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1 te by Ca(2+) critical for the suppression of photoinactivation.
2 asma membrane, cannot be re-formed after Clc photoinactivation.
3 esicle re-formation does not occur after Clc photoinactivation.
4 nt membrane internalization occurs after Clc photoinactivation.
5 y and/or protection against oxygen-dependent photoinactivation.
6 reased (approximately 2-fold) sensitivity to photoinactivation.
7 ly, 2.7- and 4-fold increased sensitivity to photoinactivation.
8 or in combination with Mg2+, protect against photoinactivation.
9 esence of 12 microM dequalinium led to rapid photoinactivation.
10  exhibiting a 3-fold increase in the rate of photoinactivation.
11  which was directly correlated to luciferase photoinactivation.
12 indicated that the mutant was susceptible to photoinactivation.
13 lumination with 405 and 488-nm light blocked photoinactivation.
14  indirect mechanism to the overall bacterial photoinactivation.
15 hing with Gly(1)-SIFamide application and LP photoinactivation.
16 ndle poles move away from regions of pai-EB1 photoinactivation.
17 d because DOM acted as an antioxidant toward photoinactivation, a phenomenon recently established for
18 erial cells, as shown by the higher bacteria photoinactivation activity retained after washing the ba
19                                We used acute photoinactivation and found that loss of Dynamin functio
20                               The results of photoinactivation and kinetic and bioluminescence studie
21 tween light-activated steps, and is prone to photoinactivation and misassembly.
22 e-C) yet all experienced similar patterns of photoinactivation and symbiont loss when heated.
23 unteract a lower intrinsic susceptibility to photoinactivation, and C. radiatus thus did not need to
24               The mutants had a high rate of photoinactivation, and many mutants showed an up to 1000
25 e retrieval has also been seen upon Clathrin photoinactivation, and superresolution imaging indicated
26 tion of these compounds and the mechanism of photoinactivation are described.
27 nthesis, nonphotochemical quenching and PSII photoinactivation arises from changes in the abundances
28 e mutant proved to be extremely sensitive to photoinactivation at high light intensities, exhibiting
29 nd these PSII centers were very sensitive to photoinactivation at high light intensities.
30         Aggregation lowers the efficiency of photoinactivation because of self-quenching of the dye.
31 olution imaging indicated that acute Dynamin photoinactivation blocked Clathrin and alpha-adaptin rel
32 enesis produced a variant, V203Y, that lacks photoinactivation but largely preserves the desirable pr
33                 Effective protection against photoinactivation by 150 microM GS-Succ-BP is provided b
34                We first demonstrate that Clc photoinactivation does not impair synaptic-vesicle fusio
35  However, in contrast to interphase, pai-EB1 photoinactivation does not inhibit microtubule growth in
36                                     Pathogen photoinactivation efficacy depends critically on UV-C do
37 e exogenous indirect mechanism by conducting photoinactivation experiments with eight health-relevant
38  indirect mechanisms contribute to bacterial photoinactivation in natural surface waters.
39  absorbance and depth, suggesting endogenous photoinactivation is a major pathway for bacterial decay
40 s of tryptophan-like fluorescence paralleled photoinactivation kinetics and because DOM acted as an a
41 cous drag impeding traveling waves; targeted photoinactivation locally interrupts this compensation.
42 gesting that although the exogenous indirect photoinactivation mechanism may be active against Ent. f
43                             A time-dependent photoinactivation occurs upon irradiation at long wavele
44 loride-limiting conditions, with a t(1/2) of photoinactivation of 2.6 min under chloride-limiting con
45 olved organic matter in marsh water enhanced photoinactivation of a laboratory strain of Enterococcus
46 ed; this learned response is reversed by the photoinactivation of a single PlB.
47 he POm influences goal-directed behavior, as photoinactivation of archaerhodopsin-expressing neurons
48 ation allowed selective and potent UV-driven photoinactivation of both homomeric (GluA2) and heterome
49                                    Moreover, photoinactivation of Dynamin in shi(ts1) animals convert
50 ynthetic photosensitizers generally enhanced photoinactivation of Gram-positive facultative anaerobes
51                                      We used photoinactivation of identified neurons and pharmacologi
52                                              Photoinactivation of MS2 was significantly lower in both
53 ng a versatile approach to characterize UV-C photoinactivation of pathogens contaminating complex sub
54  structure are significantly involved in the photoinactivation of phosphatase because a loss of trypt
55                                        Thus, photoinactivation of phosphatase can be significantly sl
56 tes but can also significantly quench direct photoinactivation of phosphatase.
57 adiance-sensitive phenotype with significant photoinactivation of photosystem II (PSII), indicated by
58 o HL benefited cells by reducing the rate of photoinactivation of PSII under high light.
59  the triple mutant revealed that the rate of photoinactivation of PSII was the same in wild-type and
60 rain of Enterococcus faecalis, but depressed photoinactivation of sewage-sourced enterococci and E. c
61                         In biological media, photoinactivation of Staphylococcus aureus was evaluated
62 e live imaging of the synapto-pHluorins with photoinactivation of Syt I, through fluorescein-assisted
63 otor and motor cortices, but was impaired by photoinactivation of the lateral superior colliculus (la
64 ease in neurotransmitter release after acute photoinactivation of the V0 a1-I subunit in neuronal pai
65     Touch-guided re-aiming was unaffected by photoinactivation of tongue sensory, premotor and motor
66 for application in cancer therapy and in the photoinactivation of viruses.
67 smaller T. pseudonana, photosystem II (PSII) photoinactivation outran the clearance of PSII protein s
68                                        Their photoinactivation performance was tested against Escheri
69 ditional investigations on the nature of the photoinactivation process strongly suggested that BPTC c
70              (1) FlAsH-FALI-mediated protein photoinactivation rapidly and specifically disrupts Clc
71 sensitizers either reduced or did not affect photoinactivation rate constants.
72  faecalis was roughly correlated with higher photoinactivation rates.
73 , a firefly luciferin analogue, was a potent photoinactivation reagent for luciferase.
74 echanism: Q69M/C70V greatly increased (~90%) photoinactivation, reminiscent of fluorescent protein fl
75 he bc(1) complex by hematoporphyrin-promoted photoinactivation resulted in the complex becoming proto
76 in live cells.(7) We find that acute pai-EB1 photoinactivation results in rapid and reversible metaph
77                                              Photoinactivation spontaneously recovered over 5 min in
78      Substrate studies, inhibition kinetics, photoinactivation studies, and photolabeling experiments
79                            3) After complete photoinactivation, the level of incorporation of radioac
80        We employ FlAsH-FALI-mediated protein photoinactivation to rapidly (3 min) and specifically di
81  mutant exhibited an enhanced sensitivity to photoinactivation under chloride-limiting conditions, wi
82  inactivation, suggesting key differences in photoinactivation under different spectral conditions.
83 ruginosa, and Escherichia coli A significant photoinactivation (up to 95%) against Gram-negative and
84 onstrate a noninvasive technique for protein photoinactivation using a transgenically encoded tag.
85 and the photoaffinity label was specific: 1) photoinactivation was inhibited in the presence of a non
86 n subjected to high light, its recovery from photoinactivation was not affected.
87                                       Direct photoinactivation was slowed by more than 50% in the pre
88 ter VL irradiation, Sigma-TiO2 showed higher photoinactivation, whereas S-TiO2 and P-25 showed modera