(Q57996196)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

title

A multilocus genotyping assay for cardiovascular disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

main subject

cardiovascular disease

1 reference

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

Sophie Visvikis-Siest

11

object named as

S Visvikis

1 reference

6 December 2019

5

H A Erlich

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

author name string

S Cheng

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

C Pallaud

2

1 reference

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6 December 2019

M A Grow

3

1 reference

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6 December 2019

S J Scharf

4

1 reference

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6 December 2019

W Klitz

6

1 reference

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6 December 2019

C R Pullinger

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

M J Malloy

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

J P Kane

9

1 reference

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6 December 2019

publication date

1 August 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

Clinical Chemistry and Laboratory Medicine

6 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

volume

36

1 reference

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6 December 2019

issue

8

1 reference

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6 December 2019

page(s)

561-566

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

Heart disease: daddies and timebombs

6 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3' untranslated region polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Restriction fragment length polymorphisms of the apolipoprotein A-I, C-III, A-IV gene locus Relationships with lipids, apolipoproteins, and premature coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

A missense mutation in the cholesteryl ester transfer protein gene with possible dominant effects on plasma high density lipoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Increased coronary heart disease in Japanese-American men with mutation in the cholesteryl ester transfer protein gene despite increased HDL levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

A mutation in the promoter of the lipoprotein lipase (LPL) gene in a patient with familial combined hyperlipidemia and low LPL activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

The molecular basis of the human serum paraoxonase activity polymorphism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Molecular basis of human hypertension: role of angiotensinogen

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Screening for mutations by expressing patient cDNA segments in E. coli: homocystinuria due to cystathionine beta-synthase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Molecular defect in a patient with pyridoxine-responsive homocystinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Characterization of a cystathionine beta-synthase allele with three mutations in cis in a patient with B6 nonresponsive homocystinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Mutation in blood coagulation factor V associated with resistance to activated protein C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

DNA polymorphisms in adhesion molecule genes--a new risk factor for early atherosclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Objectives, Design and Recruitment of a Familial and Longitudinal Cohort for Studying Gene-Environment Interactions in the Field of Cardiovascular Risk: The Stanislas Cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

Prognostic value of angiographic indices of coronary artery disease from the Coronary Artery Surgery Study (CASS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.096

21 January 2018

Identifiers

DOI

10.1515/CCLM.1998.096

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9806460%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

1 reference