戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 n the efficiency and rate of photosynthesis (photoinhibition).
2 branes, the rate of D1 protein synthesis, or photoinhibition.
3 lar body, and the repair process of D1 after photoinhibition.
4 volution, and protects photosytem II against photoinhibition.
5 was associated with increased sensitivity to photoinhibition.
6 tem II function and increases sensitivity to photoinhibition.
7 r further oxidation of ChlZ and irreversible photoinhibition.
8  when dark-grown, the effect is unrelated to photoinhibition.
9 h air, although they have less resistance to photoinhibition.
10 ge the photosynthetic apparatus and leads to photoinhibition.
11 hesis, likely driven by oxidative stress and photoinhibition.
12 ree days later (recall test), relative to no photoinhibition.
13 ical quenching, and there was no significant photoinhibition.
14 ves are exposed to excess sunlight, inducing photoinhibition.
15 reased by 109%, likely due to a release from photoinhibition.
16 tosystem II reaction center is vulnerable to photoinhibition.
17 ent formation of reactive excited states and photoinhibition.
18 Q) and its role in protecting plants against photoinhibition.
19 er UV-B stress, which mitigated UV-B-induced photoinhibition.
20 tive stress during a process that can induce photoinhibition.
21 opy architecture and the diurnal dynamics of photoinhibition.
22 onged high-light exposure caused accelerated photoinhibition.
23 y light sensitive and failed to recover from photoinhibition.
24 verreduced and photosystem I is subjected to photoinhibition.
25 nally conclude that mat decline is linked to photoinhibition.
26 volution rate and greater protection against photoinhibition.
27  and the diatom cells suffered from stronger photoinhibition.
28 es or preventing their accumulation to avoid photoinhibition.
29 n shown directly in plants in the absence of photoinhibition.
30 and to stabilize the Mn(4)Ca cluster against photoinhibition.
31 with a role for the CP43 NFK modification in photoinhibition.
32 ency within the phycobilisome and to prevent photoinhibition.
33  The mutant cells were highly susceptible to photoinhibition.
34 ll content and a reduced recovery rate after photoinhibition.
35 n increased degree of lipid peroxidation and photoinhibition.
36 thylakoid membranes, was most susceptible to photoinhibition.
37                             To avoid chronic photoinhibition, a PSII repair cycle operates to replace
38             This was reflected by a stronger photoinhibition after 24 h of high light (approximately
39                                 Moreover, S1 photoinhibition after partial adaptation blocked further
40                  Model simulations show that photoinhibition alone can result in substantial reductio
41 nthesis, biomass and yield via prevention of photoinhibition and a momentary downregulation of photos
42 on; however, increased light can also induce photoinhibition and cause physiological stress in algae
43                                              Photoinhibition and chlorophyll levels decreased upon ph
44 , meaning that any damage leads to prolonged photoinhibition and decreased growth.
45 unit of PSII but is required for repair from photoinhibition and efficient assembly of the PSII RC.
46 isms may increase biomass yields by limiting photoinhibition and increasing light penetration in dens
47 ditions, but exhibits greater sensitivity to photoinhibition and long-term mild heat stress than wild
48 ts following light stresses, linking daytime photoinhibition and nighttime GSH metabolism.
49 ic acid P in three populations, declined and photoinhibition and nighttime respiration increased in a
50 ty of cells to both high temperature-induced photoinhibition and photobleaching was ameliorated by in
51 extremely light-sensitive and susceptible to photoinhibition and photobleaching.
52  under anesthesia and in quiet waking, using photoinhibition and photoexcitation with different light
53 igh light conditions resulted in strong PSII photoinhibition and revealed the distinct light-induced
54 lated with the extent of photosystem (PS) II photoinhibition and the expression of various (1)O(2) ma
55 ast movements both during the early onset of photoinhibition and under sustained excess light.
56 naerobiosis preserves PSII from irreversible photoinhibition, and (iii) mutants with enhanced respira
57 quantum yield of photosystem II indicated no photoinhibition, and adaptations in the photosynthetic a
58  temperature on cell growth, photosynthesis, photoinhibition, and nitrate assimilation was examined i
59 of Scenedesmus obliquusbased on temperature, photoinhibition, and respiration effects at 6685 global
60         var2 mutants are hypersusceptible to photoinhibition, and VAR2 degrades unassembled polypepti
61 underlying molecular mechanisms that lead to photoinhibition are poorly understood.
62         All three isolates showed only minor photoinhibition at 15 microE m(-2) s(-1) and rapid recov
63 bation of PSII protein turnover rates during photoinhibition at elevated temperatures underlies the p
64  plastoquinone-9, resulting in near complete photoinhibition at high light intensity.
