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1 isomerized isoAsp residues upon rehydration (imbibition).
2 and redox metabolism of Arabidopsis seeds at imbibition.
3 gh in dormant grains even after five days of imbibition.
4 ly for a short period immediately after seed imbibition.
5 es beyond that at the initial stages of seed imbibition.
6 the expression of LeEXP4 within 12 hours of imbibition.
7 rly the coleorhiza) during the first 24 h of imbibition.
8 er leaf emergence at approximately 48 h post-imbibition.
9 d during seed maturation and declined during imbibition.
10 and finally disappearing after four days of imbibition.
11 abolism including the oil metabolisms during imbibition.
12 seed germination of dormant seeds upon their imbibition.
13 ing to 19,000 in Col and 17,000 in Cvi after imbibition.
14 a semi-analytical calculation of spontaneous imbibition.
15 aleurone of germinating seeds up to 24 h of imbibition.
16 ge amounts of mucilage that is released upon imbibition.
17 or seed-coat cracking that also enables seed imbibition.
18 tting phases was determined at Pc = 0 during imbibition.
19 hanced transcript levels in rdo5 during seed imbibition.
20 ainage was much less than for the AWI during imbibition.
21 athways needed later, in the early stages of imbibition.
22 d remains stable throughout seed storage and imbibition.
23 ), and is released to surround the seed upon imbibition.
24 ght/dark cycles in ambient temperatures upon imbibition.
25 ay act redundantly with TaABF1 during cereal imbibition.
26 y seeds, but is markedly induced during seed imbibition.
27 c wetting length due to capillary action and imbibition.
28 actually double during the 3 days following imbibition.
29 both the null segregant and homozygote after imbibition.
30 to 8 h after imbibition and by LOX 8 h after imbibition.
32 n samples from 6-hour, 3-day and 6-day after imbibition (6-HAI, 3-DAI, and 6-DAI) were performed to c
35 ioration, characterized by cytoplasmic lipid imbibition (accumulation), organelle disintegration, api
38 o the challenge of simultaneously monitoring imbibition and deformation with high spatial resolution,
42 script accumulates in wild-type seeds during imbibition and germination, and the transcript levels of
43 (4) a close relationship between the corneal imbibition and intraocular pressure, with potentially a
44 , also stimulated increases in uterine water imbibition and macromolecule uptake in ovariectomized ER
45 ion morphology is determined by both solvent imbibition and particle-magnetic field interactions.
46 show no significant structural change during imbibition and the amounts of specific mitochondrial pro
47 ndormant dry embryos are reawakened first by imbibition and then by perception of germination trigger
48 etained cells and the amount of drainage and imbibition, and decreased with the number of drainage an
49 in the embryo of seeds is repaired early in imbibition, and is important for germination performance
50 xpression of ABA signaling genes during seed imbibition, and thereby might contribute to the switch f
51 ow during seed development, increased during imbibition, and was even greater in seeds that had compl
52 showed that infrared thermography can detect imbibition- and germination-associated biophysical and b
54 llations seen during the first 2 d following imbibition are dependent on the clock genes LATE ELONGAT
56 bidopsis (Arabidopsis thaliana) during their imbibition at 25 degrees C in darkness, a temperature pr
57 oil interface jumps from pore-to-pore during imbibition at an approximately constant local capillary
59 results suggest a new universality class of imbibition behavior, which is expected to occur in any m
60 during the first 24 h following the onset of imbibition, both in continuous darkness and in a greenho
62 ript levels increased rapidly from 6 to 24 h imbibition, correlating with the development of peptide
67 nduction of CAT2 mRNA varied with time after imbibition, demonstrating that imbibition provides a sig
72 pression transiently increases shortly after imbibition during germination, but not in imbibed dorman
74 front inside the porous medium in a dynamic imbibition-evaporation equilibrium, as is typical for tr
75 both IS reduction and cycles of drainage and imbibition, even when the cells were retained under favo
77 The advantages associated with this droplet imbibition experiment include (1) ultra-small sample con
