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Human Gene Therapy
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August 14, 1999
Use of a liver-specific promoter reduces immune response to the transgene in adenoviral vectors
L Pastore, N Morral, H Zhou, et al.
Human Gene Therapy
|
January 5, 1999
High doses of a helper-dependent adenoviral vector yield supraphysiological levels of alpha1-antitrypsin with negligible toxicity
N Morral, R J Parks, H Zhou, et al.
Gene Therapy
|
November 23, 2007
Interleukin-12 inhibits liver-specific drug-inducible systems in vivo
M Reboredo, M Zabala, I Mauleon, et al.
Nature Genetics
|
February 14, 1998
Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity
G Schiedner, N Morral, R J Parks, et al.
Science (New York, N.Y.)
|
May 9, 2020
Response to Comment on "A noninteracting low-mass black hole-giant star binary system"
Todd A Thompson, Christopher S Kochanek, Krzysztof Z Stanek, et al.
Human Gene Therapy
|
March 1, 1997
Viral gene delivery to skeletal muscle: insights on maturation-dependent loss of fiber infectivity for adenovirus and herpes simplex type 1 viral vectors
W G Feero, J D Rosenblatt, J Huard, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 25, 2008
Genetic aspects and research development in haemostasis
E G Tuddenham, J Ingerslev, L Norengaard Sørensen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 8, 1998
An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene
M A Morsy, M Gu, S Motzel, et al.
Nature
|
October 27, 2012
Near-infrared background anisotropies from diffuse intrahalo light of galaxies
Asantha Cooray, Joseph Smidt, Francesco De Bernardis, et al.
Gene Therapy
|
April 16, 1998
Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles
S S Floyd, P R Clemens, M R Ontell, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 55) with videos related to
Sort By:
Page
of 6
Human Gene Therapy
|
August 14, 1999
Use of a liver-specific promoter reduces immune response to the transgene in adenoviral vectors
L Pastore, N Morral, H Zhou, et al.
Human Gene Therapy
|
January 5, 1999
High doses of a helper-dependent adenoviral vector yield supraphysiological levels of alpha1-antitrypsin with negligible toxicity
N Morral, R J Parks, H Zhou, et al.
Gene Therapy
|
November 23, 2007
Interleukin-12 inhibits liver-specific drug-inducible systems in vivo
M Reboredo, M Zabala, I Mauleon, et al.
Nature Genetics
|
February 14, 1998
Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity
G Schiedner, N Morral, R J Parks, et al.
Science (New York, N.Y.)
|
May 9, 2020
Response to Comment on "A noninteracting low-mass black hole-giant star binary system"
Todd A Thompson, Christopher S Kochanek, Krzysztof Z Stanek, et al.
Human Gene Therapy
|
March 1, 1997
Viral gene delivery to skeletal muscle: insights on maturation-dependent loss of fiber infectivity for adenovirus and herpes simplex type 1 viral vectors
W G Feero, J D Rosenblatt, J Huard, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 25, 2008
Genetic aspects and research development in haemostasis
E G Tuddenham, J Ingerslev, L Norengaard Sørensen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 8, 1998
An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene
M A Morsy, M Gu, S Motzel, et al.
Nature
|
October 27, 2012
Near-infrared background anisotropies from diffuse intrahalo light of galaxies
Asantha Cooray, Joseph Smidt, Francesco De Bernardis, et al.
Gene Therapy
|
April 16, 1998
Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles
S S Floyd, P R Clemens, M R Ontell, et al.
Page
of 6