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Mutagenesis|December 4, 2009
How mitochondria record the effects of UV exposure and oxidative stress using human skin as a model tissueMark A Birch-Machin, Helen Swalwell
Free Radical Biology & Medicine|December 20, 2011
Investigating the role of melanin in UVA/UVB- and hydrogen peroxide-induced cellular and mitochondrial ROS production and mitochondrial DNA damage in human melanoma cellsHelen Swalwell, Jennifer Latimer, Rachel M Haywood, et al.
Archives of Neurology|June 14, 2006
Novel mitochondrial transfer RNA(Phe) gene mutation associated with late-onset neuromuscular diseaseMarcus Deschauer, Helen Swalwell, Maria Strauss, et al.
Free Radical Research|October 15, 2010
Implications of using the fluorescent probes, dihydrorhodamine 123 and 2',7'-dichlorodihydrofluorescein diacetate, for the detection of UVA-induced reactive oxygen speciesSarahjayne Boulton, Alasdair Anderson, Helen Swalwell, et al.
Free Radical Research|June 30, 2009
Direct, real-time monitoring of superoxide generation in isolated mitochondriaJames R Henderson, Helen Swalwell, Sarahjayne Boulton, et al.
Human Mutation|September 1, 2009
Pathogenic mitochondrial tRNA mutations--which mutations are inherited and why?Joanna L Elson, Helen Swalwell, Emma L Blakely, et al.
Neuromuscular Disorders : NMD|September 11, 2007
The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathyRobert McFarland, Helen Swalwell, Emma L Blakely, et al.
Archives of Neurology|March 11, 2009
A new mitochondrial transfer RNAPro gene mutation associated with myoclonic epilepsy with ragged-red fibers and other neurological featuresEmma L Blakely, S Anand Trip, Helen Swalwell, et al.
Archives of Neurology|November 10, 2010
Mitochondrial transfer RNA(Phe) mutation associated with a progressive neurodegenerative disorder characterized by psychiatric disturbance, dementia, and akinesia-rigidityTim M Young, Emma L Blakely, Helen Swalwell, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?Helen Swalwell, Emma L Blakely, Ruth Sutton, et al.
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