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Adaptive protein synthesis in genetic models of copper deficiency and childhood neurodegeneration.
Lane AR, Scher NE, Bhattacharjee S, Zlatic SA, Roberts AM, Gokhale A, Singleton KS, Duong DM, McKenna M, Liu WL, Baiju A, Moctezuma FGR, Tran T, Patel AA, Clayton LB, Petris MJ, Wood LB, Patgiri A, Vrailas-Mortimer AD, Cox DN, Roberts BR, Werner E, Faundez V. Lane AR, et al. Among authors: werner e. bioRxiv [Preprint]. 2024 Nov 18:2024.09.09.612106. doi: 10.1101/2024.09.09.612106. bioRxiv. 2024. PMID: 39314281 Free PMC article. Preprint.
Systemic Proteome Phenotypes Reveal Defective Metabolic Flexibility in Mecp2 Mutants.
Zlatic SA, Werner E, Surapaneni V, Lee CE, Gokhale A, Singleton K, Duong D, Crocker A, Gentile K, Middleton F, Dalloul JM, Liu WL, Patgiri A, Tarquinio D, Carpenter R, Faundez V. Zlatic SA, et al. Among authors: werner e. bioRxiv [Preprint]. 2023 Sep 1:2023.04.03.535431. doi: 10.1101/2023.04.03.535431. bioRxiv. 2023. Update in: Hum Mol Genet. 2023 Dec 12;33(1):12-32. doi: 10.1093/hmg/ddad154 PMID: 37066332 Free PMC article. Updated. Preprint.
Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content.
Hartwig C, Méndez GM, Bhattacharjee S, Vrailas-Mortimer AD, Zlatic SA, Freeman AAH, Gokhale A, Concilli M, Werner E, Sapp Savas C, Rudin-Rush S, Palmer L, Shearing N, Margewich L, McArthy J, Taylor S, Roberts B, Lupashin V, Polishchuk RS, Cox DN, Jorquera RA, Faundez V. Hartwig C, et al. Among authors: werner e. J Neurosci. 2021 Jan 13;41(2):215-233. doi: 10.1523/JNEUROSCI.1284-20.2020. Epub 2020 Nov 18. J Neurosci. 2021. PMID: 33208468 Free PMC article.
APOE expression and secretion are modulated by mitochondrial dysfunction.
Wynne ME, Ogunbona O, Lane AR, Gokhale A, Zlatic SA, Xu C, Wen Z, Duong DM, Rayaprolu S, Ivanova A, Ortlund EA, Dammer EB, Seyfried NT, Roberts BR, Crocker A, Shanbhag V, Petris M, Senoo N, Kandasamy S, Claypool SM, Barrientos A, Wingo A, Wingo TS, Rangaraju S, Levey AI, Werner E, Faundez V. Wynne ME, et al. Among authors: werner e. Elife. 2023 May 12;12:e85779. doi: 10.7554/eLife.85779. Elife. 2023. PMID: 37171075 Free PMC article.
Systemic proteome phenotypes reveal defective metabolic flexibility in Mecp2 mutants.
Zlatic SA, Werner E, Surapaneni V, Lee CE, Gokhale A, Singleton K, Duong D, Crocker A, Gentile K, Middleton F, Dalloul JM, Liu WL, Patgiri A, Tarquinio D, Carpenter R, Faundez V. Zlatic SA, et al. Among authors: werner e. Hum Mol Genet. 2023 Dec 12;33(1):12-32. doi: 10.1093/hmg/ddad154. Hum Mol Genet. 2023. PMID: 37712894 Free PMC article.
The mitochondrial RNA granule modulates manganese-dependent cell toxicity.
Werner E, Gokhale A, Ackert M, Xu C, Wen Z, Roberts AM, Roberts BR, Vrailas-Mortimer A, Crocker A, Faundez V. Werner E, et al. Mol Biol Cell. 2022 Oct 1;33(12):ar108. doi: 10.1091/mbc.E22-03-0096. Epub 2022 Aug 3. Mol Biol Cell. 2022. PMID: 35921164 Free PMC article.
1,286 results