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1 oxaliplatin chemotherapy, radiotherapy, and photodynamic therapy.
2 itor, sensitizes xenotransplanted tumours to photodynamic therapy.
3 role of singlet oxygen and (1)O2 carriers in photodynamic therapy.
4 as effective and well-tolerated as daylight photodynamic therapy.
5 VEGF) interventions, dietary supplements, or photodynamic therapy.
6 econtouring, and antitumor and antimicrobial photodynamic therapy.
7 sensitizers for photocontrolled-delivery and photodynamic therapy.
8 erved between added reovirus before or after photodynamic therapy.
9 a history of choroidal neovascularization or photodynamic therapy.
10 orescence probes, as well as sensitizers for photodynamic therapy.
11 al wastewater treatment, photochemistry, and photodynamic therapy.
12 oninvasive optical imaging, optogenetics and photodynamic therapy.
13 ch as imaging combined with drug delivery or photodynamic therapy.
14 r photocoagulation, CyberKnife radiation, or photodynamic therapy.
15 therapy, hyper- or hypothermic therapy, and photodynamic therapy.
16 s, which makes them potentially suitable for photodynamic therapy.
17 s in photothermal therapy, chemotherapy, and photodynamic therapy.
18 lation of photosensitizer drugs in tumors in photodynamic therapy.
19 for light-triggered biological reactions and photodynamic therapy.
20 n of disease and any previous treatment with photodynamic therapy.
21 ential as photosensitizers for metal-organic photodynamic therapy.
22 topical or injection interferon alfa-2b, and photodynamic therapy.
23 adverse effects, and cost, limit the use of photodynamic therapy.
24 itization, a limitation often encountered in photodynamic therapy.
25 ancer-killing techniques of photothermal and photodynamic therapy.
26 Ir1-HSA are highly favorable properties for photodynamic therapy.
27 enhanced imaging, or phototoxic for improved photodynamic therapy.
28 ong candidate photosensitizer for anticancer photodynamic therapy.
29 poxic tumours are a major problem for cancer photodynamic therapy.
30 umors without relapse by taking advantage of photodynamic therapy.
31 new venues to combat current limitations of photodynamic therapy.
32 ehicles to encapsulate a photosensitizer for photodynamic therapy.
33 ith multiple morphologies and application in photodynamic therapy.
34 alfa-2b (0% vs 1%), cryotherapy (0% vs 3%), photodynamic therapy (0% vs 1%), excisional biopsy and c
35 therapy and the other half treated with AWL photodynamic therapy 1 week apart and randomly allocated
36 n nonmelanoma skin cancer were uncertain for photodynamic therapy (3 trials, 93 participants, risk ra
37 randomly assigned (1:1) to vascular-targeted photodynamic therapy (4 mg/kg padeliporfin intravenously
39 ing oxidant production by transition metals, photodynamic therapy, activated macrophages, and platele
41 bial and antiviral agents, anticancer drugs, photodynamic therapy agents, radiotherapy agents and bio
42 or 0.5 mg), sham injections plus verteporfin photodynamic therapy (ANCHOR), or sham injections alone
43 y assigned 206 patients to vascular-targeted photodynamic therapy and 207 patients to active surveill
44 e findings may help to alleviate pain during photodynamic therapy and also allow for disease modifica
45 mes were after vs before the introduction of photodynamic therapy and anti-vascular endothelial growt
47 ffectiveness and adverse effects of daylight photodynamic therapy and artificial white light (AWL) LE
49 photodynamic agent that can be used for both photodynamic therapy and image-guided surgery, allowing
51 ence for technologies including bio-imaging, photodynamic therapy and organic light-emitting diodes.
