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Mark S Sands

Showing results (61-70 of 105) with videos related to

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Journal of Neuroscience Research|September 15, 2005
Lentiviral transduction of murine oligodendrocytes in vivoSally R McIver, Chul-Sang Lee, Jin-Moo Lee, et al.
Molecular Genetics and Metabolism|June 19, 2012
Bone marrow transplantation increases efficacy of central nervous system-directed enzyme replacement therapy in the murine model of globoid cell leukodystrophyElizabeth Y Qin, Jacqueline A Hawkins-Salsbury, Xuntian Jiang, et al.
Scientific Reports|August 5, 2015
Comprehensive functional characterization of murine infantile Batten disease including Parkinson-like behavior and dopaminergic markersJoshua T Dearborn, Steven K Harmon, Stephen C Fowler, et al.
Neurobiology of Disease|October 19, 2006
Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosisCatherine Kielar, Lucy Maddox, Ellen Bible, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 21, 2005
CNS-directed AAV2-mediated gene therapy ameliorates functional deficits in a murine model of infantile neuronal ceroid lipofuscinosisMegan A Griffey, David Wozniak, Michael Wong, et al.
Journal of Lipid Research|September 6, 2013
Psychosine, the cytotoxic sphingolipid that accumulates in globoid cell leukodystrophy, alters membrane architectureJacqueline A Hawkins-Salsbury, Archana R Parameswar, Xuntian Jiang, et al.
Plos One|November 11, 2011
Exome-sequencing confirms DNAJC5 mutations as cause of adult neuronal ceroid-lipofuscinosisBruno A Benitez, David Alvarado, Yefei Cai, et al.
Scientific Reports|September 17, 2020
Comparative proteomic profiling reveals mechanisms for early spinal cord vulnerability in CLN1 diseaseHemanth R Nelvagal, Maica Llavero Hurtado, Samantha L Eaton, et al.
Stem Cells (Dayton, Ohio)|December 7, 2007
Widespread nonhematopoietic tissue distribution by transplanted human progenitor cells with high aldehyde dehydrogenase activityDavid A Hess, Timothy P Craft, Louisa Wirthlin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 25, 2010
Therapeutic efficacy of bone marrow transplant, intracranial AAV-mediated gene therapy, or both in the mouse model of MPS IIIBCoy D Heldermon, Kevin K Ohlemiller, Erik D Herzog, et al.
Pageof 11

Showing results (61-70 of 105) with videos related to

Sort By:
Pageof 11
Journal of Neuroscience Research|September 15, 2005
Lentiviral transduction of murine oligodendrocytes in vivoSally R McIver, Chul-Sang Lee, Jin-Moo Lee, et al.
Molecular Genetics and Metabolism|June 19, 2012
Bone marrow transplantation increases efficacy of central nervous system-directed enzyme replacement therapy in the murine model of globoid cell leukodystrophyElizabeth Y Qin, Jacqueline A Hawkins-Salsbury, Xuntian Jiang, et al.
Scientific Reports|August 5, 2015
Comprehensive functional characterization of murine infantile Batten disease including Parkinson-like behavior and dopaminergic markersJoshua T Dearborn, Steven K Harmon, Stephen C Fowler, et al.
Neurobiology of Disease|October 19, 2006
Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosisCatherine Kielar, Lucy Maddox, Ellen Bible, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 21, 2005
CNS-directed AAV2-mediated gene therapy ameliorates functional deficits in a murine model of infantile neuronal ceroid lipofuscinosisMegan A Griffey, David Wozniak, Michael Wong, et al.
Journal of Lipid Research|September 6, 2013
Psychosine, the cytotoxic sphingolipid that accumulates in globoid cell leukodystrophy, alters membrane architectureJacqueline A Hawkins-Salsbury, Archana R Parameswar, Xuntian Jiang, et al.
Plos One|November 11, 2011
Exome-sequencing confirms DNAJC5 mutations as cause of adult neuronal ceroid-lipofuscinosisBruno A Benitez, David Alvarado, Yefei Cai, et al.
Scientific Reports|September 17, 2020
Comparative proteomic profiling reveals mechanisms for early spinal cord vulnerability in CLN1 diseaseHemanth R Nelvagal, Maica Llavero Hurtado, Samantha L Eaton, et al.
Stem Cells (Dayton, Ohio)|December 7, 2007
Widespread nonhematopoietic tissue distribution by transplanted human progenitor cells with high aldehyde dehydrogenase activityDavid A Hess, Timothy P Craft, Louisa Wirthlin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 25, 2010
Therapeutic efficacy of bone marrow transplant, intracranial AAV-mediated gene therapy, or both in the mouse model of MPS IIIBCoy D Heldermon, Kevin K Ohlemiller, Erik D Herzog, et al.
Pageof 11