Zobrazeno 1 - 4
of 4
pro vyhledávání: '"María T. Magaña-Torres"'
Autor:
Azaria García-Ruvalcaba, Katia C. Vázquez-Ibarra, María T. Magaña-Torres, Lourdes del C. Rizo de la Torre, Lennon Meléndez-Aranda, Gabriela López-Armas, José A. Cruz-Ramos, Jorge Peregrina-Sandoval, Esther Espinoza-Jiménez, María E. Rosales-Gradilla, Josefina Y. Sánchez-López
Publikováno v:
Revista de Investigación Clínica, Vol 75, Iss 1 (2023)
Background: Reduced or null expression of E-cadherin protein is a frequent cause of diffuse gastric cancer (DGC). More than 50% of patients with DGC present somatic variants in CDH1 gene. Objectives: The objectives of this study were to study E-cadhe
Externí odkaz:
https://doaj.org/article/01449bf169ba4346a703830115845dc3
Autor:
Sofia, Dumois-Petersen, Martha P, Gallegos-Arreola, María T, Magaña-Torres, Francisco J, Perea-Díaz, John M, Ringman, Luis E, Figuera
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical geneticsREFERENCES. 184(4)
Mutations in three genes (APP, PSEN1, and PSEN2) are the main cause of the autosomal dominant early-onset Alzheimer's disease (AD-EOAD). In PSEN1, the A431E (c.1292CA, rs63750083) mutation is suspected to have exerted a founder effect in the State of
Autor:
Rentería-López, Víctor M.1 (AUTHOR), Perea-Díaz, Francisco J.1 (AUTHOR), Rizo-delaTorre, Lourdes C.1,2 (AUTHOR), Sánchez-López, Josefina Y.1 (AUTHOR), Ibarra-Cortés, Bertha2,3 (AUTHOR) bibarra@mail.udg.mx
Publikováno v:
Hemoglobin. May2017, Vol. 41 Issue 3, p180-184. 5p.
Autor:
Dumois‐Petersen, Sofia, Gallegos‐Arreola, Martha P., Magaña‐Torres, María T., Perea‐Díaz, Francisco J., Ringman, John M., Figuera, Luis E.
Publikováno v:
American Journal of Medical Genetics. Part C: Seminars in Medical Genetics; Dec2020, Vol. 184 Issue 4, p1023-1029, 7p