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Publications tagged with this subject: 14

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1. Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndrome

2. Lack of MRE11-RAD50-NBS1 (MRN) complex detection occurs frequently in low-grade epithelial ovarian cancer

3. Titanium Dioxide Nanoparticles Affect the Percentage of Free Radical Scavenging, Protein Content and DNA Mismatch Repair Genes in Zea mays L. and Triticum aestivum L.

4. A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma

5. The 116G > A MSH6 and IVS1-1121C > T PMS2 Genes Polymorphisms Modulate the Risk of the Sporadic Colorectal Cancer Development in Polish Population

6. Multilevel genomics of colorectal cancers with microsatellite instability—clinical impact of JAK1 mutations and consensus molecular subtype 1

7. Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent MLH1 hypermethylation and MSH2 somatic mutations

8. Microsatellite Instability Pathway and EMAST in Colorectal Cancer

9. The association of low penetrance genetic risk modifiers with colorectal cancer in lynch syndrome patients: a systematic review and meta-analysis

10. Metachronous colorectal carcinoma with massive submucosal invasion detected by annual surveillance in a Lynch syndrome patient: a case report

11. Success of referral to genetic counseling after positive lynch syndrome screening test

12. RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers

13. Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing

14. TGFBR2-dependent alterations of exosomal cargo and functions in DNA mismatch repair-deficient HCT116 colorectal cancer cells


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