BERNARDI, Francesco
BERNARDI, Francesco
Dipartimento di Scienze della vita e biotecnologie
A "de novo" Gene Deletion and New RFLPs Detected by von Willebrand Factor cDNA.
file con accesso da definire1989 Bernardi, Francesco; Gemmati, Donato; S., Guerra; Marchetti, Giovanna; A., Casonato; G., Ballerini
A database of polymorphisms in the von Willebrand factor gene and pseudogene
file con accesso da definire1993 Sadler, J. E.; Ginsburg, D.; Abe, T.; Anvret, M.; Batlle, J.; Bernardi, Francesco; Bonthron, D.; Bowen, D.; Eikenboom, J. C. J.; Ewenstein, B.; Falk, G.; Gralnick, H.; Inaba, H.; Inbal, A.; Lillicrap, D.; Mancuso, D.; Mazurier, C.; Meyer, D.; Michiels, J.
A De Novo and Heterozygous Gene Deletion Causing a Variant of von Willebrand Disease
1990 Bernardi, Francesco; Marchetti, Giovanna; Guerra, S; Casonato, A; Gemmati, Donato; Patracchini, P; Ballerini, G; Conconi, Francesco
A de novo antithrombin mutation found in a patient with deep vein thrombosis and vascular abnormalities
file con accesso da definire1997 Di Iasio, Mg; Gemmati, Donato; Micheletti, F; Serino, Maria Luisa; Moratelli, S; Ballerini, G; Bernardi, Francesco
A DE NOVO GENE ALTERATION CAUSING VON WILLEBRAND DISEASE
file con accesso da definire1988 Bernardi, Francesco; Marchetti, Giovanna; S., Guerra; Volinia, Stefano; Gemmati, Donato; P., Patracchini; Schwienbacher, Christine; Ballerini, Giorgio
A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype
file con accesso da definire1997 Bernardi, Francesco; Faioni, Em; Castoldi, E; Lunghi, Barbara; Castaman, G; Sacchi, E; Mannucci, Pm
A factor X variant with engineered activation peptide as innovative by-passing agent for haemophilia
file con accesso da definire2022 Tonetto, E.; Tarantino, R.; Testa, M. F.; Peretto, L.; Bernardi, F.; Pinotti, M.; Branchini, A.
A family study of FVII genotype, elevated levels of factor VII and arterial thrombotic disease
file con accesso da definire1997 Castaman, G.; Ferraresi, Paolo; Ruggieri, M.; Bernardi, Francesco; Marchetti, Giovanna
A FREQUENT FACTOR-XII GENE MUTATION IN HAGEMAN TRAIT
file con accesso da definire1988 Bernardi, Francesco; Marchetti, Giovanna; Volinia, Stefano; Patracchini, P; Casonato, A; Girolami, A; Conconi, F.
A frequent human coagulation Factor VII mutation (A294V, c152) in loop 140s affects the interaction with activators, tissue factor and substrates
file con accesso da definire2002 Toso, Raffaella; Pinotti, Mirko; High, Ka; Pollak, Es; Bernardi, Francesco
A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects
file con accesso da definire1996 Bernardi, Francesco; Legnani, C; Micheletti, Fabiola; Lunghi, Barbara; Ferraresi, Paolo; Palareti, G; Biagi, R; Marchetti, Giovanna
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders
file con accesso da definire2001 Castoldi, Elisabetta; Lunghi, Barbara; Mingozzi, Federico; Simioni, P; Girolami, A; Bernardi, Francesco
A HIND III RFLP AND A GENE LESION IN THE COAGULATION FACTOR-VIII GENE
file con accesso da definire1988 Bernardi, Francesco; Legnani, C; Volinia, Stefano; Patracchini, P; Rodorigo, G; Derosa, V; Marchetti, Giovanna
A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the italian population
file con accesso da definire2001 Castoldi, Elisabetta; Lunghi, Barbara; Mingozzi, Federico; Muleo, G; Redaelli, R; Mariani, G; Bernardi, Francesco
A NEW DISEASE-CAUSING MUTATION IN THE GAP-RELATED DOMAIN OF THE NF1 GENE
file con accesso da definire1993 Anglani, F; Murgia, A; Bedin, S; Bresin, E; Bernardi, Francesco; Clementi, M; Tenconi, R.
