TEMPIA, Filippo

TEMPIA, Filippo  

NEUROSCIENZE "RITA LEVI MONTALCINI"  

Mostra records
Risultati 1 - 20 di 25 (tempo di esecuzione: 0.023 secondi).
Titolo Data di pubblicazione Autore(i) File
A NOVEL GENE FOR SPINOCEREBELLAR ATAXIA (SCA) LINKED TO CHROMOSOME 6 AND FATTY ACID METABOLISM 2013 Eleonora Di Gregorio; Barbara Borroni; Elisa Giorgio; Daniela Lacerenza; Cecilia Mancini; Alessandro Calcia; Isabella Mura; Domenico Coviello; Nico Mitro; Marion Gaussen; Nicola Lo Buono; Ada Funaro; Giovanna Vaula; Isabelle Lagroua; Laura Orsi; Alexandra Durr; Chiara Costanzi; Alessandro Padovani; Alexis Brice; Loredana Boccone; Eriola Hoxha; Filippo Tempia; Donatella Caruso; Giovanni Stevanin; Alfredo Brusco
A NOVEL GENE FOR SPINOCEREBELLAR ATAXIA (SCA) LINKED TO CHROMOSOME 6 AND INVOLVED IN FATTY ACID METABOLISM 2013 Eleonora Di Gregorio; Barbara Borroni; Elisa Giorgio; Daniela Lacerenza; Cecilia Mancini; Alessandro Calcia; Isabella Mura; Domenico Coviello; Nico Mitro; Marion Gaussen; Nicola Lo Buono; Ada Funaro; Giovanna Vaula; Isabelle Lagroua; Laura Orsi; Alexandra Durr; Chiara Costanzi; Alessandro Padovani; Alexis Brice; Loredana Boccone; Eriola Hoxha; Filippo Tempia; Donatella Caruso; Giovanni Stevanin; Alfredo Brusco
A NOVEL GENE FOR SPINOCEREBELLAR ATAXIA (SCA) LINKED TO CHROMOSOME 6 AND INVOLVED IN FATTY ACID METABOLISM 2013 Eleonora Di Gregorio; Barbara Borroni; Elisa Giorgio; Daniela Lacerenza; Cecilia Mancini; Alessandro Calcia; Isabella Mura; Domenico Coviello; Nico Mitro; Marion Gaussen; Nicola Lo Buono; Ada Funaro; Giovanna Vaula; Isabelle Lagroua; Laura Orsi; Alexandra Durr; Chiara Costanzi; Alessandro Padovani; Alexis Brice; Loredana Boccone; Eriola Hoxha; Filippo Tempia; Donatella Caruso; Giovanni Stevanin; Alfredo Brusco
AFG3L2 mutations cause autosomal dominant ataxia SCA28 and reveal an essential role for the mitochondrial m-AAA protease complex in the cerebellum 2009 Di Bella D; Lazzaro F; Brusco A; Battaglia G; Pastore A; Finardi A; Fracasso V; Plumari M; Cagnoli C; Tempia F;Brussino A; Gellera C; Mariotti C; Pievani P;Di Donato S; Langer T; Muzi-Falconi M; Taroni F
AFG3L2 mutations cause autosomal dominant ataxia SCA28 and reveal an essential role of the m-AAA AGF3L2 homocomplex in the cerebellum 2008 DiBella D; Lazzaro F; Brusco A; Battaglia G; Pastore A; Finardi A; Fracasso V; Plumari M; Cagnoli C; Tempia F; Brussino A; Gellera C; Mariotti C; Pievani P; DiDonato S; Langer T; Muzi-Falconi M; Taroni F
Amyloid deposition during life span of APPPS1 mice, a murine model of Alzheimer's disease 2009 Montarolo F; Boda E; Hoxha E; Tempia F
Beta amyloid effects on cerebellar Purkinje cell excitability 2008 Hoxha E; Boda E; Montarolo F; Tempia F
Delayed motor learning and cerebellar electrophysiological alterations in a murine model of Alzheimer's disease with massive amyloidosis 2009 Hoxha E; Boda E; Montarolo F; Tempia F
Determinants of high frequency firing and discharge pattern modulation in cerebellar Purkinje cells 2004 Tempia F; Sacco T
Developmental time course of Kv3 voltage-gated potassium channels expression in mouse brain 2006 Boda E; Pini A; Tempia F
Effects of neuronal activity on intra- and extra-cellular beta amyloid in a transgenic murine model of Alzheimer’s disease 2011 Montarolo F; Parolisi R; Hoxha E; Tempia F
Expression pattern of the potassium channel accessory subunit Mirp2 in the mouse brain during development, in the adulthood and after lesion 2009 Boda E; Hoxha E; Montarolo F; Buffo A; Tempia F
Functional characterization of missense mutations in SCA28 patients, and development of a mouse model of the disease 2011 Mancini C; Roncaglia P; Stevanin G; Durr A; Brussino A; Cagnoli C; Krmac H; Limongi T; Montarolo F; Hoxha E; Turco E; Messana E; Altruda F; Gustincich S; Tempia F; Brusco A
GABAergic and excitability deficits in cerebellar Purkinje cells in APPPS1 mice, a murine model of Alzheimer's disease with massive amyloidosis 2009 Hoxha E; Boda E; Montarolo F; Parolisi R; Tempia F
Neurophysiology of locomotion: spinal mechanisms 2007 Tempia F
Reduced cerebellar Purkinje cell firing associated with motor impairment in Ebf2-null mice 2011 Hoxha E; Tonini R; Montarolo F; Croci L; Consalez GG; Tempia F
Spinocerebellar ataxia type 28: cellular and animal models to unravel the pathogenesis and to identify potential therapeutic targets 2015 CECILIA Mancini; ERIOLA Hoxha; EMILIA Turco; FIORELLA Altruda; FILIPPO Tempia; ALFREDO Brusco.
Studio dei meccanismi patogenetici dell’Atassia Spinocerebellare 28. 2012 Mancini C.; Roncaglia P.; Lo Buono N.; Gazzano E.; Brussino A.; Cagnoli C.; Krmac H.; Stevanin G.; Forlani S.; Hoxha E.; Funaro A.; Durr A.; Tempia F.; Altruda F.; Turco E.; Ghigo D.; Gustincich S.; Brusco A.
The GPR17 receptor participates in oligodendrocyte postnatal maturation and reaction to acute and chronic brain injury 2009 Boda E; Mantovan T; Rosa P; Tempia F; Abbracchio MP; Buffo A
The P2Y-like GPR17 receptor participates in oligodendrocyte postnatal maturation and reaction to acute and chronic brain injury 2009 Boda E; Mantovan T; Rosa P; Tempia F; Abbracchio MP; Buffo A