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1 suggesting that C. goeringii accessions were polyphyletic.
2 e, well established groups were recovered as polyphyletic.
3 the exception of Littorinimorpha, which was polyphyletic.
4 Among germplasm, the kabuli form is polyphyletic.
5 , with both type 2a and 2b viruses appearing polyphyletic.
6 e species, while others were paraphyletic or polyphyletic.
7 Further, the superfamily Rhinolophoidea is polyphyletic.
8 ught to be a unique monospecific lineage, is polyphyletic.
9 boid lineage and the subclass Gymnamoebia is polyphyletic.
10 sporina suggest that the genus Plasmodium is polyphyletic.
11 of meiosis in Brassica napus (AACC), a young polyphyletic allotetraploid crop species with closely re
12 ed morphogenera are monophyletic and 19% are polyphyletic, although certain groups appear to be probl
14 that found Triatominae to be monophyletic or polyphyletic and may be due to the more comprehensive ta
15 aces tinamous within ratites, making ratites polyphyletic and suggesting multiple losses of flight.
16 alysis confirmed the phylum Zygomycota to be polyphyletic, and the taxa conventionally classified in
20 ctural genes and trans-factors underpins the polyphyletic evolution of this highly complex trait in t
24 omella Closely related to Polytomella is the polyphyletic genus Polytoma, the members of which lost p
25 underlying metabolic processes in the latter polyphyletic group are highly constrained by evolutionar
26 onducted morphometric analyses on raptors, a polyphyletic group at the base of the landbird radiation
27 nant archaeon, Methanobrevibacter smithii, a polyphyletic group of acetogens, and sulfate-reducing ba
29 this it is suggested that Myb proteins are a polyphyletic group related only by a "Myb-box" DNA-bindi
31 llo-beta-lactamase activity is thought to be polyphyletic, having arisen on more than one occasion wi
32 t significant lignin removal (brown rot) are polyphyletic, having evolved multiple times from lignin-
34 ylogeny indicates that the genus Cambarus is polyphyletic, however we fail to reject the monophyly of
41 diverse non-typical Myb proteins exhibits a polyphyletic origin and a complex evolutionary pattern.
43 se genetically isolated strains explains the polyphyletic origin of host specificity and the emergenc
44 providing the first genomic evidence for the polyphyletic origin of methylotrophy in Betaproteobacter
45 studies dispute this, finding evidence of a polyphyletic origin of SAR11 with most strains distantly
47 prokaryotes and eukaryotes and of a possible polyphyletic origin of these proteins within eukaryotes.
49 original virus isolated in 1989, indicating polyphyletic origins and that REBOV has been circulating
50 Thus, horizontal transfer may explain the polyphyletic origins of host specificity within the genu
52 es on reduviid relationships emphasizing the polyphyletic Reduviinae and the blood-feeding, disease-v
54 In contrast, the Lepidopteran species show polyphyletic relationships for duplicated cecropin genes
55 o bacterial HSP70 are analyzed, suggesting a polyphyletic split of Trypanosoma and Leishmania protist
56 at macroglossines are either paraphyletic or polyphyletic; this implies that adaptations for pollen a
58 ate that myrmecoid rove beetles are strongly polyphyletic, with this adaptive morphological and behav
59 ) of the fungus Fusarium oxysporum are often polyphyletic within the species complex, making it impos
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