Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Roberta Parolisi 3"'
Autor:
Dario Besusso 1, 2* Roberta Schellino 3, 4, Marina Boido 3, Sara Belloli 5, 6, Roberta Parolisi 3, Paola Conforti 1, 2, Andrea Faedo 1, Manuel Cernigoj 1, Ilaria Campus 1, Angela Laporta 1, Vittoria Dickinson Bocchi 1, Valentina Murtaj 6, 7, Malin Parmar 10 Paolo Spaiardi 9, Francesca Talpo 9, Claudia Maniezzi 9, Mauro Giuseppe Toselli 9, Gerardo Biella 9, Rosa Maria Moresco 5, 8, Alessandro Vercelli 3, 4 Annalisa Buffo 3, Elena Cattaneo 1
Publikováno v:
Stem Cell Reports
Stem Cell Reports 14 (2020): 1–16. doi:10.1016/j.stemcr.2020.03.018
info:cnr-pdr/source/autori:Dario Besusso 1,2* Roberta Schellino 3,4*, Marina Boido 3,4, Sara Belloli 5,6, Roberta Parolisi 3,4, Paola Conforti 1,2, Andrea Faedo 1,2,11, Manuel Cernigoj 1,2, Ilaria Campus 1,2, Angela Laporta 1,2, Vittoria Dickinson Bocchi 1,2, Valentina Murtaj 6,7, Malin Parmar 10 Paolo Spaiardi 9, Francesca Talpo 9, Claudia Maniezzi 9, Mauro Giuseppe Toselli 9, Gerardo Biella 9, Rosa Maria Moresco 5,6,8, Alessandro Vercelli 3,4 Annalisa Buffo 3,4 and Elena Cattaneo 1,2/titolo:Stem Cell-Derived Human Striatal Progenitors Innervate Striatal Targets and Alleviate Sensorimotor Deficit in a Rat Model of Huntington Disease./doi:10.1016%2Fj.stemcr.2020.03.018/rivista:Stem Cell Reports/anno:2020/pagina_da:1/pagina_a:16/intervallo_pagine:1–16/volume:14
Stem Cell Reports 14 (2020): 1–16. doi:10.1016/j.stemcr.2020.03.018
info:cnr-pdr/source/autori:Dario Besusso 1,2* Roberta Schellino 3,4*, Marina Boido 3,4, Sara Belloli 5,6, Roberta Parolisi 3,4, Paola Conforti 1,2, Andrea Faedo 1,2,11, Manuel Cernigoj 1,2, Ilaria Campus 1,2, Angela Laporta 1,2, Vittoria Dickinson Bocchi 1,2, Valentina Murtaj 6,7, Malin Parmar 10 Paolo Spaiardi 9, Francesca Talpo 9, Claudia Maniezzi 9, Mauro Giuseppe Toselli 9, Gerardo Biella 9, Rosa Maria Moresco 5,6,8, Alessandro Vercelli 3,4 Annalisa Buffo 3,4 and Elena Cattaneo 1,2/titolo:Stem Cell-Derived Human Striatal Progenitors Innervate Striatal Targets and Alleviate Sensorimotor Deficit in a Rat Model of Huntington Disease./doi:10.1016%2Fj.stemcr.2020.03.018/rivista:Stem Cell Reports/anno:2020/pagina_da:1/pagina_a:16/intervallo_pagine:1–16/volume:14
Summary Huntington disease (HD) is an inherited late-onset neurological disorder characterized by progressive neuronal loss and disruption of cortical and basal ganglia circuits. Cell replacement using human embryonic stem cells may offer the opportu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5634e95abd3cbc8468dd02edd0c9374a
http://hdl.handle.net/10281/272196
http://hdl.handle.net/10281/272196
Autor:
Alice Bertero 1, 2, Adam Liska 1, Marco Pagani, 1, Roberta Parolisi 3, Maria Esteban Masferrer 4, Marta Gritti 5, Matteo Pedrazzoli 5, Alberto Galbusera 1, Alessia Sarica 6, Antonio Cerasa 6, 7 Mario Buffelli 8, Raffaella Tonini 5, Annalisa Buffo 3, Cornelius Gross 4, Massimo Pasqualetti 1, Alessandro Gozzi 1
Publikováno v:
Brain (Online) 141 (2018): 2055–2065. doi:10.1093/brain/awy111
info:cnr-pdr/source/autori:Alice Bertero 1,2*, Adam Liska 1*, Marco Pagani,1,* Roberta Parolisi 3, Maria Esteban Masferrer 4, Marta Gritti 5, Matteo Pedrazzoli 5, Alberto Galbusera 1, Alessia Sarica 6, Antonio Cerasa 6,7 Mario Buffelli 8, Raffaella Tonini 5, Annalisa Buffo 3, Cornelius Gross 4, Massimo Pasqualetti 1,2 and Alessandro Gozzi 1/titolo:Autism-associated 16p11.2 microdeletion impairs prefrontal functional connectivity in mouse and human/doi:10.1093%2Fbrain%2Fawy111/rivista:Brain (Online)/anno:2018/pagina_da:2055/pagina_a:2065/intervallo_pagine:2055–2065/volume:141
info:cnr-pdr/source/autori:Alice Bertero 1,2*, Adam Liska 1*, Marco Pagani,1,* Roberta Parolisi 3, Maria Esteban Masferrer 4, Marta Gritti 5, Matteo Pedrazzoli 5, Alberto Galbusera 1, Alessia Sarica 6, Antonio Cerasa 6,7 Mario Buffelli 8, Raffaella Tonini 5, Annalisa Buffo 3, Cornelius Gross 4, Massimo Pasqualetti 1,2 and Alessandro Gozzi 1/titolo:Autism-associated 16p11.2 microdeletion impairs prefrontal functional connectivity in mouse and human/doi:10.1093%2Fbrain%2Fawy111/rivista:Brain (Online)/anno:2018/pagina_da:2055/pagina_a:2065/intervallo_pagine:2055–2065/volume:141
Human genetic studies are rapidly identifying variants that increase risk for neurodevelopmental disorders. However, it remains unclear how specific mutations impact brain function and contribute to neuropsychiatric risk. Chromosome 16p11.2 deletion