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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.
4          A purified recombinant protein from Eimeria acervulina (3-1E) was used to vaccinate chickens
5 This study aimed to determine the effects of Eimeria acervulina infection on the luminal and mucosal
6 lenge studies we used the EAMZ250 antigen of Eimeria acervulina, which was previously shown to confer
7  congenital neurological birth defects), and Eimeria (an economically significant disease of poultry
8  studies on widely known coccidia, including Eimeria and Toxoplasma in addition to the emerging or re
9  the phylum Apicomplexa, such as Plasmodium, Eimeria, and Cryptosporidia.
10 ent protein kinases (CDPKs) from Plasmodium, Eimeria, and several plants, and the catalytic region of
11         The coccidian parasites of the genus Eimeria are protozoan gut pathogens that elicit a potent
12 mosomal level assembly promotes insight into Eimeria biology and evolution, hastening drug discovery
13                          Eimeria tenella and Eimeria bovis are complex parasites responsible for the
14 hich leads to significant protection against Eimeria challenge.
15   The aim of this study was to test the anti-Eimeria efficacy of maltodextrin, sodium chloride, citri
16 velopment of cost-effective vaccines against Eimeria essential.
17                                 We show that Eimeria falciformis, an apicomplexan parasite infecting
18 n by the intracellular apicomplexan parasite Eimeria falciformis.
19                     To accomplish this goal, Eimeria genes encoding the sporozoite antigen EASZ240 an
20                                  Analysis of Eimeria genes involved in basic biology and host-parasit
21 lospora is closely related to members of the Eimeria genus.
22 es in infected animals is detrimental to the Eimeria growth.
23 pments in our understanding of diversity for Eimeria in relation to its specialized life cycle, distr
24                           In Salmonella- and Eimeria-infected chickens, the expression levels of the
25  Previous studies have shown that concurrent Eimeria infection can influence the colonization and rep
26 n, requiring understanding on the effects of Eimeria infection on the gut microbiota.
27 al intracellular parasite infections such as Eimeria infection.
28  and the secondary response, we have studied Eimeria infections of a broad range of genetically alter
29  has been found to possess retrotransposons, Eimeria is home to a family of chromoviruses.
30 , caused by protozoan parasites of the genus Eimeria, is one of the most important livestock diseases
31 caused by apicomplexan protozoa of the genus Eimeria, is one of the most important poultry diseases.
32 le rabbits with intra-gastric inoculation of Eimeria magna oocytes.
33 ge), (3) Eimeria maxima (challenge), and (4) Eimeria maxima (challenge) + curcumin.
34 challenge), (2) Curcumin (no challenge), (3) Eimeria maxima (challenge), and (4) Eimeria maxima (chal
35                                   Sequential Eimeria maxima and C. perfringens challenges significant
36                                              Eimeria maxima from the chicken is characterized by high
37 -free (SPF) Leghorn chickens challenged with Eimeria maxima, with or without dietary supplementation
38 bcellular components of genetically modified Eimeria may determine the magnitude and type of immune r
39 rasites, including Plasmodium, Neospora, and Eimeria, no genetic evidence of its contribution to inva
40                 Understanding the biology of Eimeria parasites underpins development of new drugs and
41 Coccidiosis, an intestinal disease caused by Eimeria parasites, is responsible for major losses in th
42            After acquiring stable transgenic Eimeria populations, we observed EYFP expressing in expe
43                                              Eimeria pose a risk to all livestock species as a cause
44 in ovo vaccination with the recombinant 3-1E Eimeria protein induces protective intestinal immunity a
45 medical and veterinary importance, including Eimeria, Sarcocystis, Cryptosporidium, Cyclospora, and P
46  Toxoplasma gondii, Cryptosporidium sp., and Eimeria sp.
47  avian coccidiosis were developed to deliver Eimeria species antigens to the lymphoid tissues of chic
48                                              Eimeria species serve as promising eukaryotic vaccine ve
49                                              Eimeria species that infect chickens are most significan
50 inal tissues from chickens infected with two Eimeria species, E. tenella or E. maxima, that preferent
51 cies (Cyc-hu) is most closely related to the Eimeria species, which are host species-specific.
