A BamHI RFLP in the human arylsulfatase A gene

Por Polten, A., Gieselmann, V.
Publicado em 1990

Hexosaminidase--pseudodeficiency?

Por Kappler, J, Gieselmann, V, Propping, P
Publicado em 1990

Multiple mutations in a specific gene in a small geographic area: a common phenomenon?

Por Zlotogora, J., Gieselmann, V., Bach, G.
Publicado em 1996

Antibody to mannose 6-phosphate specific receptor induces receptor deficiency in human fibroblasts.

Por von Figura, K, Gieselmann, V, Hasilik, A
Publicado em 1984

Mannose 6-phosphate-specific receptor is a transmembrane protein with a C-terminal extension oriented towards the cytosol.

Por von Figura, K, Gieselmann, V, Hasilik, A
Publicado em 1985

Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic area.

Por Heinisch, U, Zlotogora, J, Kafert, S, Gieselmann, V
Publicado em 1995

Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation site.

Por Gieselmann, V, Polten, A, Kreysing, J, von Figura, K
Publicado em 1989

Recognition of human urine alpha-N-acetylglucosaminidase by rat hepatocytes. Involvement of receptors specific for galactose, mannose 6-phosphate and mannose.

Por Ullrich, K, Basner, R, Gieselmann, V, Von Figura, K
Publicado em 1979

Mutations in the arylsulfatase A pseudodeficiency allele causing metachromatic leukodystrophy.

Por Gieselmann, V, Fluharty, A L, Tønnesen, T, Von Figura, K
Publicado em 1991

Four monoclonal antibodies inhibit the recognition of arylsulphatase A by the lysosomal enzyme phosphotransferase.

Por Sommerlade, H J, Hille-Rehfeld, A, von Figura, K, Gieselmann, V
Publicado em 1994

Restoration of arylsulphatase A activity in human-metachromatic-leucodystrophy fibroblasts via retroviral-vector-mediated gene transfer.

Por Rommerskirch, W, Fluharty, A L, Peters, C, von Figura, K, Gieselmann, V
Publicado em 1991

Two new arylsulfatase A (ARSA) mutations in a juvenile metachromatic leukodystrophy (MLD) patient.

Por Fluharty, A L, Fluharty, C B, Bohne, W, von Figura, K, Gieselmann, V
Publicado em 1991

A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophy.

Por Zlotogora, J, Furman-Shaharabani, Y, Harris, A, Barth, M L, von Figura, K, Gieselmann, V
Publicado em 1994

High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophy.

Por Kreysing, J, Bohne, W, Bösenberg, C, Marchesini, S, Turpin, J C, Baumann, N, von Figura, K, Gieselmann, V
Publicado em 1993

Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase gene

Por De Deyn PP, D'Hooge R, Mansson JE, Wittke D, Franken S, Lüllmann-Rauch R, Matzner U, Gieselmann V
Publicado em 2006-08-01

Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase gene

Por Franken, S, Wittke, D, Mansson, JE, D'Hooge, R, De Deyn, PP, Lüllmann-Rauch, R, Matzner, U, Gieselmann, V
Publicado em 2006

Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease

Por Penzien, J. M., Kappler, J., Herschkowitz, N., Schuknecht, B., Leinekugel, P., Propping, P., Tønnesen, T., Lou, H., Moser, H., Zierz, S., Conzelmann, E., Gieselmann, V.
Publicado em 1993