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A mouse model demonstrates a multigenic origin of congenital hypothyroidism.
Amendola E, De Luca P, Macchia PE, Terracciano D, Rosica A, Chiappetta G, Kimura S, Mansouri A, Affuso A, Arra C, Macchia V, Di Lauro R, De Felice M. Amendola E, et al. Among authors: de luca p, de felice m. Endocrinology. 2005 Dec;146(12):5038-47. doi: 10.1210/en.2005-0882. Epub 2005 Sep 8. Endocrinology. 2005. PMID: 16150900
Conditional inactivation of the E-cadherin gene in thyroid follicular cells affects gland development but does not impair junction formation.
Calì G, Zannini M, Rubini P, Tacchetti C, D'Andrea B, Affuso A, Wintermantel T, Boussadia O, Terracciano D, Silberschmidt D, Amendola E, De Felice M, Schütz G, Kemler R, Di Lauro R, Nitsch L. Calì G, et al. Among authors: de felice m. Endocrinology. 2007 Jun;148(6):2737-46. doi: 10.1210/en.2006-1344. Epub 2007 Mar 8. Endocrinology. 2007. PMID: 17347311
Retinoic Acid Specifically Enhances Embryonic Stem Cell Metastate Marked by Zscan4.
Tagliaferri D, De Angelis MT, Russo NA, Marotta M, Ceccarelli M, Del Vecchio L, De Felice M, Falco G. Tagliaferri D, et al. Among authors: de felice m, de angelis mt. PLoS One. 2016 Feb 3;11(2):e0147683. doi: 10.1371/journal.pone.0147683. eCollection 2016. PLoS One. 2016. PMID: 26840068 Free PMC article.
Erratum to: In vivo role of different domains and of phosphorylation in the transcription factor Nkx2-1.
Silberschmidt D, Rodriguez-Mallon A, Mithboakar P, Calì G, Amendola E, Sanges R, Zannini M, Scarfò M, De Luca P, Nitsch L, Di Lauro R, De Felice M. Silberschmidt D, et al. Among authors: de luca p, de felice m. BMC Dev Biol. 2016 Aug 23;16(1):29. doi: 10.1186/s12861-016-0130-0. BMC Dev Biol. 2016. PMID: 27553860 Free PMC article. No abstract available.
369 results