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Page 1
Mitochondrial dysfunction in the development and progression of neurodegenerative diseases.
Arch Biochem Biophys. 2021 May 15;702:108698. doi: 10.1016/j.abb.2020.108698. Epub 2020 Nov 28.
Arch Biochem Biophys. 2021.
PMID: 33259796
Review.
Role of frataxin protein deficiency and metabolic dysfunction in Friedreich ataxia, an autosomal recessive mitochondrial disease.
Clark E, Johnson J, Dong YN, Mercado-Ayon E, Warren N, Zhai M, McMillan E, Salovin A, Lin H, Lynch DR.
Clark E, et al. Among authors: mercado ayon e.
Neuronal Signal. 2018 Nov 2;2(4):NS20180060. doi: 10.1042/NS20180060. eCollection 2018 Dec.
Neuronal Signal. 2018.
PMID: 32714592
Free PMC article.
Review.
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Cerebellar Pathology in an Inducible Mouse Model of Friedreich Ataxia.
Mercado-Ayón E, Warren N, Halawani S, Rodden LN, Ngaba L, Dong YN, Chang JC, Fonck C, Mavilio F, Lynch DR, Lin H.
Mercado-Ayón E, et al.
Front Neurosci. 2022 Mar 24;16:819569. doi: 10.3389/fnins.2022.819569. eCollection 2022.
Front Neurosci. 2022.
PMID: 35401081
Free PMC article.
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Frataxin controls ketone body metabolism through regulation of OXCT1.
Dong YN, Mesaros C, Xu P, Mercado-Ayón E, Halawani S, Ngaba LV, Warren N, Sleiman P, Rodden LN, Schadt KA, Blair IA, Lynch DR.
Dong YN, et al. Among authors: mercado ayon e.
PNAS Nexus. 2022 Jul 26;1(3):pgac142. doi: 10.1093/pnasnexus/pgac142. eCollection 2022 Jul.
PNAS Nexus. 2022.
PMID: 36016708
Free PMC article.
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Drp1-dependent peptide reverse mitochondrial fragmentation, a homeostatic response in Friedreich ataxia.
Johnson J, Mercado-Ayón E, Clark E, Lynch D, Lin H.
Johnson J, et al. Among authors: mercado ayon e.
Pharmacol Res Perspect. 2021 May;9(3):e00755. doi: 10.1002/prp2.755.
Pharmacol Res Perspect. 2021.
PMID: 33951329
Free PMC article.
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