(Q38569294)

4 September 2017

title

Mitochondrial DNA maintenance: an appraisal (English)

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4 September 2017

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Alexander T Akhmedov

1

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4 September 2017

José Marín-García

series ordinal

2

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4 September 2017

publication date

19 August 2015

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Molecular and Cellular Biochemistry

4 September 2017

published in

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4 September 2017

volume

409

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4 September 2017

issue

1-2

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4 September 2017

page(s)

283-305

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https://scigraph.springernature.com/pub.10.1007/s11010-015-2532-x

4 September 2017

exact match

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Structure and function of simian virus 40 large tumor antigen

21 January 2018

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A ring-opening mechanism for DNA binding in the central channel of the T7 helicase-primase protein

21 January 2018

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Bacteriophage T7 helicase/primase proteins form rings around single-stranded DNA that suggest a general structure for hexameric helicases

21 January 2018

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DNA helicases displace streptavidin from biotin-labeled oligonucleotides

21 January 2018

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Structure and function of hexameric helicases.

21 January 2018

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

21 January 2018

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Structure-function defects of the TWINKLE linker region in progressive external ophthalmoplegia.

21 January 2018

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Modular architecture of the hexameric human mitochondrial DNA helicase

21 January 2018

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The N-terminal domain of TWINKLE contributes to single-stranded DNA binding and DNA helicase activities

21 January 2018

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Twinkle, the mitochondrial replicative DNA helicase, is widespread in the eukaryotic radiation and may also be the mitochondrial DNA primase in most eukaryotes

21 January 2018

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The Arabidopsis At1g30680 gene encodes a homologue to the phage T7 gp4 protein that has both DNA primase and DNA helicase activities

21 January 2018

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Dynamic effects of cofactors and DNA on the oligomeric state of human mitochondrial DNA helicase

21 January 2018

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Human mitochondrial DNA helicase TWINKLE is both an unwinding and annealing helicase

21 January 2018

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Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling

21 January 2018

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The mitochondrial DNA helicase TWINKLE can assemble on a closed circular template and support initiation of DNA synthesis

21 January 2018

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TWINKLE Has 5' -> 3' DNA helicase activity and is specifically stimulated by mitochondrial single-stranded DNA-binding protein

21 January 2018

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Expression of catalytic mutants of the mtDNA helicase Twinkle and polymerase POLG causes distinct replication stalling phenotypes.

21 January 2018

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Physiological and biochemical defects in carboxyl-terminal mutants of mitochondrial DNA helicase

21 January 2018

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Interactions of bacteriophage T7 DNA primase/helicase protein with single-stranded and double-stranded DNAs

21 January 2018

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TWINKLE is an essential mitochondrial helicase required for synthesis of nascent D-loop strands and complete mtDNA replication

21 January 2018

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Human RECQ5beta, a protein with DNA helicase and strand-annealing activities in a single polypeptide

21 January 2018

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The Bloom's syndrome helicase promotes the annealing of complementary single-stranded DNA

21 January 2018

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RecQ family members combine strand pairing and unwinding activities to catalyze strand exchange

21 January 2018

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Dual DNA unwinding activities of the Rothmund-Thomson syndrome protein, RECQ4

21 January 2018

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Human heart mitochondrial DNA is organized in complex catenated networks containing abundant four-way junctions and replication forks

21 January 2018

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A yeast gene required for DNA replication encodes a protein with homology to DNA helicases

21 January 2018

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Assignment of the closest human homologue (DNA2L:KIAA0083) of the yeast Dna2 helicase gene to chromosome band 10q21.3-q22.1.

21 January 2018

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Identification of the Xenopus laevis homolog of Saccharomyces cerevisiae DNA2 and its role in DNA replication

21 January 2018

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Isolation of human Dna2 endonuclease and characterization of its enzymatic properties

21 January 2018

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Biochemical analysis of human Dna2

21 January 2018

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RPA governs endonuclease switching during processing of Okazaki fragments in eukaryotes

21 January 2018

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Mechanism of DNA chain growth. I. Possible discontinuity and unusual secondary structure of newly synthesized chains

21 January 2018

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Dna2 on the road to Okazaki fragment processing and genome stability in eukaryotes

21 January 2018

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The pattern of sensitivity of yeast dna2 mutants to DNA damaging agents suggests a role in DSB and postreplication repair pathways

