AMATI, FRANCESCA
AMATI, FRANCESCA
Dipartimento di Biomedicina e Prevenzione
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot
1995-01-01 Amati, F; Mari, A; Digilio, Mc; Mingarelli, R; Marino, B; Giannotti, A; Novelli, G; Dallapiccola, B
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region
1998-01-01 Mari, A; Amati, F; Conti, E; Bengala, M; Novelli, G; Dallapiccola, B
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice
2006-01-01 Cipollone, D; Amati, F; Carsetti, R; Placidi, S; Biancolella, M; D'Amati, G; Novelli, G; Siracusa, G; Marino, B
Advances in molecular analysis of congenital heart defects
1995-01-01 Dallapiccola, B; Amati, F; Gennarelli, M; Mari, A; Novelli, G
An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease
2024-05-22 Vancheri, C; Quatrana, A; Morini, E; Mariotti, C; Mongelli, A; Fichera, M; Rufini, A; Condò, I; Testi, R; Novelli, G; Malisan, F; Amati, F
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies
2003-09-01 Amati, F; Condo', I; Conti, E; Sangiuolo, Fc; Dallapiccola, B; Testi, R; Novelli, G
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome
1995-01-01 Mari, A; Amati, F; Mingarelli, R; Giannotti, A; Sebastio, G; Colloridi, V; Novelli, G; Dallapiccola, B
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death
2015-01-01 Morini, E; Sangiuolo, Fc; Caporossi, D; Novelli, G; Amati, F
Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population.
2012-01-01 Predazzi, I; Norata, G; Vecchione, L; Garlaschelli, K; Amati, F; Grigore, L; Cutuli, L; Pirillo, A; Tramontana, S; Romeo, F; Novelli, G; Catapano, Al
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22
2000-01-01 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
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia
2003-01-01 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
Association study of a promoter polymorphism of UFD1L gene with schizophrenia
2001-01-01 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
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome
1999-12-01 Amati, F; Conti, E; Novelli, A; Bengala, M; Diglio, M; Marino, B; Giannotti, A; Gabrielli, O; Novelli, G; Dallapiccola, B
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
2003-01-01 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
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models
2001-01-01 Botta, A; Amati, F; Novelli, G
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene
1996-07-01 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
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster
2001-01-01 Ratti, A; Amati, F; Bozzali, M; Conti, E; Sangiuolo, Fc; Berloco, M; Palumbo, G; Botta, A; Pizzuti, A; Novelli, G; Dallapiccola, B
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
2020-01-01 D'Apice, Mr; De Dominicis, A; Murdocca, M; Amati, F; Botta, A; Sangiuolo, F; Lattanzi, G; Federici, M; Novelli, G
Downregulation of Circulating Hsa-miR-200c-3p Correlates with Dyslipidemia in Patients with Stable Coronary Artery Disease
2023-01-01 Vancheri, C; Morini, E; Prandi, Fr; Barilla, F; Romeo, F; Novelli, G; Amati, F
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development
2007-04-15 Amati, F; Biancolella, M; Farcomeni, A; Giallonardi, S; Bueno, S; Minella, D; Vecchione, L; Chillemi, G; Desideri, A; Novelli, G
| 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 | |
| 22-mag-2024 | An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease | Vancheri, C; Quatrana, A; Morini, E; Mariotti, C; Mongelli, A; Fichera, M; Rufini, A; Condò, I; Testi, R; Novelli, G; Malisan, F; Amati, F | 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 | |
| 1-gen-2023 | Downregulation of Circulating Hsa-miR-200c-3p Correlates with Dyslipidemia in Patients with Stable Coronary Artery Disease | Vancheri, C; Morini, E; Prandi, Fr; Barilla, F; Romeo, F; Novelli, G; Amati, F | 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 |