Linda Scaramuzza

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

F. Benfenati, N. Landsberger, M. Pagani, 2020, bioRxiv.

The antidepressant tianeptine reverts synaptic AMPA receptor defects caused by deficiency of CDKL5

Tim Guilliams, D. Cavalla, F. Antonucci, 2018, Human molecular genetics.

MeCP2 Related Studies Benefit from the Use of CD1 as Genetic Background

D. Parolaro, N. Landsberger, F. Bedogni, 2016, PloS one.

Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms.

N. Landsberger, M. Pagani, G. Rossetti, 2016, Cerebral cortex.

In vitro-derived medium spiny neurons recapitulate human striatal development and complexity at single-cell resolution

E. Arenas, G. Biella, E. Cattaneo, 2022, Cell reports methods.

Lack of Methyl-CpG Binding Protein 2 (MeCP2) Affects Cell Fate Refinement During Embryonic Cortical Development

N. Landsberger, M. Pagani, M. de Simone, 2018, Cerebral cortex.

hESC-derived striatal progenitors grafted into a Huntington’s disease rat model support long-term functional motor recovery by differentiating, self-organizing and connecting into the lesioned striatum

A. Buffo, E. Cattaneo, M. Parmar, 2023, Stem Cell Research & Therapy.