Sfoglia per Autore
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML
2018-01-01 Rainero, Alessia; Angaroni, Fabrizio; Conti, Andrea; Pirrone, Cristina; Micheloni, Giovanni; Tararà, Lucia; Millefanti, Giorgia; Maserati, Emanuela; Valli, Roberto; Spinelli, Orietta; Buklijas, Ksenija; Michelato, Anna; Casalone, Rosario; Barlassina, Cristina; Barcella, Matteo; Sirchia, Silvia; Piscitelli, Eleonora; Caccia, Massimo; Porta, Giovanni
NOVEL RECURRENT CHROMOSOMAL CHANGES AND GENE EXPRESSION RELATED TO CHROMOSOME ANOMALIES
2018-01-01 Valli, Roberto
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas
2019-01-01 Millefanti, G.; Conti, A.; Pirrone, C.; Marando, A.; Rainero, A.; Tararà, L.; Pistochini, A.; Lo Curto, F.; Pasquali, F.; Castelnuovo, P.; Acquati, F.; Grimaldi, A.; Valli, R.; Porta, G.; Micheloni, G.
Novel evidence of karyotype instability in Shwachman Diamond Syndrome
2019-01-01 Valli, Roberto; Khan, ABDUL WAHEED; Porta, Giovanni; Frattini, Annalisa; Montalbano, Giuseppe; Maserati, Emanuela; Pasquali, Francesco
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability
2019-01-01 Valli, Roberto; Minelli, Antonella; Galbiati, Marta; D'Amico, Giovanna; Frattini, Annalisa; Montalbano, Giuseppe; Khan, ABDUL WAHEED; Porta, Giovanni; Millefanti, Giorgia; Olivieri, Carla; Cipolli, Marco; Cesaro, Simone; Pasquali, Francesco; Danesino, Cesare; Cazzaniga, Gianni; Maserati, Emanuela
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow
2019-01-01 Valli, Roberto; Minelli, Antonella; Khan, ABDUL WAHEED; Frattini, Annalisa; Bogni, Alessia; Porta, Giovanni; Acquati, Francesco; Danesino, Cesare; Maserati, Emanuela; Pasquali, Francesco
A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling
2020-01-01 Roggiani, F; Riva, C; Raspagliesi, F; Porta, G; Valli, R; Taramelli, R; Acquati, F; Mezzanzanica, D; Tomassetti, A.
Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype
2020-01-01 Khan, A. W.; Minelli, A.; Frattini, A.; Montalbano, G.; Bogni, A.; Fabbri, M.; Porta, G.; Acquati, F.; Pinto, R. M.; Bergami, E.; Mura, R.; Pegoraro, A.; Cesaro, S.; Cipolli, M.; Zecca, M.; Danesino, C.; Locatelli, F.; Maserati, E.; Pasquali, F.; Valli, R.
Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells
2020-01-01 Marcozzi, Cristiana; Frattini, Annalisa; Borgese, Marina; Rossi, Federica; Barone, Ludovica; Solari, Eleonora; Valli, Roberto; Gornati, Rosalba
Chromosome missegregation in single human oocytes is related to the age and gene expression profile
2020-01-01 Barone, S.; Sarogni, P.; Valli, R.; Pallotta, M. M.; Silvia, G.; Frattini, A.; Khan, A. W.; Rapalini, E.; Parri, C.; Musio, A.
Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis
2020-01-01 Bistoletti, M; Micheloni, G; Baranzini, N; Bosi, A; Conti, A; Filpa, V; Pirrone, C; Millefanti, G; Moro, E; Grimaldi, A; Valli, R; Baj, A; Crema, F; Giaroni, C; Porta, G
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects
2021-01-01 Frattini, Annalisa; Bolamperti, Simona; Valli, Roberto; Cipolli, Marco; Pinto, Rita Maria; Bergami, Elena; Frau, Maria Rita; Cesaro, Simone; Signo, Michela; Bezzerri, Valentino; Porta, Giovanni; Khan, Abdul Waheed; Rubinacci, Alessandro; Villa, Isabella
Soybean meal-dependent intestinal inflammation induces different patterns of bone-loss in adult zebrafish scale
2021-01-01 Carnovali, M.; Valli, R.; Banfi, G.; Porta, G.; Mariotti, M.
