نتائج البحث - Giacopuzzi, Edoardo
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Further Defining the Phenotypic Spectrum of B3GAT3 Mutations and Literature Review on Linkeropathy Syndromes حسب Ritelli, Marco, Cinquina, Valeria, Giacopuzzi, Edoardo, Venturini, Marina, Chiarelli, Nicola, Colombi, Marina
منشور في 2019نص -
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Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles حسب Magri, Chiara, Giacopuzzi, Edoardo, Sacco, Chiara, Bocchio-Chiavetto, Luisella, Minelli, Alessandra, Gennarelli, Massimo
منشور في 2021نص -
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Gallus gallus NEU3 sialidase as model to study protein evolution mechanism based on rapid evolving loops حسب Giacopuzzi, Edoardo, Barlati, Sergio, Preti, Augusto, Venerando, Bruno, Monti, Eugenio, Borsani, Giuseppe, Bresciani, Roberto
منشور في 2011نص -
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slc7a6os Gene Plays a Critical Role in Defined Areas of the Developing CNS in Zebrafish حسب Benini, Anna, Cignarella, Francesca, Calvarini, Laura, Mantovanelli, Silvia, Giacopuzzi, Edoardo, Zizioli, Daniela, Borsani, Giuseppe
منشور في 2015نص -
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Genome-wide analysis of consistently RNA edited sites in human blood reveals interactions with mRNA processing genes and suggests correlations with cell types and biological variab... حسب Giacopuzzi, Edoardo, Gennarelli, Massimo, Sacco, Chiara, Filippini, Alice, Mingardi, Jessica, Magri, Chiara, Barbon, Alessandro
منشور في 2018نص -
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In Silico Identification of New Putative Pathogenic Variants in the Neu1 Sialidase Gene Affecting Enzyme Function and Subcellular Localization حسب Bonardi, Dario, Ravasio, Viola, Borsani, Giuseppe, d'Azzo, Alessandra, Bresciani, Roberto, Monti, Eugenio, Giacopuzzi, Edoardo
منشور في 2014نص -
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Differential Enzymatic Activity of Rat ADAR2 Splicing Variants Is Due to Altered Capability to Interact with RNA in the Deaminase Domain حسب Filippini, Alice, Bonini, Daniela, Giacopuzzi, Edoardo, La Via, Luca, Gangemi, Fabrizio, Colombi, Marina, Barbon, Alessandro
منشور في 2018نص -
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Treatment-Resistant Schizophrenia: Genetic and Neuroimaging Correlates حسب Vita, Antonio, Minelli, Alessandra, Barlati, Stefano, Deste, Giacomo, Giacopuzzi, Edoardo, Valsecchi, Paolo, Turrina, Cesare, Gennarelli, Massimo
منشور في 2019نص -
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Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis حسب Salvi, Alessandro, Giacopuzzi, Edoardo, Bardellini, Elena, Amadori, Francesca, Ferrari, Lia, De Petro, Giuseppina, Borsani, Giuseppe, Majorana, Alessandra
منشور في 2016نص -
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Whole Blood Transcriptome Characterization of 3xTg-AD Mouse and Its Modulation by Transcranial Direct Current Stimulation (tDCS) حسب Magri, Chiara, Vitali, Erika, Cocco, Sara, Giacopuzzi, Edoardo, Rinaudo, Marco, Martini, Paolo, Barbon, Alessandro, Grassi, Claudio, Gennarelli, Massimo
منشور في 2021نص -
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Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways حسب Giacopuzzi, Edoardo, Gennarelli, Massimo, Minelli, Alessandra, Gardella, Rita, Valsecchi, Paolo, Traversa, Michele, Bonvicini, Cristian, Vita, Antonio, Sacchetti, Emilio, Magri, Chiara
منشور في 2017نص -
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Estrogen-Like Effect of Mitotane Explained by Its Agonist Activity on Estrogen Receptor-α حسب Rossini, Elisa, Giacopuzzi, Edoardo, Gangemi, Fabrizio, Tamburello, Mariangela, Cosentini, Deborah, Abate, Andrea, Laganà, Marta, Berruti, Alfredo, Grisanti, Salvatore, Sigala, Sandra
منشور في 2021نص -
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The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing حسب Stevenson, Mark, Pagnamenta, Alistair T, Mack, Heather G, Savige, Judith, Giacopuzzi, Edoardo, Lines, Kate E, Taylor, Jenny C, Thakker, Rajesh V
منشور في 2022نص -
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A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme حسب Magri, Chiara, Giacopuzzi, Edoardo, La Via, Luca, Bonini, Daniela, Ravasio, Viola, Elhussiny, Mohammed E. A., Orizio, Flavia, Gangemi, Fabrizio, Valsecchi, Paolo, Bresciani, Roberto, Barbon, Alessandro, Vita, Antonio, Gennarelli, Massimo
منشور في 2018نص -
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Author Correction: A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme حسب Magri, Chiara, Giacopuzzi, Edoardo, La Via, Luca, Bonini, Daniela, Ravasio, Viola, Elhussiny, Mohammed E. A., Orizio, Flavia, Gangemi, Fabrizio, Valsecchi, Paolo, Bresciani, Roberto, Barbon, Alessandro, Vita, Antonio, Gennarelli, Massimo
منشور في 2020نص