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of 4
pro vyhledávání: '"Angela Laporta"'
Autor:
Paola Conforti, Dario Besusso, Silvia Brocchetti, Ilaria Campus, Claudio Cappadona, Maura Galimberti, Angela Laporta, Raffaele Iennaco, Riccardo L. Rossi, Vittoria Bocchi Dickinson, Elena Cattaneo
Publikováno v:
Neurobiology of Disease, Vol 146, Iss , Pp 105140- (2020)
RUES2 cell lines represent the first collection of isogenic human embryonic stem cells (hESCs) carrying different pathological CAG lengths in the HTT gene. However, their neuronal differentiation potential has yet to be thoroughly evaluated. Here, we
Externí odkaz:
https://doaj.org/article/d8816ea5552546818bc75797b6d22185
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:
Vittoria Bocchi Dickinson, Paola Conforti, Raffaele Iennaco, Claudio Cappadona, Ilaria Campus, Riccardo L. Rossi, Silvia Brocchetti, Maura Galimberti, Dario Besusso, Elena Cattaneo, Angela Laporta
Publikováno v:
Neurobiology of Disease, Vol 146, Iss, Pp 105140-(2020)
Neurobiology_of_Disease
Neurobiology_of_Disease
RUES2 cell lines represent the first collection of isogenic human embryonic stem cells (hESCs) carrying different pathological CAG lengths in the HTT gene. However, their neuronal differentiation potential has yet to be thoroughly evaluated. Here, we
Autor:
Andrea Faedo a, b, 1, 2, Angela Laporta a, Alice Segnali a, 3, Maura Galimberti a, Dario Besusso a, Elisabetta Cesana c, Sara Belloli d, e, Rosa Maria Moresco d, Marta Tropiano f, g, Elisa Fucà f, Stefan Wild h, Andreas Bosio h, Alessandro E. Vercelli f, Gerardo Biella c, Elena Cattaneo a
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America (Online) 114 (2017): E1234–E1242. doi:10.1073/pnas.1611473114
info:cnr-pdr/source/autori:Andrea Faedo a,b,1,2, Angela Laporta a,b, Alice Segnali a,b,3, Maura Galimberti a,b, Dario Besusso a,b, Elisabetta Cesana c, Sara Belloli d,e, Rosa Maria Moresco d,e, Marta Tropiano f,g, Elisa Fucà f,g, Stefan Wild h, Andreas Bosio h, Alessandro E. Vercelli f,g, Gerardo Biella c, and Elena Cattaneo a,b,2/titolo:Differentiation of human telencephalic progenitor cells into MSNs by inducible expression of Gsx2 and Ebf1/doi:10.1073%2Fpnas.1611473114/rivista:Proceedings of the National Academy of Sciences of the United States of America (Online)/anno:2017/pagina_da:E1234/pagina_a:E1242/intervallo_pagine:E1234–E1242/volume:114
info:cnr-pdr/source/autori:Andrea Faedo a,b,1,2, Angela Laporta a,b, Alice Segnali a,b,3, Maura Galimberti a,b, Dario Besusso a,b, Elisabetta Cesana c, Sara Belloli d,e, Rosa Maria Moresco d,e, Marta Tropiano f,g, Elisa Fucà f,g, Stefan Wild h, Andreas Bosio h, Alessandro E. Vercelli f,g, Gerardo Biella c, and Elena Cattaneo a,b,2/titolo:Differentiation of human telencephalic progenitor cells into MSNs by inducible expression of Gsx2 and Ebf1/doi:10.1073%2Fpnas.1611473114/rivista:Proceedings of the National Academy of Sciences of the United States of America (Online)/anno:2017/pagina_da:E1234/pagina_a:E1242/intervallo_pagine:E1234–E1242/volume:114
Medium spiny neurons (MSNs) are a key population in the basal ganglia network, and their degeneration causes a severe neurodegenerative disorder, Huntington's disease. Understanding how ventral neuroepithelial progenitors differentiate into MSNs is c