Processing of damaged DNA ends for double-strand break repair in mammalian cells - Test2 - elhamkhani - TriplyDB

Processing of damaged DNA ends for double-strand break repair in mammalian cells

Processing of damaged DNA ends for double-strand break repair in mammalian cells

http://www.wikidata.org/entity/Q28000148

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Interactome analysis identifies a new paralogue of XRCC4 in non-homologous end joining DNA repair pathway DNA double-strand-break complexity levels and their possible contributions to the probability for error-prone processing and repair pathway choice DNA topoisomerase II-dependent control of the cell cycle progression in root meristems of Allium cepa.Microhomology-mediated end joining is activated in irradiated human cells due to phosphorylation-dependent formation of the XRCC1 repair complex.Mutational phospho-mimicry reveals a regulatory role for the XRCC4 and XLF C-terminal tails in modulating DNA bridging during classical non-homologous end joining APE1 is dispensable for S-region cleavage but required for its repair in class switch recombination.Recognition and repair of chemically heterogeneous structures at DNA ends Tetrameric Ctp1 coordinates DNA binding and DNA bridging in DNA double-strand-break repair.Fidelity of end joining in mammalian episomes and the impact of Metnase on joint processing.DNA double-strand break repair is impaired in presenescent Syrian hamster fibroblasts Unifying the DNA end-processing roles of the artemis nuclease: Ku-dependent artemis resection at blunt DNA ends.Recombinational repair of radiation-induced double-strand breaks occurs in the absence of extensive resection.Nonhomologous end joining of complex DNA double-strand breaks with proximal thymine glycol and interplay with base excision repair Trimming of damaged 3' overhangs of DNA double-strand breaks by the Metnase and Artemis endonucleases The structure of ends determines the pathway choice and Mre11 nuclease dependency of DNA double-strand break repair.The T-box transcription factor 3 is a promising biomarker and a key regulator of the oncogenic phenotype of a diverse range of sarcoma subtypes Tracking the processing of damaged DNA double-strand break ends by ligation-mediated PCR: increased persistence of 3'-phosphoglycolate termini in SCAN1 cells.DNA double-strand break repair as determinant of cellular radiosensitivity to killing and target in radiation therapy.Functional interplay between ATM/ATR-mediated DNA damage response and DNA repair pathways in oxidative stress.TDP1 deficiency sensitizes human cells to base damage via distinct topoisomerase I and PARP mechanisms with potential applications for cancer therapy.Regulation of non-homologous end joining via post-translational modifications of components of the ligation step.TDP1 promotes assembly of non-homologous end joining protein complexes on DNA.An essential developmental function for murine phosphoglycolate phosphatase in safeguarding cell proliferation Ape1 guides DNA repair pathway choice that is associated with drug tolerance in glioblastoma Polynucleotide 3'-terminal phosphate modifications by RNA and DNA ligases.The fidelity of the ligation step determines how ends are resolved during nonhomologous end joining.Tyrosyl-DNA phosphodiesterases: rescuing the genome from the risks of relaxation.Nonhomologous DNA End Joining for Repair of DNA Double-Strand Breaks.Hypericum perforatum: Synthesis of Active Principles during Flowering and Fruitification-Novel Aspects of Biological Potential.TDP1 and TDP2 process unligatable DSB ends XRCC4:LIG4 ligates DNA DSB ends during NHEJ Immunofluorescence Analysis of γ-H2AX Foci in Mammalian Fibroblasts at Different Phases of the Cell Cycle.The Interaction of the Metallo-Glycopeptide Anti-Tumour Drug Bleomycin with DNA.TDP1 suppresses mis-joining of radiomimetic DNA double-strand breaks and cooperates with Artemis to promote optimal nonhomologous end joining

P2860

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P2860

Processing of damaged DNA ends for double-strand break repair in mammalian cells

http://www.wikidata.org/entity/Q28000148

description

2012 nî lūn-bûn

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2012 թուականին հրատարակուած գիտական յօդուած

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2012 թվականին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Processing of damaged DNA ends for double-strand break repair in mammalian cells

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Processing of damaged DNA ends for double-strand break repair in mammalian cells

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Processing of damaged DNA ends for double-strand break repair in mammalian cells.

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type

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Processing of damaged DNA ends for double-strand break repair in mammalian cells

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Processing of damaged DNA ends for double-strand break repair in mammalian cells

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Processing of damaged DNA ends for double-strand break repair in mammalian cells.

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Processing of damaged DNA ends for double-strand break repair in mammalian cells

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Processing of damaged DNA ends for double-strand break repair in mammalian cells

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Processing of damaged DNA ends for double-strand break repair in mammalian cells

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Processing of damaged DNA ends for double-strand break repair in mammalian cells.

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ISRN molecular biology

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Processing of damaged DNA ends for double-strand break repair in mammalian cells

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Lawrence F Povirk

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P2860

Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damage

Molecular characterization of a human DNA kinase

The RAD2 domain of human exonuclease 1 exhibits 5' to 3' exonuclease and flap structure-specific endonuclease activities

Regulation and mechanisms of mammalian double-strand break repair

Human DNA damage checkpoint protein hRAD9 is a 3' to 5' exonuclease

Hairpin opening and overhang processing by an Artemis/DNA-dependent protein kinase complex in nonhomologous end joining and V(D)J recombination

Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1

Conversion of phosphoglycolate to phosphate termini on 3' overhangs of DNA double strand breaks by the human tyrosyl-DNA phosphodiesterase hTdp1

Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?

The SET domain protein Metnase mediates foreign DNA integration and links integration to nonhomologous end-joining repair

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1-16

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10.5402/2012/345805

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2012

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2012-01-01T00:00:00Z

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