Canlyniadau Chwilio - Pasquali, Francesco

Establishment and Study of Different Real-Time Polymerase Chain Reaction Assays for the Quantification of Cells with Deletions of Chromosome 7 gan Mattarucchi, Elia, Marsoni, Milena, Passi, Alberto, Lo Curto, Francesco, Pasquali, Francesco, Porta, Giovanni

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Molecular Monitoring of Residual Disease in Chronic Myeloid Leukemia by Genomic DNA Compared with Conventional mRNA Analysis gan Mattarucchi, Elia, Spinelli, Orietta, Rambaldi, Alessandro, Pasquali, Francesco, Lo Curto, Francesco, Campiotti, Leonardo, Porta, Giovanni

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells gan Valli, Roberto, Marletta, Cristina, Pressato, Barbara, Montalbano, Giuseppe, Lo Curto, Francesco, Pasquali, Francesco, Maserati, Emanuela

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms gan Valli, Roberto, Pressato, Barbara, Marletta, Cristina, Mare, Lydia, Montalbano, Giuseppe, Curto, Francesco Lo, Pasquali, Francesco, Maserati, Emanuela

Cael y testun llawn Cael y testun llawn Cael y testun llawn

OTX1 and OTX2 as Possible Molecular Markers of Sinonasal Carcinomas and Olfactory Neuroblastomas gan Pirrone, Cristina, Chiaravalli, Anna M., Marando, Alessandro, Conti, Andrea, Rainero, Alessia, Pistochini, Andrea, Curto, Francesco Lo, Pasquali, Francesco, Castelnuovo, Paolo, Capella, Carlo, Porta, Giovanni

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Sensing Optimum in the Raw: Leveraging the Raw-Data Imaging Capabilities of Raspberry Pi for Diagnostics Applications gan Tonelli, Alessandro, Mangia, Veronica, Candiani, Alessandro, Pasquali, Francesco, Mangiaracina, Tiziana Jessica, Grazioli, Alessandro, Sozzi, Michele, Gorni, Davide, Bussolati, Simona, Cucinotta, Annamaria, Basini, Giuseppina, Selleri, Stefano

Cael y testun llawn Cael y testun llawn Cael y testun llawn

The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes gan Marletta, Cristina, Valli, Roberto, Pressato, Barbara, Mare, Lydia, Montalbano, Giuseppe, Menna, Giuseppe, Loffredo, Giuseppe, Bernardo, Maria Ester, Vinti, Luciana, Ferrari, Simona, Di Cesare-Merlone, Alessandra, Zecca, Marco, Lo Curto, Francesco, Locatelli, Franco, Pasquali, Francesco, Maserati, Emanuela

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia gan Pagani, Ilaria S., Spinelli, Orietta, Mattarucchi, Elia, Pirrone, Cristina, Pigni, Diana, Amelotti, Elisabetta, Lilliu, Silvia, Boroni, Chiara, Intermesoli, Tamara, Giussani, Ursula, Caimi, Luigi, Bolda, Federica, Baffelli, Renata, Candi, Eleonora, Pasquali, Francesco, Lo Curto, Francesco, Lanfranchi, Arnalda, Porta, Fulvio, Rambaldi, Alessandro, Porta, Giovanni

Cael y testun llawn Cael y testun llawn

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 nor... gan Khan, Abdul Waheed, Minelli, Antonella, Frattini, Annalisa, Montalbano, Giuseppe, Bogni, Alessia, Fabbri, Marco, Porta, Giovanni, Acquati, Francesco, Pinto, Rita Maria, Bergami, Elena, Mura, Rossella, Pegoraro, Anna, Cesaro, Simone, Cipolli, Marco, Zecca, Marco, Danesino, Cesare, Locatelli, Franco, Maserati, Emanuela, Pasquali, Francesco, Valli, Roberto

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Association of unbalanced translocation der(1;7) with germline GATA2 mutations gan Kozyra, Emilia J., Göhring, Gudrun, Hickstein, Dennis D., Calvo, Katherine R., DiNardo, Courtney D., Dworzak, Michael, de Haas, Valerie, Starý, Jan, Hasle, Henrik, Shimamura, Akiko, Fleming, Mark D., Inaba, Hiroto, Lewis, Sara, Hsu, Amy P., Holland, Steven M., Arnold, Danielle E., Mecucci, Cristina, Keel, Siobán B., Bertuch, Alison A., Tawana, Kiran, Barzilai, Shlomit, Hirabayashi, Shinsuke, Onozawa, Masahiro, Lei, Shaohua, Alaiz, Helena, Andrikovics, Hajnalka, Betts, David, Beverloo, Berna H., Buechner, Jochen, Čermák, Martin, Cervera, José, Haus, Olga, Jahnukainen, Kirsi, Manola, Kalliopi N., Nebral, Karin, Pasquali, Francesco, Tchinda, Joelle, Turkiewicz, Dominik, Van Roy, Nadine, Zemanova, Zuzana, Pastor, Victor B., Strahm, Brigitte, Noellke, Peter, Niemeyer, Charlotte M., Schlegelberger, Brigitte, Yoshimi, Ayami, Wlodarski, Marcin W.

Cael y testun llawn Cael y testun llawn Cael y testun llawn