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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)

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|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

1 joint publications

Laura Monteonofrio

1 joint publications

Fabiola Moretti

1 joint publications

Alessandro Paiardini

1 joint publications

Maddalena Di Nardo

1 joint publications

Maria M Pallotta

1 joint publications

Iñigo Marcos-Alcalde

Frequent Collaborators

3 joint publications

Francesca Sardina

2 joint publications

Davide Valente

2 joint publications

Silvia Soddu

1 joint publications

Silvia Matteoni

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