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

Kevin D Foust

Showing results (11-20 of 33) with videos related to

Pageof 4
Sort By:
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 16, 2016
Self-Complementary AAV9 Gene Delivery Partially Corrects Pathology Associated with Juvenile Neuronal Ceroid Lipofuscinosis (CLN3)Megan E Bosch, Amy Aldrich, Rachel Fallet, et al.
Frontiers in Molecular Neuroscience|November 1, 2014
Intravenous AAV9 efficiently transduces myenteric neurons in neonate and juvenile miceSara E Gombash, Christopher J Cowley, Julie A Fitzgerald, et al.
Human Gene Therapy|July 31, 2012
Targeted delivery of self-complementary adeno-associated virus serotype 9 to the brain, using magnetic resonance imaging-guided focused ultrasoundEmmanuel Thévenot, Jessica F Jordão, Meaghan A O'Reilly, et al.
Human Molecular Genetics|December 22, 2011
A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mousePaul N Porensky, Chalermchai Mitrpant, Vicki L McGovern, et al.
Human Molecular Genetics|July 25, 2015
SMN expression is required in motor neurons to rescue electrophysiological deficits in the SMNΔ7 mouse model of SMAVicki L McGovern, Chitra C Iyer, W David Arnold, et al.
Human Molecular Genetics|August 16, 2015
Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMAChitra C Iyer, Vicki L McGovern, Jason D Murray, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 7, 2013
Therapeutic AAV9-mediated suppression of mutant SOD1 slows disease progression and extends survival in models of inherited ALSKevin D Foust, Desirée L Salazar, Shibi Likhite, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 23, 2013
Systemic delivery of MeCP2 rescues behavioral and cellular deficits in female mouse models of Rett syndromeSaurabh K Garg, Daniel T Lioy, Hélène Cheval, et al.
Human Gene Therapy|December 29, 2011
Adeno-associated virus serotype 9 transduction in the central nervous system of nonhuman primatesLluis Samaranch, Ernesto A Salegio, Waldy San Sebastian, et al.
Nature|July 1, 2011
A role for glia in the progression of Rett's syndromeDaniel T Lioy, Saurabh K Garg, Caitlin E Monaghan, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 16, 2016
Self-Complementary AAV9 Gene Delivery Partially Corrects Pathology Associated with Juvenile Neuronal Ceroid Lipofuscinosis (CLN3)Megan E Bosch, Amy Aldrich, Rachel Fallet, et al.
Frontiers in Molecular Neuroscience|November 1, 2014
Intravenous AAV9 efficiently transduces myenteric neurons in neonate and juvenile miceSara E Gombash, Christopher J Cowley, Julie A Fitzgerald, et al.
Human Gene Therapy|July 31, 2012
Targeted delivery of self-complementary adeno-associated virus serotype 9 to the brain, using magnetic resonance imaging-guided focused ultrasoundEmmanuel Thévenot, Jessica F Jordão, Meaghan A O'Reilly, et al.
Human Molecular Genetics|December 22, 2011
A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mousePaul N Porensky, Chalermchai Mitrpant, Vicki L McGovern, et al.
Human Molecular Genetics|July 25, 2015
SMN expression is required in motor neurons to rescue electrophysiological deficits in the SMNΔ7 mouse model of SMAVicki L McGovern, Chitra C Iyer, W David Arnold, et al.
Human Molecular Genetics|August 16, 2015
Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMAChitra C Iyer, Vicki L McGovern, Jason D Murray, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 7, 2013
Therapeutic AAV9-mediated suppression of mutant SOD1 slows disease progression and extends survival in models of inherited ALSKevin D Foust, Desirée L Salazar, Shibi Likhite, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 23, 2013
Systemic delivery of MeCP2 rescues behavioral and cellular deficits in female mouse models of Rett syndromeSaurabh K Garg, Daniel T Lioy, Hélène Cheval, et al.
Human Gene Therapy|December 29, 2011
Adeno-associated virus serotype 9 transduction in the central nervous system of nonhuman primatesLluis Samaranch, Ernesto A Salegio, Waldy San Sebastian, et al.
Nature|July 1, 2011
A role for glia in the progression of Rett's syndromeDaniel T Lioy, Saurabh K Garg, Caitlin E Monaghan, et al.
Pageof 4