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V Gieselmann

Showing results (71-80 of 87) with videos related to

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The Journal of Biological Chemistry|August 19, 1994
Glycosylation and phosphorylation of arylsulfatase AH J Sommerlade, T Selmer, A Ingendoh, et al.
Gene Therapy|July 28, 2006
Embryonic stem cell-based reduction of central nervous system sulfatide storage in an animal model of metachromatic leukodystrophyD Klein, T Schmandt, E Muth-Köhne, et al.
American Journal of Medical Genetics|April 6, 2000
Characterization of four arylsulfatase A missense mutations G86D, Y201C, D255H, and E312D causing metachromatic leukodystrophyS Hermann, F Schestag, A Polten, et al.
Neurobiology of Disease|June 15, 2004
Specific downregulation and mistargeting of the lipid raft-associated protein MAL in a glycolipid storage disorderK Saravanan, N Schaeren-Wiemers, D Klein, et al.
Human Gene Therapy|June 12, 2001
Bone marrow stem cell gene therapy of arylsulfatase A-deficient mice, using an arylsulfatase A mutant that is hypersecreted from retrovirally transduced donor-type cellsU Matzner, F Schestag, D Hartmann, et al.
American Journal of Human Genetics|August 1, 1993
High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophyJ Kreysing, W Bohne, C Bösenberg, et al.
FEBS Letters|December 13, 1982
Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease)F Steckel, V Gieselmann, A Waheed, et al.
Journal of Inherited Metabolic Disease|September 5, 1998
Metachromatic leukodystrophy: molecular genetics and an animal modelV Gieselmann, U Matzner, B Hess, et al.
Lipids in Health and Disease|August 9, 2006
Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase geneS Franken, D Wittke, J E Mansson, et al.
The Journal of Biological Chemistry|January 15, 1989
Cloning and expression of human arylsulfatase AC Stein, V Gieselmann, J Kreysing, et al.
Pageof 9

Showing results (71-80 of 87) with videos related to

Sort By:
Pageof 9
The Journal of Biological Chemistry|August 19, 1994
Glycosylation and phosphorylation of arylsulfatase AH J Sommerlade, T Selmer, A Ingendoh, et al.
Gene Therapy|July 28, 2006
Embryonic stem cell-based reduction of central nervous system sulfatide storage in an animal model of metachromatic leukodystrophyD Klein, T Schmandt, E Muth-Köhne, et al.
American Journal of Medical Genetics|April 6, 2000
Characterization of four arylsulfatase A missense mutations G86D, Y201C, D255H, and E312D causing metachromatic leukodystrophyS Hermann, F Schestag, A Polten, et al.
Neurobiology of Disease|June 15, 2004
Specific downregulation and mistargeting of the lipid raft-associated protein MAL in a glycolipid storage disorderK Saravanan, N Schaeren-Wiemers, D Klein, et al.
Human Gene Therapy|June 12, 2001
Bone marrow stem cell gene therapy of arylsulfatase A-deficient mice, using an arylsulfatase A mutant that is hypersecreted from retrovirally transduced donor-type cellsU Matzner, F Schestag, D Hartmann, et al.
American Journal of Human Genetics|August 1, 1993
High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophyJ Kreysing, W Bohne, C Bösenberg, et al.
FEBS Letters|December 13, 1982
Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease)F Steckel, V Gieselmann, A Waheed, et al.
Journal of Inherited Metabolic Disease|September 5, 1998
Metachromatic leukodystrophy: molecular genetics and an animal modelV Gieselmann, U Matzner, B Hess, et al.
Lipids in Health and Disease|August 9, 2006
Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase geneS Franken, D Wittke, J E Mansson, et al.
The Journal of Biological Chemistry|January 15, 1989
Cloning and expression of human arylsulfatase AC Stein, V Gieselmann, J Kreysing, et al.
Pageof 9