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1 rasaccharide antigen found on the Leishmania lipophosphoglycan.
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
8 ese molecules are present in L. major SEAgs, lipophosphoglycan and the molecules that associate with
13 is study, we show that L. amazonensis or its lipophosphoglycan can induce neutrophil activation, degr
18 tose- and mannose-terminating cap, procyclic lipophosphoglycan from the Indian isolate consists of be
19 xpressed and secreted molecules of L. major (lipophosphoglycan, gp46/M2/PSA-2, and gp63) revealed tha
25 hogen glycolipids, including Leishmania spp. lipophosphoglycan (LPG) and Mycobacterium tuberculosis m
26 dant surface and secreted molecules, such as lipophosphoglycan (LPG) and proteophosphoglycans (PPGs),
27 extents on abundant glycoconjugates, such as lipophosphoglycan (LPG) and related molecules, in mammal
28 of Leishmania major, including the abundant lipophosphoglycan (LPG) implicated in parasite survival
34 nt for the inhibitory activity of Leishmania lipophosphoglycan (LPG) to block endothelial adhesion to
37 e chain oligosaccharides of the cell-surface lipophosphoglycan (LPG), mutagenized Leishmania major de
38 f molecules implicated in virulence, such as lipophosphoglycan (LPG), smaller glycosylinositolphospho
39 cts of Tritrichomonas foetus and the role of lipophosphoglycan (LPG)-like cell surface glycoconjugate
48 urface through phosphatidylinositol anchors (lipophosphoglycan, LPG) or secreted as protein-containin
49 for the cell walls of Mycobacteria, for the lipophosphoglycan of Leishmania, and for other microorga
50 fts with a monoclonal antibody to the amebic lipophosphoglycan-peptidoglycan molecules can prevent or
51 oeba histolytica trophozoites are covered by lipophosphoglycan-peptidoglycan molecules which may be k
53 ance of these developmental modifications in lipophosphoglycan structure was determined using binding
54 e or heat-killed parasites, but not purified lipophosphoglycan, while that of other SOCS genes remain
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