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1 member of this family to be identified in a platyhelminth.
2 brachiopod, a phoronid, two annelids, and a platyhelminth.
3 ction appear to underlie hidden orthology in Platyhelminthes.
4 orm parasites of the class Trematoda, phylum Platyhelminthes.
5 emarkable biological properties displayed by Platyhelminthes.
6 markable biology found throughout the phylum Platyhelminthes.
8 ese helminths, also trematodes of the phylum Platyhelminthes and major human pathogens, are not carci
9 ukaryotic groups, the nematodes, arthropods, platyhelminthes, and the annelids; some of which could c
10 contains all publicly available nematode and platyhelminth annotated genome sequences, and is designe
12 interrelationships of the flatworms (phylum Platyhelminthes) are poorly resolved despite decades of
14 en-like (SmVALs)) in the medically important Platyhelminthes (class Trematoda) and describe individua
17 hey have greatest similarity to those from a platyhelminth, echiuran and mollusc with rather less to
20 riok gene family in 25 parasitic flatworms (platyhelminths) for which extensive genomic and transcri
21 ps with other microscopic spiralians, namely Platyhelminthes, Gastrotricha, and in the case of Diurod
22 tional characterisation of other schistosome/platyhelminth genomes continues to expedite anthelmintic
25 2, a Pgp homologue from Schistosoma mansoni (Platyhelminthes), in Chinese hamster ovary (CHO) cells a
27 ng flatworm orders, we provide resolution of platyhelminth interrelationships based on hundreds of nu
28 th available mitochondrial genome sequences, Platyhelminthes is the closest relative to L. thecatus,
29 tosis in a lophotrochozoan, planaria (phylum Platyhelminthes), is associated with MOMP and that cytoc
30 molecular evidence suggests the turbellarian Platyhelminthes may represent the extant basal members o
32 indicated that schistosome cathepsin D is a platyhelminth orthologue of mammalian lysosomal cathepsi
34 chistosoma mansoni are the first major human platyhelminth pathogens to have their genome sequences p
35 ng the major evolutionary transitions within Platyhelminthes: perhaps most notably, we propose a nove
38 aims that the codon UAA codes for Tyr in the Platyhelminthes rather than the standard stop codon.
39 th particularly high levels of divergence in platyhelminths relative to nematodes, arthropods or vert
42 haematobium genome that are conserved among platyhelminth species and others that are unique to S. h
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