DAC LEKIM

Metabolism of Sphingosine Bases, VIII. Distribution, Isolation and Properties of D-3-Oxosphinganine Reductase. Stereospecificity of the NADPH-dependent Reduction Reaction of 3-Oxodihydrosphingosine(2-Amino-1-hydroxyoctadecane-3-one)

Wilhelm Stoffel, DAC LEKIM, G Sticht · Hoppe-Seyler´s Zeitschrift für physiologische Chemie · 1968 · 60 citations

Studies on the Biosynthesis of Plasmalogens. Precursors in the Biosynthesis of Plasmalogens: On the Stereospecificity of the Biochemical Dehydrogenation of the 1-<i>O</i>-Alkyl Glyceryl to the 1-<i>O</i>-Alk-1’-enyl Glyceryl Ether Bond

Wilhelm Stoffel, DAC LEKIM · Hoppe-Seyler´s Zeitschrift für physiologische Chemie · 1971 · 53 citations

Biochemical Dehydrogenation, Biosynthesis, Engineering +8

Metabolism of Sphingosine Bases, IV. 2-Amino-1-hydroxyoctadecane-3-one (3-oxodihydrosphingosine), the Common Intermediate in the Biosynthesis of Dihydrosphingosine and Sphingosine and in the Degradation of Dihydrosphingosine

Wilhelm Stoffel, DAC LEKIM, G Sticht · Hoppe-Seyler´s Zeitschrift für physiologische Chemie · 1967 · 33 citations

Phosphatidylcholine Substrate Specificity of Lecithin: Cholesterol Acyltransferase

Gerd Assmann, Gerd Schmitz, N. Donath et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 1978 · 27 citations

Lipid Preparation, Labeled Fatty Acids, Engineering +9

Chemical synthesis of D,L-3-dehydrosphinganine, its C14-, C16- and C20-homologues and the resolution into the enantiomeric forms

G Sticht, DAC LEKIM, W. Stoffel · Chemistry and Physics of Lipids · 1972 · 10 citations

Biochemistry, Natural Sciences, Organic Chemistry +6