H. Gellekink

发表

Stable-isotope dilution liquid chromatography-electrospray injection tandem mass spectrometry method for fast, selective measurement of S-adenosylmethionine and S-adenosylhomocysteine in plasma.

H. Blom, M. den Heijer, E. Struys, 2005, Clinical chemistry.

Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida.

B. Franke, H. Blom, M. den Heijer, 2007, Molecular genetics and metabolism.

Molecular genetic analysis of hyperhomocysteinemia.

H. Gellekink, 2007 .

The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida

H. Blom, M. Heijer, L. Kluijtmans, 2006, Journal of Molecular Medicine.

Expression and characterization of the extracellular Ca(2+)-sensing receptor in melanotrope cells of Xenopus laevis.

B. Jenks, E. Roubos, W. Scheenen, 2003, Endocrinology.

Expression and Characterization of the Extracellular Ca 2 (cid:1) -Sensing Receptor in Melanotrope Cells of Xenopus laevis

E. Roubos, W. Scheenen, M. Bai, 2003 .

Global DNA methylation measured by liquid chromatography-tandem mass spectrometry: analytical technique, reference values and determinants in healthy subjects

T. Teerlink, C. Jakobs, Y. Smulders, 2007, Clinical chemistry and laboratory medicine.

Red blood cell folate vitamer distribution in healthy subjects is determined by the methylenetetrahydrofolate reductase C677T polymorphism and by the total folate status.

C. Stehouwer, W. Vaes, T. Teerlink, 2007, The Journal of nutritional biochemistry.

Associations of common polymorphisms in the thymidylate synthase, reduced folate carrier and 5-aminoimidazole-4-carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase genes with folate and homocysteine levels and venous thrombosis risk

H. Blom, M. den Heijer, H. Gellekink, 2007, Clinical chemistry and laboratory medicine.

Molecular genetic analysis of the human dihydrofolate reductase gene: relation with plasma total homocysteine, serum and red blood cell folate levels

H. Blom, M. Heijer, H. Gellekink, 2007, European Journal of Human Genetics.

Catechol-O-methyltransferase genotype is associated with plasma total homocysteine levels and may increase venous thrombosis risk

H. Blom, M. Heijer, S. Vermeulen, 2007, Thrombosis and Haemostasis.

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

H. Blom, M. Heijer, L. Kluijtmans, 2004, European Journal of Human Genetics.

Polymorphisms in catechol-O-methyltransferase and methylenetetrahydrofolate reductase in relation to the risk of schizophrenia

R. Kahn, R. Sinke, H. Blom, 2008, European Neuropsychopharmacology.

Expression of the cytokine leukemia inhibitory factor and pro-apoptotic insulin-like growth factor binding protein-3 in Alzheimer's disease

Irene Otte-Höller, Marcel M. Verbeek, Hans J. ten Donkelaar, 2002, Acta Neuropathologica.

Genetic determinants of plasma total homocysteine.

H. Blom, M. den Heijer, S. Heil, 2005, Seminars in vascular medicine.