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Human Mutation|January 1, 1995
Allele-specific competitive blocker PCR: a one-step method with applicability to pool screeningA Orou, B Fechner, G Utermann, et al.Human Genetics|January 1, 1988
Genetics of the quantitative Lp(a) lipoprotein trait. II. Inheritance of Lp(a) glycoprotein phenotypesG Utermann, C Duba, H J MenzelClinical Genetics|October 1, 1975
Plasma lipoprotein abnormalities in a case of primary high-density lipoprotein (HDL) deficiencyG Utermann, H J Menzel, W SchoenbornHuman Genetics|April 1, 1989
Genetics of the quantitative Lp(a) lipoprotein trait. III. Contribution of Lp(a) glycoprotein phenotypes to normal lipid variationE Boerwinkle, H J Menzel, H G Kraft, et al.Human Genetics|August 1, 1988
Human apolipoprotein A-IV polymorphism: frequency and effect on lipid and lipoprotein levelsH J Menzel, E Boerwinkle, S Schrangl-Will, et al.Human Molecular Genetics|March 21, 1998
Significant impact of the +93 C/T polymorphism in the apolipoprotein(a) gene on Lp(a) concentrations in Africans but not in Caucasians: confounding effect of linkage disequilibriumH G Kraft, M Windegger, H J Menzel, et al.Humangenetik|January 1, 1975
Lipoproteins in lecithin-cholesterol-acyltransferase(LCAT)-deficiency. II. Further studies on the abnormal high-density-lipoproteinsG Utermann, H J Menzel, K H Langer, et al.Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|March 1, 1992
Apolipoprotein (a) alleles determine lipoprotein (a) particle density and concentration in plasmaH G Kraft, C Sandholzer, H J Menzel, et al.European Journal of Biochemistry|January 1, 1980
Substitution in vitro of lecithin-cholesterol acyltransferase. Analysis of changes in plasma lipoproteinsG Utermann, H J Menzel, G Adler, et al.Clinical Genetics|June 1, 1981
Lecithin-cholesterol-acyltransferase deficiency: autosomal recessive transmission in a large kindredG Utermann, H J Menzel, P Dieker, et al.Pageof 19