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Gene Therapy
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November 1, 1996
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes
P R Clemens, S Kochanek, Y Sunada, et al.
Human Gene Therapy
|
July 31, 1999
Polylysine modification of adenoviral fiber protein enhances muscle cell transduction
K Bouri, W G Feero, M M Myerburg, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 16, 2001
Local high-capacity adenovirus-mediated mCTLA4Ig and mCD40Ig expression prolongs recombinant gene expression in skeletal muscle
Z L Jiang, D Reay, F Kreppel, et al.
Gene Therapy
|
September 10, 2003
Fetal muscle gene transfer is not enhanced by an RGD capsid modification to high-capacity adenoviral vectors
R Bilbao, D P Reay, T Hughes, et al.
American Journal of Human Genetics
|
November 1, 1991
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms
P R Clemens, R G Fenwick, J S Chamberlain, et al.
Gene Therapy
|
June 11, 2010
Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene
B M Koppanati, J Li, D P Reay, et al.
Gene Therapy
|
February 15, 2008
Full-length dystrophin gene transfer to the mdx mouse in utero
D P Reay, R Bilbao, B M Koppanati, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 22, 2001
Identification of a neuronal nitric oxide synthase in isolated cardiac mitochondria using electrochemical detection
A J Kanai, L L Pearce, P R Clemens, et al.
Gene Therapy
|
August 20, 2010
Inhibition of the IKK/NF-κB pathway by AAV gene transfer improves muscle regeneration in older mdx mice
Y Tang, D P Reay, M N Salay, et al.
Neurology
|
February 1, 1996
Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophy
K N North, G Miller, S T Iannaccone, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Gene Therapy
|
November 1, 1996
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes
P R Clemens, S Kochanek, Y Sunada, et al.
Human Gene Therapy
|
July 31, 1999
Polylysine modification of adenoviral fiber protein enhances muscle cell transduction
K Bouri, W G Feero, M M Myerburg, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 16, 2001
Local high-capacity adenovirus-mediated mCTLA4Ig and mCD40Ig expression prolongs recombinant gene expression in skeletal muscle
Z L Jiang, D Reay, F Kreppel, et al.
Gene Therapy
|
September 10, 2003
Fetal muscle gene transfer is not enhanced by an RGD capsid modification to high-capacity adenoviral vectors
R Bilbao, D P Reay, T Hughes, et al.
American Journal of Human Genetics
|
November 1, 1991
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms
P R Clemens, R G Fenwick, J S Chamberlain, et al.
Gene Therapy
|
June 11, 2010
Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene
B M Koppanati, J Li, D P Reay, et al.
Gene Therapy
|
February 15, 2008
Full-length dystrophin gene transfer to the mdx mouse in utero
D P Reay, R Bilbao, B M Koppanati, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 22, 2001
Identification of a neuronal nitric oxide synthase in isolated cardiac mitochondria using electrochemical detection
A J Kanai, L L Pearce, P R Clemens, et al.
Gene Therapy
|
August 20, 2010
Inhibition of the IKK/NF-κB pathway by AAV gene transfer improves muscle regeneration in older mdx mice
Y Tang, D P Reay, M N Salay, et al.
Neurology
|
February 1, 1996
Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophy
K N North, G Miller, S T Iannaccone, et al.
Page
of 4