ライフサイエンスコーパス: dicotyledonous

1 nd regeneration is widely applicable to both dicotyledonous and monocotyledonous plants, especially t

2 A to a wide variety of hosts, including both dicotyledonous and monocotyledonous plants.

3 Thus, nitrate assimilation in both dicotyledonous and monocotyledonous species depends on p

4 is a load-bearing primary wall component in dicotyledonous and non-graminaceous monocotyledonous pla

5 P-proteins are found in all dicotyledonous and some monocotyledonous plants, but add

6 , including representatives of the mono- and dicotyledonous angiosperms, gymnosperms, and bryophytes,

7 pecies, putative homologs were identified in dicotyledonous angiosperms, gymnosperms, and other plant

8 ly functional in partially immunocompromised dicotyledonous Arabidopsis thaliana against the barley p

9 ein-coding genes, which is 28% less than the dicotyledonous Arabidopsis thaliana and 50% less than mo

10 maize (Zea mays L.) was transferred into the dicotyledonous Brassica napus L. using Agrobacterium-med

11 Orthologous genes from monocotyledonous and dicotyledonous C(3) species also contained conserved reg

12 In leaves of Flaveria bidentis, a dicotyledonous C4 plant, ribulose 1,5-bisphosphate carbo

13 from fatty acids, are found in a variety of dicotyledonous families.

14 rly seed development in monocotyledonous and dicotyledonous flowering plants.

15 the evolution of the C4-associated CA in the dicotyledonous genus Flaveria, although the actual mutat

16 ons of proteins in a variety of experimental dicotyledonous hosts.

17 CO(2) diffusion over short distances inside dicotyledonous leaves can be important to photosynthesis

18 idization event that is conserved across the dicotyledonous lineage.

19 oth a monocotylonous plant (Poa annua) and a dicotyledonous plant (Arabidopsis [Arabidopsis thaliana]

20 CCaMK from monocotyledonous plant (lily) and dicotyledonous plant (tobacco) suggests that the autopho

21 the shoot apical region of the embryo of the dicotyledonous plant Arabidopsis thaliana using spontane

22 nsferase activity in Arabidopsis thaliana, a dicotyledonous plant of the mustard family.

23 ng a comparative genomics approach with four dicotyledonous plant species (Arabidopsis thaliana, papa

24 potentials, and SPs in monocotyledonous and dicotyledonous plant species (Hordeum vulgare, Vicia fab

25 m buckwheat (Fagopyrum esculentum Moench), a dicotyledonous plant species belonging to the Polygonace

26 In amaranth, a C(4) dicotyledonous plant, the plastid rbcL gene (encoding th

27 c and inducible expression in a heterologous dicotyledonous plant.

28 -proteins found in the sieve elements of all dicotyledonous plants and demonstrate the exceptional st

29 e in the primary cell walls of most vascular dicotyledonous plants and has important structural and p

30 Secondary walls in vessels and fibers of dicotyledonous plants are mainly composed of cellulose,

31 In dicotyledonous plants broad-spectrum resistance to patho

32 hogen that causes crown gall disease in many dicotyledonous plants by transfer of a portion of its tu

33 Stems of dicotyledonous plants consist of an outer epidermis, a c

34 Dicotyledonous plants growing under limited iron availab

35 UAS from several dicotyledonous plants has been characterized; however, i

36 ctures of the apical and floral meristems in dicotyledonous plants have been well described, little i

37 Dicotyledonous plants normally have three distinct layer

38 Because dicotyledonous plants only transport ferrous iron, we ch

39 Dicotyledonous plants possess three phage-type RNAPs, RP

40 s, which has not been observed previously in dicotyledonous plants such as Arabidopsis (Arabidopsis t

41 s and gene networks regulated by LEC1 in two dicotyledonous plants that diverged approximately 92 Mya

42 d at high levels and that their orthologs in dicotyledonous plants would be expressed at much lower l

43 abase of 40,512 orthologous intron groups of dicotyledonous plants, 28,519 orthologous intron groups

44 erified coumaric acid compared with those of dicotyledonous plants, and PAL from grasses can also pos

45 identify P3, found to date only in mono- and dicotyledonous plants, as an evolutionarily distinct P-p

46 the principal load-bearing hemicellulose of dicotyledonous plants, has a terminal fucosyl residue.