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family
2021-01-01 Micheloni, Giovanni; Carnovali, Marta; Millefanti, Giorgia; Rizzetto, Manuel; Moretti, Vittoria; Montalbano, Giuseppe; Acquati, Francesco; Giaroni, Cristina; Valli, Roberto; Costantino, Lucy; Ferrara, Fulvio; Banfi, Giuseppe; Mariotti, Massimo; Porta, Giovanni
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations
2021-01-01 Khan, Abdul Waheed; Kennedy, Alyssa; Furutani, Elissa; Myers, Kasiani; Frattini, Annalisa; Acquati, Francesco; Roccia, Pamela; Micheloni, Giovanni; Minelli, Antonella; Porta, Giovanni; Cipolli, Marco; Cesaro, Simone; Danesino, Cesare; Pasquali, Francesco; Shimamura, Akiko; Valli, Roberto
Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia
2021-01-01 Azzolini, Claudio; Donati, Simone; Micheloni, Giovanni; Moretti, Vittoria; Valli, Roberto; Acquati, Francesco; Costantino, Lucy; Ferrara, Fulvio; Borroni, Davide; Premi, Elias; Testa, Francesco; Simonelli, Francesca; Porta, Giovanni
Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman–Diamond Syndrome
2022-01-01 Taha, I.; Foroni, S.; Valli, R.; Frattini, A.; Roccia, P.; Porta, G.; Zecca, M.; Bergami, E.; Cipolli, M.; Pasquali, F.; Danesino, C.; Scotti, C.; Minelli, A.
Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis
2022-01-01 Bruno, Antonino; Mortara, Lorenzo; Noonan, Douglas M.; Valli, Roberto; Porta, Giovanni; Taramelli, Roberto; Acquati, Francesco
Donor cell acute myeloid leukemia after hematopoietic stem cell transplantation for chronic granulomatous disease: a case report and literature review
2023-01-01 Micheloni, G.; Frattini, A.; Donini, M.; Dusi, S.; Leszl, A.; Di Meglio, A.; Pigazzi, M.; Musio, A.; Zecca, M.; Mina, T.; Rabusin, M.; Roccia, P.; Bernasconi, P.; Dambruoso, I.; Minelli, A.; Montalbano, G.; Acquati, F.; Porta, G.; Valli, R.; Pasquali, F.
The Potential Role of the T2 Ribonucleases in TME-Based Cancer Therapy
2023-01-01 Campomenosi, Paola; Bruno, Antonino; Mortara, Lorenzo; Bassani, Barbara; Valli, Roberto; Porta, Giovanni; Acquati, Francesco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML | 1-gen-2018 | Rainero, Alessia; Angaroni, Fabrizio; Conti, Andrea; Pirrone, Cristina; Micheloni, Giovanni; Tararà, Lucia; Millefanti, Giorgia; Maserati, Emanuela; Valli, Roberto; Spinelli, Orietta; Buklijas, Ksenija; Michelato, Anna; Casalone, Rosario; Barlassina, Cristina; Barcella, Matteo; Sirchia, Silvia; Piscitelli, Eleonora; Caccia, Massimo; Porta, Giovanni | |
| NOVEL RECURRENT CHROMOSOMAL CHANGES AND GENE EXPRESSION RELATED TO CHROMOSOME ANOMALIES | 1-gen-2018 | Valli, Roberto | |
| Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas | 1-gen-2019 | Millefanti, G.; Conti, A.; Pirrone, C.; Marando, A.; Rainero, A.; Tararà, L.; Pistochini, A.; Lo Curto, F.; Pasquali, F.; Castelnuovo, P.; Acquati, F.; Grimaldi, A.; Valli, R.; Porta, G.; Micheloni, G. | |
| Novel evidence of karyotype instability in Shwachman Diamond Syndrome | 1-gen-2019 | Valli, Roberto; Khan, ABDUL WAHEED; Porta, Giovanni; Frattini, Annalisa; Montalbano, Giuseppe; Maserati, Emanuela; Pasquali, Francesco | |
| Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability | 1-gen-2019 | Valli, Roberto; Minelli, Antonella; Galbiati, Marta; D'Amico, Giovanna; Frattini, Annalisa; Montalbano, Giuseppe; Khan, ABDUL WAHEED; Porta, Giovanni; Millefanti, Giorgia; Olivieri, Carla; Cipolli, Marco; Cesaro, Simone; Pasquali, Francesco; Danesino, Cesare; Cazzaniga, Gianni; Maserati, Emanuela | |
| Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow | 1-gen-2019 | Valli, Roberto; Minelli, Antonella; Khan, ABDUL WAHEED; Frattini, Annalisa; Bogni, Alessia; Porta, Giovanni; Acquati, Francesco; Danesino, Cesare; Maserati, Emanuela; Pasquali, Francesco | |
