Sfoglia per Autore
Transcriptomic Profile of Human Osteoblast-like Cells Grown on Trabecular Titanium
2025 Castoldi, G; Mauri, M; D’Aliberti, D; Spinelli, S; Testa, L; Gaverina, F; Rubinacci, A; Villa, I; Bellelli, G; Zerbini, G; Piazza, R; Zatti, G
Disruption of the Autism-Associated Pcdh9 Gene Leads to Transcriptional Alterations, Synapse Overgrowth, and Defective Network Activity in the CA1
2024 Miozzo, F; Murru, L; Maiellano, G; di Iasio, I; Zippo, A; Avendano, A; Metodieva, V; Riccardi, S; D'Aliberti, D; Spinelli, S; Canu, T; Chaabane, L; Hirano, S; Kas, M; Francolini, M; Piazza, R; Moretto, E; Passafaro, M
Human Umbilical Cord-Mesenchymal Stem Cells Promote Extracellular Matrix Remodeling in Microglia
2024 Lombardo, M; Gabrielli, M; Julien-Marsollier, F; Faivre, V; Le Charpentier, T; Bokobza, C; D'Aliberti, D; Pelizzi, N; Halimi, C; Spinelli, S; Van Steenwinckel, J; Verderio, E; Gressens, P; Piazza, R; Verderio, C
Idiopathic erythrocytosis: a germline disease?
2024 Elli, E; Mauri, M; D’Aliberti, D; Crespiatico, I; Fontana, D; Redaelli, S; Pelucchi, S; Spinelli, S; Manghisi, B; Cavalca, F; Aroldi, A; Ripamonti, A; Ferrari, S; Palamini, S; Mottadelli, F; Massimino, L; Ramazzotti, D; Cazzaniga, G; Piperno, A; Gambacorti-Passerini, C; Piazza, R
First-Hit SETBP1 Mutations Cause a Myeloproliferative Disorder with Bone Marrow Fibrosis Mimicking Triple Negative Myelofibrosis
2024 Fontana, D; Crespiatico, I; Zaghi, M; Mastini, C; D’Aliberti, D; Mauri, M; Mercado, C; Spinelli, S; Crippa, V; Inzoli, E; Manghisi, B; Civettini, I; Ramazzotti, D; Sangiorgio, V; Gengotti, M; Brambilla, V; Aroldi, A; Banfi, F; Barone, C; Orsenigo, R; Riera, L; Riminucci, M; Corsi, A; Breccia, M; Morotti, A; Cilloni, D; Roccaro, A; Sacco, A; Stagno, F; Serafini, M; Mottadelli, F; Cazzaniga, G; Pagni, F; Chiarle, R; Azzoni, E; Sessa, A; Gambacorti-Passerini, C; Elli, E; Mologni, L; Piazza, R
First-hit SETBP1 mutations cause a myeloproliferative disorder with bone marrow fibrosis
2024 Crespiatico, I; Zaghi, M; Mastini, C; D'Aliberti, D; Mauri, M; Mercado, C; Fontana, D; Spinelli, S; Crippa, V; Inzoli, E; Manghisi, B; Civettini, I; Ramazzotti, D; Sangiorgio, V; Gengotti, M; Brambilla, V; Aroldi, A; Banfi, F; Barone, C; Orsenigo, R; Riera, L; Riminucci, M; Corsi, A; Breccia, M; Morotti, A; Cilloni, D; Roccaro, A; Sacco, A; Stagno, F; Serafini, M; Mottadelli, F; Cazzaniga, G; Pagni, F; Chiarle, R; Azzoni, E; Sessa, A; Gambacorti Passerini, C; Elli, E; Mologni, L; Piazza, R
Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma
2024 Villa, M; Geeta, G; Malighetti, F; Mauri, M; Arosio, G; Cordani, N; Lobello, C; Larose, H; Pirola, A; D'Aliberti, D; Massimino, L; Criscuolo, L; Pagani, L; Chinello, C; Mastini, C; Fontana, D; Bombelli, S; Meneveri, R; Lovisa, F; Mussolin, L; Janikova, A; Pospíšilová, Š; Turner, S; Inghirami, G; Magni, F; Urso, M; Pagni, F; Ramazzotti, D; Piazza, R; Chiarle, R; Gambacorti-Passerini, C; Mologni, L
First-Hit SETBP1 Mutations Cause a Myeloproliferative Disorder with Bone Marrow Fibrosis
2023 Crespiatico, I; Zaghi, M; Mastini, C; D'Aliberti, D; Mauri, M; Mercado, C; Fontana, D; Spinelli, S; Crippa, V; Inzoli, E; Manghisi, B; Civettini, I; Ramazzotti, D; Lavoro, V; Gengotti, M; Brambilla, V; Aroldi, A; Banfi, F; Barone, C; Orsenigo, R; Riera, L; Riminucci, M; Corsi, A; Breccia, M; Morotti, A; Cilloni, D; Roccaro, A; Sacco, A; Stagno, F; Serafini, M; Mottadelli, F; Cazzaniga, G; Pagni, F; Chiarle, R; Azzoni, E; Sessa, A; Gambacorti-Passerini, C; Elli, E; Mologni, L; Piazza, R
Integrating mutational profiles and single-cell transcriptional data using LASSO regularized regression to elucidate key molecular functions involved in the pathogenesis of myelodysplastic/myeloproliferative neoplasm (MDS/MPN) with neutrophilia
2023 Crippa, V; Fontana, D; Bassi, G; D’Aliberti, D; Mauri, M; Spinelli, S; Mastini, C; Bombelli, S; Civettini, I; Guglielmana, V; Ripamonti, A; Perego, R; Mologni, L; Piazza, R; Gambacorti-Passerini, C; Ramazzotti, D
