On the public citation graph

DNA polymerases in the mitochondria A critical review of the evidence

0 signed · 214 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/ddrr.105openalex-snapshot

Polymerase gamma disease through the ages

inferredcites →https://doi.org/10.1002/em.20576openalex-snapshot

DNA repair in mammalian mitochondria: Much more than we thought?

inferredcites →https://doi.org/10.1002/humu.20824openalex-snapshot

Molecular and clinical genetics of mitochondrial diseases due to POLG mutations

inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05337.xopenalex-snapshot

Yeast mitochondrial DNA mutators with deficient proofreading exonucleolytic activity.

inferredcites →https://doi.org/10.1006/abbi.1999.1590openalex-snapshot

Identification of a β-like DNA Polymerase Activity in Bovine Heart Mitochondria

inferredcites →https://doi.org/10.1006/geno.1996.0490openalex-snapshot

Cloning and Characterization of the Human Mitochondrial DNA Polymerase, DNA Polymerase γ

inferredcites →https://doi.org/10.1006/geno.1999.5843openalex-snapshot

Cloning and Chromosomal Mapping of the Human DNA Polymerase θ (POLQ), the Eighth Human DNA Polymerase

inferredcites →https://doi.org/10.1006/geno.2000.6333openalex-snapshot

Construction of Transgenic Mice with Tissue-Specific Acceleration of Mitochondrial DNA Mutagenesis

inferredcites →https://doi.org/10.1007/s10549-011-1460-zopenalex-snapshot

Genetic variation in genes encoding for polymerase ζ subunits associates with breast cancer risk, tumour characteristics and survival

inferredcites →https://doi.org/10.1016/0006-291x(87)90767-4openalex-snapshot

Evidence for a direct role of the DNA polymerase gamma in the replication of the human mitochondrial DNA in vitro

inferredcites →https://doi.org/10.1016/0092-8674(92)90431-bopenalex-snapshot

In situ hybridization to the crithidia fasciculata kinetoplast reveals two antipodal sites involved in kinetoplast DNA replication

inferredcites →https://doi.org/10.1016/j.bbrc.2012.12.119openalex-snapshot

Role of polymerase η in mitochondrial mutagenesis of Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1016/j.cell.2008.06.016openalex-snapshot

A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology

inferredcites →https://doi.org/10.1016/j.dnarep.2005.07.009openalex-snapshot

Mitochondrial DNA integrity is not dependent on DNA polymerase-β activity

inferredcites →https://doi.org/10.1016/j.dnarep.2005.08.009openalex-snapshot

Structural insight into the DNA polymerase β deoxyribose phosphate lyase mechanism

inferredcites →https://doi.org/10.1016/j.dnarep.2007.06.005openalex-snapshot

Analysis of Rev1p and Pol ζ in mitochondrial mutagenesis suggests an alternative pathway of damage tolerance

inferredcites →https://doi.org/10.1016/j.dnarep.2007.08.005openalex-snapshot

DNA polymerase θ (POLQ) can extend from mismatches and from bases opposite a (6-4) photoproduct

inferredcites →https://doi.org/10.1016/j.dnarep.2010.04.010openalex-snapshot

Crosstalk between replicative and translesional DNA polymerases: PDIP38 interacts directly with Polη

inferredcites →https://doi.org/10.1016/j.dnarep.2014.03.010openalex-snapshot

Mitochondrial genome maintenance in health and disease

inferredcites →https://doi.org/10.1016/j.gde.2016.02.007openalex-snapshot

TP53 mutation, mitochondria and cancer

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.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.2013.09.025openalex-snapshot

PrimPol, an Archaic Primase/Polymerase Operating in Human Cells

inferredcites →https://doi.org/10.1016/j.molcel.2013.10.035openalex-snapshot

PrimPol Bypasses UV Photoproducts during Eukaryotic Chromosomal DNA Replication

inferredcites →https://doi.org/10.1016/j.neurol.2013.11.005openalex-snapshot

Inherited peripheral neuropathies due to mitochondrial disorders

inferredcites →https://doi.org/10.1016/s0021-9258(17)37175-2openalex-snapshot

A beta-like DNA polymerase from the mitochondrion of the trypanosomatid Crithidia fasciculata.

inferredcites →https://doi.org/10.1016/s0021-9258(17)40396-6openalex-snapshot

DNA polymerase of mitochondria is a gamma-polymerase.

inferredcites →https://doi.org/10.1016/s0021-9258(18)67658-6openalex-snapshot

A nuclear mutant of Saccharomyces cerevisiae deficient in mitochondrial DNA replication and polymerase activity.

