Cinzia Rinaldo

6PUBLICATIONS
13CO-AUTHORS
Gene and molecular therapyNeurology and neuromuscular diseasesCell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|Mar 02, 2026
Mutation type-specific transcriptomic signatures and readthrough therapy rescue in SMC1A-related developmental and epileptic encephalopathy.

Maddalena Di Nardo, Francesca Sardina, Maria M Pallotta

|Feb 07, 2025
Targeting MDM2 affects spastin protein levels and functions: implications for HSP treatment.

Francesca Sardina, Federica Polverino, Sonia Valentini

|Mar 29, 2024
Cul-4 inhibition rescues spastin levels and reduces defects in hereditary spastic paraplegia models.

Francesca Sardina, Claudia Carsetti, Ludovica Giorgini

|Oct 27, 2020
Spastin recovery in hereditary spastic paraplegia by preventing neddylation-dependent degradation.

Francesca Sardina, Alessandra Pisciottani, Manuela Ferrara

|Feb 26, 2020
An Alternative Splice Variant of HIPK2 with Intron Retention Contributes to Cytokinesis.

Veronica Gatti, Manuela Ferrara, Ilaria Virdia

|Nov 08, 2019
Extrachromosomal Histone H2B Contributes to the Formation of the Abscission Site for Cell Division.

Laura Monteonofrio, Davide Valente, Cinzia Rinaldo

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Frequent Collaborators

3 joint publications

Francesca Sardina

2 joint publications

Davide Valente

2 joint publications

Silvia Soddu

1 joint publications

Silvia Matteoni