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P W Reymer

Showing results (1-10 of 18) with videos related to

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Clinical Chemistry|July 1, 1995
Apolipoprotein E genotyping on agarose gelsP W Reymer, B E Groenemeyer, R van de Burg, et al.
The Netherlands Journal of Medicine|February 1, 1993
Analysis of the Afrikaner mutation in exon 9 of the low-density lipoprotein receptor gene in a large Dutch kindred suffering from familial hypercholesterolaemiaJ C Defesche, P J Lansberg, P W Reymer, et al.
Nucleic Acids Research|November 25, 1991
HindIII-polymorphism in the LPL-gene detected by PCRT Bruin, P W Reymer, B E Groenemeyer, et al.
Human Genetics|December 1, 1993
South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch populationJ C Defesche, D E van Diermen, P J Lansberg, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 1, 1997
Ser447stop mutation in lipoprotein lipase is associated with elevated HDL cholesterol levels in normolipidemic malesJ A Kuivenhoven, B E Groenemeyer, J M Boer, et al.
Nature Genetics|May 1, 1995
A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosisP W Reymer, E Gagné, B E Groenemeyer, et al.
The Netherlands Journal of Medicine|November 1, 1996
Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->Asn; Ser251-->Cys) resulting in lipoprotein lipase (LPL) deficiencyS M Bijvoet, H Wiebusch, Y Ma, et al.
Circulation|March 14, 1998
A common mutation in the lipoprotein lipase gene (N291S) alters the lipoprotein phenotype and risk for cardiovascular disease in patients with familial hypercholesterolemiaM E Wittekoek, S N Pimstone, P W Reymer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 1, 1995
A common variant in the gene for lipoprotein lipase (Asp9-->Asn). Functional implications and prevalence in normal and hyperlipidemic subjectsF Mailly, Y Tugrul, P W Reymer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 1, 1995
Mutations in the gene for lipoprotein lipase. A cause for low HDL cholesterol levels in individuals heterozygous for familial hypercholesterolemiaS N Pimstone, S E Gagné, C Gagné, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Clinical Chemistry|July 1, 1995
Apolipoprotein E genotyping on agarose gelsP W Reymer, B E Groenemeyer, R van de Burg, et al.
The Netherlands Journal of Medicine|February 1, 1993
Analysis of the Afrikaner mutation in exon 9 of the low-density lipoprotein receptor gene in a large Dutch kindred suffering from familial hypercholesterolaemiaJ C Defesche, P J Lansberg, P W Reymer, et al.
Nucleic Acids Research|November 25, 1991
HindIII-polymorphism in the LPL-gene detected by PCRT Bruin, P W Reymer, B E Groenemeyer, et al.
Human Genetics|December 1, 1993
South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch populationJ C Defesche, D E van Diermen, P J Lansberg, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 1, 1997
Ser447stop mutation in lipoprotein lipase is associated with elevated HDL cholesterol levels in normolipidemic malesJ A Kuivenhoven, B E Groenemeyer, J M Boer, et al.
Nature Genetics|May 1, 1995
A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosisP W Reymer, E Gagné, B E Groenemeyer, et al.
The Netherlands Journal of Medicine|November 1, 1996
Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->Asn; Ser251-->Cys) resulting in lipoprotein lipase (LPL) deficiencyS M Bijvoet, H Wiebusch, Y Ma, et al.
Circulation|March 14, 1998
A common mutation in the lipoprotein lipase gene (N291S) alters the lipoprotein phenotype and risk for cardiovascular disease in patients with familial hypercholesterolemiaM E Wittekoek, S N Pimstone, P W Reymer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 1, 1995
A common variant in the gene for lipoprotein lipase (Asp9-->Asn). Functional implications and prevalence in normal and hyperlipidemic subjectsF Mailly, Y Tugrul, P W Reymer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 1, 1995
Mutations in the gene for lipoprotein lipase. A cause for low HDL cholesterol levels in individuals heterozygous for familial hypercholesterolemiaS N Pimstone, S E Gagné, C Gagné, et al.
Pageof 2