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Page 1
Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease.
Macias-Kauffer LR, Villamil-Ramírez H, León-Mimila P, Jacobo-Albavera L, Posadas-Romero C, Posadas-Sánchez R, López-Contreras BE, Morán-Ramos S, Romero-Hidalgo S, Acuña-Alonzo V, Del-Río-Navarro BE, Bortolini MC, Gallo C, Bedoya G, Rothhammer F, González-Jose R, Ruiz-Linares A, Stephens CR, Velazquez-Cruz R, Fernández Del Valle-Laisequilla C, Reyes-García JG, Barranco Garduño LM, Carrasco-Portugal MDC, Flores-Murrieta FJ, Vargas-Alarcón G, Aguilar-Salinas CA, Villarreal-Molina T, Canizales-Quinteros S. Macias-Kauffer LR, et al. Int J Cardiol. 2019 Mar 15;279:168-173. doi: 10.1016/j.ijcard.2018.09.107. Epub 2018 Oct 1. Int J Cardiol. 2019. PMID: 30305239
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
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
Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1.
Huertas-Vazquez A, Aguilar-Salinas C, Lusis AJ, Cantor RM, Canizales-Quinteros S, Lee JC, Mariana-Nuñez L, Riba-Ramirez RM, Jokiaho A, Tusie-Luna T, Pajukanta P. Huertas-Vazquez A, et al. Arterioscler Thromb Vasc Biol. 2005 Sep;25(9):1985-91. doi: 10.1161/01.ATV.0000175297.37214.a0. Epub 2005 Jun 23. Arterioscler Thromb Vasc Biol. 2005. PMID: 15976322
Genetic heterogeneity of autosomal dominant hypercholesterolemia in Mexico.
Robles-Osorio L, Huerta-Zepeda A, Ordóñez ML, Canizales-Quinteros S, Díaz-Villaseñor A, Gutiérrez-Aguilar R, Riba L, Huertas-Vázquez A, Rodríguez-Torres M, Gómez-Díaz RA, Salinas S, Ongay-Larios L, Codiz-Huerta G, Mora-Cabrera M, Mehta R, Gómez Pérez FJ, Rull JA, Rabès JP, Tusié-Luna MT, Durán-Vargas S, Aguilar-Salinas CA. Robles-Osorio L, et al. Arch Med Res. 2006 Jan;37(1):102-8. doi: 10.1016/j.arcmed.2005.04.018. Arch Med Res. 2006. PMID: 16314194
HNF-1alpha G574S is a functional variant with decreased transactivation activity.
Navalón-García K, Mendoza-Alcantar L, Díaz-Vargas ME, Martínez-Godínez MA, Reyna-Garfias H, Aguilar-Salinas CA, Riba L, Canizales-Quinteros S, Villarreal-Molina T, González-Chávez A, Argueta-Villamar V, Tusié-Luna MT, Miliar-García A. Navalón-García K, et al. Diabet Med. 2006 Dec;23(12):1295-300. doi: 10.1111/j.1464-5491.2006.02008.x. Diabet Med. 2006. PMID: 17116178
143 results