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Items: 1 to 50 of 63

1.

Mexican Carriers of the HNF1A p.E508K Variant Do Not Experience an Enhanced Response to Sulfonylureas.

Martagón AJ, Bello-Chavolla OY, Arellano-Campos O, Almeda-Valdés P, Walford GA, Cruz-Bautista I, Gómez-Velasco DV, Mehta R, Muñoz-Hernández L, Sevilla-González M, Viveros-Ruiz TL, Ordoñez-Sánchez ML, Rodríguez-Guillen R, Florez JC, Tusié-Luna MT, Aguilar-Salinas CA; Slim Initiative in Genomic Medicine for the Americas (SIGMA) Type 2 Diabetes Consortium.

Diabetes Care. 2018 May 29. pii: dc180384. doi: 10.2337/dc18-0384. [Epub ahead of print]

PMID:
29844095
2.

Searching for the Causal Variants of the Association Between Hypertriglyceridemia and the Genome-Wide Association Studies-Derived Signals? Take a Look in the Native American Populations.

Aguilar-Salinas CA, Sevilla González MDR, Tusie-Luna MT.

Circ Cardiovasc Genet. 2017 Dec;10(6). pii: e002010. doi: 10.1161/CIRCGENETICS.117.002010. No abstract available.

PMID:
29237696
3.

The panorama of familial hypercholesterolemia in Latin America: a systematic review.

Mehta R, Zubirán R, Martagón AJ, Vazquez-Cárdenas A, Segura-Kato Y, Tusié-Luna MT, Aguilar-Salinas CA.

J Lipid Res. 2016 Dec;57(12):2115-2129. Epub 2016 Oct 24. Review.

4.

Analysis of protein-coding genetic variation in 60,706 humans.

Lek M, Karczewski KJ, Minikel EV, Samocha KE, Banks E, Fennell T, O'Donnell-Luria AH, Ware JS, Hill AJ, Cummings BB, Tukiainen T, Birnbaum DP, Kosmicki JA, Duncan LE, Estrada K, Zhao F, Zou J, Pierce-Hoffman E, Berghout J, Cooper DN, Deflaux N, DePristo M, Do R, Flannick J, Fromer M, Gauthier L, Goldstein J, Gupta N, Howrigan D, Kiezun A, Kurki MI, Moonshine AL, Natarajan P, Orozco L, Peloso GM, Poplin R, Rivas MA, Ruano-Rubio V, Rose SA, Ruderfer DM, Shakir K, Stenson PD, Stevens C, Thomas BP, Tiao G, Tusie-Luna MT, Weisburd B, Won HH, Yu D, Altshuler DM, Ardissino D, Boehnke M, Danesh J, Donnelly S, Elosua R, Florez JC, Gabriel SB, Getz G, Glatt SJ, Hultman CM, Kathiresan S, Laakso M, McCarroll S, McCarthy MI, McGovern D, McPherson R, Neale BM, Palotie A, Purcell SM, Saleheen D, Scharf JM, Sklar P, Sullivan PF, Tuomilehto J, Tsuang MT, Watkins HC, Wilson JG, Daly MJ, MacArthur DG; Exome Aggregation Consortium.

Nature. 2016 Aug 18;536(7616):285-91. doi: 10.1038/nature19057.

5.

Factors associated with postprandial lipemia and apolipoprotein A-V levels in individuals with familial combined hyperlipidemia.

Almeda-Valdes P, Cuevas-Ramos D, Mehta R, Muñoz-Hernandez L, Cruz-Bautista I, Perez-Mendez O, Tusie-Luna MT, Gomez-Perez FJ, Pajukanta P, Matikainen N, Taskinen MR, Aguilar-Salinas CA.

BMC Endocr Disord. 2014 Nov 25;14:90. doi: 10.1186/1472-6823-14-90.

6.

[Thyroid hormone resistance (THR): a case report].

