FRATTINI, ANNALISA
FRATTINI, ANNALISA
Istituto di Ricerca Genetica e Biomedica - IRGB
Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman-Diamond syndrome cells
2024 Cipolli, M; Boni, C; Penzo, M; Villa, I; Bolamperti, S; Baldisseri, E; Frattini, A; Porta, G; Api, M; Selicato, N; Roccia, P; Pollutri, D; Marinelli Busilacchi, E; Poloni, A; Caporelli, N; D'Amico, G; Pegoraro, A; Cesaro, S; Oyarbide, U; Vella, A; Lippi, G; Corey, Sj; Valli, R; Polini, A; Bezzerri, V
The synergism of SMC1A cohesin gene silencing and bevacizumab against colorectal cancer
2024 Di Nardo, Maddalena; Astigiano, Simonetta; Baldari, Silvia; Pallotta, Maria Michela; Porta, Giovanni; Pigozzi, Simona; Antonini, Annalisa; Emionite, Laura; Frattini, Annalisa; Valli, Roberto; Toietta, Gabriele; Soddu, Silvia; Musio, Antonio
Donor cell Acute Myeloid Leukemia after hematopoietic stem cell transplantation for Chronic Granulomatous Disease: a case report and literature review
2023 Micheloni, Giovanni; Frattini, Annalisa; Donini, Marta; Dusi, Stefano; Leszl, Anna; Di Meglio, Annamaria; Pigazzi, Martina; Musio, Antonio; Zecca, Marco; Mina, Tommaso; Rabusin, Marco; Roccia, Pamela; Bernasconi, Paolo; Dambruoso, Irene; Minelli, Antonella; Montalbano, Giuseppe; Acquati, Francesco; Porta, Giovanni; Valli, Roberto; Pasquali, Francesco
Occurrence of L1M Elements in Chromosomal Rearrangements Associated to Chronic Myeloid Leukemia (CML): Insights from Patient-Specific Breakpoints Characterization
2023 Alberto L'Abbate ; Vittoria Moretti ; Ester Pungolino ; Giovanni Micheloni ; Roberto Valli ; Annalisa Frattini ; Matteo Barcella ; Francesco Acquati ; Rolland A Reinbold ; Lucy Costantino ; Fulvio Ferrara ; Alessandra Trojani ; Mario Ventura ; Giovanni Porta ; Roberto Cairoli
Case report: heterozygous germline variant in EIF6 additional to biallelic SBDS pathogenic variants in a patient with ribosomopathy Shwachman-Diamond syndrome
2022 Taha, Ibrahim; Foroni, Selena; Valli, Roberto; Frattini, Annalisa; Roccia, Pamela; Porta, Giovanni; Zecca, Marco; Bergami, Elena; Cipolli, Marco; Pasquali, Francesco; Danesino, Cesare; Scotti, Claudia; Minelli, Antonella
Enhanced p53 levels are involved in the reduced mineralization capacity of osteoblasts derived from Shwachman-Diamond syndrome subjects
2021 Frattini, Annalisa; Bolamperti, Simona; Valli, Roberto; Cipolli, Marco; Maria Pinto, Rita; Bergami, Elena; Rita Frau, Maria; Cesaro, Simone; Signo, Michela; Bezzerri, Valentino; Porta, Giovanni; Waheed Khan, Abdul; Rubinacci, Alessandro; Villa, Isabella
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations.
2021 Abdul Waheed Khan ; Alyssa Kennedy ; Elissa Furutani ; Kasiani Myers ; Annalisa Frattini ; ; Francesco Acquati ; ; Pamela Roccia ; Giovanni Micheloni ; Antonella Minelli ; Giovanni Porta ; ; Marco Cipolli ; Simone Cesaro ; Cesare Danesino ; Francesco Pasquali ; Akiko Shimamura ; Roberto Valli ;
Chromosome Missegregation in Single Human Oocytes Is Related to the Age and Gene Expression Profile
2020 Barone, Stefano; Sarogni, Patrizia; Valli, Roberto; Pallotta Maria, Michela; Silvia, Gazzi; Frattini, Annalisa; Khan Abdul, Waheed; Rapalini, Erika; Parri, Cristiana; Musio, Antonio
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 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 Marcozzi C; Frattini A; Borgese M; Rossi F; Barone L; Solari E; Valli R; Gornati R.
