ライフサイエンスコーパス: imbibe

1 , or low temperature, nitrate and light when imbibed.

2 high corresponding mRNA levels in the mature imbibed aleurone but are repressed 10-fold or more withi

3 ever, a number of mRNA species in the mature imbibed aleurone cell of barley, such as a storage globu

4 ent O(2) uptake relative to that measured in imbibed and germinated seed.

5 in the presence of Ca2+ (high calcium; HC = imbibed and raised in 10 millimolar CaCl2), in the absen

6 ly depleting them of Ca2+ (low calcium; LC = imbibed and raised in distilled H2O and subsequently tre

7 additional Ca2+ (intermediate calcium; IC = imbibed and raised in distilled H2O, calcium supply from

8 thyl acrylamide) monoliths by evaporation of imbibed aqueous solutions, adopt preferred orientations

9 regulation of primary metabolism in dry and imbibed Arabidopsis (Arabidopsis thaliana) seeds.

10 e, was sufficient to suppress germination in imbibed Arabidopsis seeds.

11 ressed between PI251246 and cv Salinas seeds imbibed at high temperature (30 degrees C).

12 tiva 'Salinas') seeds fail to germinate when imbibed at temperatures above 25 degrees C to 30 degrees

13 ion, or failure to complete germination when imbibed at warm temperatures.

14 Adult females of the genus Ixodes imbibe blood meals exceeding about 100 times their own w

15 specific cardiac teratogen in the fetus when imbibed by the maternal rat.

16 tabolic fate of NAEs in vitro and in vivo in imbibed cotton (Gossypium hirsutum) seeds.

17 The conversion of NAE 18:2 in imbibed cottonseed extracts to 12-oxo-13-hydroxy-N-(9Z)-

18 tty acids (FFA) were produced by extracts of imbibed cottonseeds.

19 er imbibition during germination, but not in imbibed dormant seeds, and genetic analyses show that CT

20 In imbibed embryos, GUS expression was limited to the cotyl

21 vity was also detected in mature embryos and imbibed embryos, in accordance with a role for FTase in

22 ve expression of TaABF1 in aleurone cells of imbibing grains completely eliminated GA-induced express

23 bolism or plastid function, are repressed in imbibed imb1 seeds.

24 When gib-1 seeds were imbibed in GA solution combined with 100 microM abscisic

25 f both genes increased when gib-1 seeds were imbibed in gibberellin.

26 RNAs differentially expressed in gib-1 seeds imbibed in the presence or absence of GA(4+7).

27 berellin-deficient (gib-1) mutant seeds were imbibed in water, LeEXP8 mRNA was not detected, but a lo

28 t the hypothesis that the remaining water is imbibed into the shale rock by capillary forces and reta

29 unted for within the shale system, with most imbibed into the shale rock matrix and retained there fo

30 The potential of imbibed mature embryos for dormancy was analysed and sho

31 d for the first time to study germination in imbibed Moravian III barley grains.

32 hogens (Anopheles gambiae and Aedes aegypti) imbibing multiple bloodmeals during a gonotrophic cycle

33 Even though imbibed mutant seeds showed no dormancy, they exhibited

34 neurotransmitter, the iridocytes reversibly imbibe or expel water commensurate with changes in refle

35 is the second most expressed PME in dry and imbibed pollen grains.

36 observed showed that they differed in newly imbibed primary dormant seeds, as commonly used in exper

37 ntrained by light-dark cycles applied to the imbibed seed and its period was shortened in the toc1-1

38 Mitochondria from dry and imbibed seed exhibited NADH-dependent O(2) uptake that w

39 haracteristics of freshly harvested seeds on imbibed seed gene expression patterns.

40 Imbibed seeds also had high PvCYP707A mRNA levels.

41 ted by the mutant phenotypes, ilr1 iar3 ill2 imbibed seeds and seedlings have lower IAA levels than w

42 riptomes for the embryonic leaves in dry and imbibed seeds every 6 h up to hour 72.

43 We showed that RGL2 protein in imbibed seeds is rapidly degraded by GA treatment and th

44 Imbibed seeds of the Arabidopsis thaliana accession Djar

45 Prolonged chilling of imbibed seeds only partially restores germination potent

46 However, LeGOLS-1 mRNA accumulated again in imbibed seeds prevented from completing germination by d

47 The levels of CDKF;1 were lower in dry or imbibed seeds than in germinating seeds or seedlings.

48 ation studies showed that the sensitivity of imbibed seeds to low temperature, nitrate and light was

49 In dormant imbibed seeds transcript levels were relatively unchange

50 morphology (size and length) of both dry and imbibed seeds was quantified by using image analysis.

51 emonstrate that this mechanism is present in imbibed seeds wherein it affects germination rate.

52 tabolisms to avoide oxidative damages to the imbibed seeds, and the seed shell played the role simili

53 the maintenance of embryo dormancy in mature imbibed seeds, but the detailed mechanisms by which this

54 In imbibed seeds, IMB1 modulates the transcription of a bat

55 ance of specific gene expression patterns in imbibed seeds.

56 of static orientation (gravistimulation) of imbibed seeds.

57 ification, a pre-chilling treatment of fully imbibed seeds.

58 ctions through control of DNA replication in imbibing seeds.

59 When dead muskmelon seeds are allowed to imbibe, solutes leaking from the embryo are retained wit

60 ing emergence from the egg, C. smithi larvae imbibe the stalk fluid, thereby possibly deriving nutrit

61 As the phengodid then imbibes the liquefied systemic contents of the dead mill

62 ed specifically in the micropylar tissues of imbibed tomato (Lycopersicon esculentum Mill.) seeds pri

63 We have isolated a cDNA from imbibed tomato seeds (LeMAN2) that shares 77% deduced am

64 vels throughout the plant but was induced in imbibing tomato seeds prior to germination and was down-

65 Tsetse flies (Glossina spp.) imbibe vertebrate blood exclusively and can be exposed t

66 This charge gradient causes the tissue to imbibe water and swell, creating a net osmotic pressure

67 le PG to force the collagenous matrix apart, imbibing water, increasing swelling and fissuring--chara

68 Macroscopic inorganic porous beads are imbibed with a "porous molecular additive" by simple sol

69 metal-exchange reactions in metallopolymers imbibed with an auxiliary metal salt.

70 ingredient of certain 'energy drinks' often imbibed with ethanol.