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Jean Bennett

Showing results (91-100 of 175) with videos related to

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Investigative Ophthalmology & Visual Science|September 6, 2014
High-resolution adaptive optics retinal imaging of cellular structure in choroideremiaJessica I W Morgan, Grace Han, Eva Klinman, et al.
Frontiers in Neuroscience|June 2, 2020
Compensatory Cross-Modal Plasticity Persists After Sight RestorationTheresa G Mowad, Aimee E Willett, Mani Mahmoudian, et al.
Frontiers in Neuroscience|September 26, 2017
Evaluating Efficiencies of Dual AAV Approaches for Retinal TargetingLivia S Carvalho, Heikki T Turunen, Sarah J Wassmer, et al.
Plos One|February 6, 2013
AAV9 targets cone photoreceptors in the nonhuman primate retinaLuk H Vandenberghe, Peter Bell, Albert M Maguire, et al.
Molecular Therapy. Nucleic Acids|January 25, 2013
Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290Rob Wj Collin, Anneke I den Hollander, Saskia D van der Velde-Visser, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 6, 2002
Pharmacological regulation of protein expression from adeno-associated viral vectors in the eyeAlberto Auricchio, Victor M Rivera, Tim Clackson, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 29, 2004
Systemic but not intraocular Epo gene transfer protects the retina from light-and genetic-induced degenerationTonia S Rex, Mariacarmela Allocca, Luciano Domenici, et al.
Cell Motility and the Cytoskeleton|February 27, 2007
Accelerated mortality from hydrocephalus and pneumonia in mice with a combined deficiency of SPAG6 and SPAG16L reveals a functional interrelationship between the two central apparatus proteinsZhibing Zhang, Waixing Tang, Rong Zhou, et al.
Molecular Therapy. Methods & Clinical Development|August 29, 2022
AAV8BP2 and AAV8 transduce the mammalian cochlear lateral wall and endolymphatic sac with high efficiencyKevin Isgrig, Yasuko Ishibashi, Hyun Jae Lee, et al.
Molecular Therapy. Methods & Clinical Development|April 27, 2019
CRISPR Activation Enhances <i>In Vitro</i> Potency of AAV Vectors Driven by Tissue-Specific PromotersDevin S McDougald, Thu T Duong, Katherine C Palozola, et al.
Pageof 18

Showing results (91-100 of 175) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|September 6, 2014
High-resolution adaptive optics retinal imaging of cellular structure in choroideremiaJessica I W Morgan, Grace Han, Eva Klinman, et al.
Frontiers in Neuroscience|June 2, 2020
Compensatory Cross-Modal Plasticity Persists After Sight RestorationTheresa G Mowad, Aimee E Willett, Mani Mahmoudian, et al.
Frontiers in Neuroscience|September 26, 2017
Evaluating Efficiencies of Dual AAV Approaches for Retinal TargetingLivia S Carvalho, Heikki T Turunen, Sarah J Wassmer, et al.
Plos One|February 6, 2013
AAV9 targets cone photoreceptors in the nonhuman primate retinaLuk H Vandenberghe, Peter Bell, Albert M Maguire, et al.
Molecular Therapy. Nucleic Acids|January 25, 2013
Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290Rob Wj Collin, Anneke I den Hollander, Saskia D van der Velde-Visser, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 6, 2002
Pharmacological regulation of protein expression from adeno-associated viral vectors in the eyeAlberto Auricchio, Victor M Rivera, Tim Clackson, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 29, 2004
Systemic but not intraocular Epo gene transfer protects the retina from light-and genetic-induced degenerationTonia S Rex, Mariacarmela Allocca, Luciano Domenici, et al.
Cell Motility and the Cytoskeleton|February 27, 2007
Accelerated mortality from hydrocephalus and pneumonia in mice with a combined deficiency of SPAG6 and SPAG16L reveals a functional interrelationship between the two central apparatus proteinsZhibing Zhang, Waixing Tang, Rong Zhou, et al.
Molecular Therapy. Methods & Clinical Development|August 29, 2022
AAV8BP2 and AAV8 transduce the mammalian cochlear lateral wall and endolymphatic sac with high efficiencyKevin Isgrig, Yasuko Ishibashi, Hyun Jae Lee, et al.
Molecular Therapy. Methods & Clinical Development|April 27, 2019
CRISPR Activation Enhances <i>In Vitro</i> Potency of AAV Vectors Driven by Tissue-Specific PromotersDevin S McDougald, Thu T Duong, Katherine C Palozola, et al.
Pageof 18