SCIANDRA, FRANCESCA
SCIANDRA, FRANCESCA
Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC
Multifunctional scaffolds for biomedical applications: Crafting versatile solutions with polycaprolactone enriched by graphene oxide
2024 Friggeri, G.; Moretti, I.; Amato, F.; Marrani, A. G.; Sciandra, F.; Colombarolli, S. G.; Vitali, A.; Viscuso, S.; Augello, A.; Cui, L.; Perini, G.; De Spirito, M.; Papi, M.; Palmieri, V.
3D-printed graphene polylactic acid devices resistant to SARS-CoV-2: Sunlight-mediated sterilization of additive manufactured objects
2022 De Maio, F; Rosa, E; Perini, G; Augello, A; Niccolini, B; Ciaiola, F; Santarelli, G; Sciandra, F; Bozzi, M; Sanguinetti, M; Sali, M; De Spirito, M; Delogu, G; Palmieri, V; Papi, M
3D Graphene Scaffolds for Skeletal Muscle Regeneration: Future Perspectives
2020 Palmieri V.; Sciandra F.; Bozzi M.; De Spirito M.; Papi M.
Identification and Modeling of a GT-A Fold in the ?-Dystroglycan Glycosylating Enzyme LARGE1
2020 Righino, B; Bozzi, M; Bozzi, M; Pirolli, D; Sciandra, F; Bigotti, Mg; Bigotti, Mg; Brancaccio, A; Brancaccio, A; DE ROSA, MARIA CRISTINA
Molecular mechanisms underlying muscle wasting in huntington's disease
2020 Bozzi, M; Sciandra, F
Punicalagin Protects Human Retinal Pigment Epithelium Cells From Ultraviolet Radiation-Induced Oxidative Damage by Activating Nrf2/HO-1 Signaling Pathway and Reducing Apoptosis
2020 Clementi, MARIA ELISABETTA; Sampaolese, Beatrice; Sciandra, Francesca; Tringali, Giuseppe
A primary dystroglycanopathy causing muscle-eye-brain disease with multicystic leukodystrophy: from cellular and biochemical analysis to a mouse model
2019 Francesca Sciandra; Manuela Bozzi; Maria Giulia Bigotti; Alberto Cassetta; Sonia Covaceuszach; Wolfgang Hübner; Thomas Huser; CarolAnn Eberle; Natalia Niemir; Sandra Blaess; Andrea Brancaccio
Molecular and structural basis of dystroglycanopathies
2019 A. Cassetta; S. Covaceuszach; F. Sciandra; M. Bozzi; M. G. Bigotti; W. Hübner; A. Brancaccio
Synchrotron Radiation as a tool for the investigation of the structural basis of primary dystroglycanopathies.
2019 Cassetta, Alberto; Covaceuszach, Sonia; Sciandra, Francesca; Bozzi, Manuela; Giulia Bigotti, Maria; Hübner, Wolfgang; Brancaccio, Andrea
A dystroglycan mutation (p.Cys667Phe) associated to muscle-eye-brain disease with multicystic leucodystrophy results in ER-retention of the mutant protein.
2018 Signorino, Giulia; Covaceuszach, Sonia; Bozzi, Manuela; Hubner, Wolfgang; Monkemoller, Viola; Konarev Petr, V; Cassetta, Alberto; Brancaccio, Andrea; Sciandra, Francesca
A dystroglycan mutation (p.Cys66uPhe) associated to muscle-eye-brain disease with multicystic leukodystrophy results in ER-retention of the mutant protein
2018 Signorino, G; Covaceuszach, S; Bozzi, M; Hübner, W; Mönkemöller, V; Konarev, Pv; Cassetta, A; Brancaccio, A; Sciandra, F
Live optical super-resolution microcospy applied to the characterization of maturation, localization and trafficking of defective dystroglycan mutants
2018 Huber, W; Bozzi, M; Kerbs, A; Monkemoller, V; Sciandra, F; Bigotti, Mg; Brancaccio, A; Huser, T
Structural model of domain 1 of the alfa-dystroglycan glycosylating enzyme LARGE
2018 Brancaccio, A; Righino, B; Bozzi, M; Sciandra, F; Bigotti, Mg; Pirolli, D; De Rosa, Mc
Structural model of domain 1 of the alfa-dystroglycan glycosylating enzyme LARGE
2018 A. Brancaccio; B. righino; M. Bozzi; F. Sciandra; M.G. Bigotti; D. Pirolli; M.C. De Rosa
The enzymatic processing of ?-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site
2018 Gioia M.; Fasciglione G.F.; Sbardella D.; Sciandra F.; Casella M.; Camerini S.; Crescenzi M.; Gori A.; Tarantino U.; Cozza P.; Brancaccio A.; Coletta M.; Bozzi M.
