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1 quinone reduction) and charge recombination (photoprotection).
2 gest that this is the principal mechanism of photoprotection.
3 may relate to processes of photosynthesis or photoprotection.
4 d are independent of tocopherol functions in photoprotection.
5 s between the two photosystems as well as in photoprotection.
6  is closely related to skin pigmentation and photoprotection.
7  PP appears to serve the function of retinal photoprotection.
8  excitation energy dissipation as a means of photoprotection.
9 a tan may not be the major factor in natural photoprotection.
10 essential role in rapid light adaptation and photoprotection.
11 og (All1123) does not seem to be involved in photoprotection.
12  Protein (OCP) is involved in cyanobacterial photoprotection.
13 etween efficient solar energy conversion and photoprotection.
14 ctivation of the OCP, that are essential for photoprotection.
15 ion with the light-harvesting antenna during photoprotection.
16 ction of singlet oxygen, indicating upgraded photoprotection.
17  an effector and regulator of cyanobacterial photoprotection.
18 f the patterns and mechanisms driving foliar photoprotection.
19 ticipate in light absorption and chloroplast photoprotection.
20 HC) is involved in both light harvesting and photoprotection.
21 he excess energy at saturating intensity for photoprotection.
22 he COCP carotenoid carrier in cyanobacterial photoprotection.
23 ence quenching (qE) has an important role in photoprotection.
24 different components of zeaxanthin-dependent photoprotection.
25  quenching (NPQ), plays an important role in photoprotection.
26 oteins, and have a major role in chloroplast photoprotection.
27  serve essential roles in photosynthesis and photoprotection.
28 noid, zeaxanthin, that was shown to increase photoprotection.
29 otoactive protein involved in cyanobacterial photoprotection.
30 ositive charge of Arg155 plays a key role in photoprotection.
31 lasia, consistent with MC1R having a role in photoprotection.
32 unscreens," MAAs are usually employed for UV photoprotection [7, 8], but mantis shrimp uniquely incor
33 stigate the respective roles of qE and qT in photoprotection, a mutant (npq4 stt7-9) was generated in
34 4 (lacking LhcSR3) backgrounds, but no clear photoprotection activity was observed.
35 vely prove that blue-blocking lenses provide photoprotection against age-related macular degeneration
36 tions is a useful early biologic endpoint of photoprotection against an important initiating event in
37 r has therefore promising potential for skin photoprotection against the deleterious effects of the U
38 riments and help elucidate melanin's role in photoprotection against ultraviolet radiation.
39 erlying maintenance of skin pigmentation and photoprotection against UV damage.
40  Sunscreens continue to be a major method of photoprotection among the public, offering numerous bene
41 e conclude that both proteins are needed for photoprotection and for survival under low oxygen, under
42 aises important clinical questions regarding photoprotection and IRR-based dermatotherapy.
43 ude that xanthophylls, besides their role in photoprotection and LHC assembly, are also needed for ph
44 eratinocytes, an event critical to epidermal photoprotection and maintenance of normal skin color.
45 cid (Asc) is a major antioxidant involved in photoprotection and photosynthetic function in plants.
46  We speculate that different efficiencies of photoprotection and repair mechanisms of algal food sour
47 vidence for a mechanistic link between plant photoprotection and the synthesis of oxylipin hormones a
48 oids play essential roles in photosynthesis, photoprotection, and as precursors to apocarotenoids.
49  such as photosynthesis, photomorphogenesis, photoprotection, and development.
50 nvolved in light harvesting, photosynthesis, photoprotection, and the heat shock response.
51 sible roles of carotenoid cation radicals in photoprotection are discussed.
