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Kalliora C, Kyriazis ID, Oka SI, Lieu MJ, Yue Y, Area-Gomez E, Pol CJ, Tian Y, Mizushima W, Chin A, Scerbo D, Schulze PC, Civelek M, Sadoshima J, Madesh M, Goldberg IJ, Drosatos K.
[2019]. Dual peroxisome-proliferator-activated-receptor-a/g activation inhibits SIRT1-PGC1a axis and causes cardiac dysfunction. JCI Insight. 2019 Aug 8;5(17):e129556. doi: 10.1172/jci.insight.129556. PMCID: PMC6777908. PMID: 31393858.
Larrea D, Pera M, Gonelli A, Cabrera RQ, Akman HO, Guardia-Laguarta C, Velasco KR, Area-Gomez E, Dal Bello F, De Stefani D, Horvath R, Shy ME, Schon EA, Giacomello M.
[2019]. MFN2 mutations in Charcot-Marie-Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics. Hum. Mol. Gen. 2019 Jun 1;28(11):1782-1800. doi: 10.1093/hmg/ddz008. PMCID: PMC6522073. PMID: 30649465
Kleiner G, Barca E, Ziosi M, Emmanuele V, Xu Y, Hidalgo-Gutierrez A, Qiao C, Tadesse S, Area-Gomez E, Lopez LC, Quinzii CM.
[2018]. CoQ10 supplementation rescues nephrotic syndrome through normalization of H2S oxidation pathway. Biochim Biophys Acta Mol Basis Dis. 2018 Nov;1864(11):3708-3722. doi: 10.1016/j.bbadis.2018.09.002. Epub 2018 Sep 6. PMCID: PMC6181133. PMID: 30251690.
Carbonell-Corvillo P, Tristán-Clavijo E, Cabrera-Serrano M, Servián-Morilla E, García-Martín G, Villarreal-Pérez L, Rivas-Infante E, Area-Gómez E, Chamorro-Muñoz MI, Gil-Gálvez A, Miranda-Vizuete A, Martinez-Mir A, Laing N, Paradas C.
[2018]. A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain. Neuromuscul Disord. 2018 Oct;28(10):828-836. doi: 10.1016/j.nmd.2018.07.006. Epub 2018 Jul 26. PMID: 30166250
Kraakman MJ, Liu Q, Postigo-Fernandez J, Ji R, Kon N, Larrea D, Namwanje M, Fan L, Chan M, Area-Gomez E, Fu W, Creusot RJ, Qiang L
[2018]. PPARγ deacetylation dissociates thiazolidinedione's metabolic benefits from its adverse effects. J Clin Invest. 2018 Jun 1;128(6):2600-2612. doi: 10.1172/JCI98709. Epub 2018 May 14. PMCID: PMC5983311. PMID: 29589839.
Pera M, Larrea D, Guardia-Laguarta C, Montesinos J., Velasco KR, Agrawal RR, Xu Y., Chan RB, Di Paolo G., Mehler MF, Perumal GS, Macaluso FP Freyberg ZZ, Acin-Perez R, Enriquez JA, Schon EA, Area-Gomez E.
[2017]. Increased localization of APP-C99 in mitochondria-associated ER membranes causes mitochodrial dysfunction in Alzheimer disease. EMBO. J 2017 Nov 15;36(22):3356-3371. doi: 10.15252/embj.201796797. Epub 2017 Oct 10. PMCID: PMC5731665. PMID: 29018038
Paradas C, Takeuchi H, Lee TV, Clarimon J, Servian E, Mavillard F, Area-Gomez E, Rivas E, Nieto JL, Cabrera M, Estrada B, Morgado Y, Suarez-Calvet X, Márquez C, Martinez-López JA, Illa I, Gallardo E, Fernández-Chacón R, Haltiwanger R, Jafar-Nejad H
[2016]. A missense mutation in POGLUT1 causes a recessive limb-girdle muscular dystrophy. EMBO Mol. Med. 2016 Nov 2;8(11):1289-1309. doi: 10.15252/emmm.201505815. Print 2016 Nov. PMCID: PMC5090660. PMID: 27807076.
Gulati S, Balderes D, Kim C, Guo ZA, Wilcox L, Area-Gomez E, Snider J, Wolinski H, Stagljar I, Granato JT, Kelly V, Ruggles KV, DiGeorgis JA, Kohlwein SD, Schon EA, Sturley SL
[2015]. ABC-transporters and sterol O-acyltransferases interact at membrane microdomains to modulate sterol uptake and esterification. FASEB J. 2015 Nov;29(11):4682-94. doi: 10.1096/fj.14-264796. Epub 2015 Jul 28. PMCID: PMC4608909. PMID: 26220175.