Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
about
Defective immunoglobulin A (IgA) glycosylation and IgA deposits in patients with IgA nephropathyThe Origin and Activities of IgA1-Containing Immune Complexes in IgA NephropathyRecent advances in the understanding and management of IgA nephropathyNew developments in the genetics, pathogenesis, and therapy of IgA nephropathyGenetic studies of IgA nephropathy: what have we learned from genome-wide association studiesThe pathophysiology of IgA nephropathyThe Genetics of IgA Nephropathy: An Overview from ChinaEffect of Immunosuppressive Drugs on the Changes of Serum Galactose-Deficient IgA1 in Patients with IgA NephropathyCumulative effects of variants identified by genome-wide association studies in IgA nephropathy.A panel of serum biomarkers differentiates IgA nephropathy from other renal diseases.The combined role of galactose-deficient IgA1 and streptococcal IgA-binding M Protein in inducing IL-6 and C3 secretion from human mesangial cells: implications for IgA nephropathy.The genetics and immunobiology of IgA nephropathy.The role of mucin-type O-glycans in eukaryotic developmentGenetic studies of IgA nephropathy: past, present, and future.Genome-wide association study identifies susceptibility loci for IgA nephropathy.Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis.Serum levels of galactose-deficient immunoglobulin (Ig) A1 and related immune complex are associated with disease activity of IgA nephropathy.Decreased circulating C3 levels and mesangial C3 deposition predict renal outcome in patients with IgA nephropathy.Down-regulation of core 1 beta1,3-galactosyltransferase and Cosmc by Th2 cytokine alters O-glycosylation of IgA1.Galactose-deficient IgA1 in African Americans with IgA nephropathy: serum levels and heritability.UMOD polymorphism rs12917707 is not associated with severe or stable IgA nephropathy in a large Caucasian cohort.Aberrantly glycosylated IgA1 as a factor in the pathogenesis of IgA nephropathyDifferent pathological roles of toll-like receptor 9 on mucosal B cells and dendritic cells in murine IgA nephropathy.Uncoupling of glomerular IgA deposition and disease progression in alymphoplasia mice with IgA nephropathyOxidative stress and galactose-deficient IgA1 as markers of progression in IgA nephropathy.Genetics of kidney failure and the evolving story of APOL1.Galectin-8 in IgA nephritis: decreased binding of IgA by galectin-8 affinity chromatography and associated increased binding in non-IgA serum glycoproteins.Serum galactose-deficient IgA1 levels in children with IgA nephropathy.Promoters of Human Cosmc and T-synthase Genes Are Similar in Structure, Yet Different in Epigenetic RegulationSerum galactose-deficient IgA1 level is not associated with proteinuria in children with IgA nephropathy.Autoantibodies targeting galactose-deficient IgA1 associate with progression of IgA nephropathyThe level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progressionNew Insights into the Pathogenesis of IgA Nephropathy.GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathwayMesangial cells from patients with IgA nephropathy have increased susceptibility to galactose-deficient IgA1.Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch-Schönlein purpura nephritis.Genetic contribution and associated pathophysiology in end-stage renal diseaseAberrant O-glycosylation and anti-glycan antibodies in an autoimmune disease IgA nephropathy and breast adenocarcinoma.In vitro-generated immune complexes containing galactose-deficient IgA1 stimulate proliferation of mesangial cells.Pathogenesis of Henoch-Schönlein purpura nephritis.
P2860
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P2860
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
description
2008 nî lūn-bûn
@nan
2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@ast
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@en
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@nl
type
label
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@ast
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@en
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@nl
prefLabel
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@ast
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@en
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@nl
P2093
P2860
P356
P1476
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
@en
P2093
Ali G Gharavi
Bruce A Julian
Catherine V Barker
Jiri Mestecky
Richard P Lifton
Susan Y Woodford
Zina Moldoveanu
P2860
P304
P356
10.1681/ASN.2007091052
P50
P577
2008-02-13T00:00:00Z