21 January 2018

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Human DNA2 is a mitochondrial nuclease/helicase for efficient processing of DNA replication and repair intermediates

21 January 2018

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Single strand annealing and ATP-independent strand exchange activities of yeast and human DNA2: possible role in Okazaki fragment maturation

21 January 2018

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Human Dna2 is a nuclear and mitochondrial DNA maintenance protein

21 January 2018

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Okazaki fragment processing-independent role for human Dna2 enzyme during DNA replication

21 January 2018

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Human nuclease/helicase DNA2 alleviates replication stress by promoting DNA end resection

21 January 2018

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Roles of Pif1-like helicases in the maintenance of genomic stability.

21 January 2018

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Unwinding the functions of the Pif1 family helicases.

21 January 2018

1 reference

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Yeast and human mitochondrial helicases

21 January 2018

1 reference

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pif mutation blocks recombination between mitochondrial rho+ and rho- genomes having tandemly arrayed repeat units in Saccharomyces cerevisiae

21 January 2018

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The Saccharomyces Pif1p DNA helicase and the highly related Rrm3p have opposite effects on replication fork progression in ribosomal DNA.

21 January 2018

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The Pif1 family in prokaryotes: what are our helicases doing in your bacteria?

21 January 2018

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Human PIF Helicase is Cell Cycle Regulated and Associates with Telomerase

21 January 2018

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Mitochondrial and nuclear localization of human Pif1 helicase.

21 January 2018

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Characterization of ATPase activity of recombinant human Pif1.

21 January 2018

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The human Pif1 helicase, a potential Escherichia coli RecD homologue, inhibits telomerase activity

21 January 2018

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Biochemical analysis of human PIF1 helicase and functions of its N-terminal domain.

21 January 2018

1 reference

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Human Pif1 helicase unwinds synthetic DNA structures resembling stalled DNA replication forks

21 January 2018

1 reference

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Determination of the biochemical properties of full-length human PIF1 ATPase

21 January 2018

1 reference

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Murine Pif1 interacts with telomerase and is dispensable for telomere function in vivo

21 January 2018

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Oxidants, antioxidants, and the degenerative diseases of aging

21 January 2018

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The sites and topology of mitochondrial superoxide production

21 January 2018

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Oxidatively generated base damage to cellular DNA.

21 January 2018

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Free radical lipid peroxidation: mechanisms and analysis

21 January 2018

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

21 January 2018

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Mitochondrial DNA replication and disease: insights from DNA polymerase γ mutations

21 January 2018

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Mitochondrial DNA polymerase gamma mutations: an ever expanding molecular and clinical spectrum.

21 January 2018

1 reference

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Clinical and molecular features of POLG-related mitochondrial disease.

21 January 2018

1 reference

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Characterization of the native and recombinant catalytic subunit of human DNA polymerase gamma: identification of residues critical for exonuclease activity and dideoxynucleotide sensitivity

21 January 2018

1 reference

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A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues

21 January 2018

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Molecular genetic aspects of human mitochondrial disorders

21 January 2018

1 reference

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Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication

21 January 2018

1 reference

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Mitochondrial point mutations do not limit the natural lifespan of mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The mtDNA mutation spectrum of the progeroid Polg mutator mouse includes abundant control region multimers

21 January 2018

1 reference

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Effect of DNA polymerases and high mobility group protein 1 on the carrier ligand specificity for translesion synthesis past platinum-DNA adducts

21 January 2018

1 reference

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Nucleotide incorporation by human DNA polymerase gamma opposite benzo[a]pyrene and benzo[c]phenanthrene diol epoxide adducts of deoxyguanosine and deoxyadenosine.

21 January 2018

1 reference

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Human mitochondrial DNA polymerase γ exhibits potential for bypass and mutagenesis at UV-induced cyclobutane thymine dimers

21 January 2018

1 reference

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Mitochondrial DNA damage and its consequences for mitochondrial gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mechanism of the neurotoxicity of MPTP. An update

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial mutations may increase oxidative stress: implications for carcinogenesis and aging?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Endogenous DNA damage in humans: a review of quantitative data

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

8,5'-Cyclopurine-2'-deoxynucleosides in DNA: mechanisms of formation, measurement, repair and biological effects

21 January 2018

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Biomarkers in toxicology and risk assessment: informing critical dose-response relationships

