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| Full Text | Issue Date | Title | Author(s) | | 2009 | Mitochondrial dynamics in human NADH:ubiquinone oxidoreductase deficiency. | Willems, P.H.G.M.; Smeitink, J.A.M.; Koopman, W.J.H. |
| 2009 | FXYD2 and Na,K-ATPase expression in isolated human proximal tubular cells: disturbed upregulation on renal hypomagnesemia? | Cairo, E.R.; Swarts, H.G.P.; Wilmer, M.J.G.; Willems, P.H.G.M.; Levtchenko, E.N.; Pont, J.J.H.H.M. de; Koenderink, J.B. |
| 2009 | The non-gastric H,K-ATPase as a tool to study the ouabain-binding site in Na,K-ATPase. | Pont, J.J.H.H.M. de; Swarts, H.G.P.; Karawajczyk, A.; Schaftenaar, G.; Willems, P.H.G.M.; Koenderink, J.B. |
| 2009 | Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder. | Janssen, R.J.R.J.; Distelmaier, F.; Smeets, R.J.P.; Wijnhoven, T.J.M.; Ostergaard, E.; Jaspers, N.G.; Raams, A.; Kemp, S.; Rodenburg, R.J.T.; Willems, P.H.G.M.; Heuvel, L.P.W.J. van den; Smeitink, J.A.M.; Nijtmans, L.G.J. |
| 2009 | Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency. | Hoefs, S.J.G.; Dieteren, C.E.J.; Rodenburg, R.J.T.; Naess, K.; Bruhn, H.; Wibom, R.; Wagena, E.; Willems, P.H.G.M.; Smeitink, J.A.M.; Nijtmans, L.G.J.; Heuvel, L.P.W.J. van den |
| 2009 | Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease. | Saada, A.; Vogel, R.O.; Hoefs, S.J.G.; Brand, M.A.M. van den; Wessels, H.J.; Willems, P.H.G.M.; Venselaar, H.; Shaag, A.; Barghuti, F.; Reish, O.; Shohat, M.; Huijnen, M.A.; Smeitink, J.A.M.; Heuvel, L.P.W.J. van den; Nijtmans, L.G.J. |
| 2009 | Parenteral medium-chain triglyceride-induced neutrophil activation is not mediated by a Pertussis Toxin sensitive receptor. | Versleijen, M.W.J.; Esterik, J.C. van; Schaap-Roelofs, H.M.J.; Emst-de Vries, S.E. van; Willems, P.H.G.M.; Wanten, G.J.A. |
| 2008 | Impaired routing of wild type FXYD2 after oligomerisation with FXYD2-G41R might explain the dominant nature of renal hypomagnesemia. | Cairo, E.R.; Friedrich, T.; Swarts, H.G.P.; Knoers, N.V.A.M.; Bindels, R.J.M.; Monnens, L.A.; Willems, P.H.G.M.; Pont, J.J.H.H.M. de; Koenderink, J.B. |
| 2008 | Mitochondrial Ca2+ homeostasis in human NADH:ubiquinone oxidoreductase deficiency. | Willems, P.H.G.M.; Valsecchi, F.; Distelmaier, F.; Verkaart, S.; Visch, H.J.; Smeitink, J.A.M.; Koopman, W.J.H. |
| 2008 | Life cell quantification of mitochondrial membrane potential at the single organelle level. | Distelmaier, F.; Koopman, W.J.; Testa, E.R.; Jong, AS de; Swarts, H.G.P.; Mayatepek, E.; Smeitink, J.A.M.; Willems, P.H.G.M. |
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