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Results: 1-10 |
Results: 10
A 31 bp VNTR in the cystathionine beta-synthase (CBS) gene is associated with reduced CBS activity and elevated post-load homocysteine levels
Authors: Lievers, KJA Kluijtmans, LAJ Heil, SG Boers, GHJ Verhoef, P van Oppenraay-Emmerzaal, D den Heijer, M Trijbels, FJM Blom, HJ
Citation: Kja. Lievers et al., A 31 bp VNTR in the cystathionine beta-synthase (CBS) gene is associated with reduced CBS activity and elevated post-load homocysteine levels, EUR J HUM G, 9(8), 2001, pp. 583-589
A second common variant in the methylenetetrahydrofolate reductase (MTHFR)gene and its relationship to MTHFR enzyme activity, homocysteine, and cardiovascular disease risk
Authors: Lievers, KJA Boers, GHJ Verhoef, P den Heijer, M Kluijtmans, LAJ van der Put, NMJ Trijbels, FJM Blom, HJ
Citation: Kja. Lievers et al., A second common variant in the methylenetetrahydrofolate reductase (MTHFR)gene and its relationship to MTHFR enzyme activity, homocysteine, and cardiovascular disease risk, J MOL MED-J, 79(9), 2001, pp. 522-528
Phase I clinical and pharmacogenetic trial of irinotecan and raltitrexed administered every 21 days to patients with cancer
Authors: Stevenson, JP Redlinger, M Kluijtmans, LAJ Sun, WJ Algazy, K Giantonio, B Haller, DG Hardy, C Whitehead, AS O'Dwyer, PJ
Citation: Jp. Stevenson et al., Phase I clinical and pharmacogenetic trial of irinotecan and raltitrexed administered every 21 days to patients with cancer, J CL ONCOL, 19(20), 2001, pp. 4081-4087
Methylenetetrahydrofolate reductase genotypes and predisposition to atherothrombotic disease - Evidence that all three MTHFR C677T genotypes confer different levels of risk
Authors: Kluijtmans, LAJ Whitehead, AS
Citation: Laj. Kluijtmans et As. Whitehead, Methylenetetrahydrofolate reductase genotypes and predisposition to atherothrombotic disease - Evidence that all three MTHFR C677T genotypes confer different levels of risk, EUR HEART J, 22(4), 2001, pp. 294-299
The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations
Authors: Gaughan, DJ Kluijtmans, LAJ Barbaux, S McMaster, D Young, IS Yarnell, JWG Evans, A Whitehead, AS
Citation: Dj. Gaughan et al., The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations, ATHEROSCLER, 157(2), 2001, pp. 451-456
The human and mouse methylenetetrahydrofolate reductase (MTHFR) genes: genomic organization, mRNA structure and linkage to the CLCN6 gene
Authors: Gaughan, DJ Barbaux, S Kluijtmans, LAJ Whitehead, AS
Citation: Dj. Gaughan et al., The human and mouse methylenetetrahydrofolate reductase (MTHFR) genes: genomic organization, mRNA structure and linkage to the CLCN6 gene, GENE, 257(2), 2000, pp. 279-289
Cystathionine beta-synthase mutations in homocystinuria
Authors: Kraus, JP Janosik, M Kozich, V Mandell, R Shih, V Sperandeo, MP Sebastio, G de Franchis, R Andria, G Kluijtmans, LAJ Blom, H Boers, GHJ Gordon, RB Kamoun, P Tsai, MY Kruger, WD Koch, HG Ohura, T Gaustadnes, M
Citation: Jp. Kraus et al., Cystathionine beta-synthase mutations in homocystinuria, HUM MUTAT, 13(5), 1999, pp. 362-375
Reduced frequency of the thermolabile methylenetetrahydrofolate reductase genotype in the elderly
Authors: Kluijtmans, LAJ Whitehead, AS
Citation: Laj. Kluijtmans et As. Whitehead, Reduced frequency of the thermolabile methylenetetrahydrofolate reductase genotype in the elderly, ATHEROSCLER, 146(2), 1999, pp. 395-397
The molecular basis of cystathionine beta-synthase deficiency in dutch patients with homocystinuria: Effect of CBS genotype on biochemical and clinical phenotype and on response to treatment
Authors: Kluijtmans, LAJ Boers, GHJ Kraus, JP van den Heuvel, LPWJ Cruysberg, JRM Trijbels, FJM Blom, HJ
Citation: Laj. Kluijtmans et al., The molecular basis of cystathionine beta-synthase deficiency in dutch patients with homocystinuria: Effect of CBS genotype on biochemical and clinical phenotype and on response to treatment, AM J HU GEN, 65(1), 1999, pp. 59-67
Methylenetetrahydrofolate reductase mutation and coronary artery disease -Response
Authors: Kluijtmans, LAJ Blom, HJ Boers, GHJ Willems, F
Citation: Laj. Kluijtmans et al., Methylenetetrahydrofolate reductase mutation and coronary artery disease -Response, CIRCULATION, 98(25), 1998, pp. 2932-2933
Risultati: 1-10 |