52 a coherent clade within the diverse group of Eimeria species.
53 ause of malaria), but related genera such as Eimeria spp. (causative agents of coccidiosis in poultry
54                                              Eimeria spp. are a group of highly successful intracellu
55                                              Eimeria spp. are intracellular parasites that have a maj
56                                              Eimeria spp. are intracellular protozoa that infect epit
57 echnologies has raised the prospect of using Eimeria spp. as recombinant vectors to express additiona
58 pyridine (Compound 1) inhibits the growth of Eimeria spp. both in vitro and in vivo.
59                  There was downregulation of Eimeria spp. genes related to gamete fusion, oocyst shed
60 known, but the intracellular growth of avian Eimeria spp. is easily shortened by serial selection for
61                       Coccidiosis, caused by Eimeria spp. presents a self-limiting intestinal infecti
62 a (Plasmodium spp.) and chicken coccidiosis (Eimeria spp.).
63 lasmodium falciparum, Toxoplasma gondii, and Eimeria spp., have significant socioeconomic impact on h
64 ivity against apicomplexan parasites such as Eimeria spp., via membrane disruption.
65 tes in their regulatory domain, the PKG from Eimeria tenella (Et-PKG) contains three putative cGMP bi
66 t infect chickens are most significant, with Eimeria tenella among the best studied and most economic
67 ffective in inducing protective immunity, of Eimeria tenella and E. acervulina sporozoites.
68                                              Eimeria tenella and Eimeria bovis are complex parasites
69 d genome sequences of the coccidian parasite Eimeria tenella and observe that, at an E-value cut-off
70 kilobase genomes of coccidians T. gondii and Eimeria tenella and the malaria parasite Plasmodium falc
71  orally with 5 x 10(4) sporulated oocysts of Eimeria tenella and treated with 60 mg/kg ZnONPs, 1% Nig
72                                              Eimeria tenella can cause the disease coccidiosis in chi
73       For antigen delivery via the T3SS, the Eimeria tenella gene encoding sporozoite antigen SO7 was
74 oparticles (ZnONPs) using Nigella sativa, on Eimeria tenella infected broilers.
75 -gamma) production in protective immunity to Eimeria tenella infection was evaluated in two inbred st
76                                              Eimeria tenella is a major cause of caecal coccidiosis i
77                                              Eimeria tenella is among the protozoan parasites that ca
78 eptides obtained from biochemically purified Eimeria tenella M1Pase was used to synthesize degenerate
79 ere, we report chromosomal scale assembly of Eimeria tenella strain APU2, a strain isolated from comm
80 coplast genome from the intestinal coccidian Eimeria tenella that may serve as a new drug target agai
81      A model to simulate natural immunity to Eimeria tenella was developed in three chicken lines whi
82 ive bacterial pathogens, the avian protozoan Eimeria tenella, and avian influenza virus.
83 inical and/or veterinary interest, including Eimeria tenella, Neospora caninum, Plasmodium falciparum
84 icient chickens challenged with the parasite Eimeria tenella, pathogen clearance was accelerated but
85 gondii) and others of veterinary importance (Eimeria tenella, Sarcocystis neurona, and Neospora canin
86 pproximately 120-kDa protein from lysates of Eimeria tenella.
87 ccidial target for the apicomplexan parasite Eimeria tenella.
88 ian parasites including Neospora caninum and Eimeria tenella.
89 s of Plasmodium falciparum and eimepsin from Eimeria tenella.
90  mannitol is present in the seven species of Eimeria that infect chickens, but is not in the avian ho
91 ted genome sequences of all seven species of Eimeria that infect domestic chickens, which reveal the
92  critically important for protection against Eimeria; thus, our approach utilizes the bacterial type
93                      To study the ability of Eimeria to secrete foreign antigens or display them on t
94 RA) in chickens infected with Salmonella and Eimeria, two major infectious agents of gastrointestinal
95 velop increased resistance to infection with Eimeria vermiformis, an abundant intestinal parasite tha
96 tion with the enteric apicomplexan parasite, Eimeria vermiformis, depends on the rapid induction of l
97         This study shows that in response to Eimeria vermiformis, mice lacking alpha beta T cells dis