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R R Williams

Showing results (201-210 of 254) with videos related to

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Genomics|November 1, 1988
Genotyping and sequence analysis of apolipoprotein E isoformsM Emi, L L Wu, M A Robertson, et al.
Japanese Heart Journal|December 28, 1999
Familial hypercholesterolemia in Utah kindred with novel 2412-6 Ins G mutations in exon 17 of the LDL receptor geneY Nobe, M Emi, H Katsumata, et al.
Atherosclerosis|January 4, 2001
Frequency of the R3500Q mutation of the apolipoprotein B-100 gene in a sample screened clinically for familial hypercholesterolemia in HungaryA Kalina, A Császár, A E Czeizel, et al.
Journal of Human Genetics|May 12, 2000
Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalitiesL L Wu, P N Hopkins, Y Xin, et al.
Circulation|January 1, 1996
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrationsP F Jacques, A G Bostom, R R Williams, et al.
Japanese Heart Journal|December 28, 1999
Familial hypercholesterolemia in Utah kindred with novel R103W mutations in exon 4 of the LDL receptor geneH Katsumata, M Emi, Y Nobe, et al.
Annals of Human Biology|May 11, 2010
Secular trends in established and novel cardiovascular risk factors in Welsh 12-13 year olds: a comparison between 2002 and 2007N E Thomas, M Jasper, D R R Williams, et al.
Biochemical and Biophysical Research Communications|January 29, 1982
Acetylcholinesterase inhibition by the ketone transition state analog phenoxyacetone and 1-halo-3-phenoxy-2-propanonesA Dafforn, J P Neenan, C E Ash, et al.
Progress in Clinical and Biological Research|January 1, 1984
The genetic epidemiology of hypertension: a review of past studies and current results for 948 persons in 48 Utah pedigreesR R Williams, M M Dadone, S C Hunt, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|September 1, 1991
Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interactionP N Hopkins, L L Wu, M C Schumacher, et al.
Pageof 26

Showing results (201-210 of 254) with videos related to

Sort By:
Pageof 26
Genomics|November 1, 1988
Genotyping and sequence analysis of apolipoprotein E isoformsM Emi, L L Wu, M A Robertson, et al.
Japanese Heart Journal|December 28, 1999
Familial hypercholesterolemia in Utah kindred with novel 2412-6 Ins G mutations in exon 17 of the LDL receptor geneY Nobe, M Emi, H Katsumata, et al.
Atherosclerosis|January 4, 2001
Frequency of the R3500Q mutation of the apolipoprotein B-100 gene in a sample screened clinically for familial hypercholesterolemia in HungaryA Kalina, A Császár, A E Czeizel, et al.
Journal of Human Genetics|May 12, 2000
Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalitiesL L Wu, P N Hopkins, Y Xin, et al.
Circulation|January 1, 1996
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrationsP F Jacques, A G Bostom, R R Williams, et al.
Japanese Heart Journal|December 28, 1999
Familial hypercholesterolemia in Utah kindred with novel R103W mutations in exon 4 of the LDL receptor geneH Katsumata, M Emi, Y Nobe, et al.
Annals of Human Biology|May 11, 2010
Secular trends in established and novel cardiovascular risk factors in Welsh 12-13 year olds: a comparison between 2002 and 2007N E Thomas, M Jasper, D R R Williams, et al.
Biochemical and Biophysical Research Communications|January 29, 1982
Acetylcholinesterase inhibition by the ketone transition state analog phenoxyacetone and 1-halo-3-phenoxy-2-propanonesA Dafforn, J P Neenan, C E Ash, et al.
Progress in Clinical and Biological Research|January 1, 1984
The genetic epidemiology of hypertension: a review of past studies and current results for 948 persons in 48 Utah pedigreesR R Williams, M M Dadone, S C Hunt, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|September 1, 1991
Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interactionP N Hopkins, L L Wu, M C Schumacher, et al.
Pageof 26