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1 e of the Moroccan plant Cladanthus arabicus (Asteraceae).
2 elf-incompatible daisy Senecio squalidus L. (Asteraceae).
3 um L. and Silphium terebinthinaceum Jacquin (Asteraceae).
4 of the Hawaiian and North American Madiinae (Asteraceae).
5 cestor of the Hawaiian silversword alliance (Asteraceae).
6 ly related woody species of the daisy group (Asteraceae).
7 rnates hosts between the Grossulariaceae and Asteraceae.
8 older than previously known records for the Asteraceae.
9 than five folds higher than to Oleaceae and Asteraceae.
10 economically important angiosperm families, Asteraceae.
11 include Myrtaceae, Lauraceae, Lamiaceae, and Asteraceae.
12 the elaborate inflorescence architecture in Asteraceae.
14 raits and habitat associations in Lasthenia (Asteraceae), a small clade of predominantly annual plant
15 ecological divergence in Achillea borealis (Asteraceae), a widespread tetraploid plant with localize
17 tetraploid populations of Achillea borealis (Asteraceae), an autopolyploid complex consisting of tetr
19 barbeyi (Ranunculaceae), Erigeron speciosus (Asteraceae), and Polemonium foliosissimum (Polemoniaceae
20 restriction site analysis of Argyranthemum (Asteraceae: Anthemideae), the largest endemic genus of p
21 us group, the paper daisy tribe Gnaphalieae (Asteraceae), based on the hitherto largest taxon samplin
24 leaves from plants of the Poaceae, Fabaceae, Asteraceae, Brassicaceae, and Cucurbitaceae that were gi
25 ide extracted from Artemisia annua L (family Asteraceae; commonly known as sweet wormwood), is highly
26 acid desaturase-like enzyme in seeds of the Asteraceae Crepis palaestina and Vernonia galamensis.
31 yza canadensis), a member of the Compositae (Asteraceae) family, was the first broadleaf weed to evol
35 the distinction of different flower types in Asteraceae is connected with their independent evolution
37 of this entrapped insect carrion on tarweed (Asteraceae: Madia elegans) plants under natural field co
39 hial inflorescences of the sunflower family, Asteraceae, mimic a solitary flower but are composed of
43 ce the evolution of woodiness in Pericallis (Asteraceae: Senecioneae), a genus endemic to the Macaron
45 iaceae (Cnidium cnidiifolium) along with two Asteraceae species (Artemisia arctica and Petasites frig
46 these results conclusively demonstrate that Asteraceae species and the Euphorbiaceae E. lagascae hav
47 ies of ethanol and water extracts from eight Asteraceae species were investigated against three Gram
48 acetylenase gene were also detected in other Asteraceae species, as revealed by PCR analysis of isola
49 we isolated homologs of these genes from an Asteraceae species, Senecio vulgaris (common groundsel).
51 e lost after ancient WGD in the same family (Asteraceae; sunflower family) [6] and with gene dosage s
53 rval survival is greater on the novel hosts (Asteraceae) than on the ancestral host (Apiaceae), but t
56 d development (apomixis) in Erigeron annuus (Asteraceae) was evaluated in a triploid (2n=3x=27) popul
58 d with those within the Senecioneae lineage (Asteraceae), where HSS expression is reproducibly found
59 on within the Chrysanthemum indicum complex (Asteraceae), which comprises diploid and polyploid plant
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