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D Brisson

Showing results (11-20 of 21) with videos related to

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Atherosclerosis|April 30, 2013
DNA methylation variations at CETP and LPL gene promoter loci: new molecular biomarkers associated with blood lipid profile variabilityS P Guay, D Brisson, B Lamarche, et al.
Biochemistry|March 25, 1975
Interaction between spin-labeled acyl-coenzyme A and the mitochondrial adenosine diphosphate carrierP F Devaux, A Bienvenüe, G Lauquin, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1975
Interaction of a spin-labeled long chain acylcholine with the cholinergic receptor protein in its membrane environmentA D Brisson, C J Scandella, A Bienvenüe, et al.
International Journal of Obesity (2005)|March 8, 2007
Genetic epistasis in the VLDL catabolic pathway is associated with deleterious variations on triglyceridemia in obese subjectsD Brisson, J St-Pierre, M Santuré, et al.
Molecular Genetics and Metabolism|March 13, 2001
A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French CanadiansJ St-Pierre, M C Vohl, D Brisson, et al.
Journal of Endocrinological Investigation|September 13, 2007
Apolipoprotein E and lipoprotein lipase gene polymorphisms interaction on the atherogenic combined expression of hypertriglyceridemia and hyperapobetalipoproteinemia phenotypesP Perron, D Brisson, M Santuré, et al.
Journal of Developmental Origins of Health and Disease|May 23, 2014
Placental lipoprotein lipase DNA methylation levels are associated with gestational diabetes mellitus and maternal and cord blood lipid profilesA A Houde, J St-Pierre, M F Hivert, et al.
Neuromuscular Disorders : NMD|October 2, 2010
Health supervision and anticipatory guidance in adult myotonic dystrophy type 1C Gagnon, M C Chouinard, L Laberge, et al.
Genetics and Molecular Biology|December 3, 2020
XRCC4 rs28360071 intronic variant is associated with increased risk for infant acute lymphoblastic leukemia with KMT2A rearrangementsOrlando Louzada-Neto, Bruno A Lopes, Gisele D Brisson, et al.
Gene Therapy|June 22, 2012
Efficacy and long-term safety of alipogene tiparvovec (AAV1-LPLS447X) gene therapy for lipoprotein lipase deficiency: an open-label trialD Gaudet, J Méthot, S Déry, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Atherosclerosis|April 30, 2013
DNA methylation variations at CETP and LPL gene promoter loci: new molecular biomarkers associated with blood lipid profile variabilityS P Guay, D Brisson, B Lamarche, et al.
Biochemistry|March 25, 1975
Interaction between spin-labeled acyl-coenzyme A and the mitochondrial adenosine diphosphate carrierP F Devaux, A Bienvenüe, G Lauquin, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1975
Interaction of a spin-labeled long chain acylcholine with the cholinergic receptor protein in its membrane environmentA D Brisson, C J Scandella, A Bienvenüe, et al.
International Journal of Obesity (2005)|March 8, 2007
Genetic epistasis in the VLDL catabolic pathway is associated with deleterious variations on triglyceridemia in obese subjectsD Brisson, J St-Pierre, M Santuré, et al.
Molecular Genetics and Metabolism|March 13, 2001
A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French CanadiansJ St-Pierre, M C Vohl, D Brisson, et al.
Journal of Endocrinological Investigation|September 13, 2007
Apolipoprotein E and lipoprotein lipase gene polymorphisms interaction on the atherogenic combined expression of hypertriglyceridemia and hyperapobetalipoproteinemia phenotypesP Perron, D Brisson, M Santuré, et al.
Journal of Developmental Origins of Health and Disease|May 23, 2014
Placental lipoprotein lipase DNA methylation levels are associated with gestational diabetes mellitus and maternal and cord blood lipid profilesA A Houde, J St-Pierre, M F Hivert, et al.
Neuromuscular Disorders : NMD|October 2, 2010
Health supervision and anticipatory guidance in adult myotonic dystrophy type 1C Gagnon, M C Chouinard, L Laberge, et al.
Genetics and Molecular Biology|December 3, 2020
XRCC4 rs28360071 intronic variant is associated with increased risk for infant acute lymphoblastic leukemia with KMT2A rearrangementsOrlando Louzada-Neto, Bruno A Lopes, Gisele D Brisson, et al.
Gene Therapy|June 22, 2012
Efficacy and long-term safety of alipogene tiparvovec (AAV1-LPLS447X) gene therapy for lipoprotein lipase deficiency: an open-label trialD Gaudet, J Méthot, S Déry, et al.
Pageof 3