bozzi, manuela
bozzi, manuela
Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC
Molecular mechanisms underlying muscle wasting in huntington's disease
2020 Bozzi, M; Sciandra, F
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
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
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
Structural flexibility of human alpha-dystroglycan
2017 Covaceuszach, Sonia; Bozzi, Manuela; Bigotti Maria, Giulia; Sciandra, Francesca; Konarev Petr, Valeryevich; Brancaccio, Andrea; Cassetta, Alberto
The effect of the pathological V72I, D109N and T190M missense mutations on the molecular structure of ?-dystroglycan
2017 Covaceuszach, S; Bozzi, M; Bigotti, Mg; Sciandra, F; Konarev, Pv; Brancaccio, A; Cassetta, A
The molecular basis of alpha-Dystroglycan hypoglycosylation: a crystallographic and SAXS study
2016 Covaceuszach, S; Bozzi, M; Konarev, ; P, V; Bigotti, ; M, G; Sciandra, F; Brancaccio, A; Cassetta, A; Lamba, Doriano; D,
The Structure of the T190M Mutant of Murine alpha-Dystroglycan at High Resolution: Insight into the Molecular Basis of a Primary Dystroglycanopathy
2015 Cassetta, A; Covaceuszach, S; Bozzi, M; Bigotti, Mg; Bannister, S; Hübner, W; Sciandra, F; Brancaccioc, A; E, ; Lamba, D
The Multiple Affinities of alpha-Dystroglycan
2013 Sciandra, Francesca; Bozzi, Manuela; Bigotti Maria, Giulia; Brancaccio, Andrea
Analysis at the molecular level of the interaction between ±-dystroglycan and ²-dystroglycan and assessment of its implication for skeletal muscle physiopathology
2009 Sciandra F.; Morlacchi S.; Desimio M.G.; Giardina B.; Bozzi M.; Brancaccio A.
Structural and functional aspects of dystroglycan: towards the elucidation of its pathophysiological role
2009 Morlacchi S.; Bozzi M.; Galtieri A.; Giardina B.; Sciandra F.; Brancaccio A.
±- and ²-dystroglycan: evaluation of processing and targeting through multiple fluorescent tagging
2009 Morlacchi S.; Bozzi M.; Galtieri A.; Giardina B.; Sciandra F.; Brancaccio A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Molecular mechanisms underlying muscle wasting in huntington's disease | 1-gen-2020 | Bozzi, M; Sciandra, F | |
| 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 | |
| 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 | |
| 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 | |
| Structural flexibility of human alpha-dystroglycan | 1-gen-2017 | Covaceuszach, Sonia; Bozzi, Manuela; Bigotti Maria, Giulia; Sciandra, Francesca; Konarev Petr, Valeryevich; Brancaccio, Andrea; Cassetta, Alberto | |
| The effect of the pathological V72I, D109N and T190M missense mutations on the molecular structure of ?-dystroglycan | 1-gen-2017 | Covaceuszach, S; Bozzi, M; Bigotti, Mg; Sciandra, F; Konarev, Pv; Brancaccio, A; Cassetta, A | |
| The molecular basis of alpha-Dystroglycan hypoglycosylation: a crystallographic and SAXS study | 1-gen-2016 | Covaceuszach, S; Bozzi, M; Konarev, ; P, V; Bigotti, ; M, G; Sciandra, F; Brancaccio, A; Cassetta, A; Lamba, Doriano; D, | |
| The Structure of the T190M Mutant of Murine alpha-Dystroglycan at High Resolution: Insight into the Molecular Basis of a Primary Dystroglycanopathy | 1-gen-2015 | Cassetta, A; Covaceuszach, S; Bozzi, M; Bigotti, Mg; Bannister, S; Hübner, W; Sciandra, F; Brancaccioc, A; E, ; Lamba, D | |
| The Multiple Affinities of alpha-Dystroglycan | 1-gen-2013 | Sciandra, Francesca; Bozzi, Manuela; Bigotti Maria, Giulia; Brancaccio, Andrea | |
| Analysis at the molecular level of the interaction between ±-dystroglycan and ²-dystroglycan and assessment of its implication for skeletal muscle physiopathology | 1-gen-2009 | Sciandra F.; Morlacchi S.; Desimio M.G.; Giardina B.; Bozzi M.; Brancaccio A. | |
| Structural and functional aspects of dystroglycan: towards the elucidation of its pathophysiological role | 1-gen-2009 | Morlacchi S.; Bozzi M.; Galtieri A.; Giardina B.; Sciandra F.; Brancaccio A. | |
| ±- and ²-dystroglycan: evaluation of processing and targeting through multiple fluorescent tagging | 1-gen-2009 | Morlacchi S.; Bozzi M.; Galtieri A.; Giardina B.; Sciandra F.; Brancaccio A. |