Search Results - "Tusie Luna, Ma Teresa"

High Adiponectin Concentrations Are Associated with the Metabolically Healthy Obese Phenotype by Aguilar-Salinas, Carlos A., García, Eduardo García, Robles, Lorena, Riaño, Daniela, Ruiz-Gomez, Doris Georgina, García-Ulloa, Ana Cristina, Melgarejo, Marco A., Zamora, Margarita, Guillen-Pineda, Luz E., Mehta, Roopa, Canizales-Quinteros, Samuel, Tusie Luna, Ma Teresa, Gómez-Pérez, Francisco J.

“…Context: In the ob/ob mice, keeping adiponectin concentrations in the physiological range (through overexpression of this gene in the adipose tissue) results…”
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A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia by 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

“…Autosomal recessive hypercholesterolemia (ARH) is characterized by elevated LDL serum levels, xanthomatosis, and premature coronary artery disease. Three loci…”
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Hypoalphalipoproteinemia in populations of Native American ancestry: an opportunity to assess the interaction of genes and the environment by Aguilar-Salinas, Carlos A, Canizales-Quinteros, Samuel, Rojas-Martínez, Rosalba, Mehta, Roopa, Villarreal-Molina, Ma Teresa, Arellano-Campos, Olimpia, Riba, Laura, Gómez-Pérez, Francisco J, Tusié-Luna, Ma Teresa

“…Our aim is to review the environmental and genetic factors associated with hypoalphalipoproteinemia in populations of Native American ancestry. We examine the…”
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Early onset type 2 diabetes in Jamaica and in Mexico. Opportunities derived from an interethnic study by Irving, Rachael, Tusié-Luna, Ma Teresa, Mills, James, Wright-Pascoe, Rosemarie, McLaughlin, Wayne, Aguilar-Salinas, Carlos A

“…Populations with Amerindian or African heritages are the one with the highest prevalence of diabetes worldwide. A large percentage of these individuals…”
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Genetic Heterogeneity of Autosomal Dominant Hypercholesterolemia in Mexico by 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.

“…Familial hypercholesterolemia (FH) and familial defective apolipoprotein B-100 (FDB) are relatively common lipid disorders caused by mutations of the…”
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Early-onset type 2 diabetes : Metabolic and genetic characterization in the Mexican population by 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

“…The objective of this study was to investigate possible defects in the insulin sensitivity and/or the acute insulin response in a group of Mexican patients…”
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Nuevas perspectivas en el síndrome de QT largo by Medeiros-Domingo, Argelia, Iturralde-Torres, Pedro, Cañizales-Quinteros, Samuel, Hernández-Cruz, Arturo, Tusié-Luna, Ma. Teresa

“…El síndrome de QT largo (SQTL) es una canalopatía que genera grave alteración en la repolarización ventricular predispone a arritmias malignas y muerte súbita…”
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New perspectives in long QT syndrome by Medeiros-Domingo, Argelia, Iturralde-Torres, Pedro, Canizales-Quinteros, Samuel, Hernández-Cruz, Arturo, Tusié-Luna, M Teresa

“…Long QT Syndrome (LQTS) is a cardiac channelopathy characterized by prolonged ventricular repolarization and increased risk to sudden death secondary to…”
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Contribution of Chromosome 1q21‐q23 to Familial Combined Hyperlipidemia in Mexican Families by 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.

“…Summary Familial combined hyperlipidemia (FCHL) is the most common familial dyslipidemia, with a prevalence of 1‐2% in the general population. A major locus…”
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The road toward molecular comprehension of diseases by Tusié Luna, Ma Teresa

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Familial Hypercholesterolemia Due to Ligand-Defective Apolipoprotein B100.: First Case Report in a Mexican Family by Robles-Osorio, Ludivina, Ordoñez, Ma.Luisa, Aguilar-Salinas, Carlos A, Aurón-Gómez, Moisés, Tusié-Luna, Ma.Teresa, Gómez-Pérez, Francisco J, Rull-Rodrigo, Juan A

“…Familial defective apolipoprotein B100 (FDB) is one of the known causes of familial hypercholesterolemia (FH). Its frequency among subjects with FH varies…”
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Early-Onset Type 2 Diabetes: Metabolic and Genetic Characterization in the Mexican Population 1 by Aguilar-Salinas, Carlos A., Reyes-RodrÍguez, Eduardo, Ordóñez-Sánchez, Ma. Luisa, Torres, Marcelo Arellano, Ramírez-Jiménez, Salvador, Domínguez-López, Aarón, MartÍnez-Francois, Juan Ramón, Velasco-Pérez, Ma. Luisa, Alpizar, Melchor, GarcÍa-GarcÍa, Eduardo, Gómez-Pérez, Francisco, Rull, Juan, Tusié-Luna, Ma. Teresa

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Early-Onset Type 2 Diabetes: Metabolic and Genetic Characterization in the Mexican Population1 by Aguilar-Salinas, Carlos A., Reyes-RodrÍguez, Eduardo, Ordóñez-Sánchez, Ma. Luisa, Torres, Marcelo Arellano, Ramírez-Jiménez, Salvador, Domínguez-López, Aarón, MartÍnez-Francois, Juan Ramón, Velasco-Pérez, Ma. Luisa, Alpizar, Melchor, GarcÍa-GarcÍa, Eduardo, Gómez-Pérez, Francisco, Rull, Juan, Tusié-Luna, Ma. Teresa

“…The objective of this study was to investigate possible defects in the insulin sensitivity and/or the acute insulin response in a group of Mexican patients…”
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Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population by 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

“…Steroid 21-hydroxylase deficiency is caused by mutations in the CYP21 gene. Approximately 95% of mutant alleles are generated by recombination events between…”
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