Sfoglia per Autore
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR
1999 L. Corrado, P. Colapietro, L. Larizza, P. Riva
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population
1999 F. Natacci, P. Colapietro, P. Riva, L. Corrado, L.N. Rossi, M.M. Maninetti, M.C. Casciati, C.A. Zambrino, G. Lanzi, L. Larizza
Genotype-phenotype correlation in patients with NF1 microdeletion syndrome : identification of candidate genes for mental retardation
2002 P. Riva, M. Venturin, P. Guarnieri, F. Orzan, F. Natacci, C. Gervasini, P. Colapietro, A. Bentivegna, R. Stabile, R. Tenconi, M. Upadhyaya, C. Hernandez, L. Larizza
NF1 exon 7 skipping by disruption of exonic splice enhancers (ESEs) in neurofibromatosis 1
2003 P. Colapietro, C. Gervasini, F. Natacci, L. Rossi, P. Riva, L. Larizza
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements
2003 P. Riva, M. Venturin, C. Gervasini, F. Orzan, A. Bentivegna, L. Corrado, P. Colapietro, R. Tenconi, M. Upadhyaya, L. Larizza
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements
2003 P. Riva, M. Venturin, C. Gervasini, F. Orzan, A. Bentivegna, L. Corrado, P. Colapietro, A. Friso, R. Tenconi, M. Upadhyaya, L. Larizza
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions
2004 M. Venturin , C. Gervasini, F. Orzan, A. Bentivegna, L. Corrado, P. Colapietro , A. Friso, R. Tenconi, M. Upadhyaya, L. Larizza, P. Riva
Smith-Magenis sindrome and growth hormone deficiency
2004 E. Spadoni, P. Colapietro, M. Bozzola, G.L. Marseglia, L. Repossi, C. Danesino, L. Larizza, P. Maraschio
KIT activating mutations : incidence in adult and pediatric AML, and identification of an internal tandem duplication
2004 A. Beghini, C.B. Ripamonti, R. Cairoli, G. Cazzaniga, P. Colapietro, F. Elice, G. Nadali, G. Grillo, O.A. Haas, A. Biondi, E. Morra, L. Larizza
Distinct expression pattern of microtubule-associated protein/microtubule affinity-regulating kinase 4 in differentiated neurons
2006 R.F. Moroni, S. De Biasi, P. Colapietro, L. Larizza, A. Beghini
Prognostic impact of c-KIT mutations in core binding factor leukemias. an Italian retrospective study
2006 R. Cairoli, A. Beghini, G. Grillo, G. Nadali, F. Elice, C.B. Ripamonti, P. Colapietro, M. Nichelatti, L. Pezzetti, M. Lunghi, A. Cuneo, A. Viola, F. Ferrara, M. Lazzarino, F. Rodeghiero, G. Pizzolo, L. Larizza, E. Morra
Rubinstein-Taybi syndrome : spectrum of CREBBP mutations in Italian patients.
2006 A. Bentivegna, D. Milani, C. Gervasini, P. Castronovo, F. Mottadelli, S. Manzini, P. Colapietro, L. Giordano, F. Atzeri, M.T. Divizia, M.L. Giovannucci Uzielli, G.i. Neri, M.F. Bedeschi, F. Faravelli, A. Selicorni, L. Larizza
Serum tryptase levels in AML at diagnosis : a multicenter retrospective study
2006 R. Cairoli, C.B. Ripamonti, S. Granata, A. Beghini, P. Colapietro, G. Grillo, G. Nadali, A. Viola, C. Cattaneo, L. Intropido, E. Ravelli, G. Bertani, L. Pezzetti, M. Nichelatti, S. Veronese, A. Marocchi, G. Rossi, G. Pizzolo, F. Ferrara, A. Nosari, E. Morra
KIT mutations in core binding factor leukemias: outcome prediction and therapeutic implications
2006 R. Cairoli, A. Beghini, G. Grillo, G. Nadali, F. Elice, C.B. Ripamonti, P. Colapietro, M. Nichelatti, L. Pezzetti, A. Cuneo, A. Viola, C. Cattaneo, A. Rossi, F. Ferrara, C. Castagnola, M. Lazzarino, F. Rodeghiero, G. Pizzolo, L. Larizza, E. Morra
Molecular screening of PDGFRA and PDGFRB genes in KIT and FLT3 negative core binding factor leukemias
2007 R. Cairoli, A. Trojani, C.B. Ripamonti, S. Penco, A. Beghini, G.P. Nadali, F. Elice, A. Viola, C. Castagnola, P. Colapietro, G. Grillo, P. Pezzetti, E. Ravelli, A. Marocchi, M.C. Patrosso, A. Cuneo, F. Ferrara, F. Rodeghiero, M. Lazzarino, G. Pizzolo, E. Morra
Prevalence and prognostic impact of KIT mutations in acute myeloid leukaemia with inv(16). A retrospective study
2007 R. Cairoli, A. Beghini, C.B. Ripamonti, G. Grillo, G. Nadali, E. Di Bona, P. Colapietro, M. Nichelatti, G. Bertani, E. Ravelli, A. Cuneo, E. Ottaviani, P. Pioltelli, F. Ferrara, M. Lazzarino, G. Rossi, F. Rodeghiero, G. Pizzolo, G.N. Martinelli, E. Morraa
IMPACT OF KIT MUTATIONS IN ACUTE MYELOID LEUKAEMIA WITH INV(16)
2008 R.C. Cairoli, A. Beghini, C.B. Ripamonti, G. Grillo, G. Nadali, E. Di Bona, P. Colapietro, G.B. Bertani, E. Ravelli, G. Nador, C. Castagnola, C. Cattaneo, E. Ottaviani, P. Pioltelli, A. Viola, A. Cuneo, F. Ferrara, G. Martinelli, M. Lazzarino, G. Rossi, G. Pizzolo, E. Morra
Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorphism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation
2008 A. Trojani, C.B. Ripamonti, S. Penco, A. Beghini, G. Nadali, E. Di Bona, A. Viola, C. Castagnola, P. Colapietro, G. Grillo, L. Pezzetti, E. Ravelli, M.C. Patrosso, A. Marocchi, A. Cuneo, F. Ferrara, M. Lazzarino, G. Pizzolo, R. Cairoli, E. Morra
Altered H19 and SNAT2 expression in type 1 IUGR (Intrauterine Growth Restriction) placentas
2008 S. Tabano, C. Mandò, P. Colapietro, S. Zanutto, S. Calabrese, P. Pileri, V. Signorelli, M.R. Miozzo, I. Cetin
Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorfism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation
2008 A. Trojani, C.B. Ripamonti, S. Penco, A. Beghini, G.P. Nadali, E. Di Bona, A. Viola, C. Castagnola, P. Colapietro, G. Grillo, L. Pezzetti, E. Ravelli, M.C. Patrosso, A. Marocchi, A. Cuneo, F. Ferrara, M. Lazzarino, G. Pizzolo, R. Cairoli, E. Morra
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