AMATI, FRANCESCA
Dettaglio
AMATI, FRANCESCA
Dipartimento di Biomedicina e prevenzione
Pubblicazioni
Risultati 1 - 20 di 60 (tempo di esecuzione: 0.003 secondi).
Data di pubblicazione | Titolo | Autore(i) | Tipo | File | |
---|---|---|---|---|---|
1 | 1995 | 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot | Amati F.,; Mari A.,; Digilio M.C.,; Mingarelli R.,; Marino B.,; Giannotti A.,; Novelli G.,; Dallapiccola B. | Articolo su rivista | - |
2 | 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 | - |
3 | 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 | - |
4 | 1995 | Advances in molecular analysis of congenital heart defects | Dallapiccola, B; Amati, F; Gennarelli, M; Mari, A; Novelli, G | Articolo su rivista | - |
5 | set-2003 | Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies | Amati, F; Condò, I; Conti, E; Sangiuolo, F; Dallapiccola, B; Testi, R; Novelli, G | Articolo su rivista | - |
6 | 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 | - |
7 | 2015 | Application of Next Generation Sequencing for personalized medicine for sudden cardiac death | Morini, E; Sangiuolo, F; Caporossi, D; Novelli, G; Amati, F | Articolo su rivista | - |
8 | 2012 | Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population. | Predazzi IM; Norata GD; Vecchione L; Garlaschelli K; Amati F; Grigore L; Cutuli L; Pirillo A; Tramontana S; Romeo F; Novelli G; Catapano AL. | Articolo su rivista | - |
9 | 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 | - |
10 | 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 | - |
11 | 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; Dallapiccola, B; Novelli, G | Articolo su rivista | - |
12 | 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, MC; Marino, B; Giannotti, A; Gabrielli, O; Novelli, G; Dallapiccola, B | Articolo su rivista | - |
13 | 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, MC; Marino, B; Aiuti, A; Amati, F; Russo, G; Novelli, G; Pandolfi, F; Luzi, G; Giovannetti, A | Articolo su rivista | - |
14 | 2001 | Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models | Botta, A; Amati, F; Novelli, G | Articolo su rivista | - |
15 | 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 | - |
16 | 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, F; Berloco, M; Palumbo, G; Botta, A; Pizzuti, A; Novelli, G; Dallapiccola, B | Articolo su rivista | - |
17 | 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 | Open Access |
18 | 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 | - |
19 | 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 | Open Access |
20 | 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 | riservati |