CUBELLIS, MARIA VITTORIA
CUBELLIS, MARIA VITTORIA
DIPARTIMENTO DI BIOLOGIA
Relaxation of Insulin-like growth factor-2 imprinting and discordant methylation at KvDMR1 in two first-cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes
2000 Sperandeo, Mp; Ungaro, P; Vernucci, M; Pedone, Pv; Cerrato, F; Perone, L; Casola, S; Cubellis, MARIA VITTORIA; Bruni, CARMELO BRUNO; Andria, Generoso; Sebastio, G; Riccio, A.
An intron-less betagamma-crystallin-type gene from the sponge Geodia cydonium.
2002 DI MARO, A; Pizzo, Eliodoro; Cubellis, MARIA VITTORIA; D'Alessio, G.
Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype-phenotype and description of a new variant (G6PD Neapolis).
1997 Alfinito, Fiorella; Cimmino, A; Ferraro, F; Cubellis, MARIA VITTORIA; Vitagliano, L; Francese, M; Zagari, A; Rotoli, B; Filosa, S; Martini, G.
The pharmacological chaperone 1-deoxynojirimycin increases the activity and lysosomal trafficking of multiple mutant forms of acid alpha-glucosidase
2009 Flanagan, Jj; Rossi, B; Tang, K; Wu, X; Mascioli, K; Donaudy, F; Tuzzi, Mr; Fontana, F; Cubellis, MARIA VITTORIA; Porto, C; Benjamin, E; Lockhart, Dj; Valenzano, Kj; Andria, Generoso; Parenti, Giancarlo; Do, Hv
Enzymes from extreme thermophilic bacteria as special catalysts: studies on a beta -galactosidase from Sulfolobus solfataricus
1991 M., Rossi; R., Rella; F. M., Pisani; Cubellis, MARIA VITTORIA; M., Moracci; R., Nucci; C. V. a. c. c. a. r., O.
Relaxation of Insulin-like Growth Factor 2 Imprinting and Discordant Methylation at KvDMR1 in Two First Cousins Affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber Syndromes
2000 Maria Pia, Sperandeo; Paola, Ungaro; Maria, Vernucci; Paolo V., Pedone; Flavia, Cerrato; Lucia, Perone; Stefano, Casola; Cubellis, MARIA VITTORIA; Carmelo B., Bruni; Generoso, Andria; Gianfranco, Sebastio; Andrea, Riccio
Cloning and expression of the receptor for human urokinase plasminogen activator, a central molecule in cell surface, plasmin dependent proteolysis.
1990 Roldan, Al; Cubellis, MARIA VITTORIA; Masucci, Mt; Behrendt, N; Lund, Lr; Danø, K; Appella, E; Blasi, F.
Frequent pathological human mutations: a survey.
2013 M., Cammisa; A., Correra; G., Andreotti; Cubellis, MARIA VITTORIA
An ORF in the intron seven of the sea urchin DNA-methyltransferase gene codes for a functional AP1 endonuclease
2002 Anna, Cioffi; Diana, Ferrara; Cubellis, MARIA VITTORIA; Aniello, Francesco; Marcella, Corrado; Francesca, Liguori; Alessandro, Amoroso; Fucci, Laura; Margherita, Branno
An EcoRI polymorphism for the PLAUR gene
1991 A. D., Børglum; A., Byskov; Cubellis, MARIA VITTORIA; T. A., Kruse
Isolation and sequencing of a new β-galactosidase-encoding archaebacterial gene
1990 Cubellis, MARIA VITTORIA; Carla, Rozzo; Piercarlo, Montecucchi; Mosè, Rossi
Accessibility of receptor-bound urokinase to type-1 plasminogen activator inhibitor.
1989 Cubellis, MARIA VITTORIA; Andreasen, P; Ragno, P; Mayer, M; Danø, K; Blasi, F.
Receptor-mediated internalization and degradation of urokinase is caused by its specific inhibitor PAI-1.
1990 Cubellis, MARIA VITTORIA; Wun, Tc; Blasi, F.
Regulation of urokinase receptors in monocytelike U937 cells by phorbol ester phorbol myristate acetate.
1989 Picone, R; Kajtaniak, El; Nielsen, Ls; Behrendt, N; Mastronicola, Mr; Cubellis, MARIA VITTORIA; Stoppelli, Mp; Pedersen, S; Danø, K; Blasi, F.
