Interplay between Ino80 and Swr1 chromatin remodeling enzymes regulates cell cycle checkpoint adaptation in response to DNA damage. - Wikidata - awgldk - TriplyDB

Interplay between Ino80 and Swr1 chromatin remodeling enzymes regulates cell cycle checkpoint adaptation in response to DNA damage.

Interplay between Ino80 and Swr1 chromatin remodeling enzymes regulates cell cycle checkpoint adaptation in response to DNA damage.

http://www.wikidata.org/entity/Q35018049

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Human INO80 chromatin-remodelling complex contributes to DNA double-strand break repair via the expression of Rad54B and XRCC3 genes A cooperative activation loop among SWI/SNF, gamma-H2AX and H3 acetylation for DNA double-strand break repair Epigenetic modifications in double-strand break DNA damage signaling and repair Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications The emerging roles of ATP-dependent chromatin remodeling enzymes in nucleotide excision repair A peek into the complex realm of histone phosphorylation Inhibition of proteasomal degradation of rpn4 impairs nonhomologous end-joining repair of DNA double-strand breaks.Global regulation of H2A.Z localization by the INO80 chromatin-remodeling enzyme is essential for genome integrity Cooperation between the INO80 complex and histone chaperones determines adaptation of stress gene transcription in the yeast Saccharomyces cerevisiae.Histone variant Htz1 promotes histone H3 acetylation to enhance nucleotide excision repair in Htz1 nucleosomes.Distinct roles for SWR1 and INO80 chromatin remodeling complexes at chromosomal double-strand breaks.Asf1 facilitates dephosphorylation of Rad53 after DNA double-strand break repair.Regulation of telomere structure and functions by subunits of the INO80 chromatin remodeling complex.Recombinational repair within heterochromatin requires ATP-dependent chromatin remodeling.A moonlighting metabolic protein influences repair at DNA double-stranded breaks.NuA4-dependent acetylation of nucleosomal histones H4 and H2A directly stimulates incorporation of H2A.Z by the SWR1 complex.The Snf2 homolog Fun30 acts as a homodimeric ATP-dependent chromatin-remodeling enzyme Differential requirement for SUB1 in chromosomal and plasmid double-strand DNA break repair The HINT1 tumor suppressor regulates both gamma-H2AX and ATM in response to DNA damage ATP-dependent chromatin remodeling shapes the DNA replication landscape Human Rvb1/Tip49 is required for the histone acetyltransferase activity of Tip60/NuA4 and for the downregulation of phosphorylation on H2AX after DNA damage.H2A.Z acidic patch couples chromatin dynamics to regulation of gene expression programs during ESC differentiation.The SWR1 histone replacement complex causes genetic instability and genome-wide transcription misregulation in the absence of H2A.Z.The NuRD chromatin-remodeling complex regulates signaling and repair of DNA damage Experimental approaches to the study of epigenomic dysregulation in ageing Mammalian Ino80 mediates double-strand break repair through its role in DNA end strand resection Proficient repair in chromatin remodeling defective ino80 mutants of Saccharomyces cerevisiae highlights replication defects as the main contributor to DNA damage sensitivity Mi-2/NuRD complex making inroads into DNA-damage response pathway The p400 ATPase regulates nucleosome stability and chromatin ubiquitination during DNA repair.Histone phosphorylation: a chromatin modification involved in diverse nuclear events.Rewiring of genetic networks in response to DNA damage.Histone chaperone CAF-1: essential roles in multi-cellular organism development.Chromatin remodelling beyond transcription: the INO80 and SWR1 complexes.Chromatin remodelling and actin organisation.The Ino80 complex prevents invasion of euchromatin into silent chromatin.Chromatin remodeling factors Isw2 and Ino80 regulate checkpoint activity and chromatin structure in S phase.SWI/SNF recruitment to a DNA double-strand break by the NuA4 and Gcn5 histone acetyltransferases Caffeine impairs resection during DNA break repair by reducing the levels of nucleases Sae2 and Dna2.ATP-dependent chromatin remodeling in the DNA-damage response.ATP-dependent chromatin remodeling factors and DNA damage repair

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Interplay between Ino80 and Swr1 chromatin remodeling enzymes regulates cell cycle checkpoint adaptation in response to DNA damage.

http://www.wikidata.org/entity/Q35018049

description

2006 nî lūn-bûn

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2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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Interplay between Ino80 and Sw ...... ion in response to DNA damage.

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Interplay between Ino80 and Sw ...... ion in response to DNA damage.

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Interplay between Ino80 and Sw ...... ion in response to DNA damage.

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Interplay between Ino80 and Sw ...... ion in response to DNA damage.

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Interplay between Ino80 and Sw ...... ion in response to DNA damage.

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Interplay between Ino80 and Sw ...... ion in response to DNA damage.

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Genes & Development

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Interplay between Ino80 and Sw ...... tion in response to DNA damage

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Craig L Peterson

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Jocelyn E Krebs

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P2860

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

Megabase chromatin domains involved in DNA double-strand breaks in vivo

A protein complex containing the conserved Swi2/Snf2-related ATPase Swr1p deposits histone variant H2A.Z into euchromatin

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

Genetic requirements for the single-strand annealing pathway of double-strand break repair in Saccharomyces cerevisiae

ATP-driven exchange of histone H2AZ variant catalyzed by SWR1 chromatin remodeling complex.

A role for Saccharomyces cerevisiae histone H2A in DNA repair.

Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair.

Binding of chromatin-modifying activities to phosphorylated histone H2A at DNA damage sites.

Histone H2A.Z has a conserved function that is distinct from that of the major H2A sequence variants.

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10.1101/GAD.1440206

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17

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20

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Manolis Papamichos-Chronakis

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2006-09-01T00:00:00Z

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