戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 lly used for targeted mutagenesis in several dicotyledonous and few monocotyledonous plants.
2                               In most NAS of dicotyledonous and monocotyledonous plants (class Ia and
3 nd regeneration is widely applicable to both dicotyledonous and monocotyledonous plants, especially t
4 A to a wide variety of hosts, including both dicotyledonous and monocotyledonous plants.
5           Thus, nitrate assimilation in both dicotyledonous and monocotyledonous species depends on p
6  is a load-bearing primary wall component in dicotyledonous and non-graminaceous monocotyledonous pla
7                  P-proteins are found in all dicotyledonous and some monocotyledonous plants, but add
8 , including representatives of the mono- and dicotyledonous angiosperms, gymnosperms, and bryophytes,
9 pecies, putative homologs were identified in dicotyledonous angiosperms, gymnosperms, and other plant
10 ly functional in partially immunocompromised dicotyledonous Arabidopsis thaliana against the barley p
11 ein-coding genes, which is 28% less than the dicotyledonous Arabidopsis thaliana and 50% less than mo
12 maize (Zea mays L.) was transferred into the dicotyledonous Brassica napus L. using Agrobacterium-med
13  Orthologous genes from monocotyledonous and dicotyledonous C(3) species also contained conserved reg
14            In leaves of Flaveria bidentis, a dicotyledonous C4 plant, ribulose 1,5-bisphosphate carbo
15 ago during the early divergence of mono- and dicotyledonous clades.
16 ck in applying virus-induced gene editing to dicotyledonous crops such as tomato and reduces the depe
17  from fatty acids, are found in a variety of dicotyledonous families.
18 rly seed development in monocotyledonous and dicotyledonous flowering plants.
19 the evolution of the C4-associated CA in the dicotyledonous genus Flaveria, although the actual mutat
20 ons of proteins in a variety of experimental dicotyledonous hosts.
21  CO(2) diffusion over short distances inside dicotyledonous leaves can be important to photosynthesis
22 idization event that is conserved across the dicotyledonous lineage.
23 we describe a new experimental system in the dicotyledonous model plant tobacco (Nicotiana tabacum) t
24 oth a monocotylonous plant (Poa annua) and a dicotyledonous plant (Arabidopsis [Arabidopsis thaliana]
25 CCaMK from monocotyledonous plant (lily) and dicotyledonous plant (tobacco) suggests that the autopho
26 the shoot apical region of the embryo of the dicotyledonous plant Arabidopsis thaliana using spontane
27 nsferase activity in Arabidopsis thaliana, a dicotyledonous plant of the mustard family.
28 ng a comparative genomics approach with four dicotyledonous plant species (Arabidopsis thaliana, papa
29  potentials, and SPs in monocotyledonous and dicotyledonous plant species (Hordeum vulgare, Vicia fab
30 m buckwheat (Fagopyrum esculentum Moench), a dicotyledonous plant species belonging to the Polygonace
31                          In amaranth, a C(4) dicotyledonous plant, the plastid rbcL gene (encoding th
32 c and inducible expression in a heterologous dicotyledonous plant.
33 t woody shells - the hardest tissues made by dicotyledonous plants - cause very minor damage to ename
34 tefly-transmitted ss-DNA viruses that infect dicotyledonous plants and contribute to major economic l
35 -proteins found in the sieve elements of all dicotyledonous plants and demonstrate the exceptional st
36 e in the primary cell walls of most vascular dicotyledonous plants and has important structural and p
37     Secondary walls in vessels and fibers of dicotyledonous plants are mainly composed of cellulose,
38                                           In dicotyledonous plants broad-spectrum resistance to patho
39 hogen that causes crown gall disease in many dicotyledonous plants by transfer of a portion of its tu
40                                     Stems of dicotyledonous plants consist of an outer epidermis, a c
41                                              Dicotyledonous plants express a type of NLR known as TIR
42                                              Dicotyledonous plants growing under limited iron availab
43                             UAS from several dicotyledonous plants has been characterized; however, i
44 ctures of the apical and floral meristems in dicotyledonous plants have been well described, little i
45                                              Dicotyledonous plants normally have three distinct layer
46                                      Because dicotyledonous plants only transport ferrous iron, we ch
47                                              Dicotyledonous plants possess three phage-type RNAPs, RP
48 s, which has not been observed previously in dicotyledonous plants such as Arabidopsis (Arabidopsis t
49 s and gene networks regulated by LEC1 in two dicotyledonous plants that diverged approximately 92 Mya
50 e report two methods to generate gene-edited dicotyledonous plants through de novo meristem induction
51 d at high levels and that their orthologs in dicotyledonous plants would be expressed at much lower l
52 abase of 40,512 orthologous intron groups of dicotyledonous plants, 28,519 orthologous intron groups
53  concentrations of dNTs in several mono- and dicotyledonous plants, a bryophyte, and three algae, rev
54 erified coumaric acid compared with those of dicotyledonous plants, and PAL from grasses can also pos
55 identify P3, found to date only in mono- and dicotyledonous plants, as an evolutionarily distinct P-p
56 on of flowering time in monocotyledonous and dicotyledonous plants, but also unveil roles in the deve
57 rabidopsis (Arabidopsis thaliana), like most dicotyledonous plants, expresses a multicomponent, heter
58  the principal load-bearing hemicellulose of dicotyledonous plants, has a terminal fucosyl residue.
