All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Expression of p53 and p53/47 are controlled by alternative mechanisms of messenger RNA translation initiation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F06%3A0000020" target="_blank" >RIV/00209805:_____/06:0000020 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Expression of p53 and p53/47 are controlled by alternative mechanisms of messenger RNA translation initiation

  • Original language description

    We have described an N-terminally truncated p53 protein (p53/47) which can interact with p53 and impose altered stability and transactivation properties to p53 complexes. Changes in synthesis of full-length p53 or p53/47 are regulated through distinct cell stress-induced pathways acting through separate regions of the p53 mRNA. We also show that some cytotoxic drugs require the presence of full-length p53 to induce apoptosis, whereas for others p53/47 is sufficient.

  • Czech name

    Exprese p53 a p53/47 je kontrolována alternativním mechanismem iniciace translace mediátorové RNA

  • Czech description

    Popsali jsme na N-konci zkrácenou formu proteinu p53 (p53/47), která může interagovat s p53 a ovlivňovat tak stabilitu a transaktivační schopnosti komplexů p53. Změny v tvorbě p53 a/nebo p53/47 jsou v buňce regulovány různými stresem indukovanými dráhami. Dále ukazujeme, že některé cytotoxické látky indukují apoptózu jen v přítomnosti p53, zatímco u jiných látek stačí k indukci apoptózy přítomnost p53/47.

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NR8338" target="_blank" >NR8338: Functional analysis of the p53-dependent pathways in breast cancer: Integration of genomic and proteomic approaches using DNA-macroarray and SELDI-TOF mass spectrometry techniques</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2006

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Oncogene

  • ISSN

    0950-9232

  • e-ISSN

  • Volume of the periodical

    25

  • Issue of the periodical within the volume

    52

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    6936-6947

  • UT code for WoS article

  • EID of the result in the Scopus database