Finding the way to Wilms tumor by comparing the primary and relapse tumor samples

por Spreafico, Filippo, Ciceri, Sara, Perotti, Daniela
Publicado 2022

Chromosomal anomalies at 1q, 3, 16q, and mutations of SIX1 and DROSHA genes underlie Wilms tumor recurrences

por Spreafico, Filippo, Ciceri, Sara, Gamba, Beatrice, Torri, Federica, Terenziani, Monica, Collini, Paola, Macciardi, Fabio, Radice, Paolo, Perotti, Daniela
Publicado 2016

Gene expression-based dissection of inter-histotypes, intra-histotype and intra-tumor heterogeneity in pediatric tumors

por Ciceri, Sara, Carenzo, Andrea, Iannó, Maria Federica, Bertolotti, Alessia, Morosi, Carlo, Luksch, Roberto, Spreafico, Filippo, Collini, Paola, Radice, Paolo, Massimino, Maura, De Cecco, Loris, Perotti, Daniela
Publicado 2022

Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors

por Roversi, Gaia, Picinelli, Chiara, Bestetti, Ilaria, Crippa, Milena, Perotti, Daniela, Ciceri, Sara, Saccheri, Fabiana, Collini, Paola, Poliani, Pietro L., Catania, Serena, Peissel, Bernard, Pagni, Fabio, Russo, Silvia, Peterlongo, Paolo, Manoukian, Siranoush, Finelli, Palma
Publicado 2015

Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of CHEK2 in Wilms tumour susceptibility

por Ciceri, Sara, Gamba, Beatrice, Corbetta, Paola, Mondini, Patrizia, Terenziani, Monica, Catania, Serena, Nantron, Marilina, Bianchi, Maurizio, D’Angelo, Paolo, Torri, Federica, Macciardi, Fabio, Collini, Paola, Di Martino, Martina, Melchionda, Fraia, Di Cataldo, Andrea, Spreafico, Filippo, Radice, Paolo, Perotti, Daniela
Publicado 2018