Almeda-Valdés P, Pérez-Enríquez B, Cuevas-Ramos D, Pérez-Díaz I, Tusié-Luna MT, Gómez-Pérez FJ.

Gac Med Mex. 2014 Sep-Oct;150(5):465-9. Spanish.

7.

PRSS1 and SPINK1 mutations in idiopathic chronic and recurrent acute pancreatitis.

Pelaez-Luna M, Robles-Diaz G, Canizales-Quinteros S, Tusié-Luna MT.

World J Gastroenterol. 2014 Sep 7;20(33):11788-92. doi: 10.3748/wjg.v20.i33.11788.

8.

The R230C variant of the ATP binding cassette protein A1 (ABCA1) gene is associated with a decreased response to glyburide therapy in patients with type 2 diabetes mellitus.

Aguilar-Salinas CA, Muñoz-Hernandez LL, Cobos-Bonilla M, Ramírez-Márquez MR, Ordoñez-Sanchez ML, Mehta R, Medina-Santillan R, Tusie-Luna MT.

Metabolism. 2013 May;62(5):638-41. doi: 10.1016/j.metabol.2012.11.006. Epub 2012 Dec 27.

PMID:
23273975
9.

Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population.

Gamboa-Meléndez MA, Huerta-Chagoya A, Moreno-Macías H, Vázquez-Cárdenas P, Ordóñez-Sánchez ML, Rodríguez-Guillén R, Riba L, Rodríguez-Torres M, Guerra-García MT, Guillén-Pineda LE, Choudhry S, Del Bosque-Plata L, Canizales-Quinteros S, Pérez-Ortiz G, Escobedo-Aguirre F, Parra A, Lerman-Garber I, Aguilar-Salinas CA, Tusié-Luna MT.

Diabetes. 2012 Dec;61(12):3314-21. doi: 10.2337/db11-0550. Epub 2012 Aug 24.

10.

Primary amenorrhea in two sisters: description of a Mexican family with 17α hydroxylase-17 lyase deficiency caused by arginine - stop mutation.

Escamilla-Márquez MA, Garduño-Garcia Jde J, Ordóñez-Sanchez ML, Reza-Albarrán A, Tusie-Luna MT, Gómez Pérez FJ, Aguilar-Salinas CA.

Gynecol Endocrinol. 2012 Sep;28(9):733-5. doi: 10.3109/09513590.2011.652718. Epub 2012 Feb 6.

PMID:
22309630
11.

[Familial homozygous hypercholesterolemia due to the c2271delT mutation in the LDL receptor gene, detected exclusively in Mexicans].

Martínez L, Ordóñez Sánchez ML, Letona R, Olvera Sumano V, Guerra MM, Tusié-Luna MT, Aguilar-Salinas CA.

Gac Med Mex. 2011 Sep-Oct;147(5):394-8. Spanish.

PMID:
22089669
12.

Early onset type 2 diabetes in Jamaica and in Mexico. Opportunities derived from an interethnic study.

Irving R, Tusié-Luna MT, Mills J, Wright-Pascoe R, McLaughlin W, Aguilar-Salinas CA.

Rev Invest Clin. 2011 Mar-Apr;63(2):198-209. Review.

PMID:
21714438
13.

Familial hypobetalipoproteinemia in a hospital survey: genetics, metabolism and non-alcoholic fatty liver disease.

Gutiérrez-Cirlos C, Ordóñez-Sánchez ML, Tusié-Luna MT, Patterson BW, Schonfeld G, Aguilar-Salinas CA.

Ann Hepatol. 2011 Apr-Jun;10(2):155-64.

14.

The non-synonymous Arg230Cys variant (R230C) of the ATP-binding cassette transporter A1 is associated with low HDL cholesterol concentrations in Mexican adults: a population based nation wide study.

Aguilar-Salinas CA, Canizales-Quinteros S, Rojas-Martínez R, Mehta R, Rodriguez-Guillén R, Ordoñez-Sanchez ML, Riba L, Tusié-Luna MT.

