Dualistic Role of BARD1 in Cancer

por Cimmino, Flora, Formicola, Daniela, Capasso, Mario
Publicado 2017

piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene

por Esposito, Teresa, Magliocca, Sara, Formicola, Daniela, Gianfrancesco, Fernando
Publicado 2011

Kinome multigenic panel identified novel druggable EPHB4‐V871I somatic variant in high‐risk neuroblastoma

por Andolfo, Immacolata, Lasorsa, Vito A., Manna, Francesco, Rosato, Barbara E., Formicola, Daniela, Iolascon, Achille, Capasso, Mario
Publicado 2020

CFDP1 is a neuroblastoma susceptibility gene that regulates transcription factors of the noradrenergic cell identity

por Formicola, Daniela, Lasorsa, Vito Alessandro, Cantalupo, Sueva, Testori, Alessandro, Cardinale, Antonella, Avitabile, Marianna, Diskin, Sharon, Iolascon, Achille, Capasso, Mario
Publicado 2022

Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility

por Formicola, Daniela, Aloia, Andrea, Sampaolo, Simone, Farina, Olimpia, Diodato, Daria, Griffiths, Lyn R, Gianfrancesco, Fernando, Di Iorio, Giuseppe, Esposito, Teresa
Publicado 2010

Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy

por Esposito, Teresa, Sampaolo, Simone, Limongelli, Giuseppe, Varone, Antonio, Formicola, Daniela, Diodato, Daria, Farina, Olimpia, Napolitano, Filomena, Pacileo, Giuseppe, Gianfrancesco, Fernando, Di Iorio, Giuseppe
Publicado 2013

The functional variant rs34330 of CDKN1B is associated with risk of neuroblastoma

por Capasso, Mario, McDaniel, Lee D., Cimmino, Flora, Cirino, Andrea, Formicola, Daniela, Russell, Mike R., Raman, Pichai, Cole, Kristina A., Diskin, Sharon J.
Publicado 2017

An 18 gene expression-based score classifier predicts the clinical outcome in stage 4 neuroblastoma

por Formicola, Daniela, Petrosino, Giuseppe, Lasorsa, Vito Alessandro, Pignataro, Piero, Cimmino, Flora, Vetrella, Simona, Longo, Luca, Tonini, Gian Paolo, Oberthuer, André, Iolascon, Achille, Fischer, Matthias, Capasso, Mario
Publicado 2016

Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship

por Sampaolo, Simone, Esposito, Teresa, Farina, Olimpia, Formicola, Daniela, Diodato, Daria, Gianfrancesco, Fernando, Cipullo, Federica, Cremone, Gaetana, Cirillo, Mario, Del Viscovo, Luca, Toscano, Antonio, Angelini, Corrado, Di Iorio, Giuseppe
Publicado 2013

ZNF687 Mutations in Severe Paget Disease of Bone Associated with Giant Cell Tumor

por Divisato, Giuseppina, Formicola, Daniela, Esposito, Teresa, Merlotti, Daniela, Pazzaglia, Laura, Del Fattore, Andrea, Siris, Ethel, Orcel, Philippe, Brown, Jacques P., Nuti, Ranuccio, Strazzullo, Pasquale, Benassi, Maria Serena, Cancela, M. Leonor, Michou, Laetitia, Rendina, Domenico, Gennari, Luigi, Gianfrancesco, Fernando
Publicado 2016

Exome and deep sequencing of clinically aggressive neuroblastoma reveal somatic mutations that affect key pathways involved in cancer progression

por Lasorsa, Vito Alessandro, Formicola, Daniela, Pignataro, Piero, Cimmino, Flora, Calabrese, Francesco Maria, Mora, Jaume, Esposito, Maria Rosaria, Pantile, Marcella, Zanon, Carlo, De Mariano, Marilena, Longo, Luca, Hogarty, Michael D., de Torres, Carmen, Tonini, Gian Paolo, Iolascon, Achille, Capasso, Mario
Publicado 2016