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Detection of the GPI-anchorless prion protein fragment PrP226 in human brain

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F13%3A10189589" target="_blank" >RIV/00216208:11110/13:10189589 - isvavai.cz</a>

  • Alternative codes found

    RIV/61389013:_____/13:00398156 RIV/00064190:_____/13:#0000663

  • Result on the web

    <a href="http://dx.doi.org/10.1186/1471-2377-13-126" target="_blank" >http://dx.doi.org/10.1186/1471-2377-13-126</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1186/1471-2377-13-126" target="_blank" >10.1186/1471-2377-13-126</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Detection of the GPI-anchorless prion protein fragment PrP226 in human brain

  • Original language description

    Background: The accumulation of the misfolded forms of cellular prion protein, i.e. prions (PrPSc), in the brain is one of the crucial characteristics of fatal neurodegenerative disorders, called transmissible spongiform encephalopathies (TSEs). Cellularprion protein is normally linked to the cell surface by the glycosylphosphatidylinositol (GPI) anchor. There is accumulating evidence that the GPI-anchorless prion protein may act as an accelerator of formation and propagation of prions. In the TSE affected human brain we have previously discovered a novel GPI-anchorless prion protein fragment, named PrP226*, which ends with the tyrosine 226. This fragment can be labeled specifically by the monoclonal antibody V5B2. Methods: We developed a DELFIA basedassay for quick and sensitive detection of the PrP226* fragment in human brain tissue homogenates. By calculating the ratio between the signals of native (N) and denatured (D) samples applied to the assay we were able to observe signific

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    EE - Microbiology, virology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach<br>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

    BMC Neurology

  • ISSN

    1471-2377

  • e-ISSN

  • Volume of the periodical

    13

  • Issue of the periodical within the volume

    September

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

  • UT code for WoS article

    000324882600002

  • EID of the result in the Scopus database