(Q42795318)

English

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

scientific article published on September 1999

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

7 November 2017

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 (English)

1 reference

Europe PubMed Central

7 November 2017

Eloisa Arbustini

5

1 reference

Europe PubMed Central

7 November 2017

Giuseppe Zanotti

9

1 reference

Europe PubMed Central

7 November 2017

author name string

L Obici

1

1 reference

Europe PubMed Central

7 November 2017

V Bellotti

2

1 reference

Europe PubMed Central

7 November 2017

P Mangione

3

1 reference

Europe PubMed Central

7 November 2017

M Stoppini

4

1 reference

Europe PubMed Central

7 November 2017

L Verga

6

1 reference

Europe PubMed Central

7 November 2017

I Zorzoli

7

1 reference

Europe PubMed Central

7 November 2017

E Anesi

8

1 reference

Europe PubMed Central

7 November 2017

C Campana

10

1 reference

Europe PubMed Central

7 November 2017

M Viganò

11

1 reference

Europe PubMed Central

7 November 2017

G Merlini

12

1 reference

Europe PubMed Central

7 November 2017

language of work or name

0 references

publication date

1 September 1999

1 reference

Europe PubMed Central

7 November 2017

The American Journal of Pathology

1 reference

Europe PubMed Central

7 November 2017

155

1 reference

Europe PubMed Central

7 November 2017

695-702

1 reference

Europe PubMed Central

7 November 2017

3

1 reference

Europe PubMed Central

7 November 2017

Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

A novel amyloidogenic variant of apolipoprotein AI: implications for a conformational change leading to cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

Crystal structure of truncated human apolipoprotein A-I suggests a lipid-bound conformation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

Molecular physiology of reverse cholesterol transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

Apolipoprotein A1-derived amyloid in human aortic atherosclerotic plaques

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

Gene structure of human apolipoprotein A1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

The plasma lecithins:cholesterol acyltransferase reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

Simplified procedures for applying the polymerase chain reaction to routinely fixed paraffin wax sections.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

Pulmonary vascular amyloidosis in aged dogs. A new form of spontaneously occurring amyloidosis derived from apolipoprotein AI

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

27 May 2018

Apolipoprotein A-I induced amyloidosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1866882

16 August 2018

Extensive intimal apolipoprotein A1-derived amyloid deposits in a patient with an apolipoprotein A1 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965167-X

7 January 2021

A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965167-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965167-X

7 January 2021

Cardiac and pleuropulmonary AL amyloid imaging with technetium-99m labelled aprotinin

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965167-X

7 January 2021

Light and electron microscopy immunohistochemical characterization of amyloid deposits

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965167-X

7 January 2021

Apolipoprotein A-I conformation in reconstituted discoidal lipoproteins varying in phospholipid and cholesterol content

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965167-X

7 January 2021

Prebeta-migrating high density lipoprotein: quantitation in normal and hyperlipidemic plasma by solid phase radioimmunoassay following electrophoretic transfer

1 reference

https://pubmed.ncbi.nlm.nih.gov/10487826

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The epitopes of apolipoprotein A-I define distinct structural domains including a mobile middle region

1 reference

https://pubmed.ncbi.nlm.nih.gov/10487826

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vivo metabolism of a mutant apolipoprotein, apoA-IIowa, associated with hypoalphalipoproteinemia and hereditary systemic amyloidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10487826

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26

1 reference

https://pubmed.ncbi.nlm.nih.gov/10487826

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S0002-9440(10)65167-X

1 reference

Europe PubMed Central

7 November 2017

1 reference

Europe PubMed Central

7 November 2017

1 reference

Europe PubMed Central

7 November 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42795318&oldid=2124242804"