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

The Osteoclast Traces the Route to Bone Tumors and Metastases

por Russo, Sharon, Scotto di Carlo, Federica, Gianfrancesco, Fernando
Publicado 2022

The identification of H3F3A mutation in giant cell tumour of the clivus and the histological diagnostic algorithm of other clival lesions permit the differential diagnosis in this...

por Scotto di Carlo, Federica, Divisato, Giuseppina, Iacoangeli, Maurizio, Esposito, Teresa, Gianfrancesco, Fernando
Publicado 2018

Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN

por De Filippo, Gianpaolo, Rendina, Domenico, Rocco, Vincenzo, Esposito, Teresa, Gianfrancesco, Fernando, Strazzullo, Pasquale
Publicado 2013

Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility

por Fernandez, Francesca, Esposito, Teresa, Lea, Rod A, Colson, Natalie J, Ciccodicola, Alfredo, Gianfrancesco, Fernando, Griffiths, Lyn R
Publicado 2008

Modulation of Endocannabinoid Tone in Osteoblastic Differentiation of MC3T3-E1 Cells and in Mouse Bone Tissue over Time

por Kostrzewa, Magdalena, Mahmoud, Ali Mokhtar, Verde, Roberta, Scotto di Carlo, Federica, Gianfrancesco, Fernando, Piscitelli, Fabiana, Ligresti, Alessia
Publicado 2021

A mutation in the ZNF687 gene that is responsible for the severe form of Paget’s disease of bone causes severely altered bone remodeling and promotes hepatocellular carcinoma onset...

por Russo, Sharon, Scotto di Carlo, Federica, Maurizi, Antonio, Fortunato, Giorgio, Teti, Anna, Licastro, Danilo, Settembre, Carmine, Mello, Tommaso, Gianfrancesco, Fernando
Publicado 2023

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

DDX11L: a novel transcript family emerging from human subtelomeric regions

por Costa, Valerio, Casamassimi, Amelia, Roberto, Roberta, Gianfrancesco, Fernando, Matarazzo, Maria R, D'Urso, Michele, D'Esposito, Maurizio, Rocchi, Mariano, Ciccodicola, Alfredo
Publicado 2009

The distinct clinical features of giant cell tumor of bone in pagetic and non-pagetic patients are associated with genetic, biochemical and histological differences

por Divisato, Giuseppina, di Carlo, Federica Scotto, Pazzaglia, Laura, Rizzo, Riccardo, Coviello, Domenico A., Benassi, Maria Serena, Picci, Piero, Esposito, Teresa, Gianfrancesco, Fernando
Publicado 2017

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

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

Profilin 1 deficiency drives mitotic defects and reduces genome stability

por Scotto di Carlo, Federica, Russo, Sharon, Muyas, Francesc, Mangini, Maria, Garribba, Lorenza, Pazzaglia, Laura, Genesio, Rita, Biamonte, Flavia, De Luca, Anna Chiara, Santaguida, Stefano, Scotlandi, Katia, Cortés-Ciriano, Isidro, Gianfrancesco, Fernando
Publicado 2023

Paget disease of bone-associated UBA domain mutations of SQSTM1 exert distinct effects on protein structure and function

por Goode, Alice, Long, Jed E., Shaw, Barry, Ralston, Stuart H., Visconti, Micaela Rios, Gianfrancesco, Fernando, Esposito, Teresa, Gennari, Luigi, Merlotti, Daniela, Rendina, Domenico, Rea, Sarah L., Sultana, Melanie, Searle, Mark S., Layfield, Robert
Publicado 2014

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

Identification of sixteen novel candidate genes for late onset Parkinson’s disease

por Gialluisi, Alessandro, Reccia, Mafalda Giovanna, Modugno, Nicola, Nutile, Teresa, Lombardi, Alessia, Di Giovannantonio, Luca Giovanni, Pietracupa, Sara, Ruggiero, Daniela, Scala, Simona, Gambardella, Stefano, Iacoviello, Licia, Gianfrancesco, Fernando, Acampora, Dario, D’Esposito, Maurizio, Simeone, Antonio, Ciullo, Marina, Esposito, Teresa
Publicado 2021