Skye L. Mcbride
Ottawa, ON, Canada
Last Updated: 09/26/2026
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Found 8 publications
PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights.
Journal: Brain : a journal of neurology
Published: May 22, 2018
Impaired activity of CCA-adding enzyme TRNT1 impacts OXPHOS complexes and cellular respiration in SIFD patient-derived fibroblasts.
Journal: Orphanet journal of rare diseases
Published: April 06, 2016
Severe Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) Deficiency.
Journal: JIMD reports
Published: November 12, 2015
DNM1L-related mitochondrial fission defect presenting as refractory epilepsy.
Journal: European journal of human genetics : EJHG
Published: June 16, 2015
Glutaredoxin-2 is required to control oxidative phosphorylation in cardiac muscle by mediating deglutathionylation reactions.
Journal: The Journal of biological chemistry
Published: April 15, 2014
Unearthing the secrets of mitochondrial ROS and glutathione in bioenergetics.
Journal: Trends in biochemical sciences
Published: July 16, 2013
Competition of nuclear factor-erythroid 2 factors related transcription factor isoforms, Nrf1 and Nrf2, in antioxidant enzyme induction.
Journal: Redox biology
Published: December 30, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026