ANDOLFO, IMMACOLATA

ANDOLFO, IMMACOLATA  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

Mostra records
Risultati 1 - 20 di 122 (tempo di esecuzione: 0.025 secondi).
Titolo Tipologia Data di pubblicazione Autore(i) File
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
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
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
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
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.
MicroRNAs and Cancer Stem Cells in Medulloblastoma 2.1 Contributo in volume (Capitolo o Saggio) 2011 Zollo, Massimo; Andolfo, Immacolata; DE ANTONELLIS, Pasqualino
Hereditary xerocytosis revisited 1.1 Articolo in rivista 2014 Archer, Natasha M.; Shmukler, Boris E.; Andolfo, Immacolata; Vandorpe, David H.; Gnanasambandam, Radhakrishnan; Higgins, John M.; Rivera, Alicia; Fleming, Mark D.; Sachs, Frederick; Gottlieb, Philip A.; Iolascon, Achille; Brugnara, Carlo; Alper, Seth L.; Nathan, David G.
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; Gambale, Antonella; Langella, Concetta; Andolfo, Immacolata; Unal, Sule; Iolascon, Achille
Correlation of NM23-H1 cytoplasmic expressionwith metastatic stage in human prostate cancer tissue 1.1 Articolo in rivista 2011 Andolfo, Immacolata; Daniela De Martino, ; Liguori, Lucia; Petrosino, Giuseppe; Troncone, Giancarlo; Tata, Nicoletta; Galasso, Alessia; Roma, Cristin; Chiancone, Francesco; Zarrilli, Stefano; Arrigoni, Gianluigi; Staibano, Stefania; Imbimbo, Ciro; Zollo, Massimo
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
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
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
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.
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
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
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