MENEVERI RAFFAELLA

Role
Full Professor  
Academic disciplines
Cellular and Experimental Biology (BIOS-10/A)
Scientific-Disciplinary Group:
CELLULAR AND EXPERIMENTAL BIOLOGY (05/BIOS-10)
Office phone
Room:
  • U08, Floor: 3, Room: 3042

Publications

  • Quattrini, G., Barone, C., Muratore, A., Zambelli, G., Timòteo Ferreira, F., Durfort, T., et al. (2025). Embryonic hematopoietic stem and progenitor cells show differential susceptibility to leukemic transformation upon acquisition of JMML-associated KrasG12D mutation. In EHA2025 Abstract Book Poster Session (pp.3125-3127). WILEY [10.1002/hem3.70152]. Detail

  • Muratore, A., Canu, G., Barone, C., Patel, S., Bonalume, V., Quattrini, G., et al. (2025). Molecular Haemopoiesis 28. Intervento presentato a: Molecular Haemopoiesis 28, London. Detail

  • Muratore, A., Canu, G., Barone, C., Patel, S., Bonalume, V., Quattrini, G., et al. (2025). Novel insights on the role of CXCL12-CXCR4 signaling in hematopoietic development. In INAUGURAL UKSCN MEETING MANCHESTER 16th-17th SEPTEMBER 2025 CONFERENCE BOOKLET. Detail

  • Muratore, A., Patel, S., Barone, C., Bonalume, V., Canu, G., Quattrini, G., et al. (2025). Novel insights on the role of CXCL12-CXCR4 signaling in hematopoietic development. Intervento presentato a: MyDev 2025, Milan. Detail

  • Villa, M., Geeta, G., Malighetti, F., Mauri, M., Arosio, G., Cordani, N., et al. (2024). Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma. BRITISH JOURNAL OF CANCER, 131(11), 1781-1795 [10.1038/s41416-024-02881-7]. Detail

Research projects

Post-genomic approaches to decipher the pathogenesis of Facioscapulohumeral dystrophy
Year: 2013
Call: 2012-065 - Call for proposal 2013
Grantors: FONDAZIONE TELETHON ETS
Analisi delle relazioni tra profili di espressione genica e organizzazione genomica, nella miogenesi normale e patologica
Year: 2008
Call: 2008-029 - PRIN 2008
Studio del fenotipo cellulare e molecolare di cellule staminali miogeniche nella distrofia facio-scapolo-omerale (FSHD) e analisi dei
meccanismi molecolari responsabili della patogenesi
Year: 2005
Call: 2005-006 - PRIN 2005