About: Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients

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About: Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients Goto Sponge NotDistinct Permalink

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scientific article published on 01 September 2001

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 2001 (uk) article scientifique publié en 2001 (fr) im September 2001 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en setiembre de 2001 (ast) scientific article published on 01 September 2001 (en)
publication date	wds:Q74452081-E061A82F-9708-4A39-85F6-46011C6C33F4
publication date	2001-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q74452081-48C1C519-9F02-4032-BE58-5549D263676B
language of work or name	English
exact match	wds:Q74452081-DDEB6E76-06D6-40F4-9293-FDD96F5CC8FB
exact match	https://scigraph.springernature.com/pub.10.1046/j.1523-1755.2001.060003969.x
author name string	wds:Q74452081-6CF1F7C5-8858-423F-99F9-0F0D322A9D17 wds:Q74452081-8FC288ED-C3B1-4E59-91F2-5B30167BF98D wds:Q74452081-952F5610-4DDB-4EF4-8179-E4877030B94A wds:Q74452081-FCE59ECA-8A25-44C7-919B-BE121F25BC84
author name string	Feehally J Bailey EM Allen AC Buck KS
rdfs:label	Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients (en) Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients (nl)
skos:prefLabel	Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients (en) Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients (nl)
name	Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients (en) Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients (nl)
author	wds:Q74452081-2BD6CC33-2534-4479-B1DA-2C722458076A wds:Q74452081-3E9B617C-D7F1-4EAA-9E02-9F0AF0A2285C
author	Paul E Brenchley Jonathan Barratt
title	wds:Q74452081-33837873-9633-42F0-985B-C560253524B5
title	Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients (en)
page(s)	wds:Q74452081-86DF1FBE-F467-4E9F-AB08-ECB905ABCFE0
page(s)	969-973
instance of	wds:Q74452081-73AA5AF0-DA37-4E26-A60A-BB53088ED42A
instance of	scholarly article
main subject	wds:Q74452081-5CC14CE2-A0BC-4BA5-9DDB-3D4471DE0CC2
main subject	kidney disease
PubMed ID	wds:Q74452081-321E23CE-1983-46E7-B6CD-8131B0F25F55
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11532091
PubMed ID	11532091
published in	wds:Q74452081-B4ECBF8A-44E2-4F9B-8B5D-C44FE1EEBAB2
published in	Kidney International
issue	wds:Q74452081-E21F2464-0FB2-4804-8339-EBAF82E17B98
volume	wds:Q74452081-8D56A65A-CE67-470B-A6BB-F4837AF69BD1
issue	3
volume	60
DOI	wds:Q74452081-74BC70BA-2EDC-4616-AEEB-EAEA6A16EE34
DOI	http://dx.doi.org/10.1046/J.1523-1755.2001.060003969.X
DOI	10.1046/J.1523-1755.2001.060003969.X
Dimensions Publication ID	wds:Q74452081-AE0CF6B3-A484-4ED5-90DD-4309732115E1
Dimensions Publication ID	1027676892
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74452081
is cites work of	Gene expression profiling analysis in nephrology: towards molecular definition of renal disease Initiation of O-glycan synthesis in IgA1 hinge region is determined by a single enzyme, UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 2 Identification and characterization of CMP-NeuAc:GalNAc-IgA1 alpha2,6-sialyltransferase in IgA1-producing cells Reactivities of N-acetylgalactosamine-specific lectins with human IgA1 proteins IgA1 immune complexes from pediatric patients with IgA nephropathy activate cultured human mesangial cells Recognition of galactose-deficient O-glycans in the hinge region of IgA1 by N-acetylgalactosamine-specific snail lectins: a comparative binding study A panel of serum biomarkers differentiates IgA nephropathy from other renal diseases The genetics and immunobiology of IgA nephropathy Aberrantly glycosylated IgA1 in IgA nephropathy patients is recognized by IgG antibodies with restricted heterogeneity Aberrant IgA1 glycosylation is inherited in familial and sporadic 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 IgA1-secreting cell lines from patients with IgA nephropathy produce aberrantly glycosylated IgA1 IgA glycosylation and IgA immune complexes in the pathogenesis of IgA nephropathy In vitro-generated immune complexes containing galactose-deficient IgA1 stimulate proliferation of mesangial cells Pathogenesis of immunoglobulin A nephropathy: recent insight from genetic studies An update on the pathogenesis and treatment of IgA nephropathy Glycosylation of IgA1 and pathogenesis of IgA nephropathy New insights into the pathogenesis of IgA nephropathy Patients with IgA nephropathy have increased serum galactose-deficient IgA1 levels Defective immunoglobulin A (IgA) glycosylation and IgA deposits in patients with IgA nephropathy Naturally occurring structural isomers in serum IgA1 o-glycosylation Role of IgA and IgA fc receptors in inflammation Antibodies: basic mechanisms and emerging concepts. Down-regulation of core 1 beta1,3-galactosyltransferase and Cosmc by Th2 cytokine alters O-glycosylation of IgA1. Aberrantly glycosylated IgA1 as a factor in the pathogenesis of IgA nephropathy Abnormal miR-148b expression promotes aberrant glycosylation of IgA1 in IgA nephropathy Pathogenetic significance of aberrant glycosylation of IgA1 in IgA nephropathy Interaction between variants of two glycosyltransferase genes in IgA nephropathy Sources of Urinary Proteins and their Analysis by Urinary Proteomics for the Detection of Biomarkers of Disease The genetics of IgA nephropathy. Different pathological roles of toll-like receptor 9 on mucosal B cells and dendritic cells in murine IgA nephropathy Pathological role of tonsillar B cells in IgA nephropathy Computational prediction of O-linked glycosylation sites that preferentially map on intrinsically disordered regions of extracellular proteins Enzymatic sialylation of IgA1 O-glycans: implications for studies of IgA nephropathy Clustered O-glycans of IgA1: defining macro- and microheterogeneity by use of electron capture/transfer dissociation. O-linked oligosaccharides of the IgA1 hinge region: roles of its aberrant structure in the occurrence and/or progression of IgA nephropathy Cytokines alter IgA1 O-glycosylation by dysregulating C1GalT1 and ST6GalNAc-II enzymes. Urinary biomarkers of IgA nephropathy and other IgA-associated renal diseases Development of immunoglobulin A nephropathy- like disease in beta-1,4-galactosyltransferase-I-deficient mice Nephrokeli, a Chinese herbal formula, may improve IgA nephropathy through regulation of the sphingosine-1-phosphate pathway Changes in nephritogenic serum galactose-deficient IgA1 in IgA nephropathy following tonsillectomy and steroid therapy Determination of severity of murine IgA nephropathy by glomerular complement activation by aberrantly glycosylated IgA and immune complexes Recent insights into the biological roles of mucin-type O-glycosylation Activated innate immunity and the involvement of CX3CR1-fractalkine in promoting hematuria in patients with IgA nephropathy. Both IgA nephropathy and alcoholic cirrhosis feature abnormally glycosylated IgA1 and soluble CD89-IgA and IgG-IgA complexes: common mechanisms for distinct diseases.

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