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Results: 1-12 |
Results: 12
A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French Canadians
Authors: St-Pierre, J Vohl, MC Brisson, D Perron, P Despres, JP Hudson, TJ Gaudet, D
Citation: J. St-pierre et al., A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French Canadians, MOL GEN MET, 72(3), 2001, pp. 209-217
Effects of the FABP2 A54T mutation on triglyceride metabolism of viscerally obese men
Authors: Berthier, MT Couillard, C Prud'homme, D Nadeau, A Bergeron, J Tremblay, A Despres, JP Vohl, MC
Citation: Mt. Berthier et al., Effects of the FABP2 A54T mutation on triglyceride metabolism of viscerally obese men, OBES RES, 9(11), 2001, pp. 668-675
Glycerol: a neglected variable in metabolic processes?
Authors: Brisson, D Vohl, MC St-Pierre, J Hudson, TJ Gaudet, D
Citation: D. Brisson et al., Glycerol: a neglected variable in metabolic processes?, BIOESSAYS, 23(6), 2001, pp. 534-542
The common PPAR gamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
Authors: Altshuler, D Hirschhorn, JN Klannemark, M Lindgren, CM Vohl, MC Nemesh, J Lane, CR Schaffner, SF Bolk, S Brewer, C Tuomi, T Gaudet, D Hudson, TJ Daly, M Groop, L Lander, ES
Citation: D. Altshuler et al., The common PPAR gamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes, NAT GENET, 26(1), 2000, pp. 76-80
HDL cholesterol and TaqIB cholesteryl ester transfer protein gene polymorphism in renal transplant recipients
Authors: Radeau, T Vohl, MC Houde, I Lachance, JG Noel, R Despres, JP Douville, P Bergeron, J
Citation: T. Radeau et al., HDL cholesterol and TaqIB cholesteryl ester transfer protein gene polymorphism in renal transplant recipients, NEPHRON, 84(4), 2000, pp. 333-341
Molecular scanning of the human PPAR alpha gene: association of the L162V mutation with hyperapobetalipoproteinemia
Authors: Vohl, MC Lepage, P Gaudet, D Brewer, CG Betard, C Perron, P Houde, G Cellier, C Faith, JM Despres, JP Morgan, K Hudson, TJ
Citation: Mc. Vohl et al., Molecular scanning of the human PPAR alpha gene: association of the L162V mutation with hyperapobetalipoproteinemia, J LIPID RES, 41(6), 2000, pp. 945-952
Glycerol as a correlate of impaired glucose tolerance: Dissection of a complex system by use of a simple genetic trait
Authors: Gaudet, D Arsenault, S Perusse, L Vohl, MC St-Pierre, J Bergeron, J Despres, JP Dewar, K Daly, MJ Hudson, T Rioux, JD
Citation: D. Gaudet et al., Glycerol as a correlate of impaired glucose tolerance: Dissection of a complex system by use of a simple genetic trait, AM J HU GEN, 66(5), 2000, pp. 1558-1568
Contribution of the cholesteryl ester transfer protein gene TaqIB polymorphism to the reduced plasma HDL-cholesterol levels found in abdominal obese men with the features of the insulin resistance syndrome
Authors: Vohl, MC Lamarche, B Pascot, A Leroux, G Prud'homme, D Bouchard, C Nadeau, A Despres, JP
Citation: Mc. Vohl et al., Contribution of the cholesteryl ester transfer protein gene TaqIB polymorphism to the reduced plasma HDL-cholesterol levels found in abdominal obese men with the features of the insulin resistance syndrome, INT J OBES, 23(9), 1999, pp. 918-925
Apolipoprotein A-I charge and conformation regulate the clearance of reconstituted high density lipoprotein in vivo
Authors: Braschi, S Neville, TAM Vohl, MC Sparks, DL
Citation: S. Braschi et al., Apolipoprotein A-I charge and conformation regulate the clearance of reconstituted high density lipoprotein in vivo, J LIPID RES, 40(3), 1999, pp. 522-532
Fine mapping of low-density lipoprotein receptor gene by genetic linkage on chromosome 19p13.1-p13.3 and study of the founder effect of four French Canadian low-density lipoprotein receptor gene mutations
Authors: Couture, P Morissette, J Gaudet, D Vohl, MC Gagne, C Bergeron, J Despres, JP Simard, J
Citation: P. Couture et al., Fine mapping of low-density lipoprotein receptor gene by genetic linkage on chromosome 19p13.1-p13.3 and study of the founder effect of four French Canadian low-density lipoprotein receptor gene mutations, ATHEROSCLER, 143(1), 1999, pp. 145-151
Contribution of receptor negative versus receptor defective mutations in the LDL-receptor gene to angiographically assessed coronary artery disease among young (25-49 years) versus middle-aged (50-64 years) men
Authors: Gaudet, D Vohl, MC Couture, P Moorjani, S Tremblay, G Perron, P Gagne, C Despres, JP
Citation: D. Gaudet et al., Contribution of receptor negative versus receptor defective mutations in the LDL-receptor gene to angiographically assessed coronary artery disease among young (25-49 years) versus middle-aged (50-64 years) men, ATHEROSCLER, 143(1), 1999, pp. 153-161
A novel lecithin-cholesterol acyltransferase antioxidant activity preventsthe formation of oxidized lipids during lipoprotein oxidation
Authors: Vohl, MC Neville, TAM Kumarathasan, R Braschi, S Sparks, DL
Citation: Mc. Vohl et al., A novel lecithin-cholesterol acyltransferase antioxidant activity preventsthe formation of oxidized lipids during lipoprotein oxidation, BIOCHEM, 38(19), 1999, pp. 5976-5981
Risultati: 1-12 |