52 igh excitation intensities in the absence of photoprotection as well as in the presence of an enzymat
53 arvesting is not the main cause of increased photoprotection, because in the absence of zeaxanthin, a
54  these shade leaves initiates a continuum of photoprotection, beyond full engagement of the Lx and V
55 utes to differences in skin pigmentation and photoprotection, but the control of these innate distrib
56  the ubiquitous biological pigment, provides photoprotection by efficient filtration of light and als
57    Further, we demonstrate the importance of photoprotection by examining the effect of photodamage o
58 fic proteins plays a major role in enhancing photoprotection by modulating the yield of potentially d
59 sted that carotenoids in chlorosomes provide photoprotection by rapidly quenching triplet excited sta
60  provide important clues to the processes of photoprotection, cancer predisposition and even human ev
61                         To account for Sepia photoprotection, continuous-wave EPR and time-resolved E
62 mical functions, including display, evasion, photoprotection, detoxification, and metal scavenging.
63  function of carotenes in photosynthesis and photoprotection, distinct from that of xanthophylls, by
64  are unclear, but hypotheses include reduced photoprotection due to less eumelanin, pheomelanin-induc
65 he appropriate induction of NPQ and level of photoprotection during exposure to high light.
66 under hazardous light conditions, sufficient photoprotection for both the reaction centre and the lig
67                            In cyanobacteria, photoprotection from overexcitation of photochemical cen
68  the importance of CEF in photosynthesis and photoprotection has been clearly established, little is
69 der fluctuating light conditions, while PSII photoprotection-impaired mutants did not.
70                       The latter operates in photoprotection in a complementary way with the orange c
71 lly important aspects of energy transfer and photoprotection in antenna complexes.
72 der to determine the role of PsbS in NPQ and photoprotection in Chlamydomonas, we generated transplas
73 rkness, setting the stage for bioengineering photoprotection in cyanobacteria as well as for developi
74 an effector of phycobilisome (PB)-associated photoprotection in cyanobacteria.
75 nergy for photochemical light conversion and photoprotection in natural environments, potentially ove
76 ay the dual function of light harvesting and photoprotection in photosynthetic organisms.
77 ral and essential role in photosynthesis and photoprotection in plants and algae.
78  switch rapidly between light harvesting and photoprotection in response to environmental fluctuation
79 than xanthophyll composition is critical for photoprotection in short-term high light, in contrast to
80 s-singlet signal was tightly correlated with photoprotection in the chloroplasts, suggesting the sign
81 verse cutaneous sequelae can be minimized by photoprotection in the form of sun avoidance, regular co
82 roviding evidence of unexpected diversity in photoprotection in the green lineage.
83  The orange carotenoid protein (OCP) governs photoprotection in the majority of cyanobacteria.
84  melanin aggregation provides an increase in photoprotection in the RPE cells that are relatively les
85 terations in the skin witnessed by increased photoprotection in the visible spectral range and reduce
86 results also show that the required level of photoprotection in vivo can be achieved by a very subtle
87 proteins that function in photosynthesis and photoprotection, including an expanded family of high-li
88  unsaturated carotenoids of higher plants in photoprotection is becoming increasingly well understood
89 liana The possible role of zeaxanthin in PSI photoprotection is discussed.
90                 The possible role of PsbS in photoprotection is discussed.
91                                              Photoprotection is essential for photosynthesis to proce
92                    We first showed that this photoprotection is related to a decrease of singlet oxyg
93 vance to skin cancer and melanoma, eumelanin photoprotection is still an enigma: What makes this pigm
94 ting environments with different demands for photoprotection is summarized.
95 s, the determining step for the induction of photoprotection is the binding of the OCP to PBs.
96 iated protein that appears to play a role in photoprotection; its transcript rapidly accumulates in r
97 roteins assigned to light-harvesting (Lhcf), photoprotection (LI818-like), and the photosystem II (PS
98                                     Vigilant photoprotection may be of lesser importance in the preve
99 of high light intensity and triggers a major photoprotection mechanism known as energy dependent nonp
100 any beta-cyanobacteria with a so far unknown photoprotection mechanism that evolved in parallel with
101  of ChlZ in intact systems may function as a photoprotection mechanism under high-light conditions an
102 tons in chlorosomes serves as an alternative photoprotection mechanism.
