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Gene Therapy|November 1, 1996
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genesP R Clemens, S Kochanek, Y Sunada, et al.Human Gene Therapy|July 31, 1999
Polylysine modification of adenoviral fiber protein enhances muscle cell transductionK 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 muscleZ 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 vectorsR 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 polymorphismsP 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 geneB M Koppanati, J Li, D P Reay, et al.Gene Therapy|February 15, 2008
Full-length dystrophin gene transfer to the mdx mouse in uteroD 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 detectionA 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 miceY Tang, D P Reay, M N Salay, et al.Neurology|February 1, 1996
Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophyK N North, G Miller, S T Iannaccone, et al.Pageof 4