FOCARELLI, Maria Luisa
FOCARELLI, Maria Luisa
Istituto di Ricerca Genetica e Biomedica - IRGB
Chromosome transplantation as a novel approach for correcting complex genomic disorders
2015 Paulis M.; Castelli A.; Susani L.; Lizier M.; Lagutina I.; Focarelli M.L.; Recordati C.; Uva P.; Faggioli F.; Neri T.; Scanziani E.; Galli C.; Lucchini F.; Villa A.; Vezzoni P.
Targeted gene correction in osteopetrotic-induced pluripotent stem cells for the generation of functional osteoclasts
2015 Neri T.; Muggeo S.; Paulis M.; Caldana M.E.; Crisafulli L.; Strina D.; Focarelli M.L.; Faggioli F.; Recordati C.; Scaramuzza S.; Scanziani E.; Mantero S.; Buracchi C.; Sobacchi C.; Lombardo A.; Naldini L.; Vezzoni P.; Villa A.; Ficara F.
Claspin inhibition leads to fragile site expression.
2009 Focarelli ML; Soza S; Mannini L; Paulis M; Montecucco A; Musio A.
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA.
2009 Revenkova E; Focarelli ML; Susani L; Paulis M; Bassi MT; Mannini L; Frattini A; Delia D; Krantz I; Vezzoni P; Jessberger R; Musio A.
X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations
2006 Musio A; Selicorni A; Focarelli ML; Gervasini C; Milani D; Russo S; Vezzoni P; Larizza L.
SMC1 involvement in fragile site expression
2005 Musio, A; Montagna, C; Mariani, T; Tilenni, M; Focarelli, Ml; Brait, L; Indino, E; Benedetti, Pa; Chessa, L; Albertini, A; Ried, T; Vezzoni, P
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Chromosome transplantation as a novel approach for correcting complex genomic disorders | 1-gen-2015 | Paulis M.; Castelli A.; Susani L.; Lizier M.; Lagutina I.; Focarelli M.L.; Recordati C.; Uva P.; Faggioli F.; Neri T.; Scanziani E.; Galli C.; Lucchini F.; Villa A.; Vezzoni P. | |
| Targeted gene correction in osteopetrotic-induced pluripotent stem cells for the generation of functional osteoclasts | 1-gen-2015 | Neri T.; Muggeo S.; Paulis M.; Caldana M.E.; Crisafulli L.; Strina D.; Focarelli M.L.; Faggioli F.; Recordati C.; Scaramuzza S.; Scanziani E.; Mantero S.; Buracchi C.; Sobacchi C.; Lombardo A.; Naldini L.; Vezzoni P.; Villa A.; Ficara F. | |
| Claspin inhibition leads to fragile site expression. | 1-gen-2009 | Focarelli ML; Soza S; Mannini L; Paulis M; Montecucco A; Musio A. | |
| Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA. | 1-gen-2009 | Revenkova E; Focarelli ML; Susani L; Paulis M; Bassi MT; Mannini L; Frattini A; Delia D; Krantz I; Vezzoni P; Jessberger R; Musio A. | |
| X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations | 1-gen-2006 | Musio A; Selicorni A; Focarelli ML; Gervasini C; Milani D; Russo S; Vezzoni P; Larizza L. | |
| SMC1 involvement in fragile site expression | 1-gen-2005 | Musio, A; Montagna, C; Mariani, T; Tilenni, M; Focarelli, Ml; Brait, L; Indino, E; Benedetti, Pa; Chessa, L; Albertini, A; Ried, T; Vezzoni, P |