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Page 1
[Identifying different susceptibility loci associated with early onset diabetes and cardiovascular disease in Mexican families].
Canizales-Quinteros S, Huertas-Vázquez A, Riba-Ramírez L, Monroy-Guzmán A, Domínguez-López A, Romero-Hidalgo S, Aguilar-Salinas C, Rodríguez-Torres M, Ramírez-Jiménez S, Tusié-Luna MT. Canizales-Quinteros S, et al. Among authors: ramirez jimenez s. Gac Med Mex. 2005 Mar-Apr;141(2):115-22. Gac Med Mex. 2005. PMID: 15892459 Spanish.
Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families.
Domínguez-López A, Miliar-García A, Segura-Kato YX, Riba L, Esparza-López R, Ramírez-Jiménez S, Rodríguez-Torres M, Canizales-Quinteros S, Cabrera-Vásquez S, Fragoso-Ontiveros V, Aguilar-Salinas CA, Altamirano-Bustamante N, Calzada-León R, Robles-Valdés C, Bravo-Ríos LE, Tusié-Luna MT. Domínguez-López A, et al. Among authors: ramirez jimenez s. JOP. 2005 May 10;6(3):238-45. JOP. 2005. PMID: 15883474
Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican families.
Huertas-Vázquez A, del Rincón JP, Canizales-Quinteros S, Riba L, Vega-Hernández G, Ramírez-Jiménez S, Aurón-Gómez M, Gómez-Pérez FJ, Aguilar-Salinas CA, Tusié-Luna MT. Huertas-Vázquez A, et al. Among authors: ramirez jimenez s. Ann Hum Genet. 2004 Sep;68(Pt 5):419-27. doi: 10.1046/j.1529-8817.2003.00116.x. Ann Hum Genet. 2004. PMID: 15469419
Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia.
Canizales-Quinteros S, Aguilar-Salinas CA, Reyes-Rodríguez E, Riba L, Rodríguez-Torres M, Ramírez-Jiménez S, Huertas-Vázquez A, Fragoso-Ontiveros V, Zentella-Dehesa A, Ventura-Gallegos JL, Vega-Hernández G, López-Estrada A, Aurón-Gómez M, Gómez-Pérez F, Rull J, Cox NJ, Bell GI, Tusié-Luna MT. Canizales-Quinteros S, et al. Among authors: ramirez jimenez s. Circ Res. 2003 Mar 21;92(5):569-76. doi: 10.1161/01.RES.0000064174.69165.66. Epub 2003 Feb 27. Circ Res. 2003. PMID: 12609970
A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia.
Canizales-Quinteros S, Aguilar-Salinas CA, Huertas-Vázquez A, Ordóñez-Sánchez ML, Rodríguez-Torres M, Venturas-Gallegos JL, Riba L, Ramírez-Jimenez S, Salas-Montiel R, Medina-Palacios G, Robles-Osorio L, Miliar-García A, Rosales-León L, Ruiz-Ordaz BH, Zentella-Dehesa A, Ferré-D'Amare A, Gómez-Pérez FJ, Tusié-Luna MT. Canizales-Quinteros S, et al. Among authors: ramirez jimenez s. Hum Genet. 2005 Jan;116(1-2):114-20. doi: 10.1007/s00439-004-1192-9. Epub 2004 Nov 17. Hum Genet. 2005. PMID: 15599766
Analysis of the glucokinase gene in Mexican families displaying early-onset non-insulin-dependent diabetes mellitus including MODY families.
del Bosque-Plata L, García-García E, Ramírez-Jiménez S, Cabello-Villegas J, Riba L, Gómez-León A, Vega-Hernández G, Altamirano-Bustamante N, Calzada-León R, Robles-Valdés C, Mendoza-Morfín F, Curiel-Pérez O, Tusié-Luna MT. del Bosque-Plata L, et al. Am J Med Genet. 1997 Nov 12;72(4):387-93. doi: 10.1002/(sici)1096-8628(19971112)72:4<387::aid-ajmg3>3.0.co;2-o. Am J Med Genet. 1997. PMID: 9375718
Early-onset type 2 diabetes: metabolic and genetic characterization in the mexican population.
Aguilar-Salinas CA, Reyes-Rodríguez E, Ordóñez-Sánchez ML, Torres MA, Ramírez-Jiménez S, Domínguez-López A, Martínez-Francois JR, Velasco-Pérez ML, Alpizar M, García-García E, Gómez-Pérez F, Rull J, Tusié-Luna MT. Aguilar-Salinas CA, et al. J Clin Endocrinol Metab. 2001 Jan;86(1):220-6. doi: 10.1210/jcem.86.1.7134. J Clin Endocrinol Metab. 2001. PMID: 11232004
Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population.
del Bosque-Plata L, Aguilar-Salinas CA, Tusié-Luna MT, Ramírez-Jiménez S, Rodríguez-Torres M, Aurón-Gómez M, Ramírez E, Velasco-Pérez ML, Ramírez-Silva A, Gómez-Pérez F, Hanis CL, Tsuchiya T, Yoshiuchi I, Cox NJ, Bell GI. del Bosque-Plata L, et al. Among authors: ramirez jimenez s. Mol Genet Metab. 2004 Feb;81(2):122-6. doi: 10.1016/j.ymgme.2003.10.005. Mol Genet Metab. 2004. PMID: 14741193
A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans.
Acuña-Alonzo V, Flores-Dorantes T, Kruit JK, Villarreal-Molina T, Arellano-Campos O, Hünemeier T, Moreno-Estrada A, Ortiz-López MG, Villamil-Ramírez H, León-Mimila P, Villalobos-Comparan M, Jacobo-Albavera L, Ramírez-Jiménez S, Sikora M, Zhang LH, Pape TD, Granados-Silvestre Mde A, Montufar-Robles I, Tito-Alvarez AM, Zurita-Salinas C, Bustos-Arriaga J, Cedillo-Barrón L, Gómez-Trejo C, Barquera-Lozano R, Vieira-Filho JP, Granados J, Romero-Hidalgo S, Huertas-Vázquez A, González-Martín A, Gorostiza A, Bonatto SL, Rodríguez-Cruz M, Wang L, Tusié-Luna T, Aguilar-Salinas CA, Lisker R, Moises RS, Menjivar M, Salzano FM, Knowler WC, Bortolini MC, Hayden MR, Baier LJ, Canizales-Quinteros S. Acuña-Alonzo V, et al. Among authors: ramirez jimenez s. Hum Mol Genet. 2010 Jul 15;19(14):2877-85. doi: 10.1093/hmg/ddq173. Epub 2010 Apr 23. Hum Mol Genet. 2010. PMID: 20418488 Free PMC article.
Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: identification of possible new mutations and high prevalence of apparent germ-line mutations.
Ordoñez-Sánchez ML, Ramírez-Jiménez S, López-Gutierrez AU, Riba L, Gamboa-Cardiel S, Cerrillo-Hinojosa M, Altamirano-Bustamante N, Calzada-León R, Robles-Valdés C, Mendoza-Morfin F, Tusié-Luna MT. Ordoñez-Sánchez ML, et al. Hum Genet. 1998 Feb;102(2):170-7. doi: 10.1007/s004390050672. Hum Genet. 1998. PMID: 9580109
17 results