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

Peter Bell

Showing results (51-60 of 105) with videos related to

Pageof 11
Sort By:
Human Gene Therapy|September 19, 2012
Adeno-associated virus serotype 8 gene therapy leads to significant lowering of plasma cholesterol levels in humanized mouse models of homozygous and heterozygous familial hypercholesterolemiaSadik H Kassim, Hui Li, Peter Bell, et al.
Molecular Genetics and Metabolism|July 23, 2011
Inverse zonation of hepatocyte transduction with AAV vectors between mice and non-human primatesPeter Bell, Lili Wang, Guangping Gao, et al.
Genes & Development|July 19, 2003
Regulated recruitment of HP1 to a euchromatic gene induces mitotically heritable, epigenetic gene silencing: a mammalian cell culture model of gene variegationKasirajan Ayyanathan, Mark S Lechner, Peter Bell, et al.
Molecular Therapy. Methods & Clinical Development|July 14, 2021
Developing a second-generation clinical candidate AAV vector for gene therapy of familial hypercholesterolemiaLili Wang, Ilayaraja Muthuramu, Suryanarayan Somanathan, et al.
Molecular Therapy. Methods & Clinical Development|June 9, 2015
Widespread gene transfer in the central nervous system of cynomolgus macaques following delivery of AAV9 into the cisterna magnaChristian Hinderer, Peter Bell, Charles H Vite, et al.
Human Gene Therapy Methods|December 2, 2016
Effects of Self-Complementarity, Codon Optimization, Transgene, and Dose on Liver Transduction with AAV8Peter Bell, Lili Wang, Shu-Jen Chen, et al.
The Journal of Clinical Investigation|May 18, 2011
The AAV9 receptor and its modification to improve in vivo lung gene transfer in miceChristie L Bell, Luk H Vandenberghe, Peter Bell, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 6, 2009
The pleiotropic effects of natural AAV infections on liver-directed gene transfer in macaquesLili Wang, Roberto Calcedo, Huan Wang, et al.
Molecular Therapy. Methods & Clinical Development|December 10, 2016
Impact of intravenous infusion time on AAV8 vector pharmacokinetics, safety, and liver transduction in cynomolgus macaquesJenny A Greig, Jayme Ml Nordin, Erin Bote, et al.
Human Gene Therapy|January 31, 2023
Neonatal Fc Receptor Inhibition Enables Adeno-Associated Virus Gene Therapy Despite Pre-Existing Humoral ImmunityMakoto Horiuchi, Christian J Hinderer, Hailey N Shankle, et al.
Pageof 11

Showing results (51-60 of 105) with videos related to

Sort By:
Pageof 11
Human Gene Therapy|September 19, 2012
Adeno-associated virus serotype 8 gene therapy leads to significant lowering of plasma cholesterol levels in humanized mouse models of homozygous and heterozygous familial hypercholesterolemiaSadik H Kassim, Hui Li, Peter Bell, et al.
Molecular Genetics and Metabolism|July 23, 2011
Inverse zonation of hepatocyte transduction with AAV vectors between mice and non-human primatesPeter Bell, Lili Wang, Guangping Gao, et al.
Genes & Development|July 19, 2003
Regulated recruitment of HP1 to a euchromatic gene induces mitotically heritable, epigenetic gene silencing: a mammalian cell culture model of gene variegationKasirajan Ayyanathan, Mark S Lechner, Peter Bell, et al.
Molecular Therapy. Methods & Clinical Development|July 14, 2021
Developing a second-generation clinical candidate AAV vector for gene therapy of familial hypercholesterolemiaLili Wang, Ilayaraja Muthuramu, Suryanarayan Somanathan, et al.
Molecular Therapy. Methods & Clinical Development|June 9, 2015
Widespread gene transfer in the central nervous system of cynomolgus macaques following delivery of AAV9 into the cisterna magnaChristian Hinderer, Peter Bell, Charles H Vite, et al.
Human Gene Therapy Methods|December 2, 2016
Effects of Self-Complementarity, Codon Optimization, Transgene, and Dose on Liver Transduction with AAV8Peter Bell, Lili Wang, Shu-Jen Chen, et al.
The Journal of Clinical Investigation|May 18, 2011
The AAV9 receptor and its modification to improve in vivo lung gene transfer in miceChristie L Bell, Luk H Vandenberghe, Peter Bell, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 6, 2009
The pleiotropic effects of natural AAV infections on liver-directed gene transfer in macaquesLili Wang, Roberto Calcedo, Huan Wang, et al.
Molecular Therapy. Methods & Clinical Development|December 10, 2016
Impact of intravenous infusion time on AAV8 vector pharmacokinetics, safety, and liver transduction in cynomolgus macaquesJenny A Greig, Jayme Ml Nordin, Erin Bote, et al.
Human Gene Therapy|January 31, 2023
Neonatal Fc Receptor Inhibition Enables Adeno-Associated Virus Gene Therapy Despite Pre-Existing Humoral ImmunityMakoto Horiuchi, Christian J Hinderer, Hailey N Shankle, et al.
Pageof 11