Croatian population data for the C677T polymorphism in methylenetetrahydrofolate reductase: frequencies in healthy and atherosclerotic study groups. (Q33188213)

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English	Croatian population data for the C677T polymorphism in methylenetetrahydrofolate reductase: frequencies in healthy and atherosclerotic study groups.	scientific article

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scholarly article

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7 November 2019

Croatian population data for the C677T polymorphism in methylenetetrahydrofolate reductase: frequencies in healthy and atherosclerotic study groups (English)

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7 November 2019

atherosclerosis

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based on heuristic

inferred from title

5

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7 November 2019

Ana-Maria Simundic

8

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7 November 2019

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Irena Zuntar

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7 November 2019

Elizabeta Topić

2

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7 November 2019

Duro Vukosavić

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7 November 2019

Vlasta Vuković

4

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7 November 2019

Antonija Begonja

6

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7 November 2019

Natasa Antoljak

7

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1 September 2003

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7 November 2019

Clinica Chimica Acta

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7 November 2019

335

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7 November 2019

1-2

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7 November 2019

95-100

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7 November 2019

Atherosclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

The pathogenesis of atherosclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

The A677V Methylenetetrahydrofolate Reductase Gene Polymorphism and Carotid Atherosclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

Relation of a common mutation in methylenetetrahydrofolate reductase to plasma homocysteine and early onset coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

Hyperhomocysteinemia in high-aged subjects: relation of B-vitamins, folic acid, renal function and the methylenetetrahydrofolate reductase mutation

1 reference

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7 January 2021

Methylene tetrahydrofolate reductase C677T genotype and stroke

1 reference

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7 January 2021

A methylenetetrahydrofolate reductase gene polymorphism in ischaemic stroke and in carotid artery stenosis

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?

1 reference

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7 January 2021

MTHFR association with arteriosclerotic vascular disease?

1 reference

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7 January 2021

Detection of CYP2D6*3 and 2D6*4 Allelic Variants by PCR-Restriction Fragment Length Polymorphism

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7 January 2021

A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506).

1 reference

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7 January 2021

Methylenetetrahydrofolate reductase mutation and neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

1 reference

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7 January 2021

Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients.

1 reference

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7 January 2021

A methylenetetrahydrofolate reductase gene polymorphism in multiple sclerosis

1 reference

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7 January 2021

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

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7 January 2021

C677T (thermolabile alanine/valine) polymorphism in methylenetetrahydrofolate reductase (MTHFR): its frequency and impact on plasma homocysteine concentration in different European populations

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

Thermolabile methylenetetrahydrofolate reductase in coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2803%2900283-3

7 January 2021

Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis

1 reference

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7 January 2021

Genetic and nongenetic factors for moderate hyperhomocyst(e)inemia

1 reference

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7 January 2021

Identifiers

10.1016/S0009-8981(03)00283-3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927690%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927690%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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