ANDOLFO, IMMACOLATA
ANDOLFO, IMMACOLATA
DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE
MicroRNAs and Cancer Stem Cells in Medulloblastoma
2011 Zollo, Massimo; Andolfo, Immacolata; DE ANTONELLIS, Pasqualino
Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: Definition of clinical and molecular spectrum and identification of new diagnostic scores
2014 Russo, Roberta; Antonella, Gambale; Concetta, Langella; Andolfo, Immacolata; Sule, Unal; Iolascon, Achille
Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma.
2011 Andolfo, I; Petrosino, Giuseppe; Vecchione, L; De Antonellis, P; Capasso, Mario; Montanaro, D; Gemei, M; Troncone, Giancarlo; Iolascon, Achille; Orditura, M; Ciardiello, F; De Vita, F; Zollo, Massimo
Correlation of NM23-H1 cytoplasmic expressionwith metastatic stage in human prostate cancer tissue
2011 Andolfo, Immacolata; Daniela De Martino, ; Lucia, Liguori; Giuseppe, Petrosino; Troncone, Giancarlo; Nicoletta, Tata; Alessia, Galasso; Cristin, Roma; Francesco, Chiancone; Zarrilli, Stefano; Gianluigi, Arrigoni; Staibano, Stefania; Imbimbo, Ciro; Zollo, Massimo
The metallophosphodiesterase Mpped2 impairs tumorigenesis in neuroblastoma.
2012 Liguori, L; Andolfo, I; De Antonellis, P; Aglio, V; di Dato, V; Marino, N; Ivan Orlotti, N; De Martino, D; Capasso, Mario; Petrosino, G; Schramm, A; Navas, Luigi; Paolo Tonini, G; Eggert, A; Iolascon, Achille; Zollo, Massimo
Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP+ as Parkinson's disease cellular model
2013 Asci, R; Vallefuoco, F; Andolfo, Immacolata; Bruno, M; DE FALCO, Luigia; Iolascon, Achille
Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells.
2010 Andolfo, I; De Falco, L; Asci, R; Russo, Roberta; Colucci, S; Gorrese, M; Zollo, Massimo; Iolascon, Achille
Rapid Cl-/HCOFormula exchange kinetics of AE1 in HEK293 cells and hereditary stomatocytosis red blood cells
2013 Frumence, E; Genetet, S; Ripoche, P; Iolascon, Achille; Andolfo, Immacolata; Le Van Kim, C; Colin, Y; Mouro Chanteloup, I; Lopez, C.
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
2013 Andolfo, I; Alper, Sl; De Franceschi, L; Auriemma, C; Russo, Roberta; De Falco, L; Vallefuoco, F; Esposito, Mr; Vandorpe, Dh; Shmukler, Be; Narayan, R; Montanaro, D; D'Armiento, Maria; Vetro, A; Limongelli, I; Zuffardi, O; Glader, Be; Schrier, Sl; Brugnara, C; Stewart, Gw; Delaunay, J; Iolascon, Achille
The micro-RNA 199b-5p regulatory circuit involves Hes1, CD15, and epigenetic modifications in medulloblastoma.
2012 Andolfo, I; Liguori, L; De Antonellis, P; Cusanelli, E; Marinaro, F; Pistollato, F; Garzia, L; De Vita, G; Petrosino, Giuseppe; Accordi, B; Migliorati, R; Basso, G; Iolascon, Achille; Cinalli, G; Zollo, Massimo
Chromosome 9q and 16q loss identified by genome-wide pooled-analysis are associated with tumor aggressiveness in patients with classic medulloblastoma.
2011 Coco, S; Valdora, F; Bonassi, S; Scaruffi, P; Stigliani, S; Oberthuer, A; Berthold, F; Andolfo, I; Servidei, T; Riccardi, R; Basso, E; Iolascon, Achille; Tonini, G. P.
Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia
2013 Andolfo, I; Alper, Sl; Delaunay, J; Auriemma, C; Russo, Roberta; Asci, R; Esposito, Mr; Sharma, Ak; Shmukler, Be; Brugnara, C; De Franceschi, L; Iolascon, Achille
Hereditary xerocytosis revisited
2014 Archer, Natasha M.; Shmukler, Boris E.; Andolfo, Immacolata; Vandorpe, David H.; Radhakrishnan, Gnanasambandam; Higgins, John M.; Alicia, Rivera; Fleming, Mark D.; Frederick, Sachs; Gottlieb, Philip A.; Iolascon, Achille; Carlo, Brugnara; Alper, Seth L.; Nathan, David G.
Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene.
2012 DE FALCO, Luigia; Bruno, M; Andolfo, Immacolata; David, Bp; Girelli, D; Noce, Fd; Camaschella, C; Iolascon, Achille
Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d inerythroid cells.