103 on donors that are believed to function in a photoprotection mechanism.
104 high zeaxanthin content, appears to underlie photoprotection mechanisms that are efficiently employed
105  required concomitant evolution of efficient photoprotection mechanisms to safeguard the photosynthet
106 tene depletion in the core complexes impairs photoprotection of both PS under high light at chilling
107 ss light-harvesting PORB::PORA complexes and photoprotection of etiolated seedlings.
108 nthophyll cycle, that play a key role in the photoprotection of photosynthesis under environmental st
109  with an operon that plays a crucial role in photoprotection of photosystem II under low carbon condi
110  known to have crucial and specific roles in photoprotection of photosystems I and II in cyanobacteri
111 native melanin can supplement native melanin photoprotection of RPE cells.
112 arotenoid protein (OCP), responsible for the photoprotection of the cyanobacterial photosynthetic app
113                                              Photoprotection of the skin is provided by melanocytes,
114 " cofactor important for photoactivation and photoprotection of the WOC-PSII complex.
115 h observations suggest irradiance-dependent 'photoprotection' of nuclear phyA in R, providing a possi
116 r diffusion-dependent electron transport and photoprotection or protein repair processes, thus fine-t
117 t because of its unique light absorption and photoprotection properties.
118 logical role for B-side electron transfer is photoprotection, rapidly quenching higher excited states
119 l proteins in E. oleoabundans, including two photoprotection-related proteins, Photosystem II Subunit
120 sm of the OCP photoconversion and associated photoprotection remains elusive.
121 red carotenoids may have both structural and photoprotection roles in green sulfur bacteria.
122                       Recent improvements in photoprotection solutions allowed us to monitor transiti
123 gronomic importance, such as photosynthesis, photoprotection, stomatal opening, and photoperiodic dev
124 ess, on the contrary, are mutually exclusive photoprotection strategies among cyanobacteria.
125 all, these results demonstrate that improved photoprotection strategies may have a profound impact on
126 iven by kinesin motor proteins using various photoprotection strategies, including a microfluidic deo
127 king of fluorescent dyes has led to improved photoprotection strategies, such as reducing and oxidizi
128 in various key components of the chloroplast photoprotection system, consistently produced greater co
129 that tocopherols have a more limited role in photoprotection than previously assumed but play crucial
130 lexes, functional antenna size, capacity for photoprotection, thermal energy dissipation and state tr
131 tenoids are essential for photosynthesis and photoprotection; they also serve as precursors to signal
132                                              Photoprotection through individual dietary components su
133 spiratory recycling of CO(2) provided little photoprotection to avocado shade leaves.
134 employs diverse strategies of regulation and photoprotection to avoid, minimize, and repair photo-oxi
135  stability of the vitamins (C+E) and doubled photoprotection to solar-simulated irradiation of skin f
136  acclimation to UV-B markedly contributes to photoprotection upon subsequent exposure to high light.
137 periments with 50-mus resolution and maximal photoprotection using a recently developed Trolox-cystea
138                                   No similar photoprotection was afforded by the addition of a high-m
139  at low concentrations of the photoprobe and photoprotection was observed in the presence of low conc
140 he more demanding effect of high altitude on photoprotection was, however, partly abolished at very h
141  To investigate the roles of xanthophylls in photoprotection, we isolated and characterized extrageni
142 ortance of melanocyte dendrites in cutaneous photoprotection, we performed functional studies examini
143                All formulations provided ANE photoprotection, were physically stable after 15months o
144  the characteristics of light absorption and photoprotection, which could be attributed to changes in
145  of light harvesting, energy channeling, and photoprotection within photosystem II.
146 ntribution of the minor antenna complexes to photoprotection would probably involve a distinct mechan

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