IgA Nephropathy Caused by Unusual Polymerization of IgA1 with Aberrant N-Glycosylation in a Patient with Monoclonal Immunoglobulin Deposition Disease
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference44 articles.
1. Analysis of IgA1 O-glycans in IgA nephropathy by fluorophore-assisted carbohydrate electrophoresis;AC Allen;J Am Soc Nephrol,1999
2. Impairment of jacalin binding to serum IgA in IgA nephropathy;PM Andre;J Clin Lab Anal,1990
3. Defective galactosylation and clearance of IgA1 molecules as a possible etiopathogenic factor in IgA nephropathy;J Mestecky;Contrib Nephrol,1993
4. Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients;AC Allen;Kidney Int,2001
5. Circulating immune complexes in IgA nephropathy consist of IgA1 with galactose-deficient hinge region and antiglycan antibodies;M Tomana;J Clin Invest,1999
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