Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 346
... lipoprotein specificities have been identified through the use of antibodies found in the sera of multi - transfused ... lipoprotein . Low - density lipoprotein was subjected to equilibrium density gradient centrifugation and each ...
... lipoprotein specificities have been identified through the use of antibodies found in the sera of multi - transfused ... lipoprotein . Low - density lipoprotein was subjected to equilibrium density gradient centrifugation and each ...
Seite 355
... lipoprotein . Although the Lp ( a ) lipoprotein is intermediate between the low density lipoprotein and high density lipoprotein as far as flotation characteristics in the ultracentrifuge are concerned , its protein part is apparently ...
... lipoprotein . Although the Lp ( a ) lipoprotein is intermediate between the low density lipoprotein and high density lipoprotein as far as flotation characteristics in the ultracentrifuge are concerned , its protein part is apparently ...
Seite 359
... 14.66 10.31 16.97 13,68 → HDL Fig . 1. Difference indices from amino acid contents comparison between a low molecular weight HL - A preparation and serum lipoproteins . lipoprotein as well as low density lipoprotein or ẞ - THE LP SYSTEM ...
... 14.66 10.31 16.97 13,68 → HDL Fig . 1. Difference indices from amino acid contents comparison between a low molecular weight HL - A preparation and serum lipoproteins . lipoprotein as well as low density lipoprotein or ẞ - THE LP SYSTEM ...
Inhalt
Clinical geneticsGénétique clinique | 25 |
Radiation geneticsRadiations ionisantes | 38 |
Données récentes sur les taux de mutations radioinduites chez | 67 |
Urheberrecht | |
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abnormal Acad acid activity alleles analysis aneuploid anti anticoagulant anticorps antigen antipyrine autosomal biochemical bishydroxycoumarin blood cell hybrids cell lines chimerism clinical clones culture Cytogenetics deficiency dehydrogenase detected deux diagnosis dose drug metabolism effect electrophoretic enzyme assay estimate été être factors Fagerhol female fibroblasts fraction G6PD gamètes gène genetic genetic control génétique hereditary heterozygotes heterozygous hexosaminidase HL-A human chromosomes individuals inheritance isozymes karyotype Level linkage lipoprotein loci locus Lp(a Lp(a+ lymphocytes lymphoid cell male marker meiosis meiotic mental retardation mouse mutation Nature Lond Negro normal observed pairs parents patients patterns peut pharmacogenetics phenotype phenylbutazone plasma polymorphism population possible Proc produit propositus protein prothrombin Pygmies rearrangement recombination red cells sera serum sibship singletons somatic cell structure studies syndrome Table Tay-Sachs disease tests tion tissues translocations twins variants Vesell vitamin vitamin K warfarin X chromosome XX/XY