Sfoglia per Autore
Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency
2021 I. Bestetti, C. Barbieri, A. Sironi, V. Specchia, S.A. Yatsenko, M.D. De Donno, C. Caslini, D. Gentilini, M. Crippa, L. Larizza, A. Marozzi, A. Rajkovic, D. Toniolo, M.P. Bozzetti, P. Finelli
Oxidative Stress Correlates with More Aggressive Features in Thyroid Cancer
2022 M. Muzza, G. Pogliaghi, C. Colombo, E. Carbone, V. Cirello, S. Palazzo, F. Frattini, D. Gentilini, G. Gazzano, L. Persani, L. Fugazzola
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects
2022 A. Brusati, A. Ratti, V. Pensato, S. Peverelli, D. Gentilini, E. Dalla Bella, M.N. Sorce, M. Meneri, D. Gagliardi, S. Corti, C. Gellera, G. Lauria Pinter, N. Ticozzi, V. Silani
Role of epigenetic therapy in the modulation of tumor growth and migration in human castration-resistant prostate cancer cells with neuroendocrine differentiation
2022 A. Dicitore, M.G. Bacalini, D. Saronni, G. Gaudenzi, M.C. Cantone, G. Gelmini, E.S. Grassi, D. Gentilini, M.O. Borghi, A.M. Di Blasio, L. Persani, P. Garagnani, C. Franceschi, G. Vitale
Molecular Characterization of Cancer Associated Fibroblasts in Prostate Cancer
2022 G. Vitale, M. Caraglia, V. Jung, J. Kamradt, D. Gentilini, M.T. Di Martino, A. Dicitore, M. Abate, P. Tagliaferri, A. Itro, M. Ferro, R. Balsamo, M. De Sio, G. Facchini, L. Persani, K. Schmitt, M. Saar, M. Stöckle, G. Unteregger, S. Zappavigna
TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis
2022 A. Manini, A. Ratti, A. Brusati, A. Maranzano, I. Fogh, S. Peverelli, S. Messina, D. Gentilini, F. Verde, B. Poletti, C. Morelli, V. Silani, N. Ticozzi
Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association study
2023 A. Brusati, S. Peverelli, L. Calzari, C. Tiloca, V. Casiraghi, M.N. Sorce, S. Invernizzi, E. Carbone, R. Cavagnola, F. Verde, V. Silani, N. Ticozzi, A. Ratti, D. Gentilini
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism
2023 D. Gentilini, M. Muzza, T. de Filippis, M.C. Vigone, G. Weber, L. Calzari, A. Cassio, M. Di Frenna, M. Bartolucci, E.S. Grassi, E. Carbone, A. Olivieri, L. Persani
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