Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Melva Gutiérrez Angulo"'
Autor:
Benedito Mauro Rossi, Edenir Inêz Palmero, Francisco López-Kostner, Carlos Sarroca, Carlos Alberto Vaccaro, Florencia Spirandelli, Patricia Ashton-Prolla, Yenni Rodriguez, Henrique de Campos Reis Galvão, Rui Manuel Reis, André Escremim de Paula, Luis Gustavo Capochin Romagnolo, Karin Alvarez, Adriana Della Valle, Florencia Neffa, Pablo German Kalfayan, Enrique Spirandelli, Sergio Chialina, Melva Gutiérrez Angulo, Maria del Carmen Castro-Mujica, Julio Sanchez de Monte, Richard Quispe, Sabrina Daniela da Silva, Norma Teresa Rossi, Claudia Barletta-Carrillo, Susana Revollo, Ximena Taborga, L. Lena Morillas, Hélène Tubeuf, Erika Maria Monteiro-Santos, Tamara Alejandra Piñero, Constantino Dominguez-Barrera, Patrik Wernhoff, Alexandra Martins, Eivind Hovig, Pål Møller, Mev Dominguez-Valentin
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-26 (2017)
Abstract Background Genetic counselling and testing for Lynch syndrome (LS) have recently been introduced in several Latin America countries. We aimed to characterize the clinical, molecular and mismatch repair (MMR) variants spectrum of patients wit
Externí odkaz:
https://doaj.org/article/1c493e85a2f64dbc8249789857b5f939
Autor:
Miguel Angel Trujillo-Rojas, María de la Luz Ayala-Madrigal, Melva Gutiérrez-Angulo, Anahí González-Mercado, José Miguel Moreno-Ortiz
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 21, Iss 1, Pp 1-8 (2023)
Abstract Background Lynch Syndrome (LS) is an autosomal dominant inheritance disorder characterized by genetic predisposition to develop cancer, caused by pathogenic variants in the genes of the mismatch repair system. Cases are detected by implement
Externí odkaz:
https://doaj.org/article/d9aa6d008d684051b1225226db1d4a4a
Autor:
Arturo Caballero-Avendaño, Melva Gutiérrez-Angulo, María de la Luz Ayala-Madrigal, José Miguel Moreno-Ortiz, Anahí González-Mercado, Jorge Peregrina-Sandoval
Publikováno v:
Genes, Vol 15, Iss 8, p 972 (2024)
CTNNB1 pathogenic variants are related to the improper functioning of the WNT/β-catenin pathway, promoting the development of different types of cancer of somatic origin. Bioinformatics analyses of genetic variation are a great tool to understand th
Externí odkaz:
https://doaj.org/article/a8e5679b4b104f1b9600e1c339faf011
Autor:
José Luis Venegas-Rodríguez, Jesús Arturo Hernández-Sandoval, Melva Gutiérrez-Angulo, José Miguel Moreno-Ortiz, Anahí González-Mercado, Jorge Peregrina-Sandoval, Helen Haydee Fernanda Ramírez-Plascencia, Beatriz Armida Flores-López, Carlos Rogelio Alvizo-Rodríguez, Jesús Alonso Valenzuela-Pérez, Sergio Cervantes-Ortiz, María de la Luz Ayala-Madrigal
Publikováno v:
Cancers, Vol 16, Iss 13, p 2323 (2024)
We searched for the prevalence of actionable somatic mutations in exon 2 of the KRAS gene in western Mexican patients with CRC. Tumor tissue DNA samples from 150 patients with sporadic CRC recruited at the Civil Hospital of Guadalajara were analyzed.
Externí odkaz:
https://doaj.org/article/b3391338fcdc4f968856a26d0d799a0c
Autor:
Martha Graciela Fuentes-Lerma, Ana Lourdes Zamora-Pérez, Cecilia Robles-Gómez, Celia Guerrero-Velázquez, Jorge Peregrina-Sandoval, Melva Gutiérrez-Angulo, Rocío Patricia Mariaud-Schmidt
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 43, Iss 1, Pp 61-68 (2023)
Introducción. La periodontitis es una enfermedad inflamatoria que afecta los tejidos de soporte dental; los efectos del exceso de óxido nítrico pueden contribuir a los síntomas de la periodontitis. Objetivo. Determinar la concentración de óxido
Externí odkaz:
https://doaj.org/article/4d56279e489e449aa83f801f467a0fde
Autor:
Arturo Caballero-Avendaño, Sergio A. Ramírez-García, Melva Gutiérrez-Angulo, Carlos E. Cabrera-Pivaral, Nory O. Dávalos-Rodríguez, Ana R. Rincón-Sánchez
Publikováno v:
Gaceta Médica de México, Vol 159, Iss 3 (2023)
El cáncer colorrectal (CCR) es una enfermedad compleja determinada por factores de riesgo genéticos, ambientales y de estilo de vida. Los factores genéticos (hereditarios) tienen gran influencia en su desarrollo, sin embargo, la mayoría de los ca
Externí odkaz:
https://doaj.org/article/e1db19c73c9d4289b1d709f697b85083
Autor:
José M. Moreno-Ortiz, Melva Gutiérrez-Angulo, Ruth Ramírez-Ramírez, Anahí González-Mercado, Alexis S. Suárez-Villanueva, Miriam Partida-Pérez, Víctor Maciel-Gutiérrez, Ma. de la Luz Ayala-Madrigal
Publikováno v:
Gaceta Médica de México, Vol 157, Iss 5 (2021)
Externí odkaz:
https://doaj.org/article/a6567ab567004dcea02db1e3820ed261
Autor:
José M. Moreno-Ortiz, Josselyn Jiménez-García, Melva Gutiérrez-Angulo, Ma. de la Luz Ayala-Madrigal, Anahí González-Mercado, Christian O. González-Villaseñor, Beatriz A. Flores-López, Carlos Alvizo-Rodríguez, Jesús A. Hernández-Sandoval, Martha A. Fernández-Galindo, Víctor Maciel-Gutiérrez, Helen Ramírez-Plascencia, Ruth Ramírez-Ramírez
Publikováno v:
Gaceta Médica de México, Vol 157, Iss 6 (2021)
Externí odkaz:
https://doaj.org/article/d053ed9f422745cd9f96adf06a1e9902
Autor:
Helen Haydee Fernanda Ramírez-Plascencia, Melva Gutiérrez-Angulo, Alexis Sayuri Suárez-Villanueva, Jorge Peregrina-Sandoval, María de la Luz Ayala-Madrigal
Publikováno v:
Revista de la Facultad de Medicina, Vol 68, Iss 1 (2020)
Dear Editor: An intra-individual somatic variation (ISV) is described as the genetic difference among different tissues of the same individual. ISV increases with age, may not manifest a defined phenotype, and is associated with neurological, hemato
Externí odkaz:
https://doaj.org/article/b2378767efc64913a95978682ba14283
Autor:
Beatriz Armida Flores-López, María de la Luz Ayala-Madrigal, José Miguel Moreno-Ortiz, Jorge Peregrina-Sandoval, Miguel Ángel Trujillo-Rojas, José Luis Venegas-Rodríguez, Rosario Hernández-Ramírez, Martha Alejandra Fernández-Galindo, Melva Gutiérrez-Angulo
Publikováno v:
Current Issues in Molecular Biology. 44:3770-3778
Colorectal cancer is a heterogeneous disease with multiple genomic changes that influence the clinical management of patients; thus, the search for new molecular targets remains necessary. The aim of this study was to identify genetic variants in tum