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
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FG - Paediatrics
OECD FORD branch
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Result continuities
Project
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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
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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
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