ライフサイエンスコーパス: imbibition

1 isomerized isoAsp residues upon rehydration (imbibition).

2 abolism including the oil metabolisms during imbibition.

3 rly the coleorhiza) during the first 24 h of imbibition.

4 er leaf emergence at approximately 48 h post-imbibition.

5 or seed-coat cracking that also enables seed imbibition.

6 tting phases was determined at Pc = 0 during imbibition.

7 hanced transcript levels in rdo5 during seed imbibition.

8 ainage was much less than for the AWI during imbibition.

9 athways needed later, in the early stages of imbibition.

10 d remains stable throughout seed storage and imbibition.

11 ), and is released to surround the seed upon imbibition.

12 ght/dark cycles in ambient temperatures upon imbibition.

13 ay act redundantly with TaABF1 during cereal imbibition.

14 aleurone of germinating seeds up to 24 h of imbibition.

15 y seeds, but is markedly induced during seed imbibition.

16 actually double during the 3 days following imbibition.

17 ge amounts of mucilage that is released upon imbibition.

18 both the null segregant and homozygote after imbibition.

19 to 8 h after imbibition and by LOX 8 h after imbibition.

20 gh in dormant grains even after five days of imbibition.

21 ly for a short period immediately after seed imbibition.

22 es beyond that at the initial stages of seed imbibition.

23 the expression of LeEXP4 within 12 hours of imbibition.

24 c competency was established about 8 h after imbibition, 11 h prior to germination.

25 During spontaneous imbibition, a wetting liquid is drawn into a porous medi

26 Upon seed imbibition, abscisic acid (ABA) levels decrease to allow

27 ioration, characterized by cytoplasmic lipid imbibition (accumulation), organelle disintegration, api

28 y amidohydrolase was observed 4 to 8 h after imbibition and by LOX 8 h after imbibition.

29 ese column studies revealed the influence of imbibition and drainage on D21g release.

30 utant lines displayed a significant delay in imbibition and germination in vitro and in vivo.

31 script accumulates in wild-type seeds during imbibition and germination, and the transcript levels of

32 , also stimulated increases in uterine water imbibition and macromolecule uptake in ovariectomized ER

33 show no significant structural change during imbibition and the amounts of specific mitochondrial pro

34 ndormant dry embryos are reawakened first by imbibition and then by perception of germination trigger

35 etained cells and the amount of drainage and imbibition, and decreased with the number of drainage an

36 in the embryo of seeds is repaired early in imbibition, and is important for germination performance

37 ow during seed development, increased during imbibition, and was even greater in seeds that had compl

38 showed that infrared thermography can detect imbibition- and germination-associated biophysical and b

39 llations seen during the first 2 d following imbibition are dependent on the clock genes LATE ELONGAT

40 bidopsis (Arabidopsis thaliana) during their imbibition at 25 degrees C in darkness, a temperature pr

41 oil interface jumps from pore-to-pore during imbibition at an approximately constant local capillary

42 y) was enhanced by priming and suppressed by imbibition at elevated temperatures.

43 results suggest a new universality class of imbibition behavior, which is expected to occur in any m

44 during the first 24 h following the onset of imbibition, both in continuous darkness and in a greenho

45 ript levels increased rapidly from 6 to 24 h imbibition, correlating with the development of peptide

46 scCO2-brine drainage and imbibition curves shifted to lower Pc relative to predic

47 Fitting universal scaled drainage and imbibition curves show that wettability alteration resul

48 nd decreased with the number of drainage and imbibition cycles.

49 nduction of CAT2 mRNA varied with time after imbibition, demonstrating that imbibition provides a sig

50 irection of the gravity vector during static imbibition, despite subsequent clinorotation.

51 pression transiently increases shortly after imbibition during germination, but not in imbibed dorman

52 In particular, imbibition efficiently released cells from the air-water

53 both IS reduction and cycles of drainage and imbibition, even when the cells were retained under favo

54 s on the relative importance of drainage and imbibition events on microorganism release.

55 may not be necessary to conduct spontaneous imbibition experiments horizontally in order to exclude

56 cellular integrity during desiccation and/or imbibition, extending longevity in the dehydrated state,

57 Expression of LsNCED4 after imbibition for 24 h at high temperature was greater in n

58 Anomalously fast imbibition front roughening is experimentally observed b

59 smoothening effect of surface tension on the imbibition front roughening is negligible.

