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Paola Torreri

Showing results (1-10 of 25) with videos related to

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Annali Dell'Istituto Superiore Di Sanita|March 30, 2006
Biomolecular interactions by Surface Plasmon Resonance technologyPaola Torreri, Marina Ceccarini, Pompeo Macioce, et al.
International Journal of Environmental Research and Public Health|July 14, 2018
The Occurrence of 275 Rare Diseases and 47 Rare Disease Groups in Italy. Results from the National Registry of Rare DiseasesDomenica Taruscio, Luciano Vittozzi, Adele Rocchetti, et al.
Annali Dell'Istituto Superiore Di Sanita|June 26, 2024
Registries or non-pharmacological observational studies? An operational attempt to draw the line and to provide some suggestions for the ethical evaluation of rare disease registriesSabina Gainotti, Paola Torreri, Chiara Mannelli, et al.
Journal of Molecular Biology|November 18, 2005
Molecular basis of dystrobrevin interaction with kinesin heavy chain: structural determinants of their bindingMarina Ceccarini, Paola Torreri, Dario Giuseppe Lombardi, et al.
Journal of Molecular Recognition : JMR|September 24, 2005
The role of loop ZA and Pro371 in the function of yeast Gcn5p bromodomain revealed through molecular dynamics and experimentFrancesco Pizzitutti, Andrea Giansanti, Paola Ballario, et al.
Human Molecular Genetics|June 14, 2014
Gaucher disease due to saposin C deficiency is an inherited lysosomal disease caused by rapidly degraded mutant proteinsMarialetizia Motta, Serena Camerini, Massimo Tatti, et al.
Plos One|March 8, 2014
Specificity of ε and non-ε isoforms of arabidopsis 14-3-3 proteins towards the H+-ATPase and other targetsRoberta Pallucca, Sabina Visconti, Lorenzo Camoni, et al.
The FEBS Journal|October 5, 2006
Concerted mutation of Phe residues belonging to the beta-dystroglycan ectodomain strongly inhibits the interaction with alpha-dystroglycan in vitroManuela Bozzi, Francesca Sciandra, Lorenzo Ferri, et al.
Plos One|June 19, 2009
Prion protein paralog doppel protein interacts with alpha-2-macroglobulin: a plausible mechanism for doppel-mediated neurodegenerationStefano Benvegnù, Diego Franciotta, Josh Sussman, et al.
The FEBS Journal|September 18, 2012
Phosphorylation on threonine 11 of β-dystrobrevin alters its interaction with kinesin heavy chainFederica Fratini, Gianfranco Macchia, Paola Torreri, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Annali Dell'Istituto Superiore Di Sanita|March 30, 2006
Biomolecular interactions by Surface Plasmon Resonance technologyPaola Torreri, Marina Ceccarini, Pompeo Macioce, et al.
International Journal of Environmental Research and Public Health|July 14, 2018
The Occurrence of 275 Rare Diseases and 47 Rare Disease Groups in Italy. Results from the National Registry of Rare DiseasesDomenica Taruscio, Luciano Vittozzi, Adele Rocchetti, et al.
Annali Dell'Istituto Superiore Di Sanita|June 26, 2024
Registries or non-pharmacological observational studies? An operational attempt to draw the line and to provide some suggestions for the ethical evaluation of rare disease registriesSabina Gainotti, Paola Torreri, Chiara Mannelli, et al.
Journal of Molecular Biology|November 18, 2005
Molecular basis of dystrobrevin interaction with kinesin heavy chain: structural determinants of their bindingMarina Ceccarini, Paola Torreri, Dario Giuseppe Lombardi, et al.
Journal of Molecular Recognition : JMR|September 24, 2005
The role of loop ZA and Pro371 in the function of yeast Gcn5p bromodomain revealed through molecular dynamics and experimentFrancesco Pizzitutti, Andrea Giansanti, Paola Ballario, et al.
Human Molecular Genetics|June 14, 2014
Gaucher disease due to saposin C deficiency is an inherited lysosomal disease caused by rapidly degraded mutant proteinsMarialetizia Motta, Serena Camerini, Massimo Tatti, et al.
Plos One|March 8, 2014
Specificity of ε and non-ε isoforms of arabidopsis 14-3-3 proteins towards the H+-ATPase and other targetsRoberta Pallucca, Sabina Visconti, Lorenzo Camoni, et al.
The FEBS Journal|October 5, 2006
Concerted mutation of Phe residues belonging to the beta-dystroglycan ectodomain strongly inhibits the interaction with alpha-dystroglycan in vitroManuela Bozzi, Francesca Sciandra, Lorenzo Ferri, et al.
Plos One|June 19, 2009
Prion protein paralog doppel protein interacts with alpha-2-macroglobulin: a plausible mechanism for doppel-mediated neurodegenerationStefano Benvegnù, Diego Franciotta, Josh Sussman, et al.
The FEBS Journal|September 18, 2012
Phosphorylation on threonine 11 of β-dystrobrevin alters its interaction with kinesin heavy chainFederica Fratini, Gianfranco Macchia, Paola Torreri, et al.
Pageof 3