A B Van Kuilenburg - JoVE Visualize

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Leukemia|August 1, 1994

The roles of uridine-cytidine kinase and CTP synthetase in the synthesis of CTP in malignant human T-lymphocytic cellsA A van den Berg, H van Lenthe, S Busch, et al.

Clinical Chemistry|December 6, 2000

Defects in pyrimidine degradation identified by HPLC-electrospray tandem mass spectrometry of urine specimens or urine-soaked filter paper stripsH van Lenthe, A B van Kuilenburg, T Ito, et al.

FEBS Letters|April 24, 1990

Demonstration of two isoforms of subunit VIIa of cytochrome c oxidase from human skeletal muscle. Implications for mitochondrial myopathiesJ J Van Beeumen, A B Van Kuilenburg, S Van Bun, et al.

European Journal of Cancer (Oxford, England : 1990)|January 1, 1995

Cytidine triphosphate (CTP) synthetase activity during cell cycle progression in normal and malignant T-lymphocytic cellsA A van den Berg, H van Lenthe, J B Kipp, et al.

European Journal of Cancer (Oxford, England : 1990)|January 1, 1995

Meta-iodobenzylguanidine (MIBG) inhibits malate and succinate driven mitochondrial ATP synthesis in the human neuroblastoma cell line SK-N-BE(2c)J Cornelissen, R J Wanders, C Van den Bogert, et al.

European Journal of Cancer (Oxford, England : 1990)|February 21, 1998

Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicityA B Van Kuilenburg, P Vreken, L V Beex, et al.

Journal of Inherited Metabolic Disease|January 1, 1996

A point mutation in an invariant splice donor site leads to exon skipping in two unrelated Dutch patients with dihydropyrimidine dehydrogenase deficiencyP Vreken, A B Van Kuilenburg, R Meinsma, et al.

European Journal of Biochemistry|August 15, 1993

Evidence for transformation-related increase in CTP synthetase activity in situ in human lymphoblastic leukemiaA A van den Berg, H van Lenthe, S Busch, et al.

Journal of Inherited Metabolic Disease|November 5, 1997

Dihydropyrimidinase deficiency and congenital microvillous atrophy: coincidence or genetic relation?B Assmann, G F Hoffmann, L Wagner, et al.

Journal of Inherited Metabolic Disease|January 24, 2002

Detection of beta-ureidopropionase deficiency with HPLC-electrospray tandem mass spectrometry and confirmation of the defect at the enzyme levelA B Van Kuilenburg, H Van Lenthe, B Assmann, et al.

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Showing results (41-50 of 60) with videos related to

Sort By:

Pageof 6

Leukemia|August 1, 1994

The roles of uridine-cytidine kinase and CTP synthetase in the synthesis of CTP in malignant human T-lymphocytic cellsA A van den Berg, H van Lenthe, S Busch, et al.

Clinical Chemistry|December 6, 2000

Defects in pyrimidine degradation identified by HPLC-electrospray tandem mass spectrometry of urine specimens or urine-soaked filter paper stripsH van Lenthe, A B van Kuilenburg, T Ito, et al.

FEBS Letters|April 24, 1990

Demonstration of two isoforms of subunit VIIa of cytochrome c oxidase from human skeletal muscle. Implications for mitochondrial myopathiesJ J Van Beeumen, A B Van Kuilenburg, S Van Bun, et al.

European Journal of Cancer (Oxford, England : 1990)|January 1, 1995

Cytidine triphosphate (CTP) synthetase activity during cell cycle progression in normal and malignant T-lymphocytic cellsA A van den Berg, H van Lenthe, J B Kipp, et al.

European Journal of Cancer (Oxford, England : 1990)|January 1, 1995

Meta-iodobenzylguanidine (MIBG) inhibits malate and succinate driven mitochondrial ATP synthesis in the human neuroblastoma cell line SK-N-BE(2c)J Cornelissen, R J Wanders, C Van den Bogert, et al.

European Journal of Cancer (Oxford, England : 1990)|February 21, 1998

Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicityA B Van Kuilenburg, P Vreken, L V Beex, et al.

Journal of Inherited Metabolic Disease|January 1, 1996

A point mutation in an invariant splice donor site leads to exon skipping in two unrelated Dutch patients with dihydropyrimidine dehydrogenase deficiencyP Vreken, A B Van Kuilenburg, R Meinsma, et al.

European Journal of Biochemistry|August 15, 1993

Evidence for transformation-related increase in CTP synthetase activity in situ in human lymphoblastic leukemiaA A van den Berg, H van Lenthe, S Busch, et al.

Journal of Inherited Metabolic Disease|November 5, 1997

Dihydropyrimidinase deficiency and congenital microvillous atrophy: coincidence or genetic relation?B Assmann, G F Hoffmann, L Wagner, et al.

Journal of Inherited Metabolic Disease|January 24, 2002

Detection of beta-ureidopropionase deficiency with HPLC-electrospray tandem mass spectrometry and confirmation of the defect at the enzyme levelA B Van Kuilenburg, H Van Lenthe, B Assmann, et al.

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