Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

V Gieselmann

Showing results (21-30 of 87) with videos related to

Pageof 9
Sort By:
Human Genetics|June 1, 1991
An 11-bp deletion in the arylsulfatase A gene of a patient with late infantile metachromatic leukodystrophyW Bohne, K von Figura, V Gieselmann
Annals of Neurology|March 1, 1992
Late-onset metachromatic leukodystrophy: molecular pathology in two siblingsJ Kappler, K von Figura, V Gieselmann
The EMBO Journal|June 1, 1984
Antibody to mannose 6-phosphate specific receptor induces receptor deficiency in human fibroblastsK von Figura, V Gieselmann, A Hasilik
American Journal of Human Genetics|January 1, 1995
Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic areaU Heinisch, J Zlotogora, S Kafert, et al.
Human Genetics|October 1, 1993
Simultaneous detection of the two most frequent metachromatic leukodystrophy mutationsJ Berger, B Molzer, V Gieselmann, et al.
Human Genetics|February 1, 1995
A missense mutation P136L in the arylsulfatase A gene causes instability and loss of activity of the mutant enzymeS Kafert, U Heinisch, J Zlotogora, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular genetics of metachromatic leukodystrophyV Gieselmann, A Polten, J Kreysing, et al.
Virchows Archiv : an International Journal of Pathology|August 14, 2001
Sulfatide storage in visceral organs of arylsulfatase A-deficient miceI Schott, D Hartmann, V Gieselmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation siteV Gieselmann, A Polten, J Kreysing, et al.
The Journal of Cell Biology|July 1, 1983
Biosynthesis and transport of cathepsin D in cultured human fibroblastsV Gieselmann, R Pohlmann, A Hasilik, et al.
Pageof 9

Showing results (21-30 of 87) with videos related to

Sort By:
Pageof 9
Human Genetics|June 1, 1991
An 11-bp deletion in the arylsulfatase A gene of a patient with late infantile metachromatic leukodystrophyW Bohne, K von Figura, V Gieselmann
Annals of Neurology|March 1, 1992
Late-onset metachromatic leukodystrophy: molecular pathology in two siblingsJ Kappler, K von Figura, V Gieselmann
The EMBO Journal|June 1, 1984
Antibody to mannose 6-phosphate specific receptor induces receptor deficiency in human fibroblastsK von Figura, V Gieselmann, A Hasilik
American Journal of Human Genetics|January 1, 1995
Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic areaU Heinisch, J Zlotogora, S Kafert, et al.
Human Genetics|October 1, 1993
Simultaneous detection of the two most frequent metachromatic leukodystrophy mutationsJ Berger, B Molzer, V Gieselmann, et al.
Human Genetics|February 1, 1995
A missense mutation P136L in the arylsulfatase A gene causes instability and loss of activity of the mutant enzymeS Kafert, U Heinisch, J Zlotogora, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular genetics of metachromatic leukodystrophyV Gieselmann, A Polten, J Kreysing, et al.
Virchows Archiv : an International Journal of Pathology|August 14, 2001
Sulfatide storage in visceral organs of arylsulfatase A-deficient miceI Schott, D Hartmann, V Gieselmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation siteV Gieselmann, A Polten, J Kreysing, et al.
The Journal of Cell Biology|July 1, 1983
Biosynthesis and transport of cathepsin D in cultured human fibroblastsV Gieselmann, R Pohlmann, A Hasilik, et al.
Pageof 9