(Q44485536)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12818402%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

title

Investigations of a common genetic variant in betaine-homocysteine methyltransferase (BHMT) in coronary artery disease (English)

1 reference

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5 November 2019

3

1 reference

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5 November 2019

9

Rima Rozen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12818402%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

author name string

Ilan S Weisberg

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12818402%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Eric Park

2

1 reference

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5 November 2019

Peter Berger

4

1 reference

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5 November 2019

Martha Nunn

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12818402%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Daniel S Suh

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12818402%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Andrew P Breksa

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12818402%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Timothy A Garrow

8

1 reference

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5 November 2019

publication date

1 April 2003

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5 November 2019

1 reference

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5 November 2019

volume

167

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12818402%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

page(s)

205-214

1 reference

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5 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12818402%20AND%20SRC:MED&resulttype=core&format=json

A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes

5 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Homocysteine and cardiovascular disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

The 1298A-->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Methylenetetrahydrofolate reductase gene polymorphism and ischemic stroke in Japanese.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Methylenetetrahydrofolate reductase genotypes and early-onset coronary artery disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Folic acid and homocyst(e)ine metabolic defects and the risk of placental abruption, pre-eclampsia and spontaneous pregnancy loss: A systematic review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Betaine-homocysteine methyltransferase expression in porcine and human tissues and chromosomal localization of the human gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Betaine-homocysteine methyltransferase is a developmentally regulated enzyme crystallin in rhesus monkey lens.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Interaction between dietary methionine and methyl donor intake on rat liver betaine-homocysteine methyltransferase gene expression and organization of the human gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Treatment of hyperhomocyst(e)inemia: physiological basis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Purification, kinetic properties, and cDNA cloning of mammalian betaine-homocysteine methyltransferase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Optimization of the single-strand conformation polymorphism (SSCP) technique for detection of point mutations.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Human betaine-homocysteine methyltransferase is a zinc metalloenzyme.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Apolipoprotein B mRNA and lipoprotein secretion are increased in McArdle RH-7777 cells by expression of betaine-homocysteine S-methyltransferase.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Betaine-homocysteine methyltransferase (BHMT): genomic sequencing and relevance to hyperhomocysteinemia and vascular disease in humans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

Common variant in betaine-homocysteine methyltransferase (BHMT) and risk for spina bifida

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2803%2900010-8

10.1016/S0021-9150(03)00010-8

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12818402%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference