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

بواسطة Mosso, Cristina, Russo, Silvia
الحاوية / القاعدة 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

بواسطة Roccato, Michele, Cavazza, Nicoletta, Colloca, Pasquale, Russo, Silvia
الحاوية / القاعدة Soc Sci Q (2020)

The Lasting Effects of the COVID‐19 Pandemic on Support for Anti‐Democratic Political Systems: A Six‐Month Longitudinal Study

بواسطة Roccato, Michele, Russo, Silvia, Colloca, Pasquale, Cavazza, Nicoletta
الحاوية / القاعدة Soc Sci Q (2021)

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

بواسطة Russo, Nunzio, Franzì, Enrico, Capilli, Gianfranco, Patané, Anella Antonietta, Russo, Silvia Paola, Evola, Rosario
الحاوية / القاعدة Case Rep Cardiol (2014)

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

بواسطة Masciadri, Maura, Ficcadenti, Anna, Milani, Donatella, Cogliati, Francesca, Divizia, Maria Teresa, Larizza, Lidia, Russo, Silvia
الحاوية / القاعدة Front Neurol (2018)

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

بواسطة Catusi, Ilaria, Bonati, Maria Teresa, Mainini, Ester, Russo, Silvia, Orlandini, Eleonora, Larizza, Lidia, Recalcati, Maria Paola
الحاوية / القاعدة Int J Mol Sci (2020)

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

بواسطة De Rasmo, Domenico, Ferretta, Anna, Russo, Silvia, Ruggieri, Maddalena, Lasorella, Piergiorgio, Paolicelli, Damiano, Trojano, Maria, Signorile, Anna
الحاوية / القاعدة Biomedicines (2020)

Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndrome

بواسطة Crippa, Milena, Rusconi, Daniela, Castronovo, Chiara, Bestetti, Ilaria, Russo, Silvia, Cereda, Anna, Selicorni, Angelo, Larizza, Lidia, Finelli, Palma
الحاوية / القاعدة Mol Cytogenet (2015)

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

بواسطة D'Apice, Maria Rosaria, Gambardella, Stefano, Bengala, Mario, Russo, Silvia, Nardone, Anna Maria, Lucidi, Vincenzina, Sangiuolo, Federica, Novelli, Giuseppe
منشور في 2004

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

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

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

بواسطة Monk, David, Morales, Joannella, den Dunnen, Johan T., Russo, Silvia, Court, Franck, Prawitt, Dirk, Eggermann, Thomas, Beygo, Jasmin, Buiting, Karin, Tümer, Zeynep
الحاوية / القاعدة Epigenetics (2018)

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

بواسطة Guzzetti, Sara, Calzari, Luciano, Buccarello, Lucia, Cesari, Valentina, Toschi, Ivan, Cattaldo, Stefania, Mauro, Alessandro, Pregnolato, Francesca, Mazzola, Silvia Michela, Russo, Silvia
الحاوية / القاعدة Int J Mol Sci (2018)

Mitochondrial Dynamics of Proximal Tubular Epithelial Cells in Nephropathic Cystinosis

بواسطة De Rasmo, Domenico, Signorile, Anna, De Leo, Ester, Polishchuk, Elena V., Ferretta, Anna, Raso, Roberto, Russo, Silvia, Polishchuk, Roman, Emma, Francesco, Bellomo, Francesco
الحاوية / القاعدة Int J Mol Sci (2019)

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

بواسطة Calzari, Luciano, Barcella, Matteo, Alari, Valentina, Braga, Daniele, Muñoz-Viana, Rafael, Barlassina, Cristina, Finelli, Palma, Gervasini, Cristina, Barco, Angel, Russo, Silvia, Larizza, Lidia
الحاوية / القاعدة Mol Neurobiol (2020)

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

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

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

بواسطة 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
منشور في 2013

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

بواسطة 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
منشور في 2012

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

بواسطة 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
الحاوية / القاعدة 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

بواسطة 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
الحاوية / القاعدة Clin Epigenetics (2020)

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

بواسطة 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
الحاوية / القاعدة Front Genet (2018)