PERETTO, LAURA
PERETTO, LAURA
Dipartimento di Scienze della vita e biotecnologie
A factor X variant with engineered activation peptide as innovative by-passing agent for haemophilia
file con accesso da definire2022 Tonetto, E.; Tarantino, R.; Testa, M. F.; Peretto, L.; Bernardi, F.; Pinotti, M.; Branchini, A.
An engineered factor X variant as a novel by-passing agent for hemophilia
file con accesso da definire2022 Tonetto, Elena; Testa, Maria Francesca; Tarantino, Rebecca; Peretto, Laura; Pinotti, Mirko; Branchini, Alessio
Counteracting the Common Shwachman-Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing
file con accesso da definire2023 Peretto, Laura; Tonetto, Elena; Maestri, Iva; Bezzerri, Valentino; Valli, Roberto; Cipolli, Marco; Pinotti, Mirko; Balestra, Dario
Deep molecular mechanisms of F8 exon 19 variants and translational approaches in Hemophilia A
2021 Lombardi, Silvia; Peretto, Laura; Merlin, Simone; Follenzi, Antonia; Mcvey, John H.; Maestri, Iva; Bernardi, Francesco; Pinotti, Mirko; Balestra, Dario
OTC intron 4 variations mediate pathogenic splicing patterns caused by the c.386G>A mutation in humans and spfash mice, and govern susceptibility to RNA-based therapies
2021 Sacchetto, Claudia; Peretto, Laura; Baralle, Francisco; Maestri, Iva; Tassi, Francesca; Bernardi, Francesco; van de Graaf, Stan F. J.; Pagani, Franco; Pinotti, Mirko; Balestra, Dario
Rescue of a FVIII splicing variant with engineered U1snRNAs
file con accesso da definire2022 Peretto, Laura; Tarantino, Rebecca; Borchiellini, Alessandra; Bernardi, Francesco; Follenzi, Antonia; Pinotti, Mirko; Balestra, Dario
Rescue of a hemophilia A-causing FVIII splicing variant via engineered U1SNRNAS
2022 Peretto, Laura; Tarantino, Rebecca; Borchiellini, Alessandra; Bernardi, Francesco; Follenzi, Antonia; Pinotti, Mirko; Balestra, Dario
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A factor X variant with engineered activation peptide as innovative by-passing agent for haemophilia | 2022 | Tonetto, E.; Tarantino, R.; Testa, M. F.; Peretto, L.; Bernardi, F.; Pinotti, M.; Branchini, A. | file con accesso da definire |
| An engineered factor X variant as a novel by-passing agent for hemophilia | 2022 | Tonetto, Elena; Testa, Maria Francesca; Tarantino, Rebecca; Peretto, Laura; Pinotti, Mirko; Branc...hini, Alessio | file con accesso da definire |
| Counteracting the Common Shwachman-Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing | 2023 | Peretto, Laura; Tonetto, Elena; Maestri, Iva; Bezzerri, Valentino; Valli, Roberto; Cipolli, Marco...; Pinotti, Mirko; Balestra, Dario | file con accesso da definire |
| Deep molecular mechanisms of F8 exon 19 variants and translational approaches in Hemophilia A | 2021 | Lombardi, Silvia; Peretto, Laura; Merlin, Simone; Follenzi, Antonia; Mcvey, John H.; Maestri, Iva...; Bernardi, Francesco; Pinotti, Mirko; Balestra, Dario | |
| OTC intron 4 variations mediate pathogenic splicing patterns caused by the c.386G>A mutation in humans and spfash mice, and govern susceptibility to RNA-based therapies | 2021 | Sacchetto, Claudia; Peretto, Laura; Baralle, Francisco; Maestri, Iva; Tassi, Francesca; Bernardi,... Francesco; van de Graaf, Stan F. J.; Pagani, Franco; Pinotti, Mirko; Balestra, Dario | |
| Rescue of a FVIII splicing variant with engineered U1snRNAs | 2022 | Peretto, Laura; Tarantino, Rebecca; Borchiellini, Alessandra; Bernardi, Francesco; Follenzi, Anto...nia; Pinotti, Mirko; Balestra, Dario | file con accesso da definire |
| Rescue of a hemophilia A-causing FVIII splicing variant via engineered U1SNRNAS | 2022 | Peretto, Laura; Tarantino, Rebecca; Borchiellini, Alessandra; Bernardi, Francesco; Follenzi, Anto...nia; Pinotti, Mirko; Balestra, Dario |