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Essential and dispensable roles of ATR in cell cycle arrest and genome maintenance

Data up to Jan 2025

Published2003
Citations489
References44

Total Citations Per Year

Abstract

References (44)

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Overexpression of a kinase-inactive ATR protein causes sensitivity to DNA-damaging agents and defects in cell cycle checkpoints

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Regulation of ATR substrate selection by Rad17-dependent loading of Rad9 complexes onto chromatin

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Two Molecularly Distinct G2/M Checkpoints Are Induced by Ionizing Irradiation

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ATR Homolog Mec1 Promotes Fork Progression, Thus Averting Breaks in Replication Slow Zones

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ATR inhibition selectively sensitizes G 1 checkpoint-deficient cells to lethal premature chromatin condensation

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The Xenopus Chk1 Protein Kinase Mediates a Caffeine-sensitive Pathway of Checkpoint Control in Cell-free Extracts

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Xenopus ATR is a replication-dependent chromatin-binding protein required for the DNA replication checkpoint

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Phosphorylation of murine p53 at Ser-18 regulates the p53 responses to DNA damage

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Checkpoint activation regulates mutagenic translesion synthesis

2003 • 159 citations

Mitotic Histone H3 Phosphorylation by the NIMA Kinase in Aspergillus nidulans

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ATR Is Not Required for p53 Activation but Synergizes with p53 in the Replication Checkpoint

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Essential and dispensable roles of ATR in cell cycle arrest and genome maintenance (2003) – Genes & Development | Metascience Observatory Explorer