(Q43723747)

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A 31 bp VNTR in the cystathionine beta-synthase (CBS) gene is associated with reduced CBS activity and elevated post-load homocysteine levels

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scholarly article

1 reference

Europe PubMed Central

26 November 2017

A 31 bp VNTR in the cystathionine beta-synthase (CBS) gene is associated with reduced CBS activity and elevated post-load homocysteine levels (English)

1 reference

Europe PubMed Central

26 November 2017

9

1 reference

Europe PubMed Central

26 November 2017

author name string

Lievers KJ

1

1 reference

Europe PubMed Central

26 November 2017

Kluijtmans LA

2

1 reference

Europe PubMed Central

26 November 2017

Heil SG

3

1 reference

Europe PubMed Central

26 November 2017

Boers GH

4

1 reference

Europe PubMed Central

26 November 2017

Verhoef P

5

1 reference

Europe PubMed Central

26 November 2017

van Oppenraay-Emmerzaal D

6

1 reference

Europe PubMed Central

26 November 2017

den Heijer M

7

1 reference

Europe PubMed Central

26 November 2017

Trijbels FJ

8

1 reference

Europe PubMed Central

26 November 2017

publication date

1 August 2001

1 reference

Europe PubMed Central

26 November 2017

European Journal of Human Genetics

1 reference

Europe PubMed Central

26 November 2017

9

1 reference

Europe PubMed Central

26 November 2017

8

1 reference

Europe PubMed Central

26 November 2017

583-589

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Europe PubMed Central

26 November 2017

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200679

0 references

The pathogenesis of atherosclerosis: a perspective for the 1990s

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Molecular genetic insights into cardiovascular disease

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Homocysteine and ischemic heart disease: results of a prospective study with implications regarding prevention

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Hyperhomocysteinemia as a risk factor for deep-vein thrombosis.

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

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

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Heterozygosity for Homocystinuria in Premature Peripheral and Cerebral Occlusive Arterial Disease

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Hyperhomocysteinemia: an independent risk factor for vascular disease

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

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

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Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation

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Plasma lipoprotein(a) levels and expression of the apolipoprotein(a) gene are dependent on the nucleotide polymorphisms in its 5'-flanking region

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The human cystathionine beta-synthase (CBS) gene: complete sequence, alternative splicing, and polymorphisms.

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Plasma total homocysteine, B vitamins, and risk of coronary atherosclerosis.

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Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?

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Three different methods for the determination of total homocysteine in plasma

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

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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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Prospective study of serum total homocysteine concentration and risk of stroke in middle-aged British men.

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Post-methionine load hyperhomocysteinemia in persons with normal fasting total plasma homocysteine: initial results from the NHLBI Family Heart Study.

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Genetic and nongenetic factors for moderate hyperhomocyst(e)inemia

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RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

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The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences

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Species-specific signals for the splicing of a short Drosophila intron in vitro

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Variable number tandem repeat in exon/intron border of the cystathionine beta-synthase gene: a single nucleotide substitution in the second repeat prevents multiple alternate splicing

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10.1038/SJ.EJHG.5200679

1 reference

Europe PubMed Central

26 November 2017

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1 reference

Europe PubMed Central

26 November 2017

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