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 l processing structure of bumblebees (Bombus impatiens).
2 fera), and common eastern bumblebees (Bombus impatiens).
3 terminal flowering and floral determinacy in Impatiens.
4 perms, the rosid Arabidopsis and the asterid Impatiens.
5 ufficient to specify meristem determinacy in Impatiens.
6 el for the action of organ identity genes in Impatiens.
7 re diffuse boundaries between organ types in Impatiens.
8 d the obligately eusocial bumble bee, Bombus impatiens.
9  size patterns for pathogen prevalence in B. impatiens.
10  Mimulus parishii attract bumblebees (Bombus impatiens), a pollinator not attracted to either of the
11                                              Impatiens, a genus of the Ericales, includes species wit
12 tinoid (imidacloprid) on bumblebees' (Bombus impatiens) ability to learn associations with visual sti
13       Here, we show that bumble bees (Bombus impatiens) account for the reliability of personally acq
14 d how these traits affect bumble bee (Bombus impatiens, an important cucumber pollinator) visitation
15 million years ago, the North American Bombus impatiens and European Bombus terrestris.
16 d strong resistance to the dipteran Bradysia impatiens and the fungus Alternaria brassicicola.
17 e bacteria in wild bumblebee workers (Bombus impatiens) and conducted laboratory experiments with gno
18                        Terminal flowering in Impatiens appears therefore to be controlled by a pathwa
19                   Flowering and reversion in Impatiens are characterised by gradual transitions of or
20                                           In Impatiens balsamina a lack of commitment of the meristem
21                                              Impatiens balsamina provides a unique opportunity to add
22      The completion of flower development in Impatiens balsamina requires continuous inductive (short
23  developing seeds of Momordica charantia and Impatiens balsamina, tissues that accumulate large amoun
24 e, we find that two of these species (Bombus impatiens, Bombus pensylvanicus) exhibit body size cline
25                      We exposed adult Bombus impatiens bumblebee workers to simulated, ecologically r
26 llen or nectar loads of equal mass to Bombus impatiens bumblebees and examined flight performance in
27 o North American plants pollinated by Bombus impatiens bumblebees.
28 re, we construct "chemosensory roadmaps" for Impatiens capensis and I. pallida, two North American pl
29              In our semifield experiments, B impatiens foragers exponentially increased their foragin
30 impact of isolation in the bumblebee, Bombus impatiens, from behavioral, molecular, and neuroanatomic
31 se findings suggest that VOC partitioning in Impatiens functions as a gustatory preference gradient t
32                          The highly invasive Impatiens glandulifera (Himalayan balsam) is one of the
33                                  Here we use Impatiens glandulifera as model case to study the impact
34                                              Impatiens glandulifera or Himalayan balsam (HB), is an i
35 ant structures such as Mimosa pudica leaves, Impatiens glandulifera seedpods, and Dionaea muscipula l
36                 The authors have isolated an Impatiens homologue of the FIM gene of Antirrhinum (UFO
37                             Here we describe Impatiens homologues of LFY, TFL1 and AG (IbLFY, IbTFL1
38            Analysis of the expression of the Impatiens homologues of the meristem identity genes flor
39                                              Impatiens (Impatiens wallerana) and wheat plants (Tritic
40 ength cDNAs for the Momordica (MomoFadX) and Impatiens (ImpFadX) enzymes in somatic soybean embryos r
41 alyzed pollen-foraging preferences of Bombus impatiens in (i) host-plant species, (ii) pollen isolate
42 ssion patterns in bumble bee workers (Bombus impatiens) in response to the presence of the queen, the
43                       Therefore reversion in Impatiens is most likely due to the failure of leaves to
44    We investigated gene expression of Bombus impatiens larvae exposed through food provisions to two
45                           Bumble bee (Bombus impatiens) microcolonies experienced reduced pollen cons
46                             The plant virus, Impatiens necrotic spot virus (INSV), is an economically
47 n crop losses due to their role in spreading Impatiens Necrotic Spot Virus (INSV).
48 , drive variation in wild bumble bee (Bombus impatiens) pathogen loads.
49           The pattern of ovule production in Impatiens requires the meristem to be maintained after t
50 n the primitively eusocial bumble bee Bombus impatiens signals information about caste, social condit
51 parison of the development of representative Impatiens species and analysis of the expression pattern
52 e transitions in integument morphology among Impatiens species suggests that control of underlying de
53 pattern in petals, together with features of Impatiens that are reminiscent of fim and ufo mutant phe
54 d laboratory experiments with gnotobiotic B. impatiens to examine factors shaping colonization by a f
55 perimentally exposed male bumblebees (Bombus impatiens) to a field-realistic concentration of a glyph
56 me sequences of Bombus terrestris and Bombus impatiens, two ecologically dominant bumblebees and wide
57 y, and nectar-collecting bumble bees (Bombus impatiens) use efficient travel routes when foraging on
58                                   Impatiens (Impatiens wallerana) and wheat plants (Triticum aestivum
59 t abundant bee species in our system, Bombus impatiens, we also evaluated the relationship between in
60 nate immune function in the bumblebee Bombus impatiens, which is an important wild and commercial pol
61 isons in the absence of other floral cues, B impatiens workers still preferred pollen with higher P:L
62 uninoculated or microbiota-inoculated Bombus impatiens workers to a field-realistic dose of 0.75 mg l