TRABETTI, Elisabetta

TRABETTI, Elisabetta  

DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO  

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1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 1-gen-2007 Rizzello, V.; Liuzzo, G.; Giannuario, G. D.; Trabetti, Elisabetta; Brugaletta, S.; Santamaria, M.; Piro, M.; Pignatti, Pierfranco; Maseri, A.; Biasucci, L. M.; Crea, F.
807 C/T polymorphism of the glycoprotein IA gene and pharmacogenetic modulation of platelet response to dual antiplatelet treatment 1-gen-2004 Angiolillo, D. J.; Fernandez-Ortis, A.; Bernardo, E.; Ramirez, C.; Escaned, J.; Moreno, R.; Hernandez-Antolin, R.; Sabat, M.; Trabetti, E.; Pignatti, P. F.; Macaya, C.
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 1-gen-2011 Costantini, Silvia; Prandini, Paola; Corradi, Massimiliano; Pasquali, Alessandra; Contreas, Giovanna; Pignatti, Pierfranco; Pinelli, Leonardo; Trabetti, Elisabetta; Maffeis, Claudio
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 1-gen-2012 Patuzzo, Cristina; Pasquali, Alessandra; Malerba, Giovanni; Trabetti, Elisabetta; Pignatti, Pierfranco; Tessari, Maddalena; Faggian, Giuseppe
A renal genetic risk score (GRS) is associated with kidney dysfunction in people with type 2 diabetes 1-gen-2018 Zusi, Chiara; Trombetta, Maddalena; Bonetti, Sara; Dauriz, Marco; Boselli, Maria L; Trabetti, Elisabetta; Malerba, Giovanni; Penno, Giuseppe; Zoppini, Giacomo; Bonora, Enzo; Solini, Anna; Bonadonna, Riccardo C
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism 1-gen-2002 Friso, S.; Girelli, D.; Trabetti, E.; Stranieri, C.; Olivieri, O.; Tinazzi, E.; Martinelli, N.; Faccini, G.; Pignatti, P. F.; Corrocher, R.
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 1-gen-2002 Friso, Simonetta; Girelli, Domenico; Trabetti, Elisabetta; Stranieri, C; Olivieri, Oliviero; Tinazzi, Elisa; Martinelli, Nicola; Faccini, G; Pignatti, Pierfranco; Corrocher, Roberto
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study. 1-gen-2009 Martinelli, Nicola; Olivieri, Oliviero; Gong Qing, Shen; Trabetti, Elisabetta; Pizzolo, Francesca; Busti, Fabiana; Friso, Simonetta; Bassi, Antonella; Lin, Li; Ying, Hu; Pignatti, Pierfranco; Corrocher, Roberto; Qing Kenneth, Wang; Girelli, Domenico
Advanced cellular models for rare disease study: exploring neural, muscle and skeletal organoids 1-gen-2024 Bombieri, Cristina; Corsi, Andrea; Trabetti, Elisabetta; Ruggiero, Alessandra; Marchetto, Giulia; Vattemi, Gaetano; Valenti, Maria Teresa; Zipeto, Donato; Romanelli, Maria Grazia
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 1-gen-1996 Martinati, L. C.; Trabetti, E.; Casartelli, A.; Boner, A. L.; Pignatti, P. F.
Allele and genotype frequencies of eight DNA polymorphisms in the Italian population 1-gen-1995 Trabetti, Elisabetta; Galavotti, Roberta; Casartelli, Alessandro; Magalini, Giovanna; DE LEO, Domenico; Pignatti, Pierfranco
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 1-gen-1998 Drmic, I.; Schanfield, M. S.; Andjelinovic, S.; Galavotti, R.; Gojanovic, M. D.; Trabetti, E.; Marasovic, D.; Primorac, D.; Pignatti, P. F.
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 1-gen-2007 Girelli, Domenico; Martinelli, Nicola; Trabetti, Elisabetta; Olivieri, Oliviero; Cavallari, Ugo Antonio Aristide; Malerba, Giovanni; Busti, Fabiana; Friso, Simonetta; Pizzolo, Francesca; Pignatti, Pierfranco; Corrocher, Roberto
Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs. 1-gen-2014 Prandini, Paola; Zusi, Chiara; Malerba, Giovanni; Itan, ; Pignatti, Pierfranco; Trabetti, Elisabetta
ApoC-III gene polymorphisms and risk of coronary artery disease 1-gen-2002 Olivieri, Oliviero; Stranieri, Chiara; A., Bassi; Zaia, Barbara; Girelli, Domenico; Pizzolo, Francesca; Trabetti, Elisabetta; S., Cheng; M. A., Grow; Pignatti, Pierfranco; Corrocher, Roberto
ApoE epsilon 2/epsilon 3/epsilon 4 polymorphism, ApoC-III/ApoE ratio and metabolic syndrome 1-gen-2007 Olivieri, Oliviero; Martinelli, Nicola; Bassi, A.; Trabetti, Elisabetta; Girelli, Domenico; Pizzolo, Francesca; Friso, Simonetta; Pignatti, Pierfranco; Corrocher, Roberto
Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease 1-gen-2003 Olivieri, Oliviero; A., Bassi; C., Stranieri; Trabetti, Elisabetta; Martinelli, Nicola; Pizzolo, Francesca; Girelli, Domenico; Friso, Simonetta; Pignatti, Pierfranco; Corrocher, Roberto
Apolipoprotein C-III, n-3 Polyunsaturated Fatty Acids, and “Insulin-Resistant” T-455C APOC3 gene polymorphism in heart disease patients: example of gene-diet interaction 1-gen-2005 Olivieri, Oliviero; Martinelli, Nicola; Sandri, M.; Bassi, A.; Guarini, Patrizia; Trabetti, Elisabetta; Pizzolo, Francesca; Girelli, Domenico; Friso, Simonetta; Pignatti, Pierfranco; Corrocher, Roberto
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 1-gen-1999 Trabetti, Elisabetta; Patuzzo, Cristina; Malerba, Giovanni; Galavotti, Roberta; L., Martinati; Boner, Attilio; Pignatti, Pierfranco
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 1-gen-2011 Belpinati, F.; Malerba, G.; Trabetti, E.; Galavotti, R.; Xumerle, L.; Pescollderungg, L.; Boner, A. L.; Pignatti, P. F.