Nuclear foci of mammalian recombination proteins are located at single-stranded DNA regions formed after DNA damage
about
The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2Regulation and localization of the Bloom syndrome protein in response to DNA damageBRCA2 and homologous recombinationE3 ligase RFWD3 participates in replication checkpoint controlPML colocalizes with and stabilizes the DNA damage response protein TopBP1The MMS22L-TONSL complex mediates recovery from replication stress and homologous recombinationFBH1 promotes DNA double-strand breakage and apoptosis in response to DNA replication stressMRE11-RAD50-NBS1 is a critical regulator of FANCD2 stability and function during DNA double-strand break repairCDK targeting of NBS1 promotes DNA-end resection, replication restart and homologous recombinationThe Rad51 paralog Rad51B promotes homologous recombinational repairThe BRCA2-interacting protein BCCIP functions in RAD51 and BRCA2 focus formation and homologous recombinational repairDirect DNA binding by Brca1Association of terminal deoxynucleotidyl transferase with KuHuman CtIP promotes DNA end resectionRAD51 localization and activation following DNA damageLoss of Geminin induces rereplication in the presence of functional p53The accumulation of MMS-induced single strand breaks in G1 phase is recombinogenic in DNA polymerase beta defective mammalian cellsImaging genome abnormalities in cancer researchRole of Saccharomyces single-stranded DNA-binding protein RPA in the strand invasion step of double-strand break repairSources of DNA double-strand breaks and models of recombinational DNA repairGenome-wide analysis of Rad52 foci reveals diverse mechanisms impacting recombination.Assembly of RecA-like recombinases: distinct roles for mediator proteins in mitosis and meiosisPredictors and Modulators of Synthetic Lethality: An Update on PARP Inhibitors and Personalized MedicineThe RNF138 E3 ligase displaces Ku to promote DNA end resection and regulate DNA repair pathway choiceXRCC2 is a nuclear RAD51-like protein required for damage-dependent RAD51 focus formation without the need for ATP bindingSpatial organization of the mammalian genome surveillance machinery in response to DNA strand breaksRegulation of replication fork progression through histone supply and demandOncogene-induced senescence is part of the tumorigenesis barrier imposed by DNA damage checkpointsChromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogsBLM helicase-dependent and -independent roles of 53BP1 during replication stress-mediated homologous recombination.RAD51AP2, a novel vertebrate- and meiotic-specific protein, shares a conserved RAD51-interacting C-terminal domain with RAD51AP1/PIR51.Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51.Etoposide induces the dispersal of DNA ligase I from replication factoriesFunctional connection between Rad51 and PML in homology-directed repair.Replication protein A (RPA) phosphorylation prevents RPA association with replication centers.Recruitment of cellular recombination and repair proteins to sites of herpes simplex virus type 1 DNA replication is dependent on the composition of viral proteins within prereplicative sites and correlates with the induction of the DNA damage respoReplication protein A and the Mre11.Rad50.Nbs1 complex co-localize and interact at sites of stalled replication forks.DNA lesion-specific co-localization of the Mre11/Rad50/Nbs1 (MRN) complex and replication protein A (RPA) to repair foci.Functions of human replication protein A (RPA): from DNA replication to DNA damage and stress responsesExtensive ssDNA end formation at DNA double-strand breaks in non-homologous end-joining deficient cells during the S phase
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P2860
Nuclear foci of mammalian recombination proteins are located at single-stranded DNA regions formed after DNA damage
description
1999 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մարտին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 1999
@ast
im März 1999 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1999/03/02)
@sk
vědecký článek publikovaný v roce 1999
@cs
wetenschappelijk artikel (gepubliceerd op 1999/03/02)
@nl
наукова стаття, опублікована в березні 1999
@uk
name
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@ast
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@en
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@nl
type
label
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@ast
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@en
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@nl
prefLabel
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@ast
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@en
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@nl
P2093
P2860
P3181
P356
P1476
Nuclear foci of mammalian reco ...... egions formed after DNA damage
@en
P2093
E. I. Golub
E. Raderschall
P2860
P304
P3181
P356
10.1073/PNAS.96.5.1921
P407
P577
1999-03-02T00:00:00Z