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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  data on photogravitropic equilibrium in oat coleoptiles.
7 mically at the Golgi of the developing maize coleoptiles.
8 us cell division (aerobic conditions) in the coleoptiles.
9 ular bundles of kernels, seedling roots, and coleoptiles.
10 en 4-day aerobically and anaerobically grown coleoptiles.
11 riptomic changes in DNA methylation in these coleoptiles.
12 light photoreception of both guard cells and coleoptiles.
13 alyses of the ExGases extracted from growing 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 ed in the endosperm of germinating seeds and coleoptiles and at lower amounts in mature shoots.
22  Ltp-like gene, Ltp6, is highly expressed in coleoptiles and embryos under normal growth conditions.
23 ti-MLG monoclonal antibody revealed that the coleoptiles and leaves retain trace amounts of MLG only
24 tracts of acetone powders were prepared from coleoptiles and mesocotyls.
25 antibodies to soluble wall antigens from the coleoptiles and primary leaves of etiolated corn (Zea ma
26 ic decrease in MLG content (97% reduction in coleoptiles and virtually undetectable in other tissues)
27 luding darkly pigmented aleurone, scutellum, coleoptile, and scutellar node [Scp(e) alleles].
28 ently normal stage 1 in which the scutellum, coleoptile, and shoot apex were clearly defined.
29 expressed in internodes and leaves, three in coleoptiles, and nine in roots, with high transcript lev
30 rasses and the ontogeny of the scutellum and coleoptile as the initial, highly modified structures of
31 nation did not reflect those seen in aerobic coleoptiles, but instead, reverted to a pattern similar
32 (ala)(GAC) gene into Zea mays bz-E2 or bz-E5 coleoptiles causes suppression of an Ala(458 )-->Val mis
33                                              Coleoptile chloroplasts also showed an enhancement by bl
34  the blue light responses of guard cells and coleoptile chloroplasts and the spectra for blue light-s
35 reception, indicates that the guard cell and coleoptile chloroplasts specialize in sensory transducti
36                                 In stems and coleoptiles, classic experiments showed that the peak re
37                                       During coleoptile development, changes in cell wall composition
38  upstream regions to drive gfp expression in coleoptiles, epicarps, and lemma/palea of developing spi
39 uggested that both control and auxin-treated coleoptiles exhibited Ca2+, and calmodulin-dependent pro
40        The rates of hydrolysis observed with coleoptile extracts were greater than those observed wit
41  is synthesized in vitro with isolated maize coleoptile Golgi membranes and the nucleotide-sugar subs
42 es induce sorghum (Sorghum bicolor var. Rio) coleoptile growth in 24-h incubations an average of 49%
43  synergistic reaction, yielding increases in coleoptile growth that average 295% above untreated cont
44 activity of the promoter was detected in the coleoptile, in the upper sheath section of the leaf, on
45 to reveal the mathematical principles of how coleoptiles integrate multiple stimuli over time.
46 ever, only XET action was observed in barley coleoptiles, leaves and roots (which all contained MLG)
47  leaf development also disrupt scutellum and coleoptile morphology, suggesting that these grass-speci
48 d by flotation centrifugation from etiolated coleoptiles of maize (Zea mays) and leaves of Arabidopsi
49 sheath cells) from ethanol:acetic acid-fixed coleoptiles of maize.
50 dependence of gravitropic responses of wheat coleoptiles on previous stimuli.
51 t essentially no indole-3-acetic acid to the coleoptile or primary leaves.
52 ositol nor IAA accumulates in the tip of the coleoptile or the mesocotyl node and thus these studies
53                          Red irradiation (of coleoptiles or extracts) sufficient to approach photocon
54 an action spectrum for blue light-stimulated coleoptile phototropism.
55                                    The cpt1 (coleoptile phototropism1) mutant, which lacks one of the
56 um prior to embryonic degeneration, but only coleoptile proliferation was observed.
57 -phytochrome immunoprecipitates of etiolated coleoptile proteins.
58 regions known from peptide sequencing of the coleoptile proteins.
59  cotyledon evolution where the scutellum and coleoptile, respectively, comprise the distal and proxim
60                  We quantitatively show that coleoptiles respond not only to sums but also to differe
61 rgan-specific differential expression in the coleoptile, root, leaf, and internode.
62 ranscript at roughly similar levels in maize coleoptiles, root meristems, and the zone of root elonga
63 mic changes in cell walls of etiolated maize coleoptiles, sampled at one-half-d intervals of growth,
64                                        Avena coleoptile sections were preincubated in either fusicocc
65 t a roughly constant velocity down a stem or coleoptile segment.
66 in phosphorylations in oat (Avena sativa L.) coleoptile segments were analyzed by sodium dodecyl sulf
67 horylation of both control and auxin-treated coleoptile segments.
68 e total RNA isolated from auxin-treated corn coleoptile segments.
69 ex: cereals produce additional organs like a coleoptile, seminal roots originating from the scutellar
70 deposition in fdl1-1 mutant seedlings at the coleoptile stage.
71 s observed in gravitropic responses of wheat coleoptiles, suggesting shoots may combine memory and mo
72 odel system, the elongating maize (Zea mays) coleoptile system, in which cell wall changes are well c
73 nd thus these studies do not explain how the coleoptile tip controls the amount of IAA in the shoot.
74  from Pima cotton (Gossypium barbadense) and coleoptile tips from corn (Zea mays).
75 wheat (Triticum aestivum cv Pennmore Winter) coleoptile (type II) walls, which showed only a negligib
76 us monocots, but was less effective on grass coleoptile walls.
77  oat (Avena sativa L.) tissues, the root and coleoptile, was compared.
78 ee sterol, whereas comparable amounts in the coleoptile were 42, 39, and 19 mole percent, respectivel
79 ls from embryonic, elongating, and senescent coleoptiles were broadly discriminated from each other b
80 longating shoot, gl-OXO is restricted to the coleoptile where it is detected only in the epidermal ce
81 ics of the germinating embryo and elongating coleoptile, which consequently enhances anaerobic germin
82 ied in both the initiating scutellum and the coleoptile, while mutations disrupting mediolateral leaf
83                                 Treatment of coleoptile with auxin for 1 hour resulted in no detectab