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1 genomic changes tended to support Tardigrada+Arthropoda.
2 the last common ancestor of Onychophora and Arthropoda.
3 thin the moulting-animal clade that includes Arthropoda.
4 onary relationships within the Myriapoda and Arthropoda.
5 unique, innate immune response in the phylum Arthropoda.
6 emiochemicals in the evolutionary biology of Arthropoda.
7 aceans, the latter belonging to the class of arthropoda.
8 that are key to understanding the origins of Arthropoda.
11 inct phyla of the Animal kingdom, insects of Arthropoda and mammals of Chordata, have different prefe
12 ric bootstrapping tests reject monophyly for Arthropoda and Nemertea but are unable to reject deutero
14 in Panarthropoda (Onychophora + Tardigrada + Arthropoda) and other molting animals (Ecdysozoa), we an
15 n marine metazoans (Mollusca, Echinodermata, Arthropoda, and Annelida; >5,400 fossils and trace fossi
16 that Platyhelminthes, Rotifera, Annelida and Arthropoda are thriving at 1.4 km depths in palaeometeor
18 igrada+Nematoda relationship over Tardigrada+Arthropoda, but rare genomic changes tended to support T
19 of the phytoseiid Metaseiulus occidentalis (Arthropoda: Chelicerata: Acari: Phytoseiidae) has been s
21 y well characterized in freshwater crayfish (Arthropoda, Crustacea), although the identity of the pre
23 hotransferase superfamily with homologues in Arthropoda (insects, spiders, mites, scorpions), Cnidari
26 ed clarify evolutionary relationships within Arthropoda, particularly among Tetraconata (i.e., crusta
27 arine and terrestrial representatives of the Arthropoda phylum, and although alpha-like OctRs have be
28 nterrelationships of major clades within the Arthropoda remain one of the most contentious issues in
29 d responsive genes exist in other members of Arthropoda such as the Crustacea, as has been demonstrat
30 tes, including several in phyla simpler than Arthropoda, the phylum containing insects such Drosophil
31 e in the radiation and ecological success of Arthropoda, which has been the most diverse and abundant
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