Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Salvador, Ramírez-Jiménez"'
Autor:
Samuel Canizales-Quinteros, Blanca H. Ruiz-Ordaz, Laura Riba, Alejandro Zentella-Dehesa, Salvador Ramírez-Jiménez, Rocío Salas-Montiel, Maribel Rodríguez-Torres, Luis Rosales-León, Giovani Medina-Palacios, Adrian R. Ferré-D'Amaré, Adriana Huertas-Vazquez, Ma. Teresa Tusié-Luna, Ángel Miliar-García, José L. Venturas-Gallegos, Ludivina Robles-Osorio, Francisco J. Gómez-Pérez, Carlos A. Aguilar-Salinas, María Luisa Ordóñez-Sánchez
Publikováno v:
Human Genetics. 116:114-120
Autosomal recessive hypercholesterolemia (ARH) is characterized by elevated LDL serum levels, xanthomatosis, and premature coronary artery disease. Three loci have been described for this condition (1p35, 15q25-q26 and 13q). Recently, the responsible
Autor:
F J Gómez-Pérez, Salvador Ramírez-Jiménez, M Aurón-Gómez, Adriana Huertas-Vazquez, Ma. Teresa Tusié-Luna, Gerardo Vega-Hernández, Laura Riba, Samuel Canizales-Quinteros, J P del Rincón, Carlos A. Aguilar-Salinas
Publikováno v:
Annals of Human Genetics. 68:419-427
Familial combined hyperlipidemia (FCHL) is the most common familial dyslipidemia, with a prevalence of 1-2% in the general population. A major locus for FCHL has been mapped to chromosome 1q21-q23 in Finnish, Chinese, German and US families. We studi
Autor:
Carlos A. Aguilar-Salinas, Ma. Luisa Velasco-Pérez, Ma. Luisa Ordonez-Sanchez, Salvador Ramírez-Jiménez, Eduardo García-García, Marcelo Arellano Torres, Melchor Alpizar, Juan A. Rull, Juan Ramón Martínez-François, Eduardo Reyes-Rodríguez, Francisco J. Gómez-Pérez, Aarón Domínguez-López, Ma. Teresa Tusié-Luna
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 86:220-226
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 displaying early-onset type 2 diabetes and to evaluate the contribution of mutations in three
Autor:
Laura Riba, Salvador Ramírez-Jiménez, M T Tusié-Luna, A U López-Gutiérrez, M Cerrillo-Hinojosa, María Luisa Ordóñez-Sánchez
Publikováno v:
Journal of Medical Genetics. 35:1014-1019
Congenital adrenal hyperplasia (CAH) is an inherited recessive disorder of adrenal steroidogenesis caused by mutations in the steroid 21-hydroxylase gene (CYP21) in more than 90% of affected patients. The CYP21 gene is located within the HLA complex
Autor:
Mabel Cerrillo-Hinojosa, Nelly Altamirano-Bustamante, Carlos Robles-Valdés, María Teresa Tusié-Luna, Raúl Calzada-León, Antonio Ulises López-Gutierrez, F. Mendoza-Morfin, María Luisa Ordóñez-Sánchez, Salvador Ramírez-Jiménez, Salvador Gamboa-Cardiel, Laura Riba
Publikováno v:
Human Genetics. 102:170-177
Steroid 21-hydroxylase deficiency is the underlying cause in over 90% of patients with congenital adrenal hyperplasia, an inherited metabolic disorder of adrenal steroidogenesis. We have characterized 94 mutant alleles from 47 unrelated Mexican patie
Autor:
Victor Acuña-Alonzo, Adriana Huertas-Vazquez, Maricela Rodríguez-Cruz, Ma Guadalupe Ortiz-López, José Bustos-Arriaga, Ana M Tito-Alvarez, Lin-Hua Zhang, Andrés Moreno-Estrada, Sandra Romero-Hidalgo, Martin Sikora, Sandro L. Bonatto, Isela Montúfar-Robles, Ma de Angeles Granados-Silvestre, Teresa Villarreal-Molina, Janine K. Kruit, Leslie J. Baier, Teresa Tusié-Luna, Michael R. Hayden, Marta Menjivar, Leonor Jacobo-Albavera, William C. Knowler, Carlos A. Aguilar-Salinas, Rodrigo Barquera-Lozano, Rubén Lisker, Antonio González-Martín, Camilo Zurita-Salinas, Leticia Cedillo-Barrón, Celta Gomez-Trejo, Teresa Flores-Dorantes, Amaya Gorostiza, Paola León-Mimila, Salvador Ramírez-Jiménez, M. Catira Bortolini, Terry D Pape, Samuel Canizales-Quinteros, Julio Granados, Regina S. Moisés, Marisela Villalobos-Comparán, Francisco M. Salzano, João P. B. Vieira-Filho, Olimpia Arellano-Campos, Hugo Villamil-Ramírez, Li Wang, Tábita Hünemeier
Publikováno v:
Human Molecular Genetics, 19(14), 2877-85. Oxford University Press
Digital.CSIC. Repositorio Institucional del CSIC
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Digital.CSIC. Repositorio Institucional del CSIC
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9 páginas, 5 figuras, 1 tabla.-- Acuña-Alonzo, Víctor et al.
