Cellular and animal models for mitochondrial complex i deficiency : A focus on the NDUFS4 subunit

by Breuer, Megan E., Willems, Peter H.G.M., Smeitink, Jan A.M., Koopman, Werner J.H., Nooteboom, Marco

Sustained accumulation of prelamin A and depletion of lamin A/C both cause oxidative stress and mitochondrial dysfunction but induce different cell fates

by Sieprath, Tom, Corne, Tobias D.J., Nooteboom, Marco, Grootaert, Charlotte, Rajkovic, Andreja, Buysschaert, Benjamin, Robijns, Joke, Broers, Jos L.V., Ramaekers, Frans C.S., Koopman, Werner J.H., Willems, Peter H.G.M., de Vos, Winnok H.

A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia

by Szklarczyk, Radek, Wanschers, Bas F.J., Nijtmans, Leo G., Rodenburg, Richard J., Zschocke, Johannes, Dikow, Nicola, Van den Brand, Mariël A.M., Hendriks-Franssen, Marthe G.M., Gilissen, Christian, Veltman, Joris A., Nooteboom, Marco, Koopman, Werner J.H., Willems, Peter H.G.M., Smeitink, Jan A.M., Huynen, Martijn A., Van den Heuvel, Lambertus P.