| A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling | 1-gen-2020 | Roggiani, F; Riva, C; Raspagliesi, F; Porta, G; Valli, R; Taramelli, R; Acquati, F; Mezzanzanica, D; Tomassetti, A. | |
| Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype | 1-gen-2020 | Khan, A. W.; Minelli, A.; Frattini, A.; Montalbano, G.; Bogni, A.; Fabbri, M.; Porta, G.; Acquati, F.; Pinto, R. M.; Bergami, E.; Mura, R.; Pegoraro, A.; Cesaro, S.; Cipolli, M.; Zecca, M.; Danesino, C.; Locatelli, F.; Maserati, E.; Pasquali, F.; Valli, R. | |
| Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells | 1-gen-2020 | Marcozzi, Cristiana; Frattini, Annalisa; Borgese, Marina; Rossi, Federica; Barone, Ludovica; Solari, Eleonora; Valli, Roberto; Gornati, Rosalba | |
| Chromosome missegregation in single human oocytes is related to the age and gene expression profile | 1-gen-2020 | Barone, S.; Sarogni, P.; Valli, R.; Pallotta, M. M.; Silvia, G.; Frattini, A.; Khan, A. W.; Rapalini, E.; Parri, C.; Musio, A. | |
| Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis | 1-gen-2020 | Bistoletti, M; Micheloni, G; Baranzini, N; Bosi, A; Conti, A; Filpa, V; Pirrone, C; Millefanti, G; Moro, E; Grimaldi, A; Valli, R; Baj, A; Crema, F; Giaroni, C; Porta, G | |
| Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects | 1-gen-2021 | Frattini, Annalisa; Bolamperti, Simona; Valli, Roberto; Cipolli, Marco; Pinto, Rita Maria; Bergami, Elena; Frau, Maria Rita; Cesaro, Simone; Signo, Michela; Bezzerri, Valentino; Porta, Giovanni; Khan, Abdul Waheed; Rubinacci, Alessandro; Villa, Isabella | |
| Soybean meal-dependent intestinal inflammation induces different patterns of bone-loss in adult zebrafish scale | 1-gen-2021 | Carnovali, M.; Valli, R.; Banfi, G.; Porta, G.; Mariotti, M. | |
| Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family | 1-gen-2021 | Micheloni, Giovanni; Carnovali, Marta; Millefanti, Giorgia; Rizzetto, Manuel; Moretti, Vittoria; Montalbano, Giuseppe; Acquati, Francesco; Giaroni, Cristina; Valli, Roberto; Costantino, Lucy; Ferrara, Fulvio; Banfi, Giuseppe; Mariotti, Massimo; Porta, Giovanni | |
| The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations | 1-gen-2021 | Khan, Abdul Waheed; Kennedy, Alyssa; Furutani, Elissa; Myers, Kasiani; Frattini, Annalisa; Acquati, Francesco; Roccia, Pamela; Micheloni, Giovanni; Minelli, Antonella; Porta, Giovanni; Cipolli, Marco; Cesaro, Simone; Danesino, Cesare; Pasquali, Francesco; Shimamura, Akiko; Valli, Roberto | |
| Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia | 1-gen-2021 | Azzolini, Claudio; Donati, Simone; Micheloni, Giovanni; Moretti, Vittoria; Valli, Roberto; Acquati, Francesco; Costantino, Lucy; Ferrara, Fulvio; Borroni, Davide; Premi, Elias; Testa, Francesco; Simonelli, Francesca; Porta, Giovanni | |
| Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman–Diamond Syndrome | 1-gen-2022 | Taha, I.; Foroni, S.; Valli, R.; Frattini, A.; Roccia, P.; Porta, G.; Zecca, M.; Bergami, E.; Cipolli, M.; Pasquali, F.; Danesino, C.; Scotti, C.; Minelli, A. | |
| Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis | 1-gen-2022 | Bruno, Antonino; Mortara, Lorenzo; Noonan, Douglas M.; Valli, Roberto; Porta, Giovanni; Taramelli, Roberto; Acquati, Francesco | |
| Donor cell acute myeloid leukemia after hematopoietic stem cell transplantation for chronic granulomatous disease: a case report and literature review | 1-gen-2023 | Micheloni, G.; Frattini, A.; Donini, M.; Dusi, S.; Leszl, A.; Di Meglio, A.; Pigazzi, M.; Musio, A.; Zecca, M.; Mina, T.; Rabusin, M.; Roccia, P.; Bernasconi, P.; Dambruoso, I.; Minelli, A.; Montalbano, G.; Acquati, F.; Porta, G.; Valli, R.; Pasquali, F. | |
| The Potential Role of the T2 Ribonucleases in TME-Based Cancer Therapy | 1-gen-2023 | Campomenosi, Paola; Bruno, Antonino; Mortara, Lorenzo; Bassani, Barbara; Valli, Roberto; Porta, Giovanni; Acquati, 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