It has been suggested that the higher susceptibility of Hispanics to metabolic disease is related to their Native American heritage. A frequent cholesterol transporter ABCA1 (ATP-bi
It has been suggested that the higher susceptibility of Hispanics to metabolic disease is related to their Native American heritage. A frequent cholesterol transporter ABCA1 (ATP-bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49c88ecc13ac85a5be11fabb8b0c0785
https://research.rug.nl/en/publications/70d79b2e-90d1-405e-a6b6-389dd572eff5
https://research.rug.nl/en/publications/70d79b2e-90d1-405e-a6b6-389dd572eff5
Autor:
Samuel, Canizales-Quinteros, Adriana, Huertas-Vázquez, Laura, Riba-Ramírez, Adriana, Monroy-Guzmán, Aarón, Domínguez-López, Sandra, Romero-Hidalgo, Carlos, Aguilar-Salinas, Maribel, Rodríguez-Torres, Salvador, Ramírez-Jiménez, María Teresa, Tusié-Luna
Publikováno v:
Gaceta medica de Mexico. 141(2)
Coronary artery disease and diabetes mellitus are among the primary mortality and morbidity causes in Mexico. Genetic factors play a fundamental role in the development of these entities. In the past few years due to the recognition and study of fami
Autor:
Aarón, Domínguez-López, Angel, Miliar-García, Yayoi X, Segura-Kato, Laura, Riba, Riba, Esparza-López, Salvador, Ramírez-Jiménez, Maribel, Rodríguez-Torres, Samuel, Canizales-Quinteros, Siraam, Cabrera-Vásquez, Verónica, Fragoso-Ontiveros, Carlos A, Aguilar-Salinas, Nelly, Altamirano-Bustamante, Raúl, Calzada-León, Carlos, Robles-Valdés, Luz E, Bravo-Ríos, Maria Teresa, Tusié-Luna
Publikováno v:
JOP : Journal of the pancreas. 6(3)
Maturity-onset diabetes of the young (MODY) is a monogenic form of diabetes mellitus characterized by autosomal dominant inheritance, early age of onset and a primary insulin secretion defect. Certain MODY gene sequence variants may be involved in po
Autor:
Erika Ramírez, Takafumi Tsuchiya, Marı́a Teresa Tusié-Luna, Nancy J. Cox, Salvador Ramírez-Jiménez, Marı́a Luisa Velasco-Pérez, Maribel Rodríguez-Torres, Issei Yoshiuchi, Alfredo Ramı́rez-Silva, Craig L. Hanis, Graeme I. Bell, Laura del Bosque-Plata, Moisés Aurón-Gómez, Carlos A. Aguilar-Salinas, Francisco J. Gómez-Pérez
Publikováno v:
Molecular genetics and metabolism. 81(2)
Variation in the calpain-10 gene (CAPN10) has been associated with risk of type 2 diabetes in the Mexican American population of Starr County, Texas. We typed five polymorphisms in the calpain-10 gene (SNP-43, -43, -63, and -110 and Indel-19) to test
Autor:
Ma. Luisa Ordonez-Sanchez, Xochitl Felix-Lopez, Ma. Teresa Tusié-Luna, Alejandro Zentella-Dehesa, Salvador Ramírez-Jiménez, José Luis Ventura-Gallegos, Laura Riba
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 16(7)
Steroid 21-hydroxylase deficiency is the major cause of congenital adrenal hyperplasia, an autosomic recessive disorder that affects the synthesis of aldosterone and cortisol. The disease presents a wide spectrum of clinical phenotypes as a result of