A new factor V gene polymorphism (His 1254 Arg) present in subjects of African origin mimics the R2 polymorphism (His 1299 Arg)
file con accesso da definire1998 Lunghi, Barbara; Castoldi, E; Mingozzi, F; Bernardi, Francesco
A new type 1 von Willebrand Disease (VWD) characterized by increased clearance of von Willebrand Factor (VWF) due to the heterozygous p.P1127S mutation: clinical phenotype and pathogenic mechanisms
file con accesso da definire2022 M. Sacco, M. Tardugno; De Cristofaro, R.; Lancellotti, S.; Bernardi, F.; Pinotti, M.; Branchini, A.; Giusti, B.; Castaman, G.
A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject
file con accesso da definire1998 Lunghi, Barbara; Castoldi, E; Mingozzi, F; Bernardi, Francesco; Castaman, G.
A novel mutation (Leu817Pro) causing type 2A von Willebrand disease
file con accesso da definire1996 Gemmati, Donato; Serino, Maria Luisa; Moratelli, S.; Ballerini, G.; Furbetta, M.; Lunghi, Barbara; Marchetti, Giovanna; Bernardi, Francesco
A novel tailored correction approach for recurrent hemophilia-causing nonsense mutations through AntiCodon-Engineered suppressor tRNAs
file con accesso da definire2023 Testa, Maria Francesca; Bernardi, Francesco; Pinotti, Mirko; Branchini, Alessio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A "de novo" Gene Deletion and New RFLPs Detected by von Willebrand Factor cDNA. | 1989 | Bernardi, Francesco; Gemmati, Donato; S., Guerra; Marchetti, Giovanna; A., Casonato; G., Ballerini | file con accesso da definire |
| A database of polymorphisms in the von Willebrand factor gene and pseudogene | 1993 | Sadler, J. E.; Ginsburg, D.; Abe, T.; Anvret, M.; Batlle, J.; Bernardi, Francesco; Bonthron, D.; ...Bowen, D.; Eikenboom, J. C. J.; Ewenstein, B.; Falk, G.; Gralnick, H.; Inaba, H.; Inbal, A.; Lillicrap, D.; Mancuso, D.; Mazurier, C.; Meyer, D.; Michiels, J. | file con accesso da definire |
| A De Novo and Heterozygous Gene Deletion Causing a Variant of von Willebrand Disease | 1990 | Bernardi, Francesco; Marchetti, Giovanna; Guerra, S; Casonato, A; Gemmati, Donato; Patracchini, P...; Ballerini, G; Conconi, Francesco | |
| A de novo antithrombin mutation found in a patient with deep vein thrombosis and vascular abnormalities | 1997 | Di Iasio, Mg; Gemmati, Donato; Micheletti, F; Serino, Maria Luisa; Moratelli, S; Ballerini, G; Be...rnardi, Francesco | file con accesso da definire |
| A DE NOVO GENE ALTERATION CAUSING VON WILLEBRAND DISEASE | 1988 | Bernardi, Francesco; Marchetti, Giovanna; S., Guerra; Volinia, Stefano; Gemmati, Donato; P., Patr...acchini; Schwienbacher, Christine; Ballerini, Giorgio | file con accesso da definire |
| A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype | 1997 | Bernardi, Francesco; Faioni, Em; Castoldi, E; Lunghi, Barbara; Castaman, G; Sacchi, E; Mannucci, Pm | file con accesso da definire |
| A factor X variant with engineered activation peptide as innovative by-passing agent for haemophilia | 2022 | Tonetto, E.; Tarantino, R.; Testa, M. F.; Peretto, L.; Bernardi, F.; Pinotti, M.; Branchini, A. | file con accesso da definire |
