Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy. - Wikidata - awgldk - TriplyDB

Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.

Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.

http://www.wikidata.org/entity/Q34655791

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Defective immunoglobulin A (IgA) glycosylation and IgA deposits in patients with IgA nephropathy The Origin and Activities of IgA1-Containing Immune Complexes in IgA Nephropathy Recent advances in the understanding and management of IgA nephropathy New developments in the genetics, pathogenesis, and therapy of IgA nephropathy Genetic studies of IgA nephropathy: what have we learned from genome-wide association studies The pathophysiology of IgA nephropathy The Genetics of IgA Nephropathy: An Overview from China Effect of Immunosuppressive Drugs on the Changes of Serum Galactose-Deficient IgA1 in Patients with IgA Nephropathy Cumulative 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 development Genetic 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 nephropathy Different 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 nephropathy Oxidative 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 Regulation Serum galactose-deficient IgA1 level is not associated with proteinuria in children with IgA nephropathy.Autoantibodies targeting galactose-deficient IgA1 associate with progression of IgA nephropathy The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression New Insights into the Pathogenesis of IgA Nephropathy.GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway Mesangial 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 disease Aberrant 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.

http://www.wikidata.org/entity/Q34655791

description

2008 nî lūn-bûn

@nan

2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի փետրվարին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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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

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Journal of the American Society of Nephrology

P1476

Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.

@en

P2093

Ali G Gharavi

http://www.w3.org/2001/XMLSchema#string

Bruce A Julian

http://www.w3.org/2001/XMLSchema#string

Catherine V Barker

http://www.w3.org/2001/XMLSchema#string

Jan Novak

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Jiri Mestecky

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Richard P Lifton

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Susan Y Woodford

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Zina Moldoveanu

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P2860

Multipoint quantitative-trait linkage analysis in general pedigrees

Mass spectrometry proves under-O-glycosylation of glomerular IgA1 in IgA nephropathy.

Molecular basis of Tn-polyagglutinability.

Circulating immune complexes in IgA nephropathy consist of IgA1 with galactose-deficient hinge region and antiglycan antibodies

Incidence of latent mesangial IgA deposition in renal allograft donors in Japan.

Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci

IgA nephropathy: current views of immune complex formation.

IgA nephropathy: characterization of IgG antibodies specific for galactose-deficient IgA1.

IgA nephropathy and Henoch-Schoenlein purpura nephritis: aberrant glycosylation of IgA1, formation of IgA1-containing immune complexes, and activation of mesangial cells.

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1008-1014

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scholarly article

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10.1681/ASN.2007091052

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5

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19

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2008-02-13T00:00:00Z

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18272841

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2386728

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