BERNARDI, Francesco
BERNARDI, Francesco
Dipartimento di Scienze della vita e biotecnologie
2 ADDITIONAL TAQI RFLPS IN VONWILLEBRAND-FACTOR GENE (VWF) AND PSEUDOGENE
file con accesso da definire1989 Marchetti, Giovanna; Sacchi, E; Patracchini, P; Randi, Am; Sampietro, M; Bernardi, Francesco
2 TAQI RFLPS IN THE HUMAN VONWILLEBRAND-FACTOR GENE
file con accesso da definire1987 Bernardi, Francesco; Marchetti, Giovanna; Bertagnolo, Valeria; Faggioli, L; DEL SENNO, Laura
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. For the Consortium on von Willebrand Factor Mutations and Polymorphisms and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
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.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 2 ADDITIONAL TAQI RFLPS IN VONWILLEBRAND-FACTOR GENE (VWF) AND PSEUDOGENE | 1989 | Marchetti, Giovanna; Sacchi, E; Patracchini, P; Randi, Am; Sampietro, M; Bernardi, Francesco | file con accesso da definire |
| 2 TAQI RFLPS IN THE HUMAN VONWILLEBRAND-FACTOR GENE | 1987 | Bernardi, Francesco; Marchetti, Giovanna; Bertagnolo, Valeria; Faggioli, L; DEL SENNO, Laura | file con accesso da definire |
| 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. For the Consortium on von Willebrand Factor Mutations and Polymorphisms and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. | 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 |