Atherosclerosis. 2011 May;216(1):146-50. doi: 10.1016/j.atherosclerosis.2010.10.049. Epub 2011 Jan 22.

PMID:
21315358
15.

[Fifty years studying hiperlipidemias: the case of familial combined hyperlipidemia].

Aguilar-Salinas C, Gómez-Díaz R, Tusié-Luna MT.

Invest Clin. 2010 Jun;51(2):145-58. Review. Spanish.

PMID:
20928976
16.

[Obesity and metabolic syndrome. A challenge for the Mexican Institutes of Health].

García-García E, De la Llata-Romero M, Kaufer-Horwitz M, Tusié-Luna MT, Calzada-León R, Vázquez-Velázquez V, Barquera-Cervera S, Caballero-Romo Ade J, Orozco L, Velázquez-Fernández D, Rosas-Peralta M, Barriguete-Meléndez A, Zacarías-Castillo R, Ortega-González C, Sotelo-Morales J.

Rev Invest Clin. 2009 Jul-Aug;61(4):337-46. Spanish.

PMID:
19848311
17.

Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes.

Florez JC, Price AL, Campbell D, Riba L, Parra MV, Yu F, Duque C, Saxena R, Gallego N, Tello-Ruiz M, Franco L, Rodríguez-Torres M, Villegas A, Bedoya G, Aguilar-Salinas CA, Tusié-Luna MT, Ruiz-Linares A, Reich D.

Diabetologia. 2009 Aug;52(8):1528-36. doi: 10.1007/s00125-009-1412-x. Epub 2009 Jun 13.

18.

Hypoalphalipoproteinemia in populations of Native American ancestry: an opportunity to assess the interaction of genes and the environment.

Aguilar-Salinas CA, Canizales-Quinteros S, Rojas-Martínez R, Mehta R, Villarreal-Molina MT, Arellano-Campos O, Riba L, Gómez-Pérez FJ, Tusié-Luna MT.

Curr Opin Lipidol. 2009 Apr;20(2):92-7. Review.

PMID:
19280764
19.

[Obesity and the metabolic syndrome as a public health problem: a reflection].

García-García E, De la Llata-Romero M, Kaufer-Horwitz M, Tusié-Luna MT, Calzada-León R, Vázquez-Velázquez V, Barquera-Cervera S, Caballero-Romo Ade J, Orozco L, Velásquez-Fernández D, Rosas-Peralta M, Barriguete-Meléndez A, Zacarías-Castillo R, Sotelo-Morales J; Grupo académico para el estudio, la prevención y el tratamiento de la obesidad y el síndrome metabólico de la Comisión Coordinadora de los Institutos Nacionales de Salud, Hospitales Federales de Referencia y Hospitales de Alta Especialidad.

Salud Publica Mex. 2008 Nov-Dec;50(6):530-47. Spanish. No abstract available.

20.

[Obesity and metabolic syndrome as public health problem. A reflection].

García-García E, De la Llata-Romero M, Kaufer-Horwitz M, Tusié-Luna MT, Calzada-León R, Vázquez-Velázquez V, Barquera-Cervera S, Caballero-Romo AJ, Orozco L, Velásquez-Fernández D, Rosas-Peralta M, Barriguete-Meléndez A, Zacarías-Castillo R, Sotelo-Morales J.

Arch Cardiol Mex. 2008 Jul-Sep;78(3):318-37. Spanish. No abstract available.

PMID:
18959021
21.

High adiponectin concentrations are associated with the metabolically healthy obese phenotype.

Aguilar-Salinas CA, García EG, Robles L, Riaño D, Ruiz-Gomez DG, García-Ulloa AC, Melgarejo MA, Zamora M, Guillen-Pineda LE, Mehta R, Canizales-Quinteros S, Tusie Luna MT, Gómez-Pérez FJ.

J Clin Endocrinol Metab. 2008 Oct;93(10):4075-9. doi: 10.1210/jc.2007-2724. Epub 2008 Aug 5.

