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
ORDONEZ-SANCHEZ, M. L, RAMIREZ-JIMENEZ, S, TUSIE-LUNA, M. T, LOPEZ-GUTIERREZ, A. U, RIBA, L, GAMBOA-CARDIEL, S, CERRILLO-HINOJOSA, M, ALTAMIRANO-BUSTAMANTE, N, CALZADA-LEON, R, ROBLES-VALDES, C, MENDOZA-MORFIN, F
Published in Human genetics (01.02.1998)
Published in Human genetics (01.02.1998)
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A cis-acting element in the promoter of human ether à go-go 1 potassium channel gene mediates repression by calcitriol in human cervical cancer cells
Cázares-Ordoñez, V, González-Duarte, R J, Díaz, L, Ishizawa, M, Uno, S, Ortíz, V, Ordoñez-Sánchez, M L, Makishima, M, Larrea, F, Avila, E
Published in Biochemistry and cell biology (01.02.2015)
Published in Biochemistry and cell biology (01.02.2015)
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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, M. L., Segura-Kato, Y., Ortíz, V., Díaz-Díaz, E., Muñoz-Hernández, L., García, A., Pérez-Méndez, O., Zentella-Dehesa, A., Aguilar-Salinas, C. A., Tusié-Luna, M. T.
Published in Journal of endocrinological investigation (01.08.2020)
Published in Journal of endocrinological investigation (01.08.2020)
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A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia
CANIZALES-QUINTEROS, Samuel, AGUILAR-SALINAS, Carlos A, ROBLES-OSORIO, Ludivina, MILIAR-GARCIA, Angel, ROSALES-LEON, Luis, RUIZ-ORDAZ, Blanca H, ZENTELLA-DEHESA, Alejandro, FERRE-D'AMARE, Adrian, GOMEZ-PEREZ, Francisco J, TUSIE-LUNA, Ma. Teresa, HUERTAS-VAZQUEZ, Adriana, ORDONEZ-SANCHEZ, Maria L, RODRIGUEZ-TORRES, Maribel, VENTURAS-GALLEGOS, José L, RIBA, Laura, RAMIREZ-JIMENEZ, Salvador, SALAS-MONTIEL, Rocio, MEDINA-PALACIOS, Giovani
Published in Human genetics (2005)
Published in Human genetics (2005)
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Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease
López-Gutiérrez, A U, Riba, L, Ordoñez-Sánchez, M L, Ramírez-Jiménez, S, Cerrillo-Hinojosa, M, Tusié-Luna, M T
Published in Journal of medical genetics (01.12.1998)
Published in Journal of medical genetics (01.12.1998)
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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, M. T., Moreno-Macías, H., Ochoa-Guzmán, A., Ordoñez-Sánchez, M. L., Rodríguez-Guillen, R., Vázquez-Cárdenas, P., Ortíz-Ortega, V. M., Peimbert-Torres, M., Aguilar-Salinas, C. A., Tusié-Luna, M. T.
Published in Journal of endocrinological investigation (01.03.2021)
Published in Journal of endocrinological investigation (01.03.2021)
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Early-onset type 2 diabetes : Metabolic and genetic characterization in the Mexican population
AGUILAR-SALINAS, Carlos A, REYES-RODRIGUEZ, Eduardo, GOMEZ-PEREZ, Francisco, RULL, Juan, TUSIE-LUNA, Ma. Teresa, ORDONEZ-SANCHEZ, Ma. Luisa, ARELLANO TORRES, Marcelo, RAMIREZ-JIMENEZ, Salvador, DOMINGUEZ-LOPEZ, Aaron, MARTINEZ-FRANCOIS, Juan Ramon, VELASCO-PEREZ, Ma. Luisa, ALPIZAR, Melchor, GARCIA-GARCIA, Eduardo
Published in The journal of clinical endocrinology and metabolism (2001)
Published in The journal of clinical endocrinology and metabolism (2001)
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Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population
Tusié-Luna, M T, Ramírez-Jiménez, S, Ordóñez-Sánchez, M L, Cabello-Villegas, J, Altamirano-Bustamante, N, Calzada-León, R, Robles-Valdés, C, Mendoza-Morfín, F, Méndez, J P, Terán-García, M
Published in Human genetics (01.09.1996)
Published in Human genetics (01.09.1996)
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Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease
Lobato, M. Natividad, Ordóñez-Sánchez, M. Luisa, Tusié-Luna, M. Teresa, Meseguer, Anna
Published in Human heredity (01.01.1999)
Published in Human heredity (01.01.1999)
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