52 ies based on oxygen free radicals, including photodynamic therapy and radiotherapy, have emerged as p
55 ad half of their scalp treated with daylight photodynamic therapy and the other half treated with AWL
56 diagnostics and analytics, photothermal and photodynamic therapies, and delivery of target molecules
57 emonstrates a highly promising new agent for photodynamic therapy, and attracts attention to photosta
58 peutics and biologics, chemotherapeutics and photodynamic therapy, and chemotherapeutics and radiothe
60 mor hypoxia for enhancement of chemotherapy, photodynamic therapy, and immunotherapy, either individu
65 ts of repeated applications of antimicrobial photodynamic therapy (aPDT) adjunctive to scaling and ro
66 ficacy of multiple sessions of antimicrobial photodynamic therapy (aPDT) as an adjunct to surgical pe
67 im of this study is to compare antimicrobial photodynamic therapy (aPDT) as an adjunctive therapy to
70 low-intensity laser (LIL); 2) antimicrobial photodynamic therapy (aPDT); or 3) toluidine blue O (TBO
71 ent singlet-oxygen generation with potential photodynamic therapy application as demonstrated by in v
72 mus) and the most promising absorptivity for photodynamic therapy application, was tested as efficien
74 Near-IR absorption, desired for potential photodynamic therapy applications, was not pursuable for
76 nor light-induced medicinal chemistry (e.g., photodynamic therapy) are covered, even if metal complex
77 ession in cancer cells and susceptibility to photodynamic therapy based on their increased ability to
78 ood coloring agent and a photosensitizer for photodynamic therapy because of its antioxidant properti
79 atoses (AKs) is as effective as conventional photodynamic therapy but has the advantage of being almo
80 e ROS not only directly kills tumor cells by photodynamic therapy but stimulates the dimeric paclitax
81 f natural systems and integral components of photodynamic therapy, but their utilization is compromis
82 er enabled the realization of self-amplified photodynamic therapy by the regulation of Ppa release us
84 cations, including therapeutic (photothermal/photodynamic therapy, chemotherapy and synergistic thera
85 is, including cryosurgery, ingenol mebutate, photodynamic therapy, colchicine, and 5-fluorouracil.
88 enkov luminescence imaging and (2) Cherenkov-photodynamic therapy (CR-PDT) on cells could be achieved
89 -VEGF therapy increased from 60.3% to 72.7%, photodynamic therapy decreased from 12.8% to 5.3%, and t
91 imaging and synergetic photothermal therapy/photodynamic therapy derived from the porphyrin-like moi
92 osensitizers into nanostructures can improve photodynamic therapy efficacy and the safety profile of
93 as photosynthesis, vision, photolithography, photodynamic therapy, etc., is yet to become a common to
94 on of photosensitizers is a key component of photodynamic therapy, exogenous photothermal contrast ag
95 re to sunlight and other patients undergoing photodynamic therapy experience similar pain, which can
96 e variety of potential applications, such as photodynamic therapy for accelerated drug screening, mag
97 therapy and artificial white light (AWL) LED photodynamic therapy for the treatment of AKs on the for
98 eporfin (VP), a light-activated drug used in photodynamic therapy for the treatment of choroidal neov
99 was 58 (28%) of 206 in the vascular-targeted photodynamic therapy group compared with 120 (58%) of 20
101 tatitis (three [2%] in the vascular-targeted photodynamic therapy group vs one [<1%] in the active su
102 rious adverse event in the vascular-targeted photodynamic therapy group was retention of urine (15 pa
106 for phototherapeutic interventions, such as photodynamic therapy, has transformed medicine and biolo
108 photodynamic therapy, named X-ray inducible photodynamic therapy, holds tremendous promise due to a
112 lar endothelial growth factor or verteporfin photodynamic therapy in combination with systemic chemot
113 o examine the responses to vascular-targeted photodynamic therapy in mice with subcutaneous xenograft
