A. Dal Mas

TBK1 mutations in Italian patients with amyotrophic lateral sclerosis: genetic and functional characterisation

L. Pozzi, F. Agosta, G. Comi, 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

Tyrosine kinase signal modulation: a matter of H2O2 membrane permeability?

R. Sitia, J. Garcia-Manteiga, M. Bertolotti, 2013, Antioxidants & redox signaling.

Improvement of SMN2 Pre-mRNA Processing Mediated by Exon-Specific U1 Small Nuclear RNA

F. Pagani, E. Bussani, M. Rogalska, 2015, American journal of human genetics.

Exon‐Specific U1s Correct SPINK5 Exon 11 Skipping Caused by a Synonymous Substitution that Affects a Bifunctional Splicing Regulatory Element

F. Pagani, L. Levati, D. Castiglia, 2015, Human mutation.

RNA‐based therapeutic approaches for coagulation factor deficiencies

F. Pagani, M. Pinotti, F. Bernardi, 2011, Journal of thrombosis and haemostasis : JTH.

An exon-specific U1 small nuclear RNA (snRNA) strategy to correct splicing defects

F. Pagani, F. Bernardi, N. Cavallari, 2012, Human molecular genetics.

Intron cleavage affects processing of alternatively spliced transcripts.

F. Pagani, T. Pastor, E. Bussani, 2011, RNA.

Stasimon/Tmem41b localizes to mitochondria-associated ER membranes and is essential for mouse embryonic development.

Meaghan Van Alstyne, L. Pellizzoni, F. Lotti, 2018, Biochemical and biophysical research communications.