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1 dling roots, developing spikes, and pericarp/testa.
2 ng to the genotype of the maternally derived testa.
3 g a lineage dependence in development of the testa.
4 tterns, e.g., in the cotyledons, radicle, or testa.
5 haliana MYB transcription factor TRANSPARENT TESTA 2 (TT2) in Medicago trunculata hairy roots induces
6    Expression of the Arabidopsis TRANSPARENT TESTA 2 (TT2) MYB family transcription factor leads to m
7 e and chalcone isomerase mutant (transparent testa 5, tt5) seedlings grown under anthocyanin inductiv
8 lated dark pigment in the cell layers of the testa above the endothelium, which itself accumulated pr
9  proteins include a family of proteins named TESTA ABUNDANT1 (TBA1) to TBA3; a less abundant fourth h
10 ed coat-specific promoters from three genes, TESTA-ABUNDANT2 (TBA2), PEROXIDASE36 (PER36), and MUCILA
11                    The toughening of the bks testa and associated poor germination were partially ove
12            By focusing on the stages between testa and endosperm rupture, we were able to circumvent
13 chanical restraints impeded the expansion of testa and endosperm, resulting in the embryo's deformati
14 ot proximity to maternal tissues such as the testa and pericarp are important for aleurone developmen
15 nibs and subsequent outward migration to the testa and the incubation solution.
16 er antioxidant activity than those with pale testa, and a positive correlation was found between tota
17  similar, with a round shape, a disorganized testa, and viviparism.
18 perm rupture, we were able to circumvent the testa barrier to the GUS substrate and observe diverse t
19  polar and non-polar metabolome of the cocoa testa (cocoa shell) and the cocoa cotyledons (cocoa nibs
20 Bio- and physicochemical analysis of the bks testa determined that it accumulated a melanic substance
21               Whole seeds, seeds lacking the testa, embryos, and isolated aleurone layers of Arabidop
22 h revealed that different seed compartments (testa, endosperm, and embryo) control germination, but l
23 g seedling epidermal patterning, TRANSPARENT TESTA GLABRA (TTG) and WEREWOLF (WER), also control the
24 RHF induced by auxin in rhd6 and transparent testa glabra (ttg) mutants.
25 kers lutescens (lu; 17.6 cM) and transparent testa glabra (ttg; 35.5 cM) on the top arm of Arabidopsi
26                       Five loci (TRANSPARENT TESTA GLABRA [TTG], GLABRA2 [GL2], ROOT HAIR DEFECTIVE6
27  (Petunia hybrida [petunia]) and TRANSPARENT TESTA GLABRA1 (TTG1) (Arabidopsis thaliana).
28 om petunia (Petunia hybrida) and TRANSPARENT TESTA GLABRA1 (TTG1) from Arabidopsis thaliana and assoc
29                              The TRANSPARENT TESTA GLABRA1 (TTG1) locus regulates several development
30                     Mutations in TRANSPARENT TESTA GLABRA1 (TTG1) result in several pleiotropic defec
31 tors, and a WD40 repeat protein, TRANSPARENT TESTA GLABRA1 (TTG1), act in concert to activate trichom
32 f the trichome promoting factors TRANSPARENT TESTA GLABRA1 (TTG1), GLABRA3 (GL3)/ENHANCER OF GL3 (EGL
33  (GL1; R2R3MYB), GL3 (bHLH), and transparent TESTA GLABRA1 (TTG1; WD40).
34 of trichome development, GL3 and TRANSPARENT TESTA GLABRA1, also impaired cuticle development and SAR
35 ranscriptional regulators MYB12, Transparent Testa Glabra1, and Production of Anthocyanin Pigment aft
36 3 (GL3)/ENHANCER OF GLABRA3, and TRANSPARENT TESTA GLABRA1.
37  the promoters of GLABRA2 (GL2), TRANSPARENT TESTA GLABRA2 (TTG2), CAPRICE (CPC) and ENHANCER OF TRIP
38 eles for endosperm growth factor transparent testa glabra2 and HAIKU1 and defense response regulators
39 t epidermal transcriptome of the transparent testa glabra2 mutant to clarify its role in the network.
40  of both the GLABROUS1 (GL1) and TRANSPARENT TESTA GLABROUS (TTG) genes.
41 abidopsis (Arabidopsis thaliana) transparent testa glabrous1 mutant.
42  of hyphae was observed between the husk and testa layer of barley after germination than raw barley
43 production in specialized cells of the outer testa layer.
44  successively after G lignin within the same testa layers, concurrently with apparent loss of the fun
45 C analyses revealed that several transparent testa lines blocked at intermediate steps of the flavono
46                       This suggests that the testa manufactures components before its demise that can
47 yo produces factors that are conveyed to the testa, mitigating this process.
48 ion pattern was also examined in transparent testa mutants blocked at different steps in the flavonoi
49 ny of the 13 flavonoid-deficient transparent testa mutants for which a map position is known.
50                              The transparent testa mutants were shown to have precursor accumulation
51 n biosynthetic pathways were analyzed in the testa of nine pecan cultivars using liquid chromatograph
52 tannins (proanthocyanidins) in the pigmented testa of some sorghum cultivars have been implicated in
53 gasse, and liquid extract of the pseudofruit testa) of cashew nut (Anacardium occidentale L.) were ch
54 oid pigment production in cells of the inner testa (or seed coat) layer and mucilage production in sp
55                            Samples with dark testa (or seed coat), namely black lentils and diavoli b
56 tment of seeds with PME resulted in enhanced testa permeability and promoted TR.
57 nsparent testa15 and displayed a transparent testa phenotype and a reduction in seed size.
58 hi mutant restores the seed coat transparent testa phenotype and the accumulation of flavonoids.
59 osynthesis is TT2, named for the transparent testa phenotype of tt2 mutant seeds that lack PAs in the
60        Mttt8 mutant seeds have a transparent testa phenotype with reduced PAs and anthocyanins.
61 mulation, but did not rescue the transparent testa phenotype, confirming that CsGSTF1 did not functio
62  in pulp, bagasse, and liquid extract of the testa, respectively.
63 some point inhibited by its contact with the testa, resulting in its formation of folds and borders.
64 atterns indicated a role for PME activity in testa rupture (TR).
65 a), PME activities peaked around the time of testa rupture but declined just before the completion of
66 mination, which was not connected to altered testa rupture morphology but to alterations of the micro
67    The ungerminated knockout seeds exhibited testa rupture, but failed to penetrate the endosperm lay
68                      This increases again at testa rupture, the start of the second transcriptional p
69 ses during germination that are separated by testa rupture.
70                     The Arabidopsis aberrant testa shape (ats) mutant produces a single integument in
71  that involves transcription factor ABERRANT TESTA SHAPE (ATS).
72 g ovule development, independent of ABERRANT TESTA SHAPE (ATS, also known as KANADI4) activity.
73                                     ABERRANT TESTA SHAPE (ATS, or KAN4) is necessary during ovule dev
74 ing the KANADI transcription factor ABERRANT TESTA SHAPE.
75 mponents before its demise that can maximize testa strength, whereas the endosperm/embryo produces fa
76 is probably due to the impermeability of the testa to the GUS substrate.
77                 Mutations in the transparent testa (tt) loci abolish pigment production in Arabidopsi
78 HA10 result in seed coats with a transparent testa (tt) phenotype (light-colored seeds).
79  by comparing wild-type (WT) and transparent testa (tt4) plants with a mutation in the gene encoding