Mice with the CHEK2*1100delC SNP are predisposed to cancer with a strong gender bias
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference47 articles.
1. Breast cancer genetics: What we know and what we need
2. Evidence for further breast cancer susceptibility genes in addition toBRCA1 andBRCA2 in a population-based study
3. A candidate gene approach to searching for low-penetrance breast and prostate cancer genes
4. Association studies for finding cancer-susceptibility genetic variants
5. Heterozygous Germ Line hCHK2 Mutations in Li-Fraumeni Syndrome
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2. Ovarian Cancer and the Environment: Rodent Models;Reference Module in Biomedical Sciences;2024
3. Breast cancer genomes from CHEK2 c.1100delC mutation carriers lack somatic TP53 mutations and display a unique structural variant size distribution profile;Breast Cancer Research;2023-05-09
4. Case report: Tisagenlecleucel for treatment of relapsed B- acute lymphoblastic leukemia in a patient with CHEK2 mutation;Frontiers in Pediatrics;2023-03-01
5. Two unrelated cases with biallelic CHEK2 variants:a novel condition with constitutional chromosomal instability?;European Journal of Human Genetics;2022-12-19
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