Xiaonan W. Wijeyeratne

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 · 118 citations · Full text

Life Sciences, Genetics, Molecular Biology +16

Gene Knockout Using Transcription Activator-like Effector Nucleases (TALENs) Reveals That Human NDUFA9 Protein Is Essential for Stabilizing the Junction between Membrane and Matrix Arms of Complex I

David A. Stroud, Luke E. Formosa, Xiaonan W. Wijeyeratne et al. · Journal of Biological Chemistry · 2012 · 84 citations · Full text

Life Sciences, Genetics, Molecular Biology +8

Deficiency in Apoptosis-Inducing Factor Recapitulates Chronic Kidney Disease via Aberrant Mitochondrial Homeostasis

Melinda T. Coughlan, Gavin C. Higgins, Tuong-Vi Nguyen et al. · Diabetes · 2016 · 58 citations · Full text

Medicine, Biochemistry, Nephrology +17

Neuronal and astrocyte dysfunction diverges from embryonic fibroblasts in the<i>Ndufs4fky/fky</i>mouse

Matthew Bird, Xiaonan W. Wijeyeratne, J.C. Komen et al. · Bioscience Reports · 2014 · 20 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17