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Modeling tumorigenesis in Drosophila: Current Advances and Future Perspectives

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F13%3A10195048" target="_blank" >RIV/00216208:11110/13:10195048 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.5772/55686" target="_blank" >http://dx.doi.org/10.5772/55686</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.5772/55686" target="_blank" >10.5772/55686</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Modeling tumorigenesis in Drosophila: Current Advances and Future Perspectives

  • Original language description

    Cancer is essentially considered as a genetic disease caused by the accumulation of multiple genetic or epigenetic lesions in tumor-suppressor genes and oncogenes [1]. Although the notion that retinoblastoma could be an inherited disease was already formulated at the end of the 19th Century a solid genetic basis was established with the discovery of both proto-oncogenes, whose gain-of function mutations or altered expression is associated with the cancerous state, and tumor suppressor genes (TSGs), whose inactivation releases the "brakes" inhibiting cell proliferation. Analysis of both proto-oncogenes and TSGs revealed also that cancer results from an alteration of the normal pathway of cell fate and differentiation. The hallmarks of cancer, as laid down by Hanahan and Weinberg to explain the complex biology of cancer, comprise six major developmental changes taking successively place in human tumors. These cancer "characteristics" include sustained proliferative signaling, evasion of

  • Czech name

  • Czech description

Classification

  • Type

    C - Chapter in a specialist book

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GAP302%2F11%2F1640" target="_blank" >GAP302/11/1640: Morphological features and molecular determinants of apocrine secretion</a><br>

  • 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

  • Book/collection name

    Future Aspects of Tumor Suppressor Gene

  • ISBN

    978-953-51-1063-7

  • Number of pages of the result

    29

  • Pages from-to

    98-127

  • Number of pages of the book

    221

  • Publisher name

    InTech

  • Place of publication

    Rijeka, Croatia

  • UT code for WoS chapter