User profiles for FRANCESCO BERNARDI
 | Bernardi FrancescoUniversità di Ferrara Verified email at unife.it Cited by 19297 |
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
…, CA Wagner, L D'Ambrosio, S Melchionda, F Bernardi… - Nature …, 1999 - nature.com
correspondence 16 nature genetics• volume 23• september 1999 light of speculation that
some form of DNA rearrangement is involved during the selective expression of individual …
some form of DNA rearrangement is involved during the selective expression of individual …
Prospective evaluation of on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention: relationship with gene polymorphisms …
…, M Tebaldi, M Miccoli, J Marchesini, F Bernardi… - Journal of the American …, 2011 - jacc.org
Objectives : This study sought to investigate the evolving pattern over time of on-clopidogrel
platelet reactivity (PR) and its relationship with genotype and clinical outcomes after …
platelet reactivity (PR) and its relationship with genotype and clinical outcomes after …
Predictive value of D-dimer test for recurrent venous thromboembolism after anticoagulation withdrawal in subjects with a previous idiopathic event and in carriers of …
…, C Legnani, B Cosmi, L Valdré, B Lunghi, F Bernardi… - Circulation, 2003 - Am Heart Assoc
Background— We have shown that normal D-dimer levels obtained after the discontinuation
of oral anticoagulant treatment (OAT) has a high negative predictive value for recurrent …
of oral anticoagulant treatment (OAT) has a high negative predictive value for recurrent …
Clinical phenotypes and factor VII genotype in congenital factor VII deficiency
…, G Auerswald, J Ingerslev, F Bernardi… - Thrombosis and …, 2005 - thieme-connect.com
To investigate the relationship between clinical phenotype, clotting activity (FVIIc) and FVII
genotype, a multi-center study of factor VII (FVII) congenital deficiency with centralized …
genotype, a multi-center study of factor VII (FVII) congenital deficiency with centralized …
[HTML][HTML] Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease
…, F Manzato, A Mazzucco, F Bernardi… - New England journal …, 2000 - Mass Medical Soc
Background High plasma levels of coagulation factor VII have been suggested to be
predictors of death due to coronary artery disease. Since polymorphisms in the factor VII gene …
predictors of death due to coronary artery disease. Since polymorphisms in the factor VII gene …
[HTML][HTML] Factor VII deficiency
G Mariani, F Bernardi - Seminars in thrombosis and hemostasis, 2009 - thieme-connect.com
The complex formed between the procoagulant serine protease activated factor VII (FVII)
and the membrane protein tissue factor, exposed on the vascular lumen upon injury, triggers …
and the membrane protein tissue factor, exposed on the vascular lumen upon injury, triggers …
Stimulation of P2 (P2X7) receptors in human dendritic cells induces the release of tissue factor‐bearing microparticles
…, S Calzavarini, P Caruso, F Bernardi… - The FASEB …, 2007 - Wiley Online Library
Receptors for extracellular nucleotides are the focus of increasing attention for their ability to
cause release of plasma membrane vesicles (micropar‐ticles, MPs). Here, we show that …
cause release of plasma membrane vesicles (micropar‐ticles, MPs). Here, we show that …
Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid …
High levels of coagulation factor VIII (FVIII) have been associated with cardiovascular disease.
Low-density lipoprotein receptor (LDLR) has been recently demonstrated to contribute to …
Low-density lipoprotein receptor (LDLR) has been recently demonstrated to contribute to …
Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma
F Bernardi, G Marchetti, M Pinotti, P Arcieri… - … , and vascular biology, 1996 - Am Heart Assoc
To assess the role of genetic variation in determining factor VII (FVII) activity and antigen
levels we studied a polymorphism located in the 5′ region of the gene (5′F7), an intronic …
levels we studied a polymorphism located in the 5′ region of the gene (5′F7), an intronic …
An exon-specific U1 small nuclear RNA (snRNA) strategy to correct splicing defects
…, N Cavallari, ME Rogalska, F Bernardi… - Human molecular …, 2012 - academic.oup.com
A significant proportion of disease-causing mutations affect precursor-mRNA splicing,
inducing skipping of the exon from the mature transcript. Using F9 exon 5, CFTR exon 12 and …
inducing skipping of the exon from the mature transcript. Using F9 exon 5, CFTR exon 12 and …