The role of genetic factors in the development of hyperhomocysteinemia (Q34281048)

1 August 2017

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title

The role of genetic factors in the development of hyperhomocysteinemia (English)

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1 August 2017

Jürgen Geisel

1

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1 August 2017

Ulrich Hübner

2

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1 August 2017

Marion Bodis

3

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1 August 2017

Heike Schorr

4

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1 August 2017

Jean-Pierre Knapp

5

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1 August 2017

Rima Obeid

6

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1 August 2017

Wolfgang Herrmann

7

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1 August 2017

1 November 2003

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Clinical Chemistry and Laboratory Medicine

1 August 2017

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1 August 2017

41

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1 August 2017

1427-1434

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1 August 2017

11

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Genetics of hyperhomocysteinaemia in cardiovascular disease

1 August 2017

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https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Genetic defects as important factors for moderate hyperhomocysteinemia

21 January 2018

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https://api.crossref.org/works/10.1515%2FCCLM.2003.219

21 January 2018

Homocysteine metabolism

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https://api.crossref.org/works/10.1515%2FCCLM.2003.219

The importance of hyperhomocysteinemia as a risk factor for diseases: an overview

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Catechol-O-Methyltransferase (COMT)-mediated methylation metabolism of endogenous bioactive catechols and modulation by endobiotics and xenobiotics: importance in pathophysiology and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobalamin and homocysteine concentration in blood

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Transcobalamin polymorphism and homocysteine

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Elevation of 2-methylcitric acid I and II levels in serum, urine, and cerebrospinal fluid of patients with cobalamin deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Homocysteine, Methylenetetrahydrofolate Reductase C677T Polymorphism and the B-Vitamins: A Facet of Nature-Nurture Interplay

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

Plasma homocysteine is regulated by phospholipid methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

3-OMD and homocysteine plasma levels in parkinsonian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.219

21 January 2018

Identifiers

DOI

10.1515/CCLM.2003.219

1 reference

1 August 2017

1 reference