Items where Author is "Dickson, G"

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Number of items: 12.

Article

Malerba, A and Klein, P and Lu-Nguyen, N and Cappellari, O and Strings-Ufombah, V and Harbaran, S and Roelvink, P and Suhy, D and Trollet, C and Dickson, G (2019) Established PABPN1 intranuclear inclusions in OPMD muscle can be efficiently reversed by AAV-mediated knock-down and replacement of mutant expanded PABPN1. HUMAN MOLECULAR GENETICS, 28 (19). pp. 3301-3308.

Harish, P and Malerba, A and Lu-Nguyen, N and Forrest, L and Cappellari, O and Roth, F and Trollet, C and Popplewell, L and Dickson, G (2019) Inhibition of myostatin improves muscle atrophy in oculopharyngeal muscular dystrophy (OPMD). Journal of Cachexia, Sarcopenia and Muscle.

Malerba, A and Roth, F and Harish, P and Dhiab, J and Lu-Nguyen, N and Cappellari, O and Jarmin, S and Mahoudeau, A and Ythier, V and Lainé, J and Negroni, E and Abgueguen, E and Simonelig, M and Guedat, P and Mouly, V and Butler-Browne, G and Voisset, C and Dickson, G and Trollet, C (2019) Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophy. HUMAN MOLECULAR GENETICS.

Koo, T and Lu-Nguyen, N B and Malerba, A and Kim, E and Kim, D and Cappellari, O and Cho, H-Y and Dickson, G and Popplewell, L and Kim, J-S (2018) Functional rescue of dystrophin deficiency in mice caused by frameshift mutations using Campylobacter jejuni Cas9. Molecular Therapy.

Cleasby, M E and Jarmin, S and Eilers, W and Elashry, M and Andersen, D K and Dickson, G and Foster, K (2014) Local overexpression of the myostatin propeptide increases glucose transporter expression and enhances skeletal muscle glucose disposal. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 306 (7). E814-E823.

Malerba, A and Graham, I and Sharp, P and Popplewell, L and Foster, K and Wells, D J and Dickson, G (2011) Chronic Systemic Therapy With Low-dose Morpholino Oligomers Ameliorates the Pathology and Normalizes Locomotor Behavior in mdx Mice. Molecular Therapy, 19 (2). pp. 345-54.

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.

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.

Foster, K and Graham, I R and Otto, A and Foster, H and Trollet, C and Yaworsky, P J and Walsh, F S and Bickham, D and Curtin, N A and Kawar, S L and Patel, K and Dickson, G (2009) Adeno-associated virus-8-mediated intravenous transfer of myostatin propeptide leads to systemic functional improvements of slow but not fast muscle. Rejuvenation Research, 12 (2). pp. 85-94.

Matsakas, A and Foster, K and Otto, A and Macharia, R G and Elashry, M I and Feist, S and Graham, I and Foster, H and Yaworsky, P and Walsh, F and Dickson, G and Patel, K (2009) Molecular, cellular and physiological investigation of myostatin propeptide-mediated muscle growth in adult mice. Neuromuscular Disorders, 19 (7). pp. 489-499.

Foster, H and Sharp, P and Trollet, C and Athanasopoulos, T and Graham, I and Foster, K and Wells, D J and Dickson, G (2008) Codon optimisation of microdystrophin improves expression and physiological outcome in dystrophic mdx mice following AAV2/8 gene transfer. Molecular Therapy, 16 (11). pp. 1825-32.

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 Sat Dec 4 07:32:08 2021 GMT.