scholarly article | Q13442814 |
P356 | DOI | 10.3762/BJOC.8.126 |
P953 | full work available online at | http://www.beilstein-journals.org/bjoc/content/8/1/126 |
https://europepmc.org/articles/PMC3458731 | ||
https://europepmc.org/articles/PMC3458731?pdf=render | ||
https://www.beilstein-journals.org/bjoc/articles/8/126 | ||
https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-8-126.pdf | ||
P932 | PMC publication ID | 3458731 |
P698 | PubMed publication ID | 23019441 |
P5875 | ResearchGate publication ID | 231225572 |
P2093 | author name string | France-Isabelle Auzanneau | |
Christopher J. Moore | |||
P2860 | cites work | Synthesis of spacer-equipped phosphorylated di-, tri- and tetrasaccharide fragments of the O-specific polysaccharide of Vibrio cholerae O139 | Q28196938 |
Immunochemical characterization of polyclonal and monoclonal Streptococcus group A antibodies by chemically defined glycoconjugates and synthetic oligosaccharides | Q28317152 | ||
Involvement of water in carbohydrate-protein binding. | Q30666622 | ||
Why are the hydroxy groups of partially protected N-acetylglucosamine derivatives such poor glycosyl acceptors, and what can be done about it? A comparative study of the reactivity of N-acetyl-, N-phthalimido-, and 2-azido-2-deoxy-glucosamine deriva | Q33423429 | ||
Convergent syntheses of Le analogues | Q33853098 | ||
Computational carbohydrate chemistry: what theoretical methods can tell us | Q34467370 | ||
Modeling protein recognition of carbohydrates | Q36185366 | ||
Localization and alteration of mono-, di-, and trifucosyl alpha 1----3 type 2 chain structures during human embryogenesis and in human cancer | Q36349361 | ||
Lewis x is highly expressed in normal tissues: a comparative immunohistochemical study and literature revision | Q36868517 | ||
Molecular Recognition of Sialyl Lewisxand Related Saccharides by Two Lectins | Q38295466 | ||
O-antigen biotin conjugates preparation and use in direct competitive enzyme immunoassays | Q38339221 | ||
Synthesis of a BSA-Le(x) glycoconjugate and recognition of Le(x) analogues by the anti-Le(x) monoclonal antibody SH1: the identification of a non-cross reactive analogue | Q38340863 | ||
Synthesis of type 2 human blood-group antigenic determinants. The H, X, and Y haptens and variations of the H type 2 determinant as probes for the combining site of the lectin I of Ulex europaeus | Q38355170 | ||
Synthesis of Lewis X trisaccharide analogues in which glucose and rhamnose replace N-acetylglucosamine and fucose, respectively | Q38355359 | ||
Total synthesis of X hapten, III3 Fuc alpha-nLc4 Cer. | Q42067267 | ||
Synthesis of a tri- and a hepta-saccharide which contain alpha-L-fucopyranosyl groups and are part of the complex type of carbohydrate moiety of glycoproteins | Q42228789 | ||
Synthesis of Le(a)Le(x) oligosaccharide fragments and efficient one-step deprotection | Q43088537 | ||
How the substituent at O-3 of N-acetylglucosamine impacts glycosylation at O-4: a comparative study | Q43265662 | ||
A highly efficient synthetic strategy for polymeric support synthesis of Le(x), Le(y), and H-type 2 oligosaccharides | Q43669118 | ||
Synthesis of building blocks of human milk oligosaccharides. Fucosylated derivatives of the lacto- and neolacto-series. | Q44120700 | ||
Complex oligosaccharide investigations: synthesis of an octasaccharide incorporating the dimeric Le(x) structure of PSGL-1. | Q44380187 | ||
Profiles of Lewisx-containing glycoproteins and glycolipids in sera of patients with adenocarcinoma | Q44387332 | ||
Assembly of a series of malarial glycosylphosphatidylinositol anchor oligosaccharides | Q45281664 | ||
Application and limitations of the methyl imidate protection strategy of N-acetylglucosamine for glycosylations at O-4: synthesis of Lewis A and Lewis X trisaccharide analogues | Q46359622 | ||
Convenient temporary methyl imidate protection of N-acetylglucosamine and glycosylation at O-4. | Q46393285 | ||
