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1 me corresponding to dusk in the absence of a diurnal cycle).
2 electron donor, with lifetimes exceeding the diurnal cycle.
3 r in guard cells of intact leaves during the diurnal cycle.
4 outheastern United States, with the expected diurnal cycle.
5 bidopsis leaves at different points during a diurnal cycle.
6 es and malate (Mal) synthesis imposed over a diurnal cycle.
7  prediction of growth properties over a full diurnal cycle.
8 re through the awake and sleep phases of the diurnal cycle.
9 he active than during the rest period of the diurnal cycle.
10 s, yet temperatures fluctuate throughout the diurnal cycle.
11 nt at the end of the illumination phase of a diurnal cycle.
12 ally expressed at distinct phases during the diurnal cycle.
13 cantly reduces mating success throughout the diurnal cycle.
14 that are later mobilized as part of a robust diurnal cycle.
15 ecessary for cycling of sxe1 mRNA during the diurnal cycle.
16  to analyze the transcriptome throughout the diurnal cycle.
17 bolism do not change appreciably through the diurnal cycle.
18 ch content than the wild-type throughout the diurnal cycle.
19 vents whose photosensitivity varies during a diurnal cycle.
20 rhythmic transcription during a circadian or diurnal cycle.
21  to 4 hours after onset of the nocturnal and diurnal cycles.
22 iolated growth, but may also function during diurnal cycles.
23 d and functions that define the seasonal and diurnal cycles.
24 uclear hormone receptors display interlinked diurnal cycling.
25 PMSR2 at the end of the night in a short-day diurnal cycle alleviates this potential burden on metabo
26 ersus form 2) appeared to change during this diurnal cycle, along with changes in the PSII monomer/di
27 Polysome loading was investigated during the diurnal cycle, an extended night, and low CO2 in Arabido
28 ine metabolism during the light phase of the diurnal cycle and evaluated the presence of diurnal and
29  spectrometry, in total leaf extracts over a diurnal cycle and when exposed to conditions that promot
30 uct-to-parent reversion mechanism results in diurnal cycling and substantial regeneration of TBA meta
31 d that LD abundance was modulated during the diurnal cycle, and characterization of LDAP misexpressio
32 s may differ functionally with regard to the diurnal cycle, and that these differences may be reflect
33      Changes in leaf starch content over the diurnal cycle are largely brought about by changes in th
34 erns in wood cell wall biosynthesis, suggest diurnal cycle as a possible cue in the regulation of car
35 n ([O2]) in all replicates exhibited regular diurnal cycles associated with daytime photosynthesis an
36 s are not solely controlled by cues from the diurnal cycle but that strain-specific intracellular met
37 sted during the light or dark portion of the diurnal cycle, but the process was significantly acceler
38 al processes that vary across the day-night (diurnal) cycle, but if and how the circadian clock regul
39 um to monitor the CO(2) levels caused by the diurnal cycles caused by the metabolism of the aquatic p
40                       The mechanism by which diurnal cycles control the transitory biosynthesis and d
41 ral chemoreception in a vigilance-state- and diurnal-cycle-dependent manner and indicate a role for o
42 the CO(2) response in a vigilance-state- and diurnal-cycle-dependent manner.
43 spheric Hg(0)g exchange resulting in typical diurnal cycles due to photochemcial reduction at the sur
44 iency is differentially regulated during the diurnal cycle for genes with 5'-Terminal Oligo Pyrimidin
45  were analyzed at various time points in the diurnal cycle in homozygous rds/rds retinas which lack p
46 xogenous fatty acid in adipose tissue over a diurnal cycle in lean (n = 9) and abdominally obese men
47 rays to measure mRNA accumulation during the diurnal cycle in the livers of (1) wild-type mice, (2) a
48 versibly modulated by the photoreceptor over diurnal cycles in Arabidopsis seedlings.
49 ocotyl cell elongation to peak at dawn under diurnal cycles in Arabidopsis thaliana.
50  either constant darkness or 12 h light/dark diurnal cycles, including several noncoding RNAs (ncRNAs
51 cription of the volatilization dynamics on a diurnal cycle (increasing efficiency factor from 0.85 to
52       Thus, Pol III transcription during the diurnal cycle is regulated both in response to nutrients
53  are U snoRNA host genes (Uhgs), a family of diurnal cycling noncoding RNAs that encode the precursor
54 ase (night) and the light phase (day) of the diurnal cycle, nor did they change between early and lat
55 ry nitrite maximum and the plausibility of a diurnal cycle of archaeal ammonia oxidation activity in
56 trial radiation is strongly modulated by the diurnal cycle of clouds (DCC).
57 ed from an emergent relationship between the diurnal cycle of the relative humidity profile and E.
58 sp70 mRNA levels in the light paralleled the diurnal cycle of total cell protein synthesis.
59 In low prey-addition treatments, the regular diurnal cycles of [O2] were disrupted, but a regime shif
60  notion that ecological features such as the diurnal cycles of light and day, sunlight exposure, seas
61 ng point at ~45 h as [O2] was decoupled from diurnal cycles of photosynthesis and respiration.
62 llations in peripheral tissues are driven by diurnal cycles of rest-activity and food intake or are a
63 grown in greenhouse conditions under natural diurnal cycles of solar irradiation, the ratio of phosph
64 ted is indicated by correlations between the diurnal cycles of the OVOC measurements and solar radiat
65 ogy of virtually all living organisms to the diurnal cycles of their environments.
66                   To investigate whether the diurnal cycling of the transcript levels is only a respo
67 icate that SBEIIa is required for the proper diurnal cycling of transitory starch within the leaf and
68 eep during both dark and light phases of the diurnal cycle only in SHRs.
69 ocioeconomic status, the underlying cortisol diurnal cycle, or subjective experience during the stres
70                                              Diurnal cycles provide a tractable system to study the r
71 to later initiation of the rest phase of the diurnal cycle seen in controls in late adolescence.
72 synchronization of biological processes with diurnal cycles such as activity and rest.
73  probably connected to the interplay between diurnal cycles that drive photosynthetic cell growth and
74                                   During the diurnal cycle, the amount of leaf starch is higher in dp
75 both the daytime and night-time phase of the diurnal cycle, the latter of which remains uncertain in
76 zes physical and metabolic activity with the diurnal cycle through a transcriptional-posttranslationa
77                            Estradiol and the diurnal cycle thus interact to induce shifts in both GAB
78 in wakefulness during the dark period of the diurnal cycle to a level observed during NREM sleep in t
79  photosystem organization changes during the diurnal cycle to favor either noncyclic electron flow, w
80 both cultivars demonstrates a high-amplitude diurnal cycle under these conditions; however, ACC oxida
81 operties of PSII were studied throughout the diurnal cycle using O2-flash-yield and pulse-amplitude-m
82    However, when the dark period in a normal diurnal cycle was cut short artificially by transferring
83 th exhibit comparable variation on a natural diurnal cycle, while PHYB1 also exhibits variation but w
84 tilization from bare soil exhibits usually a diurnal cycle with a potentially large decrease when the
85                   HO2 was observed to have a diurnal cycle with morning concentrations suppressed by
86 th (222)Rn and CO2 concentrations followed a diurnal cycle with night time concentrations higher than
87 bit abnormal fuel utilization throughout the diurnal cycle, with increased glucose oxidation near the

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