About: Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I

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

About: Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I 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 February 1998

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1998 (uk) im Februar 1998 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en febreru de 1998 (ast) artikull shkencor i botuar më 01 shkurt 1998 (sq) scientific article published on 01 February 1998 (en)
publication date	wds:Q74165052-7BDF5145-C743-40DD-8FCD-21405B9A84A7
publication date	1998-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q74165052-75093A4C-56BD-470E-BFC3-9669EC7C96B0
language of work or name	English
exact match	wds:Q74165052-771F27C4-B2FE-4F3E-9AD8-DCE692355E12
exact match	https://scigraph.springernature.com/pub.10.1046/j.1523-1755.1998.00770.x
author name string	wds:Q74165052-1EF83A90-EF11-48B3-80C0-EB789AD09679 wds:Q74165052-30C7E16F-2AB3-475C-B584-7A3BCAF52AEE wds:Q74165052-4B89B016-FF0F-439A-BCA0-1717D5B74935 wds:Q74165052-A09FB75F-8947-4488-B5C0-7E405E176E70 wds:Q74165052-AF8F1172-9A7A-462E-8586-22EAC1075C88 wds:Q74165052-D43BE68A-1079-40B6-AE9D-667A25EAEAD9 wds:Q74165052-F2954844-6113-491D-B5B2-43FF5A15AC54 wds:Q74165052-F999822D-088F-4A0B-A329-8CD18C980D9C
author name string	Booth DR van Zyl-Smit R Hawkins PN Tennent GA Booth SE Adams BK Persey MR Fattaar AB
rdfs:label	Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (en) Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (nl) Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (sq)
skos:prefLabel	Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (en) Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (nl) Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (sq)
name	Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (en) Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (nl) Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (sq)
author	wds:Q74165052-3F64D091-2887-4405-B5C2-386097D1F02B
author	Mark Pepys
title	wds:Q74165052-89B51FD0-6371-4518-A6D8-C0742E75CE4D
title	Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I (en)
page(s)	wds:Q74165052-7596CDE6-3C9C-444F-A59B-39F802E4B700
page(s)	276-281
instance of	wds:Q74165052-C62ED24D-5272-40EF-917D-2708618DCC7A
instance of	scholarly article
main subject	wds:Q74165052-4043736C-2654-4B25-863A-E98F21FD16EE
main subject	AL amyloidosis
PubMed ID	wds:Q74165052-D66AE160-6301-44C7-84B6-216AB748CF5E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9461086
PubMed ID	9461086
published in	wds:Q74165052-F9B87164-8D48-4BBE-83E7-36F89A420669
published in	Kidney International
issue	wds:Q74165052-3F819013-1775-482E-B4D9-2CD5C20440D6
volume	wds:Q74165052-47EF6ECB-54CB-4968-9B5C-E7DAF8480028
issue	2
volume	53
DOI	wds:Q74165052-E56E1325-2A6E-4CBB-8EBA-62DC1765679E
DOI	http://dx.doi.org/10.1046/J.1523-1755.1998.00770.X
DOI	10.1046/J.1523-1755.1998.00770.X
Dimensions Publication ID	wds:Q74165052-0E4C4DEB-C9AF-4728-B0FE-478CD95E8C96
Dimensions Publication ID	1019186465
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74165052
is cites work of	Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosis Amyloidogenicity and clinical phenotype associated with five novel mutations in apolipoprotein A-I. Apolipoprotein AI and transthyretin as components of amyloid fibrils in a kindred with apoAI Leu178His amyloidosis Structural Insights into High Density Lipoprotein: Old Models and New Facts The effects of altered apolipoprotein A-I structure on plasma HDL concentration Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1. Enhanced fractional catabolic rate of apo A-I and apo A-II in heterozygous subjects for apo A-I(Zaragoza) (L144R). Studies of the aggregation of mutant proteins in vitro provide insights into the genetics of amyloid diseases Familial conformational diseases and dementias The new apolipoprotein A-I variant leu(174) --> Ser causes hereditary cardiac amyloidosis, and the amyloid fibrils are constituted by the 93-residue N-terminal polypeptide Novel mass spectrometric immunoassays for the rapid structural characterization of plasma apolipoproteins APOA1 related amyloidosis: a case report and literature review Online registry for mutations in hereditary amyloidosis including nomenclature recommendations. Amyloid fibrils derived from the apolipoprotein A1 Leu174Ser variant contain elements of ordered helical structure Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens: identification of three novel mutations in the APOA1 gene A novel amyloidogenic variant of apolipoprotein AI: implications for a conformational change leading to cardiomyopathy Renal Amyloidosis Associated With 5 Novel Variants in the Fibrinogen A Alpha Chain Protein. Population-based resequencing of APOA1 in 10,330 individuals: spectrum of genetic variation, phenotype, and comparison with extreme phenotype approach Apolipoprotein A-1-related amyloidosis 2 case reports and review of the literature Renal ApoA-1 amyloidosis with Glu34Lys mutation and intra-amyloid lipid accumulation Lipoprotein abnormalities in patients with secondary renal amyloidosis
is cites work of	wds:Q26770434-3756BBE4-ED42-4993-AEF8-46F3978D96E4 wds:Q34138249-12889D65-541F-499D-8250-7A2FE2EBC587 wds:Q35754656-2A3761E2-5CA4-4469-BC3D-9124D21ECDCC wds:Q42795318-34D37D89-0CE5-45FD-BB38-0B6DD5FD71D3 wds:Q34635650-80677508-D4D7-423D-98EE-3B4DBAF7B21B wds:Q34443878-6A2E86E7-E1F4-4E8B-BAC5-ADFF4F49E1E5 wds:Q37086690-A4001B87-EDA1-430A-8856-D846323A2C61 wds:Q31029305-1C90BC5D-488B-433F-9C68-DA45446C9386 wds:Q28361328-58F0B61E-7A8F-41E1-A471-EC7E81271520 wds:Q43979090-00B5270F-DA61-466F-A34D-4D2E3039E9C7 wds:Q43030314-A45020AC-CD7D-4F64-9AD7-86CBC796CDC3 wds:Q47116927-84CD63FE-00AF-44F3-B003-1D78388AB02F wds:Q33185913-FB035446-A315-4A3F-A4F6-86C0088A275B wds:Q35754591-F32D67A3-51EA-4BF1-A0D4-21F4DB0AA627 wds:Q37164492-9429BA6C-FEC8-44B2-9F1E-D485943B1E5D wds:Q47590416-F1DAED8A-7740-4A2E-B07F-4B03CB6478E0

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