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J Samulski

Showing results (61-70 of 122) with videos related to

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Osteoarthritis and Cartilage|December 27, 2015
Adeno-associated virus gene therapy vector scAAVIGF-I for transduction of equine articular chondrocytes and RNA-seq analysisD D Hemphill, C W McIlwraith, R A Slayden, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 12, 2002
Neurological correction of lysosomal storage in a mucopolysaccharidosis IIIB mouse model by adeno-associated virus-mediated gene deliveryHaiyan Fu, Richard J Samulski, Thomas J McCown, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|December 1, 1993
Gene therapy for human hemoglobinopathiesC E Walsh, J M Liu, J L Miller, et al.
Blood|September 15, 1993
Single-copy transduction and expression of human gamma-globin in K562 erythroleukemia cells using recombinant adeno-associated virus vectors: the effect of mutations in NF-E2 and GATA-1 binding motifs within the hypersensitivity site 2 enhancerJ L Miller, C E Walsh, P A Ney, et al.
Brain Research|May 9, 1997
Adeno-associated virus (AAV) vector antisense gene transfer in vivo decreases GABA(A) alpha1 containing receptors and increases inferior collicular seizure sensitivityX Xiao, T J McCown, J Li, et al.
Journal of Neurovirology|January 7, 1998
Efficient gene transfer into primary and immortalized human fetal glial cells using adeno-associated virus vectors: establishment of a glial cell line with a functional CD4 receptorS D Keir, J Miller, G Yu, et al.
Nucleic Acids Research|January 27, 2025
AAV vector transduction restriction and attenuated toxicity in hESCs via a rationally designed inverted terminal repeatLiujiang Song, Tomoko Hasegawa, Nolan J Brown, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 11, 2003
Self-complementary adeno-associated virus serotype 2 vector: global distribution and broad dispersion of AAV-mediated transgene expression in mouse brainHaiyan Fu, Joseph Muenzer, Richard J Samulski, et al.
Human Gene Therapy|August 1, 2009
Ex vivo serotype-specific transduction of equine joint tissue by self-complementary adeno-associated viral vectorsL R Goodrich, V W Choi, B A Duda Carbone, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
Efficient expression of protein coding genes from the murine U1 small nuclear RNA promotersJ S Bartlett, M Sethna, L Ramamurthy, et al.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
Osteoarthritis and Cartilage|December 27, 2015
Adeno-associated virus gene therapy vector scAAVIGF-I for transduction of equine articular chondrocytes and RNA-seq analysisD D Hemphill, C W McIlwraith, R A Slayden, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 12, 2002
Neurological correction of lysosomal storage in a mucopolysaccharidosis IIIB mouse model by adeno-associated virus-mediated gene deliveryHaiyan Fu, Richard J Samulski, Thomas J McCown, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|December 1, 1993
Gene therapy for human hemoglobinopathiesC E Walsh, J M Liu, J L Miller, et al.
Blood|September 15, 1993
Single-copy transduction and expression of human gamma-globin in K562 erythroleukemia cells using recombinant adeno-associated virus vectors: the effect of mutations in NF-E2 and GATA-1 binding motifs within the hypersensitivity site 2 enhancerJ L Miller, C E Walsh, P A Ney, et al.
Brain Research|May 9, 1997
Adeno-associated virus (AAV) vector antisense gene transfer in vivo decreases GABA(A) alpha1 containing receptors and increases inferior collicular seizure sensitivityX Xiao, T J McCown, J Li, et al.
Journal of Neurovirology|January 7, 1998
Efficient gene transfer into primary and immortalized human fetal glial cells using adeno-associated virus vectors: establishment of a glial cell line with a functional CD4 receptorS D Keir, J Miller, G Yu, et al.
Nucleic Acids Research|January 27, 2025
AAV vector transduction restriction and attenuated toxicity in hESCs via a rationally designed inverted terminal repeatLiujiang Song, Tomoko Hasegawa, Nolan J Brown, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 11, 2003
Self-complementary adeno-associated virus serotype 2 vector: global distribution and broad dispersion of AAV-mediated transgene expression in mouse brainHaiyan Fu, Joseph Muenzer, Richard J Samulski, et al.
Human Gene Therapy|August 1, 2009
Ex vivo serotype-specific transduction of equine joint tissue by self-complementary adeno-associated viral vectorsL R Goodrich, V W Choi, B A Duda Carbone, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
Efficient expression of protein coding genes from the murine U1 small nuclear RNA promotersJ S Bartlett, M Sethna, L Ramamurthy, et al.
Pageof 13