BOVOLENTA, Matteo
BOVOLENTA, Matteo
Dipartimento di Medicina Traslazionale e per la Romagna
A naturally occurring mutation in ATP synthase subunit c is associated with increased damage following hypoxia/reoxygenation in STEMI patients
2021 Morciano, G.; Pedriali, G.; Bonora, M.; Pavasini, R.; Mikus, E.; Calvi, S.; Bovolenta, M.; Lebiedzinska-Arciszewska, M.; Pinotti, M.; Albertini, A.; Wieckowski, M. R.; Giorgi, C.; Ferrari, R.; Galluzzi, L.; Campo, G.; Pinton, P.
A new rat model for Duchenne muscular dystrophy generated by CRISPR-induced deletion of Exon 45
2019 Daoud, C; Roudaut, C; Bellec-Dyevre, J; Bovolenta, M; Richard, I
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies
2008 Bovolenta, Matteo; Neri, Marcella; Fini, Sergio; Fabris, Marina; Trabanelli, Cecilia; Venturoli, A; Martoni, Elena; Bassi, Elena; Spitali, Pietro; Brioschi, Simona; Falzarano, Maria Sofia; Rimessi, Paola; Ciccone, R; Ashton, E; Mccauley, J; Yau, S; Abbs, S; Muntoni, F; Merlini, Luciano; Gualandi, Francesca; Ferlini, Alessandra
An engineered tale-transcription factor rescues transcription of factor VII impaired by promoter mutations and enhances its endogenous expression in hepatocytes
2016 Barbon, Elena; Pignani, Silvia; Branchini, Alessio; Bernardi, Francesco; Pinotti, Mirko; Bovolenta, Matteo
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis
2015 Marchetti, Giovanna; Girelli, D; Zerbinati, Carlotta; Lunghi, Barbara; Friso, S; Meneghetti, Silvia; Coen, Matteo; Gagliano, Teresa; Guastella, Giuseppe; Bochaton Piallat, Ml; Pizzolo, F; Mascoli, Francesco; Malerba, G; Bovolenta, Matteo; Ferracin, Manuela; Olivieri, O; Bernardi, Francesco; Martinelli, N.
Antisense modulation of both exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon responsible for X-linked dilated cardiomyopathy
2010 Rimessi, Paola; Fabris, Marina; Bovolenta, Matteo; Bassi, Elena; Falzarano, Maria Sofia; Gualandi, Francesca; Rapezzi, C; Coccolo, F; Perrone, Daniela; Medici, Alessandro; Ferlini, Alessandra
Antisense oligonucleotides conjugated with lipophilic compounds: synthesis and in vitro evaluation of exon skipping in duchenne muscular dystrophy
2022 Marchesi, E.; Cortesi, R.; Preti, L.; Rimessi, P.; Sguizzato, M.; Bovolenta, M.; Perrone, D.
Antisense-Induced Messenger Depletion Corrects a COL6A2 Dominant Mutation in Ullrich Myopathy
2012 Gualandi, Francesca; Manzati, Elisa; Sabatelli, Patrizia; Passarelli, Chiara; Bovolenta, Matteo; Pellegrini, Camilla; Perrone, Daniela; Squarzoni, S; Pegoraro, E; Bonaldo, P; Ferlini, Alessandra
Autosomal recessive Bethlem myopathy
file con accesso da definire2009 Gualandi, Francesca; Urciuolo, A; Martoni, Elena; Sabatelli, Patrizia; Squarzoni, S; Bovolenta, Matteo; Messina, S; Mercuri, E; Franchella, Andrea; Ferlini, Alessandra; Bonaldo, P; Merlini, Luciano
C6orf10 low-frequency and rare variants in italian multiple sclerosis patients
2019 Ziliotto, Nicole; Marchetti, Giovanna; Scapoli, Chiara; Bovolenta, Matteo; Meneghetti, Silvia; Benazzo, Andrea; Lunghi, Barbara; Balestra, Dario; Laino, Lorenza Anna; Bozzini, Nicolò; Guidi, Irene; Salvi, Fabrizio; Straudi, Sofia; Gemmati, Donato; Menegatti, Erica; Zamboni, Paolo; Bernardi, Francesco
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse
2009 Rimessi, Paola; Sabatelli, Patrizia; Fabris, Marina; Braghetta, P; Bassi, Elena; Spitali, Pietro; Vattemi, G; Tomelleri, G; Mari, L; Perrone, Daniela; Medici, Alessandro; Neri, Marcella; Bovolenta, Matteo; Martoni, Elena; Maraldi, N; Gualandi, Francesca; Merlini, Luciano; Balestri, M; Tondelli, L; Sparnacci, K; Bonaldo, P; Caputo, Antonella; Laus, M; Ferlini, Alessandra
Chromatin configuration, RNA and protein studies identified novel DNA elements that influence the dystrophin transcription dynamics
file con accesso da definire2018 Falzarano, Ms; Gherardi, S; Bovolenta, M; Passarelli, C; Erriquez, D; Scotton, C; Armaroli, A; Rossi, R; Osman, H; Mora, M; Bernasconi, P; Maggi, L; Morandi, L; Perini, G; Ferlini, A
