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1                            Thirty days after BNCT, mice bearing TK1(+) L929 tumors had a 15x reductio
2 gliomas, which had received i.t. BSD-EGF and BNCT, had a MST of 45 +/- 5 days compared with 33 +/- 2
3 of the distribution of a clinically approved BNCT drug.
4 ty and similar or even superior potential as BNCT agents compared with different classes of 3CTAs.
5  efficacy of binary cancer therapies such as BNCT and PDT depends critically on the subcellular local
6 n surgically removed malignant tissue before BNCT.
7 ly 24 h before BPA administration (ALA + BPA-BNCT).
8 ing in improved survival compared to the BPA-BNCT group.
9  the sensitivity of malignant gliomas to BPA-BNCT.
10  fluence was the limiting factor controlling BNCT efficacy in this study.
11 therapy approach has been known for decades, BNCT failed to reach the daily clinics to date.
12                                          For BNCT experiments, tumor-bearing mice were irradiated 54
13 ered as a promising boron delivery agent for BNCT.
14 d transporters, making it an ideal agent for BNCT.
15 pment of potential boron delivery agents for BNCT as well as new bioactive compounds containing a neg
16  produce selective boron delivery agents for BNCT.
17  of high and low molecular weight agents for BNCT.
18 o not appear to be suitable boron agents for BNCT.
19              These results are important for BNCT, because clinical protocols using a 2-h infusion ha
20  make boronated aptamers as therapeutics for BNCT.
21 d to simulate a continuous infusion used for BNCT therapy.
22 er diagnosis and can potentially be used for BNCT.
23 n of tumor growth was observed in mice given BNCT vs. control mice (only 424% increase in tumor volum
24 n the characteristics of the main historical BNCT drug 4-borono-l-phenylalanine (BPA).
25                In female mice tumour models, BNCT and the controlled drug release triggered by locali
26 rug that has the potential to improve modern BNCT interventions.
27 ke of BPA and improving the effectiveness of BNCT.
28 ta are the first to show in vivo efficacy of BNCT using a high molecular weight boronated bioconjugat
29 potentially enhance the therapeutic ratio of BNCT by >25%.
30                             Also in terms of BNCT treatment, BA emerges again as an efficient boron c
31 rticular significance for clinical trials of BNCT for human glioblastoma multiforme using the drug BP
32 , it was possible to extend the follow-up of BNCT treatment groups to 16 wk after the first treatment
33 prove valuable for patient selection and pre-BNCT treatment planning.
34 of the biodistribution of BPA-Fr enables pre-BNCT calculation of expected tissue dosimetry for a sele
35  human glioblastoma tissue obtained from pre-BNCT surgical biopsy.
36                                Once-repeated BNCT treatment with readministration of liposomes at an
37            Based on these favorable results, BNCT studies were then initiated in rats bearing intrace
38               On the basis of these results, BNCT was initiated at the Brookhaven National Laboratory
39                                   Successful BNCT depends on knowledge of the distribution of boron-c
40 tron-activated boron capsule that synergizes BNCT and controlled immune adjuvants release to provoke
41 quencing unveils the fact and mechanism that BNCT heats anti-tumour immunity.
42 unds promising boron delivery agents for the BNCT of brain tumors.
43               Boron neutron capture therapy (BNCT) allows the selective elimination of malignant tumo
44 pplication of boron neutron capture therapy (BNCT) following liposomal delivery of a (10)B-enriched p
45               Boron neutron capture therapy (BNCT) is a high-LET particle radiotherapy clinically tes
46               Boron neutron capture therapy (BNCT) is a re-emerging binary cellular level cancer inte
47    Success of boron neutron capture therapy (BNCT) is dependent on cellular and molecular targeting o
48               Boron neutron capture therapy (BNCT) is dependent on the selective accumulation of boro
49 pplication of boron neutron capture therapy (BNCT) mediated by liposomes containing (10)B-enriched po
50 d N5-2OH, for boron neutron capture therapy (BNCT) of brain tumors using the RG2 rat glioma model.
51               Boron neutron capture therapy (BNCT) using 4-[10B]boronophenylalanine-fructose (BPA-Fr)
52               Boron neutron capture therapy (BNCT) was clinically approved in 2020 and exhibits remar
53               Boron neutron capture therapy (BNCT), a binary treatment modality that can potentially
54 pplication of boron neutron capture therapy (BNCT), a noninvasive approach to eliminate cancer cells.
55               Boron neutron capture therapy (BNCT), an experimental treatment for certain cancers, de
56 ry agents for boron neutron capture therapy (BNCT).
57 evaluated for boron neutron capture therapy (BNCT).
58 This suggests that ALA may sensitize GSCs to BNCT by upregulating the expression of amino acid transp
59  could sensitize glioma stem cells (GSCs) to BNCT by enhancing the uptake of BPA.
60 ) is in Phase II clinical trials to validate BNCT as a treatment for glioblastoma multiforme and mela
61 earing mice at 2-hour intervals, after which BNCT was carried out at the Massachusetts Institute of T