SDS with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability
2019 Valli, Roberto; Minelli, Antonella; Galbiati, Marta; D'Amico, Giovanna; Frattini, Annalisa; Montalbano, Giuseppe; Khan Abdul, W; Porta, Giovanni; Millefanti, Giorgia; Olivieri, Carla; Cipolli, Marco; Cesaro, Simone; Pasquali, Francesco; Danesino, Cesare; Cazzaniga, Gianni; Maserati, Emanuela
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene
2018 Valli, R; Vinti, L; Frattini, A; Fabbri, M; Montalbano, G; Olivieri, C; Minelli, A; Locatelli, F; Pasquali, F; Maserati, E
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro
2018 Scaldaferri, Debora; Bosi, Annalisa; Fabbri, Marco; Pedrini, Edoardo; Inforzato, Antonio; Valli, Roberto; Frattini, Annalisa; De Vito, Annarosaria; Noonan Douglas, M; Taramelli, Roberto; Mortara, Lorenzo; Acquati, Francesco
Toxicogenomics applied to in vitro Cell Transformation Assay reveals mechanisms of early response to cadmium
2018 Giulia, Callegaro; Matilde, Forcella; Pasquale, Melchioretto; Annalisa, Frattini; Laura, Gribaldo; Paola, Fusi; Marco, Fabbri; Chiara, Urani
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome
2017 Valli, Roberto; De Paoli, Elena; Nacci, Lucia; Frattini, Annalisa; Pasquali, Francesco; Maserati, Emanuela
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis
2017 Valli, R; Frattini, A; Minelli, A
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature
2015 Valli R.; De Bernardi F.; Frattini A.; Volpi L.; Bignami M.; Facchetti F.; Pasquali F.; Castelnuovo P.; Maserati E.
High variability of genomic instability and gene expression profiling in different HeLa clones
2015 Frattini A.; Fabbri M.; Valli R.; De Paoli E.; Montalbano G.; Gribaldo L.; Pasquali F.; Maserati E.
SMC1B is present in mammalian somatic cells and interacts with mitotic cohesin proteins.
2015 Mannini L; Cucco F; Quarantotti V; Amato C; Tinti M; Tana L; Frattini A; Delia D; Krantz ID; Jessberger R; Musio A.
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease.
2012 Gianfrancesco F; Rendina D; Di Stefano M; Mingione A; Esposito T; Merlotti D; Gallone S; Magliocca S; Goode A; Formicola D; Morello G; Layfield R; Frattini A; De Filippo G; Nuti R; Searle M; Strazzullo P; Isaia GC; Mossetti G; Gennari L.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman-Diamond syndrome cells | 1-gen-2024 | Cipolli, M; Boni, C; Penzo, M; Villa, I; Bolamperti, S; Baldisseri, E; Frattini, A; Porta, G; Api, M; Selicato, N; Roccia, P; Pollutri, D; Marinelli Busilacchi, E; Poloni, A; Caporelli, N; D'Amico, G; Pegoraro, A; Cesaro, S; Oyarbide, U; Vella, A; Lippi, G; Corey, Sj; Valli, R; Polini, A; Bezzerri, V | |
| The synergism of SMC1A cohesin gene silencing and bevacizumab against colorectal cancer | 1-gen-2024 | Di Nardo, Maddalena; Astigiano, Simonetta; Baldari, Silvia; Pallotta, Maria Michela; Porta, Giovanni; Pigozzi, Simona; Antonini, Annalisa; Emionite, Laura; Frattini, Annalisa; Valli, Roberto; Toietta, Gabriele; Soddu, Silvia; Musio, Antonio | |
| Donor cell Acute Myeloid Leukemia after hematopoietic stem cell transplantation for Chronic Granulomatous Disease: a case report and literature review | 1-gen-2023 | Micheloni, Giovanni; Frattini, Annalisa; Donini, Marta; Dusi, Stefano; Leszl, Anna; Di Meglio, Annamaria; Pigazzi, Martina; Musio, Antonio; Zecca, Marco; Mina, Tommaso; Rabusin, Marco; Roccia, Pamela; Bernasconi, Paolo; Dambruoso, Irene; Minelli, Antonella; Montalbano, Giuseppe; Acquati, Francesco; Porta, Giovanni; Valli, Roberto; Pasquali, Francesco | |
| Occurrence of L1M Elements in Chromosomal Rearrangements Associated to Chronic Myeloid Leukemia (CML): Insights from Patient-Specific Breakpoints Characterization | 1-gen-2023 | Alberto L'Abbate ; Vittoria Moretti ; Ester Pungolino ; Giovanni Micheloni ; Roberto Valli ; Annalisa Frattini ; Matteo Barcella ; Francesco Acquati ; Rolland A Reinbold ; Lucy Costantino ; Fulvio Ferrara ; Alessandra Trojani ; Mario Ventura ; Giovanni Porta ; Roberto Cairoli | |
