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Analysis of 5382insC (BRCA1) and 6174delT (BRCA2) mutations in 382 healthy Chilean women with a family history of breast cancer
(Sociedad de Biología de Chile, 2002)
Mutations in BRCA1, BRCA2 and other breast and ovarian cancer susceptibility genes in Central and South American populations
(2017)
Breast cancer (BC) is the most common malignancy among women worldwide. A major advance in the understanding of the genetic etiology of BC was the discovery of BRCA1 and BRCA2 (BRCA1/2) genes, which are considered ...
Frequency of sequence mutations and variants for the BRCA1 and BRCA2 genes in a sample of Colombian women with suspected hereditary breast cancer syndrome: Case seriesFrecuencia de mutación y de variantes de secuencia para los genes BRCA1 y BRCA2 en una muestra de mujeres colombianas con sospecha de síndrome de cáncer de mama hereditario: serie de casos
(Rev. Colomb. Obstet. Ginecol., 2015-12-21)
Objective: To describe sequence variants in the BRCA1 and BRCA2 genes in a sample of Colombian patients with a personal or family histor y of breast cancer suggestive of genetic risk. Materials and methods: Case ...
Determinación de una mutación en el gen BRCA1 en una familia que presenta cáncer de mama hereditario
(Sociedad Médica de Santiago, 2004)
Frequency of brca1 and brca2 gene mutations and risk factors related to breast cancer in women attending the Solca Cancer InstituteFrecuencia de las mutaciones en genes brca1 y brca2 y factores de riesgo relacionados con el padecimiento de cáncer de mama en mujeres que asisten al Instituto Del Cáncer Solca
(Editorial Ciencia digital Registrada en la Cámara Ecuatoriana del Libro No Afiliación 663 (Editor DrC. Efraín Velasteguí López. PhD.), 2024)
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 ...
Promoter hypermethylation of BRCA1 correlates with absence of expression in hereditary breast cancer tumors
(TAYLOR & FRANCIS INC, 2008)
Germline mutations in BRCA1 account for a low proportion of hereditary cases in diverse populations. Several efforts have been made to find new genes involved in the inheritance of breast cancer with no success until today. ...
Frecuencia de mutación y de variantes de secuencia para los genes BRCA1 y BRCA2 en una muestra de mujeres colombianas con sospecha de síndrome de cáncer de mama hereditario: serie de casos
Objective: To describe sequence variants in the BRCA1 and BRCA2 genes in a sample of Colombian patients with a personal or family histor y of breast cancer suggestive of genetic risk. Materials and methods: Case series ...