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H J Menzel

Showing results (31-40 of 58) with videos related to

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Clinical Genetics|June 1, 1981
Lecithin-cholesterol-acyltransferase deficiency: autosomal recessive transmission in a large kindredG Utermann, H J Menzel, P Dieker, et al.
Human Genetics|January 1, 1988
Genetics of the quantitative Lp(a) lipoprotein trait. I. Relation of LP(a) glycoprotein phenotypes to Lp(a) lipoprotein concentrations in plasmaG Utermann, H G Kraft, H J Menzel, et al.
American Journal of Medical Genetics|July 27, 2001
Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorderM Witsch-Baumgartner, J Loeffler, H J Menzel, et al.
Human Genetics|November 1, 1992
The apolipoprotein (a) gene: a transcribed hypervariable locus controlling plasma lipoprotein (a) concentrationH G Kraft, S Köchl, H J Menzel, et al.
The Journal of Clinical Investigation|January 1, 1989
Changes of genetic apolipoprotein phenotypes caused by liver transplantation. Implications for apolipoprotein synthesisH G Kraft, H J Menzel, F Hoppichler, et al.
The Journal of Clinical Investigation|February 1, 1986
A variant primary structure of apolipoprotein C-II in individuals of African descentH J Menzel, J P Kane, M J Malloy, et al.
Human Mutation|January 1, 1995
Apolipoprotein A-IV polymorphism in the Hungarian population: gene frequencies, effect on lipid levels, and sequence of two new variantsH J Menzel, H Dieplinger, C Sandholzer, et al.
Human Genetics|May 1, 1990
Variation in the size of human apolipoprotein(a) is due to a hypervariable region in the geneG Lindahl, E Gersdorf, H J Menzel, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 1, 1995
Apo(a) phenotypes and Lp(a) concentrations in offspring of men with and without myocardial infarction. The EARS Study. European Atherosclerosis Research StudyI C Klausen, U Beisiegel, H J Menzel, et al.
The Journal of Biological Chemistry|March 10, 1984
Human apolipoprotein A-I polymorphism. Identification of amino acid substitutions in three electrophoretic variants of the Münster-3 typeH J Menzel, G Assmann, S C Rall, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Clinical Genetics|June 1, 1981
Lecithin-cholesterol-acyltransferase deficiency: autosomal recessive transmission in a large kindredG Utermann, H J Menzel, P Dieker, et al.
Human Genetics|January 1, 1988
Genetics of the quantitative Lp(a) lipoprotein trait. I. Relation of LP(a) glycoprotein phenotypes to Lp(a) lipoprotein concentrations in plasmaG Utermann, H G Kraft, H J Menzel, et al.
American Journal of Medical Genetics|July 27, 2001
Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorderM Witsch-Baumgartner, J Loeffler, H J Menzel, et al.
Human Genetics|November 1, 1992
The apolipoprotein (a) gene: a transcribed hypervariable locus controlling plasma lipoprotein (a) concentrationH G Kraft, S Köchl, H J Menzel, et al.
The Journal of Clinical Investigation|January 1, 1989
Changes of genetic apolipoprotein phenotypes caused by liver transplantation. Implications for apolipoprotein synthesisH G Kraft, H J Menzel, F Hoppichler, et al.
The Journal of Clinical Investigation|February 1, 1986
A variant primary structure of apolipoprotein C-II in individuals of African descentH J Menzel, J P Kane, M J Malloy, et al.
Human Mutation|January 1, 1995
Apolipoprotein A-IV polymorphism in the Hungarian population: gene frequencies, effect on lipid levels, and sequence of two new variantsH J Menzel, H Dieplinger, C Sandholzer, et al.
Human Genetics|May 1, 1990
Variation in the size of human apolipoprotein(a) is due to a hypervariable region in the geneG Lindahl, E Gersdorf, H J Menzel, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 1, 1995
Apo(a) phenotypes and Lp(a) concentrations in offspring of men with and without myocardial infarction. The EARS Study. European Atherosclerosis Research StudyI C Klausen, U Beisiegel, H J Menzel, et al.
The Journal of Biological Chemistry|March 10, 1984
Human apolipoprotein A-I polymorphism. Identification of amino acid substitutions in three electrophoretic variants of the Münster-3 typeH J Menzel, G Assmann, S C Rall, et al.
Pageof 6