Glenn E. Morris

Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse

Qi Long Lu, Christopher J. Mann, Fang Lou et al. · Nature Medicine · 2003 · 388 citations

Knockout Mouse, Developmental Biology, Mdx Dystrophic Mouse +4

Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines.

T M Nguyen, J M Ellis, Donald R. Love et al. · The Journal of Cell Biology · 1991 · 259 citations · Full text

Nineteen Monoclonal Antibodies, Neuromuscular Junction, Dystrophic Skeletal Muscle +15

A novel dystrophin isoform is required for normal retinal electrophysiology

Vinita N. D'Souza, Nguyen thi Man, Glenn E. Morris et al. · Human Molecular Genetics · 1995 · 246 citations

Direct Interaction between Emerin and Lamin A

Lisa Clements, S. Manilal, Donald R. Love et al. · Biochemical and Biophysical Research Communications · 2000 · 240 citations

Protein Function, Direct Interaction, Molecular Biology +2

Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect

Tatiana Gavrilina, Vicki L. McGovern, Eileen Workman et al. · Human Molecular Genetics · 2008 · 210 citations · Full text

Genetics, Prp Results, Neuromusculoskeletal Disorder +19