116 interventions (argon laser photocoagulation, photodynamic therapy, intravitreal corticosteroids, and
117 TERPRETATION: Padeliporfin vascular-targeted photodynamic therapy is a safe, effective treatment for
121 iolet and visible light, and also to develop photodynamic therapy, it is important to resolve the mec
123 , 5% imiquimod cream, methyl aminolevulinate photodynamic therapy (MAL-PDT), or 0.015% ingenol mebuta
126 of X-rays instead of UV/Vis light to trigger photodynamic therapy, named X-ray inducible photodynamic
127 pecific interventions (acitretin, imiquimod, photodynamic therapy, nicotinamide, topical diclofenac,
134 bined with protoporphyrin IX (PpIX)-mediated photodynamic therapy on a variety of human pancreatic ca
135 gnosed as having exudative ARMD who received photodynamic therapy or anti-VEGF therapy compared with
138 ffect compared with reovirus monotherapy and photodynamic therapy (p=0.042) with 100% cell death obse
140 ing pigment (methylene blue - MB) to mediate photodynamic therapy (PDT) against Streptococcus mutans
143 development of 2 therapies: (1) verteporfin photodynamic therapy (PDT) and (2) anti-vascular endothe
144 evice has been developed to perform in vitro photodynamic therapy (PDT) and diagnostic assays for tre
145 e recently contributed to the progression of photodynamic therapy (PDT) and microbial photodynamic in
146 the design of transition metal complexes for photodynamic therapy (PDT) and photoactivated chemothera
147 ed with various therapy strategies including photodynamic therapy (PDT) and photothermal therapy (PTT
148 antigen presentation by enabling immunogenic photodynamic therapy (PDT) and promoting the maturation
150 , presumably through the combined effects of photodynamic therapy (PDT) and released chemotherapy dru
151 um behavior, leading to efficient probes for photodynamic therapy (PDT) and stochastic optical recons
152 f increasing interest as photosensitizers in photodynamic therapy (PDT) and, more recently, for photo
153 Cationic antimicrobial peptides (CAMPs) and photodynamic therapy (PDT) are attractive tools to comba
154 inical experiments addressing the effects of photodynamic therapy (PDT) as an adjunct to conventional
156 opportunities of NP imaging and therapy on a photodynamic therapy (PDT) based NP system that has been
157 namic therapy (SDT), which is different from photodynamic therapy (PDT) by the use of highly penetrat
159 we have found that addition of erlotinib to photodynamic therapy (PDT) can improve treatment respons
161 neration and exhibits significantly enhanced photodynamic therapy (PDT) efficacy on two colon cancer
169 for their potential as photosensitizers for photodynamic therapy (PDT) in P-glycoprotein (P-gp) expr
170 herapy in ancient texts and the discovery of photodynamic therapy (PDT) in the early 1900s, the landm
188 reatment of hypoxic tumors, oxygen-dependent photodynamic therapy (PDT) is considerably limited.
194 ial of this conjugate as photosensitizer for photodynamic therapy (PDT) of cancers overexpressing the
195 great potential as nanophotosensitizers for photodynamic therapy (PDT) owing to their high photosens
198 clinically approved intervention for cancer, photodynamic therapy (PDT) still suffers from limitation
200 are employed to deliver photosensitizers for photodynamic therapy (PDT) through the enhanced penetrat
201 orescence for image-guided surgery (IGS) and photodynamic therapy (PDT) to resect and ablate cancer c
202 treatment, it allowed delivery of selective photodynamic therapy (PDT) to the cancerous tissues, wit
205 e entrapped agents that harnesses sub-lethal photodynamic therapy (PDT) using a photosensitiser that
206 chanisms how the efficacy of photofrin based photodynamic therapy (PDT) was enhanced by miR-99a trans
207 racellular localization and cell response to photodynamic therapy (PDT) were analyzed in MCF10A norma
208 d visual outcomes using combination standard photodynamic therapy (PDT) with intravitreal ranibizumab
