RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage. - Wikidata - wikimedia - TriplyDB

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

http://www.wikidata.org/entity/Q33362855

about

A PP4 phosphatase complex dephosphorylates RPA2 to facilitate DNA repair via homologous recombination DNA-PK-dependent RPA2 hyperphosphorylation facilitates DNA repair and suppresses sister chromatid exchange N terminus of CtIP is critical for homologous recombination-mediated double-strand break repair Involvement of nucleotide excision and mismatch repair mechanisms in double strand break repair Managing Single-Stranded DNA during Replication Stress in Fission Yeast RPA-coated single-stranded DNA as a platform for post-translational modifications in the DNA damage response Inhibition of the mitotic exit network in response to damaged telomeres.Chromosome tips damaged in anaphase inhibit cytokinesis Mitotic crisis: the unmasking of a novel role for RPA Pot1a prevents telomere dysfunction and ATM-dependent neuronal loss.Ionizing radiation-dependent and independent phosphorylation of the 32-kDa subunit of replication protein A during mitosis Human RPA phosphorylation by ATR stimulates DNA synthesis and prevents ssDNA accumulation during DNA-replication stress The role of RPA2 phosphorylation in homologous recombination in response to replication arrest Replication protein A: directing traffic at the intersection of replication and repair.Cdk1 uncouples CtIP-dependent resection and Rad51 filament formation during M-phase double-strand break repair Phosphorylated RPA recruits PALB2 to stalled DNA replication forks to facilitate fork recovery.DNA-PK, ATM and ATR collaboratively regulate p53-RPA interaction to facilitate homologous recombination DNA repair In vitro analysis of the role of replication protein A (RPA) and RPA phosphorylation in ATR-mediated checkpoint signaling Distinct roles for DNA-PK, ATM and ATR in RPA phosphorylation and checkpoint activation in response to replication stress.Rfa2 is specifically dephosphorylated by Pph3 in Candida albicans.Zinc finger protein 668 interacts with Tip60 to promote H2AX acetylation after DNA damage Revised genetic requirements for the decatenation G2 checkpoint: the role of ATM.The DNA damage response and checkpoint adaptation in Saccharomyces cerevisiae: distinct roles for the replication protein A2 (Rfa2) N-terminus.Regulation of Rfa2 phosphorylation in response to genotoxic stress in Candida albicans.DNA damage response is suppressed by the high cyclin-dependent kinase 1 activity in mitotic mammalian cells A genome-wide RNAi screen identifies core components of the G₂-M DNA damage checkpoint.The control of DNA repair by the cell cycle.Nucleolin phosphorylation regulates PARN deadenylase activity during cellular stress response.

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P2860

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

http://www.wikidata.org/entity/Q33362855

description

2008 nî lūn-bûn

@nan

2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

name

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

@ast

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

@en

type

label

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

@ast

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

@en

prefLabel

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

@ast

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

@en

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PNAS.0803001105

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Proceedings of the National Academy of Sciences of the United States of America

P1476

RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage.

@en

P2093

Elena Sokolova

http://www.w3.org/2001/XMLSchema#string

Rachel William Anantha

http://www.w3.org/2001/XMLSchema#string

P2860

Replication Protein A (RPA): The Eukaryotic SSB

cdc2 family kinases phosphorylate a human cell DNA replication factor, RPA, and activate DNA replication

Sensing DNA damage through ATRIP recognition of RPA-ssDNA complexes

Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints

Replication protein A phosphorylation and the cellular response to DNA damage

ATM and related protein kinases: safeguarding genome integrity

Stability and nuclear distribution of mammalian replication protein A heterotrimeric complex.

DNA damage during mitosis in human cells delays the metaphase/anaphase transition via the spindle-assembly checkpoint.

RPA phosphorylation in mitosis alters DNA binding and protein-protein interactions.

Replication protein A (RPA) phosphorylation prevents RPA association with replication centers.

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12903-12908

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scholarly article

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10.1073/PNAS.0803001105

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35

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105

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James A Borowiec

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2008-08-22T00:00:00Z

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phosphorylation

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