MDC1 is required for the intra-S-phase DNA damage checkpoint (Q28212500)

8

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Jiří Bártek

7

object named as

Jiri Bartek

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author name string

Michal Goldberg

1

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Manuel Stucki

2

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Jacob Falck

3

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Damien D'Amours

4

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Dinah Rahman

ATM-dependent phosphorylation of nibrin in response to radiation exposure

5

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publication date

27 February 2003

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language of work or name

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421

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issue

6926

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page(s)

952-6

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cites work

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ATM phosphorylates p95/nbs1 in an S-phase checkpoint pathway

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Functional link between ataxia-telangiectasia and Nijmegen breakage syndrome gene products

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A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage

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

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ATM phosphorylates histone H2AX in response to DNA double-strand breaks

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Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells

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The ATM-Chk2-Cdc25A checkpoint pathway guards against radioresistant DNA synthesis

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SMC1 is a downstream effector in the ATM/NBS1 branch of the human S-phase checkpoint

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Involvement of the cohesin protein, Smc1, in Atm-dependent and independent responses to DNA damage

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Mre11 complex and DNA replication: linkage to E2F and sites of DNA synthesis

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NFBD1/KIAA0170 is a novel nuclear transcriptional transactivator with BRCT domain

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ATM phosphorylation of Nijmegen breakage syndrome protein is required in a DNA damage response

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The hMre11/hRad50 Protein Complex and Nijmegen Breakage Syndrome: Linkage of Double-Strand Break Repair to the Cellular DNA Damage Response

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Positional cloning of the gene for Nijmegen breakage syndrome

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The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder

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A single ataxia telangiectasia gene with a product similar to PI-3 kinase

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Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome

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Ataxia-telangiectasia and the Nijmegen breakage syndrome: related disorders but genes apart

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The DNA damage-dependent intra-S phase checkpoint is regulated by parallel pathways

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Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1

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hMre11 and hRad50 Nuclear Foci Are Induced During the Normal Cellular Response to DNA Double-Strand Breaks †

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p53 binding protein 1 (53BP1) is an early participant in the cellular response to DNA double-strand breaks

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