Synthesis of Lewis X and three Lewis X trisaccharide analogues in which glucose and rhamnose replace N-acetylglucosamine and fucose, respectively | Q46604814 | ||
The amide group in N-acetylglucosamine glycosyl acceptors affects glycosylation outcome | Q46623545 | ||
Unusual conformational behavior of trisaccharides containing N-acetylglucosamine | Q46768404 | ||
Differential expression of Lewis(x) and sialyl-Lewis(x) antigens in fetal human neural cells in culture | Q48169369 | ||
Location and distribution of difucoganglioside (VI3NeuAcV3III3Fuc2nLc6) in normal and tumor tissues defined by its monoclonal antibody FH6. | Q53798317 | ||
Computer simulation of histo-blood group oligosaccharides: energy maps of all constituting disaccharides and potential energy surfaces of 14 ABH and Lewis carbohydrate antigens | Q56084985 | ||
A Novel and Efficient Synthesis of a Dimeric LexOligosaccharide on Polymeric Support | Q57242579 | ||
Crystal and molecular structure of a histo-blood group antigen involved in cell adhesion: the Lewis x trisaccharide | Q57242974 | ||
Solution structure of the Lewis x oligosaccharide determined by NMR spectroscopy and molecular dynamics simulations | Q67519118 | ||
Synthesis of oligosaccharides containing the X-antigenic trisaccharide (alpha-L-Fucp-(1----3)-[beta-D-Galp-(1----4)]-beta-D-GlcpNAc) at their nonreducing ends | Q68010545 | ||
Lewisx- and sialylated Lewisx-related antigen expression in human malignant and nonmalignant colonic tissues | Q68871716 | ||
Mosaicism in the expression of tumor-associated carbohydrate antigens in human colonic and gastric cancers | Q69506209 | ||
Oligosaccharides of human milk. II. Isolation and characterization of a new pentasaccharide, lacto-N-fucopentaose 3 | Q71230172 | ||
A Sphingolipid Having a Novel Type of Ceramide and Lacto-N-Fucopentaose III | Q71760939 | ||
Total synthesis of sulfated Le(x) pentaosyl ceramide | Q72368601 | ||
Novel fucolipids accumulating in human adenocarcinoma. II. Selective isolation of hybridoma antibodies that differentially recognize mono-, di-, and trifucosylated type 2 chain | Q72728094 | ||
Active-latent glycosylation strategy toward Lewis X pentasaccharide in a form suitable for neoglycoconjugate syntheses | Q73068061 | ||
Glycosylation of N-acetylglucosamine: imidate formation and unexpected conformation | Q73685611 | ||
Selection of tumor antigens as targets for immune attack using immunohistochemistry: II. Blood group-related antigens | Q73798453 | ||
Synthesis of N-acetylglucosamine containing Lewis A and Lewis X building blocks based on N-tetrachlorophthaloyl protection--synthesis of Lewis X pentasaccharide | Q77534570 | ||
Stereospecific ester activation in nitrite-mediated carbohydrate epimerization | Q83111824 | ||
Syntheses and NMR characterizations of epimeric 4-deoxy-4-fluoro carbohydrates | Q84927536 | ||
An efficient synthesis of the Lewis X (Lex) antigen family | Q127237288 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | oligosaccharide biosynthetic process | Q21109511 |
alpha-L-Fucp-(1->3)-[beta-D-Galp4Cl-(1->4)]-beta-D-GlcpNAc-OMe | Q27146753 | ||
alpha-L-Fucp-(1->3)-[beta-D-Galp4F-(1->4)]-beta-D-GlcpNAc-OMe | Q27146754 | ||
4-chloro-4-deoxygalactose | Q106490025 | ||
P304 | page(s) | 1134-1143 | |
P577 | publication date | 2012-07-23 | |
P1433 | published in | Beilstein Journal of Organic Chemistry | Q2894008 |
P1476 | title | Synthesis of 4" manipulated Lewis X trisaccharide analogues | |
Synthesis of 4” manipulated Lewis X trisaccharide analogues | |||
P478 | volume | 8 |
Q42174680 | Multivalent glycosystems for nanoscience |
Q99591021 | Recognition of Dimeric Lewis X by Anti-Dimeric Lex Antibody SH2 |
Q91010790 | Recognition of Lewis X by Anti-Lex Monoclonal Antibody IG5F6 |
Q48262784 | Synthesis of Protected 3-Deoxy-3-fluoro- and 4-Deoxy-4-fluoro-d-galactopyranosides from Levoglucosan. |
Q64277570 | Synthesis of carbohydrate building blocks via regioselective uniform protection/deprotection strategies |
Q42709282 | Understanding the recognition of Lewis X by anti-Le(x) monoclonal antibodies |
Search more.