CICCODICOLA, Alfredo

CICCODICOLA, Alfredo  

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Titolo Data di pubblicazione Autore(i) File
Alternative Splicing in Adhesion- and Motility-Related Genes in Breast Cancer 1-gen-2016 Aversa, R; Sorrentino, A; Esposito, R; Ambrosio, Mr; Amato, A; Zambelli, A; Ciccodicola, A; D'Apice, L; Costa, V.
ANALYSIS AND SEQUENCING OF THE GENOMIC DNA REGION SPANNING THE HUMAN DBL PROTOONCOGENE 1-gen-1993 Palmieri, G; Casamassimi, A; Ciccodicola, A; Arcucci, A; DE FRANCISCIS, V; Vecchio, G; Durso, M
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 1-gen-2014 Scarpato, M; Esposito, R; Evangelista, D; Aprile, M; Ambrosio, Mr; Angelini, C; Ciccodicola, A; Costa, V.
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 1-gen-2008 Costa, V; Casamassimi, A; Villani, A; Santangelo, F; Ciccodicola, A
Analysis of SEMA6B gene expression in breast cancer: identification of a new isoform 1-gen-2013 D'Apice, L; Costa, V; Valente, C; Trovato, M; Pagani, A; Manera, S; Regolo, L; Zambelli, A; Ciccodicola, A; De Berardinis, P
Analyzing the Whole Transcriptome by RNA-Seq Data: The Tip of the Iceberg 1-gen-2010 Angelini, Claudia; Ciccodicola, Alfredo; Costa, Valerio; De Feis, Italia
Anomalie dello sviluppo 1-gen-2000 Simonelli, F; Ciccodicola, A
Anomalie dello sviluppo dell'occhio 1-gen-2004 Ciccodicola, A
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response 1-gen-2015 Sartorius, R; D'Apice, L; Trovato, M; Cuccaro, F; Costa, V; De Leo, Mg; Marzullo, Vm; Biondo, C; D'Auria, S; De Matteis, Ma; Ciccodicola, A; De Berardinis, P
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 1-gen-1997 Geschwind, Dh; Gregg, J; Karrim, J; Boone, K; Swerdloff, R; Rappold, G; Rao, E; D'Urso, M; Ciccodicola, A; Nelson, Sf
Approccio Clinico alle distrofie corneali ed ai disordini metabolici 1-gen-2007 Ciccodicola, A; Casamassimi, A; Costa, V
ASSEMBLY AND RARE-CUTTER RESTRICTION ENZYME ANALYSIS OF YACS COVERING 8.1 MB ACROSS XQ28 1-gen-1993 Palmieri, G; Ciccodicola, A; Romano, G; Cappa, V; Casamassimi, A; Campanile, C; Esposito, T; Johnson, S; Reinbold, R; Schlessinger, D; Durso, M
Association between the T239M missense variation in the FGF23 gene and renal phosphate leak 1-gen-2009 De Filippo, G; Rendina, D; Esposito, T; Gianfrancesco, F; Mossetti, G; Ciccodicola, A; Strazzullo, P
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 1-gen-1998 de Crecchio, G; Simonelli, F; Nunziata, G; Mazzeo, S; Greco, Gm; Rinaldi, E; Ventruto, V; Ciccodicola, A; Miano, Mg; Testa, F; Curci, A; D'Urso, M; Rinaldi, Mm; Cavaliere, Ml; Castelluccio, P
Characterization of a new gene expressed in an undifferentiated teratocarcinoma cell line 1-gen-1987 Ciccodicola, A; Simeone, A; Zollo, M; D'Urso, M; Persico, Mg.
Characterization of a new gene expressed in an undifferentiated teratocarcinoma cell line 1-gen-1987 Ciccodicola, A; Simeone, A; Zollo, M; D'Urso, M; Graziani, F; Malva, C; Manzi, A; Persico, Mg.
Characterization of a Novel Polymorphism in PPARG Regulatory Region Associated with Type 2 Diabetes and Diabetic Retinopathy in Italy 1-gen-2009 Costa, V; Casamassimi, A; Esposito, K; Villani, A; Capone, M; Iannella, R; Schisano, B; Ciotola, M; Di Palo, C; Corrado, Fc; Santangelo, F; Giugliano, D; Ciccodicola, A
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 1-gen-2002 Conte, I; Lestingi, M; den Hollander, A; Miano, Mg; Alfano, G; Circolo, D; Pugliese, M; Testa, F; Simonelli, F; Rinaldi, E; Baiget, M; Banfi, S; Ciccodicola, A
Characterization of Retinitis Pigmentosa GTPase (RPGR) regulator gene promoter and identification of a new allele in patients with Retinitis Pigmentosa X-linked 1-gen-2000 Miano, Mg; Conte, I; Strazzullo, M; Testa, F; Lanzara, C; Zullo, A; Simonelli, F; D'Urso, M; Wright, Af; Ciccodicola, A
Clinical and molecular genetics of Leber's congenital amaurosis: A multicenter study of Italian patients 1-gen-2007 Simonelli, F; Ziviello, C; Testa, F; Rossi, S; Fazzi, E; Bianchi, Pe; Fossarello, M; Signorini, S; Bertone, C; Galantuomo, S; Brancati, F; Valente, Em; Ciccodicola, A; Rinaldi, E; Auricchio, A; Banfi, S