Conjugates of oligonucleotides and bile acids and their derivatives for pharmaceutical active molecules delivery
file con accesso da definire2020 Palmieri, Beniamino; Bovolenta, Matteo; Braghetta, Paola; Capobianco, Massimo Luigi; Marchesi, Elena; Medici, Alessandro; Molon, Sibilla; Perrone, Daniela; Rimessi, Paola
Correction of duplications in the DMD gene by a CRISPR/Cas9 approach
file con accesso da definire2014 Bovolenta, Matteo
Correction of duplications in the DMD gene by a CRISPR/Cas9 approach
file con accesso da definire2017 Bovolenta, Matteo
Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 System
2017 Lattanzi, Annalisa; Duguez, Stephanie; Moiani, Arianna; Izmiryan, Araksya; Barbon, Elena; Martin, Samia; Mamchaoui, Kamel; Mouly, Vincent; Bernardi, Francesco; Mavilio, Fulvio; Bovolenta, Matteo
CRISPR activation on coagulation F7 or F8 promoters potentiate trascriptional activity in the normal and mutated gene context
2019 Pignani, Silvia; Zappaterra, Federico; Barbon, Elena; Bovolenta, Matteo; Bernardi, Francesco; Branchini, Alessio; Pinotti, Mirko
Crispr/Cas9-based COL7A1 editing for recessive dystrophic epidermolysis bullosa
2015 A., Izmiryan; Bovolenta, Matteo; F., Mavilio; A., Hovnanian
Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis
file con accesso da definire2010 Ferlini, Alessandra; Bovolenta, Matteo; Neri, M.; Gualandi, Francesca; Balboni, A.; Yuryev, A.; Salvi, F.; Gemmati, Donato; Liboni, Alberto; Zamboni, Paolo
D.P.12 Whole exome sequencing and RNAseq in a Duchenne-like female with no dystrophin mutations: Search for dystrophin gene modifiers
file con accesso da definire2012 S., Brioschi; Bovolenta, Matteo; M., Neri; C., Scotton; T., Castrignanò; G., Pesole; E., Bertini; B., Dallapiccola; E., Kotelnikova; F., Gualandi; Ferlini, Alessandra
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A naturally occurring mutation in ATP synthase subunit c is associated with increased damage following hypoxia/reoxygenation in STEMI patients | 2021 | Morciano, G.; Pedriali, G.; Bonora, M.; Pavasini, R.; Mikus, E.; Calvi, S.; Bovolenta, M.; Lebied...zinska-Arciszewska, M.; Pinotti, M.; Albertini, A.; Wieckowski, M. R.; Giorgi, C.; Ferrari, R.; Galluzzi, L.; Campo, G.; Pinton, P. | |
| A new rat model for Duchenne muscular dystrophy generated by CRISPR-induced deletion of Exon 45 | 2019 | Daoud, C; Roudaut, C; Bellec-Dyevre, J; Bovolenta, M; Richard, I | |
| A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies | 2008 | Bovolenta, Matteo; Neri, Marcella; Fini, Sergio; Fabris, Marina; Trabanelli, Cecilia; Venturoli, ...A; Martoni, Elena; Bassi, Elena; Spitali, Pietro; Brioschi, Simona; Falzarano, Maria Sofia; Rimessi, Paola; Ciccone, R; Ashton, E; Mccauley, J; Yau, S; Abbs, S; Muntoni, F; Merlini, Luciano; Gualandi, Francesca; Ferlini, Alessandra | |
| An engineered tale-transcription factor rescues transcription of factor VII impaired by promoter mutations and enhances its endogenous expression in hepatocytes | 2016 | Barbon, Elena; Pignani, Silvia; Branchini, Alessio; Bernardi, Francesco; Pinotti, Mirko; Bovolent...a, Matteo | |
| An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis | 2015 | Marchetti, Giovanna; Girelli, D; Zerbinati, Carlotta; Lunghi, Barbara; Friso, S; Meneghetti, Silv...ia; Coen, Matteo; Gagliano, Teresa; Guastella, Giuseppe; Bochaton Piallat, Ml; Pizzolo, F; Mascoli, Francesco; Malerba, G; Bovolenta, Matteo; Ferracin, Manuela; Olivieri, O; Bernardi, Francesco; Martinelli, N. | |
| Antisense modulation of both exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon responsible for X-linked dilated cardiomyopathy | 2010 | Rimessi, Paola; Fabris, Marina; Bovolenta, Matteo; Bassi, Elena; Falzarano, Maria Sofia; Gualandi..., Francesca; Rapezzi, C; Coccolo, F; Perrone, Daniela; Medici, Alessandro; Ferlini, Alessandra | |
