ライフサイエンスコーパス: aleurone layer

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 at shock proteins, decreased in heat-shocked aleurone layers.

10 ransposon lines identified the supernumerary aleurone layers 1-1 (sal1-1) mutant line carrying up to

11 riched in palmitic acid, while the seed coat/aleurone layer accumulated vaccenic, linoleic, and alpha

12 perm would affect the development of the two aleurone layers along the fusion plane.

13 present to different degrees in the maturing aleurone layer and embryo, but not in the starchy endosp

14 utermost cells, which differentiate into the aleurone layer and remain living in the mature seed.

15 measured, and these data show that both the aleurone layer and the embryo expressed the NO-associate

16 the level of its mRNA readily detectable in aleurone layers and embryos, yet undetectable in the sta

17 show that cPrG prevents PSV acidification in aleurone layers and prevents synthesis of secretory prot

18 When barley (Hordeum vulgare) aleurone layers are subjected to heat shock there is a s

19 general and emphasize the versatility of the aleurone layer as a model system for studying plant prot

20 istically to regulate gluconeogenesis in the aleurone layer as well as controlling the production and

21 repressible mRNA persists in the mature dry aleurone layer, but is degraded during imbibition, reple

22 rotein secretion in gibberellic acid-induced aleurone layers by two independent mechanisms, heat shoc

23 of gene constructs were introduced to barley aleurone layers by using particle bombardment: the repor

24 The aleurone layer had zeaxanthin levels 2- to 5-fold higher

25 Incubation of barley (Hordeum vulgare) aleurone layers in H2O2 causes rapid death of all cells

26 demonstrated that cycloheximide treatment of aleurone layers increased mRNA levels 4-fold, whereas a

27 Mutant kernels have several aleurone layers instead of one, indicating that Xcl1 alt

28 The cereal aleurone layer is a model system for studying the regula

29 The barley aleurone layer is a terminally differentiated secretory

30 ugh cPrG blocks many GA-induced responses of aleurone layers, it does not affect early steps in GA si

31 Barley (Hordeum vulgare) aleurone layers maintained in vitro respond to gibberell

32 as normal maize (Zea mays [Zm]) has a single aleurone layer, naked endosperm (nkd) mutants produce mu

33 The maize (Zea mays) aleurone layer occupies the single outermost layer of th

34 ted close correlation between embryo and the aleurone layer of endosperm.

35 Development of the aleurone layer of maize grains requires the activity of

36 dlings, vascular tissue of nodes, embryo and aleurone layer of seeds, and young flowers.

37 b mRNA occurred in the starchy endosperm and aleurone layer of the developing seed, but not in the em

38 ost b alleles in that it is expressed in the aleurone layer of the seed.

39 eds lacking the testa, embryos, and isolated aleurone layers of Arabidopsis (Arabidopsis thaliana) we

40 suppression of genes has been determined in aleurone layers of barley seeds.

41 sion of genes, such as alpha-amylase, in the aleurone layers of cereals.

42 en germination is triggered or when isolated aleurone layers or protoplasts are incubated in gibberel

43 Incubation of aleurone layers or protoplasts in H(2)O(2)-containing me

44 revent DNA degradation during isolation from aleurone layers or protoplasts.

45 lecular changes that occurred in embryos and aleurone layers prior to germination were measured, and

46 fluorescent probe, Hordeum vulgare (barley) aleurone layers produce NO rapidly when nitrite is added

47 ysis identified 73 glycosylation sites in 65 aleurone layer proteins, with 53 of the glycoproteins fo

48 er of starchy endosperm cells underneath the aleurone layer showed transformed cells.

49 In barley aleurone layers, the expression of genes encoding alpha-

50 2 mRNA decline rapidly following exposure of aleurone layers to GA.

51 ide dismutase are strongly down-regulated in aleurone layers treated with GA.

52 The aleurone layer was found to be the primary determinant o

53 contrast, MT4 was confined to the embryo and aleurone layer, where it appeared during tissue speciali

54 Among those yet to be studied is the aleurone layer, which produces hydrolases for mobilizati

55 RNA under anoxic conditions was decreased in aleurone layers while it increased in the embryo.

56 ed; this gene and the gene encoding the seed aleurone-layer xylanase had strict tissue-specific expre

57 ces of many microbial xylanases and a barley aleurone-layer xylanase.