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Browsing by Author Carta, Claudio
Showing results 1 to 20 of 41
| Issue Date | Title | Author(s) | | 2001 | 1. International workshop. Cell therapy: filling the gap between basic science and clinical trials. Abstract book | Migliaccio, Anna Rita; Carta, Claudio; Campisi, Silvana |
| 2001 | Accentuated response to phenylhydrazine and erythropoietin in mice genetically impaired for their GATA-1 expression (GATA-1low mice) | Vannucchi, Alessandro Maria; Bianchi, Lucia; Cellai, Cristina; Paoletti, Francesco; Carrai, Valentina; Calzolari, Anna; Centurione, Lucia; Lorenzini, Rodolfo Nello; Carta, Claudio; Alfani, Elena; Sanchez, Massimo; Migliaccio, Giovanni; Migliaccio, Anna Rita |
| 2007 | Activating mutations in SOS1 cause a distinctive form of Noonan syndrome | Tartaglia, Marco; Pennacchio, Len A; Fodale, Valentina; Lepri, Francesca Romana; Dentici, Maria Luisa; Sarkozy, Anna; Martinelli, Simone; Carta, Claudio; Pantaleoni, Francesca; Petrangeli, Valentina; Cordeddu, Viviana; et al |
| 2007 | Activating PTPN11 mutation play a minor role in pediatric and adult solid tumors | Martinelli, Simone; Carta, Claudio; Flex, Elisabetta; Binni, Francesco; Lucci Cordisco, Emanuela; Moretti, Sonia; Puxeddu, Efisio; Tonacchera, Massimo; Pinchera, Aldo; McDowell, Heather P; Dominici, Carlo; Rosolen, Angelo; Di Rocco, Concezio; Riccardi, Riccardo; Celli, Paolo; Picardo, Mauro; Genuardi, Maurizio; Grammatico, Paola; Sorcini, Mariella; Tartaglia, Marco |
| 2005 | Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors | Martinelli, Simone; Carta, Claudio; Flex, Elisabetta; Binni, Francesco; Lucci Cordisco, Emanuela; Puxeddu, Efisio; Tonacchera, Massimo; Pinchera, Aldo; Dominici, Carlo; Rosolen, Angelo; Riccardi, Riccardo; Sorcini, Mariella; Genuardi, Maurizio; Grammatico, Paola; Tartaglia, Marco |
| 2006 | Biochemical and molecular characterization of the novel BRAFv599Ins mutation detected in a classic papillary thyroid carcinoma | Moretti, Sonia; Macchiarulo, Antonio; De Falco, Valentina; Avenia, Nicola; Barbi, Flavia; Carta, Claudio; Cavaliere, Antonio; Melillo, Rosa Marina; Passeri, Lucia; Santeusanio, Fausto; Tartaglia, Marco; Santoro, Massimo; Puxeddu, Efisio |
| 2005 | Differences in the prevalence of PTPN11 mutations in FAB M5 paediatric acute myeloid leukaemia | Goemans, Bianca F; Zwaan, Ch M; Martinelli, Simone; Harrell, P; de Lange, D; Carta, Claudio; Reinhardt, D; Hahlen, Karel; Creutzig, U; Tartaglia, Marco; Heinrich, MC; Kaspers, G J L |
| 2007 | Diversity, parental germline origin and phenotypic spectrum of de novo HRAS missense change in Costello syndrome | Pantaleoni, Francesca; Zampino, Giuseppe; Carta, Claudio; Neri, Cinzia; Cobellis, Gilda; Vasta, Isabella; Pogna, Edgar Allan; De Feo, Emma; Delogu, Angelica; Sarkozy, Anna; Atzeri, Francesca; Selicorni, Angelo; Rauen, Katherine A; Cytrynbaum, Cheryl S; Weksberg, Rosanna; Dallapiccola, Bruno; Ballabio, Andrea; Gelb, Bruce D; Neri, Giovanni; Tartaglia, Marco |
| 2006 | Diversity, parental germline origin and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome | Pantaleoni, Francesca; Zampino, Giuseppe; Carta, Claudio; Neri, Cinzia; Cobellis, Gilda; Vasta, Isabella; Pogna, Edgar Allan; De Feo, Emma; Delogu, Angelica; Sarkozy, Anna; Atzeri, Francesca; Selicorni, Angelo; Rauen, Katherine A; Cytrynbaum, Cheryl S; Weksberg, Rosanna; Dallapiccola, Bruno; Ballabio, Andrea; Gelb, Bruce D; Neri, Giovanni; Tartaglia, Marco |