21 January 2018

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Quantification of DNA damage products resulting from deamination, oxidation and reaction with products of lipid peroxidation by liquid chromatography isotope dilution tandem mass spectrometry

21 January 2018

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The QPCR assay for analysis of mitochondrial DNA damage, repair, and relative copy number

21 January 2018

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Ultrasensitive simultaneous quantification of 1,N2-etheno-2'-deoxyguanosine and 1,N2-propano-2'-deoxyguanosine in DNA by an online liquid chromatography-electrospray tandem mass spectrometry assay

21 January 2018

1 reference

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Quantifying etheno-DNA adducts in human tissues, white blood cells, and urine by ultrasensitive (32)P-postlabeling and immunohistochemistry.

21 January 2018

1 reference

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Measurement of oxidatively generated base damage in cellular DNA.

21 January 2018

1 reference

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Oxidative DNA damage: mechanisms, mutation, and disease

21 January 2018

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Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain.

21 January 2018

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A method for detecting abasic sites in living cells: age-dependent changes in base excision repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Oxidative stress induces degradation of mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

DNA strand break repair and human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

DNA double-strand break repair pathways, chromosomal rearrangements and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Analysis of differential DNA damage in the mitochondrial genome employing a semi-long run real-time PCR approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Minimizing the damage: repair pathways keep mitochondrial DNA intact

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Repair of persistent strand breaks in the mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The maintenance of mitochondrial DNA integrity--critical analysis and update

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The absence of a pyrimidine dimer repair mechanism in mammalian mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Nuclear and mitochondrial DNA repair: similar pathways?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial DNA maintenance and bioenergetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial DNA repair in aging and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mechanism of homologous recombination and implications for aging-related deletions in mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Repair of alkylation and oxidative damage in mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Long patch base excision repair in mammalian mitochondrial genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Base excision repair and lesion-dependent subpathways for repair of oxidative DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Repair of 8-oxoG is slower in endogenous nuclear genes than in mitochondrial DNA and is without strand bias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Repair of oxidative DNA damage in nuclear and mitochondrial DNA, and some changes with aging in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial base excision repair of uracil and AP sites takes place by single-nucleotide insertion and long-patch DNA synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Removal of oxidative DNA damage via FEN1-dependent long-patch base excision repair in human cell mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

A unified view of base excision repair: lesion-dependent protein complexes regulated by post-translational modification

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Nuclear and mitochondrial DNA repair in selected eukaryotic aging model systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Base-excision repair of oxidative DNA damage by DNA glycosylases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

DNA base damage recognition and removal: new twists and grooves

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mechanistic comparisons among base excision repair glycosylases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

A short primer for sequencing DNA cloned in the single-stranded phage vector M13mp2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Affinity purification and comparative analysis of two distinct human uracil-DNA glycosylases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Compromised incision of oxidized pyrimidines in liver mitochondria of mice deficient in NTH1 and OGG1 glycosylases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Repair of formamidopyrimidines in DNA involves different glycosylases: role of the OGG1, NTH1, and NEIL1 enzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Role of human DNA glycosylase Nei-like 2 (NEIL2) and single strand break repair protein polynucleotide kinase 3'-phosphatase in maintenance of mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Expression and differential intracellular localization of two major forms of human 8-oxoguanine DNA glycosylase encoded by alternatively spliced OGG1 mRNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Identification and characterization of a human DNA glycosylase for repair of modified bases in oxidatively damaged DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Human DNA glycosylases of the bacterial Fpg/MutM superfamily: an alternative pathway for the repair of 8-oxoguanine and other oxidation products in DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Human DNA glycosylases involved in the repair of oxidatively damaged DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The major human abasic endonuclease: formation, consequences and repair of abasic lesions in DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Molecular and biological roles of Ape1 protein in mammalian base excision repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Differential expression of the apurinic / apyrimidinic endonuclease (APE/ref-1) multifunctional DNA base excision repair gene during fetal development and in adult rat brain and testis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Role of polynucleotide kinase/phosphatase in mitochondrial DNA repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Early steps in the DNA base excision/single-strand interruption repair pathway in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Apoptosis induced by persistent single-strand breaks in mitochondrial genome: critical role of EXOG (5'-EXO/endonuclease) in their repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

