Sfoglia per Rivista GENES, CHROMOSOMES & CANCER
Analysis of t(15;17) chromosomal breakpoint sequences in therapy-related versus de novo acute promyelocytic leukemia: association of DNA breaks with specific DNA motifs at PML and RARA loci.
2010-01-01 Hasan, Sk; Ottone, T; Schlenk, Rf; Xiao, Y; Wiemels, Jl; Mitra, Me; Bernasconi, Paolo; Di Raimondo, F; Stanghellini, Mt; Marco, P; Mays, An; Döhner, H; Sanz, Ma; Amadori, S; Grimwade, D; Lo Coco, F.
Complementary molecular approaches reveal heterogeneous CDH1 germline defects in Italian patients with hereditary diffuse gastric cancer (HDGC) syndrome.
2014-01-01 Molinaro, V; Pensotti, V; Marabelli, M; Feroce, I; Barile, M; Pozzi, S; Laghi, L; Serrano, D; Bernard, L; Bonanni, B; Ranzani, Gn.
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic and molecular data on three cases
1996-01-01 Seghezzi, L; Maserati, E; Minelli, Antonella; Dellavecchia, C; Adis, P; Locatelli, Franco; Angioni, A; Balloni, P; Miano, C; Cavalli, P; Danesino, Cesare; Pasquali, Francesco
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic and moleculardata on three cases
1996-01-01 Seghezzi, L.; Maserati, E.; Minelli, A.; Dellavecchia, C.; Addis, P.; Locatelli, Franco; Angioni, A.; Balloni, P.; Miano, C.; Cavalli, P.; Danesino, Cesare; Pasquali, F.
Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies
2004-01-01 Minelli, Antonella; Maserati, E.; Rossi, G.; Bernardo, M. E.; DE STEFANO, P.; Cecchini, M. P.; Valli, R.; Albano, V.; Pierani, P.; Leszl, A.; Sainati, L.; LO CURTO, Francesco; Danesino, Cesare; Locatelli, Franco; Pasquali, Francesco
Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase
1990-01-01 Minelli, Antonella; Piantanida, M; Maserati, E; Campagnoli, E; Pasquali, Francesco; Danesino, Cesare
Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes
1997-01-01 Pensotti, V; Radice, P; Presciuttini, S; Calistri, D; Gazzoli, I; Grimalt Perez, A; Mondini, P; Buonsanti, G; Sala, P; Rossetti, C; Ranzani, Guglielmina; Bertario, L; Pierotti, Ma
A novel APC promoter 1B deletion shows a founder effect in Italian patients with classical familial adenomatous polyposis phenotype
2017-01-01 Marabelli, Monica; Gismondi, Viviana; Ricci, Maria Teresa; Vetro, Annalisa; ABOU KHOUZAM, Raefa; Rea, Valentina; Vitellaro, Marco; Zuffardi, Orsetta; Varesco, Liliana; Ranzani, Guglielmina
Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene
2017-01-01 Nacci, Lucia; Valli, Roberto; Maria Pinto, Rita; Zecca, Marco; Cipolli, Marco; Morini, Jacopo; Cesaro, Simone; Boveri, Emanuela; Rosti, Vittorio; Corti, Paola; Ambroni, Maura; Pasquali, Francesco; Danesino, Cesare; Maserati, Emanuela; Minelli, Antonella
Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
2006-01-01 Maserati, E.; Minelli, Antonella; Pressato, B.; Valli, R.; Crescenzi, B.; Stefanelli, M.; Menna, G.; Sainati, L.; Poli, F.; Panarello, C.; Zecca, M.; Lo Curto F., Mecucci C.; Danesino, Cesare; Pasquali, F.
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases
2002-01-01 Maserati, E.; Aprili, F.; Vinante, F.; Locatelli, Franco; Amendola, G.; Zatterale, A.; Milone, G.; Minelli, Antonella; Bernardi, F.; LO CURTO, F.; Pasquali, F.
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases.
