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Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.
Requena T, Gazquez I, Moreno A, Batuecas A, Aran I, Soto-Varela A, Santos-Perez S, Perez N, Perez-Garrigues H, Lopez-Nevot A, Martin E, Sanz R, Perez P, Trinidad G, Alarcon-Riquelme ME, Teggi R, Zagato L, Lopez-Nevot MA, Lopez-Escamez JA. Requena T, et al. Immunogenetics. 2013 May;65(5):345-55. doi: 10.1007/s00251-013-0683-z. Epub 2013 Feb 1. Immunogenetics. 2013. PMID: 23370977
Familial clustering and genetic heterogeneity in Meniere's disease.
Requena T, Espinosa-Sanchez JM, Cabrera S, Trinidad G, Soto-Varela A, Santos-Perez S, Teggi R, Perez P, Batuecas-Caletrio A, Fraile J, Aran I, Martin E, Benitez J, Pérez-Fernández N, Lopez-Escamez JA. Requena T, et al. Clin Genet. 2014 Mar;85(3):245-52. doi: 10.1111/cge.12150. Epub 2013 Apr 9. Clin Genet. 2014. PMID: 23521103
Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.
Gázquez I, Moreno A, Requena T, Ohmen J, Santos-Perez S, Aran I, Soto-Varela A, Pérez-Garrigues H, López-Nevot A, Batuecas A, Friedman RA, López-Nevot MA, López-Escamez JA. Gázquez I, et al. Among authors: requena t. Eur Arch Otorhinolaryngol. 2013 Mar;270(4):1521-9. doi: 10.1007/s00405-012-2268-0. Epub 2012 Nov 21. Eur Arch Otorhinolaryngol. 2013. PMID: 23179933
Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease.
Cabrera S, Sanchez E, Requena T, Martinez-Bueno M, Benitez J, Perez N, Trinidad G, Soto-Varela A, Santos-Perez S, Martin-Sanz E, Fraile J, Perez P, Alarcon-Riquelme ME, Batuecas A, Espinosa-Sanchez JM, Aran I, Lopez-Escamez JA. Cabrera S, et al. Among authors: requena t. PLoS One. 2014 Nov 14;9(11):e112171. doi: 10.1371/journal.pone.0112171. eCollection 2014. PLoS One. 2014. PMID: 25397881 Free PMC article.
A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.
Martín-Sierra C, Requena T, Frejo L, Price SD, Gallego-Martinez A, Batuecas-Caletrio A, Santos-Pérez S, Soto-Varela A, Lysakowski A, Lopez-Escamez JA. Martín-Sierra C, et al. Among authors: requena t. Hum Mol Genet. 2016 Aug 15;25(16):3407-3415. doi: 10.1093/hmg/ddw183. Epub 2016 Jun 21. Hum Mol Genet. 2016. PMID: 27329761 Free PMC article.
Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease.
Frejo L, Requena T, Okawa S, Gallego-Martinez A, Martinez-Bueno M, Aran I, Batuecas-Caletrio A, Benitez-Rosario J, Espinosa-Sanchez JM, Fraile-Rodrigo JJ, García-Arumi AM, González-Aguado R, Marques P, Martin-Sanz E, Perez-Fernandez N, Pérez-Vázquez P, Perez-Garrigues H, Santos-Perez S, Soto-Varela A, Tapia MC, Trinidad-Ruiz G, Del Sol A, Alarcon Riquelme ME, Lopez-Escamez JA. Frejo L, et al. Among authors: requena t. Front Immunol. 2017 Dec 13;8:1739. doi: 10.3389/fimmu.2017.01739. eCollection 2017. Front Immunol. 2017. PMID: 29326686 Free PMC article.
112 results