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Molecular Therapy. Methods & Clinical Development
|
August 4, 2018
Toxicology Study of Intra-Cisterna Magna Adeno-Associated Virus 9 Expressing Iduronate-2-Sulfatase in Rhesus Macaques
Juliette Hordeaux, Christian Hinderer, Tamara Goode, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
May 6, 2009
Adeno-associated virus capsid structure drives CD4-dependent CD8+ T cell response to vector encoded proteins
Lauren E Mays, Luk H Vandenberghe, Ru Xiao, et al.
Journal of Virology
|
May 18, 2023
Vector Affinity and Receptor Distribution Define Tissue-Specific Targeting in an Engineered AAV Capsid
R Alexander Martino, Qiang Wang, Hao Xu, et al.
Molecular Genetics and Metabolism
|
March 12, 2017
AAV gene therapy corrects OTC deficiency and prevents liver fibrosis in aged OTC-knock out heterozygous mice
Lili Wang, Peter Bell, Hiroki Morizono, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 13, 2005
Biology of AAV serotype vectors in liver-directed gene transfer to nonhuman primates
Guangping Gao, You Lu, Roberto Calcedo, et al.
Plos One
|
February 6, 2013
AAV9 targets cone photoreceptors in the nonhuman primate retina
Luk H Vandenberghe, Peter Bell, Albert M Maguire, et al.
Molecular Genetics and Metabolism
|
December 3, 2011
Preclinical evaluation of a clinical candidate AAV8 vector for ornithine transcarbamylase (OTC) deficiency reveals functional enzyme from each persisting vector genome
Lili Wang, Hiroki Morizono, Jianping Lin, et al.
Molecular Therapy. Methods & Clinical Development
|
August 4, 2018
Toxicology Study of Intra-Cisterna Magna Adeno-Associated Virus 9 Expressing Human Alpha-L-Iduronidase in Rhesus Macaques
Juliette Hordeaux, Christian Hinderer, Tamara Goode, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 29, 2015
Comparative Study of Liver Gene Transfer With AAV Vectors Based on Natural and Engineered AAV Capsids
Lili Wang, Peter Bell, Suryanarayan Somanathan, et al.
Nucleic Acids Research
|
December 6, 2002
Predicting the success of primer extension genotyping assays using statistical modeling
Anton Yuryev, JianPing Huang, Mark Pohl, et al.
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of 11
Search research articles
Search
Showing results (41-50 of 105) with videos related to
Sort By:
Page
of 11
Molecular Therapy. Methods & Clinical Development
|
August 4, 2018
Toxicology Study of Intra-Cisterna Magna Adeno-Associated Virus 9 Expressing Iduronate-2-Sulfatase in Rhesus Macaques
Juliette Hordeaux, Christian Hinderer, Tamara Goode, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
May 6, 2009
Adeno-associated virus capsid structure drives CD4-dependent CD8+ T cell response to vector encoded proteins
Lauren E Mays, Luk H Vandenberghe, Ru Xiao, et al.
Journal of Virology
|
May 18, 2023
Vector Affinity and Receptor Distribution Define Tissue-Specific Targeting in an Engineered AAV Capsid
R Alexander Martino, Qiang Wang, Hao Xu, et al.
Molecular Genetics and Metabolism
|
March 12, 2017
AAV gene therapy corrects OTC deficiency and prevents liver fibrosis in aged OTC-knock out heterozygous mice
Lili Wang, Peter Bell, Hiroki Morizono, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 13, 2005
Biology of AAV serotype vectors in liver-directed gene transfer to nonhuman primates
Guangping Gao, You Lu, Roberto Calcedo, et al.
Plos One
|
February 6, 2013
AAV9 targets cone photoreceptors in the nonhuman primate retina
Luk H Vandenberghe, Peter Bell, Albert M Maguire, et al.
Molecular Genetics and Metabolism
|
December 3, 2011
Preclinical evaluation of a clinical candidate AAV8 vector for ornithine transcarbamylase (OTC) deficiency reveals functional enzyme from each persisting vector genome
Lili Wang, Hiroki Morizono, Jianping Lin, et al.
Molecular Therapy. Methods & Clinical Development
|
August 4, 2018
Toxicology Study of Intra-Cisterna Magna Adeno-Associated Virus 9 Expressing Human Alpha-L-Iduronidase in Rhesus Macaques
Juliette Hordeaux, Christian Hinderer, Tamara Goode, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 29, 2015
Comparative Study of Liver Gene Transfer With AAV Vectors Based on Natural and Engineered AAV Capsids
Lili Wang, Peter Bell, Suryanarayan Somanathan, et al.
Nucleic Acids Research
|
December 6, 2002
Predicting the success of primer extension genotyping assays using statistical modeling
Anton Yuryev, JianPing Huang, Mark Pohl, et al.
Page
of 11