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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1997 1
1998 4
2001 1
2003 2
2004 3
2005 3
2008 1
2009 1
2010 1
2014 1
2022 0
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17 results
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Page 1
[Hemophagocytic syndromes].
Herrero Hernández A, Ramírez Jiménez S, García Martín F, Martínez Valverde A. Herrero Hernández A, et al. Among authors: ramirez jimenez s. An Esp Pediatr. 1998 Sep;49(3):230-6. An Esp Pediatr. 1998. PMID: 9803544 Review. Spanish. No abstract available.
Galanin preproprotein is associated with elevated plasma triglycerides.
Plaisier CL, Kyttälä M, Weissglas-Volkov D, Sinsheimer JS, Huertas-Vazquez A, Riba L, Ramírez-Jiménez S, de Bruin TW, Tusié-Luna T, Aouizerat BE, Pullinger CR, Malloy MJ, Kane JP, Cruz-Bautista I, Herrera MF, Aguilar-Salinas C, Kuusisto J, Laakso M, Taskinen MR, van der Kallen CJ, Pajukanta P. Plaisier CL, et al. Among authors: ramirez jimenez s. Arterioscler Thromb Vasc Biol. 2009 Jan;29(1):147-52. doi: 10.1161/ATVBAHA.108.178533. Epub 2008 Nov 6. Arterioscler Thromb Vasc Biol. 2009. PMID: 18988886 Free PMC article.
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
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
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. Among authors: ramirez jimenez s. J Clin Endocrinol Metab. 2001 Jan;86(1):220-6. doi: 10.1210/jcem.86.1.7134. J Clin Endocrinol Metab. 2001. PMID: 11232004
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. Among authors: ramirez jimenez s. 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
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.
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
17 results