65 rvals, features critical for minimization of photoinhibition; (b) a microvolume (5 microL) O2 polarog
66 otodamage to the cofactor-free apo-WOC-PSII (photoinhibition).Bicarbonate does not affect the second
67 e of photosynthetic electron transport or by photoinhibition, but that inactivation of the nitrate/ni
68 me centers, suggesting that qE protects from photoinhibition by preventing overreduction of photosyst
69 ld also have provided effective reduction of photoinhibition by UV radiation.
70 d during immunization and is a suppressor of photoinhibition, cell death, and chloroplast immunity.
71 d mutant cells were similar under high-light photoinhibition conditions, as well as in media without
72 ile population increases significantly after photoinhibition, consistent with a role for protein diff
73                       Optrode recordings and photoinhibition demonstrate that LPAG(Vgat) neurons are
74 S) combination is PSII because its degree of photoinhibition depends on the balance between the rate
75 on; however, cells do not suffer substantial photoinhibition despite its near absence.
76                                      This S1 photoinhibition did not impair basic motor patterns, pos
77 n-stabilized model, we performed large-scale photoinhibition directed at (GAD-Cre) inhibitory cells a
78                                 In addition, photoinhibition-enabled lithographic patterning of front
79 urrently, FC(100) irrigation level minimizes photoinhibition, enhancing A, gs, PhiPSII, and ETR in th
80                                              Photoinhibition, exacerbated by elevated temperatures, u
81 rk, we investigated the molecular origins of photoinhibition focusing on the paradoxical energy dissi
82 of the redox component increased the rate of photoinhibition >15-fold.
83 essure at photosystem II, and no evidence of photoinhibition, implying a better dynamic regulation to
84 e required for low-temperature recovery from photoinhibition in Arabidopsis.
85                            Inspiratory-phase photoinhibition in Arch-transfected mice during inspirat
86  in thermal dissipation ability and enhanced photoinhibition in excess light conditions.
87 omponent of NPQ that is necessary to prevent photoinhibition in excess light.
88  and resistance to pathogens, and alleviates photoinhibition in immune state.
89 rong control over the rate of photosystem II photoinhibition in isolated thylakoid membranes.
90 ot in pgr5 plants, suggesting a role for PSI photoinhibition in regulating the chl-EGSH dynamics.
91                    Detailed investigation of photoinhibition in the triple mutant revealed that the r
92        However, FME facilitation during ACtx photoinhibition indicated that sound-evoked facial movem
93                                   Therefore, photoinhibition is always observed when the rate of phot
94 sustained NPQ, which 3) in concert with PSII photoinhibition, is suggested to trigger sustained NPQ i
95 increase light penetration while alleviating photoinhibition more effectively than in a flat biofilm.
96                     Moreover, we report that photoinhibition of 5HT-fDCN reduces dystonia in a1A (tot
97                                              Photoinhibition of anterolateral motor cortex impaired c
98 urons showed increased firing in response to photoinhibition of CA3.
99                                              Photoinhibition of CeM projectors impairs fear condition
100                              Dorsal striatal photoinhibition of ChIs in lesioned ChAT(cre/cre) mice e
101                        Our results show that photoinhibition of ChIs in the dorsal striatum and pharm
102                                   Unilateral photoinhibition of delay activity in the ALM or thalamus
103                                              Photoinhibition of endogenous activity of lateral hypoth
104                                              Photoinhibition of FPTase activity by Compound 1 is prev
105                                              Photoinhibition of GABAergic neurons in the MeApd inhibi
106 ac3a3b double mutants exhibit hypersensitive photoinhibition of hypocotyl elongation, suggesting that
107 ed mouse hippocampal neurons enabled precise photoinhibition of individual spikes in trains of up to
108                                 In contrast, photoinhibition of inhibitory LPO neurons did not result
109 ess-enhanced motivation for sucrose seeking, photoinhibition of IPN GABAergic neurons reduced stress-
110                                     Finally, photoinhibition of LC-CA1 terminals suppressed long-term
111                                              Photoinhibition of NAcSh neurons, whether general or cel
112 R) expression in cholinergic neurons enabled photoinhibition of pharyngeal muscle contraction in live
113  triggered changes in protein expression and photoinhibition of photosystem I (PSI) and resulted in t
114    Further, PTOX activation protects against photoinhibition of Photosystem II and reduces reactive o
115 pe exposed to mild light stress that invokes photoinhibition of photosystem II without causing photoo
116 ht stress than PSII as shown by the stronger photoinhibition of PSI and increased rate of singlet oxy
