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Neurology|September 1, 1992
Premature chain termination mutation causing Duchenne muscular dystrophyP R Clemens, P A Ward, C T Caskey, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 11, 1996
A new adenoviral vector: Replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and beta-galactosidaseS Kochanek, P R Clemens, K Mitani, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 1997
Persistence in muscle of an adenoviral vector that lacks all viral genesH H Chen, L M Mack, R Kelly, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|August 17, 2005
Promotion of long-term heart allograft survival by combination of mobilized donor plasmacytoid dendritic cells and anti-CD154 monoclonal antibodyP Björck, P T H Coates, Z Wang, et al.
Human Gene Therapy|February 27, 1999
DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscleH H Chen, L M Mack, S Y Choi, et al.
Human Gene Therapy|November 1, 1995
Recombinant truncated dystrophin minigenes: construction, expression, and adenoviral deliveryP R Clemens, T L Krause, S Chan, et al.
Muscle & Nerve|May 22, 2001
Clinical evaluator reliability for quantitative and manual muscle testing measures of strength in childrenD M Escolar, E K Henricson, J Mayhew, et al.
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