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ItalianoFUCHS, CLAUDIA
Dettaglio
FUCHS, CLAUDIA
DIPARTIMENTO DI SCIENZE BIOMEDICHE E NEUROMOTORIE
Pubblicazioni
Risultati 1 - 19 di 19 (tempo di esecuzione: 0.002 secondi).
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File | |
|---|---|---|---|---|---|---|---|
| 1 | APP-dependent alteration of GSK3β activity impairs neurogenesis in the Ts65Dn mouse model of Down syndrome. | Trazzi S;Fuchs C;De Franceschi M;Mitrugno VM;Bartesaghi R;Ciani E | 2014 | NEUROBIOLOGY OF DISEASE | 1.01 Articolo in rivista | - | |
| 2 | APP-dependent up-regulation of Ptch1 underlies proliferation impairment of neural precursors in Down syndrome. | Trazzi S.; Mitrugno V.M.; Valli E.; Fuchs C.; Rizzi S.; Guidi S.; Perini G.; Bartesaghi R.; Ciani E. | 2011 | HUMAN MOLECULAR GENETICS | 1.01 Articolo in rivista | - | |
| 3 | CDKL5 deficiency predisposes neurons to cell death through the deregulation of SMAD3 signaling (vol 29, pg 658, 2019) | Fuchs C.; Medici G.; Trazzi S.; Gennaccaro L.; Galvani G.; Berteotti C.; Ren E.; Loi M.; Ciani E. | 2019 | BRAIN PATHOLOGY | 1.01 Articolo in rivista | - | |
| 4 | CDKL5 protein substitution therapy rescues neurological phenotypes of a mouse model of CDKL5 disorder | Trazzi, Stefania; De Franceschi, Marianna; Fuchs, Claudia; Bastianini, Stefano; Viggiano, Rocchin...a; Lupori, Leonardo; Mazziotti, Raffaele; Medici, Giorgio; Martire, Viviana Lo; Ren, Elisa; Rimondini, Roberto; Zoccoli, Giovanna; Bartesaghi, Renata; Pizzorusso, Tommaso; Ciani, Elisabetta* | 2018 | HUMAN MOLECULAR GENETICS | 1.01 Articolo in rivista | - | |
| 5 | CDKL5, a novel MYCN-repressed gene, blocks cell cycle and promotes differentiation of neuronal cells | VALLI E; TRAZZI S; FUCHS C; ERRIQUEZ D; BARTESAGHI R; PERINI G; CIANI E | 2012 | BIOCHIMICA ET BIOPHYSICA ACTA. GENE REGULATORY MECHANISMS | 1.01 Articolo in rivista | - | |
| 6 | Early-occurring proliferation defects in peripheral tissues of the Ts65Dn mouse model of Down syndrome are associated with patched1 over expression | Fuchs C; Ciani E; Guidi S; Trazzi S; Bartesaghi R | 2012 | LABORATORY INVESTIGATION | 1.01 Articolo in rivista | - | |
| 7 | Functional and structural impairments in the perirhinal cortex of a mouse model of CDKL5 deficiency disorder are rescued by a TrkB agonist | Ren E.; Roncace V.; Trazzi S.; Fuchs C.; Medici G.; Gennaccaro L.; Loi M.; Galvani G.; Ye K.; Rim...ondini R.; Aicardi G.; Ciani E. | 2019 | FRONTIERS IN CELLULAR NEUROSCIENCE | 1.01 Articolo in rivista | ||
| 8 | Functional impairments in the perirhinal cortex of a mouse model of CDKL5 deficiency disorder are ameliorated by a GABAB receptor antagonist | Anna Cecilia Berardi, Claudia Fuchs, Laura Gennaccaro, Vincenzo Roncacè, Yassine Aitbali, Elisa ...Ren, Stefania Trazzi, Maurizio Giustetto, Giorgio Aicardi, Elisabetta Ciani | 2020 | 4.03 Poster | - | ||
| 9 | The green tea polyphenol epigallocatechin-3-gallate (EGCG) restores CDKL5-dependent synaptic defects in vitro and in vivo | Trovo L.; Fuchs C.; De Rosa R.; Barbiero I.; Tramarin M.; Ciani E.; Rusconi L.; Kilstrup-Nielsen C. | 2020 | NEUROBIOLOGY OF DISEASE | 1.01 Articolo in rivista | - | |
