J. Terrill

发表

Investigation of the effect of taurine supplementation on muscle taurine content in the mdx mouse model of Duchenne muscular dystrophy using chemically specific synchrotron imaging.

M. Hackett, P. Arthur, S. Webb, 2020, The Analyst.

Increasing taurine intake and taurine synthesis improves skeletal muscle function in the mdx mouse model for Duchenne muscular dystrophy

M. Grounds, P. Arthur, G. Pinniger, 2016, The Journal of physiology.

Taurine deficiency, synthesis and transport in the mdx mouse model for Duchenne Muscular Dystrophy.

M. Grounds, P. Arthur, J. Terrill, 2015, The international journal of biochemistry & cell biology.

Treatment with the cysteine precursor l-2-oxothiazolidine-4-carboxylate (OTC) implicates taurine deficiency in severity of dystropathology in mdx mice.

M. Grounds, P. Arthur, J. Terrill, 2013, The international journal of biochemistry & cell biology.

Lipid accumulation in dysferlin-deficient muscles.

M. Grounds, T. Shavlakadze, J. Papadimitriou, 2014, The American journal of pathology.

Oxidative stress and pathology in muscular dystrophies: focus on protein thiol oxidation and dysferlinopathies

M. Grounds, P. Arthur, J. Terrill, 2013, The FEBS journal.

Beneficial effects of high dose taurine treatment in juvenile dystrophic mdx mice are offset by growth restriction

M. Grounds, P. Arthur, G. Pinniger, 2017, PloS one.

Increased taurine in pre-weaned juvenile mdx mice greatly reduces the acute onset of myofibre necrosis and dystropathology and prevents inflammation

M. Grounds, P. Arthur, J. Terrill, 2016, PLoS currents.

Voluntary resistance wheel exercise from mid-life prevents sarcopenia and increases markers of mitochondrial function and autophagy in muscles of old male and female C57BL/6J mice

Robert B. White, M. Grounds, C. Mcmahon, 2016, Skeletal Muscle.

Levels of inflammation and oxidative stress, and a role for taurine in dystropathology of the Golden Retriever Muscular Dystrophy dog model for Duchenne Muscular Dystrophy

M. Grounds, P. Arthur, A. Kettle, 2016, Redox biology.

N-Acetylcysteine treatment of dystrophic mdx mice results in protein thiol modifications and inhibition of exercise induced myofibre necrosis

M. Grounds, P. Arthur, J. Terrill, 2012, Neuromuscular Disorders.

A single 30min treadmill exercise session is suitable for ‘proof-of concept studies’ in adult mdx mice: A comparison of the early consequences of two different treadmill protocols

T. Shavlakadze, M. Grounds, J. Terrill, 2012, Neuromuscular Disorders.

Screening for increased protein thiol oxidation in oxidatively stressed muscle tissue

M. Grounds, P. Arthur, J. Terrill, 2011, Free radical research.

Visualizing and quantifying oxidized protein thiols in tissue sections: a comparison of dystrophic mdx and normal skeletal mouse muscles.

M. Grounds, P. Arthur, T. Shavlakadze, 2013, Free radical biology & medicine.

Biomarkers for Duchenne muscular dystrophy: myonecrosis, inflammation and oxidative stress

M. Grounds, P. Arthur, J. Terrill, 2020, Disease Models & Mechanisms.

SHORT COMMUNICATION Lipid Accumulation in Dysferlin-Deficient Muscles

M. Grounds, T. Shavlakadze, J. Papadimitriou, 2014 .

The location of protein oxidation in dystrophic skeletal muscle from the mdx mouse model of Duchenne muscular dystrophy.

M. Grounds, Takafumi Watanabe, J. Terrill, 2022, Acta histochemica.

Dimethyl fumarate modulates the Duchenne muscular dystrophy disease program following short-term treatment in mdx mice

V. Apostolopoulos, J. D. de Haan, D. Fischer, 2022, bioRxiv.

Muscle Pathology in Dystrophic Rats and Zebrafish Is Unresponsive to Taurine Treatment, Compared to the mdx Mouse Model for Duchenne Muscular Dystrophy

R. Bryson-Richardson, M. Grounds, D. Caudal, 2023, Metabolites.

Resistance wheel exercise from mid-life has minimal effect on sciatic nerves from old mice in which sarcopenia was prevented

A. Harvey, M. Grounds, T. Shavlakadze, 2017, Biogerontology.

Oxidative damage to urinary proteins from the GRMD dog and mdx mouse as biomarkers of dystropathology in Duchenne muscular dystrophy

P. Nghiem, J. Kornegay, M. Grounds, 2020, PloS one.

Voluntary resistance wheel exercise from mid-life prevents sarcopenia and increases markers of mitochondrial function and autophagy in muscles of old male and female C57BL/6J mice

Robert B. White, M. Grounds, C. Mcmahon, 2016, Skeletal Muscle.

Three-dimensional optical coherence micro-elastography of skeletal muscle tissue.

Philip Wijesinghe, Kelsey M. Kennedy, Lixin Chin, 2014, Biomedical optics express.

Pre‐clinical evaluation of N‐acetylcysteine reveals side effects in the mdx mouse model of Duchenne muscular dystrophy

M. Grounds, P. Arthur, G. Pinniger, 2017, The Journal of physiology.

A Blood Biomarker for Duchenne Muscular Dystrophy Shows That Oxidation State of Albumin Correlates with Protein Oxidation and Damage in Mdx Muscle

M. Grounds, J. Terrill, P. Arthur, 2021, Antioxidants.

Expression patterns of regulatory RNAs, including lncRNAs and tRNAs, during postnatal growth of normal and dystrophic (mdx) mouse muscles, and their response to taurine treatment.

Robert B. White, M. Grounds, A. Filipovska, 2018, The international journal of biochemistry & cell biology.

Erratum to: Voluntary resistance wheel exercise from mid-life prevents sarcopenia and increases markers of mitochondrial function and autophagy in muscles of old male and female C57BL/6J mice

Robert B. White, M. Grounds, C. Mcmahon, 2017, Skeletal Muscle.