2002-01-01 Maserati, E; Aprili, F; Vignante, F; Locatelli, Franco; Amendola, G; Zatterale, A; Milione, G; Minelli, Antonella; Bernardi, F; LO CURTO, Francesco; Pasquali, Francesco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Analysis of t(15;17) chromosomal breakpoint sequences in therapy-related versus de novo acute promyelocytic leukemia: association of DNA breaks with specific DNA motifs at PML and RARA loci. | 1-gen-2010 | Hasan, Sk; Ottone, T; Schlenk, Rf; Xiao, Y; Wiemels, Jl; Mitra, Me; Bernasconi, Paolo; Di Raimondo, F; Stanghellini, Mt; Marco, P; Mays, An; Döhner, H; Sanz, Ma; Amadori, S; Grimwade, D; Lo Coco, F. | |
| Complementary molecular approaches reveal heterogeneous CDH1 germline defects in Italian patients with hereditary diffuse gastric cancer (HDGC) syndrome. | 1-gen-2014 | Molinaro, V; Pensotti, V; Marabelli, M; Feroce, I; Barile, M; Pozzi, S; Laghi, L; Serrano, D; Bernard, L; Bonanni, B; Ranzani, Gn. | |
| Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic and molecular data on three cases | 1-gen-1996 | Seghezzi, L; Maserati, E; Minelli, Antonella; Dellavecchia, C; Adis, P; Locatelli, Franco; Angioni, A; Balloni, P; Miano, C; Cavalli, P; Danesino, Cesare; Pasquali, Francesco | |
| Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic and moleculardata on three cases | 1-gen-1996 | Seghezzi, L.; Maserati, E.; Minelli, A.; Dellavecchia, C.; Addis, P.; Locatelli, Franco; Angioni, A.; Balloni, P.; Miano, C.; Cavalli, P.; Danesino, Cesare; Pasquali, F. | |
| Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies | 1-gen-2004 | Minelli, Antonella; Maserati, E.; Rossi, G.; Bernardo, M. E.; DE STEFANO, P.; Cecchini, M. P.; Valli, R.; Albano, V.; Pierani, P.; Leszl, A.; Sainati, L.; LO CURTO, Francesco; Danesino, Cesare; Locatelli, Franco; Pasquali, Francesco | |
| Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase | 1-gen-1990 | Minelli, Antonella; Piantanida, M; Maserati, E; Campagnoli, E; Pasquali, Francesco; Danesino, Cesare | |
| Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes | 1-gen-1997 | Pensotti, V; Radice, P; Presciuttini, S; Calistri, D; Gazzoli, I; Grimalt Perez, A; Mondini, P; Buonsanti, G; Sala, P; Rossetti, C; Ranzani, Guglielmina; Bertario, L; Pierotti, Ma | |
| A novel APC promoter 1B deletion shows a founder effect in Italian patients with classical familial adenomatous polyposis phenotype | 1-gen-2017 | Marabelli, Monica; Gismondi, Viviana; Ricci, Maria Teresa; Vetro, Annalisa; ABOU KHOUZAM, Raefa; Rea, Valentina; Vitellaro, Marco; Zuffardi, Orsetta; Varesco, Liliana; Ranzani, Guglielmina | |
| Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene | 1-gen-2017 | Nacci, Lucia; Valli, Roberto; Maria Pinto, Rita; Zecca, Marco; Cipolli, Marco; Morini, Jacopo; Cesaro, Simone; Boveri, Emanuela; Rosti, Vittorio; Corti, Paola; Ambroni, Maura; Pasquali, Francesco; Danesino, Cesare; Maserati, Emanuela; Minelli, Antonella | |
| Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies. | 1-gen-2006 | Maserati, E.; Minelli, Antonella; Pressato, B.; Valli, R.; Crescenzi, B.; Stefanelli, M.; Menna, G.; Sainati, L.; Poli, F.; Panarello, C.; Zecca, M.; Lo Curto F., Mecucci C.; Danesino, Cesare; Pasquali, F. | |
| Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases | 1-gen-2002 | Maserati, E.; Aprili, F.; Vinante, F.; Locatelli, Franco; Amendola, G.; Zatterale, A.; Milone, G.; Minelli, Antonella; Bernardi, F.; LO CURTO, F.; Pasquali, F. | |
| Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases. | 1-gen-2002 | Maserati, E; Aprili, F; Vignante, F; Locatelli, Franco; Amendola, G; Zatterale, A; Milione, G; Minelli, Antonella; Bernardi, F; LO CURTO, Francesco; Pasquali, Francesco |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile