(Q35745590)

10 August 2017

Apolipoprotein AI and transthyretin as components of amyloid fibrils in a kindred with apoAI Leu178His amyloidosis (English)

1 reference

10 August 2017

R Fernandes

4

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author name string

M M de Sousa

1

1 reference

10 August 2017

C Vital

2

1 reference

10 August 2017

D Ostler

3

1 reference

10 August 2017

J Pouget-Abadie

5

1 reference

10 August 2017

D Carles

6

1 reference

10 August 2017

M J Saraiva

7

1 reference

10 August 2017

language of work or name

English

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publication date

1 June 2000

1 reference

The American Journal of Pathology

10 August 2017

1 reference

10 August 2017

156

1 reference

10 August 2017

6

1 reference

10 August 2017

1911-1917

1 reference

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Amyloidosis: a review of recent diagnostic and therapeutic developments

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Identifying proteins from two-dimensional gels by molecular mass searching of peptide fragments in protein sequence databases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Human lysozyme gene mutations cause hereditary systemic amyloidosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Transthyretin mutations in health and disease.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C)

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

High-density lipoprotein--the clinical implications of recent studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Fibril in senile systemic amyloidosis is derived from normal transthyretin

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Mutation in gelsolin gene in Finnish hereditary amyloidosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Localization of an apolipoprotein A-I epitope critical for activation of lecithin-cholesterol acyltransferase

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Conformational analysis of apolipoprotein A-I and E-3 based on primary sequence and circular dichroism.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Microextraction and purification techniques applicable to chemical characterization of amyloid proteins in minute amounts of tissue.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac and cutaneous amyloidosis.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850097

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

25 September 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965064-X

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965064-X

Thyroxine binding to transthyretin Met 119. Comparative studies of different heterozygotic carriers and structural analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965064-X

Monoclonal antibodies to human apolipoprotein A-I: characterization and application as structural probes for apolipoprotein A-I and high density lipoprotein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965064-X

TTR exon scanning in peripheral neuropathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965064-X

Importance of central alpha-helices of human apolipoprotein A-I in the maturation of high-density lipoproteins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965064-X

An efficient salt-chloroform extraction of DNA from blood and tissues

7 January 2021

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Transthyretin in high density lipoproteins: association with apolipoprotein A-I

1 reference

12 December 2020

10.1016/S0002-9440(10)65064-X

Identifiers

DOI

1 reference

10 August 2017

1 reference

10 August 2017

1 reference