LANDSBERGER, NICOLETTA

LANDSBERGER, NICOLETTA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Advanced genetic therapies for the treatment of Rett syndrome: state of the art and future perspectives 2023 Landsberger, Nicoletta + Article (author) -
A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain 2023 De Rocco G.Albizzati E.Frasca A.Landsberger N. + Article (author) -
Complex CDKL5 translational regulation and its potential role in CDKL5 deficiency disorder 2023 Di Carlo, ValerioLandsberger, Nicoletta + Article (author) -
Not Just Loss-of-Function Variations: Identification of a Hypermorphic Variant in a Patient With a CDKL5 Missense Substitution 2022 Frasca, AngelisaLandsberger, Nicoletta + Article (author) -
Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals 2022 Albizzati E.Miramondi F.Landsberger N.Frasca A. + Article (author) -
In vivo magnetic resonance spectroscopy in the brain of Cdkl5 null mice reveals a metabolic profile indicative of mitochondrial dysfunctions 2021 De Palma, ClaraVignoli, AglaiaLandsberger, NicolettaFrasca, Angelisa + Article (author) -
The enhancement of activity rescues the establishment of Mecp2 null neuronal phenotypes 2021 Giuseppina De RoccoMassimiliano PaganiNicoletta Landsberger + Article (author) -
MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders 2020 Frasca A.Spiombi E.Palmieri M.Albizzati E.Di Carlo V.Landsberger N + Article (author) -
Fingolimod modulates dendritic architecture in a BDNF-dependent manner 2020 Spiombi E.Frasca A.Landsberger N. + Article (author) -
The DNA repair protein ATM as target in autism spectrum disorder 2020 Pizzamiglio LFocchi ECambria CMBifari FLandsberger NSala MMatteoli MMenna EAntonucci F + Article (author) -
Aminoglycoside drugs induce efficient read-through of CDKL5 nonsense mutations, slightly restoring its kinase activity 2019 Fazzari M.Frasca A.Bifari F.Landsberger N. Article (author) -
Splicing mutations impairing CDKL5 expression and activity can be efficiently rescued by U1snRNA-based therapy 2019 Balestra D.Fazzari M.Pinotti M.Landsberger N.Frasca A. + Article (author) -
Progress in the development of in vivo redox measurements: New tools for longitudinal studies in Rett syndrome 2019 Frasca A.Bedogni F.Landsberger N. Article (author) -
Rescue of prepulse inhibition deficit and brain mitochondrial dysfunction by pharmacological stimulation of the central serotonin receptor 7 in a mouse model of CDKL5 Deficiency Disorder 2019 Landsberger, Nicoletta + Article (author) -
Towards a consensus on developmental regression 2019 Bedogni F.Landsberger N. + Article (author) -
Cannabidivarin completely rescues cognitive deficits and delays neurological and motor defects in male Mecp2 mutant mice 2019 Tramarin M.Landsberger N.Rubino T.Parolaro D. + Article (author) -
A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome 2019 Bedogni FPizzamiglio LAntonucci FFrasca ALandsberger N + Article (author) -
Lack of Methyl-CpG Binding Protein 2 (MeCP2) Affects Cell Fate Refinement During Embryonic Cortical Development 2018 M. PaganiN. LandsbergerF. Bedogni + Article (author) -
Tyr120Asp mutation alters domain flexibility and dynamics of MeCP2 DNA binding domain leading to impaired DNA interaction : Atomistic characterization of a Rett syndrome causing mutation 2018 Frasca, AngelisaLandsberger, Nicoletta + Article (author) -
The neurosteroid pregnenolone reverts microtubule derangement induced by the loss of a functional CDKL5-IQGAP1 complex 2017 N. Landsberger + Article (author) -