Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Giorgia Giansante"'
Autor:
Luca Murru, Luisa Ponzoni, Anna Longatti, Sara Mazzoleni, Giorgia Giansante, Silvia Bassani, Mariaelvina Sala, Maria Passafaro
Publikováno v:
Neurobiology of Disease, Vol 148, Iss , Pp 105189- (2021)
Mutations in the TM4SF2 gene, which encodes TSPAN7, cause a severe form of intellectual disability (ID) often comorbid with autism spectrum disorder (ASD). Recently, we found that TM4SF2 loss in mice affects cognition. Here, we report that Tm4sf2−/
Externí odkaz:
https://doaj.org/article/b256e8940cbf477a9c99575d2b083f48
Autor:
Alessandra Piccini, Enrico Castroflorio, Pierluigi Valente, Fabrizia C. Guarnieri, Davide Aprile, Caterina Michetti, Mattia Bramini, Giorgia Giansante, Bruno Pinto, Annalisa Savardi, Fabrizia Cesca, Angela Bachi, Angela Cattaneo, Jonathan D. Wren, Anna Fassio, Flavia Valtorta, Fabio Benfenati, Silvia Giovedì
Publikováno v:
Cell Reports, Vol 21, Iss 12, Pp 3596-3611 (2017)
Summary: Synaptic transmission is critically dependent on synaptic vesicle (SV) recycling. Although the precise mechanisms of SV retrieval are still debated, it is widely accepted that a fundamental role is played by clathrin-mediated endocytosis, a
Externí odkaz:
https://doaj.org/article/bd9583cca84a42b3ac35a1011942d8d2
Autor:
Giorgia Giansante, Sara Mazzoleni, Antonio G. Zippo, Luisa Ponzoni, Anna Ghilardi, Greta Maiellano, Elly Lewerissa, Eline van Hugte, Nael Nadif Kasri, Maura Francolini, Mariaelvina Sala, Luca Murru, Silvia Bassani, Maria Passafaro
Mutations in PCDH19 gene, which encodes protocadherin-19 (PCDH19), cause Developmental and Epileptic Encephalopathy 9 (DEE9). Heterogeneous loss of PCDH19 expression in neurons is considered a key determinant of the disorder; however, how PCDH19 mosa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38a1ed5e212aa48375251b7cb6511c8e
https://hdl.handle.net/2434/962616
https://hdl.handle.net/2434/962616
Autor:
Giorgia Giansante, Anna Longatti, Mariaelvina Sala, Maria Passafaro, Luca Murru, Maria Nicol Colombo, Edoardo Moretto, Luisa Ponzoni, N. Lattuada, Maura Francolini
Publikováno v:
Molecular Neurobiology
Rho GTPases are a class of G-proteins involved in several aspects of cellular biology, including the regulation of actin cytoskeleton. The most studied members of this family are RHOA and RAC1 that act in concert to regulate actin dynamics. Recently,
Autor:
Franco Onofri, Giorgia Giansante, Cosimo Prestigio, Pietro Baldelli, Alessandra Romei, Antonella Marte, Pierluigi Valente, Fabio Benfenati
Publikováno v:
The Journal of Neuroscience. 40:6825-6841
Neuroinflammation is involved in the pathogenesis of several neurologic disorders, including epilepsy. Both changes in the input/output functions of synaptic circuits and cell Ca2+ dysregulation participate in neuroinflammation, but their impact on n
Autor:
Sara Mazzoleni, Giorgia Giansante, Mariaelvina Sala, Luisa Ponzoni, Maria Passafaro, Luca Murru, Anna Longatti, Silvia Bassani
Publikováno v:
Neurobiology of Disease
Neurobiology of Disease, Vol 148, Iss, Pp 105189-(2021)
Neurobiology of Disease, Vol 148, Iss, Pp 105189-(2021)
Mutations in the TM4SF2 gene, which encodes TSPAN7, cause a severe form of intellectual disability (ID) often comorbid with autism spectrum disorder (ASD). Recently, we found that TM4SF2 loss in mice affects cognition. Here, we report that Tm4sf2−/
Autor:
Giorgia, Giansante, Antonella, Marte, Alessandra, Romei, Cosimo, Prestigio, Franco, Onofri, Fabio, Benfenati, Pietro, Baldelli, Pierluigi, Valente
Publikováno v:
J Neurosci
Neuroinflammation is involved in the pathogenesis of several neurologic disorders, including epilepsy. Both changes in the input/output functions of synaptic circuits and cell Ca(2+) dysregulation participate in neuroinflammation, but their impact on
Autor:
Giorgia Giansante, Enrico Castroflorio, Anna Corradi, Floriana Fruscione, Caterina Michetti, Nicola Forte, Flavia Valtorta, Thierry Nieus, Anna Fassio, Pierluigi Valente, Federico Zara, Pietro Baldelli, Fabio Benfenati, Davide Lonardoni, Jin Wu Tsai, Bruno Sterlini, Alessandra Romei, Manuela Fadda
Publikováno v:
Cerebral Cortex
Mutations in PRoline-Rich Transmembrane protein 2 (PRRT2) underlie a group of paroxysmal disorders including epilepsy, kinesigenic dyskinesia and migraine. Most of the mutations lead to impaired PRRT2 expression and/or function, emphasizing the patho
Autor:
Simona Baldassari, Anna Corradi, Giorgia Giansante, Floriana Fruscione, Jacopo Sartorelli, Antonio Gambardella, Alessandra Romei, Anna Fassio, Alicia Rubio, Manuela Fadda, Pierluigi Valente, Bruno Sterlini, Vania Broccoli, Fabio Benfenati, Pia Irene Anna Rossi, Federico Zara, Pietro Baldelli, Thierry Nieus, Cosimo Prestigio
Publikováno v:
Brain
See Lerche (doi:10.1093/brain/awy073) for a scientific commentary on this article.Proline-rich transmembrane protein 2 (PRRT2) is the causative gene for a heterogeneous group of familial paroxysmal neurological disorders that include seizures with on