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1 resent transcription factor binding sites in Theileria.
2 ial parasite Plasmodium, the cattle parasite Theileria and the emerging human parasite Cryptosporidiu
3 mean Congo hemorrhagic fever virus, Babesia, Theileria, and Anaplasma species, identifies arboviruses
5 ion of host cells by transformation-inducing Theileria, and we propose that comparisons between cance
6 od of a dog that was naturally infected with Theileria annae at a low percentage of parasitemia was a
11 3 gene from the bovine apicomplexan parasite Theileria annulata, encodes a 46 kDa polypeptide with st
12 Some species, including Theileria parva and Theileria annulata, infect leukocytes where they induce
15 We have also generated Toxoplasma-mouse and Theileria-cow scRNA-seq datasets to highlight the functi
18 fic protein domain [frequently associated in Theileria (FAINT)] present in a large number of secreted
19 the evolution of non-coding sequences in the Theileria genome and identify conserved sequence element
22 Plasmodium, Toxoplasma, Cryptosporidium and Theileria, identifying a new protein family in the Apico
24 support a critical role of E2F signaling for Theileria-induced host cell proliferation, and its poten
26 can reveal chemotherapeutic targets against Theileria-induced pathogenesis based on cancer treatment
28 genome-wide CRISPR knockout screen targeting Theileria-infected cells to pinpoint shared vulnerabilit
31 A lineage of the protozoan parasite genus Theileria infects bovine leukocytes and induces their un
32 comparisons between cancer biology and host-Theileria interactions can reveal chemotherapeutic targe
33 Pathogens such as Plasmodium, Babesia, and Theileria invade and multiply within host red blood cell
34 , which cause veterinary and human diseases, Theileria is the only genus that transforms its mammalia
35 RNA gene was previously reported from bovine Theileria isolates from Texas and North Carolina; the ty
37 m that is important in cancer and is used by Theileria parasites to manipulate host oncogenic signall
40 tle against two immunodominant epitopes from Theileria parva (Tp1(214-224) and Tp2(49-59)) and invest
41 ve cellular and antibody immune responses to Theileria parva and antigens targeted by them that could
44 d protozoan parasites Theileria annulata and Theileria parva are important intracellular pathogens of
45 s of an experimental subunit vaccine against Theileria parva based on the 67-kDa major sporozoite sur
47 the bovine intracellular protozoan parasite Theileria parva However, the mechanism by which the spec
48 lay a key role in mediating immunity against Theileria parva in cattle (Bos taurus), and there is evi
53 xhibit cytotoxic activity against autologous Theileria parva-infected cells in vitro, and during in v
55 f the Piroplasmida hemoparasites Babesia and Theileria (pRAP-1) is structurally conserved, with the c
58 tly identified in intergenic regions of both Theileria species, and the evidence suggests that at lea
59 wn piroplasmida, including other Babesia and Theileria species, in lacking two conserved cysteines in
60 egulators of host-cell transformation, and a Theileria-specific protein domain [frequently associated
62 dium falciparum) and theileriosis (caused by Theileria spp.), profoundly impact global health and the
63 ompetitive interaction between the two ovine Theileria spp., and a substantial reduction in the risk
64 13 months during natural infections with two Theileria spp., pathogenic (T. lestoquardi) and non-path
65 parvum, Leishmania spp., Trypanosoma cruzi, Theileria spp., Toxoplasma gondii and Plasmodium spp. ha
66 in horses and are orthologues of proteins in Theileria spp., which are also tick-transmitted protozoa
68 se supporting Piroplasmida (i.e. Babesia and Theileria), the addition of large amounts of new data an
69 by IL-2 and by antigen presentation using a Theileria-transformed cell line and autologous T cells f
70 intracellular survival of P. falciparum and Theileria, while other host enzymes are only essential u