IRIS

AMATI, FRANCESCA

AMATI, FRANCESCA  

Dipartimento di Biomedicina e prevenzione  

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Risultati 1 - 20 di 64 (tempo di esecuzione: 0.023 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-1995 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot Amati, F; Mari, A; Digilio, Mc; Mingarelli, R; Marino, B; Giannotti, A; Novelli, G; Dallapiccola, B Articolo su rivista
1-gen-1998 A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region Mari, A; Amati, F; Conti, E; Bengala, M; Novelli, G; Dallapiccola, B 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-1995 Advances in molecular analysis of congenital heart defects Dallapiccola, B; Amati, F; Gennarelli, M; Mari, A; 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-1995 Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome Mari, A; Amati, F; Mingarelli, R; Giannotti, A; Sebastio, G; Colloridi, V; Novelli, G; Dallapiccola, B Articolo su rivista
1-gen-2015 Application of Next Generation Sequencing for personalized medicine for sudden cardiac death Morini, E; Sangiuolo, Fc; Caporossi, D; Novelli, G; Amati, F Articolo su rivista
1-gen-2012 Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population. Predazzi, I; Norata, G; Vecchione, L; Garlaschelli, K; Amati, F; Grigore, L; Cutuli, L; Pirillo, A; Tramontana, S; Romeo, F; Novelli, G; Catapano, Al Articolo su rivista
1-gen-2000 Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 De Luca, A; Pasini, A; Amati, F; Botta, A; Spalletta, G; Alimenti, S; Caccamo, F; Conti, E; Trakalo, J; Macciardi, F; Macciardi, B; Novelli, G Intervento a convegno
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-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-dic-1999 Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome Amati, F; Conti, E; Novelli, A; Bengala, M; Diglio, M; Marino, B; Giannotti, A; Gabrielli, O; Novelli, G; 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-2001 Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models Botta, A; Amati, F; Novelli, G Articolo su rivista
1-lug-1996 cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene Pizzuti, A; Amati, F; Calabrese, G; Mari, A; Colosimo, A; Silani, V; Giardino, L; Ratti, A; Penso, D; Calzà, L; Palka, G; Scarlato, G; Novelli, G; Dallapiccola, B Articolo su rivista
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-2020 Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome D'Apice, Mr; De Dominicis, A; Murdocca, M; Amati, F; Botta, A; Sangiuolo, F; Lattanzi, G; Federici, M; Novelli, G 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
9-feb-2015 Epidermal growth factor-like domain 7 (EGFL7) promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways. Massimiani, M; Vecchione, L; Piccirilli, D; Spitalieri, P; Amati, F; Salvi, S; Ferrazzani, S; Stuhlmann, H; Campagnolo, L Articolo su rivista
1-mag-2015 Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways Massimiani, M; Vecchione, L; Piccirilli, D; Spitalieri, P; Amati, F; Salvi, S; Ferrazzani, S; Stuhlmann, H; Campagnolo, L Articolo su rivista