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Results: 1-25 | 26-50 | 51-67
Results: 1-25/67
HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF BIOGENIC-AMINES IN CELLS AND IN CULTURE MEDIA USING ONLINE DIALYSIS AND TRACE ENRICHMENT
Authors: SLINGERLAND RJ VANKUILENBURG ABP BODAENDER JM OVERMARS H VOUTE PA VANGENNIP AH
Citation: Rj. Slingerland et al., HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF BIOGENIC-AMINES IN CELLS AND IN CULTURE MEDIA USING ONLINE DIALYSIS AND TRACE ENRICHMENT, Journal of chromatography B. Biomedical sciences and applications, 716(1-2), 1998, pp. 65-75
RAPID STABLE-ISOTOPE DILUTION ANALYSIS OF VERY-LONG-CHAIN FATTY-ACIDS, PRISTANIC ACID AND PHYTANIC ACID USING GAS-CHROMATOGRAPHY ELECTRON-IMPACT MASS-SPECTROMETRY
Authors: VREKEN P VANLINT AEM BOOTSMA AH OVERMARS H WANDERS RJA VANGENNIP AH
Citation: P. Vreken et al., RAPID STABLE-ISOTOPE DILUTION ANALYSIS OF VERY-LONG-CHAIN FATTY-ACIDS, PRISTANIC ACID AND PHYTANIC ACID USING GAS-CHROMATOGRAPHY ELECTRON-IMPACT MASS-SPECTROMETRY, Journal of chromatography B. Biomedical sciences and applications, 713(2), 1998, pp. 281-287
DIHYDROPYRIMIDINE DEHYDROGENASE PHARMACOGENETICS IN CAUCASIAN SUBJECTS
Authors: RIDGE SA SLUDDEN J BROWN O ROBERTSON L WEI XX SAPONE A FERNANDEZSALGUERO PM GONZALEZ FJ VREKEN P VANKUILENBURG ABP VANGENNIP AH MCLEOD HL
Citation: Sa. Ridge et al., DIHYDROPYRIMIDINE DEHYDROGENASE PHARMACOGENETICS IN CAUCASIAN SUBJECTS, British journal of clinical pharmacology, 46(2), 1998, pp. 151-156
MONOAMINE-OXIDASE-A DEFICIENCY - BIOGENIC-AMINE METABOLITES IN RANDOMURINE SAMPLES
Authors: ABELING NGGM VANGENNIP AH VANCRUCHTEN AG OVERMARS H BRUNNER HG
Citation: Nggm. Abeling et al., MONOAMINE-OXIDASE-A DEFICIENCY - BIOGENIC-AMINE METABOLITES IN RANDOMURINE SAMPLES, Journal of neural transmission. Supplementum, (52), 1998, pp. 9-15
SEVERE 5-FLUOROURACIL TOXICITY CAUSED BY REDUCED DIHYDROPYRIMIDINE DEHYDROGENASE-ACTIVITY DUE TO HETEROZYGOSITY FOR A G-]A POINT MUTATION (VOL 21, PG 280, 1998)
Authors: VANKUILENBURG ABP VREKEN P BEEX LVAM DEABREU RA VANGENNIP AH
Citation: Abp. Vankuilenburg et al., SEVERE 5-FLUOROURACIL TOXICITY CAUSED BY REDUCED DIHYDROPYRIMIDINE DEHYDROGENASE-ACTIVITY DUE TO HETEROZYGOSITY FOR A G-]A POINT MUTATION (VOL 21, PG 280, 1998), Journal of inherited metabolic disease, 21(7), 1998, pp. 783-783
DIHYDROPYRIMIDINE DEHYDROGENASE-DEFICIENCY - A NOVEL MUTATION AND EXPRESSION OF MISSENSE MUTATIONS IN ESCHERICHIA-COLI (VOL 21, PG 276, 1998)
Authors: VREKEN P VANKUILENBERG ABP MEINSMA R BEEMER FA DURAN M VANGENNIP AH
