Search Results - "Curzi, Paola"

Cytotoxicity and Differentiating Effect of the Poly(ADP-Ribose) Polymerase Inhibitor Olaparib in Myelodysplastic Syndromes by Faraoni, Isabella, Consalvo, Maria Irno, Aloisio, Francesca, Fabiani, Emiliano, Giansanti, Manuela, Di Cristino, Francesca, Falconi, Giulia, Tentori, Lucio, Di Veroli, Ambra, Curzi, Paola, Maurillo, Luca, Niscola, Pasquale, Lo-Coco, Francesco, Graziani, Grazia, Voso, Maria Teresa

“…Myelodysplastic syndromes (MDS) are highly heterogeneous myeloid diseases, characterized by frequent genetic/chromosomal aberrations. Olaparib is a potent,…”
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Identification of a potential topoisomerase II “hotspot” DNA region in the DEK gene in two t(6;9)-positive therapy-related myeloid neoplasms by Piredda, Maria Liliana, Catalano, Gianfranco, Ciardi, Claudia, Divona, Mariadomenica, Cicconi, Laura, Panetta, Paola, Curzi, Paola, Garza, Eduardo, Martínez-Losada, Carmen, Postorino, Massimiliano, Lo-Coco, Francesco, Noguera, Nélida I.

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Rapid detection of nucleophosmin (NPM1) mutations in acute myeloid leukemia by denaturing HPLC by AMMATUNA, Emanuele, NOGUERA, Nèlida Inès, ZANGRILLI, Daniela, CURZI, Paola, PANETTA, Paola, BENCIVENGA, Paola, AMADORI, Sergio, FEDERICI, Giorgio, LO-COCO, Francesco

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Identification of a potential "hotspot" DNA region in the RUNX1 gene targeted by mitoxantrone in therapy-related acute myeloid leukemia with t(16;21) translocation by Ottone, Tiziana, Hasan, Syed Khizer, Montefusco, Enrico, Curzi, Paola, Mays, Ashley N., Chessa, Luciana, Ferrari, Antonella, Conte, Esmeralda, Noguera, Nelida Inés, Lavorgna, Serena, Ammatuna, Emanuele, Divona, Mariadomenica, Bovetti, Katia, Amadori, Sergio, Grimwade, David, Lo-Coco, Francesco

“…The translocation t(16;21) involving RUNX1 (AML1) and resulting in the RUNX1‐CBFA2T3 fusion is a rare but recurrent abnormality mostly found in therapy‐related…”
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Diagnostic refinement of chronic myeloproliferative disorders and thrombocytoses of unknown origin by multiple RT-PCR and capillary electrophoresis of BCR-ABL rearrangements and JAK2 (V617F) mutation by Ammatuna, Emanuele, Ottone, Tiziana, Zaza, Serena, Lavorgna, Serena, Grillo, Rosa, Curzi, Paola, Panetta, Paola, Federici, Giorgio, Amadori, Sergio, Lo-Coco, Francesco

“…Detection of genetic markers improves diagnostic refinement of chronic myeloproliferative disorders (CMDs) and is helpful in discriminating reactive conditions…”
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Simultaneous occurrence of BCR/ABL1 and RUNX1/RUNX1T1 in a case of therapy-related acute myeloid leukemia by Ammatuna, Emanuele, Divona, Mariadomenica, Curzi, Paola, Panetta, Paola, Zaza, Serena, Postorino, Massimiliano, Cantonetti, Maria, Amadori, Sergio, Lo Coco, Francesco

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Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia by Storlazzi, Clelia Tiziana, Anelli, Luisa, Surace, Cecilia, Lonoce, Angelo, Zagaria, Antonella, Nanni, Mauro, Curzi, Paola, Rocchi, Mariano

“…The “golden path”, produced by the Human Genome Project effort, is composed of a collection of overlapping and fully sequenced BAC/PAC clones covering almost…”
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