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1 e degree of antimicrobial resistance through photooxidative action combats antibiotic failures.
2 uorescence bleaching of bisretinoid involves photooxidative and photodegradative processes.
3 anthin and lutein and undergoes irreversible photooxidative bleaching and cell death at moderate to h
4  damage to intracellular membranes caused by photooxidative chemistries or by phagocytosis of ground
5  but are not the longest lived species under photooxidative conditions, contrary to popular perceptio
6 tic study of each derivative under identical photooxidative conditions.
7 ogenic peptide sequences and exposed them to photooxidative conditions.
8                              On the basis of photooxidative cross-linking of the wild type but not K1
9 esence of all-trans-retinaldehyde results in photooxidative cytotoxicity.
10 nstration of protection of RPE cells against photooxidative damage by induction of phase 2 proteins m
11                                 Targeting of photooxidative damage by triplex formation extends our p
12 otection of PSII intermediate complexes from photooxidative damage during de novo assembly and repair
13 ating a role for FeSOD in protection against photooxidative damage during moderate chilling in light.
14                                   Blue-light photooxidative damage has been implicated in the etiolog
15 pective, we probe this issue by referring to photooxidative damage in one direction as the light-dark
16 n in these strains was sufficient to prevent photooxidative damage in the npq1 lor1 background.
17         A frequently occurring, irreversible photooxidative damage inhibits the PSII charge separatio
18                                              Photooxidative damage is heavily influenced by the prese
19 ere photosynthetic function is optimized and photooxidative damage is minimized in graduated response
20 e observed decreased photosynthesis and that photooxidative damage might be involved in the establish
21  was confirmed by the decreased tolerance to photooxidative damage of jasmonate-treated ch1 plants an
22 ts and may play a role in protecting against photooxidative damage of the photosynthetic apparatus du
23                         There is evidence of photooxidative damage of the photosynthetic apparatus in
24 inhibition of photosystem II without causing photooxidative damage of the plant.
25 re disrupted, the magnitude of resistance to photooxidative damage paralleled the basal levels of glu
26     Photosystem II (PSII) undergoes frequent photooxidative damage that, if not repaired, impairs pho
27  processing to the chloroplast, resulting in photooxidative damage through H(2)O(2) production.
28  various stimuli such as lipofuscin-mediated photooxidative damage to lysosomal membranes.
29 rately elevated light intensities eliminated photooxidative damage without suppressing (1)O(2) format
30 hogenesis including lipofuscin accumulation, photooxidative damage, complement activation, and RPE de
31 sponse to the high vulnerability of PS II to photooxidative damage, exacerbated by high-light (HL) st
32                                              Photooxidative damage, which occurs during anticancer ph
33 ency, higher relative water content and less photooxidative damage.
34 ation by stimuli such as lipofuscin-mediated photooxidative damage.
35 es in some process relevant to the repair of photooxidative damage.
36 ass of UVA photosensitizers, capable of skin photooxidative damage.
37 absorbed energy in the cell can cause lethal photooxidative damage.
38 ll green and displayed signs of irreversible photooxidative damage.
39 essential in protecting the chloroplast from photooxidative damage.
40 hotosynthesis and protects the plant against photooxidative damage.
41 l environment, which in turn is perturbed by photooxidative damage.
42 ane and subsequently repaired in response to photooxidative damage.
43  L-D/D-L pathways, for improved control over photooxidative damage.
44  as well as protection against pathogens and photooxidative damage.
45 e D1 subunit of photosystem II is subject to photooxidative damage.
46 a fungoid chitosan (CsG) may protect against photooxidative decay of model solutions and a sulphite-f
47 nd initiate the more rapid water-accelerated photooxidative decomposition.
48 ly benzoic acid, using a catalyst-controlled photooxidative degradation method.
49 serving 72% of a vitamin B(2) stored under a photooxidative environment.
50 ]) confer cytoprotection from oxidative- and photooxidative-induced cellular damage and to explore th
51 rging by making tumor cells more tolerant to photooxidative insult.
52 hanced plant survival and reproduction under photooxidative light conditions, evidence that the plast
53  kinase-dependent stress signaling suggest a photooxidative mechanism of skin cell photosensitization
54 photoreductive Fe-N bond breakage as well as photooxidative N-N bond breakage occur on a time scale w
55 fluorescence; this effect is consistent with photooxidative processes known to precede bisretinoid de
56 tissues, light induces primary and secondary photooxidative processes.
57 died, yellow LED lighting produced the least photooxidative production of glyoxylic acid in white win
58  in emission wavelengths but also suppresses photooxidative reactions and prevents the formation of t
59 at room temperature is achieved by using the photooxidative redox capacity of the valence band of ana
60 heptacene derivatives with varying levels of photooxidative resistance (1 < 2 < 3 < 4) have been synt
61 uantitative assessment of HOMO-LUMO gaps and photooxidative resistances for a large series of pentace
62 x1 in retinal tissue and was protective from photooxidative retinal damage.
63 r understanding of the overall scope of this photooxidative route toward substituted phenanthridines
64                                          The photooxidative self-assembly of the Mn(4)CaO(5) cluster,
65 ng absorption wavelength, lipophilicity, and photooxidative stability.
66                                        Under photooxidative stress conditions, the gene expression pr
67  from the Q(B) site in photosystem II, under photooxidative stress conditions.
68 photosynthetic organisms, protection against photooxidative stress due to singlet oxygen is provided
69    To examine the long-term effects of acute photooxidative stress in the retina, retinal pigment epi
70 senting a molecular mechanism of UVA-induced photooxidative stress potentially operative in human ski
71                           We also found that photooxidative stress signaling pathway is constitutivel
72 hat HL-induced plastid to nucleus retrograde photooxidative stress signaling takes place after loss o
73 hich limits photophosphorylation, leading to photooxidative stress, causing the chlorotic and stunted
74 re resistant to cell damage induced by acute photooxidative stress, progressive loss of cone cells co
75 esults in mutants that are hypersensitive to photooxidative stress, whereas overexpression produces p
76  known for their roles in protecting against photooxidative stress, whereas the photoprotective funct
77       Chloroplast DNA (cpDNA) is under great photooxidative stress, yet its evolution is very conserv
78                             The concept of a photooxidative stress-induced vicious cycle of increased
79                 In response to HL, H2O2- and photooxidative stress-responsive marker genes were found
80 y discussed contribution to the avoidance of photooxidative stress.
81 , an overreduced cellular state, and limited photooxidative stress.
82 t, fix CO2 , perform biosynthesis and resist photooxidative stress.
83 lorophyll precursors, which can cause deadly photooxidative stress.
84 he seedlings and adult plants susceptible to photooxidative stress.
85 herols and carotenoids in protection against photooxidative stress.
86 as associated with an increased tolerance to photooxidative stress.
87 nce and that ClpC2 might act by accelerating photooxidative stress.
88 type, implying that they experienced chronic photooxidative stress.
89 c free radicals as key mediators of cellular photooxidative stress.
90 g conferred an advantage to cells undergoing photooxidative stress.
91 melanin protects ocular retinoid stores from photooxidative stress.
92 ession, jasmonate levels, and sensitivity to photooxidative stress.
93                                In a relevant photooxidative system acetaldehyde formation was signifi
94 ronment, which are jointly necessary for the photooxidative trapping of the first stable assembly int