Using a quantitative quadruple immunofluorescent assay to detect isolated Complex I deficiency
Ahmed, S.T, Hopton, S, He, L, Alston, C.L, Hargreaves, I.P, Falkous, G, Rocha, M.C, Turnbull, D.M, Taylor, R.W
Published in Neuromuscular disorders : NMD (01.03.2017)
Published in Neuromuscular disorders : NMD (01.03.2017)
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Effect of Coenzyme Q10 supplementation on mitochondrial electron transport chain activity and mitochondrial oxidative stress in Coenzyme Q10 deficient human neuronal cells
Duberley, K.E., Heales, S.J.R., Abramov, A.Y., Chalasani, A., Land, J.M., Rahman, S., Hargreaves, I.P.
Published in The international journal of biochemistry & cell biology (01.05.2014)
Published in The international journal of biochemistry & cell biology (01.05.2014)
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O03 High-dose riboflavin therapy in Brown-Vialetto-Van Laere syndrome: clinical and biochemical improvement
Foley, A.R, Broomfield, A.A, Pandraud, A, Johnson, J.O, Singleton, A.B, Hargreaves, I.P, Land, J.M, Grunewald, S, Rahman, S, Clayton, P, Houlden, H, Reilly, M.M, Muntoni, F
Published in Neuromuscular disorders : NMD (01.03.2012)
Published in Neuromuscular disorders : NMD (01.03.2012)
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Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations
Pollard, P.J., Brière, J.J., Alam, N.A., Barwell, J., Barclay, E., Wortham, N.C., Hunt, T., Mitchell, M., Olpin, S., Moat, S.J., Hargreaves, I.P., Heales, S.J., Chung, Y.L., Griffiths, J.R., Dalgleish, A., McGrath, J.A., Gleeson, M.J., Hodgson, S.V., Poulsom, R., Rustin, P., Tomlinson, I.P.M.
Published in Human molecular genetics (01.08.2005)
Published in Human molecular genetics (01.08.2005)
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M20 - Using a quantitative quadruple immunofluorescent assay to detect isolated Complex I deficiency
Ahmed, S.T., Hopton, S., He, L., Alston, C.L., Hargreaves, I.P., Falkous, G., Rocha, M.C., Turnbull, D.M., Taylor, R.W.
Published in Neuromuscular disorders : NMD (01.03.2017)
Published in Neuromuscular disorders : NMD (01.03.2017)
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Mitochondrial dysfunction in the skeletal muscle of a mouse model of Rett syndrome (RTT): implications for the disease phenotype
Gold, W A, Williamson, S L, Kaur, S, Hargreaves, I P, Land, J M, Pelka, G J, Tam, P P L, Christodoulou, J
Published in Mitochondrion (01.03.2014)
Published in Mitochondrion (01.03.2014)
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PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutations
Yao, Z, Jones, A W E, Fassone, E, Sweeney, M G, Lebiedzinska, M, Suski, J M, Wieckowski, M R, Tajeddine, N, Hargreaves, I P, Yasukawa, T, Tufo, G, Brenner, C, Kroemer, G, Rahman, S, Szabadkai, G
Published in Oncogene (16.05.2013)
Published in Oncogene (16.05.2013)
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Chlorimipramine: A novel anticancer agent with a mitochondrial target
Daley, E., Wilkie, D., Loesch, A., Hargreaves, I.P., Kendall, D.A., Pilkington, G.J., Bates, T.E.
Published in Biochemical and biophysical research communications (11.03.2005)
Published in Biochemical and biophysical research communications (11.03.2005)
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Mitochondrial defects in Rett syndrome
Gold, W.A., Williamson, S.L., Kaur, S., Gibson, J.H., Pelka, G.J., Hargreaves, I.P., Land, J.M., Tam, P.P.L., Christodoulou, J.
Published in Mitochondrion (01.09.2012)
Published in Mitochondrion (01.09.2012)
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Inhibition of mitochondrial complex IV leads to secondary loss complex II-III activity: implications for the pathogenesis and treatment of mitochondrial encephalomyopathies
Hargreaves, I P, Duncan, A J, Wu, L, Agrawal, A, Land, J M, Heales, S J R
Published in Mitochondrion (01.07.2007)
Published in Mitochondrion (01.07.2007)
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N-acetylcysteine and Unverricht-Lundborg disease: variable response and possible side effects
Edwards, M J J, Hargreaves, I P, Heales, S J R, Jones, S J, Ramachandran, V, Bhatia, K P, Sisodiya, S
Published in Neurology (12.11.2002)
Published in Neurology (12.11.2002)
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