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1 azine; the latter removed O acetyls from the O-specific polysaccharide.
3 cholera toxin B and A subunits, V. cholerae O-specific polysaccharide and lipopolysaccharide, toxin
4 generation of the serologic response to the O-specific polysaccharide and protection against virulen
5 serotype Ogawa, which comprises in part the O-specific polysaccharide component of the native LPS, a
6 lts showed that a vaccine of E. coli O157:H7 O-specific polysaccharide conjugated to recombinant exot
7 carbohydrates, including mannose-containing O-specific polysaccharides derived from bacterial lipopo
8 tical (protective) level of serum IgG to the O-specific polysaccharide (O-SP) domain of Shigella lipo
9 hypothesis that serum IgG antibodies to the O-specific polysaccharide (O-SP) domains of the LPS of t
13 and a clinical trial with a Shigella sonnei O-specific polysaccharide (O-SP)-Pseudomonas aeruginosa
14 0-6, which are specific for Ogawa O-antigen (O-specific polysaccharide; O-SP) of V. cholerae O1, were
15 ing sequence forms the downstream end in the O-specific polysaccharide of both Vibrio cholerae O22 an
16 he case with Shigella, serum IgG against the O-specific polysaccharide of E. coli O157:H7 may confer
17 inst the surface polysaccharide antigen, the O-specific polysaccharide of lipopolysaccharide (LPS), m
19 a dimer of the basic repeating unit from the O-specific polysaccharide of Shigella flexneri 2a, a maj
20 c the terminal hexasaccharide epitope of the O-specific polysaccharide of Vibrio cholerae O1, serotyp
22 enetically modified strains deficient in the O-specific polysaccharide, we isolated fractions of core
23 prepared by covalently binding E. coli O157 O-specific polysaccharide with Pseudomonas aeruginosa re
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