Zobrazeno 1 - 10
of 27
pro vyhledávání: '"L.W. Wormhoudt"'
Publikováno v:
European Journal of Cancer. 44:819-829
This study compared the effects of early intervention with standard use of epoetin alfa on haemoglobin (Hb) levels and transfusion requirements in cancer patients receiving chemotherapy. Patients with Hb10 andor= 12 g/dL were randomised 1:1 to epoeti
Publikováno v:
The Oncologist. 11:197-205
To evaluate the effect of epoetin alfa on quality of life (QOL) in patients with solid tumors and mild-to-moderate anemia receiving platinum-based chemotherapy relative to population norms.In the original study, patients (n = 316) with hemoglobin (Hb
Publikováno v:
The Oncologist. 11:206-216
This analysis of the results of a randomized, controlled trial evaluating the effects of epoetin alfa (EPO) therapy on transfusion requirements, hemoglobin (Hb), and quality of life (QOL) in patients with cancer receiving platinum-based chemotherapy
Autor:
P.J. van Bladeren, L.W. Wormhoudt, Jan N. M. Commandeur, J.H.T.M. Ploemen, I de Waziers, M. J. Oudshoorn, Philippe Beaune, Nico P. E. Vermeulen, Guido R. M. M. Haenen, T. Watabe
Publikováno v:
Ploemen, J P H T M, Wormhoudt, L W, Haenen, G R M M, Oudshoorn, M J, Commandeur, J N M, Vermeulen, N P E, De Waziers, I, Beaune, P H, Watabe, T & van Bladeren, P J 1997, ' The use of human in vitro metabolic parameters to explore the risk assessment of hazardous compounds: The case of ethylene dibromide. ', Toxicology and Applied Pharmacology, vol. 143, pp. 56-69 . https://doi.org/10.1006/taap.1996.8004
Toxicology and Applied Pharmacology, 143, 56-69
Toxicology and Applied Pharmacology, 143, 56-69. Academic Press Inc.
Toxicology and Applied Pharmacology 143 (1997)
Toxicology and Applied Pharmacology, 143, 56-69
Toxicology and Applied Pharmacology, 143, 56-69. Academic Press Inc.
Toxicology and Applied Pharmacology 143 (1997)
Ethylene dibromide (1,2-dibromoethane, EDB) is metabolized by two routes: a conjugative route catalyzed by glutathione S -transferases (GST) and an oxidative route catalyzed by cytochrome P450 (P450). The GST route is associated with carcinogenicity.
Autor:
Jan N. M. Commandeur, L.W. Wormhoudt, Philippe Beaune, P.J. van Bladeren, Nico P. E. Vermeulen, I de Waziers, J.H.T.M. Ploemen
Publikováno v:
Chemico-Biological Interactions, 101, 175-192. Elsevier Ireland Ltd
Wormhoudt, L W, Ploemen, J P H T M, de Waziers, I, Commandeur, J N M, Beaune, P H, van Bladeren, P J & Vermeulen, N P E 1996, ' Inter-individual variability in the oxidation of 1,2-dibromoethane: use of heterologously expressed human cytochrome P450 and human liver microsomes. ', Chemico-Biological Interactions, vol. 101, pp. 175-192 . https://doi.org/10.1016/0009-2797(96)03723-4
Chemico-Biological Interactions, 3, 101, 175-192
Wormhoudt, L W, Ploemen, J P H T M, de Waziers, I, Commandeur, J N M, Beaune, P H, van Bladeren, P J & Vermeulen, N P E 1996, ' Inter-individual variability in the oxidation of 1,2-dibromoethane: use of heterologously expressed human cytochrome P450 and human liver microsomes. ', Chemico-Biological Interactions, vol. 101, pp. 175-192 . https://doi.org/10.1016/0009-2797(96)03723-4
Chemico-Biological Interactions, 3, 101, 175-192
1,2-Dibromoethane (1,2-DBE) is mainly used as an additive in leaded gasoline and as a soil fumigant and it is a suspected carcinogen in humans. In this study, the oxidative bioactivation of 1,2-DBE to 2-bromoacetaldehyde (2-BA) was studied using hete
Autor:
P.J. van Bladeren, J.H.T.M. Ploemen, Nico P. E. Vermeulen, Jan N. M. Commandeur, L.W. Wormhoudt, B. van Ommen
Publikováno v:
Chemico-Biological Interactions, 99, 41-53. Elsevier Ireland Ltd
Wormhoudt, L W, Ploemen, J P H T M, Commandeur, J N M, van Ommen, B, van Bladeren, P J & Vermeulen, N P E 1996, ' Cytochrome P450 catalyzed metabolism of 1,2-dibromoethane in liver microsomes of differentially induced rats. ', Chemico-Biological Interactions, vol. 99, pp. 41-53 . https://doi.org/10.1016/0009-2797(95)03659-8
Wormhoudt, L W, Ploemen, J P H T M, Commandeur, J N M, van Ommen, B, van Bladeren, P J & Vermeulen, N P E 1996, ' Cytochrome P450 catalyzed metabolism of 1,2-dibromoethane in liver microsomes of differentially induced rats. ', Chemico-Biological Interactions, vol. 99, pp. 41-53 . https://doi.org/10.1016/0009-2797(95)03659-8
The cytochrome P450 (P450) catalyzed oxidation of 1,2-dibromoethane (1,2-DBE) to 2-bromoacetaldehyde (2-BA) was measured in liver microsomes of both control and differentially induced rats. 2-BA formation was quantified by derivatization of 2-BA with
Autor:
G. Giaccone, Jorine H. Savonije, L.W. Wormhoudt, C.L. van Felius, C. J. van Groeningen, A. van Bochove, Aafke H. Honkoop
