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1  TRPV1 channels in the absence of additional photosensitization.
2 cal stroke injury was induced by Rose Bengal photosensitization.
3 es and thereby increase the action sphere of photosensitization.
4 sults in excess uroporphyrin I, which causes photosensitization.
5 nse (P = 0.02) without affecting normal skin photosensitization.
6 ng radiation, photoionization, oxidation, or photosensitization.
7    The major side effect of PDT is cutaneous photosensitization.
8 ins was seen in parental cells 24-48 h after photosensitization.
9 t, offering a new strategy to tackle overall photosensitization, a limitation often encountered in ph
10 ter (NOM) did not significantly impact pSi's photosensitization abilities.
11                              SOA numbers via photosensitization alone and in the absence of ozone did
12                                              Photosensitization, an exaggerated sensitivity to harmle
13 gest a photooxidative mechanism of skin cell photosensitization by 3-hydroxypyridine derivatives.
14 s of A431 squamous carcinoma cells following photosensitization by administering aminolevulinic acid
15  Thus, for three different classes of drugs, photosensitization by at least two distinct mechanisms i
16                                              Photosensitization by derivatized carbon nanotubes from
17 ure-activity relationship study of skin cell photosensitization by endogenous pyridinium derivatives
18       UVA photodamage has been attributed to photosensitization by endogenous skin chromophores leadi
19 tration of COX-2 inhibitors enhance in vitro photosensitization by increasing apoptosis and improve i
20 he hair follicle, consistent with UV-induced photosensitization by melanin in the hair shaft.
21 f 23 +/- 3 and 21 +/- 3 for ETBE obtained by photosensitization by Pahokee Peat Humic Acid (PPHA) and
22 cterized by severe PPOX deficiency, onset of photosensitization by porphyrins in early childhood, ske
23 ia cutanea tarda is a skin disease caused by photosensitization by porphyrins whose accumulation is c
24            This is in agreement with a model photosensitization by rose bengal (RB(2-)) in deoxygenat
25                                         FICZ photosensitization caused intracellular oxidative stress
26 induced HSP-70 expression, whereas identical photosensitization conditions with a porphyrin (Photofri
27                         Photosensitivity and photosensitization could be demonstrated in freshly isol
28 ilieu to reasonably interpret and/or predict photosensitization efficacies.
29 spectroscopy, which likely prevented further photosensitization events.
30 sults in peroxidation at lipid double bonds, photosensitization experiments were performed to explici
31 TPCS2a-containing particles, suggesting that photosensitization facilitated a shift from default MHC
32 ne serum albumin, unglycated collagen showed photosensitization in CF3 fibroblasts and generation of
33  key role in the degradation of ETBE by PPHA photosensitization in deoxygenated media (Lambda = 11 +/
34 pase activation, resulting in more efficient photosensitization in HT-29 cancer cells.
35 the role of singlet oxygen, an ROS formed by photosensitization, in the regulation of survival signal
36 damage by UVA, submicromolar 5-MTHF inhibits photosensitization-induced strand breaks.
37                                    Cutaneous photosensitization is a common side effect of drug treat
38 ciceptive ion-channel activity, QAQ-mediated photosensitization is a platform for understanding signa
39                                         This photosensitization is greater for pheomelanin (yellow an
40 dendritic projections together indicate that photosensitization is highly selective for OFF-RGCs.
41 naphthodianthrones fagopyrins that can cause photosensitization is low.
42                                  Remarkably, photosensitization manifests only in animals with photor
43 hemistry, it is surprising to recognize that photosensitization mechanisms to access excited-state or
44                   This article describes the photosensitization of a meso-tetraphenylporphyrin iron(I
45                          We induced the self-photosensitization of a nonphotosynthetic bacterium, Moo
46 le crystalline phase nanostructures enhances photosensitization of a proton reduction catalyst for hy
47 ch Zn(II) coordination allows 100% efficient photosensitization of azobenzene switching, while Cu(II)
48                                              Photosensitization of cultured human skin keratinocytes
49 umulation of coproporphyrin III and leads to photosensitization of Gram-positive pathogens.
50                                              Photosensitization of molecular catalysts to reduce CO2
51 n report the first instance of aqueous-phase photosensitization of semiconductor photocatalysts (WO(3
52 n explored as agents for optical imaging and photosensitization of tumors in pre-clinical studies.
53 s a result of advanced glycation end product photosensitization of ultraviolet A and solar-simulated
54                                              Photosensitization of viral membranes is a common mechan
55 dy establishes a novel concept for plasmonic photosensitization of wide band gap semiconductors, lead
56      In this study, we have investigated the photosensitization, optical, and surface properties of p
57              Singlet oxygen was generated by photosensitization or by thermal decomposition of naphth
58 could open new avenues for the assessment of photosensitization pathways.
59 ectively review current concepts relating to photosensitization, photoactivation, time of PDT applica
60 ication, historically relevant to biological photosensitization processes and some forms of photochem
61  thiothymine series account for their potent photosensitization properties.
62 diated by neutrophil infiltration induced by photosensitization (PS) because the systemic depletion o
63  that direct priming of a tumor tissue using photosensitization rapidly activates neutrophil infiltra
64                                          The photosensitization reactions are reflective of physiolog
65 findings support the notion that UVA-induced photosensitization reactions are responsible for oxidati
66 is information shows that the outcome of the photosensitization reactions is critically dependent on
67  Ras dimer formation on membranes by Type II photosensitization reactions, in which molecular oxygen
68  of this wavelength to trigger intracellular photosensitization reactions, thereby giving rise to pro
69 aps as a protectant from ultraviolet-induced photosensitization reactions.
70                           Organelle-targeted photosensitization represents a promising approach in ph
71                             However, retinal photosensitization requires a high dose of DENAQ and dis
72                                              Photosensitization, subsequent to photon absorption by c
73  photoluminescence spectroscopy, and triplet photosensitization to demonstrate intramolecular singlet
74  in vitro cytotoxic effect in tumor cells by photosensitization under two-photon irradiation.
75 iled mechanistic studies confirm the role of photosensitization via energy transfer.
76                      HSP-70 expression after photosensitization was associated with the concomitant i
77                                              Photosensitization was not observed using bovine serum a
78 singlet oxygen as the primary oxidant during photosensitization, were used in experiments under isoef
79                                              Photosensitization with Ru(bpy)(3)(2+) showed distinct F

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