GlyCosmos PubAnnotations

Recent publication annotations of glycans, cell types, and proteins, from PubAnnotation.

Displaying entries 3776 - 3800 of 24862 in total
Title ▼ Authors PubMed ID Source Publication Year
Synthesis of N-glycan oxazolines: donors for endohexosaminidase catalysed glycosylation.
  • Rising TW
  • Claridge TD
  • Davies N
  • Gamblin DP
  • Moir JW
  • Fairbanks AJ
16584712 Carbohydr Res 2006
Synthesis of N-acetylmannosamine-6-phosphate derivatives to investigate the mechanism of N-acetylmannosamine-6-phosphate 2-epimerase.
  • Arif T
  • Currie MJ
  • Dobson RCJ
  • Newson HL
  • Poonthiyil V
  • Fairbanks AJ
  • North RA
  • Rendle PM
34607125 Carbohydr Res 2021
Synthesis of N-acetyllactosamine containing a D-[6-3H]galactopyranosyl group.
  • Plessas NR
  • Blake DA
  • Goldstein IJ
6467246 Carbohydr Res 1984
Synthesis of N-acetylglucosamine derivatives as probes for specificity of chicken hepatic lectin.
  • Ichikawa Y
  • Lee RT
  • Lee YC
2136349 Glycoconj J 1990
Synthesis of N-acetylglucosamine containing Lewis A and Lewis X building blocks based on N-tetrachlorophthaloyl protection--synthesis of Lewis X pentasaccharide.
  • Lay L
  • Manzoni L
  • Schmidt RR
9809410 Carbohydr Res 1998
Synthesis of N-acetyl-4,8-dideoxyneuraminic acid-containing ganglioside GM3.
  • Yoshida M
  • Ishida H
  • Kiso M
  • Hasegawa A
8593644 Carbohydr Res 1996
Synthesis of N-(1-deoxyhexitol-1-yl)amino acids, reference compounds for the nonenzymic glycosylation of proteins.
  • Walton DJ
  • Ison ER
  • Szarek WA
6733725 Carbohydr Res 1984
Synthesis of MUC1-derived glycopeptide bearing a novel triazole STn analog.
  • Marchiori MF
  • Bortot LO
  • Carvalho I
  • Campo VL
33010570 Carbohydr Res 2020
Synthesis of Lewis(X)-O-Core-1 threonine: A building block for O-linked Lewis(X) glycopeptides.
  • Sardar MYR
  • Krishnamurthy VR
  • Park S
  • Mandhapati AR
  • Wever WJ
  • Park D
  • Cummings RD
  • Chaikof EL
29065342 Carbohydr Res 2017
Synthesis of Lewis X trisaccharide analogues in which glucose and rhamnose replace N-acetylglucosamine and fucose, respectively.
  • Asnani A
  • Auzanneau FI
12706970 Carbohydr Res 2003
Synthesis of Lewis X epitopes on plant N-glycans.
  • Rouwendal GJ
  • Florack DE
  • Hesselink T
  • Cordewener JH
  • Helsper JP
  • Bosch D
19515362 Carbohydr Res 2009
Synthesis of Lewis X and three Lewis X trisaccharide analogues in which glucose and rhamnose replace N-acetylglucosamine and fucose, respectively.
  • Asnani A
  • Auzanneau FI
18466887 Carbohydr Res 2008
Synthesis of Lewis A trisaccharide analogues in which D-glucose and L-rhamnose replace D-galactose and L-fucose, respectively.
  • Liao L
  • Auzanneau FI
16879812 Carbohydr Res 2006
Synthesis of Le(a)Le(x) oligosaccharide fragments and efficient one-step deprotection.
  • Wang A
  • Auzanneau FI
20413107 Carbohydr Res 2010
Synthesis of LacdiNAc-terminated glycoconjugates by mutant galactosyltransferase--a way to new glycodrugs and materials.
  • Bojarová P
  • Krenek K
  • Wetjen K
  • Adamiak K
  • Pelantová H
  • Bezouska K
  • Elling L
  • Kren V
19179461 Glycobiology 2009
Synthesis of L-trehalose and observations on isomer and by-product formation.
  • Haines AH
12681904 Carbohydr Res 2003
Synthesis of L-gulose, L-galactose, and their acetylated aldehydo forms from 6-S-phenyl-6-thio-D-hexoses.
  • Santoyo González F
  • Baer HH
2224894 Carbohydr Res 1990
Synthesis of L-glucose from D-gulono-1,4-lactone.
  • Hajkó J
  • Lipták A
  • Pozsgay V
10612005 Carbohydr Res 1999
Synthesis of L-fucose 2-, 3-, and 4-sulphates.
  • Forrester PF
  • Lloyd PF
  • Stuart CH
963690 Carbohydr Res 1976
Synthesis of L-arabinose 5-phosphate, 5-0-carbamoyl-D-arabinose and 6-9-carbamoyl-D-glucose.
  • Abd-el-Rahman MM
  • Hornemann U
  • Hronemann U
4447946 Carbohydr Res 1974
Synthesis of KDN-lactotetraosylceramide, KDN-neolactotetraosylceramide, and KDN-Lewis X ganglioside.
  • Terada T
  • Kiso M
  • Hasegawa A
8050096 Carbohydr Res 1994
Synthesis of Hexp-(1-->4)-beta-D-GlcpNAc-(1-->2)-alpha-D-Manp-(1-->O) (CH2)7 CH3 probes for exploration of the substrate specificity of glycosyltransferases: Part II, Hex = 3-O-methyl-beta-D-Gal, 3-deoxy-beta-D-Gal, 3-deoxy-3-fluoro-beta-D-Gal, 3-amino-3-deoxy-beta-D-Gal, beta-D-Gul, alpha-L-Alt, or beta-L-Gal.
  • van Dorst JA
  • van Heusden CJ
  • Tikkanen JM
  • Kamerling JP
  • Vliegenthart JF
9060187 Carbohydr Res 1997
Synthesis of Hex p-(1-->4)-beta-D-Glc pNAc-(1-->2)-alpha-D-Man p-(1-->O)(CH2)7CH3 probes for exploration of the substrate specificity of glycosyltransferases: Part I, Hex = beta-D-Gal, 4-deoxy-beta-D-Gal, 4-O-methyl-beta-D-Gal, 4-deoxy-4-fluoro-beta-D-Gal, or beta-D-Glc.
  • van Dorst JA
  • van Heusden CJ
  • Voskamp AF
  • Kamerling JP
  • Vliegenthart JF JF
8864224 Carbohydr Res 1996
Synthesis of Gal-beta-(1-->4)-GlcNac-beta-(1-->6)-[Gal-beta-(1-->3]-GalNAc-alpha- OBn oligosaccharides bearing O-methyl or O-sulfo groups at C-3 of the Gal residue: specific acceptors for Gal: 3-O-sulfotransferases.
  • Jain RK
  • Piskorz CF
  • Chandrasekaran EV
  • Matta KL
10211700 Glycoconj J 1998
Synthesis of Gal beta 1-3GlcNAc and Gal beta 1-3GlcNAc beta-SEt by an enzymatic method comprising the sequential use of beta-galactosidases from bovine testes and Escherichia coli.
  • Hedbys L
  • Johansson E
  • Mosbach K
  • Larsson PO
  • Gunnarsson A
  • Svensson S
  • Lönn H
2535481 Glycoconj J 1989

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