Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome-Reference-Cited by-同舟云学术

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Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome

Published:2013-05-20 Issue:23 Volume:110 Page:9403-9408
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proc Natl Acad Sci USA

Author:

Drost Mark,Lützen Anne,van Hees Sandrine,Ferreira Daniel,Calléja Fabienne,Zonneveld José B. M.,Nielsen Finn Cilius,Rasmussen Lene Juel,de Wind Niels

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference30 articles.

1. Hereditary Colorectal Cancer

2. Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

3. Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

4. Mismatch repair deficient colorectal cancer in the era of personalized treatment

5. Peltomäki P Vasen HFA (2004) Mutations associated with HNPCC predisposition — Update of ICG-HNPCC/INSiGHT mutation database. Dis Markers 20(4-5):269–276.

Cited by 20 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. Mono- and Biallelic Replication–Coupled Gene Editing Discriminates Dominant-Negative and Loss-of-Function Variants of DNA Mismatch Repair Genes;The Journal of Molecular Diagnostics;2024-09

2. A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma;Genes;2022-07-28

3. Predictive functional assay‐based classification of PMS2 variants in Lynch syndrome;Human Mutation;2022-04-28

4. Induction of mismatch repair deficiency, compromised DNA damage signaling and compound hypermutagenesis by a dietary mutagen in a cell-based model for Lynch syndrome;Carcinogenesis;2021-12-17

5. Multiplexed assays reveal effects of missense variants in MSH2 and cancer predisposition;PLOS Genetics;2021-04-22

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