KHAN, ABDUL WAHEED
KHAN, ABDUL WAHEED
DIPARTIMENTO DI BIOTECNOLOGIE E SCIENZE DELLA VITA (DBSV)
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.
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
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
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.
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: a multidisciplinary approach to better understand the pathogenesis and clinical implications
2021-01-01 Khan, ABDUL WAHEED
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
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
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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. | |
| 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 | |
| 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 | |
| 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. | |
| 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: a multidisciplinary approach to better understand the pathogenesis and clinical implications | 1-gen-2021 | Khan, ABDUL WAHEED | |
| 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 | |
| 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 |