DAZZO, EMANUELA

DAZZO, EMANUELA  

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Risultati 1 - 9 di 9 (tempo di esecuzione: 0.009 secondi).
Titolo Data di pubblicazione Autore(i) Rivista Serie Titolo libro
Selection of multipotent cells and enhanced muscle reconstruction by myogenic macrophage-secreted factors. 2009 MALERBA, ALBERTOVITIELLO, LIBEROSEGAT, DANIELADAZZO, EMANUELADE COPPI, PAOLOBOLDRIN, LUISAROMUALDI, CHIARABARONI, MAURIZIO DAVID + EXPERIMENTAL CELL RESEARCH - -
Analisi di parametri della proliferazione e del differenziamento cellulare in due modelli post-infiammatori: Metaplasia di Barrett e Rigenerazione muscolare. 2009 Dazzo, Emanuela - - -
Pericentriolar material analyses in normal esophageal mucosa, Barrett's metaplasia and adenocarcinoma 2010 SEGAT, DANIELADAZZO, EMANUELACAVALLINI, LUCIAROMUALDI, CHIARASALVADOR RVITIELLO, LIBEROFASSAN, MATTEORUGGE, MASSIMOZANINOTTO, GIOVANNIANCONA, ERMANNOBARONI, MAURIZIO DAVID + HISTOLOGY AND HISTOPATHOLOGY - -
Study of the molecular pathogenesis of arrhythmogenic cardiomyopathy due to Desmoglein-2 mutations: the zebrafish helps the mouse 2012 BEFFAGNA, GIORGIALORENZON, ALESSANDRAMILANETTO, MARTINAGRUMATI, PAOLODAZZO, EMANUELAMORO, ENRICOARGENTON, FRANCESCOBONALDO, PAOLOBRAGHETTA, PAOLARAMPAZZO, ALESSANDRA + CELL AND TISSUE RESEARCH - -
Mutations in the area composita protein alphaT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy 2013 CALORE, MARTINABAUCE, BARBARADAZZO, EMANUELAMAZZOTTI, ELISADE BORTOLI, MARZIALORENZON, ALESSANDRABEFFAGNA, GIORGIARIGATO, ILARIAZAGLIA, TANIACORRADO, DOMENICOBASSO, CRISTINATHIENE, GAETANODALIENTO, LUCIANONAVA, ANDREARAMPAZZO, ALESSANDRA + EUROPEAN HEART JOURNAL - -
Autosomal dominant lateral temporal epilepsy (ADLTE): Novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras 2015 DAZZO, EMANUELACONTI, SARADE BORTOLI, MARZIAROSA, MAURIZIOMILLINO, CATERINAPACCHIONI, BENIAMINA + EPILEPSY RESEARCH - -
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy 2015 DAZZO, EMANUELAMINERVINI, GIOVANNILUISI, CONCETTACHIAVEGATO, ANGELATOSATTO, SILVIO + AMERICAN JOURNAL OF HUMAN GENETICS - -
CNTNAP2 mutations and autosomal dominant epilepsy with auditory features 2018 Leonardi, EmanuelaDazzo, EmanuelaASPROMONTE, MARIA CRISTINATabaro, FrancescoPASCARELLI, STEFANOTosatto, Silvio C. E.Murgia, Alessandra + EPILEPSY RESEARCH - -
A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signaling and miRNA dysregulation. 2019 Calore MartinaLorenzon AlessandraVitiello LiberoPoloni GiuliaBeffagna GiorgiaDazzo EmanuelaSACCHETTO, CLAUDIABonaldo PaoloBraghetta PaolaRampazzo Alessandra + CARDIOVASCULAR RESEARCH - -