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1 ce, such as Plasmodium, Cryptosporidium, and Eimeria.
2 rotective antigens and the use of transgenic Eimeria.
3 ing to several distinct species of the genus Eimeria.
5 lenge studies we used the EAMZ250 antigen of Eimeria acervulina, which was previously shown to confer
6 congenital neurological birth defects), and Eimeria (an economically significant disease of poultry
7 studies on widely known coccidia, including Eimeria and Toxoplasma in addition to the emerging or re
9 ent protein kinases (CDPKs) from Plasmodium, Eimeria, and several plants, and the catalytic region of
19 pments in our understanding of diversity for Eimeria in relation to its specialized life cycle, distr
22 and the secondary response, we have studied Eimeria infections of a broad range of genetically alter
24 , caused by protozoan parasites of the genus Eimeria, is one of the most important livestock diseases
25 caused by apicomplexan protozoa of the genus Eimeria, is one of the most important poultry diseases.
28 rasites, including Plasmodium, Neospora, and Eimeria, no genetic evidence of its contribution to inva
31 in ovo vaccination with the recombinant 3-1E Eimeria protein induces protective intestinal immunity a
32 medical and veterinary importance, including Eimeria, Sarcocystis, Cryptosporidium, Cyclospora, and P
34 avian coccidiosis were developed to deliver Eimeria species antigens to the lymphoid tissues of chic
36 inal tissues from chickens infected with two Eimeria species, E. tenella or E. maxima, that preferent
39 ause of malaria), but related genera such as Eimeria spp. (causative agents of coccidiosis in poultry
43 echnologies has raised the prospect of using Eimeria spp. as recombinant vectors to express additiona
45 known, but the intracellular growth of avian Eimeria spp. is easily shortened by serial selection for
48 tes in their regulatory domain, the PKG from Eimeria tenella (Et-PKG) contains three putative cGMP bi
49 t infect chickens are most significant, with Eimeria tenella among the best studied and most economic
50 d genome sequences of the coccidian parasite Eimeria tenella and observe that, at an E-value cut-off
51 kilobase genomes of coccidians T. gondii and Eimeria tenella and the malaria parasite Plasmodium falc
53 -gamma) production in protective immunity to Eimeria tenella infection was evaluated in two inbred st
54 eptides obtained from biochemically purified Eimeria tenella M1Pase was used to synthesize degenerate
55 coplast genome from the intestinal coccidian Eimeria tenella that may serve as a new drug target agai
57 inical and/or veterinary interest, including Eimeria tenella, Neospora caninum, Plasmodium falciparum
58 gondii) and others of veterinary importance (Eimeria tenella, Sarcocystis neurona, and Neospora canin
63 mannitol is present in the seven species of Eimeria that infect chickens, but is not in the avian ho
64 ted genome sequences of all seven species of Eimeria that infect domestic chickens, which reveal the
65 critically important for protection against Eimeria; thus, our approach utilizes the bacterial type
67 RA) in chickens infected with Salmonella and Eimeria, two major infectious agents of gastrointestinal
68 velop increased resistance to infection with Eimeria vermiformis, an abundant intestinal parasite tha
69 tion with the enteric apicomplexan parasite, Eimeria vermiformis, depends on the rapid induction of l
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