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The Journal of Clinical Investigation
|
February 4, 2009
Antioxidant or neurotrophic factor treatment preserves function in a mouse model of neovascularization-associated oxidative stress
Michael I Dorrell, Edith Aguilar, Ruth Jacobson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 6, 2006
Viral delivery of glial cell line-derived neurotrophic factor improves behavior and protects striatal neurons in a mouse model of Huntington's disease
Jodi L McBride, Shilpa Ramaswamy, Mehdi Gasmi, et al.
Neurosurgery
|
April 8, 2009
Expression, bioactivity, and safety 1 year after adeno-associated viral vector type 2-mediated delivery of neurturin to the monkey nigrostriatal system support cere-120 for Parkinson's disease
Christopher D Herzog, Lamar Brown, Dawn Gammon, et al.
Neurobiology of Disease
|
May 29, 2007
AAV2-mediated delivery of human neurturin to the rat nigrostriatal system: long-term efficacy and tolerability of CERE-120 for Parkinson's disease
Mehdi Gasmi, Eugene P Brandon, Christopher D Herzog, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 30, 2008
Transgene expression, bioactivity, and safety of CERE-120 (AAV2-neurturin) following delivery to the monkey striatum
Christopher D Herzog, Biplob Dass, Mehdi Gasmi, et al.
Translational Vision Science & Technology
|
February 3, 2021
Long-Term Safety Evaluation of Continuous Intraocular Delivery of Aflibercept by the Intravitreal Gene Therapy Candidate ADVM-022 in Nonhuman Primates
Szilárd Kiss, Kristina Oresic Bender, Ruslan N Grishanin, et al.
Neurobiology of Disease
|
January 13, 2009
Intraspinal cord delivery of IGF-I mediated by adeno-associated virus 2 is neuroprotective in a rat model of familial ALS
Colin K Franz, Thais Federici, Jun Yang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 10, 2014
Forelimb treatment in a large cohort of dystrophic dogs supports delivery of a recombinant AAV for exon skipping in Duchenne patients
Caroline Le Guiner, Marie Montus, Laurent Servais, et al.
Page
of 3
Search research articles
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Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
The Journal of Clinical Investigation
|
February 4, 2009
Antioxidant or neurotrophic factor treatment preserves function in a mouse model of neovascularization-associated oxidative stress
Michael I Dorrell, Edith Aguilar, Ruth Jacobson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 6, 2006
Viral delivery of glial cell line-derived neurotrophic factor improves behavior and protects striatal neurons in a mouse model of Huntington's disease
Jodi L McBride, Shilpa Ramaswamy, Mehdi Gasmi, et al.
Neurosurgery
|
April 8, 2009
Expression, bioactivity, and safety 1 year after adeno-associated viral vector type 2-mediated delivery of neurturin to the monkey nigrostriatal system support cere-120 for Parkinson's disease
Christopher D Herzog, Lamar Brown, Dawn Gammon, et al.
Neurobiology of Disease
|
May 29, 2007
AAV2-mediated delivery of human neurturin to the rat nigrostriatal system: long-term efficacy and tolerability of CERE-120 for Parkinson's disease
Mehdi Gasmi, Eugene P Brandon, Christopher D Herzog, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 30, 2008
Transgene expression, bioactivity, and safety of CERE-120 (AAV2-neurturin) following delivery to the monkey striatum
Christopher D Herzog, Biplob Dass, Mehdi Gasmi, et al.
Translational Vision Science & Technology
|
February 3, 2021
Long-Term Safety Evaluation of Continuous Intraocular Delivery of Aflibercept by the Intravitreal Gene Therapy Candidate ADVM-022 in Nonhuman Primates
Szilárd Kiss, Kristina Oresic Bender, Ruslan N Grishanin, et al.
Neurobiology of Disease
|
January 13, 2009
Intraspinal cord delivery of IGF-I mediated by adeno-associated virus 2 is neuroprotective in a rat model of familial ALS
Colin K Franz, Thais Federici, Jun Yang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 10, 2014
Forelimb treatment in a large cohort of dystrophic dogs supports delivery of a recombinant AAV for exon skipping in Duchenne patients
Caroline Le Guiner, Marie Montus, Laurent Servais, et al.
Page
of 3