Citation: P. Vreken et al., DIHYDROPYRIMIDINE DEHYDROGENASE-DEFICIENCY - A NOVEL MUTATION AND EXPRESSION OF MISSENSE MUTATIONS IN ESCHERICHIA-COLI (VOL 21, PG 276, 1998), Journal of inherited metabolic disease, 21(6), 1998, pp. 623-623
AROMATIC L-AMINO-ACID DECARBOXYLASE DEFICIENCY - A NEW CASE WITH A MILD CLINICAL PRESENTATION AND UNEXPECTED LABORATORY FINDINGS
Authors: ABELING NGGM VANGENNIP AH BARTH PG VANCRUCHTEN A WESTRA M WIJBURG FA
Citation: Nggm. Abeling et al., AROMATIC L-AMINO-ACID DECARBOXYLASE DEFICIENCY - A NEW CASE WITH A MILD CLINICAL PRESENTATION AND UNEXPECTED LABORATORY FINDINGS, Journal of inherited metabolic disease, 21(3), 1998, pp. 240-242
CLINICAL VARIABILITY IN 3 DANISH PATIENTS WITH DIHYDROPYRIMIDINE DEHYDROGENASE-DEFICIENCY ALL HOMOZYGOUS FOR THE SAME MUTATION
Authors: CHRISTENSEN E CEZANNE I KJAERGAARD S HORLYK H PEDERSEN VF VREKEN P VANKUILENBURG ABP VANGENNIP AH
Citation: E. Christensen et al., CLINICAL VARIABILITY IN 3 DANISH PATIENTS WITH DIHYDROPYRIMIDINE DEHYDROGENASE-DEFICIENCY ALL HOMOZYGOUS FOR THE SAME MUTATION, Journal of inherited metabolic disease, 21(3), 1998, pp. 272-275
DIHYDROPYRIMIDINE DEHYDROGENASE-DEFICIENCY - A NOVEL MUTATION AND EXPRESSION OF MISSENSE MUTATIONS IN ESCHERICHIA-COLI
Authors: VREKEN P VANKUILENBURG ABP MEINSMA R BEEMER FA DURAN M VANGENNIP AH
Citation: P. Vreken et al., DIHYDROPYRIMIDINE DEHYDROGENASE-DEFICIENCY - A NOVEL MUTATION AND EXPRESSION OF MISSENSE MUTATIONS IN ESCHERICHIA-COLI, Journal of inherited metabolic disease, 21(3), 1998, pp. 276-279
SEVERE 5-FLUOROURACIL TOXICITY CAUSED BY REDUCED DIHYDROPYRIMIDINE DEHYDROGENASE-ACTIVITY DUE TO HETEROZYGOSITY FOR A G-]A POINT MUTATION
Authors: VANKUILENBURG ABP VREKEN P BEEX LVAM DEABREU RA VANGENNIP AH
Citation: Abp. Vankuilenburg et al., SEVERE 5-FLUOROURACIL TOXICITY CAUSED BY REDUCED DIHYDROPYRIMIDINE DEHYDROGENASE-ACTIVITY DUE TO HETEROZYGOSITY FOR A G-]A POINT MUTATION, Journal of inherited metabolic disease, 21(3), 1998, pp. 280-284
IATROGENIC ISOLATED ISOLEUCINE DEFICIENCY AS THE CAUSE OF AN ACRODERMATITIS ENTEROPATHICA-LIKE SYNDROME
Authors: BOSCH AM SMITT JHS VANGENNIP AH ABELING NGGM SCHUTGENS RBH BAKKER HD WIJBURG FA
Citation: Am. Bosch et al., IATROGENIC ISOLATED ISOLEUCINE DEFICIENCY AS THE CAUSE OF AN ACRODERMATITIS ENTEROPATHICA-LIKE SYNDROME, British journal of dermatology, 139(3), 1998, pp. 488-491
SUBCELLULAR-LOCALIZATION OF DIHYDROPYRIMIDINE DEHYDROGENASE
Authors: VANKUILENBURG ABP VANLENTHE H WANDERS RJA VANGENNIP AH
Citation: Abp. Vankuilenburg et al., SUBCELLULAR-LOCALIZATION OF DIHYDROPYRIMIDINE DEHYDROGENASE, Biological chemistry, 378(9), 1997, pp. 1047-1053
DETERMINATION OF CTP SYNTHETASE-ACTIVITY IN CRUDE CELL HOMOGENATES BYA FAST AND SENSITIVE NON-RADIOCHEMICAL ASSAY USING ANION-EXCHANGE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY
Authors: VANKUILENBURG ABP ELZINGA L VERSCHUUR AC VANDENBERG AA SLINGERLAND RJ VANGENNIP AH
Citation: Abp. Vankuilenburg et al., DETERMINATION OF CTP SYNTHETASE-ACTIVITY IN CRUDE CELL HOMOGENATES BYA FAST AND SENSITIVE NON-RADIOCHEMICAL ASSAY USING ANION-EXCHANGE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Journal of chromatography B. Biomedical sciences and applications, 693(2), 1997, pp. 287-295
THE EFFECT OF THE NEUROBLASTOMA-SEEKING AGENT METAIODOBENZYLGUANIDINE(MIBG) ON NADH-DRIVEN SUPEROXIDE FORMATION AND NADH DRIVEN LIPID-PEROXIDATION IN BEEF-HEART SUBMITOCHONDRIAL PARTICLES
Authors: CORNELISSEN J VANKUILENBURG ABP VOUTE PA VANGENNIP AH
Citation: J. Cornelissen et al., THE EFFECT OF THE NEUROBLASTOMA-SEEKING AGENT METAIODOBENZYLGUANIDINE(MIBG) ON NADH-DRIVEN SUPEROXIDE FORMATION AND NADH DRIVEN LIPID-PEROXIDATION IN BEEF-HEART SUBMITOCHONDRIAL PARTICLES, European journal of cancer, 33(3), 1997, pp. 421-424
HETEROZYGOSITY FOR A POINT MUTATION IN AN INVARIANT SPLICE DONOR SITEOF DIHYDROPYRIMIDINE DEHYDROGENASE AND SEVERE 5-FLUOROURACIL RELATED TOXICITY
Authors: VANKUILENBURG ABP VREKEN P BEEX LVAM MEINSMA R VANLENTHE H DEABREU RA VANGENNIP AH
Citation: Abp. Vankuilenburg et al., HETEROZYGOSITY FOR A POINT MUTATION IN AN INVARIANT SPLICE DONOR SITEOF DIHYDROPYRIMIDINE DEHYDROGENASE AND SEVERE 5-FLUOROURACIL RELATED TOXICITY, European journal of cancer, 33(13), 1997, pp. 2258-2264
DIHYDROPYRIMIDINE DEHYDROGENASE (DPD) DEFICIENCY - IDENTIFICATION ANDEXPRESSION OF MISSENSE MUTATIONS C29R, R886H AND R235W
Authors: VREKEN P VANKUILENBURG ABP MEINSMA R VANGENNIP AH
Citation: P. Vreken et al., DIHYDROPYRIMIDINE DEHYDROGENASE (DPD) DEFICIENCY - IDENTIFICATION ANDEXPRESSION OF MISSENSE MUTATIONS C29R, R886H AND R235W, Human genetics, 101(3), 1997, pp. 333-338
IDENTIFICATION OF A 4-BASE DELETION (DELTCAT(296-299)) IN THE DIHYDROPYRIMIDINE DEHYDROGENASE GENE WITH VARIABLE CLINICAL EXPRESSION
Authors: VREKEN P VANKUILENBURG ABP MEINSMA R DEABREU RA VANGENNIP AH
Citation: P. Vreken et al., IDENTIFICATION OF A 4-BASE DELETION (DELTCAT(296-299)) IN THE DIHYDROPYRIMIDINE DEHYDROGENASE GENE WITH VARIABLE CLINICAL EXPRESSION, Human genetics, 100(2), 1997, pp. 263-265
HBO AND THE UPTAKE AND RETENTION OF [I-125] MIBG IN HUMAN PLATELETS AND 2 NEUROENDOCRINE CELL-LINES
Authors: TYTGAT GAM CORNELISSEN J VANDENBRUG M VANKUILENBURG ABP VOUTE PA VANDERKLEIJ AJ VANGENNIP AH
Citation: Gam. Tytgat et al., HBO AND THE UPTAKE AND RETENTION OF [I-125] MIBG IN HUMAN PLATELETS AND 2 NEUROENDOCRINE CELL-LINES, Anticancer research, 17(2A), 1997, pp. 1209-1212