| Antisense oligonucleotides conjugated with lipophilic compounds: synthesis and in vitro evaluation of exon skipping in duchenne muscular dystrophy | 2022 | Marchesi, E.; Cortesi, R.; Preti, L.; Rimessi, P.; Sguizzato, M.; Bovolenta, M.; Perrone, D. | |
| Antisense-Induced Messenger Depletion Corrects a COL6A2 Dominant Mutation in Ullrich Myopathy | 2012 | Gualandi, Francesca; Manzati, Elisa; Sabatelli, Patrizia; Passarelli, Chiara; Bovolenta, Matteo; ...Pellegrini, Camilla; Perrone, Daniela; Squarzoni, S; Pegoraro, E; Bonaldo, P; Ferlini, Alessandra | |
| Autosomal recessive Bethlem myopathy | 2009 | Gualandi, Francesca; Urciuolo, A; Martoni, Elena; Sabatelli, Patrizia; Squarzoni, S; Bovolenta, M...atteo; Messina, S; Mercuri, E; Franchella, Andrea; Ferlini, Alessandra; Bonaldo, P; Merlini, Luciano | file con accesso da definire |
| C6orf10 low-frequency and rare variants in italian multiple sclerosis patients | 2019 | Ziliotto, Nicole; Marchetti, Giovanna; Scapoli, Chiara; Bovolenta, Matteo; Meneghetti, Silvia; Be...nazzo, Andrea; Lunghi, Barbara; Balestra, Dario; Laino, Lorenza Anna; Bozzini, Nicolò; Guidi, Irene; Salvi, Fabrizio; Straudi, Sofia; Gemmati, Donato; Menegatti, Erica; Zamboni, Paolo; Bernardi, Francesco | |
| Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse | 2009 | Rimessi, Paola; Sabatelli, Patrizia; Fabris, Marina; Braghetta, P; Bassi, Elena; Spitali, Pietro;... Vattemi, G; Tomelleri, G; Mari, L; Perrone, Daniela; Medici, Alessandro; Neri, Marcella; Bovolenta, Matteo; Martoni, Elena; Maraldi, N; Gualandi, Francesca; Merlini, Luciano; Balestri, M; Tondelli, L; Sparnacci, K; Bonaldo, P; Caputo, Antonella; Laus, M; Ferlini, Alessandra | |
| Chromatin configuration, RNA and protein studies identified novel DNA elements that influence the dystrophin transcription dynamics | 2018 | Falzarano, Ms; Gherardi, S; Bovolenta, M; Passarelli, C; Erriquez, D; Scotton, C; Armaroli, A; Ro...ssi, R; Osman, H; Mora, M; Bernasconi, P; Maggi, L; Morandi, L; Perini, G; Ferlini, A | file con accesso da definire |
| Conjugates of oligonucleotides and bile acids and their derivatives for pharmaceutical active molecules delivery | 2020 | Palmieri, Beniamino; Bovolenta, Matteo; Braghetta, Paola; Capobianco, Massimo Luigi; Marchesi, El...ena; Medici, Alessandro; Molon, Sibilla; Perrone, Daniela; Rimessi, Paola | file con accesso da definire |
| Correction of duplications in the DMD gene by a CRISPR/Cas9 approach | 2014 | Bovolenta, Matteo | file con accesso da definire |
| Correction of duplications in the DMD gene by a CRISPR/Cas9 approach | 2017 | Bovolenta, Matteo | file con accesso da definire |
| Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 System | 2017 | Lattanzi, Annalisa; Duguez, Stephanie; Moiani, Arianna; Izmiryan, Araksya; Barbon, Elena; Martin,... Samia; Mamchaoui, Kamel; Mouly, Vincent; Bernardi, Francesco; Mavilio, Fulvio; Bovolenta, Matteo | |
| CRISPR activation on coagulation F7 or F8 promoters potentiate trascriptional activity in the normal and mutated gene context | 2019 | Pignani, Silvia; Zappaterra, Federico; Barbon, Elena; Bovolenta, Matteo; Bernardi, Francesco; Bra...nchini, Alessio; Pinotti, Mirko | |
| Crispr/Cas9-based COL7A1 editing for recessive dystrophic epidermolysis bullosa | 2015 | A., Izmiryan; Bovolenta, Matteo; F., Mavilio; A., Hovnanian | |
| Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis | 2010 | Ferlini, Alessandra; Bovolenta, Matteo; Neri, M.; Gualandi, Francesca; Balboni, A.; Yuryev, A.; S...alvi, F.; Gemmati, Donato; Liboni, Alberto; Zamboni, Paolo | file con accesso da definire |
| D.P.12 Whole exome sequencing and RNAseq in a Duchenne-like female with no dystrophin mutations: Search for dystrophin gene modifiers | 2012 | S., Brioschi; Bovolenta, Matteo; M., Neri; C., Scotton; T., Castrignanò; G., Pesole; E., Bertini;... B., Dallapiccola; E., Kotelnikova; F., Gualandi; Ferlini, Alessandra | file con accesso da definire |