La Carpia, Francesca
La Carpia, Francesca
Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura
2018 Milillo, A; Molinario, C; Costanzi, S; Vischini, G; La Carpia, F; La Greca, F; Rigante, D; Gambaro, G; Gurrieri, F; Sangiorgi, E.
Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects.
2016 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
Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects.
2016 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
A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy.
2015 Sangiorgi, Eugenio; Gurrieri, Fiorella; Milillo, Annamaria; La Carpia, Francesca; Costanzi, Stefano; Martini, Maurizio; Larocca, Luigi Maria; Vischini, Gisella
T cell repertoire in DQ5-positive MuSK-positive myasthenia gravis patients
2014 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
PTPN22 and myasthenia gravis: replication in an Italian population and meta-analysis of literature data
2012 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
| 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 |