BOVOLENTA, Matteo

BOVOLENTA, Matteo  

Dipartimento di Medicina Traslazionale e per la Romagna  

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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