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C Motti

Showing results (31-40 of 39) with videos related to

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Coronary Artery Disease|December 22, 1999
Influence of the human paraoxonase polymorphism (PON1 192) on the carotid-wall thickening in a healthy populationM Dessì, A Gnasso, C Motti, et al.
Journal of Internal Medicine|November 1, 1990
Serum lipoproteins, apolipoproteins and very low density lipoprotein subfractions during 6-month fibrate treatment in primary hypertriglyceridaemiaP Pauciullo, G Marotta, P Rubba, et al.
Journal of Thrombosis and Thrombolysis|September 29, 1999
Serum homocysteine, MTHFR gene polymorphism, and carotid intimal-medial thickness in NIDDM subjectsA Mazza, C Motti, A Nulli, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 10, 2000
Genetic variation in human stromelysin gene promoter and common carotid geometry in healthy male subjectsA Gnasso, C Motti, C Irace, et al.
Atherosclerosis|August 14, 2001
A multiplex PCR-based DNA assay for the detection of paraoxonase gene cluster polymorphismsC Motti, M Dessì, A Gnasso, et al.
Hypertension (Dallas, Tex. : 1979)|August 24, 1999
Evaluation of common carotid hemodynamic forces. Relations with wall thickeningC Carallo, C Irace, A Pujia, et al.
Journal of the American Society of Nephrology : JASN|July 15, 1999
Pronatriodilatin gene polymorphisms, microvascular permeability, and diabetic nephropathy in type 1 diabetes mellitusM Nannipieri, G Penno, L Pucci, et al.
The Journal of Clinical Investigation|February 1, 1993
Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this diseaseH Funke, A von Eckardstein, P H Pritchard, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2000
Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotypeS Bertolini, A Cantafora, M Averna, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Coronary Artery Disease|December 22, 1999
Influence of the human paraoxonase polymorphism (PON1 192) on the carotid-wall thickening in a healthy populationM Dessì, A Gnasso, C Motti, et al.
Journal of Internal Medicine|November 1, 1990
Serum lipoproteins, apolipoproteins and very low density lipoprotein subfractions during 6-month fibrate treatment in primary hypertriglyceridaemiaP Pauciullo, G Marotta, P Rubba, et al.
Journal of Thrombosis and Thrombolysis|September 29, 1999
Serum homocysteine, MTHFR gene polymorphism, and carotid intimal-medial thickness in NIDDM subjectsA Mazza, C Motti, A Nulli, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 10, 2000
Genetic variation in human stromelysin gene promoter and common carotid geometry in healthy male subjectsA Gnasso, C Motti, C Irace, et al.
Atherosclerosis|August 14, 2001
A multiplex PCR-based DNA assay for the detection of paraoxonase gene cluster polymorphismsC Motti, M Dessì, A Gnasso, et al.
Hypertension (Dallas, Tex. : 1979)|August 24, 1999
Evaluation of common carotid hemodynamic forces. Relations with wall thickeningC Carallo, C Irace, A Pujia, et al.
Journal of the American Society of Nephrology : JASN|July 15, 1999
Pronatriodilatin gene polymorphisms, microvascular permeability, and diabetic nephropathy in type 1 diabetes mellitusM Nannipieri, G Penno, L Pucci, et al.
The Journal of Clinical Investigation|February 1, 1993
Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this diseaseH Funke, A von Eckardstein, P H Pritchard, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2000
Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotypeS Bertolini, A Cantafora, M Averna, et al.
Pageof 4