Items where Author is "Morgan, J E"

Up a level
Export as [feed] Atom [feed] RSS
Group by: Item Type | No Grouping
Number of items: 7.

Article

Ross, J and Benn, A and Jonuschies, J and Boldrin, L and Muntoni, F and Hewitt, J E and Brown, S C and Morgan, J E (2012) Defects in Glycosylation Impair Satellite Stem Cell Function and Niche Composition in the Muscles of the Dystrophic Largemyd Mouse. Stem Cells, 30 (10). pp. 2330-2341.

Cirak, S and Arechavala-Gomeza, V and Guglieri, M and Feng, L and Torelli, S and Anthony, K and Abbs, S and Garralda, M E and Wells, DJ and Dickson, G and Wood, M J A and Wilton, S D and Straub, V and Shrewsbury, S and Sewry, C and Morgan, J E and Bushby, K and Muntoni, F (2011) Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-esclation study. Lancet, 378 (9791). pp. 595-605.

Muses, S and Morgan, J E and Wells, D J (2011) A New Extensively Characterised Conditionally Immortal Muscle Cell-Line for Investigating Therapeutic Strategies in Muscular Dystrophies. PLoS One, 6 (9). e24826.

Muses, S and Morgan, J E and Wells, D J (2011) Restoration of dystrophin expression using the Sleeping Beauty transposon. PLoS Currents, 3.

Arechavala-Gomeza, V and Kinali, M and Feng, L and Brown, S C and Sewry, C and Morgan, J E and Muntoni, F (2010) Immunohistological intensity measurements as a tool to assess sarcolemma-associated protein expression. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 36 (4). pp. 265-74.

Kinali, M and Arechavala-Gomeza, V and Feng, L and Cirak, S and Hunt, D and Adkin, C and Guglieri, M and Ashton, E and Abbs, S and Nihoyannopoulos, P and Garralda, M E and Rutherford, M and McCulley, C and Popplewell, L and Graham, I R and Dickson, G and Wood, M J and Wells, D J and Wilton, S D and Kole, R and Staub, V and Bushby, K and Sewry, C and Morgan, J E and Muntoni, F (2009) Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-esclation, proof-of-concept study. Lancet Neurology, 8 (10). pp. 918-28.

Conference or Workshop Item

Cirak, S and Arechavala-Gomeza, V and Guglieri, M and Feng, L and Torelli, S and Anthony, K and Garralda, M E and Wells, D J and Dickson, G and Wood, M J A and Wilton, S D and Straub, V and Shrewsbury, S B and Sewry, C and Morgan, J E and Bushby, K and Muntoni, F (2011) EXON SKIPPING AND DYSTROPHIN RESTORATION IN DUCHENNE MUSCULAR DYSTROPHY PATIENTS AFTER SYSTEMIC PHOSPHORODIAMIDATE MORPHOLINO OLIGOMER TREATMENT. In: UNSPECIFIED.

This list was generated on Sun Dec 5 07:28:40 2021 GMT.