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European Neurology|January 1, 1994
Gene therapy prospects for Duchenne muscular dystrophyP R Clemens, C T CaskeyPhilosophical Transactions of the Royal Society of London. Series B, Biological Sciences|February 27, 1993
Gene transfer therapy for heritable disease: cell and expression targetingK Mitani, P R Clemens, A B Moseley, et al.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.Genomics|June 1, 1994
Linkage disequilibria among (CA)n polymorphisms in the human dystrophin gene and their implications in carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophiesR Chakraborty, Y Zhong, M de Andrade, 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.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.Perspectives in Nephrology and Hypertension|January 1, 1976
Inherited biochemical defects affecting the kidneyC T CaskeyAmerican Family Physician|February 1, 1975
Identifiying inherited disease through the family historyC T CaskeyPageof 26