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MEG3: A novel long noncoding potentially tumour-suppressing RNA in meningiomas (Review)

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F13%3A33146092" target="_blank" >RIV/61989592:15110/13:33146092 - isvavai.cz</a>

  • Alternative codes found

    RIV/00098892:_____/13:#0000427

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s11060-012-1038-6" target="_blank" >http://dx.doi.org/10.1007/s11060-012-1038-6</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s11060-012-1038-6" target="_blank" >10.1007/s11060-012-1038-6</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    MEG3: A novel long noncoding potentially tumour-suppressing RNA in meningiomas (Review)

  • Original language description

    Meningiomas represent one of the most common types of primary intracranial tumours. However, the specific molecular mechanisms underlying their pathogenesis remain uncertain. Loss of chromosomes 22q, 1p, and 14q have been implicated in most meningiomas.Inactivation of the NF2 gene at 22q12 has been identified as an early event in their pathogenesis, whereas abnormalities of chromosome 14 have been reported in higher-grade as well as recurrent tumours. It has long been supposed that chromosome 14q32 contains a tumour suppressor gene. However, the identity of the potential 14q32 tumour suppressor remained elusive until the Maternally Expressed Gene 3 (MEG3) was recently suggested as an ideal candidate. MEG3 is an imprinted gene located at 14q32 that encodes a non-coding RNA (ncRNA). In meningiomas, loss of MEG3 expression, its genomic DNA deletion and degree of promoter methylation have been found to be associated with aggressive tumour growth. These findings indicate that MEG3 may have

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    FH - Neurology, neuro-surgery, nuero-sciences

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Neuro-Oncology

  • ISSN

    0167-594X

  • e-ISSN

  • Volume of the periodical

    112

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    1-8

  • UT code for WoS article

  • EID of the result in the Scopus database