Zobrazeno 1 - 10
of 618
pro vyhledávání: '"A. H. van Gennip"'
Autor:
Adriaan J. M. Mackus, Erik Heijdra, Wouter J. H. van Gennip, Tahsin Faraz, Wilhelmus M. M. Kessels, Marcel A. Verheijen, Yuri G. P. Verstappen, Javier Escandon Lopez, Nicholas J. Chittock
Publikováno v:
Journal of Applied Physics, 128(21):213301. American Institute of Physics
Anisotropic plasma-enhanced atomic layer etching (ALE) requires directional ions with a well-defined ion energy to remove materials in a highly selective and self-limiting fashion. In many plasma etching systems, the ion energy is controlled using ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e96a8c1f129832cb6fcd25b4bbdfe1ea
https://doi.org/10.1063/5.0028033
https://doi.org/10.1063/5.0028033
Publikováno v:
Nucleosides, nucleotides & nucleic acids, 25(9-11), 1103-1106. Marcel Dekker Inc.
Dihydropyrimidine dehydrogenase (DPD) constitutes the first step of the pyrimidine degradation pathway in which the pyrimidine bases uracil and thymine are catabolised to beta-alanine and beta-aminoisobutyric acid (beta-AIB), respectively. The mean c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d75dc4bcef850826cdf0ba9ae06779b
https://doi.org/10.1080/15257770600894097
https://doi.org/10.1080/15257770600894097
Autor:
Rutger Meinsma, René Leen, Huib N. Caron, Albert H. van Gennip, André B.P. van Kuilenburg, Jörgen Bierau
Publikováno v:
Cancer chemotherapy and pharmacology, 57(1), 105-113. Springer Verlag
The effect of the CTP synthetase inhibitor cyclopentenyl cytosine (CPEC) on the metabolism and cytotoxicity of 2',2'-difluorodeoxycytidine (dFdC, gemcitabine) and the expression and activity of deoxycytidine kinase (dCK) was studied in human neurobla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b11320eb08bc6c44a181c5e4e4e247d6
https://doi.org/10.1007/s00280-005-0005-8
https://doi.org/10.1007/s00280-005-0005-8
Publikováno v:
Journal of inherited metabolic disease, 28(5), 793-796. Springer Netherlands
Dihydropyrimidine dehydrogenase (DPD) deficiency (McKusick 274270) is a clinically heterogeneous autosomal recessive disorder of pyrimidine metabolism. DPD is the enzyme that catalyses the first and the rate-limiting step in the catabolism of uracil,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5092a23722b5bb5f191dce2d9cc810a
https://doi.org/10.1007/s10545-005-4218-0
https://doi.org/10.1007/s10545-005-4218-0
Autor:
Ramon Martí, Michio Hirano, Jan J.G.M. Verschuuren, Alan L. Buchman, Ikuo Hirano, André B.P. van Kuilenburg, Saba Tadesse, Albert H. van Gennip, Ben J. H. M. Poorthuis
Publikováno v:
Annals of neurology, 58(4), 649-652. John Wiley and Sons Inc.
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is caused by mutations in the gene encoding thymidine phosphorylase (TP). All MNGIE patients have had severe loss of TP function and prominent plasma accumulations of the TP substrates thy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1f0cbe6c4e3040d70d9a8fa0799e574
https://doi.org/10.1002/ana.20615
https://doi.org/10.1002/ana.20615
Publikováno v:
Journal of Chromatography B. 805:339-346
A non-radioactive procedure to measure the deoxycytidine kinase (dCK) activity in crude cell free homogenates was developed. 2-Chlorodeoxyadenosine (CdA) was used as the substrate for dCK and was separated from its product 2-chlorodeoxyadenosine-5′
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::230425e00e4ff5328d5b5eba3c59119a
https://doi.org/10.1016/j.jchromb.2004.03.036
https://doi.org/10.1016/j.jchromb.2004.03.036
Publikováno v:
Obstetrics and Gynecology, 103(5), 876-880. LIPPINCOTT WILLIAMS & WILKINS
OBJECTIVE: Preeclampsia is associated with abnormal lipid metabolism, including fatty acid metabolism. Carnitine plays an indispensable role in the oxidation of fatty acids. The aim of the study was to evaluate the possible role of abnormal fatty add
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef2d21df0d0bb04a1ef9238fbc77d40f
https://doi.org/10.1097/01.aog.0000125699.60416.03
https://doi.org/10.1097/01.aog.0000125699.60416.03
Autor:
Melanie A. Manning, T. Sanger, A. H. van Gennip, A. B. P. Van Kuilenburg, Gregory M. Enns, A. J. Barkovich, D. R. Witt
Publikováno v:
Journal of inherited metabolic disease, 27(4), 513-522. Springer Netherlands
Summary: Dihydropyrimidine dehydrogenase (DPD) deficiency is a rare autosomal recessive disorder of pyrimidine metabolism. Patients may present with a wide range of neurological symptoms during the first years of life. Head imaging abnormalities have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50cab089d150ea85f19367da07afadc5
https://doi.org/10.1023/b:boli.0000037350.24142.d5
https://doi.org/10.1023/b:boli.0000037350.24142.d5
Autor:
R. D. van de Grampel, W. Ming, A. Gildenpfennig, W. J. H. van Gennip, J. Laven, J. W. Niemantsverdriet, H. H. Brongersma, G. de With, R. van der Linde
Publikováno v:
Langmuir, 20(15), 6344-6351. American Chemical Society
In this paper, we investigate the surface properties of a series of copolymers of perfluoroalkyl methacrylate (CH2 = C(CH3)COOCH2CnF(2n + 1), n = 1, 6, or 10) and methyl methacrylate (MMA) and of blends of perfluorooctyl-end-capped poly(methyl methac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5852406ed872e7b8a3384e13ffe2955b
https://research.tue.nl/en/publications/067bd5f3-ddbe-4b05-b705-7a4f0a68c4ae
https://research.tue.nl/en/publications/067bd5f3-ddbe-4b05-b705-7a4f0a68c4ae
Publikováno v:
The Plant Journal. 34:595-604
Summary In response to various environmental stress conditions, plants rapidly form the intracellular lipid second messenger phosphatidic acid (PA). It can be generated by two independent signalling pathways via phospholipase D (PLD) and via phosphol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d61e4766f79334213fe38f99742aad94
https://doi.org/10.1046/j.1365-313x.2003.01750.x
https://doi.org/10.1046/j.1365-313x.2003.01750.x