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KCNQ1 gene variants in the risk for type 2 diabetes and impaired renal function in the Spanish Renastur cohort.
Riobello C, Gómez J, Gil-Peña H, Tranche S, Reguero JR, de la Hera JM, Delgado E, Calvo D, Morís C, Santos F, Coto-Segura P, Iglesias S, Alonso B, Alvarez V, Coto E. Riobello C, et al. Among authors: reguero jr. Mol Cell Endocrinol. 2016 May 15;427:86-91. doi: 10.1016/j.mce.2016.03.007. Epub 2016 Mar 9. Mol Cell Endocrinol. 2016. PMID: 26970180
Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy.
Coto E, Reguero JR, Palacín M, Gómez J, Alonso B, Iglesias S, Martín M, Tavira B, Díaz-Molina B, Morales C, Morís C, Rodríguez-Lambert JL, Corao AI, Díaz M, Alvarez V. Coto E, et al. Among authors: reguero jr. J Mol Diagn. 2012 Sep;14(5):518-24. doi: 10.1016/j.jmoldx.2012.04.001. Epub 2012 Jul 2. J Mol Diagn. 2012. PMID: 22765922 Free article.
Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.
Palacín M, Alvarez V, Martín M, Díaz M, Corao AI, Alonso B, Díaz-Molina B, Lozano I, Avanzas P, Morís C, Reguero JR, Rodríguez I, López-Larrea C, Cannata-Andía J, Batalla A, Ruiz-Ortega M, Martínez-Camblor P, Coto E. Palacín M, et al. Among authors: reguero jr. Mitochondrion. 2011 Jan;11(1):176-81. doi: 10.1016/j.mito.2010.09.004. Epub 2010 Sep 21. Mitochondrion. 2011. PMID: 20863902
74 results