ライフサイエンスコーパス: photosensitized

1 The method is based on photosensitized activation by the fluorescent lipid anal

2 g fluorophore, whereas the second depends on photosensitized activation of a hydrophobic probe by a f

3 Photosensitized activation of VSV prebound to labeled gh

4 light exposure (633nm; 118J/cm(2)), PPIX got photosensitized, and due to higher initial amount of PPI

5 d (1)O(2) generation rates by four different photosensitized aqueous fullerene suspensions were in th

6 ud events with chamber lights on, suggesting photosensitized brown carbon formation.

7 , X = OCH3; 2, X = CH3; 3, X = H; 4, X = Br) photosensitized by 3-cyano-N-methylquinolinium perchlora

8 xidative cleavage of 1,1-dithiooxalate (DTO) photosensitized by CdSe quantum dots (QDs).

9 In this study, we evaluated photosensitized chemistry at the air-sea interface as a

10 In this paper, we show that inexpensive photosensitized copper clad circuit board substrates can

11 Photosensitized electron transfer from a variety of sing

12 Photosensitized electron-transfer processes of nanocarbo

13 ation is sufficiently robust to kill S(4)TdR-photosensitized epidermal cells.

14 (1)O(2) is most often generated through photosensitized excitation of ground-state oxygen.

15 d process is the first essential step in the photosensitized generation of H(2) from a molecular cata

16 ected against advanced glycation end product-photosensitized growth inhibition even when added follow

17 Photosensitized growth inhibition increased with the deg

18 Given the potential importance of this new photosensitized growth pathway for ambient OA, the relat

19 singlet oxygen may play a major role in the photosensitized inhibition of mitochondrial cytochrome c

20 nal concentration of 30 U, did not alter the photosensitized inhibition of mitochondrial cytochrome c

21 nal concentration of 30 U, did not alter the photosensitized inhibition of mitochondrial cytochrome c

22 singlet oxygen may play a major role in the photosensitized inhibition of mitochondrial cytochrome c

23 We report on single-molecule studies of photosensitized interfacial electron transfer (ET) proce

24 Photosensitized labeling of VSV G by DiO-125INA-ghosts w

25 Our photosensitized labeling results establish biochemical c

26 G) with biological membranes was studied by photosensitized labeling.

27 d to the site of chromophore localization by photosensitized labeling.

28 l (0.45 mol %) was ineffective in inhibiting photosensitized lipid peroxidation, whereas 4.5 mol % al

29 To probe the mechanism of the photosensitized loss of phenols by humic substances (HS)

30 However, as was previously noted for the photosensitized loss of TMP, the incomplete inhibition o

31 A Type-II (singlet oxygen) photosensitized mechanism is suggested for the di- and t

32 able isotope analysis (CSIA) to characterize photosensitized mechanisms employing fuel oxygenates, su

33 nd apoptotic cell death after irradiation of photosensitized murine leukemia L1210 or hepatoma 1c1c7

34 otochemical NO precursor, was accompanied by photosensitized NO release.

35 oduction of atmospheric organic aerosol from photosensitized origins.

36 and derived the action spectrum for melanin-photosensitized oxidant production (Phi(ox)).

37 than UVB that are thought to be mediated by photosensitized oxidant production.

38 The photosensitized oxidation of 2',3',5'-tris-(O-tert-butyl

39 The photosensitized oxidation of indole acetic acid forms a

40 ried out a detailed mechanistic study of the photosensitized oxidation of isotope-labeled imidazole d

41 were detected by low-temperature NMR in the photosensitized oxidation of the isotope-labeled imidazo

42 Photosensitized oxidation of trimethyl[2.2.1]bicyclohept

43 Photosensitized oxidation reactions damage tissue by cat

44 hylsilyl)guanosine (1), was prepared and its photosensitized oxidation was carried out in several sol

45 etramethylethylene, and sodium azide) on the photosensitized oxidation was investigated in order to f

46 -8-(13)C-guano sine, was synthesized and its photosensitized oxidation with singlet oxygen carried ou

47 d product distributions resulting from these photosensitized oxidations demonstrates that, while the

48 intracellular singlet oxygen, produced in a photosensitized process, is in fact not efficiently deac

49 droplet in a spatially localized two-photon photosensitized process.

50 Most importantly, the results indicate that photosensitized processes during high dose wastewater di

51 Photosensitized production of marine secondary organic a

52 lts of Aregahegn et al. (2013) suggests that photosensitized production of SOA from limonene, isopren

53 results confirm the hypothesis that melanin-photosensitized radical production is the major causativ

54 ly local because slowing can be induced by a photosensitized reaction in the subdomain of the organel

55 +) by EDTA is energetically unfavorable; the photosensitized reaction therefore occurs with partial c

56 were generated near the organelles through a photosensitized reaction.

57 ormation of reactive oxygen species during a photosensitized reaction.

58 However, the extent of photosensitized reactions in ambient aerosols remains po

59 Our study indicates that photosensitized reactions involving (*)OH may be a trans

60 Photosensitized reactions involving imidazole-2-carboxal

61 Here, we show that photosensitized reactions involving the sea-surface micr

62 The mechanistic aspects of the photosensitized reactions of a series of benzaldehyde ox

63 The mechanistic aspects of the photosensitized reactions of a series of oxime ethers we

64 ates of the NOM are key intermediates in the photosensitized reactions.

65 characteristics of such QDs as antennae for photosensitized release of bioactive agents (in the pres

66 kinetics of IC photochemistry, to analyze IC-photosensitized SOA formation in laboratory and ambient

67 Photosensitized transformation induced by excited triple

68 The photosensitized transformation of DMABN mainly proceeded

69 The photosensitized transformation of DMABN, the selected pr

70 The DOM photosensitized transformation rate constants of TMP dec

71 sed by determining the 4-carboxybenzophenone photosensitized transformation rate constants of two sul

72 a sulfonamide antibiotic) exhibited a marked photosensitized transformation that could be substantial

73 e a useful inhibitor even in the case of DOM-photosensitized transformations.

74 conjugates were shown to mediate ZnTPPS(4-)-photosensitized transmembrane reduction of occluded Co(b

75 omposite based on molecular triphenyldiamine photosensitized with C60.

76 tudy of photorefractive polymeric composites photosensitized with semiconductor nanocrystals has yiel

77 produced which, in turn, is reflected in the photosensitized yield of singlet oxygen.