Endonucleolytic processing of covalent protein-linked DNA double-strand breaks. - Wikidata - wikimedia - TriplyDB

Endonucleolytic processing of covalent protein-linked DNA double-strand breaks.

Endonucleolytic processing of covalent protein-linked DNA double-strand breaks.

http://www.wikidata.org/entity/Q38322004

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Clarifying the mechanics of DNA strand exchange in meiotic recombination CDK targets Sae2 to control DNA-end resection and homologous recombination DNA resection in eukaryotes: deciding how to fix the break Targeting DNA topoisomerase II in cancer chemotherapy DNA end resection: many nucleases make light work Collision of Trapped Topoisomerase 2 with Transcription and Replication: Generation and Repair of DNA Double-Strand Breaks with 5' Adducts DNA End Resection: Facts and Mechanisms DNA double-strand break repair pathway choice and cancer Repair of strand breaks by homologous recombination Mammalian BTBD12 (SLX4) protects against genomic instability during mammalian spermatogenesis Structural and functional analyses of the DMC1-M200V polymorphism found in the human population Nbs1 Flexibly Tethers Ctp1 and Mre11-Rad50 to Coordinate DNA Double-Strand Break Processing and Repair The Mre11:Rad50 Structure Shows an ATP-Dependent Molecular Clamp in DNA Double-Strand Break Repair Mre11 ATLD17/18 mutation retains Tel1/ATM activity but blocks DNA double-strand break repair Mechanism of repair of 5′-topoisomerase II–DNA adducts by mammalian tyrosyl-DNA phosphodiesterase 2 Structure of Mre11–Nbs1 complex yields insights into ataxia-telangiectasia–like disease mutations and DNA damage signaling Cdc7-dependent phosphorylation of Mer2 facilitates initiation of yeast meiotic recombination.Bidirectional resection of DNA double-strand breaks by Mre11 and Exo1 Budding yeast Pch2, a widely conserved meiotic protein, is involved in the initiation of meiotic recombination.Competing roles of DNA end resection and non-homologous end joining functions in the repair of replication-born double-strand breaks by sister-chromatid recombination.Interactions between Mei4, Rec114, and other proteins required for meiotic DNA double-strand break formation in Saccharomyces cerevisiae Yeast axial-element protein, Red1, binds SUMO chains to promote meiotic interhomologue recombination and chromosome synapsis.Phosphorylation-regulated transitions in an oligomeric state control the activity of the Sae2 DNA repair enzyme.Processing of meiotic DNA double strand breaks requires cyclin-dependent kinase and multiple nucleases.RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination.Meiotic crossover control by concerted action of Rad51-Dmc1 in homolog template bias and robust homeostatic regulation.Processing of damaged DNA ends for double-strand break repair in mammalian cells Initiation of meiotic homologous recombination: flexibility, impact of histone modifications, and chromatin remodeling Connecting by breaking and repairing: mechanisms of DNA strand exchange in meiotic recombination Relative contribution of four nucleases, CtIP, Dna2, Exo1 and Mre11, to the initial step of DNA double-strand break repair by homologous recombination in both the chicken DT40 and human TK6 cell lines A covalent protein-DNA 5'-product adduct is generated following AP lyase activity of human ALKBH1 (AlkB homologue 1)Temporally and biochemically distinct activities of Exo1 during meiosis: double-strand break resection and resolution of double Holliday junctions Collaborative action of Brca1 and CtIP in elimination of covalent modifications from double-strand breaks to facilitate subsequent break repair Numerical analysis of etoposide induced DNA breaks Integrating constitutive gene expression and chemoactivity: mining the NCI60 anticancer screen Meiotic DNA double-strand breaks and chromosome asynapsis in mice are monitored by distinct HORMAD2-independent and -dependent mechanisms Mouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPase Meiotic DNA break formation requires the unsynapsed chromosome axis-binding protein IHO1 (CCDC36) in mice The TopoVIB-Like protein family is required for meiotic DNA double-strand break formation Meiotic homologue alignment and its quality surveillance are controlled by mouse HORMAD1.

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Endonucleolytic processing of covalent protein-linked DNA double-strand breaks.

http://www.wikidata.org/entity/Q38322004

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2005 nî lūn-bûn

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Endonucleolytic processing of covalent protein-linked DNA double-strand breaks.

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Endonucleolytic processing of covalent protein-linked DNA double-strand breaks.

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Endonucleolytic processing of covalent protein-linked DNA double-strand breaks.

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Endonucleolytic processing of covalent protein-linked DNA double-strand breaks.

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Jing Pan

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Matthew J Neale

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Scott Keeney

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P2860

Cloning, characterization, and localization of mouse and human SPO11

The 3' to 5' exonuclease activity of Mre 11 facilitates repair of DNA double-strand breaks

Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage.

Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae

Tid1/Rdh54 promotes colocalization of rad51 and dmc1 during meiotic recombination

Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae

Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family

Yeast gene for a Tyr-DNA phosphodiesterase that repairs topoisomerase I complexes.

Role of yeast Rth1 nuclease and its homologs in mutation avoidance, DNA repair, and DNA replication.

Identification of residues in yeast Spo11p critical for meiotic DNA double-strand break formation.

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