molbev/msr041openalex-snapshot

Discovery of Cyanophage Genomes Which Contain Mitochondrial DNA Polymerase

inferredcites →https://doi.org/10.1093/nar/23.5.761openalex-snapshot

Misincorporation of dAMP opposite 2-hydroxyadenine, an oxidative form of adenine

inferredcites →https://doi.org/10.1093/nar/24.7.1212openalex-snapshot

Sequences Attaching Loops of Nuclear and Mitochondrial DNA to Underlying Structures in Human Cells: The Role of Transcription Units

inferredcites →https://doi.org/10.1093/nar/25.4.750openalex-snapshot

Nuclear and mitochondrial uracil-DNA glycosylases are generated by alternative splicing and transcription from different positions in the UNG gene

inferredcites →https://doi.org/10.1093/nar/26.12.2917openalex-snapshot

Mitochondrial targeting of human DNA glycosylases for repair of oxidative DNA damage

inferredcites →https://doi.org/10.1093/nar/27.18.3638openalex-snapshot

Differential subcellular localization of human MutY homolog (hMYH) and the functional activity of adenine:8-oxoguanine DNA glycosylase

inferredcites →https://doi.org/10.1093/nar/28.10.2187openalex-snapshot

Hemicatenanes form upon inhibition of DNA replication

inferredcites →https://doi.org/10.1093/nar/28.20.3880openalex-snapshot

Mitochondrial DNA ligase III function is independent of Xrcc1

inferredcites →https://doi.org/10.1093/nar/28.6.1355openalex-snapshot

Identification of human MutY homolog (hMYH) as a repair enzyme for 2-hydroxyadenine in DNA and detection of multiple forms of hMYH located in nuclei and mitochondria

inferredcites →https://doi.org/10.1093/nar/29.17.3657openalex-snapshot

Mechanism of mammalian mitochondrial DNA replication: import of mitochondrial transcription factor A into isolated mitochondria stimulates 7S DNA synthesis

inferredcites →https://doi.org/10.1093/nar/gkh165openalex-snapshot

The major human AP endonuclease (Ape1) is involved in the nucleotide incision repair pathway

inferredcites →https://doi.org/10.1093/nar/gkh594openalex-snapshot

Structural insights by molecular dynamics simulations into specificity of the major human AP endonuclease toward the benzene-derived DNA adduct, pBQ-C

inferredcites →https://doi.org/10.1093/nar/gkl177openalex-snapshot

Identification and characterization of mitochondrial abasic (AP)-endonuclease in mammalian cells

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Oxidative stress induces degradation of mitochondrial DNA

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Differential regulation of full-length genome and a single-stranded 7S DNA along the cell cycle in human mitochondria

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Role of polynucleotide kinase/phosphatase in mitochondrial DNA repair

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39 Mitochondrial DNA Replication

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Base Excision Repair

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The Maintenance of Mitochondrial DNA Integrity--Critical Analysis and Update

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Human Mitochondrial DNA Replication

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The Biologic Clock: The Mitochondria?

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Is there more to aging than mitochondrial DNA and reactive oxygen species?

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ER-mitochondria contacts couple mtDNA synthesis with mitochondrial division in human cells

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Anchoring of DNA to the bacterial cytoplasmic membrane through cotranscriptional synthesis of polypeptides encoding membrane proteins or proteins for export: a mechanism of plasmid hypernegative supercoiling in mutants deficient in DNA topoisomerase I

inferredcites →https://doi.org/10.1128/mcb.00237-17openalex-snapshot

DNA Polymerase Beta Participates in Mitochondrial DNA Repair

inferredcites →https://doi.org/10.1128/mcb.01834-08openalex-snapshot

Human Dna2 Is a Nuclear and Mitochondrial DNA Maintenance Protein

inferredcites →https://doi.org/10.1128/mcb.19.5.3869openalex-snapshot

The Human DNA Ligase III Gene Encodes Nuclear and Mitochondrial Proteins

inferredcites →https://doi.org/10.1128/mcb.26.10.3935-3941.2006openalex-snapshot

Early Embryonic Lethality Due to Targeted Inactivation of DNA Ligase III

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Maintenance and Expression of Mammalian Mitochondrial DNA

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Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases

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REPAIR OF OXIDATIVE DAMAGE TO DNA: Enzymology and Biology

inferredcites →https://doi.org/10.1146/annurev.biochem.69.1.497openalex-snapshot

DNA Replication Fidelity

inferredcites →https://doi.org/10.1146/annurev.biochem.71.110601.135425openalex-snapshot

DNA Replication in Eukaryotic Cells

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Variable penetrance of metabolic phenotypes and development of high-fat diet-induced adiposity in NEIL1-deficient mice

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Cardiac overexpression of 8-oxoguanine DNA glycosylase 1 protects mitochondrial DNA and reduces cardiac fibrosis following transaortic constriction

inferredcites →https://doi.org/10.1152/ajplung.00443.2001openalex-snapshot

Enhanced mtDNA repair capacity protects pulmonary artery endothelial cells from oxidant-mediated death

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Deficiencies in Mouse Myh and Ogg1 Result in Tumor Predisposition and G to T Mutations in Codon 12 of the K-Ras Oncogene in Lung Tumors

inferredcites →https://doi.org/10.1242/jcs.213538openalex-snapshot

Mitochondrial maintenance under oxidative stress depends on mitochondrially localised α-OGG1

inferredcites →https://doi.org/10.1371/journal.pbio.2000410openalex-snapshot

Selection for Mitochondrial Quality Drives Evolution of the Germline

inferredcites →https://doi.org/10.1371/journal.pgen.1003794openalex-snapshot

Ultra-Sensitive Sequencing Reveals an Age-Related Increase in Somatic Mitochondrial Mutations That Are Inconsistent with Oxidative Damage

inferredcites →https://doi.org/10.1371/journal.pgen.1003974openalex-snapshot

Oxidative Stress Is Not a Major Contributor to Somatic Mitochondrial DNA Mutations

inferredcites →https://doi.org/10.1371/journal.pgen.1003990openalex-snapshot

Somatic mtDNA Mutation Spectra in the Aging Human Putamen

inferredcites →https://doi.org/10.1371/journal.pgen.1004620openalex-snapshot

Clonal Expansion of Early to Mid-Life Mitochondrial DNA Point Mutations Drives Mitochondrial Dysfunction during Human Ageing

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8-Oxoguanine DNA Glycosylase (OGG1) Deficiency Increases Susceptibility to Obesity and Metabolic Dysfunction

inferredcites →https://doi.org/10.1371/journal.pone.0051776openalex-snapshot

Highly Mutagenic Exocyclic DNA Adducts Are Substrates for the Human Nucleotide Incision Repair Pathway

inferredcites →https://doi.org/10.1371/journal.pone.0075201openalex-snapshot

Deficiency in Repair of the Mitochondrial Genome Sensitizes Proliferating Myoblasts to Oxidative Damage

inferredcites →https://doi.org/10.1371/journal.pone.0106654openalex-snapshot

The Inversion of the Control Region in Three Mitogenomes Provides Further Evidence for an Asymmetric Model of Vertebrate mtDNA Replication

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Mutagenesis and carcinogenesis caused by the oxidation of nucleic acids

inferredcites →https://doi.org/10.1523/jneurosci.0852-11.2011openalex-snapshot

Mitochondrial DNA Damage Level Determines Neural Stem Cell Differentiation Fate

inferredcites →https://doi.org/10.1534/genetics.105.051029openalex-snapshot

Saccharomyces cerevisiae Polymerase ζ Functions in Mitochondria

inferredcites →https://doi.org/10.2307/3574690openalex-snapshot

Thymine Fragment Damage Retained in the DNA Polynucleotide Chain after Gamma Irradiation in Aerated Solutions. II

inferredcites →https://doi.org/10.3109/07357908409104376openalex-snapshot

Methylation of the O6Position of Guanine in DNA is the Most Likely Initiating Event in Carcinogenesis by Methylating Agents

inferredcites →https://doi.org/10.3109/19401736.2015.1089539openalex-snapshot

The efficiency of the translesion synthesis across abasic sites by mitochondrial DNA polymerase is low in mitochondria of 3T3 cells

inferredcites →https://doi.org/10.4061/2010/850234openalex-snapshot

Selective Incision of the α‐N5‐Methyl‐Formamidopyrimidine Anomer by Escherichia coli Endonuclease IV

inferredcites →https://doi.org/10.4161/23723548.2014.960754openalex-snapshot

PrimPol—A new polymerase on the block

inferredcites →https://doi.org/10.7554/elife.02935openalex-snapshot

Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3892/mmr.2025.13443openalex-snapshot

Mitochondrial DNA copy number alterations: Key players in the complexity of glioblastoma (Review)

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.