| An exon-specific U1 small nuclear RNA (snRNA) strategy to correct splicing defects E Fernandez Alanis, M Pinotti, A Dal Mas, D Balestra, N Cavallari, ... Human molecular genetics 21 (11), 2389-2398, 2012 | 116 | 2012 |
| Improvement of SMN2 pre-mRNA processing mediated by exon-specific U1 small nuclear RNA A Dal Mas, ME Rogalska, E Bussani, F Pagani The American Journal of Human Genetics 96 (1), 93-103, 2015 | 62 | 2015 |
| TBK1 mutations in Italian patients with amyotrophic lateral sclerosis: genetic and functional characterisation L Pozzi, F Valenza, L Mosca, A Dal Mas, T Domi, A Romano, C Tarlarini, ... Journal of Neurology, Neurosurgery & Psychiatry 88 (10), 869-875, 2017 | 43 | 2017 |
| Exon‐Specific U1s Correct SPINK5 Exon 11 Skipping Caused by a Synonymous Substitution that Affects a Bifunctional Splicing Regulatory Element A Dal Mas, P Fortugno, I Donadon, L Levati, D Castiglia, F Pagani Human mutation 36 (5), 504-512, 2015 | 42 | 2015 |
| RNA‐based therapeutic approaches for coagulation factor deficiencies M Pinotti, F Bernardi, A Dal Mas, F Pagani Journal of Thrombosis and Haemostasis 9 (11), 2143-2152, 2011 | 23 | 2011 |
| Intron cleavage affects processing of alternatively spliced transcripts T Pastor, A Dal Mas, G Talotti, E Bussani, F Pagani RNA 17 (8), 1604-1613, 2011 | 6 | 2011 |
| An RNA-based therapeutic approach for inherited mis-splicing diseases A Dal Mas Univerza v Novi Gorici, Fakulteta za podiplomski študij, 2014 | | 2014 |
| AN EXON-SPECIFIC U1 SMALL NUCLEAR RNA (snRNA) STRATEGY TO CORRECT SPLICING MUTATIONS ASSOCIATED TO HEMOPHILIA B D BALESTRA, N CAVALLARI, EF Alanis, A Dal Mas, ME Rogalska, ... BLOOD TRANSFUSION 10, 46-46, 2012 | | 2012 |
| RNA− based therapeutic approaches for blood coagulation factor deficiencies caused by splicing mutations M PINOTTI, F PAGANI, D BALESTRA, M BARONI, A BRANCHINI, ... XVI Scientific Convention, 98-98, 2011 | | 2011 |
