Glenn E. Morris - Concepedia

Author

Glenn E. Morris

Also Known As

G E Morris, G. E. Morris, G.E Morris, G.E. Morris, GLENN E. MORRIS, Geraint Morris, Glenn E Morris, Glenn E. MORRIS, Glenn E. Morris, Glenn E.Morris

245

Publications

9.9K

Citations

H-Index

197

Concepts

All Affiliations

Wrexham University Keele University Robert Jones and Agnes Hunt Orthopaedic Hospital Glan Clwyd Hospital University of Sussex

About

Glenn E. Morris is an author at Wrexham University specializing in medicine, cell biology, and cytoskeleton.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	41	86	5.5K
2	Natural Sciences	17	24	883
3	Health Sciences	10	10	602
4	Engineering	5	5	291
5	Business	3	3	238

Glenn E. Morris

140

Publications

9.2K

Citations

H-Index

Page 1

	Year	Citations
Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse Qi Long Lu, Christopher J. Mann, Fang Lou, Nature Medicine Knockout MouseDevelopmental BiologyMdx Dystrophic MouseDegenerative DiseaseFunctional Amounts	2003	388
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, The Journal of Cell Biology Nineteen Monoclonal AntibodiesNeuromuscular JunctionDystrophic Skeletal MuscleSkeletal MuscleMedicine	1991	259
A novel dystrophin isoform is required for normal retinal electrophysiology Vinita N. D'Souza, Nguyen thi Man, Glenn E. Morris, Human Molecular Genetics	1995	246
Direct Interaction between Emerin and Lamin A Lisa Clements, S. Manilal, Donald R. Love, Biochemical and Biophysical Research Communications Protein FunctionDirect InteractionMolecular BiologyBiomolecular InteractionCytoskeleton	2000	240
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, Human Molecular Genetics GeneticsPrp ResultsNeuromusculoskeletal DisorderSocial SciencesPhenotypic Effect	2008	210
The Relationship between SMN, the Spinal Muscular Atrophy Protein, and Nuclear Coiled Bodies in Differentiated Tissues and Cultured Cells Philip J. Young, Thanh Le, Nguyen thi Mân, Experimental Cell Research Cultured CellsNuclear Coiled BodiesDevelopmental BiologySkeletal MuscleHuman Tissue	2000	198
Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation Emanuela Gussoni, Richard Rodney Bennett, Kristina R. Muskiewicz, Journal of Clinical Investigation Regenerative MedicineMuscle FunctionTransplantationXenotransplantationDonor Nuclei	2002	197
Massive Idiosyncratic Exon Skipping Corrects the Nonsense Mutation in Dystrophic Mouse Muscle and Produces Functional Revertant Fibers by Clonal Expansion Qi Long Lu, Glenn E. Morris, Steve D. Wilton, The Journal of Cell Biology Muscle FunctionGeneticsMdx Mice MuscleCytoskeletonProtein Genetics	2000	194
Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy Thomas M. Wishart, Chantal A. Mutsaers, Michell M. Reimer, Journal of Clinical Investigation Molecular RegulationSynaptic SignalingCellular PhysiologyTranscriptional RegulationNeuroregeneration	2014	175
The dystrophin-related protein, utrophin, is expressed on the sarcolemma of regenerating human skeletal muscle fibres in dystrophies and inflammatory myopathies Timothy R. Helliwell, Man Nguyen thi, Glenn E. Morris, Neuromuscular Disorders Skeletal MuscleSarcopeniaInflammatory MyopathiesPathologyDegenerative Disease	1992	171

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