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1 t to report on carotenoid composition of the aleurone layer.
2 age oil is a major constituent in the cereal aleurone layer.
3 L gene, OsCBL2, is up-regulated by GA in the aleurone layer.
4  and in the amount of ions released from the aleurone layer.
5 sis and the endosperm is chalky and lacks an aleurone layer.
6 d phytate is inhibited by cPrG in GA-treated aleurone layers.
7 ssion have been previously defined in barley aleurone layers.
8 on of GA-inducible gene expression in cereal aleurone layers.
9 detected in spikes and nodes, but not in the aleurone layers.
10 at shock proteins, decreased in heat-shocked aleurone layers.
11 ransposon lines identified the supernumerary aleurone layers 1-1 (sal1-1) mutant line carrying up to
12 riched in palmitic acid, while the seed coat/aleurone layer accumulated vaccenic, linoleic, and alpha
13 perm would affect the development of the two aleurone layers along the fusion plane.
14 present to different degrees in the maturing aleurone layer and embryo, but not in the starchy endosp
15 e, Cu, and Zn were mainly accumulated in the aleurone layer and embryo.
16 utermost cells, which differentiate into the aleurone layer and remain living in the mature seed.
17 t the Ca and Mn were mainly localized in the aleurone layer and scutellum.
18  measured, and these data show that both the aleurone layer and the embryo expressed the NO-associate
19  with whole seed compartments: the scutellar aleurone layer and the newly named endosperm adjacent to
20  the level of its mRNA readily detectable in aleurone layers and embryos, yet undetectable in the sta
21 show that cPrG prevents PSV acidification in aleurone layers and prevents synthesis of secretory prot
22 from that of anthocyanins synthesized in the aleurone layer, and that those in the germ could increas
23                When barley (Hordeum vulgare) aleurone layers are subjected to heat shock there is a s
24 general and emphasize the versatility of the aleurone layer as a model system for studying plant prot
25 istically to regulate gluconeogenesis in the aleurone layer as well as controlling the production and
26  repressible mRNA persists in the mature dry aleurone layer, but is degraded during imbibition, reple
27 rotein secretion in gibberellic acid-induced aleurone layers by two independent mechanisms, heat shoc
28 of gene constructs were introduced to barley aleurone layers by using particle bombardment: the repor
29                                          The aleurone layer had zeaxanthin levels 2- to 5-fold higher
30       Incubation of barley (Hordeum vulgare) aleurone layers in H2O2 causes rapid death of all cells
31 demonstrated that cycloheximide treatment of aleurone layers increased mRNA levels 4-fold, whereas a
32                  Mutant kernels have several aleurone layers instead of one, indicating that Xcl1 alt
33                                   The cereal aleurone layer is a model system for studying the regula
34                                   The barley aleurone layer is a terminally differentiated secretory
35 ugh cPrG blocks many GA-induced responses of aleurone layers, it does not affect early steps in GA si
36                     Barley (Hordeum vulgare) aleurone layers maintained in vitro respond to gibberell
37 as normal maize (Zea mays [Zm]) has a single aleurone layer, naked endosperm (nkd) mutants produce mu
38                         The maize (Zea mays) aleurone layer occupies the single outermost layer of th
39 ted close correlation between embryo and the aleurone layer of endosperm.
40 ion in embryos, as well as the scutellum and aleurone layer of germinating seeds.
41                           Development of the aleurone layer of maize grains requires the activity of
42 uctive surface chemistry spectroscopy of the aleurone layer of pigmented rice integrated with ML mode
43 dlings, vascular tissue of nodes, embryo and aleurone layer of seeds, and young flowers.
44 b mRNA occurred in the starchy endosperm and aleurone layer of the developing seed, but not in the em
45 ost b alleles in that it is expressed in the aleurone layer of the seed.
46 eds lacking the testa, embryos, and isolated aleurone layers of Arabidopsis (Arabidopsis thaliana) we
47  suppression of genes has been determined in aleurone layers of barley seeds.
48 sion of genes, such as alpha-amylase, in the aleurone layers of cereals.
49 en germination is triggered or when isolated aleurone layers or protoplasts are incubated in gibberel
50                                Incubation of aleurone layers or protoplasts in H(2)O(2)-containing me
51 revent DNA degradation during isolation from aleurone layers or protoplasts.
52 lecular changes that occurred in embryos and aleurone layers prior to germination were measured, and
53  fluorescent probe, Hordeum vulgare (barley) aleurone layers produce NO rapidly when nitrite is added
54 ysis identified 73 glycosylation sites in 65 aleurone layer proteins, with 53 of the glycoproteins fo
55 er of starchy endosperm cells underneath the aleurone layer showed transformed cells.
56                                    In barley aleurone layers, the expression of genes encoding alpha-
57 ncreased Zn was broadly distributed from the aleurone layer to the inner endosperm.
58 2 mRNA decline rapidly following exposure of aleurone layers to GA.
59 ide dismutase are strongly down-regulated in aleurone layers treated with GA.
60                                          The aleurone layer was found to be the primary determinant o
61 contrast, MT4 was confined to the embryo and aleurone layer, where it appeared during tissue speciali
62         Among those yet to be studied is the aleurone layer, which produces hydrolases for mobilizati
63 RNA under anoxic conditions was decreased in aleurone layers while it increased in the embryo.
64 ed; this gene and the gene encoding the seed aleurone-layer xylanase had strict tissue-specific expre
65 ces of many microbial xylanases and a barley aleurone-layer xylanase.