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1987
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1987
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Identification of carbohydrate structures that are possible receptors for Neisseria gonorrhoeae. |
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1988
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Single-amino-acid substitution in an antigenic site of influenza virus hemagglutinin can alter the specificity of binding to cell membrane-associated gangliosides. |
1989
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Lacto- and ganglio-series glycolipids are adhesion receptors for Neisseria gonorrhoeae |
1990
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Characterization of the binding of propionibacterium granulosum to glycosphingolipids adsorbed on surfaces. An apparent recognition of lactose which is dependent on the ceramide structure |
1990
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1990
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1990
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Comparison of the glycolipid-binding specificities of cholera toxin and porcine Escherichia coli heat-labile enterotoxin: identification of a receptor-active non-ganglioside glycolipid for the heat-labile toxin in infant rabbit small intestine. |
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Glycosphingolipid receptor function is modified by fatty acid content. Verotoxin 1 and verotoxin 2c preferentially recognize different globotriaosyl ceramide fatty acid homologues. |
1994
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Multiple glycosphingolipids determine the tissue tropism of parvovirus B19. |
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1995
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Infection and Immunity, 1995; vol. 63 no. 2: 640-646
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Putative glycoprotein and glycolipid polymorphonuclear leukocyte receptors for the Actinomyces naeslundii WVU45 fimbrial lectin |
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1995
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Cystic fibrosis epithelial cells have a receptor for pathogenic bacteria on their apical surface |
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Infection and Immunity, 1998; vol. 66 no. 9: 4403-4410
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Shiga toxin binds human platelets via globotriaosylceramide (Pk antigen) and a novel platelet glycosphingolipid. |
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Applied and Environmental Microbiology, 1999 Mar; vol. 65 no. 3: 1348-51
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FEMS Immunology and Medical Microbiology, 1999 Mar 1; vol. 23 no. 3: 221-227
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Infection and Immunity, 1999; vol. 67 no. 12: 6309-6313
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