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Page 1
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
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
Steroid 21-hydroxylase (P450c21) naturally occurring mutants I172N, V281L and I236n/V237E/M239K exert a dominant negative effect on enzymatic activity when co-expressed with the wild-type protein.
Félix-López X, Riba L, Ordóñez-Sánchez ML, Ramírez-Jiménez S, Ventura-Gallegos JL, Zentella-Dehesa A, Tusié-Luna MT. Félix-López X, et al. Among authors: ramirez jimenez s. J Pediatr Endocrinol Metab. 2003 Sep;16(7):1017-24. doi: 10.1515/jpem.2003.16.7.1017. J Pediatr Endocrinol Metab. 2003. PMID: 14513879
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
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
[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.
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
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
17 results