IRIS

Sfoglia per Autore  

Opzioni
Mostrati risultati da 1 a 20 di 71
Data di pubblicazione Titolo Autore(i) Tipo File
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-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 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-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
1-gen-2011 Characterization of a novel CYP2C9 gene mutation and structural bioinformatic protein analysis in a warfarin hypersensitive patient Ciccacci, C; Falconi, M; Paolillo, N; Oteri, F; Forte, V; Novelli, G; Desideri, A; Borgiani, P Articolo su rivista
1-mar-2011 Anthropological features of the CFTR gene: Its variability in an African population Ciminelli, B; Bombieri, C; Ciccacci, C; Belpinati, F; Pompei, F; Maselli, R; Simporé, J; Pignatti, P; Modiano, G Articolo su rivista
1-giu-2011 EPHX1 Polymorphisms Are Not Associated With Warfarin Response in an Italian Population Ciccacci, C; Paolillo, N; Di Fusco, D; Novelli, G; Borgiani, P Articolo su rivista
1-dic-2012 Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis Danese, E; Montagnana, M; Johnson, J; Rettie, A; Zambon, C; Lubitz, S; Suarez Kurtz, G; Cavallari, L; Zhao, L; Huang, M; Nakamura, Y; Mushiroda, T; Kringen, M; Borgiani, P; Ciccacci, C; Au, N; Langaee, T; Siguret, V; Loriot, M; Sagreiya, H; Altman, R; Shahin, M; Scott, S; Khalifa, S; Chowbay, B; Suriapranata, I; Teichert, M; Stricker, B; Taljaard, M; Botton, M; Zhang, J; Pirmohamed, M; Zhang, X; Carlquist, J; Horne, B; Lee, M; Pengo, V; Guidi, G; Minuz, P; Fava, C Articolo su rivista
1-gen-2013 Biomarkers to predict drug efficacy and safety in neurodegenerative diseases Novelli, G; Abadie, E; Ciccacci, C; Di Fusco, D; Papaluca Amati, M; Borgiani, P Articolo su rivista
1-gen-2013 Recent advances in the genetic susceptibility to osteoarthritis Novelli, L; Ciccacci, C; Borgiani, P; Novelli, G Articolo su rivista
1-gen-2013 TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease Ciccacci, C; Biancone, L; Di Fusco, D; Ranieri, M; Condino, G; Giardina, E; Onali, S; Lepre, T; Pallone, F; Novelli, G; Borgiani, P Articolo su rivista
1-gen-2013 TCF7L2 gene polymorphisms and type 2 diabetes: Association with diabetic retinopathy and cardiovascular autonomic neuropathy Ciccacci, C; Di Fusco, D; Cacciotti, L; Morganti, R; D'Amato, C; Novelli, G; Sangiuolo, Fc; Spallone, V; Borgiani, P Articolo su rivista
1-gen-2013 ABCC10 rs2125739 polymorphism and nevirapine-induced hepatotoxicity: lack of association in a population from Mozambique Ciccacci, C; Di Fusco, D; Marazzi, M; Liotta, G; Palombi, L; Novelli, G; Borgiani, P Articolo su rivista
1-lug-2013 Resequencing of VKORC1, CYP2C9 and CYP4F2 genes in Italian patients requiring extreme low and high warfarin doses Di Fusco, D; Ciccacci, C; Rufini, S; Forte, V; Novelli, G; Borgiani, P Articolo su rivista
9-lug-2013 TRAF3IP2 gene and systemic lupus erythematosus: association with disease susceptibility and pericarditis development Perricone, C; Ciccacci, C; Ceccarelli, F; Di Fusco, D; Spinelli, F; Cipriano, E; Novelli, G; Valesini, G; Conti, F; Borgiani, P Articolo su rivista
1-gen-2014 A multilocus genetic study in a cohort of Italian SLE patients confirms the association with STAT4 gene and describes a new association with HCP5 gene Ciccacci, C; Perricone, C; Ceccarelli, F; Rufini, S; Di Fusco, D; Alessandri, C; Spinelli, F; Cipriano, E; Novelli, G; Valesini, G; Borgiani, P; Conti, F Articolo su rivista
1-mar-2014 HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons syndrome/toxic epidermal necrolysis susceptibility in a population from Mozambique Borgiani, P; Di Fusco, D; Erba, F; Marazzi, M; Mancinelli, S; Novelli, G; Palombi, L; Ciccacci, C Articolo su rivista
1-mar-2014 A family study of asymptomatic small bowel Crohn's disease Biancone, L; Calabrese, E; Petruzziello, C; Capanna, A; Zorzi, F; Onali, S; Condino, G; Lolli, E; Ciccacci, C; Borgiani, P; Pallone, F Articolo su rivista
1-ago-2014 Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes Ciccacci, C; Morganti, R; Di Fusco, D; D'Amato, C; Cacciotti, L; Greco, C; Rufini, S; Novelli, G; Sangiuolo, Fc; Marfia, Ga; Borgiani, P; Spallone, V Articolo su rivista
Mostrati risultati da 1 a 20 di 71
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile