戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

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 ut the genetic basis of these transitions in Aquilegia.
2 olution of a novel organ identity program in Aquilegia.
3 ical B class function has been elaborated in Aquilegia.
4 pression of the PRC2 and VEL PHD families in Aquilegia, a member of the lower eudicot order Ranuncula
5  genetic regulation of leaf morphogenesis in Aquilegia and other flowering plants.
6 r of these genes appear to be single copy in Aquilegia and thus variation in their expression may hav
7 ies that hybridize (Ipomopsis, Diplacus, and Aquilegia) are examined in relation to these predictions
8                                  We focus on Aquilegia as a primary example of these advantages and h
9  group (Polemoniaceae) and Aquilegia formosa-Aquilegia caerulea group (Ranunculaceae) in western Nort
10 phingophilous species: the Aquilegia formosa/Aquilegia caerulea group (Ranunculaceae), the Ipomopsis
11 pre-duplication FUL-like genes in columbine (Aquilegia coerulea).
12  ortholog AqJAG in the lower eudicot species Aquilegia coerulea.
13                            The basal eudicot Aquilegia (columbine) has an unusual floral structure th
14        Both AqSWN and AqCLF are expressed in Aquilegia endosperm but neither copy is imprinted.
15 s and sphingophilous flowers in Ipompsis and Aquilegia for nectar foraging by the hummingbird Selasph
16 pomopsis aggregata group (Polemoniaceae) and Aquilegia formosa-Aquilegia caerulea group (Ranunculacea
17 nithophilous and sphingophilous species: the Aquilegia formosa/Aquilegia caerulea group (Ranunculacea
18 ed a combination of sequence searches of the Aquilegia Gene Index, phylogenetic analyses, and the iso
19                                 We find that Aquilegia has a relatively simple PRC2 with only one hom
20                                              Aquilegia has four members of the VEL PHD family, three
21  Previous studies of the lower eudicot model Aquilegia have revealed differential expression patterns
22  this study, we have sought to determine how Aquilegia homologs of the B class genes APETALA3 (AP3) a
23                     Phylogenetic analysis of Aquilegia indicates that flower color transitions procee
24                                              Aquilegia is an emerging model organism that is phylogen
25 edicted 84 targets of these newly identified Aquilegia microRNAs including transcription factors and
26 comparative genomics approach to identify 45 Aquilegia microRNAs that comprise 20 separate plant micr
27 th during speciation events, suggesting that Aquilegia nectar spurs rapidly evolve to fit adaptive pe
28 ies demonstrate that the protein products of Aquilegia's AP3 and PI homologs can form heterodimers, m
29 netic dissection of other adaptive traits in Aquilegia should also be possible soon as genomic resour
30 In most ornithophilous taxa of Ipomopsis and Aquilegia, the floral tubes have lengths and widths in t
31                                   (i) In the Aquilegia type, which is widespread, ethological isolati
32 Mode of origin i accounts for the Salvia and Aquilegia types of isolation in nine known species group
33 ed at a relatively constant level throughout Aquilegia vulgaris development, with the VEL PHD family
34 cies-level phylogeny of the columbine genus, Aquilegia, we show a significant evolutionary trend for
35 cies and the newly identified microRNAs from Aquilegia were analyzed in a phylogenetic context reveal

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。