inferredcites →https://doi.org/10.1016/s0021-9258(19)42063-2openalex-snapshot

The Number of Mitochondrial Deoxyribonucleic Acid Genomes in Mouse L and Human HeLa Cells

inferredcites →https://doi.org/10.1016/s0021-9258(19)47098-1openalex-snapshot

Cloning and Sequencing of the Nuclear Gene MIP1 Encoding the Catalytic Subunit of the Yeast Mitochondrial DNA Polymerase

inferredcites →https://doi.org/10.1016/s0027-5107(02)00255-5openalex-snapshot

Asymmetry of DNA replication and translesion synthesis of UV-induced thymine dimers

inferredcites →https://doi.org/10.1016/s0074-7696(08)61373-xopenalex-snapshot

Animal Mitochondrial DNA: An Extreme Example of Genetic Economy

inferredcites →https://doi.org/10.1016/s0921-8777(00)00047-1openalex-snapshot

Alteration of ultraviolet-induced mutagenesis in yeast through molecular modulation of the REV3 and REV7 gene expression

inferredcites →https://doi.org/10.1016/s0960-9822(00)00724-7openalex-snapshot

Disruption of mouse polymerase ζ (Rev3) leads to embryonic lethality and impairs blastocyst development in vitro

inferredcites →https://doi.org/10.1016/s0960-9822(00)00725-9openalex-snapshot

Disruption of the developmentally regulated Rev3l gene causes embryonic lethality

inferredcites →https://doi.org/10.1016/s1097-2765(02)00571-3openalex-snapshot

Multiple Mitochondrial DNA Polymerases in Trypanosoma brucei

inferredcites →https://doi.org/10.1016/s1568-7864(01)00004-0openalex-snapshot

Polymerase η and p53 jointly regulate cell survival, apoptosis and Mre11 recombination during S phase checkpoint arrest after UV irradiation

inferredcites →https://doi.org/10.1021/bi501024uopenalex-snapshot

Kinetic Analysis of Human PrimPol DNA Polymerase Activity Reveals a Generally Error-Prone Enzyme Capable of Accurately Bypassing 7,8-Dihydro-8-oxo-2′-deoxyguanosine

inferredcites →https://doi.org/10.1021/bi980772wopenalex-snapshot

Characterization of the Native and Recombinant Catalytic Subunit of Human DNA Polymerase γ: Identification of Residues Critical for Exonuclease Activity and Dideoxynucleotide Sensitivity

inferredcites →https://doi.org/10.1021/cr0404904openalex-snapshot

Structure and Mechanism of DNA Polymerase β

inferredcites →https://doi.org/10.1038/2261209a0openalex-snapshot

Viral RNA-dependent DNA Polymerase: RNA-dependent DNA Polymerase in Virions of RNA Tumour Viruses

inferredcites →https://doi.org/10.1038/2261211a0openalex-snapshot

Viral RNA-dependent DNA Polymerase: RNA-dependent DNA Polymerase in Virions of Rous Sarcoma Virus

inferredcites →https://doi.org/10.1038/290457a0openalex-snapshot

Sequence and organization of the human mitochondrial genome

inferredcites →https://doi.org/10.1038/78169openalex-snapshot

Efficient and accurate replication in the presence of 7,8-dihydro-8-oxoguanine by DNA polymerase η

inferredcites →https://doi.org/10.1038/cr.2008.4openalex-snapshot

The fidelity of DNA synthesis by eukaryotic replicative and translesion synthesis polymerases

inferredcites →https://doi.org/10.1038/emboj.2008.281openalex-snapshot

Two‐polymerase mechanisms dictate error‐free and error‐prone translesion DNA synthesis in mammals

inferredcites →https://doi.org/10.1038/embor.2013.159openalex-snapshot

hPrimpol1/CCDC111 is a human DNA primase‐polymerase required for the maintenance of genome integrity

inferredcites →https://doi.org/10.1038/nature02517openalex-snapshot

Premature ageing in mice expressing defective mitochondrial DNA polymerase

inferredcites →https://doi.org/10.1038/nature14157openalex-snapshot

Mammalian polymerase θ promotes alternative NHEJ and suppresses recombination

inferredcites →https://doi.org/10.1038/nature14184openalex-snapshot

Homologous-recombination-deficient tumours are dependent on Polθ-mediated repair

inferredcites →https://doi.org/10.1038/nchembio.2102openalex-snapshot

Mitochondrial DNA repair and replication proteins revealed by targeted chemical probes

