| Role of frataxin protein deficiency and metabolic dysfunction in Friedreich ataxia, an autosomal recessive mitochondrial disease E Clark, J Johnson, YN Dong, E Mercado-Ayon, N Warren, M Zhai, ... Neuronal signaling 2 (4), NS20180060, 2018 | 41 | 2018 |
| Early VGLUT1-specific parallel fiber synaptic deficits and dysregulated cerebellar circuit in the KIKO mouse model of Friedreich ataxia H Lin, J Magrane, EM Clark, SM Halawani, N Warren, A Rattelle, ... Disease models & mechanisms 10 (12), 1529-1538, 2017 | 29 | 2017 |
| Frataxin controls ketone body metabolism through regulation of OXCT1 YNA Dong, C Mesaros, P Xu, E Mercado-Ayón, S Halawani, LV Ngaba, ... PNAS nexus 1 (3), pgac142, 2022 | 10 | 2022 |
| Cerebellar pathology in an inducible mouse model of Friedreich ataxia E Mercado-Ayón, N Warren, S Halawani, LN Rodden, L Ngaba, YN Dong, ... Frontiers in Neuroscience 16, 819569, 2022 | 5 | 2022 |
| A peptide derived from TID1S rescues frataxin deficiency and mitochondrial defects in FRDA cellular models YN Dong, LV Ngaba, J An, MW Adeshina, N Warren, J Wong, DR Lynch Frontiers in Pharmacology 15, 1352311, 2024 | | 2024 |
| Cerebellar endoplasmic reticulum-mitochondria calcium signal pathways are impaired in the KIKO mouse model of Friedreich ataxia (P1. 8-011) H Lin, E Clark, N Warren, YN Dong, J Magrane, D Lynch Neurology 92 (15 Supplement), 2019 | | 2019 |
