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
Published in Clinical genetics (01.02.2008)
Published in Clinical genetics (01.02.2008)
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Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma
Rasmussen, Astrid, Nava-Salazar, Sonia, Yescas, Petra, Alonso, Elisa, Revuelta, Rogelio, Ortiz, Iván, Canizales-Quinteros, Samuel, Tusié-Luna, María Teresa, López-López, Marisol
Published in Journal of neurosurgery (01.03.2006)
Published in Journal of neurosurgery (01.03.2006)
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Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population
del Bosque-Plata, Laura, Aguilar-Salinas, Carlos A, Tusié-Luna, Marı́a Teresa, Ramı́rez-Jiménez, Salvador, Rodrı́guez-Torres, Maribel, Aurón-Gómez, Moisés, Ramı́rez, Erika, Velasco-Pérez, Marı́a Luisa, Ramı́rez-Silva, Alfredo, Gómez-Pérez, Francisco, Hanis, Craig L, Tsuchiya, Takafumi, Yoshiuchi, Issei, Cox, Nancy J, Bell, Graeme I
Published in Molecular genetics and metabolism (01.02.2004)
Published in Molecular genetics and metabolism (01.02.2004)
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Genetic Heterogeneity of Autosomal Dominant Hypercholesterolemia in Mexico
Robles-Osorio, Ludivina, Huerta-Zepeda, Alejandra, Ordóñez, Ma. Luisa, Canizales-Quinteros, Samuel, Díaz-Villaseñor, Andrea, Gutiérrez-Aguilar, Ruth, Riba, Laura, Huertas-Vázquez, Adriana, Rodríguez-Torres, Maribel, Gómez-Díaz, Rita A., Salinas, Saul, Ongay-Larios, Laura, Codiz-Huerta, Guadalupe, Mora-Cabrera, Minerva, Mehta, Roopa, Gómez Pérez, Francisco J., Rull, Juan A., Rabès, Jean-Pierre, Tusié-Luna, Ma. Teresa, Durán-Vargas, Socorro, Aguilar-Salinas, Carlos A.
Published in Archives of medical research (2006)
Published in Archives of medical research (2006)
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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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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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Contribution of Chromosome 1q21‐q23 to Familial Combined Hyperlipidemia in Mexican Families
Huertas‐Vázquez, A., del Rincón, J. P., Canizales‐Quinteros, S., Riba, L., Vega‐Hernández, G., Ramírez‐Jiménez, S., Aurón‐Gómez, M., Gómez–Pérez, F. J., Aguilar‐Salinas, C. A., Tusié‐Luna, M. T.
Published in Annals of human genetics (01.09.2004)
Published in Annals of human genetics (01.09.2004)
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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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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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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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