inferredcites →https://doi.org/10.1038/ncomms5285openalex-snapshot

A role for DNA polymerase θ in the timing of DNA replication

inferredcites →https://doi.org/10.1038/ng1988openalex-snapshot

Mitochondrial point mutations do not limit the natural lifespan of mice

inferredcites →https://doi.org/10.1038/nrm3439openalex-snapshot

Minimizing the damage: repair pathways keep mitochondrial DNA intact

inferredcites →https://doi.org/10.1038/nsmb.2719openalex-snapshot

Repriming of DNA synthesis at stalled replication forks by human PrimPol

inferredcites →https://doi.org/10.1038/sj.emboj.7600424openalex-snapshot

High‐efficiency bypass of DNA damage by human DNA polymerase Q

inferredcites →https://doi.org/10.1038/sj.embor.embor765openalex-snapshot

Erroneous incorporation of oxidized DNA precursors by Y‐family DNA polymerases

inferredcites →https://doi.org/10.1038/sj.onc.1210385openalex-snapshot

Pol η is required for DNA replication during nucleotide deprivation by hydroxyurea

inferredcites →https://doi.org/10.1038/srep28942openalex-snapshot

Oxidative DNA damage stalls the human mitochondrial replisome

inferredcites →https://doi.org/10.1042/bst0310252openalex-snapshot

The RAD30 cancer susceptibility gene

inferredcites →https://doi.org/10.1073/pnas.1217425110openalex-snapshot

Dual role for mammalian DNA polymerase ζ in maintaining genome stability and proliferative responses

inferredcites →https://doi.org/10.1073/pnas.1308760110openalex-snapshot

DNA polymerase δ-interacting protein 2 is a processivity factor for DNA polymerase λ during 8-oxo-7,8-dihydroguanine bypass

inferredcites →https://doi.org/10.1073/pnas.69.2.452openalex-snapshot

A New Synthetic RNA-Dependent DNA Polymerase from Human Tissue Culture Cells

inferredcites →https://doi.org/10.1073/pnas.71.7.2777openalex-snapshot

The Absence of a Pyrimidine Dimer Repair Mechanism in Mammalian Mitochondria

inferredcites →https://doi.org/10.1073/pnas.76.5.2316openalex-snapshot

Functional roles of DNA polymerases beta and gamma.

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/10.1074/jbc.270.8.3495openalex-snapshot

A DNA Polymerase β in the Mitochondrion of the Trypanosomatid Crithidia fasciculata

inferredcites →https://doi.org/10.1074/jbc.273.18.11121openalex-snapshot

Functional Analysis of the Amino-terminal 8-kDa Domain of DNA Polymerase β as Revealed by Site-directed Mutagenesis

inferredcites →https://doi.org/10.1074/jbc.273.24.15263openalex-snapshot

Human DNA Polymerase β Deoxyribose Phosphate Lyase

inferredcites →https://doi.org/10.1074/jbc.m000559200openalex-snapshot

In Vivo Functional Analysis of the Human Mitochondrial DNA Polymerase POLG Expressed in Cultured Human Cells

inferredcites →https://doi.org/10.1074/jbc.m114.556977openalex-snapshot

A Role for DNA Polymerase θ in Promoting Replication through Oxidative DNA Lesion, Thymine Glycol, in Human Cells

inferredcites →https://doi.org/10.1074/jbc.m308565200openalex-snapshot

Trypanosoma brucei Has Two Distinct Mitochondrial DNA Polymerase β Enzymes

inferredcites →https://doi.org/10.1074/jbc.m414597200openalex-snapshot

Further Characterization of Human DNA Polymerase δ Interacting Protein 38

inferredcites →https://doi.org/10.1074/jbc.m611849200openalex-snapshot

DNA Polymerases η and θ Function in the Same Genetic Pathway to Generate Mutations at A/T during Somatic Hypermutation of Ig Genes

inferredcites →https://doi.org/10.1074/jbc.r100056200openalex-snapshot

Eukaryotic DNA Polymerases: Proposal for a Revised Nomenclature

inferredcites →https://doi.org/10.1080/07352680701252817openalex-snapshot

Multiple Functions of DNA Polymerases

inferredcites →https://doi.org/10.1089/ars.2010.3650openalex-snapshot

p53, Aerobic Metabolism, and Cancer

inferredcites →https://doi.org/10.1093/hmg/ddi184openalex-snapshot

Mitochondrial DNA polymerase gamma is essential for mammalian embryogenesis

inferredcites →https://doi.org/10.1093/hmg/dds506openalex-snapshot

Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenance

inferredcites →https://doi.org/10.1093/hmg/ddv240openalex-snapshot

POLG2disease variants: analyses reveal a dominant negative heterodimer, altered mitochondrial localization and impaired respiratory capacity

inferredcites →https://doi.org/10.1093/jb/mvi169openalex-snapshot

PDIP38 Associates with Proteins Constituting the Mitochondrial DNA Nucleoid

inferredcites →https://doi.org/10.1093/nar/18.22.6716openalex-snapshot

Yeast mitochondrial DNA polymerase is related to the family A DNA polymerases

inferredcites →https://doi.org/10.1093/nar/19.15.4045openalex-snapshot

Compilation and alignment of DNA polymerase sequences

inferredcites →https://doi.org/10.1093/nar/24.14.2753openalex-snapshot

Mitochondrial DNA Polymerase is Expressed and Translated in the Absence of Mitochondrial DNA Maintenance and Replication

