M. Colombo

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Endothelial Function and Carotid Intima-Media Thickness in Young Healthy Subjects Among Endothelial Nitric Oxide

U. Paradossi, A. Biagini, A. Clerico, 2012 .

Endothelial Function and Carotid Intima-Media Thickness in Young Healthy Subjects Among Endothelial Nitric Oxide Synthase Glu 298 3 Asp and T 786 3 C Polymorphisms

U. Paradossi, A. Biagini, A. Clerico, 2004 .

polymorphism) to the presence, extent, and severity of coronary artery disease

S. Masetti, M. Andreassi, U. Paradossi, 2002 .

Prothrombotic mutations, family history and the risk of thrombosis in postmenopausal women: implications for hormone replacement therapy

M. Andreassi, A. Mazzone, S. Maffei, 2011, Climacteric : the journal of the International Menopause Society.

ET-1 Lys198Asn and ETA Receptor H323H Polymorphisms in Heart Failure

U. Paradossi, A. Biagini, S. Bevilacqua, 2006, Cardiology.

Possibility of age regulation of the natriuretic peptide C-receptor in human platelets

M. Andreassi, D. Giannessi, A. Clerico, 2001, Journal of endocrinological investigation.

oxide synthase gene is associated with insulin resistance in patients with ischemic or non ischemic cardiomyopathy

D. Neglia, C. Carpeggiani, M. Andreassi, 2012 .

T−786→C polymorphism of the endothelial nitric oxide synthase gene is associated with insulin resistance in patients with ischemic or non ischemic cardiomyopathy

D. Neglia, A. L'Abbate, C. Carpeggiani, 2012, BMC Medical Genetics.

Interactive effect of the glutathione S-transferase genes and cigarette smoking on occurrence and severity of coronary artery risk

S. Masetti, M. Andreassi, C. Vassalle, 2003, Journal of Molecular Medicine.

A novel LMNA mutation (R189W) in familial dilated cardiomyopathy: evidence for a 'hot spot' region at exon 3: a case report

G. Aquaro, M. Andreassi, U. Paradossi, 2010, Cardiovascular ultrasound.

Deoxyribonucleic acid damage in human lymphocytes after percutaneous transluminal coronary angioplasty.

S. Masetti, M. Andreassi, C. Palmieri, 2002, Journal of the American College of Cardiology.

High density of endothelin binding sites in the hearts of infants and children.

V. Nardini, M. Andreassi, D. Giannessi, 1999, Life sciences.

Efficacy of an amphipathic oligopeptide to shuttle and release a cis-acting DNA decoy into human cells.

L. Poliseno, P. Rovero, G. Rainaldi, 2002, BioTechniques.

The Sensitivity of MCF10A Breast Epithelial Cells to Alkylating Drugs is Enhanced by the Inhibition of O6-Methylguanine-DNA Methyltransferase Transcription with a Synthetic Double Strand DNA Oligonucleotide

L. Poliseno, G. Rainaldi, L. Mariani, 2002, Breast Cancer Research and Treatment.

Differential Ability of Human Endothelial Cells to Internalize and Express Exogenous DNA

R. de Caterina, G. Basta, A. Biagini, 2004, Cardiovascular Drugs and Therapy.

Evidence for DNA damage in patients with coronary artery disease.

S. Masetti, M. Andreassi, A. Mazzone, 2001, Mutation research.

Chronic long-term nitrate therapy: possible cytogenetic effect in humans?

E. Picano, M. Andreassi, D. Giannessi, 2001, Mutagenesis.

Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease

S. Masetti, M. Andreassi, A. Biagini, 2003, Human Genetics.

p53 codon 72 polymorphism in coronary artery disease: No evidence for association with increased risk or micronucleus frequency

S. Masetti, M. Andreassi, C. Vassalle, 2002, Environmental and molecular mutagenesis.

Genetic instability and atherosclerosis: can somatic mutations account for the development of cardiovascular diseases?

M. Andreassi, A. Biagini, A. Clerico, 2000, Environmental and Molecular Mutagenesis.

Endothelial nitric oxide synthase gene polymorphisms and risk of coronary artery disease.

S. Masetti, M. Andreassi, U. Paradossi, 2003, Clinical chemistry.

Clinical utility of genetic tests for inherited hypertrophic and dilated cardiomyopathies

M. Andreassi, U. Paradossi, N. Botto, 2008, Cardiovascular ultrasound.

Weight is an independent predictor of vascular injury in healthy volunteers with aspartate allele

C. Pizzi, U. Paradossi, O. Manfrini, 2012, Journal of cardiovascular medicine.

Endothelial Function and Carotid Intima-Media Thickness in Young Healthy Subjects Among Endothelial Nitric Oxide Synthase Glu298→Asp and T−786→C Polymorphisms

U. Paradossi, A. Biagini, A. Clerico, 2004, Stroke.

Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage

S. Masetti, M. Andreassi, A. Biagini, 2003, European Journal of Human Genetics.

Verapamil prevents cyclosporine-induced hypertension by modulating endothelin A receptor expression in rat kidney membranes.

V. Panichi, M. Andreassi, R. Palla, 1998, Transplantation proceedings.

Evidence for association of a common variant of the endothelial nitric oxide synthase gene (Glu298→Asp polymorphism) to the presence, extent, and severity of coronary artery disease

S. Masetti, M. Andreassi, U. Paradossi, 2002, Heart.

ET-1 Lys198Asn and ET(A) receptor H323H polymorphisms in heart failure. A case-control study.

U. Paradossi, A. Biagini, S. Bevilacqua, 2006, Cardiology.

Methylenetetrahydrofolate reductase gene C 677 T polymorphism , homocysteine , vitamin B 12 , and DNA damage in coronary artery disease

S. Masetti, M. Andreassi, A. Biagini, 2022 .

Clinical utility of genetic tests for inherited hypertrophic and dilated cardiomyopathies

M. Andreassi, U. Paradossi, N. Botto, 2008, Cardiovascular ultrasound.

Clinical utility of genetic tests for inherited hypertrophic and dilated cardiomyopathies.

M. Andreassi, U. Paradossi, N. Botto, 2008 .

A novel LMNA mutation (R189W) in familial dilated cardiomyopathy: evidence for a 'hot spot' region at exon 3: a case report

M. Andreassi, U. Paradossi, N. Botto, 2010, Cardiovascular ultrasound.