Buscar
Mostrando ítems 1-8 de 8
Cáncer colorrectal hereditario no asociado a poliposis o síndrome de Lynch
Hereditary nonpolyposis colorectal cancer, also known as Lynch syndrome is recognized as an autosomal dominant hereditary syndrome of incomplete penetrance characterized by mutations in DNA repair genes. It is the most ...
Predisposición hereditaria de padecer melanoma en familias uruguayas.: Resultados preliminares
(Sindicato Médico del Uruguay, 2007)
Mutational analysis of BRCA 1 and BRCA 2 genes in Peruvian families with hereditary breast and ovarian cancer
(Wiley Periodicals, Inc., 2017-06-28)
Background
Breast cancer is one of the most prevalent malignancies in the world. In Peru, breast cancer is the second cause of death among women. Five to ten percent of patients present a high genetic predisposition due ...
Polimorfismos del gen P53 en cáncer mamario familiar en una población colombiana
Introduction: Gen p53 codifies a 53 KD protein, an important regulator of cell processes such as proliferation, cellular death (apoptosis), and the preservation of the genetic material. It is known as the guardian of the ...
Prevalence of BRCA1 and BRCA2 Mutations in Unselected Breast Cancer Patients from Medellín, Colombia
(BMC (BioMed Central)Genética MédicaPoznań, Polonia, 2023)
From colorectal cancer pattern to the characterization of individuals at risk: picture for genetic research in Latin America
(John Wiley & Sons Ltd, 2019-05-17)
Colorectal cancer (CRC) is one of the most common cancers in Latin America and the Caribbean, with the highest rates reported for Uruguay, Brazil and Argentina. We provide a global snapshot of the CRC patterns, how screening ...
Análise da expressão de hsa-miR-9 e CDH1 em adenocarcinoma gástricoExpression analisys of hsa-miR-9 and CDH1 in gastric adenocarcinoma
(Universidade Federal do ParáBrasilNúcleo de Pesquisas em OncologiaUFPAPrograma de Pós-Graduação em Oncologia e Ciências Médicas, 2017)