Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Maria Luisa Ordoñez-Sánchez"'
Autor:
Magdalena Sevilla-González, Maria Fernanda Garibay-Gutiérrez, Arsenio Vargas-Vázquez, Andrea Celeste Medina-García, Maria Luisa Ordoñez-Sánchez, Clary B Clish, Paloma Almeda-Valdes, Teresa Tusie-Luna
Publikováno v:
Current Developments in Nutrition, Vol 8, Iss 9, Pp 104444- (2024)
Background: A risk haplotype in SLC16A11 characterized by alterations in fatty acid metabolism emerged as a genetic risk factor associated with increased susceptibility to type 2 diabetes (T2D) in Mexican population. Its role on treatment responses i
Externí odkaz:
https://doaj.org/article/00026c60dbba4e9d9cf10fa8c7287ee8
Autor:
Laura E. Martínez-Gómez, Carlos Martinez-Armenta, Daniel Medina-Luna, María Luisa Ordoñez-Sánchez, Tere Tusie-Luna, Silvestre Ortega-Peña, Brígida Herrera-López, Carlos Suarez-Ahedo, Guadalupe Elizabeth Jimenez-Gutierrez, Alberto Hidalgo-Bravo, Paola Vázquez-Cárdenas, Rosa P. Vidal-Vázquez, Juan P. Ramírez-Hinojosa, Pilar Miyoko Martinez Matsumoto, Gilberto Vargas-Alarcón, Rosalinda Posadas-Sánchez, José-Manuel Fragoso, Felipe de J. Martínez-Ruiz, Dulce M. Zayago-Angeles, Mónica Maribel Mata-Miranda, Gustavo Jesús Vázquez-Zapién, Adriana Martínez-Cuazitl, Javier Andrade-Alvarado, Julio Granados, Luis Ramos-Tavera, María del Carmen Camacho-Rea, Yayoi Segura-Kato, José Manuel Rodríguez-Pérez, Roberto Coronado-Zarco, Rafael Franco-Cendejas, Luis Esau López-Jácome, Jonathan J. Magaña, Marcela Vela-Amieva, Carlos Pineda, Gabriela Angélica Martínez-Nava, Alberto López-Reyes
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 56, Iss 5, Pp 939-950 (2023)
Background/purpose(s): During a viral infection, the immune response is mediated by the toll-like receptors and myeloid differentiation Factor 88 (MyD88) that play an important role sensing infections such as SARS-CoV-2 which has claimed the lives of
Externí odkaz:
https://doaj.org/article/088b5f42a8be4673ab7c6b2e4ae1cc27
Autor:
Ivette Cruz-Bautista, Alicia Huerta-Chagoya, Hortensia Moreno-Macías, Rosario Rodríguez-Guillén, María Luisa Ordóñez-Sánchez, Yayoi Segura-Kato, Roopa Mehta, Paloma Almeda-Valdés, Lizeth Gómez-Munguía, Ximena Ruiz-De Chávez, Ximena Rosas-Flota, Arali Andrade-Amado, Bárbara Bernal-Barroeta, María Guadalupe López-Carrasco, Luz Elizabeth Guillén-Pineda, Angelina López-Estrada, Daniel Elías-López, Alexandro J. Martagón-Rosado, Donají Gómez-Velasco, Cesar Ernesto Lam-Chung, Omar Yaxmehen Bello-Chavolla, Fabiola Del Razo-Olvera, Lucely D. Cetina-Pérez, José Luis Acosta-Rodríguez, María Teresa Tusié-Luna, Carlos A. Aguilar-Salinas
Publikováno v:
Lipids in Health and Disease, Vol 20, Iss 1, Pp 1-13 (2021)
Abstract Background Familial hypertriglyceridemia (FHTG) is a partially characterized primary dyslipidemia which is frequently confused with other forms hypertriglyceridemia. The aim of this work is to search for specific features that can help physi
Externí odkaz:
https://doaj.org/article/65d5c8711dd447cab13487fcecca3748
Autor:
Alicia Huerta-Chagoya, Hortensia Moreno-Macías, Juan Carlos Fernández-López, María Luisa Ordóñez-Sánchez, Rosario Rodríguez-Guillén, Alejandra Contreras, Alfredo Hidalgo-Miranda, Luis Alberto Alfaro-Ruíz, Edgar Pavel Salazar-Fernandez, Andrés Moreno-Estrada, Carlos Alberto Aguilar-Salinas, Teresa Tusié-Luna
Publikováno v:
BMC Genetics, Vol 20, Iss 1, Pp 1-11 (2019)
Abstract Background Association studies are useful to unravel the genetic basis of common human diseases. However, the presence of undetected population structure can lead to both false positive results and failures to detect genuine associations. Ev
Externí odkaz:
https://doaj.org/article/ba897d81a80f47dd95f13ef840a8f202
Autor:
Carlos Gutiérrez-Cirlos, María Luisa Ordóñez-Sánchez, María Teresa Tusié-Luna, Bruce W. Patterson, Gustav Schonfeld, Carlos A. Aguilar-Salinas
Publikováno v:
Annals of Hepatology, Vol 10, Iss 2, Pp 155-164 (2011)
Introduction. Familial hypobetalipoproteinemia (FHBL) is an autosomal dominant disease characterized by abnormally low levels of apolipoprotein-B (apoB) containing lipoproteins. FHBL is caused by APOB, PCSK9 or ANGPTL3 mutations or is associated with
Externí odkaz:
https://doaj.org/article/2f4ecaf779014c18bb02ebd1e00d59f3