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Serum galactose-deficient-IgA1 and IgG autoantibodies correlate in patients with IgA nephropathy
IgA nephropathy is an autoimmune disease characterized by IgA1-containing glomerular immune deposits. We previously proposed a multi-hit pathogenesis model in which patients with IgA nephropathy have elevated levels of circulatory IgA1 with some O-glycans deficient in galactose (Gd-IgA1, autoantigen...
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| Izdano u: | PLoS One |
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| Glavni autori: | , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Public Library of Science
2018
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5764330/ https://ncbi.nlm.nih.gov/pubmed/29324897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0190967 |
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