ライフサイエンスコーパス: coleoptile

1 the endosperm is not a source of IAA for the coleoptile.

2 en different tissues of the maize (Zea mays) coleoptile.

3 ased by staining the peripheral cells of the coleoptile.

4 PM was more than double the activity in the coleoptile.

5 ed indole-3-acetic acid to the mesocotyl and coleoptile.

6 us cell division (aerobic conditions) in the coleoptiles.

7 mically at the Golgi of the developing maize coleoptiles.

8 en 4-day aerobically and anaerobically grown coleoptiles.

9 ular bundles of kernels, seedling roots, and coleoptiles.

10 riptomic changes in DNA methylation in these coleoptiles.

11 light photoreception of both guard cells and coleoptiles.

12 alyses of the ExGases extracted from growing coleoptiles.

13 data on photogravitropic equilibrium in oat coleoptiles.

14 ranscription levels in S. nodorum-challenged coleoptiles, although their pattern of accumulation vari

15 Unlike the coleoptile and first leaf sheath, EOD-FR-mediated elonga

16 e roots) and stem-borne tissues (tillers and coleoptile and leaf node axile roots) plus branch roots.

17 Coleoptile and mesocotyl length increased by up to 31 an

18 SafBP is most abundant in the coleoptile and scarcest in the leaves, consistent with t

19 The coleoptile and scutellar node phenotypes are unique from

20 ons, documented by the lack of any growth of coleoptiles and any increase of alpha-amylase and beta-g

21 Ltp-like gene, Ltp6, is highly expressed in coleoptiles and embryos under normal growth conditions.

22 ti-MLG monoclonal antibody revealed that the coleoptiles and leaves retain trace amounts of MLG only

23 tracts of acetone powders were prepared from coleoptiles and mesocotyls.

24 antibodies to soluble wall antigens from the coleoptiles and primary leaves of etiolated corn (Zea ma

25 ic decrease in MLG content (97% reduction in coleoptiles and virtually undetectable in other tissues)

26 luding darkly pigmented aleurone, scutellum, coleoptile, and scutellar node [Scp(e) alleles].

27 ently normal stage 1 in which the scutellum, coleoptile, and shoot apex were clearly defined.

28 expressed in internodes and leaves, three in coleoptiles, and nine in roots, with high transcript lev

29 nation did not reflect those seen in aerobic coleoptiles, but instead, reverted to a pattern similar

30 (ala)(GAC) gene into Zea mays bz-E2 or bz-E5 coleoptiles causes suppression of an Ala(458 )-->Val mis

31 Coleoptile chloroplasts also showed an enhancement by bl

32 the blue light responses of guard cells and coleoptile chloroplasts and the spectra for blue light-s

33 reception, indicates that the guard cell and coleoptile chloroplasts specialize in sensory transducti

34 In stems and coleoptiles, classic experiments showed that the peak re

35 During coleoptile development, changes in cell wall composition

36 upstream regions to drive gfp expression in coleoptiles, epicarps, and lemma/palea of developing spi

37 uggested that both control and auxin-treated coleoptiles exhibited Ca2+, and calmodulin-dependent pro

38 The rates of hydrolysis observed with coleoptile extracts were greater than those observed wit

39 is synthesized in vitro with isolated maize coleoptile Golgi membranes and the nucleotide-sugar subs

40 es induce sorghum (Sorghum bicolor var. Rio) coleoptile growth in 24-h incubations an average of 49%

41 synergistic reaction, yielding increases in coleoptile growth that average 295% above untreated cont

42 activity of the promoter was detected in the coleoptile, in the upper sheath section of the leaf, on

43 ever, only XET action was observed in barley coleoptiles, leaves and roots (which all contained MLG)

44 sheath cells) from ethanol:acetic acid-fixed coleoptiles of maize.

45 t essentially no indole-3-acetic acid to the coleoptile or primary leaves.

46 ositol nor IAA accumulates in the tip of the coleoptile or the mesocotyl node and thus these studies

47 Red irradiation (of coleoptiles or extracts) sufficient to approach photocon

48 an action spectrum for blue light-stimulated coleoptile phototropism.

49 The cpt1 (coleoptile phototropism1) mutant, which lacks one of the

50 um prior to embryonic degeneration, but only coleoptile proliferation was observed.

51 -phytochrome immunoprecipitates of etiolated coleoptile proteins.

52 regions known from peptide sequencing of the coleoptile proteins.

53 rgan-specific differential expression in the coleoptile, root, leaf, and internode.

54 ranscript at roughly similar levels in maize coleoptiles, root meristems, and the zone of root elonga

55 mic changes in cell walls of etiolated maize coleoptiles, sampled at one-half-d intervals of growth,

56 Avena coleoptile sections were preincubated in either fusicocc

57 t a roughly constant velocity down a stem or coleoptile segment.

58 in phosphorylations in oat (Avena sativa L.) coleoptile segments were analyzed by sodium dodecyl sulf

59 horylation of both control and auxin-treated coleoptile segments.

60 e total RNA isolated from auxin-treated corn coleoptile segments.

61 odel system, the elongating maize (Zea mays) coleoptile system, in which cell wall changes are well c

62 nd thus these studies do not explain how the coleoptile tip controls the amount of IAA in the shoot.

63 from Pima cotton (Gossypium barbadense) and coleoptile tips from corn (Zea mays).

64 wheat (Triticum aestivum cv Pennmore Winter) coleoptile (type II) walls, which showed only a negligib

65 us monocots, but was less effective on grass coleoptile walls.

66 oat (Avena sativa L.) tissues, the root and coleoptile, was compared.

67 ee sterol, whereas comparable amounts in the coleoptile were 42, 39, and 19 mole percent, respectivel

68 ls from embryonic, elongating, and senescent coleoptiles were broadly discriminated from each other b

69 longating shoot, gl-OXO is restricted to the coleoptile where it is detected only in the epidermal ce

70 ics of the germinating embryo and elongating coleoptile, which consequently enhances anaerobic germin

71 Treatment of coleoptile with auxin for 1 hour resulted in no detectab