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Anup Kumar Misra
Researcher at Bose Institute
Publications - 252
Citations - 2897
Anup Kumar Misra is an academic researcher from Bose Institute. The author has contributed to research in topics: Glycosyl & Glycosylation. The author has an hindex of 26, co-authored 247 publications receiving 2582 citations. Previous affiliations of Anup Kumar Misra include University of Debrecen & Central Drug Research Institute.
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Journal ArticleDOI
The α(1,3)fucosyltransferases FucT-IV and FucT-VII Exert Collaborative Control over Selectin-Dependent Leukocyte Recruitment and Lymphocyte Homing
Jonathon W. Homeister,Aron D. Thall,Bronia Petryniak,Petr Malý,Clare E. Rogers,Peter L. Smith,Robert Kelly,Kevin M. Gersten,Sanaz Askari,Guiying Cheng,Glennda Smithson,Rory M. Marks,Anup Kumar Misra,Ole Hindsgaul,Ulrich H. von Andrian,John B. Lowe,John B. Lowe +16 more
TL;DR: It is shown here that inflammation-dependent leukocyte recruitment retained in FucT-VII deficiency is extinguished in FucaT-IV(-/-)/FucT -VII(-/-) mice, and essential Fuct-IV-dependent contributions to E-, P-, and L-selectin ligand synthesis and to the control of leukocytes recruitment and lymphocyte homing are revealed.
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Ferrier Rearrangement Catalyzed by HClO4-SiO2: Synthesis of 2,3-Unsaturated Glycopyranosides
TL;DR: Alkyl 2,3-unsaturated glycopyranosides have been prepared by the Ferrier rearrangement of acetyl protected glycals catalyzed by HClO 4 -SiO 2 as discussed by the authors.
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Poly-N-acetyllactosamine Extension inN-Glycans and Core 2- and Core 4-branchedO-Glycans Is Differentially Controlled by i-Extension Enzyme and Different Members of the β1,4-Galactosyltransferase Gene Family *
TL;DR: It is found that poly-N-acetyllactosamine synthesis in N-glycans and core 2- and core 4-branchedO- glycans is achieved by iGnT and distinct members of the β4Gal-T gene family.
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One-pot synthesis of per-O-acetylated thioglycosides from unprotected reducing sugars.
TL;DR: A sequential per-O-acetylation and thioglycosidation of unprotected reducing sugars using a stoichiometric quantity of acetic anhydride and alkyl- or arylthiols is reported.
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HClO4-SiO2 catalyzed per-O-acetylation of carbohydrates.
TL;DR: An efficient per-O-acetylation of carbohydrates catalyzed by HClO4-SiO2 is reported using a stoichiometric quantity of acetic anhydride avoiding the use of pyridine and excess aceticAnhydride under solvent-free conditions.