Projects

Cellular and molecular mechanisms of spinocerebellar ataxia type (SCA38)
2016-2017 | University of Turin, Local Grants

Role of neuronal excitability in the prefrontal cortex of mouse models of pasychiatric diseases
2015-2016 | University of Turin, Local Grants

Translating molecular pathology into a therapeutic strategy in SCA38, a newly identified form of spinocerebellar ataxia
2014-2017 | Telethon Italy Foundation (call 2014)

Filippo Tempia Co-Principal Investigator

Spinocerebellar ataxia type 28: cellular and animal models to unravel the pathogenesis and to identify potential therapeutic targets
October 2012- September 2015 | Telethon Italy Foundation (call 2012)

Filippo Tempia Co-Principal Investigator

Morphological and functional alterations in knock-in mice, model of spinocerebellar ataxia SCA28
2012-2015 | PRIN 2010-2011 Ministry of University and Research (prog. PRIN 20108WT59Y)

Filippo Tempia Co-Principal Investigator

Cerebellar symptoms and cellular mechanisms in a model of spinocerebellar ataxia SCA38(SCA38)
2014-2015 | University of Turin – Local Grants

Integration of healthy embryonic nervous tissue in the adult brain of mice models of Alzheimer's disease
2013-2014 | University of Turin – Local Grants