Mitochondrial content is preserved throughout disease progression in the mdx mouse model of Duchenne muscular dystrophy, regardless of taurine supplementation

Preservation of skeletal muscle mitochondrial content in older adults: relationship between mitochondria, fibre type and high-intensity exercise training

(2017) Victoria L. Wyckelsma et al.   JOURNAL OF PHYSIOLOGY-LONDON

Mfn2 deficiency links age‐related sarcopenia and impaired autophagy to activation of an adaptive mitophagy pathway

(2016) David Sebastián et al.   EMBO JOURNAL

Cooperative and independent roles of the Drp1 adaptors Mff, MiD49 and MiD51 in mitochondrial fission

(2016) Laura D. Osellame et al.   JOURNAL OF CELL SCIENCE

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

(2016) Jessica R. Terrill et al.   JOURNAL OF PHYSIOLOGY-LONDON

Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy

(2016) David G. Allen et al.   PHYSIOLOGICAL REVIEWS

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

(2015) Jessica R. Terrill et al.   INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY

Taurine: the appeal of a safe amino acid for skeletal muscle disorders

(2015) Annamaria De Luca et al.   Journal of Translational Medicine

Metabolic Dysfunction and Altered Mitochondrial Dynamics in the Utrophin-Dystrophin Deficient Mouse Model of Duchenne Muscular Dystrophy

(2015) Meghna Pant et al.   PLoS One

Structural and functional analysis of MiD51, a dynamin receptor required for mitochondrial fission

(2014) Viviane Richter et al.   JOURNAL OF CELL BIOLOGY

Defects in Mitochondrial ATP Synthesis in Dystrophin-Deficient Mdx Skeletal Muscles May Be Caused by Complex I Insufficiency

(2014) Emma Rybalka et al.   PLoS One

L-type Ca2+ channel contributes to alterations in mitochondrial calcium handling in the mdx ventricular myocyte

(2013) Helena M. Viola et al.   AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY

Important considerations for protein analyses using antibody based techniques: down-sizing Western blotting up-sizes outcomes

(2013) Robyn M. Murphy et al.   JOURNAL OF PHYSIOLOGY-LONDON

Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission

(2013) Oliver C. Losón et al.   MOLECULAR BIOLOGY OF THE CELL

Defects in mitochondrial localization and ATP synthesis in the mdx mouse model of Duchenne muscular dystrophy are not alleviated by PDE5 inhibition

(2012) J. M. Percival et al.   HUMAN MOLECULAR GENETICS

Biomarkers of mitochondrial content in skeletal muscle of healthy young human subjects

(2012) Steen Larsen et al.   JOURNAL OF PHYSIOLOGY-LONDON

Mechanism underlying the antioxidant activity of taurine: prevention of mitochondrial oxidant production

(2011) Chian Ju Jong et al.   AMINO ACIDS

Understanding mitochondrial complex I assembly in health and disease

(2011) Masakazu Mimaki et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

Enhanced technique to measure proteins in single segments of human skeletal muscle fibers: fiber-type dependence of AMPK-α1 and -β1

(2010) Robyn M. Murphy   JOURNAL OF APPLIED PHYSIOLOGY

Evaluation of potential synergistic action of a combined treatment with alpha-methyl-prednisolone and taurine on the mdx mouse model of Duchenne muscular dystrophy

(2010) A. Cozzoli et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Are genuine changes in protein expression being overlooked? Reassessing Western blotting

(2009) Janelle P. Mollica et al.   ANALYTICAL BIOCHEMISTRY

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management

(2009) Katharine Bushby et al.   LANCET NEUROLOGY

Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy

(2008) Douglas P Millay et al.   NATURE MEDICINE

Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy

(2008) Miranda D. Grounds et al.   NEUROBIOLOGY OF DISEASE