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Antigen selection in B-cell lymphomas-Tracing the evidence

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F13%3A00072727" target="_blank" >RIV/00216224:14740/13:00072727 - isvavai.cz</a>

  • Result on the web

    <a href="http://ac.els-cdn.com/S1044579X1300076X/1-s2.0-S1044579X1300076X-main.pdf?_tid=53d1b2dc-bfba-11e3-91ac-00000aab0f6b&acdnat=1397029454_a5ad89568b55191984c5a6ad89549a75" target="_blank" >http://ac.els-cdn.com/S1044579X1300076X/1-s2.0-S1044579X1300076X-main.pdf?_tid=53d1b2dc-bfba-11e3-91ac-00000aab0f6b&acdnat=1397029454_a5ad89568b55191984c5a6ad89549a75</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.semcancer.2013.07.006" target="_blank" >10.1016/j.semcancer.2013.07.006</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Antigen selection in B-cell lymphomas-Tracing the evidence

  • Original language description

    While signaling through the B cell receptor (BcR) facilitates B cell development and maintenance, it also carries intertwined risks for the development of lymphomas since malignant B cells can exploit these pathways in order to trigger and fuel clonal expansion. This corruption of the normal B cell response to antigens, leading to sustained BcR signaling, has given great impulse to investigate in detail the role of antigen in lymphomas. Suffice it to conclude from such studies, largely immunogenetics based, that the evidence implicating antigens (exogenous or self) in lymphoma development is substantial and that lymphomagenesis is functionally driven and dynamic, rather than a simple stochastic process. As the paradigm of antigen-driven lymphoma evolves, further investigation will be paramount to the identification of the inciting agent(s) that may be responsible for immunoproliferative neoplasms and also for the development of therapeutic agents targeting effectors of the BcR signalin

  • Czech name

  • Czech description

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

  • 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

    Seminars in Cancer Biology

  • ISSN

    1044-579X

  • e-ISSN

  • Volume of the periodical

    23

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    11

  • Pages from-to

    399-409

  • UT code for WoS article

    000329011000002

  • EID of the result in the Scopus database