Search research articles
Contact Us
Filters
Showing results (71-80 of 87) with videos related to
Page
of 9
Sort By:
The Journal of Biological Chemistry
|
August 19, 1994
Glycosylation and phosphorylation of arylsulfatase A
H 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 leukodystrophy
D 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 leukodystrophy
S 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 disorder
K 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 cells
U 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 leukodystrophy
J 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 model
V 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 gene
S Franken, D Wittke, J E Mansson, et al.
The Journal of Biological Chemistry
|
January 15, 1989
Cloning and expression of human arylsulfatase A
C Stein, V Gieselmann, J Kreysing, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 87) with videos related to
Sort By:
Page
of 9
The Journal of Biological Chemistry
|
August 19, 1994
Glycosylation and phosphorylation of arylsulfatase A
H 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 leukodystrophy
D 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 leukodystrophy
S 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 disorder
K 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 cells
U 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 leukodystrophy
J 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 model
V 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 gene
S Franken, D Wittke, J E Mansson, et al.
The Journal of Biological Chemistry
|
January 15, 1989
Cloning and expression of human arylsulfatase A
C Stein, V Gieselmann, J Kreysing, et al.
Page
of 9