117    The flv4-2/OE mutant is more resistant to photoinhibition of PSII and exhibits a more oxidized sta
118                  Increased susceptibility to photoinhibition of PSII in stm6 demonstrates that the MO
119             We found that temporally precise photoinhibition of somatosensory cortex (S1) applied con
120                                   Similarly, photoinhibition of the ALM diminished thalamic activity.
121                                 In contrast, photoinhibition of the BLA->Acb pathway augmented fear l
122                                              Photoinhibition of the BLA->CeA pathway during the foots
123 H) promoter, memory updating was impaired by photoinhibition of the CA1 catecholaminergic terminals f
124  (DA) and noradrenaline (NA) decreased after photoinhibition of the LC-CA1 terminals (but not VTA-CA1
125 induced decrease in feeding was abolished by photoinhibition of the LH-glutamatergic inputs to VTA.
126                        Finally, we show that photoinhibition of the POMC(ARH)->VTA circuit in mice in
127                                              Photoinhibition of the thalamus caused a short-latency a
128 nic approaches to demonstrate that selective photoinhibition of these neurons affects mystacial pad a
129 rmal firing rates in the left mPFC; however, photoinhibition of these neurons induced social avoidanc
130 teral hypothalamic area (LHA) and found that photoinhibition of this input decreases escape responses
131                                              Photoinhibition of VGAT neurons in the MeApd decreased L
132  quotient (LQ) was measured following either photoinhibition of VGAT or photoexcitation of VGluT2 neu
133             Here, we evaluate the effects of photoinhibition on long-term carbon gain (over 1 d) in t
134 comes about, explore the consequences of PSI photoinhibition on photosynthesis and growth, discuss re
135                                  Significant photoinhibition only occurred at Chl concentrations belo
136 f light level and occurred in the absence of photoinhibition or lipid peroxidation suggests that the
137 of ATP and NADPH must be balanced to prevent photoinhibition or photodamage.
138 ) or SST(+) interneuron activity, via either photoinhibition or photoexcitation, led to a decrease in
139 in NM-3, NM 69, NM-70, and C-76-16 indicated photoinhibition or saturation of the photosynthetic appa
140 tein deficiency did not significantly affect photoinhibition or turnover of photosystem II-associated
141  an acute, noxious thermal stimulus, whereas photoinhibition potentiates thermal nociception.
142  inactivation results from an FtsH-sensitive photoinhibition process.
143                                          RTN photoinhibition reduced breathing equally during non-REM
144                                              Photoinhibition reduces photosynthetic productivity; how
145 52L, and W352A, exhibit an increased rate of photoinhibition relative to wild type.
146          During persistent apneas, prolonged photoinhibition restored rhythmic breathing.
147 bic potentiometric titrations of the rate of photoinhibition revealed a redox component with a midpoi
148 osses to the atmosphere, and a lower risk of photoinhibition, roles that justify its vast presence in
149 mpensate for the impaired photosynthesis and photoinhibition sensitivity.
150 spiratory duration, whereas expiratory-phase photoinhibition shortened the latency until the next ins
151 ates that potato may be a useful species for photoinhibition studies.
152 h increased DHAR expression experienced less photoinhibition than did wild-type plants following expo
153 d show that younger leaves are less prone to photoinhibition than older leaves.
154 had higher degrees of lipid peroxidation and photoinhibition than the vtc2 mutant.
155 th higher qE capacity were more resistant to photoinhibition than the wild type.
156 ow light growth, but it is more sensitive to photoinhibition than the wild type.
157 fad8 triple mutant, were more susceptible to photoinhibition than wild-type Arabidopsis, whereas one
158                                              Photoinhibition, the light-dependent decrease of PSII ac
159 e pre-steady-state lag phase and to suppress photoinhibition, thereby improving the accuracy of t(lag
160                The mutant was susceptible to photoinhibition under pulsing but not constant light.
161 ae decreased simultaneously, indicating that photoinhibition underlies the observed decreased photosy
162 lastly reveal the heterogeneity of PSII upon photoinhibition using structure-function modeling of exc
163                                 We monitored photoinhibition using the chlorophyll fluorescence param
164                                  Significant photoinhibition was also observed following exposure to
165                                       Such a photoinhibition was paralleled by significant damage to
166                                The extent of photoinhibition was the same in all of the mutants, sugg
167 nts showed impaired growth and photosystem I photoinhibition when exposed to fluctuating light, demon
168 amage of photosystem II (PSII) thus avoiding photoinhibition which can decrease plant fitness and pro
169 es: subsets of cells increased firing during photoinhibition, while other cells decreased firing duri

 
Page Top