FIORINI, Maurilia
FIORINI, Maurilia
Dipartimento Materno Infantile e Tecnologie Biomediche (attivo dal 01/01/1900 al 31/12/2012)
Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome.
1998-01-01 Facchetti, Fabio; Blanzuoli, Laura; Vermi, William; Notarangelo, Luigi Daniele; Giliani, Silvia Clara; Fiorini, Maurilia; Fasth, A; Stewart, Dm; Nelson, D. L.
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency.
2002-01-01 Fiorini, Maurilia; Vermi, William; Facchetti, Fabio; Moratto, Daniele; Alessandri, Giulio; Notarangelo, L.; Caruso, Arnaldo; Grigolato, Pier Giovanni; Ugazio, Alberto Giovanni; Notarangelo, Luigi Daniele; Badolato, Raffaele
Major histocompatibility class II molecole deficiency (bare lymphocyte sindrome): Cell type specific residual expression of classical MHC protein on dendritic cells and endothelium.
2002-01-01 Vermi, William; Facchetti, Fabio; Fiorini, Maurilia; RODRIGUEZ PÉREZ, C; Franceschini, F; Badolato, Raffaele; Notarangelo, Luigi Daniele
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia.
2007-01-01 Ferrari, Samantha; Puntini, R; Lougaris, Vassilios; Soresina, A; Surkova, V; Fiorini, Maurilia; Martino, S; Rossi, Paola; Pietrogrande, Mc; Martire, B; Spadaio, G; Cardinale, F; Cossu, F; Pievani, P; Quinti, I; Rossi, Cecilia; Plebani, Alessandro
Monocytes from Wiskott-Aldrich patients display reduced chemotaxis and lack of cell polarization in response to monocyte chemoattractant protein-1 and formyl-methionyl-leucyl-phenylalanine
1998-01-01 Badolato, R.; Sozzani, S.; Malacarne, F.; Bresciani, S.; Fiorini, M.; Borsatti, A.; Albertini, A.; Mantovani, A.; Ugazio, A. G.; Notarangelo, L. D.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome. | 1-gen-1998 | Facchetti, Fabio; Blanzuoli, Laura; Vermi, William; Notarangelo, Luigi Daniele; Giliani, Silvia Clara; Fiorini, Maurilia; Fasth, A; Stewart, Dm; Nelson, D. L. | |
| Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. | 1-gen-2002 | Fiorini, Maurilia; Vermi, William; Facchetti, Fabio; Moratto, Daniele; Alessandri, Giulio; Notarangelo, L.; Caruso, Arnaldo; Grigolato, Pier Giovanni; Ugazio, Alberto Giovanni; Notarangelo, Luigi Daniele; Badolato, Raffaele | |
| Major histocompatibility class II molecole deficiency (bare lymphocyte sindrome): Cell type specific residual expression of classical MHC protein on dendritic cells and endothelium. | 1-gen-2002 | Vermi, William; Facchetti, Fabio; Fiorini, Maurilia; RODRIGUEZ PÉREZ, C; Franceschini, F; Badolato, Raffaele; Notarangelo, Luigi Daniele | |
| Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. | 1-gen-2007 | Ferrari, Samantha; Puntini, R; Lougaris, Vassilios; Soresina, A; Surkova, V; Fiorini, Maurilia; Martino, S; Rossi, Paola; Pietrogrande, Mc; Martire, B; Spadaio, G; Cardinale, F; Cossu, F; Pievani, P; Quinti, I; Rossi, Cecilia; Plebani, Alessandro | |
| Monocytes from Wiskott-Aldrich patients display reduced chemotaxis and lack of cell polarization in response to monocyte chemoattractant protein-1 and formyl-methionyl-leucyl-phenylalanine | 1-gen-1998 | Badolato, R.; Sozzani, S.; Malacarne, F.; Bresciani, S.; Fiorini, M.; Borsatti, A.; Albertini, A.; Mantovani, A.; Ugazio, A. G.; Notarangelo, L. D. |