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Molecular Genetics and Metabolism
|
November 25, 2015
Histochemical localization of palmitoyl protein thioesterase-1 activity
Joshua T Dearborn, Subramania Ramachandran, Charles Shyng, et al.
Science (New York, N.Y.)
|
July 28, 2007
AAV vector integration sites in mouse hepatocellular carcinoma
Anthony Donsante, Daniel G Miller, Yi Li, et al.
Journal of Inherited Metabolic Disease
|
February 8, 2012
Combination small molecule PPT1 mimetic and CNS-directed gene therapy as a treatment for infantile neuronal ceroid lipofuscinosis
Marie S Roberts, Shannon L Macauley, Andrew M Wong, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 5, 2017
Synergistic effects of treating the spinal cord and brain in CLN1 disease
Charles Shyng, Hemanth R Nelvagal, Joshua T Dearborn, et al.
Behavioural Brain Research
|
June 25, 2016
Behavioral deficits and cholinergic pathway abnormalities in male Sanfilippo B mice
Shih-Hsin Kan, Steven Q Le, Quang D Bui, et al.
Stem Cells (Dayton, Ohio)
|
April 26, 2008
Lentiviral-transduced human mesenchymal stem cells persistently express therapeutic levels of enzyme in a xenotransplantation model of human disease
Todd E Meyerrose, Marie Roberts, Kevin K Ohlemiller, et al.
Annals of Neurology
|
February 28, 2012
Synergistic effects of central nervous system-directed gene therapy and bone marrow transplantation in the murine model of infantile neuronal ceroid lipofuscinosis
Shannon L Macauley, Marie S Roberts, Andrew M Wong, et al.
Acta Neuropathologica Communications
|
August 10, 2018
Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis
Jenny Lange, Luke J Haslett, Emyr Lloyd-Evans, et al.
Molecular Genetics and Metabolism
|
April 28, 2004
Neonatal retroviral vector-mediated hepatic gene therapy reduces bone, joint, and cartilage disease in mucopolysaccharidosis VII mice and dogs
Robert L Mango, Lingfei Xu, Mark S Sands, et al.
Acta Neuropathologica Communications
|
November 28, 2015
Clinically early-stage CSPα mutation carrier exhibits remarkable terminal stage neuronal pathology with minimal evidence of synaptic loss
Bruno A Benitez, Nigel J Cairns, Robert E Schmidt, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 105) with videos related to
Sort By:
Page
of 11
Molecular Genetics and Metabolism
|
November 25, 2015
Histochemical localization of palmitoyl protein thioesterase-1 activity
Joshua T Dearborn, Subramania Ramachandran, Charles Shyng, et al.
Science (New York, N.Y.)
|
July 28, 2007
AAV vector integration sites in mouse hepatocellular carcinoma
Anthony Donsante, Daniel G Miller, Yi Li, et al.
Journal of Inherited Metabolic Disease
|
February 8, 2012
Combination small molecule PPT1 mimetic and CNS-directed gene therapy as a treatment for infantile neuronal ceroid lipofuscinosis
Marie S Roberts, Shannon L Macauley, Andrew M Wong, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 5, 2017
Synergistic effects of treating the spinal cord and brain in CLN1 disease
Charles Shyng, Hemanth R Nelvagal, Joshua T Dearborn, et al.
Behavioural Brain Research
|
June 25, 2016
Behavioral deficits and cholinergic pathway abnormalities in male Sanfilippo B mice
Shih-Hsin Kan, Steven Q Le, Quang D Bui, et al.
Stem Cells (Dayton, Ohio)
|
April 26, 2008
Lentiviral-transduced human mesenchymal stem cells persistently express therapeutic levels of enzyme in a xenotransplantation model of human disease
Todd E Meyerrose, Marie Roberts, Kevin K Ohlemiller, et al.
Annals of Neurology
|
February 28, 2012
Synergistic effects of central nervous system-directed gene therapy and bone marrow transplantation in the murine model of infantile neuronal ceroid lipofuscinosis
Shannon L Macauley, Marie S Roberts, Andrew M Wong, et al.
Acta Neuropathologica Communications
|
August 10, 2018
Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis
Jenny Lange, Luke J Haslett, Emyr Lloyd-Evans, et al.
Molecular Genetics and Metabolism
|
April 28, 2004
Neonatal retroviral vector-mediated hepatic gene therapy reduces bone, joint, and cartilage disease in mucopolysaccharidosis VII mice and dogs
Robert L Mango, Lingfei Xu, Mark S Sands, et al.
Acta Neuropathologica Communications
|
November 28, 2015
Clinically early-stage CSPα mutation carrier exhibits remarkable terminal stage neuronal pathology with minimal evidence of synaptic loss
Bruno A Benitez, Nigel J Cairns, Robert E Schmidt, et al.
Page
of 11