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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 markable biology found throughout the phylum Platyhelminthes.
4 orm parasites of the class Trematoda, phylum Platyhelminthes.
5 ing has yet to be reported in species of the Platyhelminthes.
6 emarkable biological properties displayed by Platyhelminthes.
7 ed clade gathering annelids, nemerteans, and platyhelminthes.
8 omorphic organisms, primarily Arthropoda and Platyhelminthes.
9 ction appear to underlie hidden orthology in Platyhelminthes.
10  derived and diversified group of the phylum Platyhelminthes.(1)(,)(2) The four major lineages of Neo
11 y analyses of multiple species of flatworms (Platyhelminthes; among which schistosomes recently evolv
12 o distinct SCP/TAPS protein types within the Platyhelminthes and across taxa.
13 ese helminths, also trematodes of the phylum Platyhelminthes and major human pathogens, are not carci
14 ukaryotic groups, the nematodes, arthropods, platyhelminthes, and the annelids; some of which could c
15 contains all publicly available nematode and platyhelminth annotated genome sequences, and is designe
16                                              Platyhelminthes are excellent models for the study of st
17                                   Flatworms (Platyhelminthes) are a basally branching phylum that har
18  interrelationships of the flatworms (phylum Platyhelminthes) are poorly resolved despite decades of
19 fe cycles, reproduction is a central part of platyhelminth biology.
20 en-like (SmVALs)) in the medically important Platyhelminthes (class Trematoda) and describe individua
21          Our phylogenetic analyses show that Platyhelminthes consist of the two clades Catenulida and
22       Studies on transcription regulation in platyhelminth development are scarce, especially for par
23 exhibited by other spiralians, including the Platyhelminthes (e.g., polyclad turbellarians).
24 hey have greatest similarity to those from a platyhelminth, echiuran and mollusc with rather less to
25  three animal phyla: chordates (fish, frog), platyhelminthes (flatworm), and arthropods (crustacean).
26                                              Platyhelminthes (flatworms) have captivated the imaginat
27 a based on morphological features, including Platyhelminthes (flatworms)(2), Priapulida (penis worms)
28 l genetic code, to define a clade within the Platyhelminthes (flatworms), the Rhabditophora.
29  riok gene family in 25 parasitic flatworms (platyhelminths) for which extensive genomic and transcri
30 ps with other microscopic spiralians, namely Platyhelminthes, Gastrotricha, and in the case of Diurod
31 tional characterisation of other schistosome/platyhelminth genomes continues to expedite anthelmintic
32 omosomal assignment, of existing schistosome/platyhelminth genomes.
33 ids, nemerteans, entoprocts, and some marine platyhelminth groups (reviewed in [12, 13]).
34 2, a Pgp homologue from Schistosoma mansoni (Platyhelminthes), in Chinese hamster ovary (CHO) cells a
35  immunopathology and egg transmission during platyhelminth infection.
36 ng flatworm orders, we provide resolution of platyhelminth interrelationships based on hundreds of nu
37 tify orthologous genes to those for VP/OT in Platyhelminthes, intertidal planarians that have a simpl
38 th available mitochondrial genome sequences, Platyhelminthes is the closest relative to L. thecatus,
39 tosis in a lophotrochozoan, planaria (phylum Platyhelminthes), is associated with MOMP and that cytoc
40 molecular evidence suggests the turbellarian Platyhelminthes may represent the extant basal members o
41 ultienzyme proteolytic complexes in malaria, platyhelminths, nematodes, and ticks.
42  indicated that schistosome cathepsin D is a platyhelminth orthologue of mammalian lysosomal cathepsi
43 d link the cytosine methylation machinery to platyhelminth oviposition processes.
44 conventional perspective on the evolution of platyhelminth parasitism, rejecting a common origin for
45 chistosoma mansoni are the first major human platyhelminth pathogens to have their genome sequences p
46 ng the major evolutionary transitions within Platyhelminthes: perhaps most notably, we propose a nove
47 ly from Schistosoma mansoni, a member of the Platyhelminthes phylum.
48  cell development in the strikingly colorful Platyhelminthes phylum.
49 aims that the codon UAA codes for Tyr in the Platyhelminthes rather than the standard stop codon.
50 th particularly high levels of divergence in platyhelminths relative to nematodes, arthropods or vert
51                         In case of parasitic platyhelminths, reproductive processes can also contribu
52 rn coast by species of Arthropoda, Nematoda, Platyhelminthes, Rotifera and Tardigrada.
53                           We identified that Platyhelminthes, Rotifera, Annelida and Arthropoda are t
54 ns well-supported phylum-specific clades for Platyhelminthes, Rotifera, Nematoda, Porifera/Cnidaria,
55  haematobium genome that are conserved among platyhelminth species and others that are unique to S. h
56                   Schistosomes are parasitic platyhelminthes that cause schistosomiasis, which is a l
57                   Schistosomes are parasitic platyhelminths that constitute an important public healt
58                   Monogeneans are flatworms (Platyhelminthes) that are primarily found on gills and s
59 nd Myriapods) and even phyla (Arthropods and Platyhelminthes), that dampens the slow nanoscopic dynam
60       Sixteen new NRs were identified in the Platyhelminth trematode, Schistosoma mansoni.
61 ical roles have come from archaebacteria and platyhelminths, which present opsin-like proteins that l