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V Gieselmann

Showing results (61-70 of 87) with videos related to

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Neurochemical Research|August 23, 2008
Lysosulfatide regulates the motility of a neural precursor cell line via calcium-mediated process collapseM Hans, A Pusch, L Dai, et al.
Clinical Genetics|October 1, 1992
Ring chromosome 22 and neurofibromatosisN Tommerup, M Warburg, V Gieselmann, et al.
European Journal of Pediatrics|February 1, 1991
Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophyJ Kappler, R W Watts, E Conzelmann, et al.
American Journal of Medical Genetics|August 15, 1994
Arylsulfatase A pseudodeficiency: a common polymorphism which is associated with a unique haplotypeJ Zlotogora, Y Furman-Shaharabani, S Goldenfum, et al.
Journal of Medical Genetics|September 1, 1994
A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophyJ Zlotogora, Y Furman-Shaharabani, A Harris, et al.
American Journal of Medical Genetics|March 31, 1997
Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophyJ Berger, B Löschl, H Bernheimer, et al.
Acta Biochimica Polonica|January 1, 1986
Human tartrate-inhibitable lysosomal acid phosphatase. Purification, characterization, biosynthesis and intracellular transportV Gieselmann, P Lemansky, A Hasilik, et al.
The New England Journal of Medicine|January 3, 1991
Molecular basis of different forms of metachromatic leukodystrophyA Polten, A L Fluharty, C B Fluharty, et al.
Genomics|January 15, 1994
Structure of the mouse arylsulfatase A gene and cDNAJ Kreysing, A Polten, B Hess, et al.
Biochemistry|April 2, 1998
Crystal structure of human arylsulfatase A: the aldehyde function and the metal ion at the active site suggest a novel mechanism for sulfate ester hydrolysisG Lukatela, N Krauss, K Theis, et al.
Pageof 9

Showing results (61-70 of 87) with videos related to

Sort By:
Pageof 9
Neurochemical Research|August 23, 2008
Lysosulfatide regulates the motility of a neural precursor cell line via calcium-mediated process collapseM Hans, A Pusch, L Dai, et al.
Clinical Genetics|October 1, 1992
Ring chromosome 22 and neurofibromatosisN Tommerup, M Warburg, V Gieselmann, et al.
European Journal of Pediatrics|February 1, 1991
Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophyJ Kappler, R W Watts, E Conzelmann, et al.
American Journal of Medical Genetics|August 15, 1994
Arylsulfatase A pseudodeficiency: a common polymorphism which is associated with a unique haplotypeJ Zlotogora, Y Furman-Shaharabani, S Goldenfum, et al.
Journal of Medical Genetics|September 1, 1994
A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophyJ Zlotogora, Y Furman-Shaharabani, A Harris, et al.
American Journal of Medical Genetics|March 31, 1997
Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophyJ Berger, B Löschl, H Bernheimer, et al.
Acta Biochimica Polonica|January 1, 1986
Human tartrate-inhibitable lysosomal acid phosphatase. Purification, characterization, biosynthesis and intracellular transportV Gieselmann, P Lemansky, A Hasilik, et al.
The New England Journal of Medicine|January 3, 1991
Molecular basis of different forms of metachromatic leukodystrophyA Polten, A L Fluharty, C B Fluharty, et al.
Genomics|January 15, 1994
Structure of the mouse arylsulfatase A gene and cDNAJ Kreysing, A Polten, B Hess, et al.
Biochemistry|April 2, 1998
Crystal structure of human arylsulfatase A: the aldehyde function and the metal ion at the active site suggest a novel mechanism for sulfate ester hydrolysisG Lukatela, N Krauss, K Theis, et al.
Pageof 9