| A family study of FVII genotype, elevated levels of factor VII and arterial thrombotic disease | 1997 | Castaman, G.; Ferraresi, Paolo; Ruggieri, M.; Bernardi, Francesco; Marchetti, Giovanna | file con accesso da definire |
| A FREQUENT FACTOR-XII GENE MUTATION IN HAGEMAN TRAIT | 1988 | Bernardi, Francesco; Marchetti, Giovanna; Volinia, Stefano; Patracchini, P; Casonato, A; Girolami..., A; Conconi, F. | file con accesso da definire |
| A frequent human coagulation Factor VII mutation (A294V, c152) in loop 140s affects the interaction with activators, tissue factor and substrates | 2002 | Toso, Raffaella; Pinotti, Mirko; High, Ka; Pollak, Es; Bernardi, Francesco | file con accesso da definire |
| A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects | 1996 | Bernardi, Francesco; Legnani, C; Micheletti, Fabiola; Lunghi, Barbara; Ferraresi, Paolo; Palareti..., G; Biagi, R; Marchetti, Giovanna | file con accesso da definire |
| A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders | 2001 | Castoldi, Elisabetta; Lunghi, Barbara; Mingozzi, Federico; Simioni, P; Girolami, A; Bernardi, Fra...ncesco | file con accesso da definire |
| A HIND III RFLP AND A GENE LESION IN THE COAGULATION FACTOR-VIII GENE | 1988 | Bernardi, Francesco; Legnani, C; Volinia, Stefano; Patracchini, P; Rodorigo, G; Derosa, V; Marche...tti, Giovanna | file con accesso da definire |
| A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the italian population | 2001 | Castoldi, Elisabetta; Lunghi, Barbara; Mingozzi, Federico; Muleo, G; Redaelli, R; Mariani, G; Ber...nardi, Francesco | file con accesso da definire |
| A NEW DISEASE-CAUSING MUTATION IN THE GAP-RELATED DOMAIN OF THE NF1 GENE | 1993 | Anglani, F; Murgia, A; Bedin, S; Bresin, E; Bernardi, Francesco; Clementi, M; Tenconi, R. | file con accesso da definire |
| A new factor V gene polymorphism (His 1254 Arg) present in subjects of African origin mimics the R2 polymorphism (His 1299 Arg) | 1998 | Lunghi, Barbara; Castoldi, E; Mingozzi, F; Bernardi, Francesco | file con accesso da definire |
| A new type 1 von Willebrand Disease (VWD) characterized by increased clearance of von Willebrand Factor (VWF) due to the heterozygous p.P1127S mutation: clinical phenotype and pathogenic mechanisms | 2022 | M. Sacco, M. Tardugno; De Cristofaro, R.; Lancellotti, S.; Bernardi, F.; Pinotti, M.; Branchini, ...A.; Giusti, B.; Castaman, G. | file con accesso da definire |
| A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject | 1998 | Lunghi, Barbara; Castoldi, E; Mingozzi, F; Bernardi, Francesco; Castaman, G. | file con accesso da definire |
| A novel mutation (Leu817Pro) causing type 2A von Willebrand disease | 1996 | Gemmati, Donato; Serino, Maria Luisa; Moratelli, S.; Ballerini, G.; Furbetta, M.; Lunghi, Barbara...; Marchetti, Giovanna; Bernardi, Francesco | file con accesso da definire |
| A novel tailored correction approach for recurrent hemophilia-causing nonsense mutations through AntiCodon-Engineered suppressor tRNAs | 2023 | Testa, Maria Francesca; Bernardi, Francesco; Pinotti, Mirko; Branchini, Alessio | file con accesso da definire |