C. Motti

发表

A multiplex PCR-based DNA assay for the detection of paraoxonase gene cluster polymorphisms.

A. Gnasso, G. Federici, S. Bernardini, 2001, Atherosclerosis.

Association between wall shear stress and flow-mediated vasodilation in healthy men.

A. Gnasso, C. Cortese, C. Irace, 2001, Atherosclerosis.

In vivo association between low wall shear stress and plaque in subjects with asymmetrical carotid atherosclerosis.

A. Gnasso, C. Irace, C. Carallo, 1997, Stroke.

Apolipoprotein E genotyping: a comparative study between restriction endonuclease mapping and allelic discrimination with the LightCycler.

G. Federici, S. Bernardini, C. Cortese, 2002, Clinica chimica acta; international journal of clinical chemistry.

Clinical Expression of Familial Hypercholesterolemia in Clusters of Mutations of the LDL Receptor Gene That Cause a Receptor-Defective or Receptor-Negative Phenotype

I. Rabbone, C. Cortese, A. Cantafora, 2000, Arteriosclerosis, thrombosis, and vascular biology.

Apolipoprotein E genotype and cholesterogenesis in polygenic hypercholesterolemia.

C. Cortese, C. Motti, G. Menzinger, 1998, Metabolism: clinical and experimental.

Using mutagenic polymerase chain reaction primers to detect carriers of familial defective apolipoprotein B-100.

G. Assmann, C. Motti, H. Funke, 1991, Clinical chemistry.

Identification of an alternative transcript of ABCA1 gene in different human cell types.

S. Bernardini, C. Cortese, S. Bertolini, 2001, Biochemical and biophysical research communications.

Modulation of GST P1‐1 activity by polymerization during apoptosis

G. Melino, F. Bernassola, G. Federici, 2000, Journal of cellular biochemistry.

Carotid atherosclerosis in subjects with different hyperlipidaemia phenotypes.

A. Gnasso, C. Irace, C. Motti, 1998, International angiology : a journal of the International Union of Angiology.

Deletion polymorphism in angiotensin converting enzyme gene associated with carotid wall thickening in a healthy male population

A. Gnasso, G. Federici, C. Cortese, 1996, Coronary artery disease.

The Arg allele in position 192 of PON1 is associated with carotid atherosclerosis in subjects with elevated HDLs.

A. Gnasso, G. Federici, S. Bernardini, 2002, Atherosclerosis.

Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease.

A. von Eckardstein, M. Hayden, H. Wiebusch, 1993, The Journal of clinical investigation.

Expression of co-factors (SMRT and Trip-1) for retinoic acid receptors in human neuroectodermal cell lines.

G. Melino, M. Annicchiarico-Petruzzelli, G. Federici, 1997, Biochemical and biophysical research communications.

Whole blood viscosity and haematocrit are associated with internal carotid atherosclerosis in men

A. Gnasso, C. Irace, C. Carallo, 1998, Coronary artery disease.

Fully automated assay for total homocysteine, cysteine, cysteinylglycine, glutathione, cysteamine, and 2-mercaptopropionylglycine in plasma and urine.

G. Federici, C. Cortese, R. Massoud, 1998, Clinical chemistry.

Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine and other risk factors for vascular disease.

A. Gnasso, G. Federici, S. Bernardini, 1998, Atherosclerosis.

A nonsense mutation in the apolipoprotein A-I gene is associated with high-density lipoprotein deficiency and periorbital xanthelasmas.

A. von Eckardstein, G. Assmann, G. Noseda, 1994, Arteriosclerosis and thrombosis : a journal of vascular biology.

Serum Homocysteine, MTHFR Gene Polymorphism, and Carotid Intimal-Medial Thickness in NIDDM Subjects

G. Federici, F. Andreotti, C. Cortese, 1999, Journal of Thrombosis and Thrombolysis.

Lack of association between carotid intima-media thickness and methylenetetrahydrofolate reductase gene polymorphism or serum homocysteine in non-insulin-dependent diabetes mellitus.

A. Gnasso, G. Federici, C. Cortese, 2000, Metabolism: clinical and experimental.

Serum Homocysteine, MTHFR Gene Polymorphism, and

G. Federici, F. Andreotti, C. Cortese, 1999 .

MTHFR gene polymorphism, homocysteine and cardiovascular disease

C. Cortese, C. Motti, 2001, Public Health Nutrition.

Genetic variation in human stromelysin gene promoter and common carotid geometry in healthy male subjects.

A. Gnasso, G. Federici, S. Bernardini, 2000, Arteriosclerosis, thrombosis, and vascular biology.

, in Healthy Male Subjects Genetic Variation in Human Stromelysin Gene Promoter and Common Carotid Geometry

A. Gnasso, G. Federici, S. Bernardini, 2000 .

Pronatriodilatin gene polymorphisms, microvascular permeability, and diabetic nephropathy in type 1 diabetes mellitus.

M. Nannipieri, H. Colhoun, L. Rizzo, 1999, Journal of the American Society of Nephrology : JASN.

Evaluation of common carotid hemodynamic forces. Relations with wall thickening.

A. Gnasso, C. Cortese, C. Irace, 1999, Hypertension.

NIDDM is associated with lower wall shear stress of the common carotid artery.

A. Gnasso, C. Irace, C. Carallo, 1999, Diabetes.

Alternative splicing of human plasma cholesteryl ester transfer protein mRNA in Caco-2 cells and its modulation by oleic acid

G. Federici, C. Cortese, C. Motti, 1997, Molecular and Cellular Biochemistry.

Influence of the human paraoxonase polymorphism (PON1 192) on the carotid-wall thickening in a healthy population.

A. Gnasso, G. Federici, C. Cortese, 1999, Coronary Artery Disease.

Characterization and screening of a point mutation in LDL receptor gene found in southern Italy (FHAvellino).

C. Cortese, A. Cantafora, S. Bertolini, 2000, Annali dell'Istituto superiore di sanita.

Glycemia, MTHFR genotype and low homocysteine in uncomplicated type 2 diabetic patients.

D. Giugliano, F. Andreotti, C. Cortese, 2000, Atherosclerosis.

Recognition by human sera and immunogenicity of HBsAg mimotopes selected from an M13 phage display library.

A. Meola, F. Felici, G. Galfré, 1994, Gene.

[Dyslipoproteinemia and monoclonal gammopathy: a case report].

A. Gnasso, C. Motti, V. Spagnuolo, 1996, Annali italiani di medicina interna : organo ufficiale della Societa italiana di medicina interna.

Receptor Gene That Cause a Receptor-defective or Receptor-negative Phenotype Clinical Expression of Familial Hypercholesterolemia in Clusters of Mutations of the Ldl

I. Rabbone, C. Cortese, A. Cantafora, 2022 .