78 may not be necessary to conduct spontaneous imbibition experiments horizontally in order to exclude
79 cellular integrity during desiccation and/or imbibition, extending longevity in the dehydrated state,
82 e final expansion is absent when we stop the imbibition front inside the porous medium in a dynamic i
85 different sorghum lines during 72 h of grain imbibition, germination and early seedling development,
86 n older seedlings (approximately 9 days post-imbibition) gl-OXO activity is detected in leaves, but o
89 udy primary drainage followed by spontaneous imbibition in a carbonate specimen under increasing isot
91 d oval morphology were evident after 12 h of imbibition in continuous light (following 48 h of strati
92 actin cytoskeleton was not involved because imbibition in Latrunculin B did not affect the onset of
95 The proteins necessary for translation upon imbibition in orthodox seeds may be particularly importa
103 beta-HCH-loaded animals also increased water imbibition in the uterus; there was no effect from fasti
110 dered, namely, the critical time for solvent imbibition into the substrate (t(im)), the time it takes
111 tion, and that the Laplace contribution upon imbibition is precisely half that of vapor sorption, due
115 acceleration was achieved through a droplet imbibition mass spectrometry (MS) experiment that allows
119 cribed in the current study showcase droplet imbibition MS to be a powerful and high-throughput alter
121 lthough TaABF1 mRNA was downregulated during imbibition of afterripened grains, transcript levels wer
123 m.s-1, with predicted and designed capillary imbibition of monomers into nanopores enabling high fill
126 phases within the pores of AAMs were made by imbibition of the latter solutions followed by solvent e
127 tion to seedling establishment, i.e. between imbibition of the mature dry seed and opening of the cot
130 athways exist for NAE metabolism during seed imbibition: one to hydrolyze NAEs in a manner similar to
134 parate hydration systems for maintaining the imbibition pressure (vertical static hydration) and corn
135 Clinical observation shows that the stromal imbibition pressure is "too high" in Fuchs endothelial d
136 l stromal edema, indicating that the corneal imbibition pressure is relatively "too high." RESULTS: T
137 ous humor are governed, respectively, by the imbibition pressure of the stromal matrix and the transe
138 uggests that these observations apply to any imbibition process in nanopores, regardless of the liqui
139 ly explained based on the Wenzel's model and imbibition process, revealing that the dimensions of the
140 seeds were linked to the regulation of SEED IMBIBITION PROTEIN1 Proteomic analysis confirmed that a
141 th time after imbibition, demonstrating that imbibition provides a signal capable of resetting the ci
142 is activated in the earliest stages of water imbibition, providing evidence for the accumulation of c
144 rived analytically was used to calculate the imbibition rates in porous media with different permeabi
146 e dry aleurone layer, but is degraded during imbibition, replenished by de novo transcription, and ma
147 contents strongly increased just after seed imbibition, so that germinating seeds contained 5- and 1
150 ponse to low-salinity water in a spontaneous imbibition test, aiming (1) to identify suitable indicat
152 l design was carried out at 12 h and 24 h of imbibition to analyze the effects of temperature, light,
154 chia coli D21g during cycles of drainage and imbibition under various solution chemistry and initial
155 seeds maintained LeGOLS-1 mRNA amounts after imbibition unless supplied with gibberellin, whereas abs
157 ed that the effect of gravity on spontaneous imbibition was governed by the hydraulic conductivity of
158 the porous ceramic substrate, whereas water imbibition was observed for superhydrophilic coating dur
159 sativum) seed, 4 days from the initiation of imbibition, was determined by the use of specific protea
160 ng maize leaves from dry seeds to 192 h post imbibition, we studied gene up- and down-regulation and
161 acing brine (drainage), and brine rewetting (imbibition) were studied to understand CO2 transport and
163 nd AR stages but diverged significantly upon imbibition, with Col showing enrichment in 40S ribosomal
164 cross-linking transepithelial iontophoresis imbibition yielded greater and deeper riboflavin saturat