About: Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis

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About: Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis Goto Sponge NotDistinct Permalink

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scientific article published on 01 April 1982

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 1982 (uk) article scientifique publié en 1982 (fr) im April 1982 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'abril de 1982 (ast) scientific article published on 01 April 1982 (en)
publication date	wds:Q70248269-00DD518C-7AEA-409C-B7EE-C07993FFB71C
publication date	1982-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q70248269-01239BDD-A09D-488D-B377-6BC9447DE598
language of work or name	English
exact match	wds:Q70248269-31BB9726-0CE5-4D05-9914-385C97CB33C3
exact match	https://scigraph.springernature.com/pub.10.1038/ki.1982.72
cites work	wds:Q70248269-139AF434-1666-433B-8CD7-FFC534418987 wds:Q70248269-214DA298-0DD7-4FAD-AE1D-D4F5EF34A66D wds:Q70248269-408E4DF8-9E2E-4722-A554-9F4C1C08C219 wds:Q70248269-54B51174-D61B-4843-86C5-CC879EC7DD2E wds:Q70248269-7EDAA7E8-77AA-472F-8F79-E5793A2E0155 wds:Q70248269-7EF7135F-7AEB-4700-BA9C-29792AEC5525 wds:Q70248269-84E05847-9D37-4DF5-8E61-1974C337B090 wds:Q70248269-923040EA-971A-4082-A2D7-00C6A1C34E54 wds:Q70248269-966D4A26-A3D7-44B8-989E-C55B2C3A4E06 wds:Q70248269-A3056A7E-B5BA-4E1A-BE59-97F5EAA22805 wds:Q70248269-B1566F12-48C4-4B42-89F3-CD43EB2BF8EA wds:Q70248269-B484B47F-492F-495C-8370-9B7B0660EE54 wds:Q70248269-BD006B62-F152-45A1-9102-B12284A8F215 wds:Q70248269-C4BAB9D1-392B-4363-A24F-F15A107B1BB0 wds:Q70248269-E903E977-92E0-4400-85CB-49B508E8B0CB
cites work	Hereditary nephritis with nerve deafness. Immunofluorescent studies on the kidney, with a consideration of discordant immunoglobulin-complement immunofluorescent reactions HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS. Diagnosis of hereditary nephritis by failure of glomeruli to bind anti-glomerular basement membrane antibodies Isolation and immunological characterization of human glomerular basement membrane antigens The cross-linking of proteins with glutaraldehyde and its use for the preparation of immunoadsorbents. Hereditary Nephritis: A Re-examination of its Clinical and Genetic Features Urinary excretion of glomerular basement membrane antigens in Alport's syndrome. A new diagnostic approach Antitubular basement membrane antibodies after renal transplantation Hereditary nephropathy, deafness and renal foam cells. Changes in glomerular basement membrane antigen(s) with age Induction of antitubular basement membrane antibodies in rats by renal transplantation. Familial and nonfamilial benign hematuria Composition of the glomerular basement membrane in the congenital nephrotic syndrome of the Finnish type Progressive and nonprogressive hereditary chronic nephritis The spectrum of hereditary renal diseases
author name string	wds:Q70248269-02C4493E-4C10-4510-B8C4-E2CC515F2800 wds:Q70248269-D63313E0-24F8-43A9-AFAC-CF9CC0754A58 wds:Q70248269-E306BB2B-8090-4DD7-8AAD-2E01FCC31039 wds:Q70248269-FFCDF721-151A-4568-91D4-2BD84B4C8430
author name string	C B Wilson W J Stone H K Johnson R C McCoy
rdfs:label	Absence of nephritogenic GBM antigen (nl) Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis (en)
skos:prefLabel	Absence of nephritogenic GBM antigen (nl) Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis (en)
name	Absence of nephritogenic GBM antigen (nl) Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis (en)
title	wds:Q70248269-179DA2C4-A936-4667-B2B3-2736855DA586
title	Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis (en)
page(s)	wds:Q70248269-80255CF1-B561-4D7E-A3DA-03BE2F803A86
page(s)	642-652
instance of	wds:Q70248269-F476066D-1CFB-4C39-BB6B-EC803B279C27
instance of	scholarly article
PubMed ID	wds:Q70248269-7ECD4002-6EBA-4111-8342-4BFAC82E4262
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7047864
PubMed ID	7047864
published in	wds:Q70248269-29283D1D-848C-492D-8AEB-6B152E5DBE15
published in	Kidney International
issue	wds:Q70248269-661E6A4C-7630-48EE-8545-412D4B34B0EA
volume	wds:Q70248269-94629C9D-0660-448A-AA1A-484BD44BF8E6
issue	4
volume	21
DOI	wds:Q70248269-4BA39DAD-B359-4F43-9B27-5467748B585D
DOI	http://dx.doi.org/10.1038/KI.1982.72
DOI	10.1038/KI.1982.72
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70248269
is cites work of	Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis Human tissue distribution of novel basement membrane collagen The Goodpasture antigen in Alport's syndrome: studies with a monoclonal antibody The glomerular basement membrane abnormality in Alport's syndrome. Goodpasture's syndrome Animal model of human disease: hereditary nephritis in Samoyed dogs. The pathogenesis of Alport syndrome involves type IV collagen molecules containing the alpha 3(IV) chain: evidence from anti-GBM nephritis after renal transplantation Molecular cloning of the human Goodpasture antigen demonstrates it to be the alpha 3 chain of type IV collagen Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane The development of anti-glomerular basement membrane nephritis in two children with Alport's syndrome after renal transplantation: characterization of the antibody target Autoimmunity in rapidly progressive glomerulonephritis Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis Alport syndrome: from bedside to genome to bedside Immunohistochemical study of alpha 1-5 chains of type IV collagen in hereditary nephritis Samoyed hereditary glomerulopathy (SHG). Evolution of splitting of glomerular capillary basement membranes The NC1 domain of collagen type IV in neonatal dog glomerular basement membranes. Significance in Samoyed hereditary glomerulopathy Renal disease in carrier female dogs with X-linked hereditary nephritis. Implications for female patients with this disease The clinical spectrum of hereditary nephritis Alport's syndrome: specificity and pathogenesis of glomerular basement membrane alterations Alport syndrome Urinary 3-hydroxyproline excretion in Alport's syndrome: a non-invasive screening test? NON-INVASIVE DIAGNOSIS OF ALPORT'S SYNDROME Clinical, histopathologic, and genetic studies in nine families with focal segmental glomerulosclerosis. Antibody-negative Goodpasture's disease

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