The Perception of Instability and Legitimacy of Status Differences Enhances the Infrahumanization Bias among High Status Groups

Por Mosso, Cristina, Russo, Silvia
Publicado no Eur J Psychol (2019)

A Democratic Emergency After a Health Emergency? Exposure to COVID‐19, Perceived Economic Threat and Support for Anti‐Democratic Political Systems

Por Roccato, Michele, Cavazza, Nicoletta, Colloca, Pasquale, Russo, Silvia
Publicado no Soc Sci Q (2020)

The Drop That Spilled the Cup: Acute Myocardial Infarction in a Young Woman with Underlying Thrombophilic Polymorphisms and Oral Contraceptive Use

Por Russo, Nunzio, Franzì, Enrico, Capilli, Gianfranco, Patané, Anella Antonietta, Russo, Silvia Paola, Evola, Rosario
Publicado no Case Rep Cardiol (2014)

Recurrence and Familial Inheritance of Intronic NIPBL Pathogenic Variant Associated With Mild CdLS

Por Masciadri, Maura, Ficcadenti, Anna, Milani, Donatella, Cogliati, Francesca, Divizia, Maria Teresa, Larizza, Lidia, Russo, Silvia
Publicado no Front Neurol (2018)

Recombinant Chromosome 7 Driven by Maternal Chromosome 7 Pericentric Inversion in a Girl with Features of Silver-Russell Syndrome

Por Catusi, Ilaria, Bonati, Maria Teresa, Mainini, Ester, Russo, Silvia, Orlandini, Eleonora, Larizza, Lidia, Recalcati, Maria Paola
Publicado no Int J Mol Sci (2020)

PBMC of Multiple Sclerosis Patients Show Deregulation of OPA1 Processing Associated with Increased ROS and PHB2 Protein Levels

Por De Rasmo, Domenico, Ferretta, Anna, Russo, Silvia, Ruggieri, Maddalena, Lasorella, Piergiorgio, Paolicelli, Damiano, Trojano, Maria, Signorile, Anna
Publicado no Biomedicines (2020)

Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndrome

Por Crippa, Milena, Rusconi, Daniela, Castronovo, Chiara, Bestetti, Ilaria, Russo, Silvia, Cereda, Anna, Selicorni, Angelo, Larizza, Lidia, Finelli, Palma
Publicado no Mol Cytogenet (2015)

Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy

Por D'Apice, Maria Rosaria, Gambardella, Stefano, Bengala, Mario, Russo, Silvia, Nardone, Anna Maria, Lucidi, Vincenzina, Sangiuolo, Federica, Novelli, Giuseppe
Publicado em 2004

The Steady-State Serum Concentration of Genistein Aglycone Is Affected by Formulation: A Bioequivalence Study of Bone Products

Por Bitto, Alessandra, Burnett, Bruce P., Polito, Francesca, Russo, Silvia, D'Anna, Rosario, Pillai, Lakshmi, Squadrito, Francesco, Altavilla, Domenica, Levy, Robert M.
Publicado em 2013

Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains

Por Monk, David, Morales, Joannella, den Dunnen, Johan T., Russo, Silvia, Court, Franck, Prawitt, Dirk, Eggermann, Thomas, Beygo, Jasmin, Buiting, Karin, Tümer, Zeynep
Publicado no Epigenetics (2018)

Taurine Administration Recovers Motor and Learning Deficits in an Angelman Syndrome Mouse Model

Por Guzzetti, Sara, Calzari, Luciano, Buccarello, Lucia, Cesari, Valentina, Toschi, Ivan, Cattaldo, Stefania, Mauro, Alessandro, Pregnolato, Francesca, Mazzola, Silvia Michela, Russo, Silvia
Publicado no Int J Mol Sci (2018)

Mitochondrial Dynamics of Proximal Tubular Epithelial Cells in Nephropathic Cystinosis

Por De Rasmo, Domenico, Signorile, Anna, De Leo, Ester, Polishchuk, Elena V., Ferretta, Anna, Raso, Roberto, Russo, Silvia, Polishchuk, Roman, Emma, Francesco, Bellomo, Francesco
Publicado no Int J Mol Sci (2019)

Transcriptome Analysis of iPSC-Derived Neurons from Rubinstein-Taybi Patients Reveals Deficits in Neuronal Differentiation

Por Calzari, Luciano, Barcella, Matteo, Alari, Valentina, Braga, Daniele, Muñoz-Viana, Rafael, Barlassina, Cristina, Finelli, Palma, Gervasini, Cristina, Barco, Angel, Russo, Silvia, Larizza, Lidia
Publicado no Mol Neurobiol (2020)

Overall and allele-specific expression of the SMC1A gene in female Cornelia de Lange syndrome patients and healthy controls

Por Parenti, Ilaria, Rovina, Davide, Masciadri, Maura, Cereda, Anna, Azzollini, Jacopo, Picinelli, Chiara, Limongelli, Giuseppe, Finelli, Palma, Selicorni, Angelo, Russo, Silvia, Gervasini, Cristina, Larizza, Lidia
Publicado em 2014

Genomic imbalances in patients with a clinical presentation in the spectrum of Cornelia de Lange syndrome

Por Gervasini, Cristina, Picinelli, Chiara, Azzollini, Jacopo, Rusconi, Daniela, Masciadri, Maura, Cereda, Anna, Marzocchi, Cinzia, Zampino, Giuseppe, Selicorni, Angelo, Tenconi, Romano, Russo, Silvia, Larizza, Lidia, Finelli, Palma
Publicado em 2013

Intragenic and large NIPBL rearrangements revealed by MLPA in Cornelia de Lange patients

Por Russo, Silvia, Masciadri, Maura, Gervasini, Cristina, Azzollini, Jacopo, Cereda, Anna, Zampino, Giuseppe, Haas, Oskar, Scarano, Gioacchino, Di Rocco, Maja, Finelli, Palma, Tenconi, Romano, Selicorni, Angelo, Larizza, Lidia
Publicado em 2012

A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation

Por Demond, Hannah, Anvar, Zahra, Jahromi, Bahia Namavar, Sparago, Angela, Verma, Ankit, Davari, Maryam, Calzari, Luciano, Russo, Silvia, Jahromi, Mojgan Akbarzadeh, Monk, David, Andrews, Simon, Riccio, Andrea, Kelsey, Gavin
Publicado no Genome Med (2019)

Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance

Por Cubellis, Maria Vittoria, Pignata, Laura, Verma, Ankit, Sparago, Angela, Del Prete, Rosita, Monticelli, Maria, Calzari, Luciano, Antona, Vincenzo, Melis, Daniela, Tenconi, Romano, Russo, Silvia, Cerrato, Flavia, Riccio, Andrea
Publicado no Clin Epigenetics (2020)

Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features

Por Cirello, Valentina, Giorgini, Valentina, Castronovo, Chiara, Marelli, Susan, Mainini, Ester, Sironi, Alessandra, Recalcati, Maria Paola, Pessina, Marco, Giardino, Daniela, Larizza, Lidia, Persani, Luca, Finelli, Palma, Russo, Silvia, Fugazzola, Laura
Publicado no Front Genet (2018)

Genetic investigations on 8 patients affected by ring 20 chromosome syndrome

Por Giardino, Daniela, Vignoli, Aglaia, Ballarati, Lucia, Recalcati, Maria Paola, Russo, Silvia, Camporeale, Nicole, Marchi, Margherita, Finelli, Palma, Accorsi, Patrizia, Giordano, Lucio, La Briola, Francesca, Chiesa, Valentina, Canevini, Maria Paola, Larizza, Lidia
Publicado em 2010