Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ingrid P, Dávalos"'
Autor:
Martha Patricia Gallegos-Arreola, Asbiel Felipe Garibaldi-Ríos, María Teresa Magaña-Torres, Luis E. Figuera, Belinda Claudia Gómez-Meda, Guillermo Moisés Zúñiga-González, Ana María Puebla-Pérez, Irving Alejandro Carrillo-Dávila, Mónica Alejandra Rosales-Reynoso, Ingrid Patricia Dávalos-Rodríguez, Jorge I. Delgado-Saucedo, Marco Uriel López-Monroy
Publikováno v:
Diseases, Vol 12, Iss 11, p 276 (2024)
Background/Objectives: This study investigated the association between the rs13306703 and rs8192288 variants of the superoxide dismutase 3 (SOD3) gene and breast cancer (BC) in the Mexican population, conducting both genetic and in silico analyses. M
Externí odkaz:
https://doaj.org/article/aba55136705540a4866a65aab1be650c
Autor:
Valeria Peralta-Leal, Evelia Leal-Ugarte, Juan P. Meza-Espinoza, Ingrid P. Dávalos-Rodríguez, Anabel Bocanegra-Alonso, Rosa I. Acosta-González, Enrique Gonzales, Saraswathy Nair, Jorge Durán-González
Publikováno v:
Genetics and Molecular Biology, Vol 35, Iss 3, Pp 589-593 (2012)
The serotonergic system has been hypothesized to contribute to the biological susceptibility to type 2 diabetes mellitus (T2DM) and body-mass index (BMI) categories. We investigate a possible association of 5-HTTLPR polymorphism (L and S alleles) in
Externí odkaz:
https://doaj.org/article/d344bf945f1f4079934b5402142db90f
Autor:
Alberto Daniel Rocha-Muñoz, Aniel Jessica Leticia Brambila-Tapia, María Guadalupe Zavala-Cerna, José Clemente Vásquez-Jiménez, Liliana Faviola De la Cerda-Trujillo, Mónica Vázquez-Del Mercado, Norma Alejandra Rodriguez-Jimenez, Valeria Díaz-Rizo, Viviana Díaz-González, Ernesto German Cardona-Muñoz, Ingrid Patricia Dávalos-Rodríguez, Mario Salazar-Paramo, Jorge Ivan Gamez-Nava, Arnulfo Hernan Nava-Zavala, Laura Gonzalez-Lopez
Publikováno v:
Journal of Immunology Research, Vol 2015 (2015)
Objective. To evaluate the effect of anti-TNF agents plus synthetic disease modifying antirheumatic drugs (DMARDs) versus DMARDs alone for ankylosing spondylitis (AS) with reduced pulmonary function vital capacity (FVC%). Methods. In an observational
Externí odkaz:
https://doaj.org/article/499897296f314dcb9bfd39f02293c380
Autor:
Wendoline Rojo-Contreras, Valeria Diaz-Rizo, Xochitl Trujillo, Miguel Huerta, Alberto D. Rocha-Muñoz, Benjamin Trujillo-Hernandez, Alicia Rivera-Cameras, Ingrid P. Dávalos-Rodríguez, Mario Salazar-Páramo
Publikováno v:
Healthcare; Volume 10; Issue 10; Pages: 1825
We estimate the prevalence and identified the associated factors of sexual dysfunction in Mexican women with rheumatoid arthritis (RA). A cross-sectional survey was applied to 100 women with RA and compared with 100 healthy, sexually active, adult wo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ad50d971d2232f1fae52ec739dcb3e8
https://doi.org/10.3390/healthcare10101825
https://doi.org/10.3390/healthcare10101825
Autor:
Ricardo Medina-Coss y León, M. Patricia Gallegos-Arreola, Mirna Gisel González-Mercado, Laura Gonzalez-Lopez, M. Cristina Morán-Moguel, J. Iván Gámez-Nava, Ingrid P. Dávalos, J. Francisco Muñoz-Valle, Mario Salazar-Páramo, Agustín Macías-Chumacera, Fernando Rivas, Nory Omayra Dávalos, Anahí González-Mercado, Mario Alberto Aceves Aceves
Publikováno v:
Genetic Testing and Molecular Biomarkers
