Koopman 2013 Abstract MiP2013
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| Koopman WJH (2013) Developing novel treatment strategies for mitochondrial disease. Mitochondr Physiol Network 18.08. |
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Koopman WJH (2013)
Event: MiP2013
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Affiliations and author contributions
1 - Dept of Biochemistry, Radboud University Medical Centre, Nijmegen, The Netherlands.
Email: [email protected]
References
- Nijtmans LGJ, Rodenburg RJ, Szklarcyk R, Willems PHGM, Koopman WJH, Smeitink JAM (2013) Assembly of OXPHOS complexes. Cell Metabolism (in press).
- Willems, P.H.G.M., Wanschers, B., Esseling, J., Szklarzyk, R., Kudla, U., Duarte I., Nooteboom, M., Forkink, M., Swarts H, Gloerich J, Nijtmans LJ, Koopman WJH, Huynen M (2013) BOLA1 is an aerobic protein that prevents mitochondrial morphology changes induced by glutathione depletion. Antioxidants and redox signaling therapeutics 18:129-138.
- Koopman WJH, Distelmaier F, Smeitink JAM, Willems PHGM (2013) OXPHOS mutations and neurodegeneration. EMBO J 32: 9-29.
- Distelmaier F, Valsecchi F, Forkink M, Van Emst-de Vries S, Swarts H, Rodenburg R, Verwiel E, Smeitink J, Willems PHGM, Koopman WJH (2012) Trolox-sensitive ROS regulate mitochondrial morphology, oxidative phosphorylation and cytosolic calcium handling in healthy cells. Antioxidants and redox signaling 17: 1657-1669.
- Koopman WJH, Willems PHGM, Smeitink JAM (2012) Monogenic mitochondrial disorders. N Eng J Med 366: 1132-1141.
- Dieteren CEJ, Gielen SCAM, Nijtmans LGJ, Smeitink JAM, Swarts HG, Brock R, Willems PHGM, Koopman WJH (2011) Solute diffusion is hindered in the mitochondrial matrix. Proc Natl Acad Sci USA 108: 8657-8662.
- Koopman WJH, Nijtmans LG, Dieteren CEJ, Roestenberg P, Valsecchi F, Smeitink JAM, Willems PHGM (2010) Mammalian mitochondrial complex I: Biogenesis, Regulation and Reactive Oxygen Species generation. Antioxidants and redox signaling 12:1431-1470.
- Distelmaier F, Koopman WJH, Van den Heuvel LW, Rodenburg RJ, Mayatepek E, Willems PHGM, Smeitink JAM (2009) Mitochondrial complex I deficiency: from organelle dysfunction to clinical disease. Brain 132: 833-842.
- Eisenberg I, Noversthern N, Itzaki Z, Becker-Cohen M, Sadeh M, Willems PHGM, Friedman N, Koopman WJH, Mitrani-Rosenbaum S (2008) Mitochondrial processes are impaired in hereditary inclusion body myopathy. Hum Mol Genet 17: 3663-3674.