Cloning and sequencing of the gene coding for aspartate aminotransferase from the thermoacidophilic archaebacterium Sulfolobus solfataricus
1989 Cubellis, MARIA VITTORIA; Carla, Rozzo; Gianpaolo, Nitti; Maria Immacolata, Arnone; Gennaro, Marino; Giovanni, Sannia
Biochemical phenotype of a common disease-causing mutation and a possible therapeutic approach for the phosphomannomutase 2-associated disorder of glycosylation
2013 G., Andreotti; E., Pedone; A., Giordano; Cubellis, MARIA VITTORIA
Fabry_CEP: a tool to identify Fabry mutations responsive to pharmacological chaperones.
2013 Cammisa, M; Correra, A; Andreotti, G; Cubellis, MARIA VITTORIA
Inherited and Sporadic Epimutations at the IGF2-H19 Locus in Beckwith-Wiedemann Syndrome and Wilms’ Tumor. In: Endocrine Involvement in Developmental Syndromes.
2008 Riccio, A.; Sparago, A.; Verde, G.; DE CRESCENZO, A.; Citro, V.; Cubellis, MARIA VITTORIA; Ferrero, G. B.; CIRILLO SILENGO, M.; Russo, S.; Larizza, L.; Cerrato, F.
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.
2009 Bliek, J.; Verde, G.; Callaway, J.; Maas, S.; DE CRESCENZO, A.; Sparago, A.; Cerrato, F.; Russo, S.; Ferraiuolo, S.; Rinaldi, M. M.; Fischetto, R.; Lalatta, F.; Giordano, L.; Ferrari, P.; Cubellis, MARIA VITTORIA; Larizza, L.; Temple, I. K.; Mannens, M.; Mackay, D. J. G.; Riccio, A.
Prediction of the responsiveness to pharmacological chaperones: lysosomal human alpha-galactosidase, a case of study
2010 Andreotti, G; Guarracino, M. R.; Marco Cammisa, M.; Antonella Correra, A.; Cubellis, MARIA VITTORIA
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| Relaxation of Insulin-like growth factor-2 imprinting and discordant methylation at KvDMR1 in two first-cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes | 1.1 Articolo in rivista | 2000 | Sperandeo, Mp; Ungaro, P; Vernucci, M; Pedone, Pv; Cerrato, F; Perone, L; Casola, S; Cubellis, MARIA VITTORIA; Bruni, CARMELO BRUNO; Andria, Generoso; Sebastio, G; Riccio, A. | |
| An intron-less betagamma-crystallin-type gene from the sponge Geodia cydonium. | 1.1 Articolo in rivista | 2002 | DI MARO, A; Pizzo, Eliodoro; Cubellis, MARIA VITTORIA; D'Alessio, G. | |
| Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype-phenotype and description of a new variant (G6PD Neapolis). | 1.1 Articolo in rivista | 1997 | Alfinito, Fiorella; Cimmino, A; Ferraro, F; Cubellis, MARIA VITTORIA; Vitagliano, L; Francese, M; Zagari, A; Rotoli, B; Filosa, S; Martini, G. | |
| The pharmacological chaperone 1-deoxynojirimycin increases the activity and lysosomal trafficking of multiple mutant forms of acid alpha-glucosidase | 1.1 Articolo in rivista | 2009 | Flanagan, Jj; Rossi, B; Tang, K; Wu, X; Mascioli, K; Donaudy, F; Tuzzi, Mr; Fontana, F; Cubellis, MARIA VITTORIA; Porto, C; Benjamin, E; Lockhart, Dj; Valenzano, Kj; Andria, Generoso; Parenti, Giancarlo; Do, Hv | |
| Enzymes from extreme thermophilic bacteria as special catalysts: studies on a beta -galactosidase from Sulfolobus solfataricus | 3.1 Monografia o trattato scientifico | 1991 | M., Rossi; R., Rella; F. M., Pisani; Cubellis, MARIA VITTORIA; M., Moracci; R., Nucci; C. V. a. c. c. a. r., O. | |
| Relaxation of Insulin-like Growth Factor 2 Imprinting and Discordant Methylation at KvDMR1 in Two First Cousins Affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber Syndromes | 1.1 Articolo in rivista | 2000 | Maria Pia, Sperandeo; Paola, Ungaro; Maria, Vernucci; Paolo V., Pedone; Flavia, Cerrato; Lucia, Perone; Stefano, Casola; Cubellis, MARIA VITTORIA; Carmelo B., Bruni; Generoso, Andria; Gianfranco, Sebastio; Andrea, Riccio | |