| 10 | HDAC4: a key factor underlying brain developmental alterations in CDKL5 disorder | Trazzi, Stefania; Fuchs, Claudia; Viggiano, Rocchina; De Franceschi, Marianna; Valli, Emanuele; J...edynak, Paulina; Hansen, Finn K; Perini, Giovanni; Rimondini, Roberto; Kurz, Thomas; Bartesaghi, Renata; Ciani, Elisabetta | 2016 | HUMAN MOLECULAR GENETICS | 1.01 Articolo in rivista | - | |
| 11 | Heterozygous CDKL5 Knockout Female Mice Are a Valuable Animal Model for CDKL5 Disorder | Fuchs, Claudia; Gennaccaro, Laura; Trazzi, Stefania; Bastianini, Stefano; Bettini, Simone; Martir...e, Viviana Lo; Ren, Elisa; Medici, Giorgio; Zoccoli, Giovanna; Rimondini, Roberto; Ciani, Elisabetta* | 2018 | NEURAL PLASTICITY | 1.01 Articolo in rivista | ||
| 12 | Increased DNA Damage and Apoptosis in CDKL5-Deficient Neurons | Loi M.; Trazzi S.; Fuchs C.; Galvani G.; Medici G.; Gennaccaro L.; Tassinari M.; Ciani E. | 2020 | MOLECULAR NEUROBIOLOGY | 1.01 Articolo in rivista | - | |
| 13 | Inhibition of GSK3β rescues hippocampal development and learning in a mouse model of CDKL5 disorder | Fuchs, C.; Rimondini, R.; Viggiano, R.; Trazzi, S.; De Franceschi, M.; Bartesaghi, R.; Ciani, E. | 2015 | NEUROBIOLOGY OF DISEASE | 1.01 Articolo in rivista | - | |
| 14 | Loss of CDKL5 impairs survival and dendritic growth of newborn neurons by altering AKT/GSK-3β signaling. | Fuchs C;Trazzi S;Torricella R;Viggiano R;De Franceschi M;Amendola E;Gross C;Calzà L;Bartesaghi R;...Ciani E | 2014 | NEUROBIOLOGY OF DISEASE | 1.01 Articolo in rivista | - | |
| 15 | Mapping pathological phenotypes in a mouse model of CDKL5 disorder. | Amendola E;Zhan Y;Mattucci C;Castroflorio E;Calcagno E;Fuchs C;Lonetti G;Silingardi D;Vyssotski A...L;Farley D;Ciani E;Pizzorusso T;Giustetto M;Gross CT | 2014 | PLOS ONE | 1.01 Articolo in rivista | ||
| 16 | Pharmacotherapy with sertraline rescues brain development and behavior in a mouse model of CDKL5 deficiency disorder | Fuchs C.; Gennaccaro L.; Ren E.; Galvani G.; Trazzi S.; Medici G.; Loi M.; Conway E.; Devinsky O....; Rimondini R.; Ciani E. | 2020 | NEUROPHARMACOLOGY | 1.01 Articolo in rivista | - | |
| 17 | Site-specific abnormalities in the visual system of a mouse model of CDKL5 deficiency disorder | Lupori L.; Sagona G.; Fuchs C.; Mazziotti R.; Stefanov A.; Putignano E.; Napoli D.; Strettoi E.; ...Ciani E.; Pizzorusso T. | 2019 | HUMAN MOLECULAR GENETICS | 1.01 Articolo in rivista | ||
| 18 | The amyloid precursor protein (APP) triplicated gene impairs neuronal precursor differentiation and neurite development through two different domains in the Ts65Dn mouse model for down syndrome. | Trazzi S; Fuchs C; Valli E; Perini G; Bartesaghi R; Ciani E. | 2013 | THE JOURNAL OF BIOLOGICAL CHEMISTRY | 1.01 Articolo in rivista | - | |
| 19 | Treatment with the GSK3-beta inhibitor Tideglusib improves hippocampal development and memory performance in juvenile, but not adult, Cdkl5 knockout mice | Fuchs, Claudia; Fustini, Norma; Trazzi, Stefania; Gennaccaro, Laura; Rimondini, Roberto; Ciani, E...lisabetta* | 2018 | EUROPEAN JOURNAL OF NEUROSCIENCE | 1.01 Articolo in rivista | - |
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