EXOG, a novel paralog of Endonuclease G in higher eukaryotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Identification of a novel human mitochondrial endo-/exonuclease Ddk1/c20orf72 necessary for maintenance of proper 7S DNA levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial DNA ligase III function is independent of Xrcc1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Structure and function of the DNA ligases encoded by the mammalian LIG3 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Antisense-mediated decrease in DNA ligase III expression results in reduced mitochondrial DNA integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Crucial role for DNA ligase III in mitochondria but not in Xrcc1-dependent repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Intrinsic mitochondrial DNA repair defects in Ataxia Telangiectasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

RECQL4 localizes to mitochondria and preserves mitochondrial DNA integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

RECQL4 is essential for the transport of p53 to mitochondria in normal human cells in the absence of exogenous stress.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Rising from the RecQ-age: the role of human RecQ helicases in genome maintenance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

RecQ helicases: multifunctional genome caretakers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

RecQ helicases: guardian angels of the DNA replication fork

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Homologous recombination and maintenance of genome integrity: cancer and aging through the prism of human RecQ helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

DNA helicase activity in purified human RECQL4 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Conserved helicase domain of human RecQ4 is required for strand annealing-independent DNA unwinding

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

RECQL4-deficient cells are hypersensitive to oxidative stress/damage: Insights for osteosarcoma prevalence and heterogeneity in Rothmund-Thomson syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The Rothmund-Thomson gene product RECQL4 localizes to the nucleolus in response to oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Nuclear import and retention domains in the amino terminus of RECQL4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The involvement of human RECQL4 in DNA double-strand break repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Assembly of the Cdc45-Mcm2-7-GINS complex in human cells requires the Ctf4/And-1, RecQL4, and Mcm10 proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Direct and indirect roles of RECQL4 in modulating base excision repair capacity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

MCM10 mediates RECQ4 association with MCM2-7 helicase complex during DNA replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Aprataxin, poly-ADP ribose polymerase 1 (PARP-1) and apurinic endonuclease 1 (APE1) function together to protect the genome against oxidative damage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial localization of PARP-1 requires interaction with mitofilin and is involved in the maintenance of mitochondrial DNA integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

p53 functions in the incorporation step in DNA base excision repair in mouse liver mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Novel role of p53 in maintaining mitochondrial genetic stability through interaction with DNA Pol gamma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The p53 pathway promotes efficient mitochondrial DNA base excision repair in colorectal cancer cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Accumulation of mitochondrial DNA damage and bioenergetic dysfunction in CSB defective cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Molecular and clinical genetics of mitochondrial diseases due to POLG mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Defects in mitochondrial DNA replication and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Polymerase gamma disease through the ages

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial DNA polymerase gamma deficiency and mtDNA depletion in a child with Alpers' syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Molecular diagnosis of Alpers syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Dominant inheritance of premature ovarian failure associated with mutant mitochondrial DNA polymerase gamma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The common A467T mutation in the human mitochondrial DNA polymerase (POLG) compromises catalytic efficiency and interaction with the accessory subunit.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Genetic and chemical rescue of the Saccharomyces cerevisiae phenotype induced by mitochondrial DNA polymerase mutations associated with progressive external ophthalmoplegia in humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

A single mutation in human mitochondrial DNA polymerase Pol gammaA affects both polymerization and proofreading activities of only the holoenzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

A cluster of pathogenic mutations in the 3'-5' exonuclease domain of DNA polymerase gamma defines a novel module coupling DNA synthesis and degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Active site mutation in DNA polymerase gamma associated with progressive external ophthalmoplegia causes error-prone DNA synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Finding twinkle in the eyes of a 71-year-old lady: a case report and review of the genotypic and phenotypic spectrum of TWINKLE-related dominant disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Recessive twinkle mutations cause severe epileptic encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Structure-function defects of the twinkle amino-terminal region in progressive external ophthalmoplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Differential phenotypes of active site and human autosomal dominant progressive external ophthalmoplegia mutations in Drosophila mitochondrial DNA helicase expressed in Schneider cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Disease variants of the human mitochondrial DNA helicase encoded by C10orf2 differentially alter protein stability, nucleotide hydrolysis, and helicase activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

A genomewide screen for suppressors of Alu-mediated rearrangements reveals a role for PIF1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Precise determination of mitochondrial DNA copy number in human skeletal and cardiac muscle by a PCR-based assay: lack of change of copy number with age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

