Elyshia McNamara

Substrate and inhibitor specificities differ between human cytosolic and mitochondrial thioredoxin reductases: Implications for development of specific inhibitors

Oliver Rackham, Anne-Marie J. Shearwood, Ross Thyer et al. · Free Radical Biology and Medicine · 2010 · 123 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +13

Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients

Steven B. Marston, Massimiliano Memo, Andrew E. Messer et al. · Human Molecular Genetics · 2013 · 82 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Mouse models of dominant ACTA1 disease recapitulate human disease and provide insight into therapies

Gianina Ravenscroft, Connie Jackaman, Scott Bringans et al. · Brain · 2011 · 69 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca2+ sensitivity

Massimiliano Memo, Man Ching Leung, Douglas G. Ward et al. · Cardiovascular Research · 2013 · 68 citations · Full text

Life Sciences, Biochemistry, Cardiology +10

A mutation in an alternative untranslated exon of hexokinase 1 associated with Hereditary Motor and Sensory Neuropathy – Russe (HMSNR)

Janina Hantke, David Chandler, R. H. M. King et al. · European Journal of Human Genetics · 2009 · 67 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15