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Browsing by Author Tartaglia, Marco

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Issue DateTitleAuthor(s)
2002Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndromeIon, Andra; Tartaglia, Marco; Song, Xiaoling; Kalidas, Kamini; van der Burgt, Ineke; Shaw, Adam; Ming, Jeffrey E.; Zampino, Giuseppe; Zackai, Elaine H.; Dean, John C.S.; Somer, Mirja; Parenti, Giancarlo; Crosby, Andrew H.; Patton, Michael A.; Gelb, Bruce D; Jeffery, Steve
2005Acquired PTPN11 mutations occur rarely in adult patients with myelodyspalstic syndromes and chronic myelomonocytic leukemiaLoh, Mignon L; Martinelli, Simone; Cordeddu, Viviana; Reynolds, Melissa G; Vattikuti, Shashaank; Wulfert, Micheal; Niemeyer, Charlotte M; Beran, Miloslav E; Strom, Sara; Haas, Peter; Sorcini, Mariella; Estey, Elihu H; Lubbert, Micheal; Gattermann, Norbert; Tartaglia, Marco
2005Acquired PTPN11 mutations occur rarely in adult patients with myelodysplastic syndromes and chronic myelomonocytic leukemiaLoh, Mignon L; Martinelli, Simone; Cordeddu, Viviana; Reynolds, Melissa G; Vattikuti, Shashaank; Lee, Connie M.; Wulfert, Micheal; Germing, Ulrich; Haas, Peter; Niemeyer, Charlotte M; Beran, Miloslav E; Strom, Sara; Lubbert, Micheal; Sorcini, Mariella; Estey, Elihu H; Gattermann, Norbert; Tartaglia, Marco
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
2006Acute lymphoblasic leukaemia in Noonan syndromeRoti, Giovanni; La Starza, Roberta; Ballanti, Stelvio; Crescenzi, Barbara; Romoli, Silvia; Foà, Robin; Tartaglia, Marco; Aversa, Franco; Martelli, Massimo Fabrizio; Mecucci, Cristina
2009Acute lymphoblastic leukemia-associated JAK1 mutants activate the Janus Kinase/STAT pathway via interleukin-9 receptor a homodimersHornakova, Tekla; Staerk, Judith; Royer, Yohan; Flex, Elisabetta; Tartaglia, Marco; Constantinescu, Stefan N; Knoops, Laurent; Renauld, Jean-Christophe
2010ALL-associated JAK1 mutations confer hypersensitivity to the anti-proliferative effect of type I interferonHornakova, Tekla; Chiaretti, Sabina; Lemaire, Muriel M.; Foà, Robin; Abdelali, Raouf Ben; Asnafi, Vahid; Tartaglia, Marco; Renauld, Jean-Christophe; Knoops, Laurent
2002Analysis of three RFLPs of the COL1A2 (Type I Collagen) in the Amhara and the Oromo of EthiopiaDe Stefano, G.F.; Martinez-Labarga, C.; Casalotti, R.; Tartaglia, Marco; Novelletto, A; Pepe, Gennaro; Rickards, O.
2013Atrioventricular canal defect in patients with RASopathiesDigilio, Maria Cristina; Lepri, Francesca Romana; Dentici, Maria Luisa; Henderson, Alex; Baban, Anwar; Roberti, Maria Cristina; Capolino, Rossella; Versacci, Paolo; Surace, Cecilia; Angioni, Adriano; Tartaglia, Marco; Marino, Bruno; Dalla Piccola, Bruno
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
2002Clinical characteristics of children with juvenile myelomonocytic leukemia (JMML) and germline or somatic PTPN11 mutations, Ras mutations or neurofibromatosis type 1Niemeyer, Charlotte M; Tartaglia, Marco; Buechner, Jochen; Jung, Andreas; Baumann, Irith; Harbott, Jochen; Rogge, Tim; Gerecke, Anja; Fischer, Alexandra; Gelb, Bruce D; Nollke, Peter
2007Clinical lumping and molecular splitting of LEOPARD and NF1/NF1-Noonan SyndromesSarkozy, Anna; Schirinzi, Annalisa; Lepri, Francesca Romana; De Luca, Alessandro; Pizzuti, Antonio; Tartaglia, Marco; Digilio, Maria Cristina; Dallapiccola, Bruno
2009Cognitive profile of disorders associated with dysregulation of the RAS/MAPK signaling cascadeCesarini, Laura; Alfieri, Paolo; Pantaleoni, Francesca; Vasta, Isabella; Cerutti, Marta; Petrangeli, Valentina; Mariotti, Paolo; Leoni, Chiara; Ricci, Daniela; Vicari, Stefano; Selicorni, Angelo; Tartaglia, Marco; Mercuri, Eugenio; Zampino, Giuseppe
2001A competitive PCR-based method to measure human fibroblast growth factor receptor 1-4 (FGFR1-4) gene expressionTartaglia, Marco; Fragale, Alessandra; Battaglia, Piero Augusto
2003A competitive polymerase chain reaction-based approach for the identification and semiquantification of mitochondrial DNA in differently heat-treated bovine meat and bone mealFrezza, Domenico; Favaro, Marco; Vaccari, Gabriele; von-Holst, Christoph; Giambra, Vincenzo; Anklam, Elke; Bove, Daniela; Battaglia, Piero Augusto; Agrimi, Umberto; Brambilla, Gianfranco; Ajmone-Marsan, Paolo; Tartaglia, Marco
2003A competitive polymerase chain reaction-based approach for the identification and semiquantification of mitochondrial DNA in differently heat-treated bovine meat and bone mealFrezza, Domenico; Favaro, Marco; Vaccari, Gabriele; von-Holst, Christoph; Giambra, Vincenzo; Anklam, Elke; Bove, Daniela; Battaglia, Piero Augusto; Agrimi, Umberto; Brambilla, Gianfranco; Ajmone-Marsan, Paolo; Tartaglia, Marco
2012Counteracting effects operating on Src-homology 2 domain-containing protein tyrosine phosphatase 2 (SHP2) function drive selection of the recurrent Y62D and Y63C substitutions in Noonan syndromeMartinelli, Simone; Nardozza, Aurelio P; Delle Vigne, Silvia; Sabetta, Gilda; Torreri, Paola; Bocchinfuso, Gianfranco; Flex, Elisabetta; Venanzi, Serenella; Palleschi, Antonio; Gelb, Bruce D; Cesareni, Gianni; Stella, Lorenzo; Castagnoli, Luisa; Tartaglia, Marco
2009Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutationsKratz, Christian P; Zampino, Giuseppe; Kriek, Marjolein; Kant, Sarina G; Leoni, Chiara; Pantaleoni, Francesca; Oudesluys-Murphy, Anne Marie; Di Rocco, Concezio; Kloska, Stephan P; Tartaglia, Marco; Zenker, Martin
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