| 2007 | Diversity, parental germline origin and phenotypic spectrum of de novo RAS missense changes in Costello syndrome | Zampino, Giuseppe; Pantaleoni, Francesca; Carta, Claudio; Cobellis, Gilda; Vasta, Isabella; Neri, Cinzia; Pogna, Edgar Allan; De Feo, Emma; Delogu, Angelica; Sarkozy, Anna; Atzeri, Francesca; Selicorni, Angelo; Rauen, Katherine A; Cytrynbaum, Cheryl S; Weksberg, Rosanna; Dallapiccola, Bruno; Ballabio, Andrea; Gelb, Bruce D; Neri, Giovanni; Tartaglia, Marco |
| 2008 | Dysregulated ras signaling in Noonan syndrome and related disorders: disease gene discovery and functional studies | Carta, Claudio; Cordeddu, Viviana; Flex, Elisabetta; Fodale, Valentina; Pantaleoni, Francesca; Petrangeli, Valentina; Torreri, Paola; Lepri, Francesca Romana; Zampino, Giuseppe; Digilio, Maria Cristina; Castagnoli, Luisa; Petrucci, Tamara Corinna; Sarkozy, Anna; Gelb, Bruce D; Martinelli, Simone; Stella, Lorenzo; Dallapiccola, Bruno; Tartaglia, Marco |
| 2010 | Dysregulated RAS signalling in Noonan syndrome and related disorders: disease gene discovery and functional studies | Cordeddu, Viviana; Martinelli, Simone; Carta, Claudio; Fodale, Valentina; Flex, Elisabetta; Pantaleoni, Francesca; Sarkozy, Anna; Lepri, Francesca; Zampino, Giuseppe; Digilio, Maria Cristina; Mazzanti, Laura; Ferrero, Giovanni Battista; Rossi, Cesare; Stella, Lorenzo; Pennacchio, Len A; Gelb, Bruce D; Dallapiccola, Bruno; Tartaglia, Marco |
| 2000 | Erythropoietin-dependent suppression of the expression of the beta subunits of the interleukin-3 receptor during erythroid differentiation | Carta, Claudio; Campisi, Silvana; Migliaccio, Giovanni; Migliaccio, Anna Rita |
| 2008 | Gain-of-function RAF1 mutations cause Noonan and Leopard syndromes with hypertrophic cardiomyopathy | Pandit, Bhaswati; Sarkozy, Anna; Pennacchio, Len A; Carta, Claudio; Martinelli, Simone; Schackwitz, Wendy; Ustaszewska, A; Esposito, Giorgia; Lepri, Francesca Romana; Mundel, Peter; Rossi, Cesare; Mazzanti, Laura; Marino, Benedetto; Digilio, Maria Cristina; Zampino, Giuseppe; Ackerman, M J; Dallapiccola, Bruno; Tartaglia, Marco; Gelb, Bruce D |
| 2007 | Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy | Pandit, Bhaswati; Sarkozy, Anna; Pennacchio, Len A; Carta, Claudio; Oishi, Kimihiko; Martinelli, Simone; Pogna, Edgar Allan; Tartaglia, Marco; et al |
| 2007 | Gain-of-function RAF1 mutations cause Noonan and Leopard syndromes with hypertrophic cardiomyopathy | Pandit, Bhaswati; Sarkozy, Anna; Pennacchio, Len A; Carta, Claudio; Oishi, Kimihiko; Martinelli, Simone; Pogna, Edgar Allan; Pantaleoni, Francesca; Petrangeli, Valentina; Tartaglia, Marco; et al |
| 2007 | Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome | Tartaglia, Marco; Pennacchio, Len A; Zhao, Chen; Yadav, Kamlesh K; Fodale, Valentina; Sarkozy, Anna; Martinelli, Simone; Carta, Claudio; et al |
| 2004 | Genetic evidence for lineage-related and differentiation stage related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemia | Martinelli, Simone; Cazzaniga, Giovanni; Cordeddu, Viviana; Iavarone, Ivano; Spinelli, Monica; Palmi, Chiara; Carta, Claudio; Pession, Andrea; Aricò, Maurizio; Masera, Giuseppe; Basso, Giuseppe; Gelb, Bruce D; Sorcini, Mariella; Biondi, Andrea; Tartaglia, Marco |
| 2004 | Genetic evidence for lineage and differentiation stage-related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemia | Tartaglia, Marco; Martinelli, Simone; Cazzaniga, Giovanni; Cordeddu, Viviana; Spinelli, Monica; Palmi, Chiara; Carta, Claudio; Pession, Andrea; Aricò, Maurizio; Masera, Giuseppe; Basso, Giuseppe; Sorcini, Mariella; Gelb, Bruce D; Biondi, Andrea |
| 2009 | Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome | Graham, John M; Kramer, Nancy; Bejjani, Bassem A; Thiel, Christian T; Carta, Claudio; Neri, Giovanni; Tartaglia, Marco; Zenker, Martin |
Showing results 1 to 20 of 41
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