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1 designed, synthesized, and evaluated against Trypanosoma brucei brucei .
2 e glycerol kinase and alternative oxidase of Trypanosoma brucei brucei.
3 rized that protects humans from infection by Trypanosoma brucei brucei.
4 oodstream and procyclic life cycle stages of Trypanosoma brucei brucei.
5 he purine-specific nucleoside hydrolase from Trypanosoma brucei brucei.
6 LF2) that are lytic for the African parasite Trypanosoma brucei brucei.
7 de hydrolase (IAG-nucleoside hydrolase) from Trypanosoma brucei brucei.
8 rate and an auxiliary ubiquinol oxidase from Trypanosoma brucei brucei.
9 B-cells in the brains of mice infected with Trypanosoma brucei brucei.
10 ts: I172V, I172A, L232A, and P168A (TIM from Trypanosoma brucei brucei); a 208-TGAG for 208-YGGS loop
11 postmitochondrial supernatants prepared from Trypanosoma brucei brucei and Crithidia fasciculata, we
12 (HDL) found in human serum that is toxic to Trypanosoma brucei brucei and may be critical in prevent
13 e mitochondrial DNA (kinetoplast or kDNA) of Trypanosoma brucei brucei and related kinetoplastid prot
15 nd to be a potent inhibitor against cultured Trypanosoma brucei brucei and Trypanosoma brucei rhodesi
16 were evaluated against bloodstream forms of Trypanosoma brucei brucei and Trypanosoma brucei rhodesi
17 against the parasites Plasmodium falciparum, Trypanosoma brucei brucei, and Trypanosoma cruzi will be
18 olstein-Friesian calves were inoculated with Trypanosoma brucei brucei AnTat 1.1 (n = 5) or T. congol
19 lipid-free Hpr and apoL-I were both toxic to Trypanosoma brucei brucei but with specific activities a
20 everal African trypanosome species including Trypanosoma brucei brucei, but not the human-infective p
21 al immunity of humans to the cattle pathogen Trypanosoma brucei brucei, but not to the morphologicall
22 GAP for wildtype TIM from muscle sources and Trypanosoma brucei brucei, but partitioning of the enedi
24 cells but were effective in cell cultures of Trypanosoma brucei brucei (EC(50) = 1-15 muM) and elimin
25 h a single-digit micromolar activity against Trypanosoma brucei brucei (EC50 = 2.97 muM), thus being
26 on by several protozoan parasites, including Trypanosoma brucei brucei Endocytosis and acidification
27 ine transport activities in bloodstream form Trypanosoma brucei brucei found that these cells express
28 resistance of humans to the cattle pathogen Trypanosoma brucei brucei has been attributed to the pre
29 al immunity of humans to the cattle pathogen Trypanosoma brucei brucei has been attributed to the pre
31 een of approximately 87000 compounds against Trypanosoma brucei brucei identified a number of promisi
33 responses in the penetration of T cells and Trypanosoma brucei brucei into the brain was studied in
34 ate immunity against the veterinary pathogen Trypanosoma brucei brucei is conferred by trypanosome ly
35 serum that protects from infection by lysing Trypanosoma brucei brucei, is also bound and endocytosed
36 against most African trypanosomes, including Trypanosoma brucei brucei, is mediated by a minor subcla
37 st four strains of African trypanosomes, one Trypanosoma brucei brucei isolate, and several clinical
38 desiense LouTat 1 with the 117 VSG gene from Trypanosoma brucei brucei MiTat 1.4 in order to produce
40 d low micromolar levels of inhibition of the Trypanosoma brucei brucei parasite grown in culture.
41 tion in triosephosphate isomerase (TIM) from Trypanosoma brucei brucei results in a small 6-fold decr
42 d by wildtype triosephosphate isomerase from Trypanosoma brucei brucei (Tbb TIM) and a monomeric vari
43 HAP) by triosephosphate isomerase (TIM) from Trypanosoma brucei brucei (Tbb) has been investigated.
44 Glu-167 of triosephosphate isomerase from Trypanosoma brucei brucei (TbbTIM) acts as the base to d
45 certain mammalian trypanosomes, most notably Trypanosoma brucei brucei, the causative agent of a wast
47 xperimental-model species of Kinetoplastida -Trypanosoma brucei brucei, Trypanosoma cruzi and Leishma
48 or activity against the pathogenic parasites Trypanosoma brucei brucei, Trypanosoma cruzi, and Leishm
49 31-fold more active against bloodstream-form Trypanosoma brucei brucei trypomastigotes engineered to
50 cyclic and long slender bloodstream forms of Trypanosoma brucei brucei was investigated by means of s
51 een of approximately 87000 compounds against Trypanosoma brucei brucei, we recently identified eight