Hereditary colorectal cancer.
By H. Lynch, A. de la Chapelle. New England Journal of Medicine, 2003
828 citations recorded by the source corpus.
Subfields: Cancer Research, Oncology, Pathology and Forensic Medicine
View Paper: https://www.semanticscholar.org/paper/13f9e51529c94a67a9f1cd37350c7f013aa5759a
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In Cancer Research
In Oncology
In Pathology and Forensic Medicine
Citations in the corpus
- Variation in cancer risk among tissues can be explained by the number of stem cell divisions (2015, background): “Colorectal adenocarcinoma in patients with HNPCC HNPCC (Hereditary Non-polyposis Colorectal Cancer, also called Lynch Syndrome) accounts for 1-3% of colorectal cancers, and the lifetime risk of colorectal cancer for those with HNPCC has been estimated to be ~50% (61), (62).”
- Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1 (2009, background): “283" language="eng" relation="no"> Lynch syndrome patients are susceptible to colorectal and endometrial cancers owing to inactivating germline mutations in mismatch repair genes, including MSH2 (ref”