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R J Samulski

Showing results (71-80 of 107) with videos related to

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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.
Gene Therapy|November 20, 2003
Adeno-associated virus terminal repeat (TR) mutant generates self-complementary vectors to overcome the rate-limiting step to transduction in vivoD M McCarty, H Fu, P E Monahan, et al.
Gene Therapy|November 12, 2016
Direct interaction of human serum proteins with AAV virions to enhance AAV transduction: immediate impact on clinical applicationsM Wang, J Sun, A Crosby, et al.
Transplantation|April 13, 2000
Delivery of Cu/Zn-superoxide dismutase genes with a viral vector minimizes liver injury and improves survival after liver transplantation in the ratT G Lehmann, M D Wheeler, R Schoonhoven, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1992
Regulated high level expression of a human gamma-globin gene introduced into erythroid cells by an adeno-associated virus vectorC E Walsh, J M Liu, X Xiao, et al.
Journal of Virology|March 23, 2000
Kinetics of recombinant adeno-associated virus-mediated gene transferA K Malik, P E Monahan, D L Allen, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
Recombinant adeno-associated virus (rAAV)-mediated expression of a human gamma-globin gene in human progenitor-derived erythroid cellsJ L Miller, R E Donahue, S E Sellers, et al.
The EMBO Journal|December 1, 1991
Targeted integration of adeno-associated virus (AAV) into human chromosome 19R J Samulski, X Zhu, X Xiao, et al.
Human Gene Therapy|March 21, 2000
The use of adeno-associated virus to circumvent the maturation-dependent viral transduction of muscle fibersR Pruchnic, B Cao, Z Q Peterson, et al.
Pageof 11

Showing results (71-80 of 107) with videos related to

Sort By:
Pageof 11
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.
Gene Therapy|November 20, 2003
Adeno-associated virus terminal repeat (TR) mutant generates self-complementary vectors to overcome the rate-limiting step to transduction in vivoD M McCarty, H Fu, P E Monahan, et al.
Gene Therapy|November 12, 2016
Direct interaction of human serum proteins with AAV virions to enhance AAV transduction: immediate impact on clinical applicationsM Wang, J Sun, A Crosby, et al.
Transplantation|April 13, 2000
Delivery of Cu/Zn-superoxide dismutase genes with a viral vector minimizes liver injury and improves survival after liver transplantation in the ratT G Lehmann, M D Wheeler, R Schoonhoven, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1992
Regulated high level expression of a human gamma-globin gene introduced into erythroid cells by an adeno-associated virus vectorC E Walsh, J M Liu, X Xiao, et al.
Journal of Virology|March 23, 2000
Kinetics of recombinant adeno-associated virus-mediated gene transferA K Malik, P E Monahan, D L Allen, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
Recombinant adeno-associated virus (rAAV)-mediated expression of a human gamma-globin gene in human progenitor-derived erythroid cellsJ L Miller, R E Donahue, S E Sellers, et al.
The EMBO Journal|December 1, 1991
Targeted integration of adeno-associated virus (AAV) into human chromosome 19R J Samulski, X Zhu, X Xiao, et al.
Human Gene Therapy|March 21, 2000
The use of adeno-associated virus to circumvent the maturation-dependent viral transduction of muscle fibersR Pruchnic, B Cao, Z Q Peterson, et al.
Pageof 11