inferredcites →https://doi.org/10.1093/nar/gkg814openalex-snapshot

POLQ (Pol ), a DNA polymerase and DNA-dependent ATPase in human cells

inferredcites →https://doi.org/10.1093/nar/gki702openalex-snapshot

Origin and evolution of the archaeo-eukaryotic primase superfamily and related palm-domain proteins: structural insights and new members

inferredcites →https://doi.org/10.1093/nar/gkn310openalex-snapshot

Low-fidelity DNA synthesis by human DNA polymerase theta

inferredcites →https://doi.org/10.1093/nar/gku1321openalex-snapshot

Human PrimPol is a highly error-prone polymerase regulated by single-stranded DNA binding proteins

inferredcites →https://doi.org/10.1093/nar/gku214openalex-snapshot

Molecular dissection of the domain architecture and catalytic activities of human PrimPol

inferredcites →https://doi.org/10.1093/nar/gku879openalex-snapshot

Human PrimPol mutation associated with high myopia has a DNA replication defect

inferredcites →https://doi.org/10.1093/nar/gkv1003openalex-snapshot

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins

inferredcites →https://doi.org/10.1093/nar/gkw123openalex-snapshot

PrimPol prevents APOBEC/AID family mediated DNA mutagenesis

inferredcites →https://doi.org/10.1093/nar/gkw175openalex-snapshot

PolDIP2 interacts with human PrimPol and enhances its DNA polymerase activities

inferredcites →https://doi.org/10.1100/tsw.2003.09openalex-snapshot

DNA Polymerase Gamma in Mitochondrial DNA Replication and Repair

inferredcites →https://doi.org/10.1101/gad.1872810openalex-snapshot

Error-free replicative bypass of (6–4) photoproducts by DNA polymerase ζ in mouse and human cells

inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06521.xopenalex-snapshot

DNA polymerase kappa from Trypanosoma cruzi localizes to the mitochondria, bypasses 8‐oxoguanine lesions and performs DNA synthesis in a recombination intermediate

inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07061.xopenalex-snapshot

Mitochondrial DNA polymerase POLIB is essential for minicircle DNA replication in African trypanosomes

inferredcites →https://doi.org/10.1111/j.1432-1033.1975.tb02416.xopenalex-snapshot

Nomenclature of Eukaryotic DNA Polymerases

inferredcites →https://doi.org/10.1111/j.1550-7408.1998.tb05091.xopenalex-snapshot

Identification and Characterization of Two DNA Polymerase Activities Present in Trypanosoma brucei Mitochondria

inferredcites →https://doi.org/10.1126/science.1112125openalex-snapshot

Mitochondrial DNA Mutations, Oxidative Stress, and Apoptosis in Mammalian Aging

inferredcites →https://doi.org/10.1126/science.1148242openalex-snapshot

Bypass of DNA Lesions Generated During Anticancer Treatment with Cisplatin by DNA Polymerase η

inferredcites →https://doi.org/10.1126/science.1179222openalex-snapshot

Nomenclature of Eukaryotic DNA Polymerases

inferredcites →https://doi.org/10.1126/science.283.5407.1482openalex-snapshot

Mitochondrial Diseases in Man and Mouse

inferredcites →https://doi.org/10.1126/science.285.5425.263openalex-snapshot

hRAD30 Mutations in the Variant Form of Xeroderma Pigmentosum

inferredcites →https://doi.org/10.1126/science.7516580openalex-snapshot

Structures of Ternary Complexes of Rat DNA Polymerase β, a DNA Template-Primer, and ddCTP

inferredcites →https://doi.org/10.1126/science.7516581openalex-snapshot

Crystal Structure of Rat DNA Polymerase β: Evidence for a Common Polymerase Mechanism

inferredcites →https://doi.org/10.1128/aac.02270-15openalex-snapshot

Insights into the Molecular Mechanism of Polymerization and Nucleoside Reverse Transcriptase Inhibitor Incorporation by Human PrimPol

inferredcites →https://doi.org/10.1128/mcb.00457-08openalex-snapshot

Removal of Oxidative DNA Damage via FEN1-Dependent Long-Patch Base Excision Repair in Human Cell Mitochondria

inferredcites →https://doi.org/10.1128/mcb.20.19.7205-7213.2000openalex-snapshot

Identification and Functional Analysis of Human Tom22 for Protein Import into Mitochondria

