Glenn E. Morris

Robert Jones and Agnes Hunt Orthopaedic Hospital — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

58h-index9.9kcitations245works0.02yr avg
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Research Topics

Muscle Physiology and Disorders(93), RNA Research and Splicing(58), Nuclear Structure and Function(41), Cardiomyopathy and Myosin Studies(26), Monoclonal and Polyclonal Antibodies Research(26)

Publications245 total

An interaction of heart disease-associated proteins POPDC1/2 with XIRP1 in transverse tubules and intercalated discs
BMC Molecular and Cell Biology·2020· 14 citedOpen Access
Muscle cell differentiation and development pathway defects in Emery-Dreifuss muscular dystrophy
Neuromuscular Disorders·2020· 17 cited
Additional file 1 of An interaction of heart disease-associated proteins POPDC1/2 with XIRP1 in transverse tubules and intercalated discs
Figshare·2020Open Access
Nesprin-1-alpha2 associates with kinesin at myotube outer nuclear membranes, but is restricted to neuromuscular junction nuclei in adult muscle
Scientific Reports·2019· 21 citedOpen Access
Report of a TREAT-NMD/World Duchenne Organisation Meeting on Dystrophin Quantification Methodology
Journal of Neuromuscular Diseases·2019· 55 citedOpen Access
Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation
Scientific Reports·2018· 17 citedOpen Access
Congenital and Acquired Heart Disease
2018· 3 cited
Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis
Human Molecular Genetics·2017· 98 citedOpen Access
Specific localization of nesprin-1-α2, the short isoform of nesprin-1 with a KASH domain, in developing, fetal and regenerating muscle, using a new monoclonal antibody
BMC Cell Biology·2016· 31 citedOpen Access
Spinal Muscular Atrophy Patient iPSC-Derived Motor Neurons Have Reduced Expression of Proteins Important in Neuronal Development
Frontiers in Cellular Neuroscience·2016· 75 citedOpen Access
Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery–Dreifuss muscular dystrophy
Neuromuscular Disorders·2014
A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core protein in some, but not all, dystroglycanopathy patients
Neuromuscular Disorders·2014· 10 citedOpen Access
G.P.27
Neuromuscular Disorders·2014
G.P.321
Neuromuscular Disorders·2014Open Access
G.P.147
Neuromuscular Disorders·2014
Nesprins: Tissue-Specific Expression of Epsilon and Other Short Isoforms
PLoS ONE·2014· 88 citedOpen Access
Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy
Journal of Clinical Investigation·2014· 175 citedOpen Access
P22 High content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC independent pathway in myotonic dystrophy cell lines
Neuromuscular Disorders·2014· 1 cited
Characterization of 65 Epitope-Specific Dystrophin Monoclonal Antibodies in Canine and Murine Models of Duchenne Muscular Dystrophy by Immunostaining and Western Blot
PLoS ONE·2014· 25 citedOpen Access
Monoclonal antibodies for clinical trials of Duchenne muscular dystrophy therapy
Neuromuscular Disorders·2013· 4 cited
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Frequent Co-authors

Ian Holt(8), Kay E. Davies(7), Caroline A. Sewry(7), Nguyen thi Mân(6), Donald R. Love(5), Arthur H.M. Burghes(5), George Dickson(4), Philip J. Young(4), Denis Furling(4), Steve D. Wilton(3), J M Ellis(3), S. Manilal(3), Thanh Le(3), Timothy R. Helliwell(3), Qi Long Lu(2), Terence A. Partridge(2), T M Nguyen(2), Kevin C. Gatter(2), Nguyen thi Man(2), Emanuela Gussoni(2)