PMID:
18682512
22.

[Succesful collaborations between three Mexican institutions for research on dislipidemias, obesity and diabetes].

Aguilar-Salinas CA, Canizales-Quinteros S, Rojas-Martínez R, García-García E, Olaiz-Fernández G, Gómez-Pérez FJ, Tusié-Luna MT.

Gac Med Mex. 2007 Sep-Oct;143(5):355-64. Spanish.

PMID:
18246928
23.

The ATP-binding cassette transporter subfamily A member 1 (ABC-A1) and type 2 diabetes: an association beyond HDL cholesterol.

Salinas CA, Cruz-Bautista I, Mehta R, Villarreal-Molina MT, Pérez FJ, Tusié-Luna MT, Canizales-Quinteros S.

Curr Diabetes Rev. 2007 Nov;3(4):264-7. Review.

PMID:
18220685
24.

High frequency of T130I mutation of HNF4A gene in Mexican patients with early-onset type 2 diabetes.

Menjívar M, Granados-Silvestre MA, Montúfar-Robles I, Herrera M, Tusié-Luna MT, Canizales-Quinteros S, Aguilar-Salinas CA, Ortiz-López MG.

Clin Genet. 2008 Feb;73(2):185-7. Epub 2007 Nov 19. No abstract available.

PMID:
18028455
25.

Association of the ATP-binding cassette transporter A1 R230C variant with early-onset type 2 diabetes in a Mexican population.

Villarreal-Molina MT, Flores-Dorantes MT, Arellano-Campos O, Villalobos-Comparan M, Rodríguez-Cruz M, Miliar-García A, Huertas-Vazquez A, Menjivar M, Romero-Hidalgo S, Wacher NH, Tusie-Luna MT, Cruz M, Aguilar-Salinas CA, Canizales-Quinteros S; Metabolic Study Group.

Diabetes. 2008 Feb;57(2):509-13. Epub 2007 Nov 14.

26.

Association of PPARG2 Pro12Ala variant with larger body mass index in Mestizo and Amerindian populations of Mexico.

Canizales-Quinteros S, Aguilar-Salinas CA, Ortiz-López MG, Rodríguez-Cruz M, Villarreal-Molina MT, Coral-Vázquez R, Huertas-Vázquez A, Hernández-Caballero A, López-Alarcón M, Brito-Zurita OR, Domínguez-Banda A, Martinez-Sánchez LR, Canto-de Cetina T, Vilchis-Dorantes G, Rosas-Vargas H, Granados-Silvestre MA, Medeiros-Domingo A, Menjivar M, Tusié-Luna MT.

Hum Biol. 2007 Feb;79(1):111-9.

PMID:
17985660
27.

SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome.

Medeiros-Domingo A, Kaku T, Tester DJ, Iturralde-Torres P, Itty A, Ye B, Valdivia C, Ueda K, Canizales-Quinteros S, Tusié-Luna MT, Makielski JC, Ackerman MJ.

Circulation. 2007 Jul 10;116(2):134-42. Epub 2007 Jun 25.

28.

[New perspectives in long QT syndrome].

Medeiros-Domingo A, Iturralde-Torres P, Canizales-Quinteros S, Hernández-Cruz A, Tusié-Luna MT.

Rev Invest Clin. 2007 Jan-Feb;59(1):57-72. Review. Spanish.

PMID:
17569301
29.

The ATP-binding cassette transporter A1 R230C variant affects HDL cholesterol levels and BMI in the Mexican population: association with obesity and obesity-related comorbidities.

Villarreal-Molina MT, Aguilar-Salinas CA, Rodríguez-Cruz M, Riaño D, Villalobos-Comparan M, Coral-Vazquez R, Menjivar M, Yescas-Gomez P, Königsoerg-Fainstein M, Romero-Hidalgo S, Tusie-Luna MT, Canizales-Quinteros S; Metabolic Study Group.

Diabetes. 2007 Jul;56(7):1881-7. Epub 2007 Feb 7.