Characterization of SARS-CoV-2 Mutational Signatures from 1.5+ Million Raw Sequencing Samples
2023 Aroldi, A; Angaroni, F; D’Aliberti, D; Spinelli, S; Crespiatico, I; Crippa, V; Piazza, R; Graudenzi, A; Ramazzotti, D
Balanced SET levels favor the correct enhancer repertoire during cell fate acquisition
2023 Zaghi, M; Banfi, F; Massimino, L; Volpin, M; Bellini, E; Brusco, S; Merelli, I; Barone, C; Bruni, M; Bossini, L; Lamparelli, L; Pintado, L; D'Aliberti, D; Spinelli, S; Mologni, L; Colasante, G; Ungaro, F; Cioni, J; Azzoni, E; Piazza, R; Montini, E; Broccoli, V; Sessa, A
Targeting the immune microenvironment in Waldenström Macroglobulinemia via halting the CD40/CD40-ligand axis
2023 Sacco, A; Desantis, V; Celay, J; Giustini, V; Rigali, F; Savino, F; Cea, M; Soncini, D; Cagnetta, A; Solimando, A; D'Aliberti, D; Spinelli, S; Ramazzotti, D; Almici, C; Todoerti, K; Neri, A; Anastasia, A; Tucci, A; Motta, M; Chiarini, M; Kawano, Y; Martinez-Climent, J; Piazza, R; Roccaro, A
Targeting CCR7-PI3Kγ overcomes resistance to tyrosine kinase inhibitors in ALK-rearranged lymphoma
2023 Mastini, C; Campisi, M; Patrucco, E; Mura, G; Ferreira, A; Costa, C; Ambrogio, C; Germena, G; Martinengo, C; Peola, S; Mota, I; Vissio, E; Molinaro, L; Arigoni, M; Olivero, M; Calogero, R; Prokoph, N; Tabbò, F; Shoji, B; Brugieres, L; Geoerger, B; Turner, S; Cuesta-Mateos, C; D’Aliberti, D; Mologni, L; Piazza, R; Gambacorti Passerini, C; Inghirami, G; Chiono, V; Kamm, R; Hirsch, E; Koch, R; Weinstock, D; Aster, J; Voena, C; Chiarle, R
Clinical and Molecular features of the patients with Idiopathic Erythrocytosis
2022 Elli, E; Mauri, M; D’Aliberti, D; Crespiatico, I; Fontana, D; Redaelli, S; Pelucchi, S; Manghisi, B; Cavalca, F; Ripamonti, A; Brioschi, F; Palamini, S; Mottadelli, F; Ramazzotti, D; Piperno, A; Gambacorti Passerini, C; Piazza, R
Large-Scale Analysis of SARS-CoV-2 Synonymous Mutations Reveals the Adaptation to the Human Codon Usage During the Virus Evolution
2022 Ramazzotti, D; Angaroni, F; Maspero, D; Mauri, M; D’Aliberti, D; Fontana, D; Antoniotti, M; Elli, E; Graudenzi, A; Piazza, R
Characterization of the transcriptional landscape of atypical Chronic Myeloid Leukemia at single-cell resolution
2022 Fontana, D; Crippa, V; Bassi, G; D'Aliberti, D; Mauri, M; Spinelli, S; Mastini, C; Bombelli, S; Civettini, I; Guglielmana, V; Perego, R; Ramazzotti, D; Mologni, L; Piazza, R; Gambacorti Passerini, C
Liquid Biopsy in Cancer: Focus on Lymphoproliferative Disorders
2022 Savino, F; Rigali, F; Giustini, V; D'Aliberti, D; Spinelli, S; Piazza, R; Sacco, A; Roccaro, A
ETNK1 mutations in atypical chronic myeloid leukemia induce a mutator phenotype that can be reverted with phosphoethanolamine
2020 Fontana, D; Mauri, M; Renso, R; Docci, M; Crespiatico, I; Rost, L; Jang, M; Niro, A; D'Aliberti, D; Massimino, L; Bertagna, M; Zambrotta, G; Bossi, M; Citterio, S; Crescenzi, B; Fanelli, F; Cassina, V; Corti, R; Salerno, D; Nardo, L; Chinello, C; Mantegazza, F; Mecucci, C; Magni, F; Cavaletti, G; Bruheim, P; Rea, D; Larsen, S; Piazza, R; Gambacorti-Passerini, C
ETNK1 mutations induce a mutator phenotype that can be reverted with phosphoethanolamine
2020 Fontana, D; Mauri, M; Renso, R; Docci, M; Crespiatico, I; Rost, L; Jang, M; Niro, A; D'Aliberti, D; Massimino, L; Bertagna, M; Zambrotta, G; Bossi, M; Citterio, S; Crescenzi, B; Fanelli, F; Cassina, V; Corti, R; Salerno, D; Nardo, L; Chinello, C; Mantegazza, F; Mecucci, C; Magni, F; Cavaletti, G; Bruheim, P; Rea, D; Larsen, S; Gambacorti-Passerini, C; Piazza, R
A fatal case of TEMPI syndrome, refractory to proteasome inhibitors and autologous stem cell transplantation
2020 Diral, E; Parma, M; Renso, R; Pezzatti, S; Terruzzi, E; Perfetti, P; D'Aliberti, D; Gambacorti Passerini, C; Piazza, R; Elli, E
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