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1 nates the outer surface of a human parasitic flatworm.
2 in Schistosoma mansoni, a derived, dioecious flatworm.
3 ls, has an important role in regeneration in flatworms.
4 o defend the germline integrity of parasitic flatworms.
5 ution of the complex life cycle of parasitic flatworms.
6 of amidated neuropeptides in these parasitic flatworms.
7 and it was initially linked to turbellarian flatworms.
9 ted regenerative capabilities make planarian flatworms an ideal system with which to investigate thes
13 by gastropod-borne helminths, predominantly flatworms and roundworms, whose life cycles are characte
15 ll-known regenerative abilities of planarian flatworms are attributed to a population of adult stem c
20 an, should serve to reignite interest in the flatworm as an experimental model for studying the probl
21 This set of unique properties makes many flatworms attractive organisms for studying the evolutio
22 and epidermal ultrastructure, to acoelomorph flatworms based on body plan and ciliary ultrastructure
23 e model for regeneration, with the planarian flatworm being one of the most important model species.
24 ed tropical diseases worldwide, is caused by flatworms (blood flukes or schistosomes) that live in th
31 molluscs, annelids, nemerteans, and polyclad flatworms) display a well-conserved early developmental
32 in other eukaryotes, the loss of RIOK-3 from flatworms does not result in an evolutionary disadvantag
34 tissue maintenance in long-lived free-living flatworms (for example, planarians), and neoblast-like c
35 ents, we show that TTXs do not protect these flatworms from some predators but instead are used to ca
39 roup may be closely related to the ancestral flatworm; however, polyclad embryos have been the subjec
40 sly unknown prey item (soft-bodied planarian flatworms in the genus Dugesia) made up the majority of
41 he abundance of larval trematodes (parasitic flatworms) in the declining northern leopard frog Rana p
45 olytic secretions from schistosome parasitic flatworm larvae and a pancreatic cancer cell line were d
46 case study, we used 35 transcriptomes of 29 flatworm lineages to recover 3427 putative hidden orthol
47 e evolutionary relationships among the major flatworm lineages, suggesting new roots and conflicting
50 phylogenies have suggested that acoelomorph flatworms might provide insights into the nature of the
52 the first cell-lineage fate map for an acoel flatworm, Neochildia fusca, using modern intracellular l
54 Asian tapeworms, respectively) are parasitic flatworms of major public health and food safety importa
56 transcriptomes representing all free-living flatworm orders, we provide resolution of platyhelminth
57 ed to the dissemination of data from flukes, flatworm parasites of the class Trematoda, phylum Platyh
58 deficits have prevented similar advances in flatworm parasites since those driven by bioimaging, imm
59 yses robustly support a modern hypothesis of flatworm phylogeny, one which emphasizes the primacy of
61 ific island of Guam, we found an undescribed flatworm (planocerid sp. 1) that contains high levels of
63 ysis of the riok gene family in 25 parasitic flatworms (platyhelminths) for which extensive genomic a
64 between free-living and vertebrate-parasitic flatworms, providing new opportunities to shed light on
65 ificant proportion of the gene repertoire in flatworms, qualifying the impact of gene losses and gain
68 ther, these results elucidate key aspects of flatworm reproductive biology and will be relevant for b
69 ef Gelei proposed that chromosome pairing in flatworms resulted from the formation of a telomere bouq
72 logical agents of this disease are trematode flatworms (Schistosoma) that live and lay eggs within th
73 ng an ommochrome body pigment, the planarian flatworm Schmidtea mediterranea generates porphyrins in
75 atial expression of SL RNAs in the planarian flatworm Schmidtea mediterranea, with the goal of identi
77 ral schistosome stages demonstrated that the flatworm SL AUG can serve as a translation initiator met
80 e provided evidence that another function of flatworm spliced leader trans-splicing is to provide som
81 nssplicing metazoan groups (e.g. nematodes), flatworm spliced leaders are variable in both sequence a
82 solutely conserved and unique feature of all flatworm spliced leaders is the presence of a 3'-termina
83 elop a concept for an in vivo test, based on flatworm stem cell dynamics, to detect and classify carc
85 tion structure of an sHsp from the parasitic flatworm Taenia saginata Tsp36, the first metazoan cryst
86 cids with less than 28% missing data from 27 flatworm taxa in 11 orders covering all major clades.
87 fferences from the pattern observed in other flatworm taxa in regard to the number of neurons that ex
90 Schistosomes are intravascular, parasitic flatworms that cause debilitating disease afflicting >20
95 odes are a large, complex group of parasitic flatworms that infect an incredible diversity of organis
96 criptomes of major cell types of planarians--flatworms that regenerate from nearly any injury--and id
98 ontrast, three other classes of turbellarian flatworm, the Acoela, Nemertodermatida, and Catenulida,
100 an important role in the ability of certain flatworms to identify wounds that require the production
101 is a small protein secreted by the parasitic flatworm (trematode) Fasciola hepatica that belongs to a
102 ces for parasitic roundworms (nematodes) and flatworms (trematodes), collectively known as helminths.
105 lecular phylogenies however, place the acoel flatworms, which have only one opening to their digestiv
107 o reverse-engineer systems such as planaria: flatworms with a complex bodyplan and nervous system tha
108 e we study the telomere biology of planarian flatworms with apparently limitless regenerative capacit
111 from single-celled bacteria to multicellular flatworms-yet share many common features in their life h
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