HYPERBARIC-OXYGEN ENHANCES THE EFFECTS OF METAIODOBENZYLGUANIDINE (MIBG) ON ENERGY-METABOLISM AND LIPID-PEROXIDATION IN THE HUMAN NEUROBLASTOMA CELL-LINE SK-N-BE (2C)
Authors: CORNELISSEN J VANKUILENBURG ABP ELZINGA L VANDERKLEIJ AJ VOUTE PA VANGENNIP AH
Citation: J. Cornelissen et al., HYPERBARIC-OXYGEN ENHANCES THE EFFECTS OF METAIODOBENZYLGUANIDINE (MIBG) ON ENERGY-METABOLISM AND LIPID-PEROXIDATION IN THE HUMAN NEUROBLASTOMA CELL-LINE SK-N-BE (2C), Anticancer research, 17(1A), 1997, pp. 259-264
SPECIFICATION OF THE INHIBITORY-ACTION OF MIBG ON THE RESPIRATORY-CHAIN BY EPR SCANNING
Authors: CORNELISSEN J VANBELZEN R VANGENNIP AH VOUTE PA VANKUILENBURG ABP
Citation: J. Cornelissen et al., SPECIFICATION OF THE INHIBITORY-ACTION OF MIBG ON THE RESPIRATORY-CHAIN BY EPR SCANNING, Anticancer research, 17(1A), 1997, pp. 265-268
IN-SITU CYTIDINE-DEAMINASE ACTIVITY AND CHROMOSOME 1P DELETION IN HUMAN NEUROBLASTOMA-CELLS
Authors: SLINGERLAND RJ VANGENNIP AH BODLAENDER JM VOUTE PA VANKUILENBURG ABP
Citation: Rj. Slingerland et al., IN-SITU CYTIDINE-DEAMINASE ACTIVITY AND CHROMOSOME 1P DELETION IN HUMAN NEUROBLASTOMA-CELLS, Anticancer research, 17(1A), 1997, pp. 457-459
DIHYDROPYRIMIDINASE DEFICIENCY, A PROGRESSIVE NEUROLOGICAL DISORDER
Authors: PUTMAN CWMM ROTTEVEEL JJ WEVERS RA VANGENNIP AH BAKKEREN JAJM DEABREU RA
Citation: Cwmm. Putman et al., DIHYDROPYRIMIDINASE DEFICIENCY, A PROGRESSIVE NEUROLOGICAL DISORDER, Neuropediatrics, 28(2), 1997, pp. 106-110
MENADIONE INHIBITS MIBG UPTAKE IN 2 NEUROENDOCRINE CELL-LINES
Authors: CORNELISSEN J TYTGAT GAM VANDENBRUG M VANKUILENBURG ABP VOUTE PA VANGENNIP AH
Citation: J. Cornelissen et al., MENADIONE INHIBITS MIBG UPTAKE IN 2 NEUROENDOCRINE CELL-LINES, Journal of neuro-oncology, 31(1-2), 1997, pp. 147-151
THE DUTCH UNIFORM MULTICENTER REGISTRATION SYSTEM FOR GENETIC-DISORDERS AND MALFORMATION SYNDROMES
Authors: ZWAMBORNHANSSEN AMN BIJLSMA JB HENNEKAM EFAM LINDHOUT D BEEMER FA BAKKER E KLEIJER WJ DEFRANCE HF DEDIESMULDERS CEM DURAN M VANGENNIP AH VANMENS JT PEARSON PL MANTEL G VERHAGE RE GERAEDTS JPM
Citation: Amn. Zwambornhanssen et al., THE DUTCH UNIFORM MULTICENTER REGISTRATION SYSTEM FOR GENETIC-DISORDERS AND MALFORMATION SYNDROMES, American journal of medical genetics, 70(4), 1997, pp. 444-447
DIHYDROPYRIDMIDINASE DEFICIENCY AND CONGENITAL MICROVILLOUS ATROPHY -COINCIDENCE OR GENETIC RELATION
Authors: ASSMANN B HOFFMANN GF WAGNER L BRAUTIGAM C SEYBERTH HW DURAN M VANKUILENBURG ABP WEVERS R VANGENNIP AH
Citation: B. Assmann et al., DIHYDROPYRIDMIDINASE DEFICIENCY AND CONGENITAL MICROVILLOUS ATROPHY -COINCIDENCE OR GENETIC RELATION, Journal of inherited metabolic disease, 20(5), 1997, pp. 681-688
Risultati: 1-25 | 26-50 | 51-67