Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Ingrid Patricia Dávalos Rodríguez"'
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:
Aniel Jessica Leticia Brambila-Tapia, Fabiola Macías-Espinoza, Yesica Arlae Reyes-Domínguez, María Luisa Ramírez-García, Aris Judit Miranda-Lavastida, Blanca Estela Ríos-González, Ana Miriam Saldaña-Cruz, Yussef Esparza-Guerrero, Francisco Fabián Mora-Moreno, Ingrid Patricia Dávalos-Rodríguez
Publikováno v:
Healthcare; Volume 10; Issue 6; Pages: 1048
Somatization and number of diseases are interrelated variables, whose association with stress-coping strategies, according to sex, has not been investigated. Therefore, the aim of this study was to investigate such association in a sample of the Mexi
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:
Mario Alberto Aceves-Aceves, Jorge I. Gamez-Nava, Ana Lilia Díaz-Pérez, Ingrid Patricia Dávalos-Rodríguez, Mario Salazar-Páramo, Laura Gonzalez-Lopez, María Cristina Morán-Moguel, Christian Michel Enríquez-Barajas, Daniel Efraín Silva-Castro, Martha Rocio Hernández-Preciado, Juan Paulo Valdovinos-Maravilla
Publikováno v:
Genetic Testing and Molecular Biomarkers
Aim: The present study looked for variation in the miRNA-24 sequence, and evaluated the associations between the dihydrofolate reductase (DHFR) gene-829 C-T polymorphism and plasma DHFR concentrations with response to methotrexate (MTX) treatment in
Publikováno v:
Journal of Clinical Laboratory Analysis
Background Non‐acrocentric satellited chromosomes mostly result from familial balanced insertions or translocations with p12 or p13 of any acrocentric. Although all non‐acrocentrics have been involved, only 12 instances of chromosome 6 involvemen
Autor:
Alejandro Marín-Medina, Moisés Alejandro Alatorre-Jiménez, José Juan Gómez-Ramos, Sergio Emilio Prieto-Miranda, Ingrid Patricia Dávalos-Rodríguez, Eduardo Esteban-Zubero
Publikováno v:
The American Journal of Emergency Medicine. 36:1418-1422
To determine the validity of plasma lactate in the emergency department for the early detection of tissue hypoperfusion in septic patients.Longitudinal descriptive study. Non probabilistic sampling for convenience. Plasma lactate levels were determin
Autor:
Azubel, Ramírez-Velazco, Thania Alejandra, Aguayo-Orozco, Luis, Figuera, Horacio, Rivera, Luis, Jave-Suárez, Adriana, Aguilar-Lemarroy, Luis A, Torres-Reyes, Carlos, Córdova-Fletes, Patricio, Barros-Núñez, Saturnino, Delgadillo-Pérez, Ingrid Patricia, Dávalos-Rodríguez, José Elías, García-Ortiz, María G, Domínguez
Publikováno v:
Journal of genetics. 98(2)
Williams-Beuren syndrome (WBS) has a prevalence of 1/7500-20000 live births and results principally from a
Autor:
Luis E. Figuera, Carlos Córdova-Fletes, José Elías García-Ortiz, Ingrid Patricia Dávalos-Rodríguez, Saturnino Delgadillo-Pérez, M G Domínguez, Horacio Rivera, Patricio Barros-Núñez, Luis A Torres-Reyes, Luis Felipe Jave-Suárez, Azubel Ramírez-Velazco, Adriana Aguilar-Lemarroy, Thania Alejandra Aguayo-Orozco
Publikováno v:
Journal of Genetics. 98
Williams-Beuren syndrome (WBS) has a prevalence of 1/7500-20000 live births and results principally from a de novo deletion in 7q11.23 with a length of 1.5 Mb or 1.8 Mb. This study aimed to determine the frequency of 7q11.23 deletion, size of the seg
Autor:
Sergio Alberto Ramírez-García, Diana García-Cruz, Iván Cervantes-Aragón, Wadih Emilio Bitar-Alatorre, Ingrid Patricia Dávalos-Rodríguez, Nory Omayra Dávalos-Rodríguez, Jorge Román Corona-Rivera, José Sánchez-Corona
Publikováno v:
Cirugia y cirujanos. 86(1)
Achondrogenesis is a skeletal dysplasia characterized primarily by short stature, severe micromelia, short and narrow chest, prematurity, polyhydramnios, fetal hydrops, and in utero or neonatal death. Based on the radiological and histopathological f
Autor:
Wadih Emilio Bitar-Alatorre, José Sánchez-Corona, Iván Cervantes-Aragón, Ingrid Patricia Dávalos-Rodríguez, Jorge Román Corona-Rivera, Diana García-Cruz, Nory Omayra Dávalos-Rodríguez, Sergio Alberto Ramirez-Garcia
Publikováno v:
Cirugía y Cirujanos. 86
Background Achondrogenesis is a skeletal dysplasia characterized primarily by short stature, severe micromelia, short and narrow chest, prematurity, polyhydramnios, fetal hydrops, and in utero or neonatal death. Based on the radiological and histopat