Browse by RVC Staff

Up a level
Export as [feed] Atom [feed] RSS
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 10.

Article

Hildyard, J C W and Finch, A M and Wells, D J (2019) Identification of qPCR reference genes suitable for normalizing gene expression in the mdx mouse model of Duchenne muscular dystrophy. PLoS One, 14 (1). e0211384.

Amoasii, L and Hildyard, J C W and Li, H and Sanchez-Ortiz, E and Mireault, A and Caballero, D and Harron, R and Stathopoulou, T-R and Massey, C A and Shelton, J M and Bassel-Duby, R and Piercy, R J and Olson, E N (2018) Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy. SCIENCE, 362 (6410). pp. 86-91.

Hildyard, J C W and Taylor-Brown, F E and Massey, C and Wells, D J and Piercy, R J (2018) Determination of qPCR Reference Genes Suitable for Normalizing Gene Expression in a Canine Model of Duchenne Muscular Dystrophy. Journal of Neuromuscular Diseases, 5 (2). pp. 177-191.

Kondori, N R and Paul, P and Robbins, J P and Liu, K and Hildyard, J C W and Wells, D J and De Belleroche, J S (2018) Focus on the Role of D-serine and D-amino Acid Oxidase in Amyotrophic Lateral Sclerosis/Motor Neuron Disease (ALS). Frontiers in Molecular Biosciences, 5 (8).

Hildyard, J C W and Rawson, F and Harron, R and Riddell, D and Massey, C A and Taylor-Brown, F E and Wells, D J and Piercy, R J (2018) CHARACTERISING THE SKELETAL MUSCLE HISTOLOGICAL PHENOTYPE OF THE DELTAE50-MD DOG, A PRECLINICAL MODEL OF DUCHENNE MUSCULAR DYSTROPHY. Neuromuscular Disorders, 28. S18.

Kondori, N R and Paul, P and Robbins, J P and Liu, K and Hildyard, J C W and Wells, D J and De Belleroche, J S (2017) Characterisation of the pathogenic effects of the in vivo expression of an ALS-linked mutation in D-amino acid oxidase: Phenotype and loss of spinal cord motor neurons. PLoS One, 12. e0188912.

Hildyard, J C W and Lacey, E and Booler, H and Hopkinson, M and Wells, D J and Brown, S C (2016) Transgenic Rescue of the LARGEmyd Mouse: A LARGE Therapeutic Window? PLoS One, 11 (7). e0159853.

Hildyard, J C W and Wells, D J (2016) Investigating synthetic oligonucleotide targeting of miR31 in Duchenne muscular dystrophy. PLoS Currents.

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.

Hildyard, J C W and Wells, D J (2014) Identification and validation of quantitative PCR reference genes suitable for normalising expression in normal and dystrophic cell culture models of myogenesis. PLoS Currents, 6.

This list was generated on Sat Dec 7 07:41:58 2019 GMT.