Aim: To investigate the relationships of polymorphisms in genes whose protein products are related in the metabolic pathway of folic acid, particularly MTRR A66G, RFC1 G80A, and MTHFR C677T and A1298C, and disease activity in Mexican patients with rh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a8e10651bcaa1b8086ebc1a1155b449
https://pubmed.ncbi.nlm.nih.gov/28994615
https://pubmed.ncbi.nlm.nih.gov/28994615
Autor:
María Teresa Magaña, Ingrid P. Dávalos, Vaca G, Bertha Marìn, Gabriela Carrillo, Esperanza Pérez Martínez, María Lourdes Ramirez, Alejandra Vàzquez
Publikováno v:
Atherosclerosis. 218:391-396
The goal of this project was to identify families with autosomal dominant hypercholesterolemia (ADH) to facilitate early detection and treatment and to provide genetic counselling as well as to approximate the mutational diversity of ADH in Mexico. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::238929139f9fbd594f4fe91c8fc9306c
https://doi.org/10.1016/j.atherosclerosis.2011.06.006
https://doi.org/10.1016/j.atherosclerosis.2011.06.006
Autor:
D. García-Cruz, Zamira Nazará, M O García-Cruz, Ingrid P. Dávalos, Victor Castañeda, José Elias García-Ortiz, Leonel Gutiérrez-Mendivil, José Sánchez-Corona
Publikováno v:
Clinical Dysmorphology. 16:15-20
Three siblings with postaxial polydactyly type A, congenital heart defect (single atrium), mental retardation, microcephaly, a distinctive facial appearance, skeletal anomalies and neonatal macrosomy were studied. Comparison with other cardiomelic sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a3485246eba061112c0fbacc961f1ac
https://doi.org/10.1097/01.mcd.0000198929.24577.a5
https://doi.org/10.1097/01.mcd.0000198929.24577.a5
Autor:
Ingrid P. Dávalos, Esperanza Martínez-Abundis, Luis E. Figuera, Manuel González-Ortiz, J.M. Oliva, V. Machorro, Silvia Esperanza Flores-Martínez, J.P. Mena, J A Tlacuilo-Parra, Mario Salazar-Páramo, José Sánchez-Corona, M.C. Moran, Lucila Sandoval
Publikováno v:
Blood Cells, Molecules, and Diseases. 35:66-69
The etiology of preeclampsia is still a matter of controversy. An association between hyperhomocysteinemia and preeclamptic patients has been described. A common missense mutation in the methylenetetrahydrofolate reductase (MTHFR) gene is associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c43c7d795dde3d8db52009f8db1c7f2d
https://doi.org/10.1016/j.bcmd.2005.03.008
https://doi.org/10.1016/j.bcmd.2005.03.008
Publikováno v:
Clinical Dysmorphology. 11:243-247
A Mexican family is presented with the main clinical features of camptodactyly, a distinctive facial appearance because of ocular hypertelorism, telecanthus, symblepharon and spinal defects. Other clinical manifestations included: multiple nevi, simp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7335cfc3bafc5ac3c325ac3f1c189efd
https://doi.org/10.1097/00019605-200210000-00003
https://doi.org/10.1097/00019605-200210000-00003
Publikováno v:
American Journal of Medical Genetics. 103:289-294
We report on a man with mental retardation and a complex karyotype with cells containing up to three morphologically distinct supernumerary marker chromosomes (SMCs) in most metaphases. Fluorescence in situ hybridisation studies using chromosome 15-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::182b7d54470120b90adcab9b125bf4c9
https://doi.org/10.1002/ajmg.1516
https://doi.org/10.1002/ajmg.1516