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European Neurology
|
January 1, 1994
Gene therapy prospects for Duchenne muscular dystrophy
P R Clemens, C T Caskey
Current Neurology and Neuroscience Reports
|
March 20, 2002
Progress in gene therapy for Duchenne muscular dystrophy
P R Clemens, F J Duncan
Current Opinion in Rheumatology
|
November 1, 1996
HyperCKemic, proximal muscular dystrophies and the dystrophin membrane cytoskeleton, including dystrophinopathies, sarcoglycanopathies, and merosinopathies
E P Hoffman, P R Clemens
Annals of Neurology
|
October 1, 1990
Adult phosphorylase b kinase deficiency
P R Clemens, M Yamamoto, A G Engel
Neurology
|
November 1, 1991
Mitochondrial DNA deletions in mitochondrial cytopathies: observations in 19 patients
M Yamamoto, P R Clemens, A G Engel
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 27, 2001
Transfer of full-length Dmd to the diaphragm muscle of Dmd(mdx/mdx) mice through systemic administration of plasmid DNA
F Liu, M Nishikawa, P R Clemens, et al.
Gene Therapy
|
May 29, 2009
Systemic delivery of AAV8 in utero results in gene expression in diaphragm and limb muscle: treatment implications for muscle disorders
B M Koppanati, J Li, X Xiao, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
February 27, 1993
Gene transfer therapy for heritable disease: cell and expression targeting
K Mitani, P R Clemens, A B Moseley, et al.
Human Molecular Genetics
|
November 1, 1994
Human muscle glycogenosis due to phosphorylase kinase deficiency associated with a nonsense mutation in the muscle isoform of the alpha subunit
M Wehner, P R Clemens, A G Engel, et al.
Gene Therapy
|
July 23, 2004
CTLA4Ig delivered by high-capacity adenoviral vector induces stable expression of dystrophin in mdx mouse muscle
Z Jiang, G Schiedner, S C Gilchrist, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
European Neurology
|
January 1, 1994
Gene therapy prospects for Duchenne muscular dystrophy
P R Clemens, C T Caskey
Current Neurology and Neuroscience Reports
|
March 20, 2002
Progress in gene therapy for Duchenne muscular dystrophy
P R Clemens, F J Duncan
Current Opinion in Rheumatology
|
November 1, 1996
HyperCKemic, proximal muscular dystrophies and the dystrophin membrane cytoskeleton, including dystrophinopathies, sarcoglycanopathies, and merosinopathies
E P Hoffman, P R Clemens
Annals of Neurology
|
October 1, 1990
Adult phosphorylase b kinase deficiency
P R Clemens, M Yamamoto, A G Engel
Neurology
|
November 1, 1991
Mitochondrial DNA deletions in mitochondrial cytopathies: observations in 19 patients
M Yamamoto, P R Clemens, A G Engel
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 27, 2001
Transfer of full-length Dmd to the diaphragm muscle of Dmd(mdx/mdx) mice through systemic administration of plasmid DNA
F Liu, M Nishikawa, P R Clemens, et al.
Gene Therapy
|
May 29, 2009
Systemic delivery of AAV8 in utero results in gene expression in diaphragm and limb muscle: treatment implications for muscle disorders
B M Koppanati, J Li, X Xiao, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
February 27, 1993
Gene transfer therapy for heritable disease: cell and expression targeting
K Mitani, P R Clemens, A B Moseley, et al.
Human Molecular Genetics
|
November 1, 1994
Human muscle glycogenosis due to phosphorylase kinase deficiency associated with a nonsense mutation in the muscle isoform of the alpha subunit
M Wehner, P R Clemens, A G Engel, et al.
Gene Therapy
|
July 23, 2004
CTLA4Ig delivered by high-capacity adenoviral vector induces stable expression of dystrophin in mdx mouse muscle
Z Jiang, G Schiedner, S C Gilchrist, et al.
Page
of 4