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Neuromuscular Disorders : NMD|August 26, 1998
Expression of truncated utrophin improves pH recovery in exercising muscles of dystrophic mdx mice: a 31P NMR studyJ F Goudemant, N Deconinck, J M Tinsley, et al.Human Molecular Genetics|November 1, 1993
The utrophin and dystrophin genes share similarities in genomic structureM Pearce, D J Blake, J M Tinsley, et al.Neuromuscular Disorders : NMD|October 12, 2001
Non-toxic ubiquitous over-expression of utrophin in the mdx mouseR Fisher, J M Tinsley, S R Phelps, et al.The Journal of Biological Chemistry|March 28, 1997
Local transcriptional control of utrophin expression at the neuromuscular synapseA O Gramolini, C L Dennis, J M Tinsley, et al.Human Molecular Genetics|August 1, 1994
Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell linesJ N Schofield, D J Blake, C Simmons, et al.Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Induction of utrophin gene expression by heregulin in skeletal muscle cells: role of the N-box motif and GA binding proteinA O Gramolini, L M Angus, L Schaeffer, et al.Journal of Cell Science|January 1, 1995
Utrophin actin binding domain: analysis of actin binding and cellular targetingS J Winder, L Hemmings, S K Maciver, et al.Human Gene Therapy|June 12, 1999
Adenovirus-mediated utrophin gene transfer mitigates the dystrophic phenotype of mdx mouse musclesR Gilbert, J Nalbantoglu, B J Petrof, et al.The Journal of Biological Chemistry|February 14, 1998
Muscle and neural isoforms of agrin increase utrophin expression in cultured myotubes via a transcriptional regulatory mechanismA O Gramolini, E A Burton, J M Tinsley, et al.The Journal of Cell Biology|February 24, 1997
Postsynaptic abnormalities at the neuromuscular junctions of utrophin-deficient miceA E Deconinck, A C Potter, J M Tinsley, et al.Pageof 4