inferredcites →https://doi.org/10.1128/mcb.20.21.8001-8007.2000openalex-snapshot

Replication past O 6 -Methylguanine by Yeast and Human DNA Polymerase η

inferredcites →https://doi.org/10.1128/mcb.21.10.3558-3563.2001openalex-snapshot

Role of DNA Polymerase η in the Bypass of a (6-4) TT Photoproduct

inferredcites →https://doi.org/10.1128/mcb.22.7.2159-2169.2002openalex-snapshot

Involvement of Mouse Rev3 in Tolerance of Endogenous and Exogenous DNA Damage

inferredcites →https://doi.org/10.1128/mcb.25.13.5396-5403.2005openalex-snapshot

The Cotranscriptional Assembly of snoRNPs Controls the Biosynthesis of H/ACA snoRNAs in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1128/mmbr.00034-08openalex-snapshot

Eukaryotic Translesion Polymerases and Their Roles and Regulation in DNA Damage Tolerance

inferredcites →https://doi.org/10.1146/annurev.med.59.053006.104646openalex-snapshot

Inherited Mitochondrial Diseases of DNA Replication

inferredcites →https://doi.org/10.1146/annurev.mi.49.100195.001001openalex-snapshot

THE STRUCTURE AND REPLICATION OF KINETOPLAST DNA

inferredcites →https://doi.org/10.1215/15228517-2009-015openalex-snapshot

REV3L confers chemoresistance to cisplatin in human gliomas: The potential of its RNAi for synergistic therapy

inferredcites →https://doi.org/10.1371/journal.pgen.1004654openalex-snapshot

Mechanism of Suppression of Chromosomal Instability by DNA Polymerase POLQ

inferredcites →https://doi.org/10.1371/journal.pone.0034322openalex-snapshot

Overexpression of DNA Polymerase Zeta Reduces the Mitochondrial Mutability Caused by Pathological Mutations in DNA Polymerase Gamma in Yeast

inferredcites →https://doi.org/10.1371/journal.pone.0140409openalex-snapshot

Human REV3 DNA Polymerase Zeta Localizes to Mitochondria and Protects the Mitochondrial Genome

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

Saccharomyces cerevisiae Polymerase ζ Functions in Mitochondria

inferredcites →https://doi.org/10.1593/neo.11828openalex-snapshot

Inhibition of REV3 Expression Induces Persistent DNA Damage and Growth Arrest in Cancer Cells

inferredcites →https://doi.org/10.2210/pdb2bpf/pdbopenalex-snapshot

STRUCTURES OF TERNARY COMPLEXES OF RAT DNA POLYMERASE BETA, A DNA TEMPLATE-PRIMER, AND DDCTP

inferredcites →https://doi.org/10.3109/10409238.2011.632763openalex-snapshot

Defects in mitochondrial DNA replication and human disease

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

PrimPol—A new polymerase on the block

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.3155512openalex-extracted

DNA Polymerase Mediates Robust Base Lesion Repair in Mammalian Mitochondria

inferred← citeshttps://doi.org/10.1002/1873-3468.13440openalex-snapshot

Ribonucleotides in mitochondrial DNA

inferred← citeshttps://doi.org/10.1002/adhm.202200742openalex-snapshot

Inhibition of Mitochondrial Biosynthesis Using a “Right‐Side‐Out” Membrane‐Camouflaged Micelle to Facilitate the Therapeutic Effects of Shikonin on Triple‐Negative Breast Cancer

inferred← citeshttps://doi.org/10.1002/bies.201800102openalex-snapshot

Known Unknowns of Mammalian Mitochondrial DNA Maintenance

inferred← citeshttps://doi.org/10.1002/em.22319openalex-snapshot

Mitochondrial DNA: Epigenetics and environment

inferred← citeshttps://doi.org/10.1002/iub.2770openalex-snapshot

The Saccharomyces cerevisiae mitochondrial DNA polymerase and its contribution to the knowledge about human POLG ‐related disorders

inferred← citeshttps://doi.org/10.1002/iub.2801openalex-snapshot

Schizosaccharomyces pombe as a fundamental model for research on mitochondrial gene expression: Progress, achievements and outlooks

inferred← citeshttps://doi.org/10.1002/jez.2646openalex-snapshot

High‐fat diet affects autophagy and mitochondrial compartment in rat Harderian gland

inferred← citeshttps://doi.org/10.1002/mds.28475openalex-snapshot

Nuclear Genes Associated with Mitochondrial DNA Processes as Contributors to Parkinson's Disease Risk

inferred← citeshttps://doi.org/10.1007/978-1-0716-1433-4_8openalex-snapshot

PCR-Based Determination of Mitochondrial DNA Copy Number in Multiple Species

inferred← citeshttps://doi.org/10.1007/978-1-0716-3064-8_4openalex-snapshot

Mitochondrial Inheritance Following Nuclear Transfer: From Cloned Animals to Patients with Mitochondrial Disease

