74 results on '"Blom, Henk J."'
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2. Effect of BTD gene variants on in vitro biotinidase activity
3. Cytokines levels in late-diagnosed Classical Homocystinuria patients
4. Leptin concentrations and SCD-1 indices in classical homocystinuria: Evidence for the role of sulfur amino acids in the regulation of lipid metabolism
5. Homocysteine and disease: Causal associations or epiphenomenons?
6. S-adenosylhomocysteine induces inflammation through NFkB: A possible role for EZH2 in endothelial cell activation
7. Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism
8. Inhibition of Cellular Methyltransferases Promotes Endothelial Cell Activation by Suppressing Glutathione Peroxidase 1 Protein Expression
9. Global protein and histone arginine methylation are affected in a tissue-specific manner in a rat model of diet-induced hyperhomocysteinemia
10. Metabolic syndrome components are associated with DNA hypomethylation
11. A liquid chromatography mass spectrometry method for the measurement of cystathionine β-synthase activity in cell extracts
12. Simultaneous determination of asymmetric and symmetric dimethylarginine, l-monomethylarginine, l-arginine, and l-homoarginine in biological samples using stable isotope dilution liquid chromatography tandem mass spectrometry
13. Asymmetric dimethylarginine in adults with cystathionine β-synthase deficiency
14. S-Adenosylhomocysteine induces apoptosis and phosphatidylserine exposure in endothelial cells independent of homocysteine
15. Maternal homocysteine and small-for-gestational-age offspring: systematic review and meta-analysis
16. Adenosine Kinase Deficiency Disrupts the Methionine Cycle and Causes Hypermethioninemia, Encephalopathy, and Abnormal Liver Function
17. Identification and Characterization of an Inborn Error of Metabolism Caused by Dihydrofolate Reductase Deficiency
18. Maternal homocysteine and related B vitamins as risk factors for low birthweight
19. Does global hypomethylation contribute to susceptibility to neural tube defects?
20. Inhibition of methylation decreases osteoblast differentiation via a non-DNA-dependent methylation mechanism
21. Polymorphisms in catechol-O-methyltransferase and methylenetetrahydrofolate reductase in relation to the risk of schizophrenia
22. Diet-induced hyperhomocysteinemia does not lead to large gene-expression differences in rat aorta
23. DNA methylation status is not impaired in treated cystathionine beta-synthase (CBS) deficient patients
24. Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida
25. Low vitamin B6, and not plasma homocysteine concentration, as risk factor for abdominal aortic aneurysm: A retrospective case–control study
26. Effect of oral vitamin B-12 with or without folic acid on cognitive function in older people with mild vitamin B-12 deficiency: a randomized, placebo-controlled trial
27. Effect of oral vitamin B-12 with or without folic acid on cognitive function in older people with mild vitamin B-12 deficiency: a randomized, placebo-controlled trial1–3
28. Elevated oxidized glutathione in cystinotic proximal tubular epithelial cells
29. Aberrant folate status in schizophrenic patients: What is the evidence?
30. Effect of supplementation with cobalamin carried either by a milk product or a capsule in mildly cobalamin-deficient elderly Dutch persons
31. Inhibition of transmethylation disturbs neurulation in chick embryos
32. Total homocysteine and its predictors in Dutch children1–3
33. Bioavailability of polyglutamyl folic acid relative to that of monoglutamyl folic acid in subjects with different genotypes of the glutamate carboxypeptidase II gene
34. Vitamin and homocysteine status of mothers and infants and the risk of nonsyndromic orofacial clefts
35. The 2756A>G variant in the gene encoding methionine synthase: its relation with plasma homocysteine levels and risk of coronary heart disease in a Dutch case-control study
36. Effect of the methylenetetrahydrofolate reductase 677C→T mutation on the relations among folate intake and plasma folate and homocysteine concentrations in a general population sample
37. Coronary heart disease mortality, plasma homocysteine, and B-vitamins: a prospective study
38. The H475Y Polymorphism in the Glutamate Carboxypeptidase II Gene Increases Plasma Folate without Affecting the Risk for Neural Tube Defects in Humans
39. Influence of a glutamate carboxypeptidase II (GCPII) polymorphism (1561C→T) on plasma homocysteine, folate and vitamin B12 levels and its relationship to cardiovascular disease risk
40. Hyperhomocysteinemia as risk factor for ischemic and hemorrhagic stroke in newborn infants
41. Coronary endothelial function in hyperhomocysteinemia: improvement after treatment with folic acid and cobalamin in patients with coronary artery disease
42. Quantification of plasma S-adenosylmethionine and S-adenosylhomocysteine as their fluorescent 1,N6-etheno derivatives: an adaptation of previously described methodology
43. Why are homocysteine levels increased in kidney failure? A metabolic approach
44. Association between B vitamin intake and plasma homocysteine concentration in the general Dutch population aged 20–65 y
45. Is Mutated Serine Hydroxymethyltransferase (SHMT) Involved in the Etiology of Neural Tube Defects?
46. The homocysteine distribution
47. Hyperhomocysteinemia and recurrent early pregnancy loss: a meta-analysis
48. Betaine-Homocysteine Methyltransferase (BHMT): Genomic Sequencing and Relevance to Hyperhomocysteinemia and Vascular Disease in Humans
49. Neural tube defects and a disturbed folate dependent homocysteine metabolism
50. A common mutation in the 5,10-methylenetetrahydrofolate reductase gene as a new risk factor for placental vasculopathy
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