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1 ently identified a murine commensal protist, Tritrichomonas arnold, that protects against reovirus-in
2 s in the previously characterized IMPDH from Tritrichomonas foetus ( TfIMPDH).
3  is a sexually transmitted disease caused by Tritrichomonas foetus and characterized by early embryo
4 amine prevalence and risk factors for feline Tritrichomonas foetus and Giardia infection.
5 rmed multiple inhibitor experiments with the Tritrichomonas foetus and human type 2 IMPDHs using tiaz
6 loped to study the cytopathogenic effects of Tritrichomonas foetus and the role of lipophosphoglycan
7 richomonad highly similar to bovine venereal Tritrichomonas foetus but having a unique tropism for th
8 ae) formed one, while Monocercomonas sp. and Tritrichomonas foetus formed the other.
9                Likewise, the bovine parasite Tritrichomonas foetus had no cytotoxic effects on hVECs.
10 e phosphoribosyltransferase (HGXPRTase) from Tritrichomonas foetus has been determined and refined ag
11 e phosphoribosyltransferase (HGXPRTase) from Tritrichomonas foetus has been proven to be a target for
12 mplexes of IMPDH from the protozoan parasite Tritrichomonas foetus have been solved: with its substra
13 with the high K(m) for PPi (165.5 microM) in Tritrichomonas foetus HGXPRTase-catalyzed reverse reacti
14 butane-2,3-dione irreversibly inactivate the Tritrichomonas foetus hypoxanthine-guanine-xanthine phos
15 crystal structures of the protozoan parasite Tritrichomonas foetus IMPDH complexed with the inhibitor
16 al structure of the catalytic core domain of Tritrichomonas foetus IMPDH in complex with IMP and beta
17                An X-ray crystal structure of Tritrichomonas foetus IMPDH with mizoribine monophosphat
18 uctures of IMPDH from the protozoan parasite Tritrichomonas foetus in the apo form at 2.3 A resolutio
19 sferase (HGXPRT) from the protozoan parasite Tritrichomonas foetus is a rational target for antiparas
20                                              Tritrichomonas foetus is a serious veterinary pathogen,
21          One reason is because inhibition of Tritrichomonas foetus ODC results in growth arrest, dest
22 he complete kinetic mechanism for IMPDH from Tritrichomonas foetus using ligand binding, isotope effe
23 ine phosphoribosyltransferase (HGXPRTase) of Tritrichomonas foetus was inactivated by the thiol reage
24                                              Tritrichomonas foetus, a venereal pathogen of cattle, wa
25                                              Tritrichomonas foetus, an anaerobic flagellated protozoa
26 ansferase (HGXPRTase), a type I PRTase, from Tritrichomonas foetus, is a potential target for antitri
27 thermore, T. vaginalis LPG (but not LPG from Tritrichomonas foetus, the causative agent of bovine tri
28 ed by the genome of the trichomonad parasite Tritrichomonas foetus, this otherwise highly conserved h
29 ) and its analogue in the protozoan parasite Tritrichomonas foetus.
30 e salvage pathway of the parasitic protozoan Tritrichomonas foetus.
31 ite Trichomonas gallinae and cattle parasite Tritrichomonas foetus.
32  complex of this protozoan, and the costa of Tritrichomonas foetus; c) the flagellulm of trypanosomat
33 ng site of resistant IMPDH from the parasite Tritrichomonas foetuscontains two residues that differ f
34 th is recapitulated with cecal extracts from Tritrichomonas-infected mice but not purified protozoa,
35                                In agreement, Tritrichomonas infection causes a shift in the microbiot
36 stinal epithelium via Tamoxifen injection in Tritrichomonas muris (Tm) infected mice, tuft cells, IL-
37 ponse to the infection of parasites, such as Tritrichomonas muris and Nippostrongylus brasiliensis.
38                  We identified the protozoan Tritrichomonas muris as the disease-exacerbating element
39  Succinate produced by the commensal protist Tritrichomonas musculis (T. mu) stimulates chemosensory
40 nt colonization with the protozoan commensal Tritrichomonas musculis (T.mu) promotes T cell-dependent
41 e, we show that the gut commensal protozoan, Tritrichomonas musculis (T.mu), remotely shapes the lung
42             Here, we show that the protozoan Tritrichomonas musculis activates the host epithelial in
43                                              Tritrichomonas musculis, a protozoan gut commensal, stre
44 t al. (2016) identify a commensal protozoan, Tritrichomonas musculis, that can enhance anti-bacterial
45                                              Tritrichomonas protists initiate a Bacteroides bloom and
46                    Here, we demonstrate that Tritrichomonas protozoa induce thickening of the colonic
47 alyses of murine parabasalids from the genus Tritrichomonas revealed species-level differences in exc
48                Metabolic differences between Tritrichomonas species also determine their ecological n
49 itro protist culture, we show that different Tritrichomonas species prefer dietary polysaccharides or
50 pitopes with proteins in data banks, such as Tritrichomonas suis, Candida albicans, and Saccharomyces
51 e discovered that the gut-colonizing protist Tritrichomonas (T.) arnold promotes oral tolerance and p