The Common Germline TP53-R337H Mutation Is Hypomorphic and Confers Incomplete Penetrance and Late Tumor Onset in a Mouse Model
Author:
Funder
NIHNCINCI
ALSAC
Publisher
American Association for Cancer Research (AACR)
Subject
Cancer Research,Oncology
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. AI-guided identification of risk variants for adrenocortical tumours in TP53 p.R337H carrier children: a genetic association study;The Lancet Regional Health - Americas;2024-10
2. Tumor Spectrum and Temporal Cancer Trends in adult carriers of Li-Fraumeni syndrome: Implications for Personalized Screening Strategies inTP53R337H carriers;2024-06-08
3. Functional pri-miR-34b/c rs4938723 and KRAS 3′UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?;Gene;2024-03
4. LFSPROShiny: An Interactive R/Shiny App for Prediction and Visualization of Cancer Risks in Families With Deleterious Germline TP53 Mutations;JCO Clinical Cancer Informatics;2024-03
5. Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility;Human Genetics and Genomics Advances;2024-01
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