Aberrantly glycosylated IgA1 in IgA nephropathy patients is recognized by IgG antibodies with restricted heterogeneity
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F09%3A4983" target="_blank" >RIV/00216208:11110/09:4983 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Aberrantly glycosylated IgA1 in IgA nephropathy patients is recognized by IgG antibodies with restricted heterogeneity
Original language description
IgA nephropathy is characterized by circulating immune complexes composed of galactose-deficient IgA1 and glycan-specific IgG antibody, their deposit in the glomerular mesangium and mesangioproliferative glomerulonephritis. We found that the secreted IgGformed complexes with galactose-deficient IgA1 in a glycan-dependent manner. We developed a dot-blot assay for the glycan-specific IgG antibody.
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
EC - 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
2009
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 Clinical Investigation
ISSN
0021-9738
e-ISSN
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Volume of the periodical
119
Issue of the periodical within the volume
6
Country of publishing house
US - UNITED STATES
Number of pages
10
Pages from-to
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UT code for WoS article
000266601000031
EID of the result in the Scopus database
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