209 integration of fluorescence imaging (FL) and photodynamic therapy (PDT) with positron emission tomogr
211 nstrate that benzoporphyrin derivative-based photodynamic therapy (PDT), a photochemical cytotoxic mo
213 f cancer and dermatological diseases through photodynamic therapy (PDT), and advanced materials for e
214 , 0.09, and 0.07 LogMAR in the no-treatment, photodynamic therapy (PDT), bevacizumab, and ranibizumab
215 rossing (ISC) are highly promising for smart photodynamic therapy (PDT), but achieving this goal rema
216 rates cytotoxic singlet oxygen ((1)O(2)) for photodynamic therapy (PDT), but also triggers a spontane
218 additional limitations of porphyrin-mediated photodynamic therapy (PDT), including low depths of tiss
219 ent procedures, such as laser irradiation or photodynamic therapy (PDT), may provide some additional
220 each clinical treatment tool (chemotherapy, photodynamic therapy (PDT), radiotherapy (RT)) by contro
223 ptake of photosensitizers by cancer cells in photodynamic therapy (PDT), we designed a smart plasma m
246 MRI contrasting agents, and sensitizers for photodynamic therapy (PDT); and more recently as models
247 (MARINA), or were randomized to verteporfin photodynamic therapy (PDT; n=143), 0.3-mg ranibizumab mo
249 atform for the high-throughput assessment of photodynamic therapy photosensitizer (PDT) efficacy on E
250 addition, light activation has potential in photodynamic therapy, photothermal therapy, radiotherapy
251 , which is used as an antimicrobial agent in photodynamic therapy, potentiates tellurite toxicity.
252 gated as cytotoxic agents and inhibitors, in photodynamic therapy, radiation therapy, drug/gene deliv
253 rapies were identified: electrochemotherapy, photodynamic therapy, radiotherapy, intralesional therap
255 es applications in bioimaging and diagnosis, photodynamic therapy regimes, in addition to photovoltai
259 vely killing beta-cells by receptor-targeted photodynamic therapy (rtPDT) with exendin-4-IRDye700DX,
260 tionic and anionic phthalocyanines (Pcs) for photodynamic therapy suggest systematically significant
262 d radical ions (Type I reaction); whereas in photodynamic therapy, the tumor destruction is mainly ca
263 , photoreformation, photoredox catalysis and photodynamic therapy, they are being developed in surpri
264 hogonal reactions as an original strategy in photodynamic therapy to achieve conditional phototoxicit
266 scular endothelial growth factor injections, photodynamic therapy, topical dorzolamide, oral dosing o
271 on with Photodynamic Therapy; Verteporfin in Photodynamic Therapy; VEGF Inhibition Study in Ocular Ne
272 ent of Age-Related Macular Degeneration with Photodynamic Therapy; Verteporfin in Photodynamic Therap
273 anic framework, Zr-TBB, for highly effective photodynamic therapy via both type I and type II mechani
274 vitreal anti-VEGF injection; (3) verteporfin photodynamic therapy (vPDT); or (4) laser photocoagulati
275 xamine the hypothesis that vascular-targeted photodynamic therapy (VTP) with WST11 and clinically rel
282 rcumvent the limitations of chemotherapy and photodynamic therapy, we have engineered a robust and sm
283 s as photosensitizers for oxygen sensing and photodynamic therapy, we investigated the potential beta
284 ects of reovirus combined with PpIX-mediated photodynamic therapy were analysed in methylthiazoltetra
287 omy, cryotherapy, laser photocoagulation, or photodynamic therapy, were excluded from the analysis.
288 in rare diseases, such as porphyrias, and in photodynamic therapy where short-term toxicity is intend
289 itization represents a promising approach in photodynamic therapy where the design of the active phot
291 photothermal therapy and porphyrin-mediated photodynamic therapy which results in complete tumor eli
292 mour cells with low or no PTEN expression to photodynamic therapy, which is based on the ability of p
300 to achieve efficient low-dose X-ray-induced photodynamic therapy (X-PDT) with negligible side effect