59                                           In dicotyledonous plants, hypocotyl folds to form hooks aft
60 in that causes necrosis when applied to many dicotyledonous plants, including invasive weed species.
61 gene expression in both monocotyledonous and dicotyledonous plants, pointing to a potential for explo
62                                           In dicotyledonous plants, such as Nicotinana tabacum (tobac
63 roteins in a variety of monocotyledonous and dicotyledonous plants, suggesting broad utility for the
64 Rubiaceae family in the euasterid I clade of dicotyledonous plants, to which the Solanaceae family al
65 ole-5-one (MIO) domain compared with that of dicotyledonous plants.
66 exa is a stem holoparasite that infests most dicotyledonous plants.
67 LS2) and activate MAMP-triggered immunity in dicotyledonous plants.
68 umulation in vegetative tissues of different dicotyledonous plants.
69  new iron transport system may be generic to dicotyledonous plants.
70  important group of seed storage proteins in dicotyledonous plants.
71 llulose present in the primary cell walls of dicotyledonous plants.
72 ent biological functions of AP2 orthologs in dicotyledonous plants.
73 nalysis of two powdery mildews pathogenic on dicotyledonous plants.
74 e parenchymatous nature of the pith cells in dicotyledonous plants.
75 A) from its tumor-inducing (Ti) plasmid into dicotyledonous plants.
76  wide variety of transformation recalcitrant dicotyledonous plants.
77 genic elements to efficiently transform most dicotyledonous plants.
78 e arguably the most devastating pathogens of dicotyledonous plants.
79 n), from 4 other Glycine species, and across dicotyledonous plants.
80 nically related proteins are present in many dicotyledonous plants.
81 oteins (R proteins) in Arabidopsis and other dicotyledonous plants.
82 ble in sequence since the early radiation of dicotyledonous plants.
83 ins of C(4) photosynthetic mechanisms within dicotyledonous plants.
84  the regulation of growth and development of dicotyledonous plants.
85 ic developmental juncture is the response of dicotyledonous seedlings to light.
86 e atlases for two independently evolved C(4) dicotyledonous species - Gynandropsis gynandra (NAD-mali
87 ch has not been widely adopted for the model dicotyledonous species Arabidopsis (Arabidopsis thaliana
88 organic ions in recently mature leaves of 45 dicotyledonous species at midafternoon.
89                            Experiments on 45 dicotyledonous species identified the predicted loading
90 thesis that reduced root secondary growth of dicotyledonous species improves phosphorus acquisition.
91 ea mays, with Arabidopsis thaliana and other dicotyledonous species reveals that the CesA genes clust
92 ces was substantial and very similar in five dicotyledonous species with different vascular anatomies
93 r to Solanum lycopersicon (tomato) and other dicotyledonous species yet distinct from the monocotyled
94 ter-selectable genes have been tested in six dicotyledonous species, whereas there are no data availa
95 Da acetylatable protein is only found in the dicotyledonous species, while all plant species tested c
96 alues in gymnosperms are similar to those of dicotyledonous species.
97 ocotyledonous species, -107 per thousand for dicotyledonous species.
98 gene function is conserved between mono- and dicotyledonous species.
99 ne expression and disease resistance in many dicotyledonous species.
100 e of methylomes in both monocotyledonous and dicotyledonous species.
101 research has suggested that the epidermis of dicotyledonous stems is the primary site of auxin action
102 rmis is not the sole site of auxin action in dicotyledonous stems.
103 a universal gene silencing mechanism both in dicotyledonous tobacco plants and monocotyledonous rice
104 uced bleaching of new growth on a variety of dicotyledonous weeds and was a potent inhibitor of Arabi
105 s, is currently marketed as racemate against dicotyledonous weeds in cereals.
106 icide currently marketed as racemate against dicotyledonous weeds in cereals.

 
Page Top