Nicoletta Landsberger

Full Professor of Molecular Biology

Università degli Studi di Torino

Italy

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About

Nicoletta Landsberger is a Full Professor of Molecular Biology at Università degli Studi di Milano, Italy. Her research focuses on molecular mechanisms related to Rett syndrome, including the effects of genetic therapies, synaptogenesis, and specific alterations in astrocytes. Recent publications highlight her investigations into the role of the MeCP2 protein and its implications in autism spectrum disorders and metabolic dysfunctions in neural contexts.

Articles (12)

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2024

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2023

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2023

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2023

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2022

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2022

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2021

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2021

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2021

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2021

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2020

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2020

Collaborators (8)

Yunan Gao

University College London

UNITED KINGDOM

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Dario Balestra

Associate Professor of Molecular Biology

University of Ferrara

ITALY

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LAURA MAURI

Associate Professor

University of Milan

ITALY

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EFTERPI PAVLIDOU

Assistant Professor of Pediatrics

University of Ioannina

GREECE

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Michela Palmieri

Lecturer

Università Cattolica del Sacro Cuore Facoltà di Medicina e Chirurgia

ITALY

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Maria Fazzari

ITALY

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Nico Mitro

Università degli Studi di Perugia Dipartimento di Scienze Farmaceutiche

ITALY

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Angelisa Frasca

Assistant Professor

University of Milan

ITALY

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Nicoletta Landsberger

Research Interests

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About

Articles (12)

GM1 Oligosaccharide Ameliorates Rett Syndrome Phenotypes In Vitro and In Vivo via Trk Receptor Activation

A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain

Advanced genetic therapies for the treatment of Rett syndrome: state of the art and future perspectives

Mecp2 knock-out astrocytes affect synaptogenesis by IL-6 dependent mechanisms

Not Just Loss-of-Function Variations Identification of a Hypermorphic Variant in a Patient With a CDKL5 Missense Substitution

Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals

Brain phosphorylation of MeCP2 at serine 164 is developmentally regulated and globally alters its chromatin association (vol 6, 28295, 2016)

In vivo magnetic resonance spectroscopy in the brain of Cdkl5 null mice reveals a metabolic profile indicative of mitochondrial dysfunctions

The DNA repair protein ATM as a target in autism spectrum disorder

The enhancement of activity rescues the establishment of Mecp2 null neuronal phenotypes

Fingolimod Modulates Dendritic Architecture in a BDNF-Dependent Manner

<i>MECP2</i> mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders

Collaborators (8)

Yunan Gao

Dario Balestra

LAURA MAURI

EFTERPI PAVLIDOU

Michela Palmieri

Maria Fazzari

Nico Mitro

Angelisa Frasca

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