inferred← citeshttps://doi.org/10.1007/s00018-019-03368-yopenalex-snapshot

Structure and function relationships in mammalian DNA polymerases

inferred← citeshttps://doi.org/10.1007/s00441-019-03164-xopenalex-snapshot

Patient-specific neural progenitor cells derived from induced pluripotent stem cells offer a promise of good models for mitochondrial disease

inferred← citeshttps://doi.org/10.1007/s10072-021-05380-2openalex-snapshot

Novel biallelic mutations in POLG gene: large deletion and missense variant associated with PEO

inferred← citeshttps://doi.org/10.1007/s12551-021-00891-wopenalex-snapshot

Uncovering the important role of mitochondrial dynamics in oogenesis: impact on fertility and metabolic disorder transmission

inferred← citeshttps://doi.org/10.1007/s40572-021-00329-1openalex-snapshot

Mitochondrial DNA Mutagenesis: Feature of and Biomarker for Environmental Exposures and Aging

inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64219-8openalex-snapshot

Mitochondrial Genomics and Targeted Toxicities

inferred← citeshttps://doi.org/10.1016/b978-0-12-821751-1.00011-7openalex-snapshot

Genetics of mitochondrial diseases: Current approaches for the molecular diagnosis

inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00128-5openalex-snapshot

Causes and Consequences of Perturbations of the Mitochondrial Genome

inferred← citeshttps://doi.org/10.1016/bs.enz.2019.08.002openalex-snapshot

DNA polymerase beta and other gap-filling enzymes in mammalian base excision repair

inferred← citeshttps://doi.org/10.1016/bs.enz.2019.08.004openalex-snapshot

Mitochondrial DNA degradation: A quality control measure for mitochondrial genome maintenance and stress response

inferred← citeshttps://doi.org/10.1016/j.cell.2025.04.012openalex-snapshot

Extrachromosomal DNA replication and maintenance couple with DNA damage pathway in tumors

inferred← citeshttps://doi.org/10.1016/j.celrep.2020.02.105openalex-snapshot

SFTSV Infection Induces BAK/BAX-Dependent Mitochondrial DNA Release to Trigger NLRP3 Inflammasome Activation

inferred← citeshttps://doi.org/10.1016/j.dnarep.2017.10.011openalex-snapshot

DNA polymerase β: A missing link of the base excision repair machinery in mammalian mitochondria

inferred← citeshttps://doi.org/10.1016/j.dnarep.2017.11.002openalex-snapshot

POLB: A new role of DNA polymerase beta in mitochondrial base excision repair

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118572openalex-snapshot

Effects and mechanisms of aflatoxin B1 on oocytes and embryo development

inferred← citeshttps://doi.org/10.1016/j.jbc.2021.101523openalex-snapshot

Oxidative stress induces Z-DNA-binding protein 1–dependent activation of microglia via mtDNA released from retinal pigment epithelial cells

inferred← citeshttps://doi.org/10.1016/j.jhepr.2022.100508openalex-snapshot

A new mouse model of radiation-induced liver disease reveals mitochondrial dysfunction as an underlying fibrotic stimulus

inferred← citeshttps://doi.org/10.1016/j.jmb.2025.169433openalex-snapshot

Phosphomimetic Experiments Do Not Support a Causal Role for TFAM Phosphorylation in mtDNA Elimination in Sperm

inferred← citeshttps://doi.org/10.1016/j.mito.2018.11.004openalex-snapshot

The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort

inferred← citeshttps://doi.org/10.1016/j.phrs.2026.108106openalex-snapshot

Mitochondrial semi-autonomous inheritance in cardiovascular pathology: Emerging mechanisms and therapeutic opportunities

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.07.349openalex-snapshot

Toxicity response of silkworm intestine to Bacillus cereus SW7-1 pathogen

inferred← citeshttps://doi.org/10.1016/j.semcdb.2024.01.007openalex-snapshot

The role of mitochondrial dynamics in oocyte and early embryo development

inferred← citeshttps://doi.org/10.1021/acs.jafc.8b05194openalex-snapshot

Cytotoxicity and DNA Damage Caused from Diazinon Exposure by Inhibiting the PI3K-AKT Pathway in Porcine Ovarian Granulosa Cells

inferred← citeshttps://doi.org/10.1021/acschembio.8b00072openalex-snapshot

DNA Polymerase θ Increases Mutational Rates in Mitochondrial DNA

inferred← citeshttps://doi.org/10.1038/s41467-021-24317-zopenalex-snapshot

Structural basis of DNA synthesis opposite 8-oxoguanine by human PrimPol primase-polymerase