30.

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.

Diabet Med. 2006 Dec;23(12):1295-300.

PMID:
17116178
31.

Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families.

Yescas P, Huertas-Vazquez A, Villarreal-Molina MT, Rasmussen A, Tusié-Luna MT, López M, Canizales-Quinteros S, Alonso ME.

Neurogenetics. 2006 Jul;7(3):195-200. Epub 2006 Apr 21.

PMID:
16628450
32.

Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma.

Rasmussen A, Nava-Salazar S, Yescas P, Alonso E, Revuelta R, Ortiz I, Canizales-Quinteros S, Tusié-Luna MT, López-López M.

J Neurosurg. 2006 Mar;104(3):389-94.

PMID:
16572651
33.

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.

Arch Med Res. 2006 Jan;37(1):102-8. Erratum in: Arch Med Res. 2006 Feb;37(2):297.

PMID:
16314194
34.

GENEHUNTER versus SimWalk2 in the context of an extended kindred and a qualitative trait locus.

Romero-Hidalgo S, Rodrigues ER, Gutiérrez-Peña E, Riba L, Tusié-Luna MT.

Genetica. 2005 Mar;123(3):235-44.

PMID:
15954494
35.

Genes and type 2 diabetes mellitus.

Tusié Luna MT.

Arch Med Res. 2005 May-Jun;36(3):210-22. Review.

PMID:
15925011
36.

[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.

Gac Med Mex. 2005 Mar-Apr;141(2):115-22. Spanish.

PMID:
15892459
37.

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.

JOP. 2005 May 10;6(3):238-45.

38.

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.

Hum Genet. 2005 Jan;116(1-2):114-20. Epub 2004 Nov 17.

PMID:
15599766
39.

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.

Ann Hum Genet. 2004 Sep;68(Pt 5):419-27.

40.

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.

Mol Genet Metab. 2004 Feb;81(2):122-6.

PMID:
14741193
41.

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.

J Pediatr Endocrinol Metab. 2003 Sep;16(7):1017-24.

PMID:
14513879
42.

With the finished human genome in hand, what next?

Collado-Vides J, Medrano-Soto A, Tusié-Luna MT.

Genome Biol. 2003;4(7):328. Epub 2003 Jun 27. No abstract available.

43.

[The road toward molecular comprehension of diseases].

Tusié Luna MT.

Rev Invest Clin. 2003 Mar-Apr;55(2):143-7. Review. Spanish. No abstract available.

PMID:
12827917
44.

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.

Circ Res. 2003 Mar 21;92(5):569-76. Epub 2003 Feb 27.

45.

Familial hypercholesterolemia due to ligand-defective apolipoprotein B100: first case report in a Mexican family.

Robles-Osorio L, Ordoñez ML, Aguilar-Salinas CA, Aurón-Gómez M, Tusié-Luna MT, Gómez-Pérez FJ, Rull-Rodrigo JA.

Arch Med Res. 2003 Jan-Feb;34(1):70-5.

PMID:
12604379
46.

[The human genetic variability map, single nucleotide polymorphisms (SNP's) and some of their applications to medicine].

Tusié Luna MT.

Rev Invest Clin. 2001 Jul-Aug;53(4):308-10. Spanish. No abstract available.

PMID:
11599476
47.

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.

J Clin Endocrinol Metab. 2001 Jan;86(1):220-6.

PMID:
11232004
48.

[Role of the allelic E4 variant of apolipoprotein E in lipid concentrations in a Mexican rural indigenous population predisposed to type 2 diabetes mellitus].

Canizales Quinteros S, Tusié Luna MT.

Rev Invest Clin. 2000 May-Jun;52(3):314-7. Spanish. No abstract available.

PMID:
10953615
49.

[Genetics of type 2 diabetes mellitus: genes implicated in early onset diabetes].

Tusié Luna MT.

Rev Invest Clin. 2000 May-Jun;52(3):296-305. Spanish.

PMID:
10953613

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