Formation of AR-SMRT binding in prostate cancer cells treated with natural histone deacetylase inhibitor
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F10%3A33140357" target="_blank" >RIV/61989592:15110/10:33140357 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.3233/CBM-2010-0150" target="_blank" >http://dx.doi.org/10.3233/CBM-2010-0150</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3233/CBM-2010-0150" target="_blank" >10.3233/CBM-2010-0150</a>
Alternative languages
Result language
angličtina
Original language name
Formation of AR-SMRT binding in prostate cancer cells treated with natural histone deacetylase inhibitor
Original language description
Signaling through the androgen receptor (AR) plays a critical role in prostate cancer progression. The AR is a classical nuclear receptor (NR) providing a link between signaling molecule and transcription response. Histone deacetylase inhibitors (HDACI)have antiproliferative and proapoptotic effects on prostate cancer cells and their implication in silence AR signaling may have potential therapeutic use.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2010
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cancer Biomarkers
ISSN
1574-0153
e-ISSN
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Volume of the periodical
7
Issue of the periodical within the volume
2
Country of publishing house
US - UNITED STATES
Number of pages
12
Pages from-to
79-90
UT code for WoS article
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EID of the result in the Scopus database
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