Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases. (Q51564037)

7 April 2018

title

Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases. (English)

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author

Michael Y. Tsai

1

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author name string

Welge BG

2

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Hanson NQ

3

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Bignell MK

4

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Vessey J

5

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Schwichtenberg K

6

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Yang F

7

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Bullemer FE

8

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Rasmussen R

9

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Graham KJ

10

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publication date

1 March 1999

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published in

Atherosclerosis

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volume

143

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issue

1

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page(s)

163-170

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Association between Plasma Homocysteine Concentrations and Extracranial Carotid-Artery Stenosis

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Hyperhomocysteinemia: an independent risk factor for vascular disease

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Molecular and biochemical approaches in the identification of heterozygotes for homocystinuria

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Excess prevalence of fasting and postmethionine-loading hyperhomocysteinemia in stable renal transplant recipients.

7 January 2021

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

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

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Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians

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A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction.

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7 January 2021

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7 January 2021

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

7 January 2021

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High frequency (71%) of cystathionine β-synthase mutation G307S in Irish homocystinuria patients

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

7 January 2021

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7 January 2021

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

7 January 2021

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Estimates of heritability of plasma homocyst(e)ine levels in aging adult male twins

7 January 2021

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10.1016/S0021-9150(98)00271-8

7 January 2021

Identifiers

DOI

1 reference

7 April 2018

release_76dylcn3ifcf5d7hxfk42kv2le

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/76dylcn3ifcf5d7hxfk42kv2le

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

10208491

1 reference

7 April 2018