inferred← citeshttps://doi.org/10.1038/s41576-020-00284-xopenalex-snapshot

Extreme heterogeneity of human mitochondrial DNA from organelles to populations

inferred← citeshttps://doi.org/10.1038/s41598-020-66153-zopenalex-snapshot

Identifying the role of PrimPol in TDF-induced toxicity and implications of its loss of function mutation in an HIV+ patient

inferred← citeshttps://doi.org/10.1042/bcj20200920openalex-snapshot

Mitochondrial genome stability in human: understanding the role of DNA repair pathways

inferred← citeshttps://doi.org/10.1042/bcj20230262openalex-snapshot

Mechanisms and pathologies of human mitochondrial DNA replication and deletion formation

inferred← citeshttps://doi.org/10.1042/ebc20170100openalex-snapshot

Mitochondrial DNA replication in mammalian cells: overview of the pathway

inferred← citeshttps://doi.org/10.1080/10409238.2020.1818684openalex-snapshot

Mammalian mitochondrial DNA replication and mechanisms of deletion formation

inferred← citeshttps://doi.org/10.1080/21678707.2018.1540979openalex-snapshot

An update on Alpers-Huttenlocher syndrome: pathophysiology of disease and rational treatment designs

inferred← citeshttps://doi.org/10.1093/gbe/evab003openalex-snapshot

Phage Origin of Mitochondrion-Localized Family A DNA Polymerases in Kinetoplastids and Diplonemids

inferred← citeshttps://doi.org/10.1093/nar/gkac666openalex-snapshot

Resistance of mitochondrial DNA to cadmium and Aflatoxin B1 damage-induced germline mutation accumulation in C. elegans

inferred← citeshttps://doi.org/10.1093/nar/gkad037openalex-snapshot

Mechanism of strand displacement DNA synthesis by the coordinated activities of human mitochondrial DNA polymerase and SSB

inferred← citeshttps://doi.org/10.1093/nar/gkz056openalex-snapshot

PrimPol is required for the maintenance of efficient nuclear and mitochondrial DNA replication in human cells

inferred← citeshttps://doi.org/10.1096/fj.201801591ropenalex-snapshot

Increased dNTP pools rescue mtDNA depletion in human POLG‐deficient fibroblasts

inferred← citeshttps://doi.org/10.1111/febs.15032openalex-snapshot

Plasmodium falciparum Apn1 homolog is a mitochondrial base excision repair protein with restricted enzymatic functions

inferred← citeshttps://doi.org/10.1146/annurev-biochem-013118-111315openalex-snapshot

Eukaryotic Base Excision Repair: New Approaches Shine Light on Mechanism

inferred← citeshttps://doi.org/10.1146/annurev-biochem-052621-092014openalex-snapshot

Replication and Transcription of Human Mitochondrial DNA

inferred← citeshttps://doi.org/10.1159/000550301openalex-snapshot

Ultrarare Variants in DNA Damage Repair and Mitochondrial Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome and Acute Behavioral Regression in Neurodevelopmental Disorders

inferred← citeshttps://doi.org/10.1186/s12943-026-02571-3openalex-snapshot

Targeting mitochondrial homeostasis as a cancer treatment strategy: current status and future prospects

inferred← citeshttps://doi.org/10.1242/dmm.048912openalex-snapshot

Mitochondrial function in development and disease

inferred← citeshttps://doi.org/10.1371/journal.pgen.1007315openalex-snapshot

The presence of rNTPs decreases the speed of mitochondrial DNA replication

inferred← citeshttps://doi.org/10.18297/etd/3748openalex-snapshot

Investigation of mitochondrial inheritance in the smut fungus sporisorium reilianum.

inferred← citeshttps://doi.org/10.20517/jtgg.2023.0openalex-snapshot

Mechanisms regulating mitochondrial DNA quality control

inferred← citeshttps://doi.org/10.20517/jtgg.2023.08openalex-snapshot

Mechanisms regulating mitochondrial DNA quality control

inferred← citeshttps://doi.org/10.21203/rs.3.rs-3708982/v1openalex-snapshot

Extrachromosomal DNA Couples with ATM-mediated DNA Damage Response for Genome Instability in Tumors

inferred← citeshttps://doi.org/10.2147/tcrm.s153895openalex-snapshot

Mitochondrial genome variability: the effect on cellular functional activity

inferred← citeshttps://doi.org/10.2174/0929867324666171116123345openalex-snapshot

G4-Interacting DNA Helicases and Polymerases: Potential Therapeutic Targets

inferred← citeshttps://doi.org/10.2174/1381612826666200826165735openalex-snapshot

