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1 syl residues of N-acetyllactosamine close to nonreducing terminals.
2 , which preferentially binds to a cluster of nonreducing terminal alpha1,3-linked mannosyl residues,
3 rom additional favorable interactions of the nonreducing terminal galactose, as well as of the fucose
4 llactosamine antenane, neuraminic acids, and nonreducing terminal GlcNAc monosaccharides, commonly su
5 ulfotransferases can transfer sulfate to the nonreducing terminal GlcNAc of short carbohydrate substr
6 thod, which revealed that it was composed of nonreducing terminal glucopyranosyl, 6-linked glucopyran
7 nd of beta(1-->6)-glucan is connected to the nonreducing terminal glucose of beta(1-->3)-glucan throu
9 branched, primarily with double branches of nonreducing terminal l-arabinosyl units at the O-2 and O
10 I preferentially cleaves exolytically at the nonreducing terminal linkage of the HLGAG chain, althoug
11 to Ca(2+) in a primary binding site and the nonreducing terminal mannose residue occupying an adjace
13 proteins are involved in the assembly of the nonreducing terminal motif of arabinogalactan and EmbC i
14 beta1,4-galactosylation is the presence of a nonreducing terminal N-acetylglucosamine; however, this
15 bits highest specificity and affinity toward nonreducing terminal Neu5Acalpha2, 6Galbeta1,4Glc/GlcNAc
17 inding patterns, confirmed the presence of a nonreducing terminal repeating LacNAc ((Galbeta1-->4GlcN
18 onal immunoglobulin A (IgA) specific for the nonreducing terminal residue of Ogawa O-polysaccharide (
19 For IgG1s S-20-4, A-20-6, and IgA 2D6, the nonreducing terminal residue of Ogawa O-PS is the domina
21 The rhamnogalacturonan I has numerous single nonreducing terminal residues of the rare sugar l-galact
22 id chromatography to separate and quantitate nonreducing terminal structures, in addition to internal
24 dase digestion confirmed the identity of the nonreducing terminal sugar of the disaccharide and estab
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