| Cloning and expression of the receptor for human urokinase plasminogen activator, a central molecule in cell surface, plasmin dependent proteolysis. | 1.1 Articolo in rivista | 1990 | Roldan, Al; Cubellis, MARIA VITTORIA; Masucci, Mt; Behrendt, N; Lund, Lr; Danø, K; Appella, E; Blasi, F. | |
| Frequent pathological human mutations: a survey. | 4.2 Abstract in Atti di convegno | 2013 | M., Cammisa; A., Correra; G., Andreotti; Cubellis, MARIA VITTORIA | |
| An ORF in the intron seven of the sea urchin DNA-methyltransferase gene codes for a functional AP1 endonuclease | 1.1 Articolo in rivista | 2002 | Anna, Cioffi; Diana, Ferrara; Cubellis, MARIA VITTORIA; Aniello, Francesco; Marcella, Corrado; Francesca, Liguori; Alessandro, Amoroso; Fucci, Laura; Margherita, Branno | |
| An EcoRI polymorphism for the PLAUR gene | 1.1 Articolo in rivista | 1991 | A. D., Børglum; A., Byskov; Cubellis, MARIA VITTORIA; T. A., Kruse | |
| Isolation and sequencing of a new β-galactosidase-encoding archaebacterial gene | 1.1 Articolo in rivista | 1990 | Cubellis, MARIA VITTORIA; Carla, Rozzo; Piercarlo, Montecucchi; Mosè, Rossi | |
| Accessibility of receptor-bound urokinase to type-1 plasminogen activator inhibitor. | 1.1 Articolo in rivista | 1989 | Cubellis, MARIA VITTORIA; Andreasen, P; Ragno, P; Mayer, M; Danø, K; Blasi, F. | |
| Receptor-mediated internalization and degradation of urokinase is caused by its specific inhibitor PAI-1. | 1.1 Articolo in rivista | 1990 | Cubellis, MARIA VITTORIA; Wun, Tc; Blasi, F. | |
| Regulation of urokinase receptors in monocytelike U937 cells by phorbol ester phorbol myristate acetate. | 1.1 Articolo in rivista | 1989 | Picone, R; Kajtaniak, El; Nielsen, Ls; Behrendt, N; Mastronicola, Mr; Cubellis, MARIA VITTORIA; Stoppelli, Mp; Pedersen, S; Danø, K; Blasi, F. | |
| Cloning and sequencing of the gene coding for aspartate aminotransferase from the thermoacidophilic archaebacterium Sulfolobus solfataricus | 1.1 Articolo in rivista | 1989 | Cubellis, MARIA VITTORIA; Carla, Rozzo; Gianpaolo, Nitti; Maria Immacolata, Arnone; Gennaro, Marino; Giovanni, Sannia | |
| Biochemical phenotype of a common disease-causing mutation and a possible therapeutic approach for the phosphomannomutase 2-associated disorder of glycosylation | 1.1 Articolo in rivista | 2013 | G., Andreotti; E., Pedone; A., Giordano; Cubellis, MARIA VITTORIA | |
| Fabry_CEP: a tool to identify Fabry mutations responsive to pharmacological chaperones. | 1.1 Articolo in rivista | 2013 | Cammisa, M; Correra, A; Andreotti, G; Cubellis, MARIA VITTORIA | |
| Inherited and Sporadic Epimutations at the IGF2-H19 Locus in Beckwith-Wiedemann Syndrome and Wilms’ Tumor. In: Endocrine Involvement in Developmental Syndromes. | 4.1 Articoli in Atti di convegno | 2008 | Riccio, A.; Sparago, A.; Verde, G.; DE CRESCENZO, A.; Citro, V.; Cubellis, MARIA VITTORIA; Ferrero, G. B.; CIRILLO SILENGO, M.; Russo, S.; Larizza, L.; Cerrato, F. | |
| Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome. | 1.1 Articolo in rivista | 2009 | Bliek, J.; Verde, G.; Callaway, J.; Maas, S.; DE CRESCENZO, A.; Sparago, A.; Cerrato, F.; Russo, S.; Ferraiuolo, S.; Rinaldi, M. M.; Fischetto, R.; Lalatta, F.; Giordano, L.; Ferrari, P.; Cubellis, MARIA VITTORIA; Larizza, L.; Temple, I. K.; Mannens, M.; Mackay, D. J. G.; Riccio, A. | |
| Prediction of the responsiveness to pharmacological chaperones: lysosomal human alpha-galactosidase, a case of study | 1.1 Articolo in rivista | 2010 | Andreotti, G; Guarracino, M. R.; Marco Cammisa, M.; Antonella Correra, A.; Cubellis, MARIA VITTORIA |