(Q44969272)

English

Effect of genetic variation in the human S-adenosylhomocysteine hydrolase gene on total homocysteine concentrations and risk of recurrent venous thrombosis

scientific article published in November 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Effect of genetic variation in the human S-adenosylhomocysteine hydrolase gene on total homocysteine concentrations and risk of recurrent venous thrombosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

0 references

genetic variation

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

author name string

Henkjan Gellekink

1

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Martin den Heijer

2

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Leo A J Kluijtmans

3

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

publication date

1 November 2004

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

European Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

942-948

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201237

0 references

Homocysteine and cardiovascular disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

Increased homocysteine and S-adenosylhomocysteine concentrations and DNA hypomethylation in vascular disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

S-Adenosylhomocysteine hydrolase from human placenta. Affinity purification and characterization

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

Family and population studies of SAHH and ADA polymorphisms. A possible pitfall in the ascertainment of SAHH electrophoretic phenotypes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

Isozyme and DNA analysis of human S-adenosyl-L-homocysteine hydrolase (AHCY).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

Sequence of full length cDNA for human S-adenosylhomocysteine hydrolase

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

The homocysteine distribution: (mis)judging the burden

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

Potential role for adenosine in the pathogenesis of the vascular complications of hyperhomocysteinemia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

Local hypomethylation in atherosclerosis found in rabbit ec-sod gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

DNA hypomethylation and methyltransferase expression in atherosclerotic lesions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

Homocysteine and cardiovascular disease: evidence on causality from a meta-analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

21 January 2018

Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

7 January 2021

based on heuristic

inferred from DOI database lookup

Homocysteine and risk of ischemic heart disease and stroke: a meta-analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

7 January 2021

based on heuristic

inferred from DOI database lookup

Hyperhomocysteinemia: an independent risk factor for vascular disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

7 January 2021

based on heuristic

inferred from DOI database lookup

Elevation in S-Adenosylhomocysteine and DNA Hypomethylation: Potential Epigenetic Mechanism for Homocysteine-Related Pathology

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

7 January 2021

based on heuristic

inferred from DOI database lookup

Increase in plasma homocysteine associated with parallel increases in plasma S-adenosylhomocysteine and lymphocyte DNA hypomethylation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of human S-adenosylhomocysteine hydrolase. A new polymorphism in man

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

7 January 2021

based on heuristic

inferred from DOI database lookup

Three different methods for the determination of total homocysteine in plasma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

7 January 2021

based on heuristic

inferred from DOI database lookup

Plasma S-adenosylhomocysteine is a more sensitive indicator of cardiovascular disease than plasma homocysteine

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201237

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5201237

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

ResearchGate publication ID

0 references

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