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Title
Genetics and Immunopathogenesis of IgA Nephropathy
Authors
Keywords
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Journal
CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
Volume 41, Issue 2, Pages 198-213
Publisher
Springer Nature
Online
2010-12-28
DOI
10.1007/s12016-010-8232-0
References
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Note: Only part of the references are listed.- Megsin 2093T-2180C haplotype at the 3 untranslated region is associated with poor renal survival in Korean IgA nephropathy patients
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- Altered modulation of WNT–β-catenin and PI3K/Akt pathways in IgA nephropathy
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- The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88
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- Can a dysregulated mucosal immune system in IgA nephropathy be controlled by tonsillectomy?
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- Down-regulation of core 1 1,3-galactosyltransferase and Cosmc by Th2 cytokine alters O-glycosylation of IgA1
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- IgA nephropathy: Challenges and opportunities
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- Toll-like receptor 4 expression is increased in circulating mononuclear cells of patients with immunoglobulin A nephropathy
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- Role of IgA and IgA Fc Receptors in Inflammation
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- Spontaneous animal model, ddY mouse, for studying the pathogenesis and treatment in patients with immunoglobulin A nephropathy
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- Genetic variation in the transforming growth factor- 1 gene is associated with susceptibility to IgA nephropathy
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- No evidence for a role of cosmc-chaperone mutations in European IgA nephropathy patients
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