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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
2003 3
2004 7
2005 6
2006 3
2007 3
2008 5
2009 7
2010 5
2011 6
2012 5
2013 5
2014 3
2015 8
2016 5
2017 6
2018 4
2019 7
2020 7
2021 8
2022 4
2023 6
2024 1

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105 results

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Page 1
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: faundez v. Elife. 2023 May 12;12:e85779. doi: 10.7554/eLife.85779. Elife. 2023. PMID: 37171075 Free PMC article.
Trafficking mechanisms of P-type ATPase copper transporters.
Hartwig C, Zlatic SA, Wallin M, Vrailas-Mortimer A, Fahrni CJ, Faundez V. Hartwig C, et al. Among authors: faundez v. Curr Opin Cell Biol. 2019 Aug;59:24-33. doi: 10.1016/j.ceb.2019.02.009. Epub 2019 Mar 29. Curr Opin Cell Biol. 2019. PMID: 30928671 Free PMC article. Review.
Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion.
Purcell RH, Sefik E, Werner E, King AT, Mosley TJ, Merritt-Garza ME, Chopra P, McEachin ZT, Karne S, Raj N, Vaglio BJ, Sullivan D, Firestein BL, Tilahun K, Robinette MI, Warren ST, Wen Z, Faundez V, Sloan SA, Bassell GJ, Mulle JG. Purcell RH, et al. Among authors: faundez v. Sci Adv. 2023 Aug 18;9(33):eadh0558. doi: 10.1126/sciadv.adh0558. Epub 2023 Aug 16. Sci Adv. 2023. PMID: 37585521 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: faundez v. Hum Mol Genet. 2023 Dec 12;33(1):12-32. doi: 10.1093/hmg/ddad154. Hum Mol Genet. 2023. PMID: 37712894
Rare Genetic Diseases: Nature's Experiments on Human Development.
Lee CE, Singleton KS, Wallin M, Faundez V. Lee CE, et al. Among authors: faundez v. iScience. 2020 May 22;23(5):101123. doi: 10.1016/j.isci.2020.101123. Epub 2020 May 1. iScience. 2020. PMID: 32422592 Free PMC article. Review.
Neuronal and immune synapses on the move at traffic.
Billadeau DD, Faundez V. Billadeau DD, et al. Among authors: faundez v. Traffic. 2015 Mar;16(3):227-8. doi: 10.1111/tra.12251. Traffic. 2015. PMID: 25524292 Free article. No abstract available.
Translating molecular advances in Down syndrome and Fragile X syndrome into therapies.
Faundez V, De Toma I, Bardoni B, Bartesaghi R, Nizetic D, de la Torre R, Cohen Kadosh R, Herault Y, Dierssen M, Potier MC; Down Syndrome and Other Genetic Developmental Disorders ECNP Network. Faundez V, et al. Eur Neuropsychopharmacol. 2018 Jun;28(6):675-690. doi: 10.1016/j.euroneuro.2018.03.006. Epub 2018 Jun 7. Eur Neuropsychopharmacol. 2018. PMID: 29887288 Review.
105 results