Mitochondrial-induced Epigenetic Modifications: From Biology to Clinical Translation

inferred← citeshttps://doi.org/10.2478/jtim-2021-0049openalex-snapshot

New insights of epigenetics in vascular and cellular senescence

inferred← citeshttps://doi.org/10.24920/003697openalex-snapshot

POLG Mutations Are Probably Rare in the Han Chinese Population

inferred← citeshttps://doi.org/10.3389/fcell.2022.984245openalex-snapshot

Dynamic features of human mitochondrial DNA maintenance and transcription

inferred← citeshttps://doi.org/10.3389/fendo.2018.00177openalex-snapshot

Deoxyribonucleotide Triphosphate Metabolism in Cancer and Metabolic Disease

inferred← citeshttps://doi.org/10.3389/fgene.2020.00439openalex-snapshot

“Mitochondrial Toolbox” – A Review of Online Resources to Explore Mitochondrial Genomics

inferred← citeshttps://doi.org/10.3389/fmolb.2017.00074openalex-snapshot

Off-Target Effects of Drugs that Disrupt Human Mitochondrial DNA Maintenance

inferred← citeshttps://doi.org/10.3389/fonc.2022.850883openalex-snapshot

Recent Advances in the Development of Non-PIKKs Targeting Small Molecule Inhibitors of DNA Double-Strand Break Repair

inferred← citeshttps://doi.org/10.3390/biology7010005openalex-snapshot

Family A and B DNA Polymerases in Cancer: Opportunities for Therapeutic Interventions

inferred← citeshttps://doi.org/10.3390/biom15070969openalex-snapshot

Methionine Restriction Differentially Modulates Expression of Genes in the Base Excision Repair Pathway in Rat Brain and Liver

inferred← citeshttps://doi.org/10.3390/books978-3-0365-3052-9openalex-snapshot

Kinetoplastid Phylogenomics and Evolution

inferred← citeshttps://doi.org/10.3390/cells8070686openalex-snapshot

Mitochondrial Homeostasis and Cellular Senescence

inferred← citeshttps://doi.org/10.3390/cells9010017openalex-snapshot

Mitochondrial Gene Expression and Beyond—Novel Aspects of Cellular Physiology

inferred← citeshttps://doi.org/10.3390/dna2020010openalex-snapshot

Mitochondrial DNA: Consensuses and Controversies

inferred← citeshttps://doi.org/10.3390/genes12111668openalex-snapshot

Gaining Insight into Mitochondrial Genetic Variation and Downstream Pathophysiology: What Can i(PSCs) Do?

inferred← citeshttps://doi.org/10.3390/genes13050879openalex-snapshot

Polymerase ζ Is Involved in Mitochondrial DNA Maintenance Processes in Concert with APE1 Activity

inferred← citeshttps://doi.org/10.3390/genes17010082openalex-snapshot

Mitochondrial DNA Instability and Neuroinflammation: Connecting the Dots Between Base Excision Repair and Neurodegenerative Disease

inferred← citeshttps://doi.org/10.3390/ijms20112770openalex-snapshot

Organization of DNA in Mammalian Mitochondria

inferred← citeshttps://doi.org/10.3390/ijms21051706openalex-snapshot

One, No One, and One Hundred Thousand: The Many Forms of Ribonucleotides in DNA

inferred← citeshttps://doi.org/10.3390/ijms21113883openalex-snapshot

Mitochondrial Inheritance in Phytopathogenic Fungi—Everything Is Known, or Is It?

inferred← citeshttps://doi.org/10.3390/ijms26135986openalex-snapshot

Aging in the Skeletal Muscle Revealed by Molecular Immunohistochemical Imaging

inferred← citeshttps://doi.org/10.3390/jof9040476openalex-snapshot

Uniparental Inheritance and Recombination as Strategies to Avoid Competition and Combat Muller’s Ratchet among Mitochondria in Natural Populations of the Fungus Amanita phalloides

inferred← citeshttps://doi.org/10.3390/molecules25122857openalex-snapshot

The Similarities between Human Mitochondria and Bacteria in the Context of Structure, Genome, and Base Excision Repair System

inferred← citeshttps://doi.org/10.3390/molecules26227042openalex-snapshot

The Influence of 5′,8-Cyclo-2′-deoxypurines on the Mitochondrial Repair of Clustered DNA Damage in Xrs5 Cells: The Preliminary Study

inferred← citeshttps://doi.org/10.3390/pathogens9040257openalex-snapshot

Inventory and Evolution of Mitochondrion-localized Family A DNA Polymerases in Euglenozoa

inferred← citeshttps://doi.org/10.3390/pharmaceutics17040471openalex-snapshot

Targeting Regulatory Noncoding RNAs in Human Cancer: The State of the Art in Clinical Trials

inferred← citeshttps://doi.org/10.7554/elife.69916openalex-snapshot

Unleashing a novel function of Endonuclease G in mitochondrial genome instability

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.