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1 rasaccharide antigen found on the Leishmania lipophosphoglycan.
2                      Despite the presence of lipophosphoglycan, a TLR2 ligand capable of eliciting ho
3  TLR2 short hairpin RNA or anti-TLR2 or anti-lipophosphoglycan Abs reversed the L. major-altered N-Ra
4 TvLG), that differs markedly from Leishmania lipophosphoglycan and Entamoeba lipopeptidophosphoglycan
5 her-lipid derivatives and virulence factors, lipophosphoglycan and GPI-anchored proteins, gp63, and i
6     Since Leishmania major mutants that lack lipophosphoglycan and other secreted phosphoglycans, ter
7 lerance to stress, and altered expression of lipophosphoglycan and proteophosphoglycan.
8 d permit discrimination between the roles of lipophosphoglycan and related glycoconjugates.
9 ese molecules are present in L. major SEAgs, lipophosphoglycan and the molecules that associate with
10 h parasite surface phosphoglycans, including lipophosphoglycan, are not required for IgMn-induced par
11        The Leishmania surface glycoconjugate lipophosphoglycan, as well as related glycoinositol phos
12                     LPG2 (a gene involved in lipophosphoglycan assembly) encodes the Golgi GDP-Man tr
13          Pretreatment with purified parasite lipophosphoglycan before IFN-gamma stimulation had no ef
14                           When two different lipophosphoglycan biosynthetic genes from Leishmania maj
15 is study, we show that L. amazonensis or its lipophosphoglycan can induce neutrophil activation, degr
16                               The Leishmania lipophosphoglycan conveys the ability for the parasites
17 jor lpg2(-), instead resembling the L. major lipophosphoglycan-deficient lpg1(-) mutant.
18  promastigotes from cutaneous, visceral, and lipophosphoglycan-deficient strains of Leishmania.
19 lpg1-knockout parasites expressing defective lipophosphoglycan did not induce autophagy, indicating t
20                    We have characterized the lipophosphoglycan from an Indian L. donovani isolate.
21 tose- and mannose-terminating cap, procyclic lipophosphoglycan from the Indian isolate consists of be
22 xpressed and secreted molecules of L. major (lipophosphoglycan, gp46/M2/PSA-2, and gp63) revealed tha
23                                     Membrane lipophosphoglycan increased in size as parasites develop
24                                Structurally, lipophosphoglycan is a multidomain glycoconjugate whose
25                                              Lipophosphoglycan is a prominent member of the phosphogl
26 an did not induce autophagy, indicating that lipophosphoglycan is necessary for interaction with the
27        We found that L. chagasi infection or lipophosphoglycan isolated from promastigotes triggered
28       Of biological significance, metacyclic lipophosphoglycan lacks the glucose residues while doubl
29 hogen glycolipids, including Leishmania spp. lipophosphoglycan (LPG) and Mycobacterium tuberculosis m
30 dant surface and secreted molecules, such as lipophosphoglycan (LPG) and proteophosphoglycans (PPGs),
31 extents on abundant glycoconjugates, such as lipophosphoglycan (LPG) and related molecules, in mammal
32  of Leishmania major, including the abundant lipophosphoglycan (LPG) implicated in parasite survival
33                We have shown that Leishmania lipophosphoglycan (LPG) inhibits IL-1 beta gene expressi
34                                   Leishmania lipophosphoglycan (LPG) is a key virulence factor, initi
35                                              Lipophosphoglycan (LPG) is an abundant surface molecule
36 ds known to be prominent constituents of the lipophosphoglycan (LPG) of T. foetus.
37 facilitated its use as a donor substrate for lipophosphoglycan (LPG) synthesis.
38 nt for the inhibitory activity of Leishmania lipophosphoglycan (LPG) to block endothelial adhesion to
39         The abundant cell surface glycolipid lipophosphoglycan (LPG) was implicated in many steps of
40        We examined the mechanism(s) by which lipophosphoglycan (LPG), a major glycolipid of Leishmani
41 e chain oligosaccharides of the cell-surface lipophosphoglycan (LPG), mutagenized Leishmania major de
42 f molecules implicated in virulence, such as lipophosphoglycan (LPG), smaller glycosylinositolphospho
43 cts of Tritrichomonas foetus and the role of lipophosphoglycan (LPG)-like cell surface glycoconjugate
44 oconjugate of the parasite, the T. vaginalis lipophosphoglycan (LPG).
45 or for the stage-specific Leishmania adhesin lipophosphoglycan (LPG).
46  modifications of the stage-specific adhesin lipophosphoglycan (LPG).
47 glycan repeats of the major surface adhesin, lipophosphoglycan (LPG).
48 nositol (GPI)-anchored polysaccharide called lipophosphoglycan (LPG).
49 e (CPI-GC) of the dominant surface protozoan lipophosphoglycan (LPG).
50 iphile known to alter membrane properties is lipophosphoglycan (LPG).
51 xpression of the key surface glycoconjugate, lipophosphoglycan (LPG).
52 urface through phosphatidylinositol anchors (lipophosphoglycan, LPG) or secreted as protein-containin
53  for the cell walls of Mycobacteria, for the lipophosphoglycan of Leishmania, and for other microorga
54 fts with a monoclonal antibody to the amebic lipophosphoglycan-peptidoglycan molecules can prevent or
55 oeba histolytica trophozoites are covered by lipophosphoglycan-peptidoglycan molecules which may be k
56                                              Lipophosphoglycan plays an integral role during this tra
57 ance of these developmental modifications in lipophosphoglycan structure was determined using binding
58 -gamma binding on the 11betaHSD1 promoter by lipophosphoglycan, which drives cortisol production.
59 2 play a role in side-chain modifications of lipophosphoglycan, while gene deletion studies here show
60 attachment involves galectins and Leishmania lipophosphoglycan, while in permissive species like Lutz
61 e or heat-killed parasites, but not purified lipophosphoglycan, while that of other SOCS genes remain