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

J M Quirk

Showing results (11-20 of 25) with videos related to

Pageof 3
Sort By:
The Journal of Biological Chemistry|June 10, 1974
Isolation and relationship of human hexosaminidasesJ F Tallman, R O Brady, J M Quirk, et al.
Chemistry and Physics of Lipids|December 15, 1986
Animal and cellular models of sphingolipid storage disorders of humansA E Gal, A L Weis, J M Quirk, et al.
Neurology|August 1, 1984
Delivery of active hexosaminidase across the blood-brain barrier in ratsE A Neuwelt, J A Barranger, M A Pagel, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 23, 1996
Correction in trans for Fabry disease: expression, secretion and uptake of alpha-galactosidase A in patient-derived cells driven by a high-titer recombinant retroviral vectorJ A Medin, M Tudor, R Simovitch, et al.
The New England Journal of Medicine|July 5, 1973
Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry's diseaseR O Brady, J F Tallman, W G Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1981
Delivery of hexosaminidase A to the cerebrum after osmotic modification of the blood--brain barrierE A Neuwelt, J A Barranger, R O Brady, et al.
Gene|December 12, 1995
Structural organization and expression of the mouse gene encoding alpha-galactosidase AT Ohshima, G J Murray, J W Nagle, et al.
Biochimica Et Biophysica Acta|September 8, 1980
A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidaseP G Pentchev, A E Gal, A D Booth, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 7, 2000
Long-term enzyme correction and lipid reduction in multiple organs of primary and secondary transplanted Fabry mice receiving transduced bone marrow cellsT Takenaka, G J Murray, G Qin, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1987
Niemann-pick variant disorders: comparison of errors of cellular cholesterol homeostasis in group D and group C fibroblastsJ D Butler, M E Comly, H S Kruth, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
The Journal of Biological Chemistry|June 10, 1974
Isolation and relationship of human hexosaminidasesJ F Tallman, R O Brady, J M Quirk, et al.
Chemistry and Physics of Lipids|December 15, 1986
Animal and cellular models of sphingolipid storage disorders of humansA E Gal, A L Weis, J M Quirk, et al.
Neurology|August 1, 1984
Delivery of active hexosaminidase across the blood-brain barrier in ratsE A Neuwelt, J A Barranger, M A Pagel, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 23, 1996
Correction in trans for Fabry disease: expression, secretion and uptake of alpha-galactosidase A in patient-derived cells driven by a high-titer recombinant retroviral vectorJ A Medin, M Tudor, R Simovitch, et al.
The New England Journal of Medicine|July 5, 1973
Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry's diseaseR O Brady, J F Tallman, W G Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1981
Delivery of hexosaminidase A to the cerebrum after osmotic modification of the blood--brain barrierE A Neuwelt, J A Barranger, R O Brady, et al.
Gene|December 12, 1995
Structural organization and expression of the mouse gene encoding alpha-galactosidase AT Ohshima, G J Murray, J W Nagle, et al.
Biochimica Et Biophysica Acta|September 8, 1980
A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidaseP G Pentchev, A E Gal, A D Booth, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 7, 2000
Long-term enzyme correction and lipid reduction in multiple organs of primary and secondary transplanted Fabry mice receiving transduced bone marrow cellsT Takenaka, G J Murray, G Qin, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1987
Niemann-pick variant disorders: comparison of errors of cellular cholesterol homeostasis in group D and group C fibroblastsJ D Butler, M E Comly, H S Kruth, et al.
Pageof 3