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The Biochemical Journal|February 1, 2024
The Parkinson's disease related mutant VPS35 (D620N) amplifies the LRRK2 response to endolysosomal stressKaty R McCarron, Hannah Elcocks, Heather Mortiboys, et al.Nature Neuroscience|August 18, 2009
Rapamycin activation of 4E-BP prevents parkinsonian dopaminergic neuron lossLuke S Tain, Heather Mortiboys, Ran N Tao, et al.Brain : a Journal of Neurology|May 15, 2009
Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio)Laura Flinn, Heather Mortiboys, Katrin Volkmann, et al.International Journal of Molecular Sciences|December 1, 2020
Peripheral Glycolysis in Neurodegenerative DiseasesSimon M Bell, Toby Burgess, James Lee, et al.Neurobiology of Aging|January 21, 2014
Superoxide dismutase 1 mutation in a cellular model of amyotrophic lateral sclerosis shifts energy generation from oxidative phosphorylation to glycolysisScott P Allen, Sandeep Rajan, Lynn Duffy, et al.The European Journal of Neuroscience|September 18, 2021
Persistent DNA damage alters the neuronal transcriptome suggesting cell cycle dysregulation and altered mitochondrial functionIrina Vazquez-Villasenor, Claire J Garwood, Julie E Simpson, et al.Scientific Reports|June 25, 2026
Variable mitochondrial phenotypes and reduced complex IV assembly factor SCO2 in LRRK2-G2019S fibroblastsRuby Wallis, Ella Simmonite, Harry Cooper, et al.Plos Genetics|November 21, 2014
The complex I subunit NDUFA10 selectively rescues Drosophila pink1 mutants through a mechanism independent of mitophagyJoe H Pogson, Rachael M Ivatt, Alvaro Sanchez-Martinez, et al.Life Science Alliance|November 30, 2021
Benchmarking a highly selective USP30 inhibitor for enhancement of mitophagy and pexophagyEmma V Rusilowicz-Jones, Francesco G Barone, Fernanda Martins Lopes, et al.Brain Research|September 30, 2018
TIGAR inclusion pathology is specific for Lewy body diseasesKarla L Robles López, Julie E Simpson, Lisa C Watson, et al.Pageof 6