Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 291
... activity of hexosaminidase B is probably due to stimulation of lysosomes secondary to cerebral ganglioside storage , since the activities of the other lyso- somal hydrolases including ẞ - glucosidase , B - galactosidase , and acid ...
... activity of hexosaminidase B is probably due to stimulation of lysosomes secondary to cerebral ganglioside storage , since the activities of the other lyso- somal hydrolases including ẞ - glucosidase , B - galactosidase , and acid ...
Seite 433
... activity and is plotted as a function of a single oral dose of sodium warfarin on a logarithmic scale . Regression lines were fitted to the data by the method of least squares . bishydroxycoumarin ( Dicumarol ) , as well as to the ...
... activity and is plotted as a function of a single oral dose of sodium warfarin on a logarithmic scale . Regression lines were fitted to the data by the method of least squares . bishydroxycoumarin ( Dicumarol ) , as well as to the ...
Seite 434
... ACTIVITY ( % ) 40 20 NORMAL RANGE FOR PROTHROMBIN COMPLEX ACTIVITY O HOURS 1 BEFORE TREATMENT 48 HOURS AFTER TREATMENT NORMALI RESPONSE ATO 48 HOURS MEAN 35.D. AT 48 HOURS- 4 8 10 12 WARFARIN CONCENTRATION ( mg / L PLASMA ) Fig . 7 ...
... ACTIVITY ( % ) 40 20 NORMAL RANGE FOR PROTHROMBIN COMPLEX ACTIVITY O HOURS 1 BEFORE TREATMENT 48 HOURS AFTER TREATMENT NORMALI RESPONSE ATO 48 HOURS MEAN 35.D. AT 48 HOURS- 4 8 10 12 WARFARIN CONCENTRATION ( mg / L PLASMA ) Fig . 7 ...
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