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The EMBO Journal|August 1, 1996

Reduced replication of 3TC-resistant HIV-1 variants in primary cells due to a processivity defect of the reverse transcriptase enzymeN K Back, M Nijhuis, W Keulen, et al.

Leukemia Research|September 5, 2001

Cyclopentenyl cytosine induces apoptosis and increases cytarabine-induced apoptosis in a T-lymphoblastic leukemic cell-lineA C Verschuur, J Brinkman, A H Van Gennip, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 15, 2001

Lethal outcome of a patient with a complete dihydropyrimidine dehydrogenase (DPD) deficiency after administration of 5-fluorouracil: frequency of the common IVS14+1G>A mutation causing DPD deficiencyA B van Kuilenburg, E W Muller, J Haasjes, et al.

Biochemical Pharmacology|September 28, 1995

The IMP dehydrogenase inhibitor mycophenolic acid antagonizes the CTP synthetase inhibitor 3-deazauridine in MOLT-3 human leukemia cells: a central role for phosphoribosyl pyrophosphateA A van Berg, P A Mooyer, H van Lenthe, et al.

Anticancer Research|March 1, 1997

HBO and the uptake and retention of [125I] MIBG in human platelets and two neuroendocrine cell linesG A Tytgat, J Cornelissen, M Van den Brug, et al.

Biochimica Et Biophysica Acta|November 5, 1999

cDNA cloning, genomic structure and chromosomal localization of the human BUP-1 gene encoding beta-ureidopropionaseP Vreken, A B van Kuilenburg, N Hamajima, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 13, 2001

Clinical implications of dihydropyrimidine dehydrogenase (DPD) deficiency in patients with severe 5-fluorouracil-associated toxicity: identification of new mutations in the DPD geneA B van Kuilenburg, J Haasjes, D J Richel, et al.

British Journal of Clinical Pharmacology|September 2, 1998

Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjectsS A Ridge, J Sludden, O Brown, et al.

Magnetic Resonance in Medicine|October 25, 2001

beta-Ureidopropionase deficiency: a novel inborn error of metabolism discovered using NMR spectroscopy on urineS H Moolenaar, G Göhlich-Ratmann, U F Engelke, et al.

Human Genetics|March 10, 1999

Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiencyA B Van Kuilenburg, P Vreken, N G Abeling, et al.

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Showing results (51-60 of 60) with videos related to

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You have reached the last page of results.This site can display upto 60 results.

The EMBO Journal|August 1, 1996

Reduced replication of 3TC-resistant HIV-1 variants in primary cells due to a processivity defect of the reverse transcriptase enzymeN K Back, M Nijhuis, W Keulen, et al.

Leukemia Research|September 5, 2001

Cyclopentenyl cytosine induces apoptosis and increases cytarabine-induced apoptosis in a T-lymphoblastic leukemic cell-lineA C Verschuur, J Brinkman, A H Van Gennip, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 15, 2001

Lethal outcome of a patient with a complete dihydropyrimidine dehydrogenase (DPD) deficiency after administration of 5-fluorouracil: frequency of the common IVS14+1G>A mutation causing DPD deficiencyA B van Kuilenburg, E W Muller, J Haasjes, et al.

Biochemical Pharmacology|September 28, 1995

The IMP dehydrogenase inhibitor mycophenolic acid antagonizes the CTP synthetase inhibitor 3-deazauridine in MOLT-3 human leukemia cells: a central role for phosphoribosyl pyrophosphateA A van Berg, P A Mooyer, H van Lenthe, et al.

Anticancer Research|March 1, 1997

HBO and the uptake and retention of [125I] MIBG in human platelets and two neuroendocrine cell linesG A Tytgat, J Cornelissen, M Van den Brug, et al.

Biochimica Et Biophysica Acta|November 5, 1999

cDNA cloning, genomic structure and chromosomal localization of the human BUP-1 gene encoding beta-ureidopropionaseP Vreken, A B van Kuilenburg, N Hamajima, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 13, 2001

Clinical implications of dihydropyrimidine dehydrogenase (DPD) deficiency in patients with severe 5-fluorouracil-associated toxicity: identification of new mutations in the DPD geneA B van Kuilenburg, J Haasjes, D J Richel, et al.

British Journal of Clinical Pharmacology|September 2, 1998

Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjectsS A Ridge, J Sludden, O Brown, et al.

Magnetic Resonance in Medicine|October 25, 2001

beta-Ureidopropionase deficiency: a novel inborn error of metabolism discovered using NMR spectroscopy on urineS H Moolenaar, G Göhlich-Ratmann, U F Engelke, et al.

Human Genetics|March 10, 1999

Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiencyA B Van Kuilenburg, P Vreken, N G Abeling, et al.

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