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Journal of Neuroscience Research
|
September 15, 2005
Lentiviral transduction of murine oligodendrocytes in vivo
Sally 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 leukodystrophy
Elizabeth 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 markers
Joshua 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 lipofuscinosis
Catherine 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 lipofuscinosis
Megan 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 architecture
Jacqueline 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-lipofuscinosis
Bruno 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 disease
Hemanth 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 activity
David 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 IIIB
Coy D Heldermon, Kevin K Ohlemiller, Erik D Herzog, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 105) with videos related to
Sort By:
Page
of 11
Journal of Neuroscience Research
|
September 15, 2005
Lentiviral transduction of murine oligodendrocytes in vivo
Sally 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 leukodystrophy
Elizabeth 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 markers
Joshua 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 lipofuscinosis
Catherine 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 lipofuscinosis
Megan 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 architecture
Jacqueline 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-lipofuscinosis
Bruno 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 disease
Hemanth 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 activity
David 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 IIIB
Coy D Heldermon, Kevin K Ohlemiller, Erik D Herzog, et al.
Page
of 11