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Simona M Monti

Showing results (1-10 of 27) with videos related to

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Current Topics in Medicinal Chemistry|April 14, 2016
L-Histidinol Dehydrogenase as a New Target for Old DiseasesSimona M Monti, Giuseppina De Simone, Katia D'Ambrosio
Current Topics in Medicinal Chemistry|July 29, 2016
Editorial (Thematic Issue: Bacterial Metallo-Enzymes as Drug Targets)Simona M Monti, Katia D'Ambrosio, Giuseppina De Simone
Journal of Peptide Science : an Official Publication of the European Peptide Society|May 4, 2011
A new FcεRI receptor-mimetic peptide (PepE) that blocks IgE binding to its high affinity receptor and prevents mediator release from RBL 2H3 cellsAnnamaria Sandomenico, Simona M Monti, Rosanna Palumbo, et al.
International Journal of Molecular Sciences|July 18, 2015
Thermostable Carbonic Anhydrases in Biotechnological ApplicationsAnna Di Fiore, Vincenzo Alterio, Simona M Monti, et al.
Oxidative Medicine and Cellular Longevity|August 30, 2018
Protective Role of Carbonic Anhydrases III and VII in Cellular Defense Mechanisms upon Redox UnbalanceAnna Di Fiore, Daria M Monti, Andrea Scaloni, et al.
Molecular Immunology|August 25, 2009
IgE-binding properties and selectivity of peptide mimics of the FcvarepsilonRI binding siteAnnamaria Sandomenico, Simona M Monti, Daniela Marasco, et al.
Advances in Experimental Medicine and Biology|April 30, 2009
Peptides binding the type E immunoglobulinsAnnamaria Sandomenico, Daniela Marasco, Simona M Monti, et al.
Biopolymers|August 5, 2006
The chemical synthesis of the GstI protein by NCL on a X-Met siteAngela Saporito, Daniela Marasco, Angela Chambery, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 29, 2015
A Combined Crystallographic and Theoretical Study Explains the Capability of Carboxylic Acids to Adopt Multiple Binding Modes in the Active Site of Carbonic AnhydrasesEmma Langella, Katia D'Ambrosio, Melissa D'Ascenzio, et al.
Biopolymers|December 31, 2013
The structural comparison between membrane-associated human carbonic anhydrases provides insights into drug design of selective inhibitorsVincenzo Alterio, Peiwen Pan, Seppo Parkkila, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Current Topics in Medicinal Chemistry|April 14, 2016
L-Histidinol Dehydrogenase as a New Target for Old DiseasesSimona M Monti, Giuseppina De Simone, Katia D'Ambrosio
Current Topics in Medicinal Chemistry|July 29, 2016
Editorial (Thematic Issue: Bacterial Metallo-Enzymes as Drug Targets)Simona M Monti, Katia D'Ambrosio, Giuseppina De Simone
Journal of Peptide Science : an Official Publication of the European Peptide Society|May 4, 2011
A new FcεRI receptor-mimetic peptide (PepE) that blocks IgE binding to its high affinity receptor and prevents mediator release from RBL 2H3 cellsAnnamaria Sandomenico, Simona M Monti, Rosanna Palumbo, et al.
International Journal of Molecular Sciences|July 18, 2015
Thermostable Carbonic Anhydrases in Biotechnological ApplicationsAnna Di Fiore, Vincenzo Alterio, Simona M Monti, et al.
Oxidative Medicine and Cellular Longevity|August 30, 2018
Protective Role of Carbonic Anhydrases III and VII in Cellular Defense Mechanisms upon Redox UnbalanceAnna Di Fiore, Daria M Monti, Andrea Scaloni, et al.
Molecular Immunology|August 25, 2009
IgE-binding properties and selectivity of peptide mimics of the FcvarepsilonRI binding siteAnnamaria Sandomenico, Simona M Monti, Daniela Marasco, et al.
Advances in Experimental Medicine and Biology|April 30, 2009
Peptides binding the type E immunoglobulinsAnnamaria Sandomenico, Daniela Marasco, Simona M Monti, et al.
Biopolymers|August 5, 2006
The chemical synthesis of the GstI protein by NCL on a X-Met siteAngela Saporito, Daniela Marasco, Angela Chambery, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 29, 2015
A Combined Crystallographic and Theoretical Study Explains the Capability of Carboxylic Acids to Adopt Multiple Binding Modes in the Active Site of Carbonic AnhydrasesEmma Langella, Katia D'Ambrosio, Melissa D'Ascenzio, et al.
Biopolymers|December 31, 2013
The structural comparison between membrane-associated human carbonic anhydrases provides insights into drug design of selective inhibitorsVincenzo Alterio, Peiwen Pan, Seppo Parkkila, et al.
Pageof 3