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Sara Guglieri

Showing results (1-10 of 8) with videos related to

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Organic & Biomolecular Chemistry|June 9, 2009
Exploiting the cross-metathesis reaction in the synthesis of pseudo-oligosaccharidesPaolo Ronchi, Stefano Vignando, Sara Guglieri, et al.
Seminars in Thrombosis and Hemostasis|July 17, 2007
Low molecular weight heparins: structural differentiation by bidimensional nuclear magnetic resonance spectroscopyMarco Guerrini, Sara Guglieri, Annamaria Naggi, et al.
Analytical Biochemistry|January 15, 2005
Complex glycosaminoglycans: profiling substitution patterns by two-dimensional nuclear magnetic resonance spectroscopyMarco Guerrini, Annamaria Naggi, Sara Guglieri, et al.
The Biochemical Journal|June 27, 2006
Conformational transitions induced in heparin octasaccharides by binding with antithrombin IIIMarco Guerrini, Sara Guglieri, Daniela Beccati, et al.
Seminars in Thrombosis and Hemostasis|July 17, 2007
Structural modification induced in heparin by a Fenton-type depolymerization processElena Vismara, Monica Pierini, Sara Guglieri, et al.
The Journal of Biological Chemistry|July 22, 2008
Antithrombin-binding octasaccharides and role of extensions of the active pentasaccharide sequence in the specificity and strength of interaction. Evidence for very high affinity induced by an unusual glucuronic acid residueMarco Guerrini, Sara Guglieri, Benito Casu, et al.
Journal of Medicinal Chemistry|February 6, 2004
Undersulfated and glycol-split heparins endowed with antiangiogenic activityBenito Casu, Marco Guerrini, Sara Guglieri, et al.
Nature Biotechnology|April 26, 2008
Oversulfated chondroitin sulfate is a contaminant in heparin associated with adverse clinical eventsMarco Guerrini, Daniela Beccati, Zachary Shriver, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Organic & Biomolecular Chemistry|June 9, 2009
Exploiting the cross-metathesis reaction in the synthesis of pseudo-oligosaccharidesPaolo Ronchi, Stefano Vignando, Sara Guglieri, et al.
Seminars in Thrombosis and Hemostasis|July 17, 2007
Low molecular weight heparins: structural differentiation by bidimensional nuclear magnetic resonance spectroscopyMarco Guerrini, Sara Guglieri, Annamaria Naggi, et al.
Analytical Biochemistry|January 15, 2005
Complex glycosaminoglycans: profiling substitution patterns by two-dimensional nuclear magnetic resonance spectroscopyMarco Guerrini, Annamaria Naggi, Sara Guglieri, et al.
The Biochemical Journal|June 27, 2006
Conformational transitions induced in heparin octasaccharides by binding with antithrombin IIIMarco Guerrini, Sara Guglieri, Daniela Beccati, et al.
Seminars in Thrombosis and Hemostasis|July 17, 2007
Structural modification induced in heparin by a Fenton-type depolymerization processElena Vismara, Monica Pierini, Sara Guglieri, et al.
The Journal of Biological Chemistry|July 22, 2008
Antithrombin-binding octasaccharides and role of extensions of the active pentasaccharide sequence in the specificity and strength of interaction. Evidence for very high affinity induced by an unusual glucuronic acid residueMarco Guerrini, Sara Guglieri, Benito Casu, et al.
Journal of Medicinal Chemistry|February 6, 2004
Undersulfated and glycol-split heparins endowed with antiangiogenic activityBenito Casu, Marco Guerrini, Sara Guglieri, et al.
Nature Biotechnology|April 26, 2008
Oversulfated chondroitin sulfate is a contaminant in heparin associated with adverse clinical eventsMarco Guerrini, Daniela Beccati, Zachary Shriver, et al.
Pageof 1