2014 - Hellman Fellow
His primary areas of investigation include Polypeptide N-acetylgalactosaminyltransferase, Molecular biology, Biochemistry, Glycosylation and Gene. His work carried out in the field of Polypeptide N-acetylgalactosaminyltransferase brings together such families of science as C-type lectin, C-terminus, Isozyme and O-linked glycosylation. His Molecular biology study combines topics from a wide range of disciplines, such as Complementary DNA, Cellular differentiation, DNA methylation and Coding region.
He combines topics linked to Cell culture with his work on Biochemistry. His Glycosylation research includes elements of Cancer research, Endocrinology, Glycoprotein, HeLa and Tandem repeat. As a part of the same scientific study, Eric P. Bennett usually deals with the Gene, concentrating on Serine and frequently concerns with N-linked glycosylation.
Eric P. Bennett spends much of his time researching Biochemistry, Glycosylation, Molecular biology, Gene and Glycoprotein. His Glycosylation research incorporates elements of Tandem repeat, Glycan, Cell biology, Peptide and Gene isoform. His study on Glycome is often connected to Context as part of broader study in Glycan.
His biological study spans a wide range of topics, including Polypeptide N-acetylgalactosaminyltransferase, Coding region, Galactosyltransferase, Molecular cloning and Monoclonal antibody. His Gene research is under the purview of Genetics. His work deals with themes such as Cell, MUC1 and Cell culture, which intersect with Glycoprotein.
Eric P. Bennett mostly deals with Cell biology, Glycosylation, Gene, CRISPR and Cas9. His studies in Glycosylation integrate themes in fields like Phenotype, Enzyme, Glycan, Glycoconjugate and Secretory pathway. His Gene study is concerned with the field of Genetics as a whole.
His work on Human genome, Glycoprotein and Glycoside hydrolase as part of his general Genetics study is frequently connected to Genetic association and Genome-wide association study, thereby bridging the divide between different branches of science. Eric P. Bennett works mostly in the field of CRISPR, limiting it down to concerns involving Gene targeting and, occasionally, Glycome and Gene family. His Cas9 research integrates issues from Genome editing and Computational biology.
Cell biology, Gene, Glycosylation, Glycan and Gene isoform are his primary areas of study. His Cell biology research is multidisciplinary, incorporating elements of Receptor and Isogenic human disease models. His Gene study results in a more complete grasp of Genetics.
His research ties Glycoconjugate and Glycosylation together. Eric P. Bennett has researched Glycan in several fields, including Glycosyltransferase Gene, Computational biology and Chinese hamster ovary cell. As part of the same scientific family, he usually focuses on Gene isoform, concentrating on HEK 293 cells and intersecting with Secretory pathway, Glycoproteomics and Function.
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Precision mapping of the human O-GalNAc glycoproteome through SimpleCell technology
Catharina Steentoft;Sergey Vakhrushev;Hiren Jitendra Joshi;Hiren Jitendra Joshi;Yun Kong.
The EMBO Journal (2013)
Control of mucin-type O-glycosylation: A classification of the polypeptide GalNAc-transferase gene family
Eric P Bennett;Ulla Mandel;Henrik Clausen;Thomas A Gerken.
Polypeptide GalNAc-transferase T3 and Familial Tumoral Calcinosis SECRETION OF FIBROBLAST GROWTH FACTOR 23 REQUIRES O-GLYCOSYLATION
Kentaro Kato;Charlotte Jeanneau;Mads Agervig Tarp;Anna Benet-Pagès.
Journal of Biological Chemistry (2006)
Substrate Specificities of Three Members of the Human UDP-N-Acetyl-α-d-galactosamine:Polypeptide N-Acetylgalactosaminyltransferase Family, GalNAc-T1, -T2, and -T3
Hans H. Wandall;Helle Hassan;Ekaterina Mirgorodskaya;Anne K. Kristensen.
Journal of Biological Chemistry (1997)
Mining the O-glycoproteome using zinc-finger nuclease-glycoengineered SimpleCell lines
Catharina Steentoft;Sergey Y Vakhrushev;Malene B Vester-Christensen;Katrine T-B G Schjoldager.
Nature Methods (2011)
Bacterial glycosidases for the production of universal red blood cells
Qiyong P Liu;Gerlind Sulzenbacher;Huaiping Yuan;Eric P Bennett.
Nature Biotechnology (2007)
A family of UDP-GalNAc: polypeptide N-acetylgalactosaminyl-transferases control the initiation of mucin-type O-linked glycosylation
Henrik Clausen;Eric P. Bennett.
Cloning of a human UDP-N-acetyl-alpha-D-Galactosamine:polypeptide N-acetylgalactosaminyltransferase that complements other GalNAc-transferases in complete O-glycosylation of the MUC1 tandem repeat.
Eric Paul Bennett;Helle Hassan;Ulla Mandel;Ekatarina Mirgorodskaya.
Journal of Biological Chemistry (1998)
Localization of three human polypeptide GalNAc-transferases in HeLa cells suggests initiation of O-linked glycosylation throughout the Golgi apparatus
Sabine Röttger;Jamie White;Hans H. Wandall;Jean-Christophe Olivo.
Journal of Cell Science (1998)
cDNA cloning and expression of a novel human UDP-N-acetyl-alpha-D-galactosamine. Polypeptide N-acetylgalactosaminyltransferase, GalNAc-t3.
Eric Paul Bennett;Helle Hassan;Henrik Clausen.
Journal of Biological Chemistry (1996)
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