| 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, Ibrahim; Foroni, Selena; Valli, Roberto; Frattini, Annalisa; Roccia, Pamela; Porta, Giovanni; Zecca, Marco; Bergami, Elena; Cipolli, Marco; Pasquali, Francesco; Danesino, Cesare; Scotti, Claudia; Minelli, Antonella | |
| 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; Maria Pinto, Rita; Bergami, Elena; Rita Frau, Maria; Cesaro, Simone; Signo, Michela; Bezzerri, Valentino; Porta, Giovanni; Waheed Khan, Abdul; Rubinacci, Alessandro; Villa, Isabella | |
| 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 | Abdul Waheed Khan ; Alyssa Kennedy ; Elissa Furutani ; Kasiani Myers ; Annalisa Frattini ; ; Francesco Acquati ; ; Pamela Roccia ; Giovanni Micheloni ; Antonella Minelli ; Giovanni Porta ; ; Marco Cipolli ; Simone Cesaro ; Cesare Danesino ; Francesco Pasquali ; Akiko Shimamura ; Roberto Valli ; | |
| Chromosome Missegregation in Single Human Oocytes Is Related to the Age and Gene Expression Profile | 1-gen-2020 | Barone, Stefano; Sarogni, Patrizia; Valli, Roberto; Pallotta Maria, Michela; Silvia, Gazzi; Frattini, Annalisa; Khan Abdul, Waheed; Rapalini, Erika; Parri, Cristiana; Musio, Antonio | |
| 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 C; Frattini A; Borgese M; Rossi F; Barone L; Solari E; Valli R; Gornati R. | |
| SDS 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, W; Porta, Giovanni; Millefanti, Giorgia; Olivieri, Carla; Cipolli, Marco; Cesaro, Simone; Pasquali, Francesco; Danesino, Cesare; Cazzaniga, Gianni; Maserati, Emanuela | |
| Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene | 1-gen-2018 | Valli, R; Vinti, L; Frattini, A; Fabbri, M; Montalbano, G; Olivieri, C; Minelli, A; Locatelli, F; Pasquali, F; Maserati, E | |
| The human RNASET2 protein affects the polarization pattern of human macrophages in vitro | 1-gen-2018 | Scaldaferri, Debora; Bosi, Annalisa; Fabbri, Marco; Pedrini, Edoardo; Inforzato, Antonio; Valli, Roberto; Frattini, Annalisa; De Vito, Annarosaria; Noonan Douglas, M; Taramelli, Roberto; Mortara, Lorenzo; Acquati, Francesco | |
| Toxicogenomics applied to in vitro Cell Transformation Assay reveals mechanisms of early response to cadmium | 1-gen-2018 | Giulia, Callegaro; Matilde, Forcella; Pasquale, Melchioretto; Annalisa, Frattini; Laura, Gribaldo; Paola, Fusi; Marco, Fabbri; Chiara, Urani | |
| Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome | 1-gen-2017 | Valli, Roberto; De Paoli, Elena; Nacci, Lucia; Frattini, Annalisa; Pasquali, Francesco; Maserati, Emanuela | |
| Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis | 1-gen-2017 | Valli, R; Frattini, A; Minelli, A | |
| Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature | 1-gen-2015 | Valli R.; De Bernardi F.; Frattini A.; Volpi L.; Bignami M.; Facchetti F.; Pasquali F.; Castelnuovo P.; Maserati E. | |
| High variability of genomic instability and gene expression profiling in different HeLa clones | 1-gen-2015 | Frattini A.; Fabbri M.; Valli R.; De Paoli E.; Montalbano G.; Gribaldo L.; Pasquali F.; Maserati E. | |
| SMC1B is present in mammalian somatic cells and interacts with mitotic cohesin proteins. | 1-gen-2015 | Mannini L; Cucco F; Quarantotti V; Amato C; Tinti M; Tana L; Frattini A; Delia D; Krantz ID; Jessberger R; Musio A. | |
| A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. | 1-gen-2012 | Gianfrancesco F; Rendina D; Di Stefano M; Mingione A; Esposito T; Merlotti D; Gallone S; Magliocca S; Goode A; Formicola D; Morello G; Layfield R; Frattini A; De Filippo G; Nuti R; Searle M; Strazzullo P; Isaia GC; Mossetti G; Gennari L. |