47 in that causes necrosis when applied to many dicotyledonous plants, including invasive weed species.

48 gene expression in both monocotyledonous and dicotyledonous plants, pointing to a potential for explo

49 In dicotyledonous plants, such as Nicotinana tabacum (tobac

50 roteins in a variety of monocotyledonous and dicotyledonous plants, suggesting broad utility for the

51 Rubiaceae family in the euasterid I clade of dicotyledonous plants, to which the Solanaceae family al

52 exa is a stem holoparasite that infests most dicotyledonous plants.

53 LS2) and activate MAMP-triggered immunity in dicotyledonous plants.

54 umulation in vegetative tissues of different dicotyledonous plants.

55 new iron transport system may be generic to dicotyledonous plants.

56 important group of seed storage proteins in dicotyledonous plants.

57 llulose present in the primary cell walls of dicotyledonous plants.

58 ent biological functions of AP2 orthologs in dicotyledonous plants.

59 nalysis of two powdery mildews pathogenic on dicotyledonous plants.

60 e parenchymatous nature of the pith cells in dicotyledonous plants.

61 ole-5-one (MIO) domain compared with that of dicotyledonous plants.

62 A) from its tumor-inducing (Ti) plasmid into dicotyledonous plants.

63 wide variety of transformation recalcitrant dicotyledonous plants.

64 genic elements to efficiently transform most dicotyledonous plants.

65 e arguably the most devastating pathogens of dicotyledonous plants.

66 n), from 4 other Glycine species, and across dicotyledonous plants.

67 nically related proteins are present in many dicotyledonous plants.

68 oteins (R proteins) in Arabidopsis and other dicotyledonous plants.

69 ble in sequence since the early radiation of dicotyledonous plants.

70 ins of C(4) photosynthetic mechanisms within dicotyledonous plants.

71 the regulation of growth and development of dicotyledonous plants.

72 ic developmental juncture is the response of dicotyledonous seedlings to light.

73 ch has not been widely adopted for the model dicotyledonous species Arabidopsis (Arabidopsis thaliana

74 organic ions in recently mature leaves of 45 dicotyledonous species at midafternoon.

75 Experiments on 45 dicotyledonous species identified the predicted loading

76 thesis that reduced root secondary growth of dicotyledonous species improves phosphorus acquisition.

77 ea mays, with Arabidopsis thaliana and other dicotyledonous species reveals that the CesA genes clust

78 ces was substantial and very similar in five dicotyledonous species with different vascular anatomies

79 r to Solanum lycopersicon (tomato) and other dicotyledonous species yet distinct from the monocotyled

80 ter-selectable genes have been tested in six dicotyledonous species, whereas there are no data availa

81 Da acetylatable protein is only found in the dicotyledonous species, while all plant species tested c

82 gene function is conserved between mono- and dicotyledonous species.

83 ne expression and disease resistance in many dicotyledonous species.

84 alues in gymnosperms are similar to those of dicotyledonous species.

85 ocotyledonous species, -107 per thousand for dicotyledonous species.

86 research has suggested that the epidermis of dicotyledonous stems is the primary site of auxin action

87 rmis is not the sole site of auxin action in dicotyledonous stems.

88 a universal gene silencing mechanism both in dicotyledonous tobacco plants and monocotyledonous rice

89 uced bleaching of new growth on a variety of dicotyledonous weeds and was a potent inhibitor of Arabi

90 s, is currently marketed as racemate against dicotyledonous weeds in cereals.

91 icide currently marketed as racemate against dicotyledonous weeds in cereals.