Items where Author is "Wells, K E"

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Number of items: 11.

Article

Betts, C A and McClorey, G and Healicon, R and Hammond, S M and Manzano, R and Muses, S and Ball, V and Godfrey, C and Merritt, T M and Westering, T and O'Donovan, L and Wells, K E and Gait, M J and Wells, D J and Tyler, D and Wood, M J (2019) Cmah-dystrophin deficient mdx mice display an accelerated cardiac phenotype that is improved following peptide-PMO exon skipping treatment. HUMAN MOLECULAR GENETICS, 28 (3). pp. 396-406.

Maffioletti, S M and Sarcar, S and Henderson, A B H and Mannhardt, I and Pinton, L and Moyle, L A and Steele-Stallard, H and Cappellari, O and Wells, K E and Ferrari, G and Mitchell, J S and Tyzack, G E and Kotiadis, V N and Khedr, M and Ragazzi, M and Wang, W and Duchen, M R and Patani, R and Zammit, P S and Wells, D J and Eschenhagen, T and Tedesco, F S (2018) Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering. Cell Reports, 23 (3). pp. 899-908.

Maffioletti, S M and Sarcar, S and Henderson, A and Mannhardt, I and Pinton, L and Moyle, L A and Steele-Stallard, H and Cappellari, O and Wells, K E and Ragazzi, M and Wang, W and Zammit, P and Wells, D J and Eschenhagen, T and Tedesco, F S (2017) GENERATION OF THREE-DIMENSIONAL HUMAN ARTIFICIAL SKELETAL MUSCLE TISSUE FROM IPS CELLS ENABLES COMPLEX DISEASE MODELLING FOR MUSCULAR DYSTROPHY. HUMAN GENE THERAPY, 28 (12). A2-A2.

Muses, S and Godfrey, C and McClorey, G and Wells, K E and Coursindel, T and Terry, R L and Betts, C and Cappellari, O and Hammond, S and O'Donovan, E and Hildyard, J C W and El Andaloussi, S and Gait, M and Wood, M and Wells, D J (2015) THE PHYSIOLOGICAL CONSEQUENCES OF DIFFERENT LEVELS OF DYSTROPHIN FOLLOWING ANTISENSE BASED EXON-SKIPPING IN THE MDX MOUSE. Neuromuscular Disorders, 25. S312-S313.

Godfrey, C and Muses, S and McClorey, G and Wells, K E and Coursindel, T and Terry, R L and Betts, C and Hammond, S and O'Donovan, L and Hildyard, J C W and El Andaloussi, S and Gait, M J and Wood, M J and Wells, D J (2015) How much dystrophin is enough: the physiological consequences of different levels of dystrophin in the mdx mouse. HUMAN MOLECULAR GENETICS, 24 (15). pp. 4225-4237.

Betts, C A and Saleh, A F and Carr, C A and Muses, S and Wells, K E and Hammond, S M and Godfrey, C and McClorey, G and Woffindale, C and Clarke, K and Wells, D J, Gait, M J and Wood, M J A (2015) Implications for Cardiac Function Following Rescue of the Dystrophic Diaphragm in a Mouse Model of Duchenne Muscular Dystrophy. Scientific Reports (Nature), 5 (11632).

van Putten, M and Terry, R L and Hulsker, M and Wells, K E and Aartsma-Rus, A and Wells, D J (2014) MUSCLE PHYSIOLOGY PROPERTIES OF MOUSE MODELS FOR DUCHENNE MUSCULAR DYSTROPHY. Neuromuscular Disorders, 24 (9-10). pp. 819-820.

Whitmore, C and Fernandez-Fuente, M and Booler, H and Parr, C and Kavishwar, M and Ashraf, A and Lacey, E and Kim, J and Terry, R and Ackroyd, M R and Wells, K E and Muntoni, F and Wells, D J and Brown, S C (2014) The transgenic expression of LARGE exacerbates the muscle phenotype of dystroglycanopathy mice. HUMAN MOLECULAR GENETICS, 23 (7). pp. 1842-1855.

van Putten, M and Terry, R and Hulsker, M and Wells, K E and Aartsma-Rus, A and Wells, D J (2013) MUSCLE PHYSIOLOGY PROPERTIES OF MOUSE MODELS FOR DUCHENNE MUSCULAR DYSTROPHY. Neuromuscular Disorders, 23 (9-10). p. 840.

Wells, K E and Muses, S and Ruberg, A and Terry, R and Shihab, N K and Wells, D J (2012) OVER EXPRESSION OF THE LARGE TRANSGENE EXACERBATES MUSCLE PATHOLOGY IN THE MDX MOUSE. Neuromuscular Disorders, 22 (9-10). p. 813.

Conference or Workshop Item

Wells, K E and Muses, S and Terry, R L and Wood, M J and Gait, M J and Wells, D J (2013) PEPTIDE-PMO INDUCED EXON-SKIPPING RESTORES MUSCLE PHYSIOLOGY IN THE MDX MOUSE. In: UNSPECIFIED.

This list was generated on Sun Feb 16 07:25:00 2020 GMT.