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1 sion, indicating the compound functions as a radiosensitizer.
2 idate for further development as a potential radiosensitizer.
3 cancer demonstrating the role of RK-33 as a radiosensitizer.
4 Our studies identify MMAE as a potent radiosensitizer.
5 now shows promise as an anticancer drug and radiosensitizer.
6 super-repressor constructs) to function as a radiosensitizer.
7 ile, either as a chemotherapeutic agent or a radiosensitizer.
8 eta-lap may warrant clinical evaluation as a radiosensitizer.
9 eatment of pancreatic cancer and is a potent radiosensitizer.
10 d who have not received prior cisplatin as a radiosensitizer.
11 sistance, and the EGFR KI GW572016 acts as a radiosensitizer.
12 of the head and neck (SCCHN) and an in vitro radiosensitizer.
13 ting that 6-aminonicotinamide is acting as a radiosensitizer.
14 y and the potential use of ATM inhibitors as radiosensitizers.
15 anism of Cu-Cy for cancer treatment as a new radiosensitizers.
16 mall peptides as specific ATM inhibitors and radiosensitizers.
17 all molecules that could function as thermal radiosensitizers.
18 d docetaxel are being extensively studied as radiosensitizers.
20 tter understand the interaction of these two radiosensitizers, additional studies on DNA repair and c
21 b should be considered a potential cutaneous radiosensitizer and an inducer of radiation recall derma
22 rected conjugate, could function as a potent radiosensitizer and be selectively delivered to tumors u
23 tive component of soy isoflavones, acts as a radiosensitizer and potentiates prostate tumor cell kill
25 articles (NPs) are studied as drug carriers, radiosensitizers and imaging agents, and characterizing
26 iation regimens, the use of new hypoxic cell radiosensitizers and monoclonal antibodies that inhibit
28 hroughput screening method to identify novel radiosensitizers and suggest that NS-123 and similar nit
29 perimental data show that glucoazomycins are radiosensitizers and that they competitively inhibit glu
30 ted therapeutic compounds, NU7441 - a potent radiosensitizer, and gemcitabine - an FDA approved chemo
31 plore combinations of FU with cisplatin, new radiosensitizers, and active drugs combined with RT to r
32 e have demonstrated that POH is an effective radiosensitizer at clinically relevant doses of radiatio
33 ere selected as candidate Notch-1-regulating radiosensitizers based on the results of assay screening
34 w a significant increase in the ratio of the radiosensitizer bromodeoxyuridine (BUdR) in tumors versu
35 Here we show that hyperthermia, an effective radiosensitizer, can induce several steps associated wit
37 cantly more effective than the commonly used radiosensitizer cisplatin in vitro in three cancer cell
39 nly on physical improvements in delivery, as radiosensitizer development to target tumor cells has ye
41 easibility of administering carboplatin as a radiosensitizer during craniospinal radiation therapy (C
42 These data support testing of curcumin as a radiosensitizer for the clinical treatment of alveolar r
43 ncept for use of MLN4924 as a novel class of radiosensitizer for the treatment of pancreatic cancer.
44 larger than that of the most popularly used radiosensitizers, gold nanoparticles (1.19), and paclita
45 particular, the use of biological agents as radiosensitizers has led to the investigation of new com
46 t clear yet and Cu-Cy nanoparticles as novel radiosensitizers have never been tested on colorectal ca
48 ext, we have addressed new avenues including radiosensitizers, hypoxia, metabolism, angiogenesis, inv
53 oRNA (miR)-24 acts as a tumor suppressor and radiosensitizer in NPC cells and xenografts by targeting
56 nical utilization of beta-lap (Arq 501) as a radiosensitizer in prostate cancers that overexpress NQO
58 ical utility of pharmacologic ascorbate as a radiosensitizer in the treatment of pancreatic cancer.
60 idine; dFdCyd) has been shown to be a potent radiosensitizer in tumor cells both in vitro and in vivo
62 one (beta-lap; Arq 501), can act as a potent radiosensitizer in vitro through an unknown mechanism.
63 inally, NP Wtmn was shown to be an effective radiosensitizer in vivo using two murine xenograft model
65 Caffeine and okadaic acid, both established radiosensitizers, inhibit the incorporation of BrdU in G
67 diation that can serve as a highly effective radiosensitizer is reported here, significantly sensitiz
70 4'-bromo-3'-nitropropiophenone (NS-123) as a radiosensitizer of human glioma cells in vitro and in vi
71 combination with radiation was an effective radiosensitizer of murine NIH-3T3 fibroblasts, with a se
73 on inhibitors may prove clinically useful as radiosensitizers of tumors that depend on ras function.
74 ancer cells and evaluated its potential as a radiosensitizer on cell lines and prostate tumor xenogra
76 inase inhibitors may be more potent cellular radiosensitizers than ATM kinase inhibitors, and that th
77 (Cu-Cy) is a new photosensitizer and a novel radiosensitizer that can be activated by light, X-ray an
78 herapeutic relevance of EphB4 targeting as a radiosensitizer that can be exploited for the treatment
79 ngal metabolite, wortmannin, is an effective radiosensitizer that irreversibly inhibits certain membe
81 rhamnetin and cirsiliol can act as promising radiosensitizers that enhance the radiotherapeutic effic
86 assess the interaction of these two types of radiosensitizers, we compared treatment responses to the
87 ne cancer antigen 19-9, and gemcitabine as a radiosensitizer were associated with a major pathologic
88 vel less than 200 U/mL, and gemcitabine as a radiosensitizer were associated with a major response.
89 rapy, but DA was also equally effective as a radiosensitizer when given only 2 hours before fractiona
90 dR) and caffeine are recognized as potential radiosensitizers with different mechanisms of interactio
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