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HPV-mediated inactivation of tumor suppressor p53.

作者信息

Travé Gilles, Zanier Katia

机构信息

a Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM U964, CNRS UMR 7104, Université de Strasbourg , Illkirch , France.

b Biotechnologie et Signalisation Cellulaire (UMR 7242), Ecole Superieure de Biotechnologie de Strasbourg , Illkirch , France.

出版信息

Cell Cycle. 2016 Sep;15(17):2231-2. doi: 10.1080/15384101.2016.1191257. Epub 2016 May 31.

Abstract
摘要

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本文引用的文献

1
Structure of the E6/E6AP/p53 complex required for HPV-mediated degradation of p53.
Nature. 2016 Jan 28;529(7587):541-5. doi: 10.1038/nature16481. Epub 2016 Jan 20.
2
Intracellular Analysis of the Interaction between the Human Papillomavirus Type 16 E6 Oncoprotein and Inhibitory Peptides.
PLoS One. 2015 Jul 7;10(7):e0132339. doi: 10.1371/journal.pone.0132339. eCollection 2015.
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Structural basis for hijacking of cellular LxxLL motifs by papillomavirus E6 oncoproteins.
Science. 2013 Feb 8;339(6120):694-8. doi: 10.1126/science.1229934.
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Peptide interactions stabilize and restructure human papillomavirus type 16 E6 to interact with p53.
J Virol. 2012 Oct;86(20):11386-91. doi: 10.1128/JVI.01236-12. Epub 2012 Aug 15.
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The common mechanisms of transformation by the small DNA tumor viruses: The inactivation of tumor suppressor gene products: p53.
Virology. 2009 Feb 20;384(2):285-93. doi: 10.1016/j.virol.2008.09.034. Epub 2008 Dec 11.
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Association of human papillomavirus types 16 and 18 E6 proteins with p53.
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