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Mostrati risultati da 21 a 40 di 69
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2001 Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster Ratti, A; Amati, F; Bozzali, M; Conti, E; Sangiuolo, Fc; Berloco, M; Palumbo, G; Botta, A; Pizzuti, A; Novelli, G; Dallapiccola, B Articolo su rivista
1-gen-2001 Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models Botta, A; Amati, F; Novelli, G Articolo su rivista
1-gen-2001 Association study of a promoter polymorphism of UFD1L gene with schizophrenia De Luca, A; Pasini, A; Amati, F; Botta, A; Spalletta, G; Alimenti, S; Caccamo, F; Conti, E; Trakalo, J; Macciardi, F; DALLA PICCOLA, B; Novelli, G Articolo su rivista
1-gen-2001 Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit Berti, L; Mittler, G; Przemeck, G; Stelzer, G; Gunzler, B; Amati, F; Conti, E; Dallapiccola, B; Hrabe de Angelis, M; Novelli, G; Meisterernst, M Articolo su rivista
1-gen-2002 Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre Giardina, E; Capon, F; D'Apice, Mr; Amati, F; Arturi, A; Filetti, S; Bonifazi, E; Pucci, S; Conte, C; Novelli, G Articolo su rivista
1-gen-2002 Functional characterization of the 5′ flanking region of human Ubiquitin Fusion Degradation 1 Like gene (UFD1L) Amati, F; Conti, E; Botta, A; Amicucci, P; Dallapiccola, B; Novelli, G Articolo su rivista
1-gen-2003 Mutations of ZFPM2/FOG2 gene in sporadic cases of Tetralogy of Fallot Pizzuti, A; Sarkozy, A; Newton, A; Conti, E; Flex, E; Digilio, M; Amati, F; Gianni, D; Tandoi, C; Marino, B; Crossley, M; Dallapiccola, B Articolo su rivista
1-gen-2003 Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) Pierdominici, M; Mazzetta, F; Caprini, E; Marziali, M; Digilio, M; Marino, B; Aiuti, A; Amati, F; Russo, G; Novelli, G; Pandolfi, F; Luzi, G; Giovannetti, A Articolo su rivista
1-gen-2003 Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia De Luca, A; Conti, E; Grifone, N; Amati, F; Spalletta, G; Caltagirone, C; Bonaviri, G; Pasini, A; Gennarelli, M; Stefano, B; Berti, L; Mittler, G; Meisterernst, M; Dallapiccola, B; Novelli, G Articolo su rivista
1-set-2003 Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies Amati, F; Condo', I; Conti, E; Sangiuolo, Fc; Dallapiccola, B; Testi, R; Novelli, G Articolo su rivista
1-gen-2004 Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays Amati, F; Biancolella, M; D'Apice, Mr; Gambardella, S; Mango, R; Sbraccia, P; D'Adamo, M; Margiotti, K; Nardone, A; Lewis, M; Novelli, G Articolo su rivista
1-mar-2004 Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. Contino, G; Amati, F; Pucci, S; Pontieri, E; Picchiorri, F; Novelli, A; Botta, A; Mango, R; Nardone, A; Sangiuolo, Fc; Citro, G; Spagnoli, Lg; Novelli, G Articolo su rivista
22-lug-2005 In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction Mango, R; Biocca, S; Del Vecchio, F; Clementi, F; Sangiuolo, Fc; Amati, F; Filareto, A; Grelli, S; Spitalieri, P; Filesi, I; Favalli, C; Lauro, R; Mehta, J; Romeo, F; Novelli, G Articolo su rivista
1-gen-2006 A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice Cipollone, D; Amati, F; Carsetti, R; Placidi, S; Biancolella, M; D'Amati, G; Novelli, G; Siracusa, G; Marino, B Articolo su rivista
1-gen-2006 Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation Bucci, B; Misiti, S; Cannizzaro, A; Marchese, R; Raza, Gh; Miceli, R; Stigliano, A; Amendola, D; Monti, O; Biancolella, M; Amati, F; Novelli, G; Vecchione, A; Brunetti, E; De Paula, U Articolo su rivista
1-dic-2006 Gene expression profile study in CFTR mutated bronchial cell lines Gambardella, S; Biancolella, M; D'Apice, M; Amati, F; Sangiuolo, Fc; Farcomeni, A; Chillemi, G; Bueno, S; Desideri, A; Novelli, G Articolo su rivista
1-gen-2007 Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. Botta, A; Vallo, L; Rinaldi, F; Bonifazi, E; Amati, F; Biancolella, M; Gambardella, S; Mancinelli, E; Angelini, C; Meola, G; Novelli, G Articolo su rivista
1-gen-2007 Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line Valentini, A; Biancolella, M; Amati, F; Gravina, P; Miano, R; Chillemi, G; Farcomeni, A; Bueno, S; Vespasiani, G; Desideri, A; Federici, G; Novelli, G; Bernardini, S Articolo su rivista
15-apr-2007 Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development Amati, F; Biancolella, M; Farcomeni, A; Giallonardi, S; Bueno, S; Minella, D; Vecchione, L; Chillemi, G; Desideri, A; Novelli, G Articolo su rivista
1-gen-2009 MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 Menghini, R; Casagrande, V; Cardellini, M; Martelli, E; Terrinoni, A; Amati, F; Vasa Nicotera, M; Ippoliti, A; Novelli, G; Melino, G; Lauro, R; Federici, M Articolo su rivista
Mostrati risultati da 21 a 40 di 69
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