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Prevalent polymorphism in thyroid hormone-activating enzyme leaves a genetic fingerprint that underlies associated clinical syndromes.
McAninch EA, Jo S, Preite NZ, Farkas E, Mohácsik P, Fekete C, Egri P, Gereben B, Li Y, Deng Y, Patti ME, Zevenbergen C, Peeters RP, Mash DC, Bianco AC. McAninch EA, et al. Among authors: jo s. J Clin Endocrinol Metab. 2015 Mar;100(3):920-33. doi: 10.1210/jc.2014-4092. Epub 2015 Jan 8. J Clin Endocrinol Metab. 2015. PMID: 25569702 Free PMC article.
Type 2 deiodinase polymorphism causes ER stress and hypothyroidism in the brain.
Jo S, Fonseca TL, Bocco BMLC, Fernandes GW, McAninch EA, Bolin AP, Da Conceição RR, Werneck-de-Castro JP, Ignacio DL, Egri P, Németh D, Fekete C, Bernardi MM, Leitch VD, Mannan NS, Curry KF, Butterfield NC, Bassett JHD, Williams GR, Gereben B, Ribeiro MO, Bianco AC. Jo S, et al. J Clin Invest. 2019 Jan 2;129(1):230-245. doi: 10.1172/JCI123176. Epub 2018 Dec 3. J Clin Invest. 2019. PMID: 30352046 Free PMC article.
The Foxo1-Inducible Transcriptional Repressor Zfp125 Causes Hepatic Steatosis and Hypercholesterolemia.
Fernandes GW, Bocco BMLC, Fonseca TL, McAninch EA, Jo S, Lartey LJ, O-Sullivan I, Unterman TG, Preite NZ, Voigt RM, Forsyth CB, Keshavarzian A, Sinkó R, Goldfine AB, Patti ME, Ribeiro MO, Gereben B, Bianco AC. Fernandes GW, et al. Among authors: jo s. Cell Rep. 2018 Jan 9;22(2):523-534. doi: 10.1016/j.celrep.2017.12.053. Cell Rep. 2018. PMID: 29320745 Free PMC article.
2,650 results