Geert-Jan Boons mostly deals with Biochemistry, Stereochemistry, Glycosylation, Organic chemistry and Combinatorial chemistry. His Glycan, Glycopeptide, Glycoprotein, Peptidoglycan and Glycosyltransferase study are his primary interests in Biochemistry. Geert-Jan Boons has included themes like Sialic acid and Binding site in his Glycan study.
Geert-Jan Boons interconnects Azide, Click chemistry, Viral protein and Cycloaddition in the investigation of issues within Sialic acid. His Stereochemistry study frequently draws connections between related disciplines such as Stereoselectivity. The concepts of his Combinatorial chemistry study are interwoven with issues in Glycoprotein synthesis, Trisaccharide, Transferase and Solid-phase synthesis.
His primary areas of study are Stereochemistry, Biochemistry, Glycosylation, Glycan and Organic chemistry. His Stereochemistry research is multidisciplinary, incorporating elements of Protecting group and Stereoselectivity. His Biochemistry study frequently draws parallels with other fields, such as Epitope.
Geert-Jan Boons combines subjects such as Disaccharide and Glycoside with his study of Glycosylation. His Glycan research includes elements of Sialic acid and Binding site. His Organic chemistry study often links to related topics such as Combinatorial chemistry.
Geert-Jan Boons mainly investigates Glycan, Biochemistry, Heparan sulfate, Virology and Oligosaccharide. Geert-Jan Boons has researched Glycan in several fields, including Ion-mobility spectrometry, Mass spectrometry, Binding site and Ligand. The Biochemistry study combines topics in areas such as Epitope and Bacillus anthracis.
His studies deal with areas such as Sulfation, Stereochemistry, Glucosamine and Enzyme as well as Heparan sulfate. His research integrates issues of Residue and Transferase in his study of Stereochemistry. Geert-Jan Boons studied Virology and Sialic acid that intersect with Receptor, Viral protein and Viral entry.
Glycan, Heparan sulfate, Oligosaccharide, Coronavirus and Biochemistry are his primary areas of study. His Glycan research is multidisciplinary, relying on both Receptor, Computational biology and Binding site. His Computational biology study combines topics in areas such as Glycosylation and Enzymatic synthesis.
His work carried out in the field of Heparan sulfate brings together such families of science as Sulfation and Stereochemistry. His research investigates the connection between Stereochemistry and topics such as Chondroitin sulfate that intersect with issues in Glycomics. His research in Oligosaccharide focuses on subjects like Enzyme, which are connected to Heparitin Sulfate, Carbohydrate conformation, Epimer, Residue and Cell biology.
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Visualizing metabolically labeled glycoconjugates of living cells by copper-free and fast huisgen cycloadditions.
Xinghai Ning;Jun Guo;Margreet A. Wolfert;Geert-Jan Boons.
Angewandte Chemie (2008)
Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research
Thomas J. Boltje;Therese Buskas;Geert-Jan Boons.
Nature Chemistry (2009)
Strategies in Oligosaccharide Synthesis
Structural basis for human coronavirus attachment to sialic acid receptors.
M. Alejandra Tortorici;M. Alejandra Tortorici;M. Alejandra Tortorici;Alexandra C. Walls;Yifei Lang;Chunyan Wang.
Nature Structural & Molecular Biology (2019)
Recent advances in o-sialylation.
Geert-Jan Boons;Alexei V. Demchenko.
Chemical Reviews (2000)
Selective Labeling of Living Cells by a Photo-Triggered Click Reaction
Andrei A. Poloukhtine;Ngalle Eric Mbua;Margreet A. Wolfert;Geert-Jan Boons.
Journal of the American Chemical Society (2009)
Immune recognition of tumor-associated mucin MUC1 is achieved by a fully synthetic aberrantly glycosylated MUC1 tripartite vaccine
Vani Lakshminarayanan;Pamela Thompson;Margreet A. Wolfert;Therese Buskas.
Proceedings of the National Academy of Sciences of the United States of America (2012)
Robust immune responses elicited by a fully synthetic three-component vaccine
Sampat Ingale;Margreet A Wolfert;Jidnyasa Gaekwad;Therese Buskas.
Nature Chemical Biology (2007)
A General Strategy for the Chemoenzymatic Synthesis of Asymmetrically Branched N-Glycans
Zhen Wang;Zoeisha S. Chinoy;Shailesh G. Ambre;Wenjie Peng.
An Angiogenic Switch in Macrophages Involving Synergy between Toll-Like Receptors 2, 4, 7, and 9 and Adenosine A2A Receptors
Grace Pinhal-Enfield;Madhuri Ramanathan;Gyorgy Hasko;Stefanie N. Vogel.
American Journal of Pathology (2003)
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