Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamicsERRICO, Alessia; BALLABIO, Andrea; RUGARLI, Elena I et al.Human molecular genetics (Print). 2002, Vol 11, Num 2, pp 153-163, issn 0964-6906Article

Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axonERRICO, Alessia; CLAUDIANI, Pamela; D'ADDIO, Marilena et al.Human molecular genetics (Print). 2004, Vol 13, Num 18, pp 2121-2132, issn 0964-6906, 12 p.Article

Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degenerationMARTINELLI, Paola; LA MATTINA, Veronica; BERNACCHIA, Andrea et al.Human molecular genetics (Print). 2009, Vol 18, Num 11, pp 2001-2013, issn 0964-6906, 13 p.Article

Senataxin modulates neurite growth through fibroblast growth factor 8 signallingVANTAGGIATO, Chiara; BONDIONI, Sara; AIROLDI, Giovanni et al.Brain. 2011, Vol 134, pp 1808-1828, issn 0006-8950, 21 p., 6Article

The product of X-linked Kallmann's syndrome gene (KAL1) affects the migratory activity of gonadotropin-releasing hormone (GnRH)-producing neuronsCARIBONI, Anna; PIMPINELLI, Federica; COLAMARINO, Sophia et al.Human molecular genetics (Print). 2004, Vol 13, Num 22, pp 2781-2791, issn 0964-6906, 11 p.Article