An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis
about
Common fragile sites: genomic hotspots of DNA damage and carcinogenesisFATS is a transcriptional target of p53 and associated with antitumor activityThe value of FATS expression in predicting sensitivity to radiotherapy in breast cancerA functional genetic variant in fragile-site gene FATS modulates the risk of breast cancer in triparous womenStabilization of p21 (Cip1/WAF1) following Tip60-dependent acetylation is required for p21-mediated DNA damage responseFATS is an E2-independent ubiquitin ligase that stabilizes p53 and promotes its activation in response to DNA damage.
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An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis
description
2010 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2010 թվականի մայիսին հրատարակված գիտական հոդված
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artículu científicu espublizáu en 2010
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im Mai 2010 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 2010/05/06)
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vědecký článek publikovaný v roce 2010
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wetenschappelijk artikel (gepubliceerd op 2010/05/06)
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наукова стаття, опублікована в травні 2010
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مقالة علمية (نشرت في 6-5-2010)
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name
An HDAC1-binding domain within ...... adiation-induced tumorigenesis
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An HDAC1-binding domain within ...... adiation-induced tumorigenesis
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An HDAC1-binding domain within ...... adiation-induced tumorigenesis
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type
label
An HDAC1-binding domain within ...... adiation-induced tumorigenesis
@ast
An HDAC1-binding domain within ...... adiation-induced tumorigenesis
@en
An HDAC1-binding domain within ...... adiation-induced tumorigenesis
@nl
prefLabel
An HDAC1-binding domain within ...... adiation-induced tumorigenesis
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An HDAC1-binding domain within ...... adiation-induced tumorigenesis
@en
An HDAC1-binding domain within ...... adiation-induced tumorigenesis
@nl
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An HDAC1-binding domain within ...... adiation-induced tumorigenesis
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P2093
A. Balmain
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10.1038/ONC.2010.19
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P577
2010-05-06T00:00:00Z
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1026271272