MANNA, FRANCESCO
MANNA, FRANCESCO
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Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway
2020 Andolfo, I.; Rosato, B. E.; Manna, F.; De Rosa, G.; Marra, R.; Gambale, A.; Girelli, D.; Russo, R.; Iolascon, A.
Rap-011 rescues the disease phenotype in a cellular model of congenital dyserythropoietic anemia type ii by inhibiting the smad2-3 pathway
2020 De Rosa, G.; Andolfo, I.; Marra, R.; Manna, F.; Rosato, B. E.; Iolascon, A.; Russo, R.
Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene
2020 Russo, R.; Marra, R.; Andolfo, I.; Manna, F.; De Rosa, G.; Rosato, B. E.; Radhakrishnan, K.; Fahey, M.; Iolascon, A.
Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locus
2020 Andolfo, I.; Martone, S.; Ribersani, M.; Bianchi, S.; Manna, F.; Genesio, R.; Gambale, A.; Pignataro, P.; Testi, A. M.; Iolascon, A.; Russo, R.
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway | 1.1 Articolo in rivista | 2020 | Andolfo, I.; Rosato, B. E.; Manna, F.; De Rosa, G.; Marra, R.; Gambale, A.; Girelli, D.; Russo, R.; Iolascon, A. | |
| Rap-011 rescues the disease phenotype in a cellular model of congenital dyserythropoietic anemia type ii by inhibiting the smad2-3 pathway | 1.1 Articolo in rivista | 2020 | De Rosa, G.; Andolfo, I.; Marra, R.; Manna, F.; Rosato, B. E.; Iolascon, A.; Russo, R. | |
| Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene | 1.1 Articolo in rivista | 2020 | Russo, R.; Marra, R.; Andolfo, I.; Manna, F.; De Rosa, G.; Rosato, B. E.; Radhakrishnan, K.; Fahey, M.; Iolascon, A. | |
| Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locus | 1.1 Articolo in rivista | 2020 | Andolfo, I.; Martone, S.; Ribersani, M.; Bianchi, S.; Manna, F.; Genesio, R.; Gambale, A.; Pignataro, P.; Testi, A. M.; Iolascon, A.; Russo, R. |