MASSA, VALENTINA
MASSA, VALENTINA
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
Portrait of a spectrum: clinical and genetic characterization of a large cohort of chromatinopathies—30 years' experience from a third level center
2025 G.B. Marchetti, E. Rosina, C. Meossi, M. Mura, L. Pezzani, A. Selicorni, M.F. Bedeschi, R. Tenconi, C. Agostoni, P. Finelli, S. De Matteis, E. Di Fede, V. Massa, L. Pezzoli, C. Gervasini, M. Iascone, D. Milani
Targeting senescence in Lymphangioleyomyomatosis through senomorphic-like molecules as a paradigm to counteract senescence in lung tumor microenvironment
2025 C. Bernardelli, P. Selvaggio, G. Cappello, S. Rosa, E. Di Fede, E. Taci, C. Gervasini, V. Massa, E. Lesma
Cohesins: Crossroad Between Cornelia de Lange Spectrum and Cancer Predisposition
2025 L. Rigotti, S. Rebellato, A. Lettieri, S. Castiglioni, M. Mariani, S. Totaro, C. Saitta, C. Gervasini, G. Fazio, V. Massa, G. Cazzaniga, A. Selicorni
Exploring senescence-driven miscommunication in the lung microenvironment
2025 C. Bernardelli, P. Selvaggio, G. Cappello, S. Rosa, E. Di Fede, E. Taci, C. Gervasini, V. Massa, E. Lesma
Exploring the uncharted role of cell senescence in rare diseases
2025 P. Selvaggio, E. Taci, A. Barassi, V. Massa, C. Gervasini, E. Lesma, C. Bernardelli, E. Di Fede
Prevention of stillbirths associated with umbilical cord abnormalities: A clinico‐pathological overview
2025 L. Avagliano, C. Parodi, V. Massa, G. Bulfamante
Targeting senescence as a novel pharmacological approach in Lymphangioleiomyomatosis
2024 C. Bernardelli, P. Selvaggio, S. Rosa, E. Di Fede, E. Taci, V. Massa, C. Gervasini, E. Lesma
SMC1A epilepsy syndrome: clinical data from a large international cohort
2024 E. Gibellato, P. Cianci, M. Mariani, B. Parma, S. Huisman, R. Śmigiel, A. Bisgaard, V. Massa, C. Gervasini, A. Moretti, A. Cattoni, A. Biondi, A. Selicorni
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
Extracellular vesicles from II trimester human amniotic fluid as paracrine conveyors counteracting oxidative stress
2024 G. Senesi, L. Guerricchio, M. Ghelardoni, N. Bertola, S. Rebellato, N. Grinovero, M. Bartolucci, A. Costa, A. Raimondi, C. Grange, S. Bolis, V. Massa, D. Paladini, D. Coviello, A. Pandolfi, B. Bussolati, A. Petretto, G. Fazio, S. Ravera, L. Barile, C. Balbi, S. Bollini
Long-Term Effects of SARS-CoV-2 Infection in Hospitalized Children: Findings from an Italian Single-Center Study
2024 V. Calcaterra, V.M. Tagi, E. D'Auria, A. Lai, S. Zanelli, C. Montanari, E. Maria Biganzoli, G. Marano, E. Borghi, V. Massa, A. Riva, G. Zuccotti
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear
2023 C. Chiereghin, M. Robusto, M.A. Lewis, S. Caetano, V. Massa, P. Castorina, U. Ambrosetti, K.P. Steel, S. Duga, R. Asselta, G. Soldà
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
Editorial: Maternal-foetal crosstalk impacts on offspring development
2023 P. Ybot-Gonzalez, N.D.E. Greene, A.J. Copp, D.J. Henderson, V. Massa
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
Maternal risk factors associated with antepartum stillbirth
2022 S. Raimondi, V. Massa, C. Ravaldi, A. Vannacci, G. Bulfamante, A. Marconi, L. Avagliano
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