All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Microheterogeneity of some serum glycoproteins in neurodegenerative diseases

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F12%3A10108107" target="_blank" >RIV/00179906:_____/12:10108107 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11150/12:10108107

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S0022510X11006587" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0022510X11006587</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jns.2011.11.006" target="_blank" >10.1016/j.jns.2011.11.006</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Microheterogeneity of some serum glycoproteins in neurodegenerative diseases

  • Original language description

    Protein polymorphism and aberrant protein glycosylation may play important roles in human disorders, including neurodegenerative diseases. The aim of the study was to examine possible involvement of protein genetic variants and degree of glycosylation ofsome serum glycoproteins in the manifestation of neurodegenerative disorders in a Czech population sample. Apolipoprotein (Apo) E and three main serum markers of glycosylation defects (transferrin, Tf, alpha1-antitrypsin, aAT and ApoCIII) in patients with Alzheimer's dementia (AD), Parkinson disease (PD) and vascular dementia (n=62, 139 and 44, respectively) were analyzed by isoelectric focusing. Children with serious neurological symptoms (n=55) and three age-matched control groups (n=45, 45 and 42) were examined for comparison. Of the supposedly pathognomonic protein variants Tf C2, aAT ZM and ApoE e4 only the latter was detected with higher frequency in AD patients; significant synergy of the C2/e4 allelic combination was not confir

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    FG - Paediatrics

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2012

  • 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 the Neurological Sciences

  • ISSN

    0022-510X

  • e-ISSN

  • Volume of the periodical

    314

  • Issue of the periodical within the volume

    1-2

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    6

  • Pages from-to

    20-25

  • UT code for WoS article

    000301273000004

  • EID of the result in the Scopus database