CASTIGLIONI, VALENTINA
CASTIGLIONI, VALENTINA
Dipartimento di Bioscienze
Dynamic and Cell-Specific DACH1 Expression in Human Neocortical and Striatal Development
2019 V. Castiglioni, A. Faedo, M. Onorati, V.D. Bocchi, Z. Li, R. Iennaco, R. Vuono, G.P. Bulfamante, L. Muzio, G. Martino, N. Sestan, R.A. Barker, E. Cattaneo
Molecular and functional definition of the developing human striatum
2014 M. Onorati, V. Castiglioni, D. Biasci, E. Cesana, R. Menon, R. Vuono, F. Talpo, R. Goya, P. Lyons, G. Bulfamante, L. Muzio, G. Martino, M. Toselli, C. Farina, R. Barker, G. Biella, E. Cattaneo
UN APPROCCIO TRASCRIZIONALE, MOLECOLARE E FUNZIONALE PER DEFINIRE L¿ONTOGENIA DEI NEURONI STRIATALI UMANI
2014 V. Castiglioni
EZ spheres: a stable and expandable culture system for the generation of pre-rosette multipotent stem cells from human ESCs and iPSCs
2013 A. Ebert, B. Shelley, A. Hurley, M. Onorati, V. Castiglioni, T. Patitucci, S. Svendsen, V. Mattis, J. Mcgivern, A. Schwab, D. Sareen, H. Kim, E. Cattaneo, C. Svendsen
Developmentally coordinated extrinsic signals drive human pluripotent stem cell differentiation toward authentic DARPP-32(+) medium-sized spiny neurons
2013 A. Delli Carri, M. Onorati, M.J. Lelos, V. Castiglioni, A. Faedo, R. Menon, S. Camnasio, R. Vuono, P. Spaiardi, F. Talpo, M. Toselli, G. Martino, R.A. Barker, S.B. Dunnett, G. Biella, E. Cattaneo
Human pluripotent stem cell differentiation into authentic striatal projection neurons
2013 A. Delli Carri, M. Onorati, V. Castiglioni, A. Faedo, S. Camnasio, M. Toselli, G. Biella, E. Cattaneo
The first reported generation of several induced pluripotent stem cell lines from homozygous and heterozygous Huntington’s disease patients demonstrates mutation related enhanced lysosomal activity
2012 S. Camnasio, A. DELLI CARRI, A. Lombardo, I. Grad, C. Margotti, C. Castucci, B. Rozell, P. Lo Riso, V. Castiglioni, C. Zuccato, C. Rochon, Y. Takashima, G. Diaferia, I. Biunno, C. Gellera, M. Jaconi, A. Smith, O. Hovatta, L. Naldini, S. Di Donato, A. Feki, E. Cattaneo
Induced pluripotent stem cells from patients with Huntington’s disease: show CAG repeat-expansion-associated phenotypes
2012 V.B. Mattis, A. Ebert, S.P. Svendsen, C.N. Svendsen, A. King, M. Casale, S.T. Winokur, G. Batugedara, M. Vawter, P.J. Donovan, L.F. Lock, L.M. Thompson, Y. Zhu, E. Fossale, R. Singh, T. Gillis, J. Mysore, J. Li, I. Seong, Y. Shen, X. Chen, V. Wheeler, M. Macdonald, J.F. Guselia, S. Akimov, N. Arbez, T. Juoppen, T. Ratoviski, J.H. Chiang, W.R. Kim, E. Chighladze, E. Watkin, C. Zhong, G. Makri, R.N. Cole, R.L. Margolis, H. Song, G. Ming, C.A. Ross, J.A. Kaye, A. Daub, P. Sharma, A.R. Mason, S. Finkbeiner, J. Yu, J.A. Thmson, D. Rushton, S.P. Brazier, A.A. Battersby, A. Redfern, H. Tseng, A.W. Harrison, P.J. Kemp, N.D. Allen, M. Onorati, V. Castiglioni, E. Cattaneo, J. Arjomand, C. Svendsen
Induced pluripotent stem cell lines from Huntington's disease mice undergo neuronal differentiation while showing alterations in the lysosomal pathway
2012 V. Castiglioni, M. Onorati, C. Rochon, E. Cattaneo