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

Mark S Sands

Showing results (21-30 of 105) with videos related to

Pageof 11
Sort By:
The Journal of Biological Chemistry|October 4, 2007
Lysosomal dysfunction results in altered energy balanceJosh C Woloszynek, Trey Coleman, Clay F Semenkovich, et al.
Molecular Therapy. Methods & Clinical Development|August 1, 2015
Generation of a stable packaging cell line producing high-titer PPT-deleted integration-deficient lentiviral vectorsPeirong Hu, Yedda Li, Mark S Sands, et al.
JIMD Reports|February 19, 2017
Widespread Expression of a Membrane-Tethered Version of the Soluble Lysosomal Enzyme Palmitoyl Protein Thioesterase-1Charles Shyng, Shannon L Macauley, Joshua T Dearborn, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 28, 2005
AAV2-mediated ocular gene therapy for infantile neuronal ceroid lipofuscinosisMegan Griffey, Shannon L Macauley, Judith M Ogilvie, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 5, 2022
Preclinical studies in Krabbe disease: A model for the investigation of novel combination therapies for lysosomal storage diseasesGregory Heller, Allison M Bradbury, Mark S Sands, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 10, 2007
A murine model of infantile neuronal ceroid lipofuscinosis-ultrastructural evaluation of storage in the central nervous system and visceraNancy Galvin, Carole Vogler, Beth Levy, et al.
Journal of Clinical Apheresis|October 20, 2004
Collection of a mobilized peripheral blood apheresis product from a patient with mucopolysaccharidosis type VII and subsequent CD34+ cell isolationA Alex Hofling, Mark S Sands, Douglas M Lublin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2006
Central nervous system-directed AAV2/5-mediated gene therapy synergizes with bone marrow transplantation in the murine model of globoid-cell leukodystrophyDarshong Lin, Anthony Donsante, Shannon Macauley, et al.
The Journal of Biological Chemistry|August 25, 2009
Metabolic adaptations to interrupted glycosaminoglycan recyclingJosh C Woloszynek, Atilla Kovacs, Kevin K Ohlemiller, et al.
Plos One|June 12, 2013
Central nervous system pathology progresses independently of KC and CXCR2 in globoid-cell leukodystrophyAdarsh S Reddy, Jigisha R Patel, Carole Vogler, et al.
Pageof 11

Showing results (21-30 of 105) with videos related to

Sort By:
Pageof 11
The Journal of Biological Chemistry|October 4, 2007
Lysosomal dysfunction results in altered energy balanceJosh C Woloszynek, Trey Coleman, Clay F Semenkovich, et al.
Molecular Therapy. Methods & Clinical Development|August 1, 2015
Generation of a stable packaging cell line producing high-titer PPT-deleted integration-deficient lentiviral vectorsPeirong Hu, Yedda Li, Mark S Sands, et al.
JIMD Reports|February 19, 2017
Widespread Expression of a Membrane-Tethered Version of the Soluble Lysosomal Enzyme Palmitoyl Protein Thioesterase-1Charles Shyng, Shannon L Macauley, Joshua T Dearborn, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 28, 2005
AAV2-mediated ocular gene therapy for infantile neuronal ceroid lipofuscinosisMegan Griffey, Shannon L Macauley, Judith M Ogilvie, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 5, 2022
Preclinical studies in Krabbe disease: A model for the investigation of novel combination therapies for lysosomal storage diseasesGregory Heller, Allison M Bradbury, Mark S Sands, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 10, 2007
A murine model of infantile neuronal ceroid lipofuscinosis-ultrastructural evaluation of storage in the central nervous system and visceraNancy Galvin, Carole Vogler, Beth Levy, et al.
Journal of Clinical Apheresis|October 20, 2004
Collection of a mobilized peripheral blood apheresis product from a patient with mucopolysaccharidosis type VII and subsequent CD34+ cell isolationA Alex Hofling, Mark S Sands, Douglas M Lublin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2006
Central nervous system-directed AAV2/5-mediated gene therapy synergizes with bone marrow transplantation in the murine model of globoid-cell leukodystrophyDarshong Lin, Anthony Donsante, Shannon Macauley, et al.
The Journal of Biological Chemistry|August 25, 2009
Metabolic adaptations to interrupted glycosaminoglycan recyclingJosh C Woloszynek, Atilla Kovacs, Kevin K Ohlemiller, et al.
Plos One|June 12, 2013
Central nervous system pathology progresses independently of KC and CXCR2 in globoid-cell leukodystrophyAdarsh S Reddy, Jigisha R Patel, Carole Vogler, et al.
Pageof 11