Genetic defects in common variable immunodeficiency
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F07%3A00003838" target="_blank" >RIV/00216208:11150/07:00003838 - isvavai.cz</a>
Alternative codes found
RIV/00179906:_____/07:00000384
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Genetic defects in common variable immunodeficiency
Original language description
CVID is a heterogenous group of diseases. The defects of molecules regulating activation and terminal differentiation of B lymfocytes have been described in some patients with CVID. In this study, we show the overview of deficiencies of ICOS, TACI, CD19molecules, their genetic basis, pathogenesis and clinical manifestations of humoral deficiency.
Czech name
Genetické defekty při běžné variabilní imunodeficienci
Czech description
CVID je skupina heterogenních chorob. U některých případů CVID byla popsána mutace molekul regulujících aktivaci a diferenciaci B lymfocytů. V tomto přehledu je diskutována deficience molekul ICOS, TACI, CD19 a jejich receptorů na podkladě mutací, patogeneze a jejich klinické manifestace.
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FN - Epidemiology, infection diseases and clinical immunology
OECD FORD branch
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Result continuities
Project
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Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2007
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
International Journal of Immunogenetics
ISSN
1744-3121
e-ISSN
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Volume of the periodical
34
Issue of the periodical within the volume
4
Country of publishing house
GB - UNITED KINGDOM
Number of pages
5
Pages from-to
225-229
UT code for WoS article
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EID of the result in the Scopus database
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