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1 in building the main capsule polysaccharide, glucuronoxylomannan.
2 ted with higher serum titers of cryptococcal glucuronoxylomannan.
3 mAb 2H1 binds C. neoformans glucuronoxylomannan.
4 or the major type-specific capsular antigen, glucuronoxylomannan.
5 survival, reducing CFU, and reducing tissue glucuronoxylomannan Ag. mAb administration was associate
6 tococcus neoformans capsular polysaccharides glucuronoxylomannan and galactoxylomannan (GalXM) elicit
12 the MAb was not cross-reactive with purified glucuronoxylomannan derived from either serotypes A or D
13 1, one of a large family of mAbs against the glucuronoxylomannan fraction (GXM), is highly protective
14 n V region usage for Cryptococcus neoformans glucuronoxylomannan, glucuronoxylomannan peptide mimetic
15 sis of the two main capsule polysaccharides, glucuronoxylomannan (GXM) and galactoxylomannan (GalXM),
16 l for virulence and is composed primarily of glucuronoxylomannan (GXM) and galactoxylomannan (GalXM).
17 eactive with the cryptococcal polysaccharide glucuronoxylomannan (GXM) are present in sera from both
18 sma levels of immunoglobulins, C. neoformans glucuronoxylomannan (GXM) capsule-specific and laminarin
19 ine monoclonal antibodies (MAbs) against the glucuronoxylomannan (GXM) component of the C. neoformans
20 ith a glycoconjugate vaccine composed of the glucuronoxylomannan (GXM) component of the cryptococcal
21 ith a glycoconjugate vaccine composed of the glucuronoxylomannan (GXM) component of the cryptococcal
22 pertoire of human antibodies to cryptococcal glucuronoxylomannan (GXM) elicited by the investigationa
23 or (PAF) content in mice given C. neoformans glucuronoxylomannan (GXM) followed by specific Ab of IgG
24 o biological function of human antibodies to glucuronoxylomannan (GXM) from individuals immunized wit
25 ptococcus neoformans capsular polysaccharide glucuronoxylomannan (GXM) have been rigorously investiga
26 ptococcus neoformans capsular polysaccharide glucuronoxylomannan (GXM) have been shown to be protecti
27 to the C. neoformans capsular polysaccharide glucuronoxylomannan (GXM) have demonstrated that patient
28 response to Cryptococcus neoformans capsular glucuronoxylomannan (GXM) in BALB/c mice frequently expr
29 antibodies (Abs) to Cryptococcus neoformans glucuronoxylomannan (GXM) is dependent on Ab fine specif
31 Most mAbs to the capsular polysaccharide glucuronoxylomannan (GXM) of Cryptococcus neoformans are
33 GXM10-Ac(3) was designed as an extension of glucuronoxylomannan (GXM) polysaccharide motif (M2) whic
34 IgA to the Cryptococcus neoformans capsular glucuronoxylomannan (GXM) promote complement-independent
35 epitope in Cryptococcus neoformans capsular glucuronoxylomannan (GXM) that can elicit protective ant
36 l constituents of native and de-O-acetylated glucuronoxylomannan (GXM) was determined by one-dimensio
38 ypes of cryptococcal capsular polysaccharide glucuronoxylomannan (GXM) was studied, followed by an as
40 or the major capsular polysaccharide, termed glucuronoxylomannan (GXM), can markedly suppress the abi
41 mAbs that recognize two epitopes of capsular glucuronoxylomannan (GXM), defined by the IgG1 mAbs 2H1
42 with cryptococcal capsular polysaccharide, a glucuronoxylomannan (GXM), exhibit increased survival ti
43 of CneF and its individual components, i.e., glucuronoxylomannan (GXM), galactoxylomannan (GalXM), an
44 rmine if cryptococcal polysaccharides, i.e., glucuronoxylomannan (GXM), galactoxylomannan, and mannop
45 ptococcus neoformans capsular polysaccharide glucuronoxylomannan (GXM), in mice that produce human an
46 r polysaccharide of Cryptococcus neoformans, glucuronoxylomannan (GXM), is recognized by Toll-like re
47 immunoglobulin M (IgM) and IgG responses to glucuronoxylomannan (GXM), lack of IgE regulation during
48 2H1, which binds to Cryptococcus neoformans glucuronoxylomannan (GXM), on pulmonary infection in imm
49 of the cryptococcal capsular polysaccharide glucuronoxylomannan (GXM), the key C. neoformans virulen
50 Monoclonal antibodies (MAbs) reactive with glucuronoxylomannan (GXM), the major capsular polysaccha
51 the host response to Cryptococcus neoformans glucuronoxylomannan (GXM), the major capsular polysaccha
52 urine macrophages treated with extracellular glucuronoxylomannan (GXM), the major Cn capsular polysac
54 ed that the 18B7 monoclonal antibody against glucuronoxylomannan (GXM), the major component of the Cr
65 ropriate for a role in the synthesis of this glucuronoxylomannan is active in cryptococcal membranes.
66 that the main fungal capsule polysaccharide glucuronoxylomannan is responsible for these alterations
67 ed the conservation of previously identified glucuronoxylomannan motifs only in the sonicated CPS.
68 Cryptococcus neoformans glucuronoxylomannan, glucuronoxylomannan peptide mimetics, and anti-Id mAbs.
70 t have specificity appropriate for a role in glucuronoxylomannan synthesis, it may participate in pro
71 cryptococcal capsular polysaccharide vaccine glucuronoxylomannan-tetanus toxoid (GXM-TT) have been sh
74 saccharide capsule composed predominantly of glucuronoxylomannan, which constitutes approximately 90%