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Methods in Molecular Biology (Clifton, N.J.)
|
November 28, 2015
Systemic Gene Therapy for Targeting the CNS
Sara E Gombash, Kevin D Foust
Cell Cycle (Georgetown, Tex.)
|
December 2, 2009
Over the barrier and through the blood: to CNS delivery we go
Kevin D Foust, Brian K Kaspar
Methods in Molecular Biology (Clifton, N.J.)
|
October 29, 2011
Recombinant AAV delivery to the central nervous system
Olivier Bockstael, Kevin D Foust, Brian Kaspar, et al.
Journal of Visualized Experiments : Jove
|
November 20, 2014
Intravenous injections in neonatal mice
Sara E Gombash Lampe, Brian K Kaspar, Kevin D Foust
Current Gene Therapy
|
October 29, 2009
AAV as a gene transfer vector for the treatment of neurological disorders: novel treatment thoughts for ALS
Mark E Hester, Kevin D Foust, Rita W Kaspar, et al.
Human Gene Therapy
|
December 13, 2007
Recombinant adeno-associated virus-mediated global anterograde delivery of glial cell line-derived neurotrophic factor to the spinal cord: comparison of rubrospinal and corticospinal tracts in the rat
Kevin D Foust, Terence R Flotte, Paul J Reier, et al.
Human Gene Therapy
|
December 7, 2007
Neonatal intraperitoneal or intravenous injections of recombinant adeno-associated virus type 8 transduce dorsal root ganglia and lower motor neurons
Kevin D Foust, Amy Poirier, Christina A Pacak, et al.
Neuron
|
July 17, 2015
Endolysosomal Deficits Augment Mitochondria Pathology in Spinal Motor Neurons of Asymptomatic fALS Mice
Yuxiang Xie, Bing Zhou, Mei-Yao Lin, et al.
Nature Biotechnology
|
December 23, 2008
Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes
Kevin D Foust, Emily Nurre, Chrystal L Montgomery, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 18, 2006
Recombinant adeno-associated viral vectors as therapeutic agents to treat neurological disorders
Ronald J Mandel, Fredric P Manfredsson, Kevin D Foust, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 4
Methods in Molecular Biology (Clifton, N.J.)
|
November 28, 2015
Systemic Gene Therapy for Targeting the CNS
Sara E Gombash, Kevin D Foust
Cell Cycle (Georgetown, Tex.)
|
December 2, 2009
Over the barrier and through the blood: to CNS delivery we go
Kevin D Foust, Brian K Kaspar
Methods in Molecular Biology (Clifton, N.J.)
|
October 29, 2011
Recombinant AAV delivery to the central nervous system
Olivier Bockstael, Kevin D Foust, Brian Kaspar, et al.
Journal of Visualized Experiments : Jove
|
November 20, 2014
Intravenous injections in neonatal mice
Sara E Gombash Lampe, Brian K Kaspar, Kevin D Foust
Current Gene Therapy
|
October 29, 2009
AAV as a gene transfer vector for the treatment of neurological disorders: novel treatment thoughts for ALS
Mark E Hester, Kevin D Foust, Rita W Kaspar, et al.
Human Gene Therapy
|
December 13, 2007
Recombinant adeno-associated virus-mediated global anterograde delivery of glial cell line-derived neurotrophic factor to the spinal cord: comparison of rubrospinal and corticospinal tracts in the rat
Kevin D Foust, Terence R Flotte, Paul J Reier, et al.
Human Gene Therapy
|
December 7, 2007
Neonatal intraperitoneal or intravenous injections of recombinant adeno-associated virus type 8 transduce dorsal root ganglia and lower motor neurons
Kevin D Foust, Amy Poirier, Christina A Pacak, et al.
Neuron
|
July 17, 2015
Endolysosomal Deficits Augment Mitochondria Pathology in Spinal Motor Neurons of Asymptomatic fALS Mice
Yuxiang Xie, Bing Zhou, Mei-Yao Lin, et al.
Nature Biotechnology
|
December 23, 2008
Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes
Kevin D Foust, Emily Nurre, Chrystal L Montgomery, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 18, 2006
Recombinant adeno-associated viral vectors as therapeutic agents to treat neurological disorders
Ronald J Mandel, Fredric P Manfredsson, Kevin D Foust, et al.
Page
of 4