Werner Fürst

Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene.

Dirk Schnabel, Maria Schröder, Werner Fürst et al. · Journal of Biological Chemistry · 1992 · 149 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

The human GM2 activator protein. A substrate specific cofactor of beta-hexosaminidase A

Elke Meier, Günter Schwarzmann, Werner Fürst et al. · Journal of Biological Chemistry · 1991 · 114 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +15

The Precursor of Sulfatide Activator Protein is Processed to Three Different Proteins

Werner Fürst, Werner Machleidt, Konrad Sandhoff · Biological Chemistry Hoppe-Seyler · 1988 · 112 citations

Life Sciences, Biochemistry, Molecular Biology +17

The complete amino‐acid sequences of human ganglioside GM2 activator protein and cerebroside sulfate activator protein

Werner Fürst, Jörg Schubert, Werner Machleidt et al. · European Journal of Biochemistry · 1990 · 58 citations

Life Sciences, Biochemistry, Molecular Biology +10

Hydrolysis of lactosylceramide by human galactosylceramidase and GM1‐β‐galactosidase in a detergent‐free system and its stimulation by sphingolipid activator proteins, <i>sap</i>‐B and <i>sap</i>‐C Activator proteins stimulate lactosylceramide hydrolysis

Alexandra Zschoche, Werner Fürst, Günter Schwarzmann et al. · European Journal of Biochemistry · 1994 · 51 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17