Publikováno v:
European journal of cancer (Oxford, England : 1990). 41(11)
This work was conducted to evaluate the effect of early intervention with epoetin alfa (EPO) on transfusion requirements, hemoglobin level (Hb), quality of life (QOL) and to explore a possible relationship between the use of EPO and survival, in pati
Autor:
L.W. Wormhoudt, Q.J Li, S Ramnatshing, Nico P. E. Vermeulen, E.J. Groot, J. P. G. Brakenhoff, Jan N. M. Commandeur
Publikováno v:
Chemico-Biological Interactions, 110, 139-158. Elsevier Ireland Ltd
Vrije Universiteit Amsterdam
Chemico-Biological Interactions, 110(3), 139-58. Elsevier Ireland Ltd
Vermeulen, N P, Commandeur, J N, Groot, E J, Wormhoudt, L W, Ramnatshing, S, Li, Q J & Brakenhoff, J P 1998, ' Toxicity of fotemustine in rat hepatocytes and mechanism-based protection against it ', Chemico-Biological Interactions, vol. 110, no. 3, pp. 139-58 . https://doi.org/10.1016/S0009-2797(98)00004-0
Vermeulen, N P E, Commandeur, J N M, Groot, E J, Wormhoudt, L W, Ramnathsing, S, Li, Q J & Brakenhoff, J P G 1998, ' Toxicity of fotemustine in rat hepatocytes and mechanism-based protection against it. ', Chemico-Biological Interactions, vol. 110, pp. 139-158 . https://doi.org/10.1016/S0009-2797(98)00004-0
Vrije Universiteit Amsterdam
Chemico-Biological Interactions, 110(3), 139-58. Elsevier Ireland Ltd
Vermeulen, N P, Commandeur, J N, Groot, E J, Wormhoudt, L W, Ramnatshing, S, Li, Q J & Brakenhoff, J P 1998, ' Toxicity of fotemustine in rat hepatocytes and mechanism-based protection against it ', Chemico-Biological Interactions, vol. 110, no. 3, pp. 139-58 . https://doi.org/10.1016/S0009-2797(98)00004-0
Vermeulen, N P E, Commandeur, J N M, Groot, E J, Wormhoudt, L W, Ramnathsing, S, Li, Q J & Brakenhoff, J P G 1998, ' Toxicity of fotemustine in rat hepatocytes and mechanism-based protection against it. ', Chemico-Biological Interactions, vol. 110, pp. 139-158 . https://doi.org/10.1016/S0009-2797(98)00004-0
Fotemustine is a relatively novel DNA-alkylating 2-chloroethyl-substituted N-nitrosourea (CENU) drug, clinically used for the treatment of disseminated malignant melanoma in different visceral and non-visceral tissues. Thrombocytopenia has been obser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::400d9c813a5c8e84696c89ad1af9cd64
https://research.vu.nl/en/publications/03fbe49f-c862-40d1-848a-e14fa9c13e8a
https://research.vu.nl/en/publications/03fbe49f-c862-40d1-848a-e14fa9c13e8a
Publikováno v:
Brakenhoff, J P G, Commandeur, J N M, Wormhoudt, L W, Groot, E J & Vermeulen, N P E 1996, ' Molecular mechanisms of toxic effects of fotemustine in rat hepatocytes and subcellular rat liver fractions. ', Carcinogenesis, vol. 17, no. 4, pp. 715-724 . https://doi.org/10.1093/carcin/17.4.715
Carcinogenesis, 17(4), 715-724. Oxford University Press
Carcinogenesis, 17(4), 715-724. Oxford University Press
Fotemustine is a clinically used DNA-alkylating 2-chloro-ethyl-substituted N-nitrosourea, which sometimes shows signs of haematotoxicity and reversible liver and renal toxicity as toxic side-effects. Mechanistic data on these side-effects are scarce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec3dfa4bda31551a3c505b9e643f17b7
https://research.vu.nl/ws/files/1739822/134715.pdf
https://research.vu.nl/ws/files/1739822/134715.pdf
Autor:
P.J. van Bladeren, Nico P. E. Vermeulen, M. van Iersel, Jan N. M. Commandeur, J.H.T.M. Ploemen, L.W. Wormhoudt
Publikováno v:
Ploemen, J P H T M, van Iersel, M, Wormhoudt, L W, Commandeur, J N M, Vermeulen, N P E & van Bladeren, P J 1996, ' In vitro inhibition of rat and human glutathione S-transferase isoenzymes by disulfiram and diethyldithiocarbamate. ', Biochemical Pharmacology, vol. 52, pp. 197-204 . https://doi.org/10.1016/0006-2952(96)00142-6
Biochemical Pharmacology 52 (1996)
Biochemical Pharmacology, 52, 197-204
Biochemical Pharmacology, 2, 52, 197-204
Biochemical Pharmacology, 52, 197-204. Elsevier Inc.
Biochemical Pharmacology 52 (1996)
Biochemical Pharmacology, 52, 197-204
Biochemical Pharmacology, 2, 52, 197-204
Biochemical Pharmacology, 52, 197-204. Elsevier Inc.
The drug disulfiram (DSF, Antabuse) has been used in the therapy of alcohol abuse. It is a potent inhibitor of aldehyde dehydrogenase. Its reduced form, diethyldithiocarbamate (DDTC), and further metabolites show similar activities. DSF and DDTC have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1019d53dec0451bc9dd5ff4571a6233
https://research.vu.nl/en/publications/db901fc4-3409-471c-967d-6d4b148ab51a
https://research.vu.nl/en/publications/db901fc4-3409-471c-967d-6d4b148ab51a