Cargando…
RAD51 and Breast Cancer Susceptibility: No Evidence for Rare Variant Association in the Breast Cancer Family Registry Study
BACKGROUND: Although inherited breast cancer has been associated with germline mutations in genes that are functionally involved in the DNA homologous recombination repair (HRR) pathway, including BRCA1, BRCA2, TP53, ATM, BRIP1, CHEK2 and PALB2, about 70% of breast cancer heritability remains unexpl...
Autores principales: | Le Calvez-Kelm, Florence, Oliver, Javier, Damiola, Francesca, Forey, Nathalie, Robinot, Nivonirina, Durand, Geoffroy, Voegele, Catherine, Vallée, Maxime P., Byrnes, Graham, Registry, Breast Cancer Family, Hopper, John L., Southey, Melissa C., Andrulis, Irene L., John, Esther M., Tavtigian, Sean V., Lesueur, Fabienne |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531476/ https://www.ncbi.nlm.nih.gov/pubmed/23300655 http://dx.doi.org/10.1371/journal.pone.0052374 |
Ejemplares similares
-
Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study
por: Le Calvez-Kelm, Florence, et al.
Publicado: (2011) -
Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study
por: Damiola, Francesca, et al.
Publicado: (2014) -
ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry
por: Renault, Anne-Laure, et al.
Publicado: (2016) -
Detecting differential allelic expression using high-resolution melting curve analysis: application to the breast cancer susceptibility gene CHEK2
por: Nguyen-Dumont, Tú, et al.
Publicado: (2011) -
Multigene testing of moderate-risk genes: be mindful of the missense
por: Young, E L, et al.
Publicado: (2016)