2010 Andolfo, I; De Falco, L; Asci, R; Russo, R; Colucci, S; Gorrese, M; Zollo, Massimo; Iolascon, Achille
MiR-34a Targeting of Notch Ligand Delta-Like 1 ImpairsCD15+/CD133+ Tumor-Propagating Cells and SupportsNeural Differentiation in
2011 de Antonellis, P.; Medaglia, C.; Cusanelli, E.; Andolfo, I.; Liguori, L.; DE VITA, Gennaro; Carotenuto, M.; Bello, A.; Formiggini, F.; Galeone, Aldo; DE ROSA, Giuseppe; Virgilio, Antonella; Scognamiglio, I.; Sciro, M.; Basso, G.; Schulte, J. H.; Cinalli, G.; Iolascon, Achille; Zollo, Massimo
Diagnosis and management of congenital dyserythropoietic anemias
2016 Gambale, Antonella; Iolascon, Achille; Andolfo, Immacolata; Russo, Roberta
Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia
2016 Andolfo, Immacolata; Russo, Roberta; Manna, Francesco; De Rosa, Gianluca; Gambale, Antonella; Zouwail, Soha; Detta, Nicola; Pardo, Catia Lo; Alper, Seth L; Brugnara, Carlo; Sharma, Alok K; De Franceschi, Lucia; Iolascon, Achille
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)
2015 Andolfo, Immacolata; Russo, Roberta; Manna, Francesco; Shmukler, Boris E; Gambale, Antonella; Vitiello, Giuseppina; DE ROSA, Gianluca; Brugnara, Carlo; Alper, Seth L; Snyder, L. Michael; Iolascon, Achille
SOCS3 and IRS-1 gene expression differs between genotype 1 and genotype 2 hepatitis C virus-infected HepG2 cells.
2009 Persico, M.; Russo, Roberta; Persico, E.; Svelto, M.; Spano, D.; Andolfo, I.; La Mura, V.; Capasso, Mario; Tiribelli, C.; Torella, R.; Iolascon, Achille
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| MicroRNAs and Cancer Stem Cells in Medulloblastoma | 2.1 Contributo in volume (Capitolo o Saggio) | 2011 | Zollo, Massimo; Andolfo, Immacolata; DE ANTONELLIS, Pasqualino | |
| Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: Definition of clinical and molecular spectrum and identification of new diagnostic scores | 1.1 Articolo in rivista | 2014 | Russo, Roberta; Antonella, Gambale; Concetta, Langella; Andolfo, Immacolata; Sule, Unal; Iolascon, Achille | |
| Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma. | 1.1 Articolo in rivista | 2011 | Andolfo, I; Petrosino, Giuseppe; Vecchione, L; De Antonellis, P; Capasso, Mario; Montanaro, D; Gemei, M; Troncone, Giancarlo; Iolascon, Achille; Orditura, M; Ciardiello, F; De Vita, F; Zollo, Massimo | |
| Correlation of NM23-H1 cytoplasmic expressionwith metastatic stage in human prostate cancer tissue | 1.1 Articolo in rivista | 2011 | Andolfo, Immacolata; Daniela De Martino, ; Lucia, Liguori; Giuseppe, Petrosino; Troncone, Giancarlo; Nicoletta, Tata; Alessia, Galasso; Cristin, Roma; Francesco, Chiancone; Zarrilli, Stefano; Gianluigi, Arrigoni; Staibano, Stefania; Imbimbo, Ciro; Zollo, Massimo | |
| The metallophosphodiesterase Mpped2 impairs tumorigenesis in neuroblastoma. | 1.1 Articolo in rivista | 2012 | Liguori, L; Andolfo, I; De Antonellis, P; Aglio, V; di Dato, V; Marino, N; Ivan Orlotti, N; De Martino, D; Capasso, Mario; Petrosino, G; Schramm, A; Navas, Luigi; Paolo Tonini, G; Eggert, A; Iolascon, Achille; Zollo, Massimo | |
| Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP+ as Parkinson's disease cellular model | 1.1 Articolo in rivista | 2013 | Asci, R; Vallefuoco, F; Andolfo, Immacolata; Bruno, M; DE FALCO, Luigia; Iolascon, Achille | |
| Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells. | 1.1 Articolo in rivista | 2010 | Andolfo, I; De Falco, L; Asci, R; Russo, Roberta; Colucci, S; Gorrese, M; Zollo, Massimo; Iolascon, Achille | |
| Rapid Cl-/HCOFormula exchange kinetics of AE1 in HEK293 cells and hereditary stomatocytosis red blood cells | 1.1 Articolo in rivista | 2013 | Frumence, E; Genetet, S; Ripoche, P; Iolascon, Achille; Andolfo, Immacolata; Le Van Kim, C; Colin, Y; Mouro Chanteloup, I; Lopez, C. | |
| Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1 | 1.1 Articolo in rivista | 2013 | Andolfo, I; Alper, Sl; De Franceschi, L; Auriemma, C; Russo, Roberta; De Falco, L; Vallefuoco, F; Esposito, Mr; Vandorpe, Dh; Shmukler, Be; Narayan, R; Montanaro, D; D'Armiento, Maria; Vetro, A; Limongelli, I; Zuffardi, O; Glader, Be; Schrier, Sl; Brugnara, C; Stewart, Gw; Delaunay, J; Iolascon, Achille | |
| The micro-RNA 199b-5p regulatory circuit involves Hes1, CD15, and epigenetic modifications in medulloblastoma. | 1.1 Articolo in rivista | 2012 | Andolfo, I; Liguori, L; De Antonellis, P; Cusanelli, E; Marinaro, F; Pistollato, F; Garzia, L; De Vita, G; Petrosino, Giuseppe; Accordi, B; Migliorati, R; Basso, G; Iolascon, Achille; Cinalli, G; Zollo, Massimo | |
| Chromosome 9q and 16q loss identified by genome-wide pooled-analysis are associated with tumor aggressiveness in patients with classic medulloblastoma. | 1.1 Articolo in rivista | 2011 | Coco, S; Valdora, F; Bonassi, S; Scaruffi, P; Stigliani, S; Oberthuer, A; Berthold, F; Andolfo, I; Servidei, T; Riccardi, R; Basso, E; Iolascon, Achille; Tonini, G. P. | |
| Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia | 1.1 Articolo in rivista | 2013 | Andolfo, I; Alper, Sl; Delaunay, J; Auriemma, C; Russo, Roberta; Asci, R; Esposito, Mr; Sharma, Ak; Shmukler, Be; Brugnara, C; De Franceschi, L; Iolascon, Achille | |
| Hereditary xerocytosis revisited | 1.1 Articolo in rivista | 2014 | Archer, Natasha M.; Shmukler, Boris E.; Andolfo, Immacolata; Vandorpe, David H.; Radhakrishnan, Gnanasambandam; Higgins, John M.; Alicia, Rivera; Fleming, Mark D.; Frederick, Sachs; Gottlieb, Philip A.; Iolascon, Achille; Carlo, Brugnara; Alper, Seth L.; Nathan, David G. | |
| Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene. | 1.1 Articolo in rivista | 2012 | DE FALCO, Luigia; Bruno, M; Andolfo, Immacolata; David, Bp; Girelli, D; Noce, Fd; Camaschella, C; Iolascon, Achille | |
| Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d inerythroid cells. | 1.1 Articolo in rivista | 2010 | Andolfo, I; De Falco, L; Asci, R; Russo, R; Colucci, S; Gorrese, M; Zollo, Massimo; Iolascon, Achille | |
| MiR-34a Targeting of Notch Ligand Delta-Like 1 ImpairsCD15+/CD133+ Tumor-Propagating Cells and SupportsNeural Differentiation in | 1.1 Articolo in rivista | 2011 | de Antonellis, P.; Medaglia, C.; Cusanelli, E.; Andolfo, I.; Liguori, L.; DE VITA, Gennaro; Carotenuto, M.; Bello, A.; Formiggini, F.; Galeone, Aldo; DE ROSA, Giuseppe; Virgilio, Antonella; Scognamiglio, I.; Sciro, M.; Basso, G.; Schulte, J. H.; Cinalli, G.; Iolascon, Achille; Zollo, Massimo | |
| Diagnosis and management of congenital dyserythropoietic anemias | 1.1 Articolo in rivista | 2016 | Gambale, Antonella; Iolascon, Achille; Andolfo, Immacolata; Russo, Roberta | |
| Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia | 1.1 Articolo in rivista | 2016 | Andolfo, Immacolata; Russo, Roberta; Manna, Francesco; De Rosa, Gianluca; Gambale, Antonella; Zouwail, Soha; Detta, Nicola; Pardo, Catia Lo; Alper, Seth L; Brugnara, Carlo; Sharma, Alok K; De Franceschi, Lucia; Iolascon, Achille | |
| Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis) | 1.1 Articolo in rivista | 2015 | Andolfo, Immacolata; Russo, Roberta; Manna, Francesco; Shmukler, Boris E; Gambale, Antonella; Vitiello, Giuseppina; DE ROSA, Gianluca; Brugnara, Carlo; Alper, Seth L; Snyder, L. Michael; Iolascon, Achille | |
| SOCS3 and IRS-1 gene expression differs between genotype 1 and genotype 2 hepatitis C virus-infected HepG2 cells. | 1.1 Articolo in rivista | 2009 | Persico, M.; Russo, Roberta; Persico, E.; Svelto, M.; Spano, D.; Andolfo, I.; La Mura, V.; Capasso, Mario; Tiribelli, C.; Torella, R.; Iolascon, Achille |