What is he best known for?
The fields of study he is best known for:
Terry D. Butters mostly deals with Biochemistry, Substrate reduction therapy, Glycosphingolipid, Immunology and Enzyme.
His research on Biochemistry frequently links to adjacent areas such as Stereochemistry.
His biological study spans a wide range of topics, including Glucocerebrosidase, GM2 gangliosidoses, Gangliosidosis and Miglustat.
He has researched Glycosphingolipid in several fields, including Chromatography, Pharmacology, In vivo and Cell biology.
His study looks at the relationship between Immunology and fields such as Sandhoff disease, as well as how they intersect with chemical problems.
His study in Enzyme is interdisciplinary in nature, drawing from both High-performance liquid chromatography, Glycobiology, Anthranilic acid, Digestion and Monosaccharide.
His most cited work include:
- Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis (640 citations)
- N-butyldeoxynojirimycin is a novel inhibitor of glycolipid biosynthesis. (404 citations)
- Targeting glycosylation as a therapeutic approach (343 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Biochemistry, Stereochemistry, Enzyme, Glycosphingolipid and Glycosylation.
His Biochemistry study is mostly concerned with Endoplasmic reticulum, Glycan, Glycolipid, Ceramide and Oligosaccharide.
His Stereochemistry study combines topics in areas such as Iminosugar, Biosynthesis, Alkyl and Glycoside hydrolase.
His Glycosphingolipid research is multidisciplinary, incorporating perspectives in Immunology, Miglustat, Ganglioside, Cell biology and Substrate reduction therapy.
His studies in Ganglioside integrate themes in fields like HEXB, Sandhoff disease, Endocrinology and Internal medicine.
His Glycosylation research includes elements of Mannose and Glycoprotein.
He most often published in these fields:
- Biochemistry (42.86%)
- Stereochemistry (28.57%)
- Enzyme (12.86%)
What were the highlights of his more recent work (between 2011-2020)?
- Biochemistry (42.86%)
- Stereochemistry (28.57%)
- Iminosugar (8.57%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Biochemistry, Stereochemistry, Iminosugar, Glycoprotein and Glycan.
His Biochemistry study frequently draws connections between related disciplines such as Miglustat.
His research in Stereochemistry intersects with topics in Mannosidase, Glycoside hydrolase and Enzyme.
His Iminosugar research is multidisciplinary, incorporating elements of Cystic fibrosis, Dengue virus, Dengue fever, Alkyl and In vivo.
His Glycoprotein research integrates issues from Golgi apparatus, Ubiquitin and Glycosylation.
The various areas that he examines in his Glycan study include In vitro and Endoplasmic reticulum.
Between 2011 and 2020, his most popular works were:
- An iminosugar with potent inhibition of dengue virus infection in vivo. (65 citations)
- Small molecule inhibitors of ER α-glucosidases are active against multiple hemorrhagic fever viruses (62 citations)
- Structural and mechanistic insight into N-glycan processing by endo-α-mannosidase (58 citations)
In his most recent research, the most cited papers focused on:
- Enzyme
- Gene
- Organic chemistry
His primary areas of investigation include Stereochemistry, Biochemistry, Iminosugar, Enzyme and Enantiomer.
Terry D. Butters combines subjects such as Mannosidase, Miglitol, Cleavage and Disaccharidase with his study of Stereochemistry.
His studies in Protein folding, Cystic fibrosis transmembrane conductance regulator, Glucosidases, RNA and Secretion are all subfields of Biochemistry research.
His work deals with themes such as Prodrug, Enzyme assay, Acetylation and Alkyl, which intersect with Iminosugar.
Terry D. Butters interconnects Cell culture, Fibroblast and Molecular biology in the investigation of issues within Enzyme.
His studies deal with areas such as Miglustat, Maltase, Hydroxymethyl and Maltose as well as Enantiomer.
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