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1 cial APC, in a pattern we refer to as a 'CD2 corolla'.
2 ntral genes in an intermediary region of the corolla.
3 he M. lewisii flower, thus prepatterning the corolla.
4 al to the lateral and abaxial regions of the corolla.
5 ression analyses in different regions of the corolla.
6 es examined and could extend into sepals and corolla.
7 identity and are highly expressed in petunia corollas.
8 st-pollination ethylene synthesis in petunia corollas.
9 ight hours, paralleling PhCCD1 expression in corollas.
10  sensitivity and ABA accumulation in petunia corollas.
11                                          The corolla amplified active phosphorylated Src-family kinas
12  a role in specifying dorsal identity in the corolla and androecium of monosymmetric (bilateral) flow
13                 Engaged PD-1 invaded the CD2 corolla and buffered CD2-mediated amplification of TCR s
14  revealed that PhCCD1 is highly expressed in corollas and leaves, where it constitutes approximately
15 af petiole, flower and fruit pedicel, flower corolla, and fruit calyx.
16  such as the thickened calyx and sympetalous corolla, are ineffective in deterring orioles.
17 rioles target the zygomorphic trumpet-shaped corollas at the 11:00 h or 01:00 h positions with a clos
18                 CD2-CD58 interactions in the corolla boosted signaling by 77% as compared with centra
19          The capitulum constituents (stigma, corolla, bracts, pappus, and receptacle) of seven cardoo
20 as induced by pollination in both WT and IPT corollas, but this increase was delayed in IPT flowers.
21                                          The corolla captured engaged CD28, ICOS, CD226 and SLAM-F1 c
22  senescence, was significantly greater in WT corollas, confirming that floral senescence was delayed
23 sociation between mouthparts' length and the corolla depth of the visited flowers, thus favouring tra
24 ber of cell divisions that took place during corolla development.
25                                              Corolla diameter and corolla tube length were larger and
26    Such pleiotropic effects may underlie the corolla dimorphism frequently observed in gynodioecious
27          Flies and bees defecated inside the corolla (flower) more frequently than other plant locati
28 nd motifs in its cytoplasmic tail controlled corolla formation.
29 in floral design by scoring floral symmetry, corolla fusion, floral orientation and stamen number.
30 concentration of phenolic compounds, and the corolla had the greatest variety.
31  character states (bilateral symmetry, fused corollas, horizontal orientation and reduced stamen numb
32 espite seasonal pulses of flowers with short-corollas, hummingbirds consistently foraged on well-matc
33 ogies in both parties, and flowers with long corollas hypothesized to be pollinated only by individua
34 n emerging model featuring a bullseye on its corolla, is prepatterned as the bullseye boundary positi
35 gth and nectar consumption (fly benefit) and corolla length and pollen deposition (plant benefit).
36                            Selection between corolla length and proboscis length was reciprocal at th
37 the major driving force for the evolution of corolla length of R. purpurea and proboscis length of P.
38 loral display area, inflorescence height and corolla length of R. purpurea by comparing selection gra
39    Visitation also peaked at an intermediate corolla length, while its relationship to corolla width
40 hat (1) JA-Ile/COR-based signaling regulates corolla limb opening and a JA-negative feedback loop; (2
41 le-sterile flowers had significantly smaller corollas, longer styles and greater stigmatic exsertion
42        We studied hummingbird bill and plant corolla matching during seasonal variation in flower ava
43 lis purpurea shows rapid recent evolution of corolla morphology but not nectar traits following a ran
44                                          The corolla of F1-34-1 cultivar showed higher antihaemolytic
45                                          The corolla of F4-1-4 and F1-34-1 cultivars, and bracts of F
46                                          The corolla of flowering plants provides pivotal functions f
47 lling anthocyanin pigmentation in the entire corolla of M. lewisii and two R2R3-MYB genes, PELAN and
48 ate pathway to the synthesis of FVBPs in the corolla of Petunia x hybrida cv. 'Mitchell Diploid'.
49 76% decrease in beta-ionone synthesis in the corollas of selected petunia lines, indicating a signifi
50 t flower), which differs from Antirrhinum in corolla (petal) symmetry and pollination mode.
51 ned, such as floral phenology, display size, corolla pigment, and inflorescence height.
52 es to induce endogenous ethylene production, corolla senescence, and up-regulation of the senescence-
53    While most floral trait values, including corolla size and nectar, increased linearly with increas
54 at male sterility is associated with reduced corolla size.
55 lor, in addition to nectar concentration and corolla size.
56 or two dimensional traits, pistil length and corolla size.
57 ve but may not correlate with transitions in corolla symmetry.
58 ike genes are thought to affect evolution of corolla symmetry.
59 ed via changes to multiple components of the corolla that are only recognised in geometric morphometr
60  duet for the main function of a sympetalous corolla, that of advertising for and rewarding pollinato
61  white region (i.e., light areas) around the corolla throat of M. lewisii flowers by diverting dihydr
62 70%, and total chorismate mutase activity in corolla tissue is reduced by 80-85% compared to control
63 lls within the ventral petal which adapt the corolla to specialised functions in pollination.
64  we focus on petals, which together form the corolla, to examine the mechanisms patterning floral sur
65                  The various elaborations of corolla tube attributes, such as length, width and curva
66 e genetic and developmental control of these corolla tube attributes.
67                            Different axes of corolla tube complexity can be disentangled at the devel
68 me, the Petunia axillaris fused and proximal corolla tube expresses several genes that in A. thaliana
69                    Developmental genetics of corolla tube formation and elaboration 697 VI.
70 entation patterns, developmental genetics of corolla tube formation and elaboration, and the molecula
71                                              Corolla tube length and anther filament length were larg
72 g linear selection imposed by pollinators on corolla tube length at all sites, but there was no consi
73                                        Local corolla tube length was correlated with local fly probos
74                         Corolla diameter and corolla tube length were larger and pollen total nitroge
75 idy on floral morphology in Nicotiana, using corolla tube measurements and geometric morphometrics to
76 loral traits (e.g., carotenoid pigmentation, corolla tube structure, nectar volume, pistil and stamen
77 ulus lewisii, with a substantial decrease in corolla tube width but no change in tube length.
78 s also located in the inner epidermis of the corolla tube with little BAMT protein detected in the ou
79  three functions: trichome production in the corolla tube, conical cell development in the petal hing
80  and between lower and upper portions of the corolla tube, defined by the stamen insertion boundary.
81 ies produce flowers with petals fused into a corolla tube.
82 small pollen from anthers located within the corolla tube.
83             Pollination of flowers with long corolla tubes by long-tongued hawkmoths has been invoked
84 s and is the sole pollinator of a plant with corolla tubes of matching length.
85  polyploids tend to evolve shorter and wider corolla tubes, suggesting that allopolyploidy could prov
86  pollinators specialize on flowers with deep corolla tubes, whereas shorter-tongued pollinators gener
87 ctar traits, and the proximal section of the corolla, which regulates access to nectar and underwent
88 te corolla length, while its relationship to corolla width varied across sites.
89 rect effects and vice versa for the trait of corolla width, which may be due, at least in part, to th
90 ls are only known as flowers, more precisely corollas with stamens and styles.
91 henylethyl benzoate, both present in petunia corollas, with similar catalytic efficiencies.
92 CYC2-like genes correlate with the origin of corolla zygomorphy are poorly understood.
93 YC2-like genes correlates with the origin of corolla zygomorphy.
94 es are probably crucial for the evolution of corolla zygomorphy.