Current gene panels account for nearly all homologous recombination repair-associated multiple-case breast cancer families
Abstract It was hypothesized that variants in underexplored homologous recombination repair (HR) genes could explain unsolved multiple-case breast cancer (BC) families. We investigated HR deficiency (HRD)-associated mutational signatures and second hits in tumor DNA from familial BC cases. No candid...
Guardado en:
Autores principales: | Thibaut S. Matis, Nadia Zayed, Bouchra Labraki, Manon de Ladurantaye, Théophane A. Matis, José Camacho Valenzuela, Nancy Hamel, Adrienne Atayan, Barbara Rivera, Yuval Tabach, Patricia N. Tonin, Alexandre Orthwein, Anne-Marie Mes-Masson, Zaki El Haffaf, William D. Foulkes, Paz Polak |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/cbb6acef8a0543f6b4e46805a7d21ec0 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Founder BRCA1/BRCA2/PALB2 pathogenic variants in French-Canadian breast cancer cases and controls
por: Supriya Behl, et al.
Publicado: (2020) -
Energy Dissipation Pathways in Few-Layer MoS2 Nanoelectromechanical Systems
por: Bernard R. Matis, et al.
Publicado: (2017) -
Investigating the causal role of MRE11A p.E506* in breast and ovarian cancer
por: Islam E. Elkholi, et al.
Publicado: (2021) -
The genomic landscape of TP53 and p53 annotated high grade ovarian serous carcinomas from a defined founder population associated with patient outcome.
por: Paulina M Wojnarowicz, et al.
Publicado: (2012) -
Homological scaffold via minimal homology bases
por: Marco Guerra, et al.
Publicado: (2021)