The enzymatic processing of ?-dystroglycan by MMP-2 is controller by two anchoring sites distinct from the active site
2018 Gioia, M; Fasciglione, Gf; Sbardella, D; Sciandra, F; Casella, M; Camerini, S; Crescenzi, M; Gori, A; Tarantino, U; Cozza, P; Brancaccio, A; Coletta, M; Bozzi, M
?-Dystroglycan hypoglycosylation affects cell migration by influencing ?-dystroglycan membrane clustering and filopodia length: A musticale confocal microscopi analysis
2017 Palmieri, V; Bozzi, M; Signorino, G; Papi, M; De Spirito, M; Brancaccio, A; Maulucci, G; Sciandra, F
Evaluation of the effect of a floxed Neo cassette within the dystroglycan (Dag1) gene
2017 Sciandra, F; Scicchitano, Bm; Signorino, G; Bigotti, Mg; Tavazzi, B; Lombardi, F; Bozzi, M; Sica, G; Giardina, B; Blaess, S; Brancaccio, A
optical nanoscopy applied to the characterization of maturation and localization of defective dystroglycan mutants
2017 Hubner W.; Bozzi M.; Bannister S.; Signorino G.; Frommann J.F.; Wilking A.; Monkemoller V.; Sciandra F.; Brancaccio a.; Huser T.
Structural flexibility of human ?lpha-dystroglycan
2017 Covaceuszach, S; Bozzi, M; Bigotti, Mg; Sciandra, F; Konarev, Pv; Brancaccio, A; Cassetta, A
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Multifunctional scaffolds for biomedical applications: Crafting versatile solutions with polycaprolactone enriched by graphene oxide | 1-gen-2024 | Friggeri, G.; Moretti, I.; Amato, F.; Marrani, A. G.; Sciandra, F.; Colombarolli, S. G.; Vitali, A.; Viscuso, S.; Augello, A.; Cui, L.; Perini, G.; De Spirito, M.; Papi, M.; Palmieri, V. | |
| 3D-printed graphene polylactic acid devices resistant to SARS-CoV-2: Sunlight-mediated sterilization of additive manufactured objects | 1-gen-2022 | De Maio, F; Rosa, E; Perini, G; Augello, A; Niccolini, B; Ciaiola, F; Santarelli, G; Sciandra, F; Bozzi, M; Sanguinetti, M; Sali, M; De Spirito, M; Delogu, G; Palmieri, V; Papi, M | |
| 3D Graphene Scaffolds for Skeletal Muscle Regeneration: Future Perspectives | 1-gen-2020 | Palmieri V.; Sciandra F.; Bozzi M.; De Spirito M.; Papi M. | |
| Identification and Modeling of a GT-A Fold in the ?-Dystroglycan Glycosylating Enzyme LARGE1 | 1-gen-2020 | Righino, B; Bozzi, M; Bozzi, M; Pirolli, D; Sciandra, F; Bigotti, Mg; Bigotti, Mg; Brancaccio, A; Brancaccio, A; DE ROSA, MARIA CRISTINA | |
| Molecular mechanisms underlying muscle wasting in huntington's disease | 1-gen-2020 | Bozzi, M; Sciandra, F | |
| Punicalagin Protects Human Retinal Pigment Epithelium Cells From Ultraviolet Radiation-Induced Oxidative Damage by Activating Nrf2/HO-1 Signaling Pathway and Reducing Apoptosis | 1-gen-2020 | Clementi, MARIA ELISABETTA; Sampaolese, Beatrice; Sciandra, Francesca; Tringali, Giuseppe | |
| A primary dystroglycanopathy causing muscle-eye-brain disease with multicystic leukodystrophy: from cellular and biochemical analysis to a mouse model | 1-gen-2019 | Francesca Sciandra; Manuela Bozzi; Maria Giulia Bigotti; Alberto Cassetta; Sonia Covaceuszach; Wolfgang Hübner; Thomas Huser; CarolAnn Eberle; Natalia Niemir; Sandra Blaess; Andrea Brancaccio | |
| Molecular and structural basis of dystroglycanopathies | 1-gen-2019 | A. Cassetta; S. Covaceuszach; F. Sciandra; M. Bozzi; M. G. Bigotti; W. Hübner; A. Brancaccio | |
