Magliocca, Sara
Magliocca, Sara
Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.
2013 Esposito, T; Lea, Ra; Maher, Bh; Moses, D; Cox, Hc; Magliocca, S; Angius, A; Nyholt, Dr; Titus, T; Kay, T; Gray, Na; Rastaldi, Mp; Parnham, A; Gianfrancesco, F; Griffiths, Lr
A functional allelic variant of the FGF23 gene is associated with renal phospate leak in calcium nephrolithiasis.
2012 Rendina D; Esposito T; Mossetti G; De Filippo G; Gianfrancesco F; Perfetti A; Magliocca S; Formisano P; Prié D;Strazzullo P.
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease
2012 Gianfrancesco, F; Rendina, D; Di Stefano, M; Mingione, A; Esposito, T; Merlotti, D; Gallone, S; Magliocca, S; Goode, A; Formicola, D; Morello, G; Layfield, R; Frattini, A; De Filippo, G; Nuti, R; Searle, M; Strazzullo, P; Isaia, G; Mossetti, G; Gennari, L
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease.
2012 Gianfrancesco F; Rendina D; Di Stefano M; Mingione A; Esposito T; Merlotti D; Gallone S; Magliocca S; Goode A; Formicola D; Morello G; Layfield R; Frattini A; De Filippo G; Nuti R; Searle M; Strazzullo P; Isaia GC; Mossetti G; Gennari L.
A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease
2012 Gianfrancesco, F; Rendina, D; Di Stefano, M; Mingione, A; Esposito, T; Merlotti, D; Gallone, S; Magliocca, S; Goode, A; Formicola, D; Morello, G; Layfield, R; Frattini, A; De Filippo, G; Nuti, R; Searle, M; Strazzullo, P; Isaia, Gc; Mossetti, G; Gennari, L A
Ruolo della Melatonina nelle Patologie Metaboliche osee
2012 Gianfrancesco F; Magliocca S
The melatonin receptor 1a (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis
2012 Esposito T; Rendina D; Aloia A; Formicola D; Magliocca S; De Filippo G; Muscariello R; Mossetti G; Gianfrancesco F; Strazzullo P
piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene
2011 Esposito, T; Magliocca, S; Formicola, D; Gianfrancesco, F
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. | 1-gen-2013 | Esposito, T; Lea, Ra; Maher, Bh; Moses, D; Cox, Hc; Magliocca, S; Angius, A; Nyholt, Dr; Titus, T; Kay, T; Gray, Na; Rastaldi, Mp; Parnham, A; Gianfrancesco, F; Griffiths, Lr | |
| A functional allelic variant of the FGF23 gene is associated with renal phospate leak in calcium nephrolithiasis. | 1-gen-2012 | Rendina D; Esposito T; Mossetti G; De Filippo G; Gianfrancesco F; Perfetti A; Magliocca S; Formisano P; Prié D;Strazzullo P. | |
| A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease | 1-gen-2012 | Gianfrancesco, F; Rendina, D; Di Stefano, M; Mingione, A; Esposito, T; Merlotti, D; Gallone, S; Magliocca, S; Goode, A; Formicola, D; Morello, G; Layfield, R; Frattini, A; De Filippo, G; Nuti, R; Searle, M; Strazzullo, P; Isaia, G; Mossetti, G; Gennari, L | |
| A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. | 1-gen-2012 | Gianfrancesco F; Rendina D; Di Stefano M; Mingione A; Esposito T; Merlotti D; Gallone S; Magliocca S; Goode A; Formicola D; Morello G; Layfield R; Frattini A; De Filippo G; Nuti R; Searle M; Strazzullo P; Isaia GC; Mossetti G; Gennari L. | |
| A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease | 1-gen-2012 | Gianfrancesco, F; Rendina, D; Di Stefano, M; Mingione, A; Esposito, T; Merlotti, D; Gallone, S; Magliocca, S; Goode, A; Formicola, D; Morello, G; Layfield, R; Frattini, A; De Filippo, G; Nuti, R; Searle, M; Strazzullo, P; Isaia, Gc; Mossetti, G; Gennari, L A | |
| Ruolo della Melatonina nelle Patologie Metaboliche osee | 1-gen-2012 | Gianfrancesco F; Magliocca S | |
| The melatonin receptor 1a (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis | 1-gen-2012 | Esposito T; Rendina D; Aloia A; Formicola D; Magliocca S; De Filippo G; Muscariello R; Mossetti G; Gianfrancesco F; Strazzullo P | |
| piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene | 1-gen-2011 | Esposito, T; Magliocca, S; Formicola, D; Gianfrancesco, F |