DIS3 depletion in multiple myeloma causes extensive perturbation in cell cycle progression and centrosome amplification
Favasuli, Vanessa K, Ronchetti, Domenica, Silvestris, Ilaria, Puccio, Noemi, Fabbiano, Giuseppina, Traini, Valentina, Todoerti, Katia, Erratico, Silvia, Ciarrocchi, Alessia, Fragliasso, Valentina, Giannandrea, Domenica, Tumiatti, Francesca, Chiaramonte, Raffaella, Torrente, Yvan, Finelli, Palma, Morelli, Eugenio, Munshi, Nikhil C, Bolli, Niccolò, Neri, Antonino, Taìana, Elisa
Published in Haematologica (Roma) (01.01.2024)
Published in Haematologica (Roma) (01.01.2024)
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Journal Article
Long-read sequencing reveals chromothripsis in a molecularly unsolved case of Cornelia de Lange syndrome
Bestetti, Ilaria, Crippa, Milena, Sironi, Alessandra, Bellini, Matteo, Tumiatti, Francesca, Ballabio, Sara, Ceriotti, Ferruccio, Memo, Luigi, Iascone, Maria, Larizza, Lidia, Finelli, Palma
Published in Frontiers in genetics (13.03.2024)
Published in Frontiers in genetics (13.03.2024)
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Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome
Bestetti, Ilaria, Crippa, Milena, Sironi, Alessandra, Tumiatti, Francesca, Masciadri, Maura, Smeland, Marie Falkenberg, Naik, Swati, Murch, Oliver, Bonati, Maria Teresa, Spano, Alice, Cattaneo, Elisa, Mariani, Milena, Gotta, Fabio, Crosti, Francesca, Cavalli, Pietro, Pantaleoni, Chiara, Natacci, Federica, Bedeschi, Maria Francesca, Milani, Donatella, Maitz, Silvia, Selicorni, Angelo, Spaccini, Luigina, Peron, Angela, Russo, Silvia, Larizza, Lidia, Low, Karen, Finelli, Palma
Published in International journal of molecular sciences (25.05.2022)
Published in International journal of molecular sciences (25.05.2022)
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A unique Smith-Magenis patient with a de novo intragenic deletion on the maternally inherited overexpressed RAI1 allele
Sironi, Alessandra, Bestetti, Ilaria, Masciadri, Maura, Tumiatti, Francesca, Crippa, Milena, Pantaleoni, Chiara, Russo, Silvia, D'Arrigo, Stefano, Milani, Donatella, Larizza, Lidia, Finelli, Palma
Published in European journal of human genetics : EJHG (01.11.2022)
Published in European journal of human genetics : EJHG (01.11.2022)
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