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1 ation are only beginning to be elucidated in Mollusca.
2 s as possibly having multiple origins within Mollusca.
3 a) and recover a well-supported topology for Mollusca.
4 binding protein is not limited to the phylum Mollusca.
5 s are among the rarest members of the phylum Mollusca.
6 NA transposon to be identified in the phylum Mollusca.
7 f mitochondrial gene order across the phylum Mollusca.
8 ave important implications for the origin of Mollusca and for morphological evolution within the grou
9 ion of mitochrondrial gene order amongst the Mollusca and suggests that radical mitochondrial DNA gen
10 abalone, Haliotis discus hannai (Gastropoda, Mollusca), and the sand worm Perinereis aibuhitensis (Po
12 s been allied to such disparate phyla as the Mollusca, Annelida or Chordata, it remains enigmatic.
13 While the seven classes within the phylum Mollusca are clearly defined morphologically and molecul
15 otrochozoa, a form of Ecdysozoa, Vertebrata, Mollusca, Bivalvia, Gastropoda, Arachnida, Hexapoda, Col
17 r knowledge, of changes in marine metazoans (Mollusca, Echinodermata, Arthropoda, and Annelida; >5,40
21 BA-ir) neurons in four species of sea slugs (Mollusca, Gastropoda, Opisthobranchia, Nudibranchia): Tr
24 ationships among the eight major lineages of Mollusca have remained unresolved despite their diversit
27 simple swimming behavior in two nudibranchs (Mollusca, Opisthobranchia), Melibe leonina and Dendronot
28 rpions), Cnidaria (Hydra, sea anemones), and Mollusca (oysters) but not in most other animal phyla.
30 tic or monophyletic group at the base of the Mollusca, proximate to other derived clades such as Ceph
32 ytilus californianus (class Bivalvia, phylum Mollusca) that contains two complete (ND2 and ND3) and t
33 Pacific oyster, Crassostrea gigas (Bivalvia, Mollusca), the Pacific abalone, Haliotis discus hannai (
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