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The functional interactions between CD98, beta 1-integrins, and CD147 in the induction of U937 homotypic aggregation.

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F01%3A23010304" target="_blank" >RIV/68378050:_____/01:23010304 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    The functional interactions between CD98, beta 1-integrins, and CD147 in the induction of U937 homotypic aggregation.

  • Original language description

    Several of the CD98 antibodies induced homotypic aggregation of U937 cells without affecting cellular viability or growth. Some CD29 antibodies partially inhibited CD98-induced aggregation. Some CD98 antibodies were potent inhibitors of CD29-induced aggregation. Two antibodies to CD147 were also potent inhibitors of both the aggregation and the protein tyrosine phosphorylation induced via CD98 ligation. The results support a role for CD98 within a multimolecular unit that regulates cell aggregation.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GA310%2F99%2F0349" target="_blank" >GA310/99/0349: Low-affinity monoclonal antibodies as specific tolls targeting functionally important subsets of leukocyte surface receptors</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2001

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Blood

  • ISSN

    0006-4971

  • e-ISSN

  • Volume of the periodical

    98

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    374-382

  • UT code for WoS article

  • EID of the result in the Scopus database