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Journal of Inherited Metabolic Disease|October 2, 2003
Primary pyruvate dehydrogenase E3 binding protein deficiency with mild hyperlactataemia and hyperalaninaemiaI P Hargreaves, S J R Heales, A Briddon, et al.The International Journal of Biochemistry & Cell Biology|February 19, 2014
Effect of Coenzyme Q10 supplementation on mitochondrial electron transport chain activity and mitochondrial oxidative stress in Coenzyme Q10 deficient human neuronal cellsK E Duberley, S J R Heales, A Y Abramov, et al.Cell Death & Disease|May 27, 2016
'Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich's ataxia'R Abeti, M H Parkinson, I P Hargreaves, et al.Neurology|November 13, 2002
N-acetylcysteine and Unverricht-Lundborg disease: variable response and possible side effectsM J J Edwards, I P Hargreaves, S J R Heales, et al.Mitochondrion|March 12, 2014
Mitochondrial dysfunction in the skeletal muscle of a mouse model of Rett syndrome (RTT): implications for the disease phenotypeW A Gold, S L Williamson, S Kaur, et al.Oncogene|July 11, 2012
PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutationsZ Yao, A W E Jones, E Fassone, et al.Human Molecular Genetics|July 1, 2005
Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutationsP J Pollard, J J Brière, N A Alam, et al.Pageof 2