About: Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 December 1984

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1984 (uk) article scientifique publié en 1984 (fr) im Dezember 1984 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 December 1984 (en) artículu científicu espublizáu n'avientu de 1984 (ast)
publication date	wds:Q70775616-C906B144-8D10-4FAE-A3AF-80F439950740
publication date	1984-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q70775616-5EAC34D5-6986-4D4D-9EFA-E04360FDB333
language of work or name	English
exact match	wds:Q70775616-F4AB2615-F126-46BE-88B4-AD590506D251
exact match	https://scigraph.springernature.com/pub.10.1038/ki.1984.228
cites work	wds:Q70775616-06D8C81C-A294-414A-B16B-7A59DE239290 wds:Q70775616-0CC3FE58-935F-4545-8FFA-E6B2CDC0ECFC wds:Q70775616-0D03F181-735D-44FD-B2BF-03FC2573066E wds:Q70775616-0DF9F78D-D1B7-479A-BECE-A80532849C24 wds:Q70775616-20A31DAE-B8A0-4C4C-962E-6E61CE6E2735 wds:Q70775616-2271DE5E-B7DC-41C4-A896-C335EA6824F5 wds:Q70775616-25EB954C-6507-4AF5-96A7-BA11692318EA wds:Q70775616-2DD002EC-48CF-47FD-A70B-7FEA7017C64F wds:Q70775616-31CF010F-493A-447F-836B-98FCBBD21DC2 wds:Q70775616-33FBD4EE-D879-437D-964C-9C965D77624F wds:Q70775616-432C4572-A201-4718-A23F-DE4CE7B1F034 wds:Q70775616-47D5A3AA-245E-4D0D-8FFF-A37705EAD4BE wds:Q70775616-51379A4D-BA5C-49E9-A18A-1561AF318540 wds:Q70775616-519F3802-4DC7-488B-BE2E-A38E1332D909 wds:Q70775616-5243B6F3-2F3A-4110-9B56-7A6230A14D48 wds:Q70775616-5A209AC4-7CF8-4A66-958B-7E4B2F3C28E9 wds:Q70775616-7B8E102D-FAC3-4AFD-AAA8-1D377812133E wds:Q70775616-9964FFA2-DD3D-4E23-920F-DB89C49D0217 wds:Q70775616-A5F9519F-A50D-4A7F-8F8A-B455F335EF01 wds:Q70775616-B373E3D5-3F59-4D29-9605-96CE672111B0 wds:Q70775616-BE944DC3-F8E2-41BC-A59B-4474F27C1577 wds:Q70775616-C7F5E084-6B17-45D1-A1F2-67590209AB56 wds:Q70775616-E951E3E9-DE84-4818-9DA2-2D09B20EC249
cites work	Statement on the nomenclature of human C4 allotypes. Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility Genetic polymorphism of human complement C4 and detection of heterozygotes Two HLA-linked loci controlling the fourth component of human complement Structural polymorphism of the fourth component of human complement The complement system in chronic glomerulonephritis: Three newly associated aberrations Inherited structural polymorphism of the fourth component of human complement Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man. Genetic deficiency of C4 presenting with recurrent infections and a SLE-like disease. Genetic and immunologic studies HLA-Bw35 and Mesangial IgA Glomerulonephritis Inherited deficiency of the second component of complement (C2) with membranoproliferative glomerulonephritis Higher Prevalence of HLA-B12 in Patients with IgA Nephropathy IGA nephropathy in HLA-identical siblings Family study in IgA nephritis: the possible role of HLA antigens BF types and the mode of inheritance of insulin-dependent diabetes mellitus (IDDM) HLA antigen in three types of glomerulonephritis Severe systemic lupus erythematosus with nephritis in a boy with deficiency of the fourth component of complement Selective deficiency of the second component of complement in a patient with anaphylactoid purpura Partial H (beta 1H) deficiency and glomerulonephritis in two families Inherited complement component deficiencies in membranoproliferative glomerulonephritis Homozygous deficiency of C4 in a child with a lupus erythematosus syndrome Human C4 polymorphism: pedigree analysis of qualitative, quantitative, and functional parameters as a basis for phenotype interpretations C4 polymorphism and HLA linkage: studies in a family with hereditary C4 deficiency
author name string	wds:Q70775616-35DE9980-4D07-4B0A-B5DF-227A606B8EB0 wds:Q70775616-4A7E2A28-BD48-4289-AFF5-4597B1163D5E wds:Q70775616-4E93324D-8134-4469-996A-A90E33C84532
author name string	R J Wyatt B A Julian R H McLean
rdfs:label	Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura (en) Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura (nl)
skos:prefLabel	Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura (en) Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura (nl)
name	Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura (en) Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura (nl)
title	wds:Q70775616-B3FE1F4F-4166-4452-A0B3-ED4A5E5E650F
title	Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura (en)
page(s)	wds:Q70775616-E8EA9F4E-CD82-4A84-A5E4-F743DF6C9E95
page(s)	855-860
instance of	wds:Q70775616-D7702310-3392-46B0-B143-D383C7465E72
instance of	scholarly article
main subject	wds:Q70775616-2BEA4BB0-3401-4301-AD05-9FA9B1004E44 wds:Q70775616-5DBF3EF9-0AE2-4024-BFE7-38CD9168213D wds:Q70775616-9B41F527-EA1C-41F8-977C-026F77728C6B
main subject	phenotype kidney disease homozygosity
PubMed ID	wds:Q70775616-07B862D3-7BFF-4F3A-A378-32F08049E888
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6533396
PubMed ID	6533396
published in	wds:Q70775616-B24156DF-E05A-4801-9B04-9661082C204E
published in	Kidney International
issue	wds:Q70775616-29AE4521-7E08-4DAC-916C-B3BA978E3FFD
volume	wds:Q70775616-C5F4C895-9DAA-4D66-A4CE-A1840687A00C
issue	6
volume	26
DOI	wds:Q70775616-1D8D439B-DC38-455B-A603-803F58D76D69
DOI	http://dx.doi.org/10.1038/KI.1984.228
DOI	10.1038/KI.1984.228
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70775616
is cites work of	Characterization of two hybrid C4 allotypes (C4A12andC4B3) by electrophoretic, serological and restriction fragment length polymorphism analyses Pathogenesis of Henoch-Schönlein purpura nephritis CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency Null alleles of the fourth component of complement and HLA haplotypes in familial systemic lupus erythematosus.

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 188 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software