CAPASSO, Mario

CAPASSO, Mario  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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Histone Chaperone CHAF1A Inhibits Differentiation and Promotes Aggressive Neuroblastoma 1.1 Articolo in rivista 2014 Barbieri, E1; De Preter, K; Capasso, Mario; Chen, Z; Hsu, Dm; Tonini, Gp; Lefever, S; Hicks, J; Versteeg, R; Pession, A; Speleman, F; Kim, Es; Shohet, J. M.
Decreased concentration of adiponectin together with a selective reduction of its high molecular weight oligomers is involved in metabolic complications of myotonic dystrophy type 1 1.1 Articolo in rivista 2011 Daniele, A1; De Rosa, A; De Cristofaro, M; Monaco, Ml; Masullo, M; Porcile, C; Capasso, Mario; Tedeschi, G; Oriani, G; Di Costanzo, A.
Homozygosis for (12) CA repeats in the first intron of the human IFN-gamma gene is significantly associated with the risk of aplastic anaemia in Caucasian population 1.1 Articolo in rivista 2004 C., Dufour; Capasso, Mario; J., Svahn; A., Marrone; R., Haupt; A., Bacigalupo; L., Giordani; D., Longoni; M., Pillon; A., Pistorio; P. D., Michele; A. P., Iori; C., Pongiglione; M., Lanciotti; Iolascon, Achille
Mannose-binding lectin genetic analysis: possible protective role of the HYPA haplotype in the development of recurrent urinary tract infections in men 1.1 Articolo in rivista 2014 Scudiero, Olga; Maria Ludovica Monaco, ; Ersilia, Nigro; Capasso, Mario; Guida, Maurizio; DI SPIEZIO SARDO, Attilio; Prezioso, Domenico; Daniele, Aurora; Castaldo, Giuseppe
Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10 -1082 G/A polymorphism and respiratory distress syndrome. 1.1 Articolo in rivista 2007 Capasso, Mario; Avvisati, Ra; Piscopo, C; Laforgia, N; Raimondi, Francesco; de Angelis, F; Iolascon, Achille
Gene expression analysis in HBV transgenic mouse liver: a model to study early events related tohepatocarcinogenesis 1.1 Articolo in rivista 2006 Barone, M; Spano, D; D'Apolito, M; Centra, M; Lasalandra, C; Capasso, Mario; Di Leo, A; Volinia, S; Arcelli, D; Rosso, N; Francavilla, A; Tiribelli, C; Iolascon, Achille
Combinations of genetic data in a study of neuroblastoma risk genotypes 1.1 Articolo in rivista 2014 Capasso, Mario; Francesco Maria, Calabrese; Iolascon, Achille; Erling, Mellerup
Integrative genomics identifies LMO1 as a neuroblastoma oncogene. 1.1 Articolo in rivista 2011 Wang, K; Diskin, Sj; Zhang, H; Attiyeh, Ef; Winter, C; Hou, C; Schnepp, Rw; Diamond, M; Bosse, K; Mayes, Pa; Glessner, J; Kim, C; Frackelton, E; Garris, M; Wang, Q; Glaberson, W; Chiavacci, R; Nguyen, L; Jagannathan, J; Saeki, N; Sasaki, H; Grant, Sf; Iolascon, Achille; Mosse, Yp; Cole, Ka; Li, H; Devoto, M; Mcgrady, Pw; London, Wb; Capasso, Mario; Rahman, N; Hakonarson, H; Maris, J. M.
Proteomic Analysis of Sera from Common Variable Immunodeficiency Patients Undergoing Replacement Intravenous Immunoglobulin Therapy 1.1 Articolo in rivista 2011 Spadaro, Giuseppe; C., D'Orio; Genovese, Arturo; A., Galeotafiore; C., D'Ambrosio; S., Di Giovanni; Vitale, Monica; Capasso, Mario; V., Lamberti; A., Scaloni; Marone, Gianni; Zambrano, Nicola
Impact of interleukin-6 -174 G>C gene promoter polymorphism on neuroblastoma. 1.1 Articolo in rivista 2013 Totaro, F; Cimmino, F; Pignataro, P; Acierno, G; De Mariano, M; Longo, L; Tonini, Gp; Iolascon, Achille; Capasso, Mario
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
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma. 1.1 Articolo in rivista 2012 S. J., Diskin; Capasso, Mario; R. W., Schnepp; K. A., Cole; E. F., Attiyeh; C., Hou; M., Diamond; E. L., Carpenter; C., Winter; H., Lee; J., Jagannathan; V., Latorre; Iolascon, Achille; H., Hakonarson; M., Devoto; J. M. M. a. r. i., S.
A p53 drug response signature identifies prognostic genes in high-risk neuroblastoma. 1.1 Articolo in rivista 2014 Barbieri, E; De Preter, K; Capasso, Mario; Johansson, P; Man, Tk; Chen, Z; Stowers, P; Tonini, Gp; Speleman, F; Shohet, J. M.
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci. 1.1 Articolo in rivista 2011 Nguyen le, B; Diskin, Sj; Capasso, Mario; Wang, K; Diamond, Ma; Glessner, J; Kim, C; Attiyeh, Ef; Mosse, Yp; Cole, K; Iolascon, Achille; Devoto, M; Hakonarson, H; Li, Hk; Maris, J. M.
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
Common variation at BARD1 results in the expression of an oncogenic isoform that influences neuroblastoma susceptibility and oncogenicity 1.1 Articolo in rivista 2012 Bosse, Kr1; Diskin, Sj; Cole, Ka; Wood, Ac; Schnepp, Rw; Norris, G; Nguyen le, B; Jagannathan, J; Laquaglia, M; Winter, C; Diamond, M; Hou, C; Attiyeh, Ef; Mosse, Yp; Pineros, V; Dizin, E; Zhang, Y; Asgharzadeh, S; Seeger, Rc; Capasso, Mario; Pawel, Br; Devoto, M; Hakonarson, H; Rappaport, Ef; Irminger Finger, I; Maris, J. M.
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility 1.1 Articolo in rivista 2013 Capasso, Mario; Diskin, Sj; Totaro, F; Longo, L; Mariano, Md; Russo, Roberta; Cimmino, F; Hakonarson, H; Tonini, Gp; Devoto, M; Maris, Jm; Iolascon, Achille
Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10 -1082 G/A polymorphism and respiratory distress syndrome. 1.1 Articolo in rivista 2007 Capasso, Mario; Avvisati, Ra; Piscopo, C; Laforgia, N; Raimondi, Francesco; DE ANGELIS, F; Iolascon, Achille
Comparative proteomic expression profile in all-trans retinoic acid differentiated neuroblastoma cellline. 1.1 Articolo in rivista 2007 Cimmino, F; Spano, D; Capasso, Mario; Zambrano, Nicola; Russo, Roberta; Zollo, Massimo; Iolascon, Achille
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population. 1.1 Articolo in rivista 2011 Russo, Roberta; Gambale, A; Esposito, Mr; Serra, Ml; Troiano, A; De Maggio, I; Capasso, Mario; Luzzatto, L; Delaunay, J; Tamary, H; Iolascon, Achille