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The -514C>T polymorphism in the LIPC gene modifies type 2 diabetes risk through modulation of HDL-cholesterol levels in Mexicans.
Guerra-García MT, Moreno-Macías H, Ochoa-Guzmán A, Ordoñez-Sánchez ML, Rodríguez-Guillen R, Vázquez-Cárdenas P, Ortíz-Ortega VM, Peimbert-Torres M, Aguilar-Salinas CA, Tusié-Luna MT. Guerra-García MT, et al. J Endocrinol Invest. 2021 Mar;44(3):557-565. doi: 10.1007/s40618-020-01346-x. Epub 2020 Jul 2. J Endocrinol Invest. 2021. PMID: 32617858
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
Prevalence and characteristics of early-onset type 2 diabetes in Mexico.
Aguilar-Salinas CA, Rojas R, Gómez-Pérez FJ, García E, Valles V, Ríos-Torres JM, Franco A, Olaiz G, Sepúlveda J, Rull JA. Aguilar-Salinas CA, et al. Am J Med. 2002 Nov;113(7):569-74. doi: 10.1016/s0002-9343(02)01314-1. Am J Med. 2002. PMID: 12459403
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. 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
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. Mol Genet Metab. 2004 Feb;81(2):122-6. doi: 10.1016/j.ymgme.2003.10.005. Mol Genet Metab. 2004. PMID: 14741193
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. 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
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. JOP. 2005 May 10;6(3):238-45. JOP. 2005. PMID: 15883474
440 results