(Q41858956)

English

The C677 mutation in methylene tetrahydrofolate reductase gene: correlation with uric acid and cardiovascular risk factors in elderly Korean men.

scientific article published on April 2004

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scholarly article

1 reference

Europe PubMed Central

13 October 2017

The C677 mutation in methylene tetrahydrofolate reductase gene: correlation with uric acid and cardiovascular risk factors in elderly Korean men. (English)

1 reference

Europe PubMed Central

13 October 2017

author name string

Young Seoub Hong

1

1 reference

Europe PubMed Central

13 October 2017

Myeong Jin Lee

2

1 reference

Europe PubMed Central

13 October 2017

Kyeong Hee Kim

3

1 reference

Europe PubMed Central

13 October 2017

Sang Hwa Lee

4

1 reference

Europe PubMed Central

13 October 2017

Yong Hwan Lee

5

1 reference

Europe PubMed Central

13 October 2017

Byoung Gwon Kim

6

1 reference

Europe PubMed Central

13 October 2017

Baekgeun Jeong

7

1 reference

Europe PubMed Central

13 October 2017

Hyeong Ryeol Yoon

8

1 reference

Europe PubMed Central

13 October 2017

Hisahide Nishio

9

1 reference

Europe PubMed Central

13 October 2017

Joon Youn Kim

10

1 reference

Europe PubMed Central

13 October 2017

publication date

1 April 2004

1 reference

Europe PubMed Central

13 October 2017

Journal of Korean Medical Science

1 reference

Europe PubMed Central

13 October 2017

19

1 reference

Europe PubMed Central

13 October 2017

2

1 reference

Europe PubMed Central

13 October 2017

209-213

1 reference

Europe PubMed Central

13 October 2017

copyright license

Creative Commons Attribution-NonCommercial 3.0 Unported

1 January 2004

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Correlation of polymorphisms to coagulation and biochemical risk factors for cardiovascular diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822300

5 June 2018

Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine and other risk factors for vascular disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822300

5 June 2018

Serum urate and the risk of major coronary heart disease events.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822300

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=2822300

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=2822300

5 June 2018

Hyperuricemia as a risk factor of coronary heart disease: The Framingham Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822300

5 June 2018

Protein-bound homocyst(e)ine. A possible 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=2822300

5 June 2018

Uric acid: a risk factor for coronary heart disease?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822300

5 June 2018

Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage 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=2822300

18 August 2018

Mutations in the methylene-tetrahydrofolate reductase gene and Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822300

18 August 2018

Relation of serum uric acid to mortality and ischemic heart disease. The NHANES I Epidemiologic Follow-up Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822300

18 August 2018

Elevated plasma homocyst(e)ine concentration as a possible independent risk factor for stroke

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822300

18 August 2018

Serum Uric Acid and Risk for Cardiovascular Disease and Death: The Framingham Heart Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15082892

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relationship of serum uric acid to hypertension and ischemic heart disease in Hisayama population, Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/15082892

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of blood pressure, uric acid, and hemorheological parameters on plasma homocyst(e)ine concentration

1 reference

https://pubmed.ncbi.nlm.nih.gov/15082892

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Features, symptoms, and neurophysiological findings in stroke associated with hyperhomocysteinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15082892

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum uric acid is a strong predictor of stroke in patients with non-insulin-dependent diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/15082892

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine and atherothrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15082892

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15082892

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3346/JKMS.2004.19.2.209

1 reference

Europe PubMed Central

13 October 2017

1 reference

Europe PubMed Central

13 October 2017

1 reference

Europe PubMed Central

13 October 2017

ResearchGate publication ID

0 references

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