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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
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
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. 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
The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytes.
Almeda-Valdes P, Gómez Velasco DV, Arellano Campos O, Bello-Chavolla OY, Del Rocío Sevilla-González M, Viveros Ruiz T, Martagón Rosado AJ, Bautista CJ, Muñoz Hernandez L, Cruz-Bautista I, Moreno-Macias H, Huerta-Chagoya A, Rodríguez-Álvarez KG, Walford GA, Jacobs SBR, Guillen Pineda LE, Ordoñez-Sánchez ML, Roldan-Valadez E, Azpiroz J, Furuzawa-Carballeda J, Clark P, Herrera-Hernández MF, Zambrano E, Florez JC, Tusié Luna MT, Aguilar-Salinas CA. Almeda-Valdes P, et al. Eur J Endocrinol. 2019 Feb 1;180(2):99-107. doi: 10.1530/EJE-18-0677. Eur J Endocrinol. 2019. PMID: 30475225
R230C but not - 565C/T variant of the ABCA1 gene is associated with type 2 diabetes in Mexicans through an effect on lowering HDL-cholesterol levels.
Ochoa-Guzmán A, Moreno-Macías H, Guillén-Quintero D, Chávez-Talavera O, Ordoñez-Sánchez ML, Segura-Kato Y, Ortíz V, Díaz-Díaz E, Muñoz-Hernández L, García A, Pérez-Méndez O, Zentella-Dehesa A, Aguilar-Salinas CA, Tusié-Luna MT. Ochoa-Guzmán A, et al. Among authors: ordonez sanchez ml. J Endocrinol Invest. 2020 Aug;43(8):1061-1071. doi: 10.1007/s40618-020-01187-8. Epub 2020 Feb 3. J Endocrinol Invest. 2020. PMID: 32016916
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. Among authors: ordonez sanchez ml. 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
A novel nonsense mutation in the insulin receptor gene in a patient with HAIR-AN syndrome and endometrial cancer.
Cuenca D, Ventura-Gallegos JL, Almeda-Valdes P, Tusié-Luna MT, Reza-Albarran A, Ventura-Ayala L, Ordoñez-Sánchez ML, Segura-Kato Y, Gomez-Perez FJ, Conte MP, Gonzalez LR, Zentella-Dehesa A. Cuenca D, et al. Among authors: ordonez sanchez ml. Mol Genet Metab Rep. 2023 Mar 13;35:100965. doi: 10.1016/j.ymgmr.2023.100965. eCollection 2023 Jun. Mol Genet Metab Rep. 2023. PMID: 36941956 Free PMC article.
40 results