Associated Papers
BRCA2 and NF2-Mutated High-Grade Renal Cell Carcinoma: A Case Report and Literature Review.
Talafha MM et al.
International Journal of Surgical Pathology, 2026
Positive and negative regulators of RAD51/DMC1 in homologous recombination and DNA replication.
Ito M et al.
Dna Repair, 2024
Sequencing-based functional assays for classification of BRCA2 variants in mouse ESCs.
Biswas K et al.
Cell Reports Methods, 2023
The pathogenic role of the BRCA2 c.7847C>T (p.Ser2616Phe) variant in breast and ovarian cancer predisposition.
Yamazawa K et al.
Cancer Science, 2023
37067535 (PubMed )
Supplement: CAS-114-2993-s001.pdf
BRCA2 BRC missense variants disrupt RAD51-dependent DNA repair.
Jimenez-Sainz J et al.
Elife, 2022
High-throughput functional evaluation of BRCA2 variants of unknown significance.
Ikegami M et al.
Nature Communications, 2020
32444794 (PubMed )
Supplement: 41467_2020_16141_MOESM6_ESM.xlsx › Information_of_244_variants
Genetics of breast cancer in African populations: a literature review.
Abbad A et al.
Global Health, Epidemiology and Genomics, 2018
Monoallelic characteristic-bearing heterozygous L1053X in BRCA2 gene among Sudanese women with breast cancer.
Elimam AA et al.
Bmc Medical Genetics, 2017
Contribution of BRCA1 and BRCA2 Germline Mutations to Early Algerian Breast Cancer.
Henouda S et al.
Disease Markers, 2016
Cancer-associated mutations in BRC domains of BRCA2 affect homologous recombination induced by Rad51.
Tal A et al.
Journal of Molecular Biology, 2009
Stabilization of RAD51 nucleoprotein filaments by the C-terminal region of BRCA2.
Esashi F et al.
Nature Structural & Molecular Biology, 2007
Sequence fingerprints in BRCA2 and RAD51: implications for DNA repair and cancer.
Lo T et al.
Dna Repair, 2003
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