M. Henseler

Expression of the Three Alternative Forms of the Sphingolipid Activator Protein Precursor in Baby Hamster Kidney Cells and Functional Assays in a Cell Culture System (*)

K. Sandhoff, A. Klein, M. Henseler, 1996, The Journal of Biological Chemistry.

Sphingolipid activator protein D (sap-D) stimulates the lysosomal degradation of ceramide in vivo.

K. Sandhoff, K. Suzuki, A. Klein, 1994, Biochemical and biophysical research communications.

Sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses: an immunological study

M. Baumann, K. Sandhoff, M. Haltia, 2004, Acta Neuropathologica.

Sphingolipid activator proteins (SAPs) are stored together with glycosphingolipids in the infantile neuronal ceroid-lipofuscinosis (INCL).

M. Baumann, K. Sandhoff, M. Haltia, 1995, American journal of medical genetics.

Immunological studies on sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses.

M. Baumann, K. Sandhoff, M. Haltia, 1995, Gerontology.

Analysis of a splice-site mutation in the sap-precursor gene of a patient with metachromatic leukodystrophy.

K. Sandhoff, P. Landrieu, M. Vanier, 1996, American journal of human genetics.

A non-glycosylated and functionally deficient mutant (N215H) of the sphingolipid activator protein B (SAP-B) in a novel case of metachromatic leukodystrophy (MLD)

K. Sandhoff, A. Chabás, M. Henseler, 2000, Journal of Inherited Metabolic Disease.

Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids.

N. Maeda, K. Sandhoff, B. Popko, 1996, Human molecular genetics.