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Mostrati risultati da 21 a 40 di 134
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2003 Role of genetics in prevention of coronary atherosclerosis Novelli, G; Borgiani, P; Giardina, E; Mango, R; Contino, G; Romeo, F; Mehta, J Articolo su rivista
1-gen-2003 Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. Mango, R; Clementi, F; Borgiani, P; Forleo, G; Federici, M; Contino, G; Giardina, E; Garza, L; Fahdi, I; Lauro, R; Mehta, J; Novelli, G; Romeo, F Articolo su rivista
1-mar-2004 CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease Vavassori, P; Borgiani, P; Biancone, L; D'Apice, M; Blanco, G; Vallo, L; De Nigris, F; Monteleone, I; Monteleone, G; Pallone, F; Novelli, G Articolo su rivista
1-mag-2004 Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population Giardina, E; Novelli, G; Costanzo, A; Nisticò, S; Bulli, C; Sinibaldi, C; Sorgi, M; Chimenti, S; Pallone, F; Taccari, E; Borgiani, P Articolo su rivista
1-ago-2004 Type 2 diabetes and the genetics of signal transduction: a study of interaction between adenosine deaminase and acid phosphatase locus 1 polymorphisms Bottini, N; Gloria Bottini, F; Borgiani, P; Antonacci, E; Lucarelli, P; Bottini, E Articolo su rivista
1-gen-2005 Neonatal screening, clinical features and genetic testing for galactosemia [3] Zaffanello, M; Zamboni, G; Schadewaldt, P; Borgiani, P; Novelli, G Articolo su rivista
1-feb-2005 Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population Vallo, L; Bonifazi, E; Borgiani, P; Novelli, G; Botta, A Articolo su rivista
1-dic-2005 Pharmacogenomics in cardiovascular disease: the role of single nucleotide polymorphisms in improving drug therapy Mango, R; Vecchione, L; Raso, Bfmc; Borgiani, P; Brunetti, E; Mehta, J; Lauro, R; Romeo, F; Novelli, G Articolo su rivista
1-gen-2006 OLR1 gene and coronary artery disease/acute myocardial infarction: Replication in an independently collected sample [1] Novelli, G; Borgiani, P; Mango, R; Romeo, F; Mehta, J Articolo su rivista
1-gen-2007 Interleukin-23R Arg381Gln Is Associated With Susceptibility to Crohn's Disease But Not With Phenotype in an Italian Population Borgiani, P; Perricone, C; Ciccacci, C; Romano, S; Novelli, G; Biancone, L; Petruzziello, C; Pallone, F Articolo su rivista
1-gen-2007 Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians Borgiani, P; Ciccacci, C; Forte, V; Romano, S; Federici, G; Novelli, G Articolo su rivista
1-gen-2007 Genotyping OLR1 gene: A genomic biomarker for cardiovascular diseases Vecchione, L; Gargiul, E; Borgiani, P; Predazzi, I; Mango, R; Romeo, F; Magnani, M; Novelli, G Articolo su rivista
1-gen-2007 New insights in atherosclerosis research: LOX-1, leading actor of cardiovascular diseases [Nuovi approfondimenti nella ricerca su l'ateroslerosi: LOX-1, un primo attore nelle malattie cardiovascolari] Novelli, G; Mango, R; Vecchione, L; Mariotti, E; Borgiani, P; Mehta, J; Romeo, F Articolo su rivista
1-mar-2007 Further evidence that polymorphisms of the OLR1 gene are associated with susceptibility to coronary artery disease and myocardial infarction Novelli, G; Borgiani, P; Mango, R; Lauro, R; Romeo, F Articolo su rivista
1-gen-2008 Genetic tests and genomic biomarkers: regulation, qualification and validation Novelli, G; Ciccacci, C; Borgiani, P; Papaluca Amati, M; Abadie, E Articolo su rivista
1-gen-2008 Ala197Thr is not associated with susceptibility to Crohn’s Disease or with phenotype in an Italian population. Perricone, C; Borgiani, P; Romano, S; Ciccacci, C; Fusco, G; Novelli, G; Biancone, L; Calabrese, E; Pallone, F Articolo su rivista
1-gen-2008 ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn's Disease or With Phenotype in an Italian Population Perricone, C; Borgiani, P; Romano, S; Ciccacci, C; Fusco, G; Novelli, G; Biancone, L; Calabrese, E; Pallone, F Articolo su rivista
1-ott-2008 Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome Lombardi, F; Fasciglione, G; D'Apice, M; Vielle, A; D'Adamo, M; Sbraccia, P; Marini, S; Borgiani, P; Coletta, M; Novelli, G Articolo su rivista
1-gen-2009 Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice Cipollone, D; Carsetti, R; Tagliani, A; Rosado, M; Borgiani, P; Novelli, G; D'Amati, G; Fumagalli, L; Marino, B; Businaro, R Articolo su rivista
1-feb-2009 CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population Borgiani, P; Ciccacci, C; Forte, V; Sirianni, E; Novelli, L; Bramanti, P; Novelli, G Articolo su rivista
Mostrati risultati da 21 a 40 di 134
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