GRAZIOLI, PAOLO
GRAZIOLI, PAOLO
Dipartimento di Scienze della Salute
p300 inhibition delays premature cellular senescence
2025 E. Di Fede, E. Taci, S. Castiglioni, S. Rebellato, S. Ancona, P. Grazioli, C. Parodi, E.A. Colombo, C. Bernardelli, E. Lesma, I. Daniel Krantz, S. Corti, A. Priori, G. Fazio, C. Gervasini, V. Massa, A. Lettieri
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies
2024 E. Di Fede, A. Lettieri, E. Taci, S. Castiglioni, S. Rebellato, C. Parodi, E.A. Colombo, P. Grazioli, F. Natacci, P. Marchisio, L. Pezzani, G. Fazio, D. Milani, V. Massa, C. Gervasini
Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matter
2024 S. Castiglioni, L. Pezzoli, L. Pezzani, A. Lettieri, E. Di Fede, A. Cereda, S. Ancona, A. Gallina, E.A. Colombo, C. Parodi, P. Grazioli, E. Taci, D. Milani, M. Iascone, V. Massa, C. Gervasini
Intrauterine growth in chromatinopathies: A long road for better understanding and for improving clinical management
2024 L. Avagliano, S. Castiglioni, A. Lettieri, C. Parodi, E. Di Fede, E. Taci, P. Grazioli, E.A. Colombo, C. Gervasini, V. Massa
Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency
2023 R. Oleari, A. Lettieri, S. Manzini, A. Paganoni, V. André, P. Grazioli, M. Busnelli, P. Duminuco, A. Vitobello, C. Philippe, V. Bizaoui, H.L. Storr, F. Amoruso, F. Memi, V. Vezzoli, V. Massa, P. Scheiffele, S.R. Howard, A. Cariboni
KMT2A : umbrella gene for multiple diseases
2022 S. Castiglioni, E. Di Fede, C. Bernardelli, A. Lettieri, C. Parodi, P. Grazioli, E.A. Colombo, S. Ancona, D. Milani, E. Ottaviano, E. Borghi, V. Massa, F. Ghelma, A. Vignoli, E. Lesma, C. Gervasini
Epigenetic disorders: Lessons from the animals-animal models in chromatinopathies
2022 E. Di Fede, P. Grazioli, A. Lettieri, C. Parodi, S. Castiglioni, E. Taci, E.A. Colombo, S. Ancona, A. Priori, C. Gervasini, V. Massa
Lithium as a possible therapeutic strategy for Cornelia de Lange syndrome
2021 P. Grazioli, C. Parodi, M. Mariani, D. Bottai, E. Di Fede, A. Zulueta, L. Avagliano, A. Cereda, R. Tenconi, J. Wierzba, R. Adami, M. Iascone, P.F. Ajmone, T. Vaccari, C. Gervasini, A. Selicorni, V. Massa
IN VITRO AND IN VIVO MODELLING OF CORNELIA DE LANGE SYNDROME CAUSATIVE MUTATIONS: WNT ACTIVATION AS A POSSIBLE THERAPEUTIC APPROACH
2021 P. Grazioli
Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies
2021 C. Parodi, E. Di Fede, A. Peron, I. Viganò, P. Grazioli, S. Castiglioni, R.H. Finnell, C. Gervasini, A. Vignoli, V. Massa
Insights into the role of the microbiota and of short-chain fatty acids in Rubinstein–Taybi syndrome
2021 E. Di Fede, E. Ottaviano, P. Grazioli, C. Ceccarani, A. Galeone, C. Parodi, E.A. Colombo, G. Bassanini, G. Fazio, M. Severgnini, D. Milani, E. Verduci, T. Vaccari, V. Massa, E. Borghi, C. Gervasini
Chromatinopathies: a focus on Cornelia de Lange Syndrome
2020 L. Avagliano, I. Parenti, P. Grazioli, E. Di Fede, C. Parodi, M. Mariani, F.J. Kaiser, A. Selicorni, C. Gervasini, V. Massa
Dynamic acetylation profile during mammalian neurulation
2019 V. Massa, L. Avagliano, P. Grazioli, S.C.P. De Castro, C. Parodi, D. Savery, P. Vergani, S. Cuttin, P. Doi, G. Bulfamante, A.J. Copp, N.D.E. Greene
The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes
2019 N. Luna-Peláez, R. March-Díaz, M. Ceballos-Chávez, J.A. Guerrero-Martínez, P. Grazioli, P. García-Gutiérrez, T. Vaccari, V. Massa, J.C. Reyes, M. García-Domínguez
Microbial colonization during early phases of amphibian life
2019 G. Bassanini, F. Di Renzo, V. Massa, C. Ceccarani, P. Grazioli, R. Bacchetta, E. Ottaviano, E. Menegola, E. Borghi
Modeling Cornelia de Lange Syndrome in vitro and in vivo reveals a role for cohesin complex in neuronal survival and differentiation
2019 D. Bottai, M. Spreafico, A.S. Pistocchi, G. Fazio, R. Adami, P. Grazioli, A. Canu, C. Bragato, S. Rigamonti, C. Parodi, G. Cazzaniga, A. Biondi, F. Cotelli, A. Selicorni, V. Massa
Lithium as a positive modulator of defective WNT pathway in Cornelia de Lange Syndrome models
2018 C. Parodi, P. Grazioli, D. Bottai, E. DI FEDE, T. Vaccari, C.C.G. Gervasini, V. Massa
Drosophila melanogaster as a model to study WNT pathway alteration in Cornelia de Lange Syndrome
2018 P. Grazioli, A. Selicorni, C.C.G. Gervasini, T. Vaccari, V. Massa
Modulating the WNT pathway in Drosophila models of Cornelia de Lange Syndrome
2018 P. Grazioli, T. Vaccari, V. Massa
Cornelia de Lange Syndrome: different models and strategies to study the disease
2018 P. Grazioli, D. Bottai, G. Fazio, A. Pistocchi, T. Vaccari, V. Massa