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1 e, formed nuclear foci in cells treated with floxuridine.
4 a CRISPR knockout screen in the presence of floxuridine, a chemotherapeutic agent that incorporates
5 um-labile prodrug of the nucleoside analogue floxuridine, a potent antineoplastic drug used in the cl
6 erial infusion pump (HAIP) chemotherapy with floxuridine aims to control the liver disease and improv
8 the effectiveness of HAIP chemotherapy with floxuridine and concurrent systemic gem-cis in patients
9 ates with the phosphorylated 5-FU nucleoside Floxuridine and demonstrated their enhanced activity aga
10 six cycles of hepatic arterial infusion with floxuridine and dexamethasone plus intravenous fluoroura
11 re enrolled onto a phase I protocol with HAI floxuridine and dexamethasone plus systemic chemotherapy
13 combination of hepatic arterial infusion of floxuridine and intravenous fluorouracil improves the ou
15 ition of chemotherapy, such as capecitabine, floxuridine, and vinblastine, may increase the effective
16 its metabolite 5-fluorodeoxyuridine (FdUrd, floxuridine) are chemotherapy agents that are converted
18 patients) or postoperative hepatic arterial floxuridine combined with intravenous continuous-infusio
19 dengue virus replication in the presence of floxuridine, consistent with thymidine-less stress trigg
20 CONCLUSION The combination of regional HAI floxuridine/dexamethasone and systemic oxaliplatin and i
22 ara-guanosine (AraG), gemcitabine (Ge), and floxuridine (FdU), to replace all natural nucleosides in
24 followed by hepatic artery infusion (HAI) of floxuridine (FUDR) alternating with systemic fluorouraci
25 every 2 weeks concurrent with 2 weeks of HAI floxuridine (FUDR) and dexamethasone (Dex) every 28 days
27 biliary toxicity may permit salvage HAI with floxuridine (FUDR) in patients whose liver tumors fail t
28 MTD) of systemic irinotecan (CPT-11) and HAI floxuridine (FUDR) plus dexamethasone (DEX) as combinati
29 efit of adjuvant hepatic arterial infusional floxuridine (HAI-FUDR) in addition to modern systemic ch
30 acil (5-FU) and 5-fluorodeoxyuridine (FdUrd, floxuridine) have activity in multiple tumors, and both
32 ylation facilitates UNG2-dependent repair of floxuridine-induced DNA lesions and promotes tumor cell
33 molecules, we observed that methotrexate and floxuridine inhibited dengue virus infections at low mic
36 g patients with hepatic arterial infusion of floxuridine plus systemic fluorouracil after liver resec
37 focal liver irradiation with hepatic artery floxuridine prolongs survival in patients with unresecta
38 otrexate and by thymidine in the presence of floxuridine, suggesting an unexpected role for thymidine
39 n cancer cell line that is hypersensitive to floxuridine, we show that GSK-3 phosphorylation facilita
40 re highly sensitive to both methotrexate and floxuridine, whereas other RNA viruses (Sindbis virus an
41 On univariate analysis, receipt of HAI-FUDR (floxuridine) within 1 year of IHP was the only factor as
42 e radiation with concurrent hepatic arterial floxuridine would improve survival in patients with unre