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1 osphingolipid, or a synthetic agonist, alpha-galactosyl ceramide.
2 aired following in vivo challenge with alpha-galactosyl ceramide.
3 of a precursor lipid, galactosyl-(alpha1-2)-galactosyl ceramide.
4 bes a short and efficient synthesis of alpha-galactosyl ceramide.
5 ns (MLR), anti-CD3, and the glycolipid alpha-galactosyl ceramide.
6 using the previously cloned cDNA encoding a galactosyl ceramide 3-O-sulfotransferase, which we term
8 the CD1d molecule to bind and present alpha-galactosyl ceramide after lysosomal processing of a prec
11 her species can present the glycolipid alpha-galactosyl ceramide (alpha-GalCer) to mouse natural kill
12 ll responses to the glycolipid antigen alpha-galactosyl ceramide (alpha-GalCer) were dampened by prio
13 ogs of the well known NKT cell agonist alpha-galactosyl ceramide (alpha-GalCer), bacterial glycolipid
14 aded with a synthetic NKT cell ligand, alpha-galactosyl-ceramide (alpha-GalCer; KRN-7000) in five pat
15 ion with the NKT cell-specific agonist alpha-galactosyl ceramide (alphaGC), Sh2d1a-/- splenocytes did
16 in response to the model iNKT cell Ag alpha-galactosyl ceramide and expressed lower amounts of the T
18 simple strategy for the synthesis of beta-C-galactosyl ceramide and its new aza-variant analogue is
19 le for assembly or the ability to bind alpha-galactosyl ceramide and to present it to human NKT cells
21 Cell surface expression was detected for galactosyl ceramide but not for CC-chemokine receptor 5,
23 The preparation of the glycosphingolipid galactosyl ceramide from an orthogonally protected five-
24 ugh both Gal3ST-2 and Gal3ST-3 do not act on galactosyl ceramide, Gal3ST-3 is only moderately more ho
28 ion factor 21 and GATA3 expression and alpha-galactosyl ceramide-induced cytokine production in vivo.
29 1) and recognize lipid antigens (e.g., alpha-galactosyl ceramide) presented by nonpolymorphic CD1 mol
30 levels of IL-4 following TCR ligation, alpha-galactosyl ceramide-stimulated NKT cells from the livers
32 er T (NKT) cells mobilizing glycolipid alpha-galactosyl ceramide, used to mature splenic DCs, served
34 In vivo stimulation of iNKT cells by alpha-galactosyl-ceramide was effective in both preventing and
35 nistration of concanavalin A (ConA) or alpha-galactosyl-ceramide, which induce liver inflammation and
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