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2 Escherichia coli O86 possesses high human blood group B activity because of its O-antigen structur
3 ipients of allograft expressing incompatible blood group B also produce anti-Gal B antibody, which bi
5 ng kidneys from A2 donors into patients with blood group B and O recipients has been used to alleviat
6 explanation for contrasts in associations of blood groups B and AB between CagA-endemic and -nonendem
8 d to a series of oligomannose compounds, the blood group B antigen, and a fragment of beta-glucan rev
9 minant alpha1,3-linked galactose residues of blood group B antigens, we recently identified a novel p
10 have increased the transplantation rate for blood group B cadaveric waiting list candidates by trans
13 specificity of anti-alphaGal antibodies; (3) blood group B human and baboon sera have lower levels of
16 The median waiting times for patients with blood groups B or O were 1329 and 1007 days, respectivel
21 e carbohydrate binding properties, including blood group B-specific agglutination and preferential bi
23 isite substrate specificity for the branched blood group B structure Galalpha1-3(Fucalpha1-2)Gal, whe
24 have exclusive specificity for the branched blood group B structures, whereas members of a newly ide
26 Moreover, we found that the genetic-inferred blood group B was associated with a decreased risk (OR =
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