Francesca Amati
Francesca Amati
Ricercatore confermato Genetica Medica, Università Tor Vergata Roma
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MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1
R Menghini, V Casagrande, M Cardellini, E Martelli, A Terrinoni, F Amati, ...
American Heart Association, 2009
Practical guidelines for managing patients with 22q11. 2 deletion syndrome
AS Bassett, DM McDonald-McGinn, K Devriendt, MC Digilio, ...
The Journal of pediatrics 159 (2), 332-339. e1, 2011
Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot
A Pizzuti, A Sarkozy, AL Newton, E Conti, E Flex, M Cristina Digilio, ...
Human mutation 22 (5), 372-377, 2003
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot
F Amati, A Mari, MC Digilio, R Mingarelli, B Marino, A Giannotti, G Novelli, ...
Human genetics 95 (5), 479-482, 1995
In Vivo and In Vitro Studies Support That a New Splicing Isoform of OLR1 Gene Is Protective Against Acute Myocardial Infarction
R Mango, S Biocca, F Del Vecchio, F Clementi, F Sangiuolo, F Amati, ...
Circulation research 97 (2), 152-158, 2005
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome
A Pizzuti, G Novelli, A Ratti, F Amati, A Mari, G Calabrese, S Nicolis, ...
Human molecular genetics 6 (2), 259-265, 1997
Atypical deletions suggest five 22q11. 2 critical regions related to the DiGeorge/velo-cardio-facial syndrome
F Amati, E Conti, A Novelli, M Bengala, MC Digilio, B Marino, A Giannotti, ...
European Journal of Human Genetics 7 (8), 903, 1999
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene
A Pizzuti, F Amati, G Calabrese, A Mari, A Colosimo, V Silani, L Giardino, ...
Human molecular genetics 5 (7), 953-958, 1996
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome
A Mari, F Amati, R Mingarelli, A Giannotti, G Sebastio, V Colloridi, ...
Human genetics 96 (4), 444-448, 1995
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.
A Pizzuti, G Novelli, A Mari, A Ratti, A Colosimo, F Amati, D Penso, ...
American journal of human genetics 58 (4), 722, 1996
Biased T‐cell receptor repertoires in patients with chromosome 22q11. 2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
M Pierdominici, F Mazzetta, E Caprini, M Marziali, MC Digilio, B Marino, ...
Clinical & Experimental Immunology 132 (2), 323-331, 2003
Association study of a promoter polymorphism of UFD1L gene with schizophrenia
A De Luca, A Pasini, F Amati, A Botta, G Spalletta, S Alimenti, F Caccamo, ...
American journal of medical genetics 105 (6), 529-533, 2001
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit
L Berti, G Mittler, GKH Przemeck, G Stelzer, B Günzler, F Amati, E Conti, ...
Genomics 74 (3), 320-332, 2001
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2
A Botta, L Vallo, F Rinaldi, E Bonifazi, F Amati, M Biancolella, ...
Gene Expression, The Journal of Liver Research 13 (6), 339-351, 2006
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line
A Valentini, M Biancolella, F Amati, P Gravina, R Miano, G Chillemi, ...
Drug metabolism and disposition 35 (6), 968-972, 2007
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.
R Wadey, J McKie, C Papapetrou, H Sutherland, F Lohman, J Osinga, ...
American journal of human genetics 65 (1), 247, 1999
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation
B Bucci, S Misiti, A Cannizzaro, R Marchese, GH Raza, R Miceli, ...
Anticancer research 26 (6B), 4549-4557, 2006
Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways
M Massimiani, L Vecchione, D Piccirilli, P Spitalieri, F Amati, S Salvi, ...
MHR: Basic science of reproductive medicine 21 (5), 435-451, 2015
Structure and expression of the human ubiquitin fusion–degradation gene (UFD1L)
G Novelli, A Mari, F Amati, A Colosimo, F Sangiuolo, M Bengala, E Conti, ...
Biochimica et Biophysica Acta (BBA)-Gene Structure and Expression 1396 (2 …, 1998
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice
D Cipollone, F Amati, R Carsetti, S Placidi, M Biancolella, G D'Amati, ...
Cardiovascular Pathology 15 (4), 194-202, 2006
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