(Q41936983)

English

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

scientific article published on January 1996

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scholarly article

1 reference

Europe PubMed Central

14 October 2017

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease (English)

1 reference

Europe PubMed Central

14 October 2017

0 references

cardiovascular disease

1 reference

based on heuristic

inferred from title

10

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Europe PubMed Central

14 October 2017

author name string

Kluijtmans LA

1

1 reference

Europe PubMed Central

14 October 2017

van den Heuvel LP

2

1 reference

Europe PubMed Central

14 October 2017

Boers GH

3

1 reference

Europe PubMed Central

14 October 2017

Frosst P

4

1 reference

Europe PubMed Central

14 October 2017

Stevens EM

5

1 reference

Europe PubMed Central

14 October 2017

van Oost BA

6

1 reference

Europe PubMed Central

14 October 2017

den Heijer M

7

1 reference

Europe PubMed Central

14 October 2017

Trijbels FJ

8

1 reference

Europe PubMed Central

14 October 2017

Rozen R

9

1 reference

Europe PubMed Central

14 October 2017

language of work or name

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publication date

1 January 1996

1 reference

Europe PubMed Central

14 October 2017

American Journal of Human Genetics

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Europe PubMed Central

14 October 2017

58

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Europe PubMed Central

14 October 2017

1

1 reference

Europe PubMed Central

14 October 2017

35-41

1 reference

Europe PubMed Central

14 October 2017

Protein measurement with the Folin phenol reagent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Homocyst(e)ine and arterial occlusive diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Komrower Lecture. Molecular basis of phenotype expression in homocystinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Human cystathionine beta-synthase cDNA: sequence, alternative splicing and expression in cultured cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Two novel missense mutations in the cystathionine beta-synthase gene in homocystinuric patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Hyperhomocysteinemia in premature arterial disease: examination of cystathionine beta-synthase alleles at the molecular level.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

A study of cardiovascular risk in heterozygotes for homocystinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Improved identification of heterozygotes for homocystinuria due to cystathionine synthase deficiency by the combination of methionine loading and enzyme determination in cultured fibroblasts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Impaired homocysteine metabolism in early-onset cerebral and peripheral occlusive arterial disease. Effects of pyridoxine and folic acid treatment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Effect of vitamin B-6 deficiency on fasting plasma homocysteine concentrations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Hyperhomocyst(e)inemia as a risk factor for occlusive vascular disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

The pathogenesis of coronary artery disease. A possible role for methionine metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Homocystinuria. Evidence for three distinct classes of cystathionine beta-synthase mutants in cultured fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

5 June 2018

Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

18 August 2018

Plasma concentrations of homocysteine and other aminothiol compounds are related to food intake in healthy human subjects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

18 August 2018

Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914961

18 August 2018

Three different methods for the determination of total homocysteine in plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8554066

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE

1 reference

https://pubmed.ncbi.nlm.nih.gov/8554066

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinaemia: a metabolic risk factor for coronary heart disease determined by both genetic and environmental influences?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8554066

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vitamin status and intake as primary determinants of homocysteinemia in an elderly population

1 reference

https://pubmed.ncbi.nlm.nih.gov/8554066

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thermolabile methylenetetrahydrofolate reductase in patients with coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8554066

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia: an independent risk factor for vascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8554066

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

14 October 2017

1 reference

Europe PubMed Central

14 October 2017

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