DNA damage is an early event in doxorubicin-induced cardiac myocyte death

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Role of mtDNA lesions in anthracycline cardiotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial pathology in cardiac failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Defective DNA replication impairs mitochondrial biogenesis in human failing hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Induction of mitochondrial biogenesis is a maladaptive mechanism in mitochondrial cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Control by circulating factors of mitochondrial function and transcription cascade in heart failure: a role for endothelin-1 and angiotensin II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Prominent mitochondrial DNA recombination intermediates in human heart muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Developmental and pathological changes in the human cardiac muscle mitochondrial DNA organization, replication and copy number

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Of circles, forks and humanity: Topological organisation and replication of mammalian mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

The overexpression of Twinkle helicase ameliorates the progression of cardiac fibrosis and heart failure in pressure overload model in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Overexpression of Twinkle-helicase protects cardiomyocytes from genotoxic stress caused by reactive oxygen species

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Premature ageing in mice expressing defective mitochondrial DNA polymerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

Replication stalling by catalytically impaired Twinkle induces mitochondrial DNA rearrangements in cultured cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-015-2532-X

A gene with specific and global effects on recombination of sequences from tandemly repeated genes in Saccharomyces cerevisiae

21 January 2018

1 reference

12 December 2020

Characterization of the Enzymatic Properties of the Yeast Dna2 Helicase/Endonuclease Suggests a New Model for Okazaki Fragment Processing

1 reference

12 December 2020

The oxidative DNA lesion 8,5'-(S)-cyclo-2'-deoxyadenosine is repaired by the nucleotide excision repair pathway and blocks gene expression in mammalian cells

1 reference

12 December 2020

Repair of 8-oxodeoxyguanosine lesions in mitochondrial dna depends on the oxoguanine dna glycosylase (OGG1) gene and 8-oxoguanine accumulates in the mitochondrial dna of OGG1-defective mice

1 reference

12 December 2020

Asbestos increases mammalian AP-endonuclease gene expression, protein levels, and enzyme activity in mesothelial cells

1 reference

12 December 2020

Purification and characterization of a mitochondrial thymine glycol endonuclease from rat liver

1 reference

12 December 2020

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

1 reference

12 December 2020

Kearns-Sayre syndrome with a novel mitochondrial DNA deletion

1 reference

12 December 2020

Preferential formation and decreased removal of cisplatin-DNA adducts in Chinese hamster ovary cell mitochondrial DNA as compared to nuclear DNA

1 reference

12 December 2020

DNA repair of UV photoproducts and mutagenesis in human mitochondrial DNA

1 reference

12 December 2020

PIF1: a DNA helicase in yeast mitochondria

1 reference

12 December 2020

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Overexpression of mitochondrial transcription factor a ameliorates mitochondrial deficiencies and cardiac failure after myocardial infarction

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Preferential attack of mitochondrial DNA by aflatoxin B1 during hepatocarcinogenesis

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Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy

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Twinkle helicase(PEO1)gene mutation causes mitochondrial DNA depletion

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Dna2 requirement for normal reproduction of Caenorhabditis elegans is temperature-dependent

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The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability

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Functional organization of mammalian mitochondrial DNA in nucleoids: history, recent developments, and future challenges.

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Reactive species and mitochondrial dysfunction: mechanistic significance of 4-hydroxynonenal

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Decreased mtDNA, oxidative stress, cardiomyopathy, and death from transgenic cardiac targeted human mutant polymerase gamma.

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Coupling of DNA Helicase and Endonuclease Activities of Yeast Dna2 Facilitates Okazaki Fragment Processing

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Endogenous apurinic/apyrimidinic sites in genomic DNA of mammalian tissues

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Repair of oxidative damage within the mitochondrial DNA of RINr 38 cells

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DNA wrapping and bending by a mitochondrial high mobility group-like transcriptional activator protein

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Unwinding and rewinding: double faces of helicase?

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The presence of nuclear and mitochondrial uracil-DNA glycosylase in extracts of human KB cells

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Protein sliding and DNA denaturation are essential for DNA organization by human mitochondrial transcription factor A

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10.1007/S11010-015-2532-X

Identifiers

DOI

1 reference

Dimensions Publication ID

4 September 2017

1045889807

0 references

1 reference