DSpace ISS DSpace ISS DSpace ISS
 

DSpace ISS >

Browsing by Author Carta, Claudio

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:   
Sort by: In order: Results/Page Authors/Record:
Showing results 1 to 20 of 43
 next >
Issue DateTitleAuthor(s)
20011. International workshop. Cell therapy: filling the gap between basic science and clinical trials. Abstract bookMigliaccio, Anna Rita; Carta, Claudio; Campisi, Silvana
2001Accentuated 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
2007Activating mutations in SOS1 cause a distinctive form of Noonan syndromeTartaglia, 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
2007Activating PTPN11 mutation play a minor role in pediatric and adult solid tumorsMartinelli, 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
2005Activating PTPN11 mutations play a minor role in pediatric and adult solid tumorsMartinelli, 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
2006Biochemical and molecular characterization of the novel BRAFv599Ins mutation detected in a classic papillary thyroid carcinomaMoretti, 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
2012Complete sequencing of an IncH plasmid carrying the blaNDM-1, blaCTX-M-15, and qnrB1 genesVilla, Laura; Poirel, Laurent; Nordmann, Patrice; Carta, Claudio; Carattoli, Alessandra
2005Differences in the prevalence of PTPN11 mutations in FAB M5 paediatric acute myeloid leukaemiaGoemans, 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
2007Diversity, parental germline origin and phenotypic spectrum of de novo HRAS missense change in Costello syndromePantaleoni, 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
2006Diversity, parental germline origin and phenotypic spectrum of de novo HRAS missense changes in Costello syndromePantaleoni, 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
2007Diversity, parental germline origin and phenotypic spectrum of de novo RAS missense changes in Costello syndromeZampino, 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
2008Dysregulated ras signaling in Noonan syndrome and related disorders: disease gene discovery and functional studiesCarta, 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
2010Dysregulated RAS signalling in Noonan syndrome and related disorders: disease gene discovery and functional studiesCordeddu, 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
2000Erythropoietin-dependent suppression of the expression of the beta subunits of the interleukin-3 receptor during erythroid differentiationCarta, Claudio; Campisi, Silvana; Migliaccio, Giovanni; Migliaccio, Anna Rita
2007Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathyPandit, Bhaswati; Sarkozy, Anna; Pennacchio, Len A; Carta, Claudio; Oishi, Kimihiko; Martinelli, Simone; Pogna, Edgar Allan; Tartaglia, Marco; et al
2008Gain-of-function RAF1 mutations cause Noonan and Leopard syndromes with hypertrophic cardiomyopathyPandit, 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, Michael J; Dallapiccola, Bruno; Tartaglia, Marco; Gelb, Bruce D
2007Gain-of-function RAF1 mutations cause Noonan and Leopard syndromes with hypertrophic cardiomyopathyPandit, Bhaswati; Sarkozy, Anna; Pennacchio, Len A; Carta, Claudio; Oishi, Kimihiko; Martinelli, Simone; Pogna, Edgar Allan; Pantaleoni, Francesca; Petrangeli, Valentina; Tartaglia, Marco; et al
2007Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndromeTartaglia, Marco; Pennacchio, Len A; Zhao, Chen; Yadav, Kamlesh K; Fodale, Valentina; Sarkozy, Anna; Martinelli, Simone; Carta, Claudio; et al
2004Genetic evidence for lineage-related and differentiation stage related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemiaMartinelli, 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
2004Genetic evidence for lineage and differentiation stage-related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemiaTartaglia, 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
Showing results 1 to 20 of 43
 next >

 

Valid XHTML 1.0! DSpace ISS  Istituto Superiore di Sanità  - Feedback