Bas F.J. Wanschers

Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression

Elena J. Tucker, Bas F.J. Wanschers, Radek Szklarczyk et al. · PLoS Genetics · 2013 · 117 citations · Full text

Protein Function, Complex Iii Deficiency, Mitochondrial Function +15

Iterative orthology prediction uncovers new mitochondrial proteins and identifies C12orf62 as the human ortholog of COX14, a protein involved in the assembly of cytochrome coxidase

Radek Szklarczyk, Bas F.J. Wanschers, Thomas D. Cuypers et al. · Genome biology · 2012 · 94 citations · Full text

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

Radek Szklarczyk, Bas F.J. Wanschers, Leo Nijtmans et al. · Human Molecular Genetics · 2012 · 91 citations · Full text

Genetics, Molecular Biology, Pathology +20

Rab6 family proteins interact with the dynein light chain protein DYNLRB1

Bas F.J. Wanschers, Rinske van de Vorstenbosch, Mietske Wijers et al. · Cell Motility and the Cytoskeleton · 2007 · 77 citations

A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stability

Bas F.J. Wanschers, Radek Szklarczyk, Mariël A.M. van den Brand et al. · Human Molecular Genetics · 2014 · 76 citations · Full text

Protein Function, Mendelian Disorder, Complex Iii Deficiency +13