La Carpia, Francesca

La Carpia, Francesca  

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Data di pubblicazione Titolo Autore(i) File
1-gen-2018 Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura Milillo, A; Molinario, C; Costanzi, S; Vischini, G; La Carpia, F; La Greca, F; Rigante, D; Gambaro, G; Gurrieri, F; Sangiorgi, E.
1-gen-2016 Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects. La Carpia, Francesca; Rendeli, Claudia; Molinario, Clelia; Milillo, Annamaria; Farroni, C; Cannelli, Natalia; Ausili, Emanuele; Paolucci, V; Neri, Giovanni; Romagnoli, Costantino; Sangiorgi, Eugenio; Gurrieri, Fiorella
1-gen-2016 Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects. La Carpia, Francesca; Rendeli, Claudia; Molinario, Clelia; Milillo, Annamaria; Farroni, C.; Cannelli, Natalia; Ausili, Emanuele; Paolucci, V.; Neri, Giovanni; Romagnoli, Costantino; Sangiorgi, Eugenio; Gurrieri, Fiorella
1-gen-2015 A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy. Sangiorgi, Eugenio; Gurrieri, Fiorella; Milillo, Annamaria; La Carpia, Francesca; Costanzi, Stefano; Martini, Maurizio; Larocca, Luigi Maria; Vischini, Gisella
1-gen-2014 T cell repertoire in DQ5-positive MuSK-positive myasthenia gravis patients Marino, Mariapaola; Maiuri, Mt; Di Sante, Gabriele; Scuderi, Flavia; La Carpia, Francesca; Trakas, N; Provenzano, Carlo; Zisimopoulou, P; Ria, Francesco; Tzartos, Sj; Evoli, Amelia; Bartoccioni, Emanuela
1-gen-2012 PTPN22 and myasthenia gravis: replication in an Italian population and meta-analysis of literature data Provenzano, Carlo; Ricciardi, R; Scuderi, Flavia; Maiuri, Mt; Maestri, M; La Carpia, Francesca; Sferrazza, Antonella; Marino, Mariapaola; Leone, Lucia; Lucchi, M; Mussi, A; Zollino, Marcella; Evoli, Amelia; Bartoccioni, Emanuela