(Q35754591)

10 August 2017

title

Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1. (English)

1 reference

10 August 2017

main subject

Amyloid cardiomyopathy

1 reference

L Hamidi Asl

1

1 reference

10 August 2017

J J Liepnieks

2

1 reference

10 August 2017

K Hamidi Asl

3

1 reference

10 August 2017

T Uemichi

4

1 reference

10 August 2017

G Moulin

5

1 reference

10 August 2017

E Desjoyaux

6

1 reference

10 August 2017

R Loire

7

1 reference

10 August 2017

M Delpech

8

1 reference

10 August 2017

G Grateau

9

1 reference

10 August 2017

M D Benson

10

1 reference

10 August 2017

language of work or name

English

0 references

publication date

1 January 1999

1 reference

The American Journal of Pathology

10 August 2017

published in

1 reference

10 August 2017

volume

154

1 reference

10 August 2017

issue

1

1 reference

10 August 2017

page(s)

221-227

1 reference

The presenilin 2 mutation (N141I) linked to familial Alzheimer disease (Volga German families) increases the secretion of amyloid beta protein ending at the 42nd (or 43rd) residue

10 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Primary localized amyloidosis of the eyelid: two cases of immunoglobulin light chain-derived proteins, subtype lambda V respectively lambda VI.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Human lysozyme gene mutations cause hereditary systemic amyloidosis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

The x-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val-30-->Met variant to 1.7-A resolution

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Isolation and DNA Sequence of Full-Length cDNA and of the Entire Gene for Human Apolipoprotein AI—Discovery of a New Genetic Polymorphism in the apo AI Gene

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

The characterization of soluble amyloid prepared in water

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Fibril in senile systemic amyloidosis is derived from normal transthyretin

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Clinical features of cutaneous amyloidoses

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Mutation in gelsolin gene in Finnish hereditary amyloidosis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Mutation of the beta-amyloid precursor protein in familial Alzheimer's disease increases beta-protein production

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Characterization of amyloid fibril proteins from medullary carcinoma of the thyroid

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Inherited predisposition to generalized amyloidosis. Clinical and pathological study of a family with neuropathy, nephropathy, and peptic ulcer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

[Familial primary disseminated amyloidosis (a new clinical form?)]

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Skin deposits in hereditary cystatin C 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=1853430

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Characterization of amyloid fibril beta-peptide in familial Alzheimer's disease with APP717 mutations.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

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=1853430

Apolipoprotein A1-derived amyloid in human aortic atherosclerotic plaques

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853430

Transthyretin amyloidosis

25 September 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965268-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965268-6

Hereditary cerebral amyloid angiopathy: the amyloid fibrils contain a protein which is a variant of cystatin C, an inhibitor of lysosomal cysteine proteases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965268-6

Local synthesis of amyloid fibril precursor in AL amyloidosis of the urinary tract

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965268-6

Skin involvement in familial amyloidotic polyneuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965268-6

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%2965268-6

Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965268-6

Familial primary cutaneous amyloidosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965268-6

Familial lichen amyloidosis. Report of 19 cases in 4 generations of a Chinese family in Malaysia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965268-6

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

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9916936

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9916936

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)65268-6

1 reference

10 August 2017

1 reference

10 August 2017

1 reference