60 n older seedlings (approximately 9 days post-imbibition) gl-OXO activity is detected in leaves, but o

61 Spontaneous imbibition happens in many natural and chemical engineer

62 Clock function is detected within 2 d of imbibition (hydration of the dried seed).

63 Here we investigate water imbibition in a nanoporous glass (Vycor) in which the po

64 d oval morphology were evident after 12 h of imbibition in continuous light (following 48 h of strati

65 actin cytoskeleton was not involved because imbibition in Latrunculin B did not affect the onset of

66 The proteins necessary for translation upon imbibition in orthodox seeds may be particularly importa

67 The effect of gravity on imbibition in porous media can be modeled theoretically.

68 The effect of gravity on spontaneous imbibition in porous media was investigated both theoret

69 In the lesions after imbibition in quinoline, remineralization was also appar

70 light photomicrographs of each section after imbibition in several media.

71 was seen in dry seeds and immediately after imbibition in the entire seedling.

72 beta-HCH-loaded animals also increased water imbibition in the uterus; there was no effect from fasti

73 desiccated seeds but declined within 8 h of imbibition in wild-type seeds.

74 Induction of NCED6 during imbibition increased ABA levels more than 20-fold and wa

75 Our results indicate that, upon seed imbibition, increased GA levels reduce DELLA protein abu

76 same order as that of the gravity and liquid imbibition-induced dry spot rewetting timescale.

77 Imbibition-inducible 1 (IMB1) appears to be a nuclear pr

78 Imbibition is sufficient to synchronize individuals in a

79 Upon imbibition, leaf expansion occurs rapidly with new KSs i

80 However, during imbibition mitochondria in the heavy fraction (37%-42% [

81 Upon grain imbibition, mobilisation of arabinoxylan and starch spre

82 d lipid is broken down over 6 days following imbibition of ABA-treated seed.

83 lthough TaABF1 mRNA was downregulated during imbibition of afterripened grains, transcript levels wer

84 ABF transcripts increased transiently during imbibition of dormant grains.

85 s to an undetectable level within 12 h after imbibition of non-dormant grains.

86 phases within the pores of AAMs were made by imbibition of the latter solutions followed by solvent e

87 tion to seedling establishment, i.e. between imbibition of the mature dry seed and opening of the cot

88 nstrate mechanisms of shape selection during imbibition of the texture.

89 Imbibition on gibberellin(4 + 7) did not ameliorate germ

90 athways exist for NAE metabolism during seed imbibition: one to hydrolyze NAEs in a manner similar to

91 ial movements which are not identified under imbibition or drainage conditions.

92 Hysteretic drainage and imbibition Pc-Sw curves were measured in limestone sands

93 ous humor are governed, respectively, by the imbibition pressure of the stromal matrix and the transe

94 seeds were linked to the regulation of SEED IMBIBITION PROTEIN1 Proteomic analysis confirmed that a

95 th time after imbibition, demonstrating that imbibition provides a signal capable of resetting the ci

96 is activated in the earliest stages of water imbibition, providing evidence for the accumulation of c

97 rived analytically was used to calculate the imbibition rates in porous media with different permeabi

98 Cycles of drainage and imbibition removed cells from the SWI and the AWI, respe

99 e dry aleurone layer, but is degraded during imbibition, replenished by de novo transcription, and ma

100 illing process and provide estimates for the imbibition speed and electrocapillary pressure.

101 ity of the porous media (permeability of the imbibition systems).

102 in recovery of the defending fluid from weak imbibition to intermediate-wet conditions.

103 chia coli D21g during cycles of drainage and imbibition under various solution chemistry and initial

104 seeds maintained LeGOLS-1 mRNA amounts after imbibition unless supplied with gibberellin, whereas abs

105 Release of cells during drainage and imbibition was found to be more pronounced in the presen

106 ed that the effect of gravity on spontaneous imbibition was governed by the hydraulic conductivity of

107 sativum) seed, 4 days from the initiation of imbibition, was determined by the use of specific protea

108 ng maize leaves from dry seeds to 192 h post imbibition, we studied gene up- and down-regulation and

109 acing brine (drainage), and brine rewetting (imbibition) were studied to understand CO2 transport and

110 Ten corneas underwent imbibition with epi-on (n = 3), epi-off (n = 3), iontoph

111 cross-linking transepithelial iontophoresis imbibition yielded greater and deeper riboflavin saturat