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1 reased pyrimidine catabolism at the level of dihydropyrimidine dehydrogenase.
2 tumours, consistent with the inactivation of dihydropyrimidine dehydrogenase: a selective decrease in
3 Eniluracil (776C85), a potent inactivator of dihydropyrimidine dehydrogenase, allows fluorouracil (5-
4 ples include thiopurine S-methyltransferase, dihydropyrimidine dehydrogenase and flavin monooxygenase
5             5-Fluorouracil is inactivated by dihydropyrimidine dehydrogenase and targets thymidylate
6                                              Dihydropyrimidine dehydrogenase catalyzes the rate-limit
7 bolite 5-methyl tetrahydrofolate (MTHF), and dihydropyrimidine dehydrogenase (DPD) activity in periph
8                                              Dihydropyrimidine dehydrogenase (DPD) activity was deter
9                                              Dihydropyrimidine dehydrogenase (DPD) catabolizes endoge
10                                              Dihydropyrimidine dehydrogenase (DPD) deficiency constit
11 cause of intolerance to fluoropyrimidines is dihydropyrimidine dehydrogenase (DPD) deficiency, which
12 rt that macrophages specifically overexpress dihydropyrimidine dehydrogenase (DPD) in hypoxia, leadin
13                                              Dihydropyrimidine dehydrogenase (DPD) is a major determi
14                                              Dihydropyrimidine dehydrogenase (DPD) is the initial and
15                                              Dihydropyrimidine dehydrogenase (DPD) is the initial, ra
16 ve reported a correlation between intratumor dihydropyrimidine dehydrogenase (DPD) messenger RNA (mRN
17 ected dose of 5-FU is rapidly inactivated by dihydropyrimidine dehydrogenase (DPD) to therapeutically
18 ficiency of the pyrimidine catabolic enzyme, dihydropyrimidine dehydrogenase (DPD), has been shown to
19 e uracil in UFT slows degradation of 5-FU by dihydropyrimidine dehydrogenase (DPD), which results in
20 e pair, we identified an enhancer region for dihydropyrimidine dehydrogenase (DPD, DPYD gene) express
21                                              Dihydropyrimidine dehydrogenase (DPD, encoded by DPYD) r
22  in the fluoropyrimidine metabolizing enzyme dihydropyrimidine dehydrogenase (DPD; ie, DPYD*2A) is st
23 ral regimen of eniluracil (which inactivates dihydropyrimidine dehydrogenase [DPD]), 5-FU, and leucov
24  enzyme in the pyrimidine catabolic pathway, dihydropyrimidine dehydrogenase (DPYD) and its effect on
25                                              Dihydropyrimidine dehydrogenase (DPYD) is an enzyme resp
26 n addition, AEG-1 enhances the expression of dihydropyrimidine dehydrogenase (DPYD) that catalyzes th
27                                              Dihydropyrimidine dehydrogenase (DPYD), a pyrimidine-deg
28 sly unreported gene affecting sleep duration-dihydropyrimidine dehydrogenase (Dpyd).
29 red study with eniluracil, an inactivator of dihydropyrimidine dehydrogenase, enabling catabolite cor
30                        Thus, by inactivating dihydropyrimidine dehydrogenase, EU prolonged the half-l
31                                      Tumoral dihydropyrimidine dehydrogenase expression is a promisin
32 acy; in the XELOX group, for high versus low dihydropyrimidine dehydrogenase expression levels, DFS H
33  shown the prognostic impact of several rare dihydropyrimidine dehydrogenase gene (DPYD) variants on
34                                          The dihydropyrimidine dehydrogenase gene (DPYD) was isolated
35 xia induces HIF2a-mediated overexpression of dihydropyrimidine dehydrogenase in TAMs, leading to chem
36 e to progression (TTP) of an oral regimen of dihydropyrimidine dehydrogenase inhibitory fluoropyrimid
37                      Low tumor expression of dihydropyrimidine dehydrogenase may be predictive for XE
38 pidermal growth factor receptor mutation, or dihydropyrimidine dehydrogenase polymorphism) may differ
39  and other drug metabolizing enzymes such as dihydropyrimidine dehydrogenase represents a major innov
40 acil (776C85) is an effective inactivator of dihydropyrimidine dehydrogenase that allows continuous l
41 acil is being developed as an inactivator of dihydropyrimidine dehydrogenase, the enzyme that brings
42 routine use of p53, ras, thymidine synthase, dihydropyrimidine dehydrogenase, thymidine phosphorylase