Giangiacomo Torri spends much of his time researching Heparin, Sulfation, Stereochemistry, Biochemistry and Heparan sulfate. The concepts of his Heparin study are interwoven with issues in Computational chemistry and Divalent. His studies examine the connections between Sulfation and genetics, as well as such issues in Uronic acid, with regards to Chorioallantoic membrane, Angiogenesis and Iduronic acid.
His work carried out in the field of Stereochemistry brings together such families of science as Residue, Aminoglycoside and Antithrombin. Biochemistry is closely attributed to Anticoagulant in his study. His work deals with themes such as Molecular biology and Cancer research, which intersect with Heparan sulfate.
Giangiacomo Torri focuses on Heparin, Biochemistry, Stereochemistry, Sulfation and Nuclear magnetic resonance spectroscopy. Giangiacomo Torri has included themes like Chromatography and Glycosaminoglycan in his Heparin study. The Biochemistry study combines topics in areas such as Anticoagulant and Thrombin.
His work in Stereochemistry tackles topics such as Organic chemistry which are related to areas like Medicinal chemistry. His study in Sulfation is interdisciplinary in nature, drawing from both Uronic acid, Glucuronic acid, Chemical modification, Dissociation constant and Chondroitin sulfate. Nuclear magnetic resonance spectroscopy is often connected to Polymer chemistry in his work.
His primary scientific interests are in Heparin, Adsorption, Environmental science, Cyclodextrin and Biosorption. His research in the fields of Low molecular weight heparin overlaps with other disciplines such as Severe acute respiratory syndrome coronavirus 2. His biological study spans a wide range of topics, including Molecule, Metal ions in aqueous solution, Aqueous solution and Nuclear chemistry.
Giangiacomo Torri interconnects Nanoporous, Textile production and Silanol in the investigation of issues within Cyclodextrin. His Biosorption study combines topics from a wide range of disciplines, such as Self-healing hydrogels, Cross linked chitosan and Effluent. Giangiacomo Torri has researched Inflammation in several fields, including Heparan sulfate, Cell, Heparanase and Cancer research, Myeloid leukemia.
His primary areas of study are Research groups, Molecule, Cyclodextrin, Biosorption and Adsorption. A majority of his Research groups research is a blend of other scientific areas, such as Nanotechnology, Textile production and Polymer science. His studies in Molecule integrate themes in fields like Nanoporous, Metal ions in aqueous solution, Surface modification and Silanol.
As a member of one scientific family, he mostly works in the field of Biosorption, focusing on Self-healing hydrogels and, on occasion, Chitosan. Giangiacomo Torri combines subjects such as Cosmetics, Biotechnology and Nutraceutical with his study of Chitosan. His Adsorption study frequently draws connections between related disciplines such as Pollutant.
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Oversulfated chondroitin sulfate is a contaminant in heparin associated with adverse clinical events.
Marco Guerrini;Daniela Beccati;Zachary Shriver;Annamaria Naggi.
Nature Biotechnology (2008)
Alkaline N-deacetylation of chitin enhanced by flash treatments. Reaction kinetics and structure modifications
B. Focher;P.L. Beltrame;A. Naggi;G. Torri.
Carbohydrate Polymers (1990)
Total synthesis of a heparin pentasaccharide fragment having high affinity for antithrombin III
Pierre Sinaÿ;Jean-Claude Jacquinet;Maurice Petitou;Philippe Duchaussoy.
Carbohydrate Research (1984)
Conformer populations of L-iduronic acid residues in glycosaminoglycan sequences.
Dino R. Ferro;Augusto Provasoli;Massimo Ragazzi;Benito Casu.
Carbohydrate Research (1990)
Modulation of the heparanase-inhibiting activity of heparin through selective desulfation, graded N-acetylation, and glycol splitting.
Annamaria Naggi;Benito Casu;Marta Perez;Giangiacomo Torri.
Journal of Biological Chemistry (2005)
Evidence for conformational equilibrium of the sulfated L-iduronate residue in heparin and in synthetic heparin mono- and oligo-saccharides: NMR and force-field studies
Dino R. Ferro;Augusto. Provasoli;Massimo. Ragazzi;Giangiacomo. Torri.
Journal of the American Chemical Society (1986)
SST0001, a chemically modified heparin, inhibits myeloma growth and angiogenesis via disruption of the heparanase/ syndecan-1 axis
Joseph P. Ritchie;Vishnu C. Ramani;Yongsheng Ren;Annamaria Naggi.
Clinical Cancer Research (2011)
Structural differences between chitin polymorphs and their precipitates from solutions—evidence from CP-MAS 13C-NMR, FT-IR and FT-Raman spectroscopy
B. Focher;A. Naggi;G. Torri;A. Cosani.
Carbohydrate Polymers (1992)
Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes-6.
Arduino A. Mangoni;Catherine Guillou;Jean Jacques Vanden Eynde;Christopher Hulme.
1H and 13C NMR spectral assignments of the major sequences of twelve systematically modified heparin derivatives.
Edwin A. Yates;Francesco Santini;Marco Guerrini;Annamaria Naggi.
Carbohydrate Research (1996)
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