Temporally coordinated assembly and disassembly of replication factories in the absence of DNA synthesis - Wikidata - wikimedia - TriplyDB

Temporally coordinated assembly and disassembly of replication factories in the absence of DNA synthesis

Temporally coordinated assembly and disassembly of replication factories in the absence of DNA synthesis

http://www.wikidata.org/entity/Q30939848

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CDK targeting of NBS1 promotes DNA-end resection, replication restart and homologous recombination Activation of mammalian Chk1 during DNA replication arrest: a role for Chk1 in the intra-S phase checkpoint monitoring replication origin firing Stability, chromatin association and functional activity of mammalian pre-replication complex proteins during the cell cycle Stabilization of stalled DNA replication forks by the BRCA2 breast cancer susceptibility protein Preventing replication fork collapse to maintain genome integrity Checking in on Cds1 (Chk2): A checkpoint kinase and tumor suppressor Regulation of cellular and SV40 virus origins of replication by Chk1-dependent intrinsic and UVC radiation-induced checkpoints Gli1 protein regulates the S-phase checkpoint in tumor cells via Bid protein, and its inhibition sensitizes to DNA topoisomerase 1 inhibitors HCLK2 is essential for the mammalian S-phase checkpoint and impacts on Chk1 stability Regulation of replication timing in fission yeast.ATR: an essential regulator of genome integrity Regulation of DNA replication fork progression through damaged DNA by the Mec1/Rad53 checkpoint The DNA replication checkpoint response stabilizes stalled replication forks Replication independent ATR signalling leads to G2/M arrest requiring Nbs1, 53BP1 and MDC1.The effect of the intra-S-phase checkpoint on origins of replication in human cells.Replication foci dynamics: replication patterns are modulated by S-phase checkpoint kinases in fission yeast.Retinoblastoma tumor suppressor protein signals through inhibition of cyclin-dependent kinase 2 activity to disrupt PCNA function in S phase.Etoposide induces the dispersal of DNA ligase I from replication factories Checkpoint independence of most DNA replication origins in fission yeast Global regulation of genome duplication in eukaryotes: an overview from the epifluorescence microscope.The role of the Fanconi anemia network in the response to DNA replication stress.H3 k36 methylation helps determine the timing of cdc45 association with replication origins Hyperphosphorylation of replication protein A in cisplatin-resistant and -sensitive head and neck squamous cell carcinoma cell lines Single-molecule analysis reveals that DNA replication dynamics vary across the course of schizogony in the malaria parasite Plasmodium falciparum.cAMP-mediated inhibition of DNA replication and S phase progression: involvement of Rb, p21Cip1, and PCNA.Mammalian nuclei become licensed for DNA replication during late telophase Evidence for sequential and increasing activation of replication origins along replication timing gradients in the human genome Dimerization of the ATRIP protein through the coiled-coil motif and its implication to the maintenance of stalled replication forks Cell cycle-dependent phosphorylation of human DNA ligase I at the cyclin-dependent kinase sites.Multiple roles for kinases in DNA replication.Transfection with thymidine kinase permits bromodeoxyuridine labelling of DNA replication in the human malaria parasite Plasmodium falciparum.Epstein-Barr virus (EBV) nuclear antigen 1 colocalizes with cellular replication foci in the absence of EBV plasmids.DNA replication: a complex matter.5-ASA affects cell cycle progression in colorectal cells by reversibly activating a replication checkpoint.The breast cancer susceptibility gene BRCA2 is required for the maintenance of telomere homeostasis.Checking on DNA damage in S phase.The Replication Checkpoint Prevents Two Types of Fork Collapse without Regulating Replisome Stability.Open sesame: activating dormant replication origins in the mouse immunoglobulin heavy chain (Igh) locus Mismatch repair-dependent processing of methylation damage gives rise to persistent single-stranded gaps in newly replicated DNA.Overexpression of hepatocyte nuclear factor-4α initiates cell cycle entry, but is not sufficient to promote β-cell expansion in human islets

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Temporally coordinated assembly and disassembly of replication factories in the absence of DNA synthesis

http://www.wikidata.org/entity/Q30939848

description

2000 nî lūn-bûn

@nan

2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2000年の論文

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2000年論文

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2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

@zh-tw

2000年论文

@wuu

name

Temporally coordinated assembl ...... n the absence of DNA synthesis

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Temporally coordinated assembl ...... n the absence of DNA synthesis

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type

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Temporally coordinated assembl ...... n the absence of DNA synthesis

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Temporally coordinated assembl ...... n the absence of DNA synthesis

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Temporally coordinated assembl ...... n the absence of DNA synthesis

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Temporally coordinated assembl ...... n the absence of DNA synthesis

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Nature Cell Biology

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Temporally coordinated assembl ...... n the absence of DNA synthesis

@en

P2093

D M Gilbert

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

D S Dimitrova

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

P2860

A role for ATR in the DNA damage-induced phosphorylation of p53

A suppressor of two essential checkpoint genes identifies a novel protein that negatively affects dNTP pools.

Recovery from DNA replicational stress is the essential function of the S-phase checkpoint pathway.

Caffeine inhibits the checkpoint kinase ATM

A Mec1- and Rad53-dependent checkpoint controls late-firing origins of DNA replication

Chromosome architecture can dictate site-specific initiation of DNA replication in Xenopus egg extracts.

Radiation effects on DNA synthesis in a defined chromosomal replicon.

The Chinese hamster dihydrofolate reductase origin consists of multiple potential nascent-strand start sites

Defining origins of replication in mammalian cells.

ATR is a caffeine-sensitive, DNA-activated protein kinase with a substrate specificity distinct from DNA-PK.

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P304

686-694

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scholarly article

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10.1038/35036309

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10

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2

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1006757017

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11025658

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1255923

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