| Synchrotron Radiation as a tool for the investigation of the structural basis of primary dystroglycanopathies. | 1-gen-2019 | Cassetta, Alberto; Covaceuszach, Sonia; Sciandra, Francesca; Bozzi, Manuela; Giulia Bigotti, Maria; Hübner, Wolfgang; Brancaccio, Andrea | |
| A dystroglycan mutation (p.Cys667Phe) associated to muscle-eye-brain disease with multicystic leucodystrophy results in ER-retention of the mutant protein. | 1-gen-2018 | Signorino, Giulia; Covaceuszach, Sonia; Bozzi, Manuela; Hubner, Wolfgang; Monkemoller, Viola; Konarev Petr, V; Cassetta, Alberto; Brancaccio, Andrea; Sciandra, Francesca | |
| A dystroglycan mutation (p.Cys66uPhe) associated to muscle-eye-brain disease with multicystic leukodystrophy results in ER-retention of the mutant protein | 1-gen-2018 | Signorino, G; Covaceuszach, S; Bozzi, M; Hübner, W; Mönkemöller, V; Konarev, Pv; Cassetta, A; Brancaccio, A; Sciandra, F | |
| Live optical super-resolution microcospy applied to the characterization of maturation, localization and trafficking of defective dystroglycan mutants | 1-gen-2018 | Huber, W; Bozzi, M; Kerbs, A; Monkemoller, V; Sciandra, F; Bigotti, Mg; Brancaccio, A; Huser, T | |
| Structural model of domain 1 of the alfa-dystroglycan glycosylating enzyme LARGE | 1-gen-2018 | Brancaccio, A; Righino, B; Bozzi, M; Sciandra, F; Bigotti, Mg; Pirolli, D; De Rosa, Mc | |
| Structural model of domain 1 of the alfa-dystroglycan glycosylating enzyme LARGE | 1-gen-2018 | A. Brancaccio; B. righino; M. Bozzi; F. Sciandra; M.G. Bigotti; D. Pirolli; M.C. De Rosa | |
| The enzymatic processing of ?-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site | 1-gen-2018 | Gioia M.; Fasciglione G.F.; Sbardella D.; Sciandra F.; Casella M.; Camerini S.; Crescenzi M.; Gori A.; Tarantino U.; Cozza P.; Brancaccio A.; Coletta M.; Bozzi M. | |
| The enzymatic processing of ?-dystroglycan by MMP-2 is controller by two anchoring sites distinct from the active site | 1-gen-2018 | Gioia, M; Fasciglione, Gf; Sbardella, D; Sciandra, F; Casella, M; Camerini, S; Crescenzi, M; Gori, A; Tarantino, U; Cozza, P; Brancaccio, A; Coletta, M; Bozzi, M | |
| ?-Dystroglycan hypoglycosylation affects cell migration by influencing ?-dystroglycan membrane clustering and filopodia length: A musticale confocal microscopi analysis | 1-gen-2017 | Palmieri, V; Bozzi, M; Signorino, G; Papi, M; De Spirito, M; Brancaccio, A; Maulucci, G; Sciandra, F | |
| Evaluation of the effect of a floxed Neo cassette within the dystroglycan (Dag1) gene | 1-gen-2017 | Sciandra, F; Scicchitano, Bm; Signorino, G; Bigotti, Mg; Tavazzi, B; Lombardi, F; Bozzi, M; Sica, G; Giardina, B; Blaess, S; Brancaccio, A | |
| optical nanoscopy applied to the characterization of maturation and localization of defective dystroglycan mutants | 1-gen-2017 | Hubner W.; Bozzi M.; Bannister S.; Signorino G.; Frommann J.F.; Wilking A.; Monkemoller V.; Sciandra F.; Brancaccio a.; Huser T. | |
| Structural flexibility of human ?lpha-dystroglycan | 1-gen-2017 | Covaceuszach, S; Bozzi, M; Bigotti, Mg; Sciandra, F; Konarev, Pv; Brancaccio, A; Cassetta, A |