The polymorphism ApoB/4311 in patients with myocardial infarction and controls: the ECTIM Study (Q68127459)

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22 September 2019

title

The polymorphism ApoB/4311 in patients with myocardial infarction and controls: the ECTIM Study (English)

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22 September 2019

main subject

myocardial infarction

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J F Moreel

1

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22 September 2019

G Roizes

2

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22 September 2019

A E Evans

3

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22 September 2019

D Arveiler

4

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22 September 2019

J P Cambou

5

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22 September 2019

C Souriau

6

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22 September 2019

H J Parra

7

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22 September 2019

E Desmarais

8

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22 September 2019

J C Fruchart

9

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22 September 2019

P Ducimetière

10

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22 September 2019

publication date

1 May 1992

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22 September 2019

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22 September 2019

volume

89

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22 September 2019

issue

2

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22 September 2019

page(s)

169-175

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https://scigraph.springernature.com/pub.10.1007/bf00217118

22 September 2019

exact match

0 references

cites work

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12 December 2020

A three codon insertion/deletion polymorphism in the signal peptide region of the human apolipoprotein B (APOB) gene directly typed by the polymerase chain reaction

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DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory

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Two amino acid substitutions in apolipoprotein B are in complete allelic association with the antigen group (x/y) polymorphism: evidence for little recombination in the 3' end of the human gene

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12 December 2020

Quantification of two different types of apolipoprotein A-I containing lipoprotein particles in plasma by enzyme-linked differential-antibody immunosorbent assay

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12 December 2020

Relation of parental history of early myocardial infarction to the level of apoprotein B in men

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12 December 2020

A worldwide population study of the Ag-system haplotypes, a genetic polymorphism of human low-density lipoprotein

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12 December 2020

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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12 December 2020

Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred

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12 December 2020

Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the f

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12 December 2020

Two distinct truncated apolipoprotein B species in a kindred with hypobetalipoproteinemia

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12 December 2020

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12 December 2020

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12 December 2020

Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hypelipidaemic individuals

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12 December 2020

Two common low density lipoprotein receptor gene mutations cause familial hypercholesterolemia in Afrikaners

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12 December 2020

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12 December 2020

Detection by denaturing gradient gel electrophoresis of a new polymorphism in the apolipoprotein B gene

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12 December 2020

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12 December 2020

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12 December 2020

DNA sequence of the human apolipoprotein B gene

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12 December 2020

The World Health Organization MONICA Project (monitoring trends and determinants in cardiovascular disease): a major international collaboration. WHO MONICA Project Principal Investigators

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12 December 2020

Heritable allele-specific differences in amounts of apoB and low-density lipoproteins in plasma

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12 December 2020

Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region

1 reference

12 December 2020

A selective bi-site immunoenzymatic procedure for human Lp[a] lipoprotein quantification using monoclonal antibodies against apo[a] and apoB.

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12 December 2020

Identifiers

DOI

10.1007/BF00217118

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1587527%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

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