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 MSH2 Syndrome MLH1 DNA mismatch repair Colorectal cancer Protein Microsatellite instability Gene Exon DNA MSH6 Obesity Hypertension Phenotype Chemotherapy Metastasis Colonoscopy Messenger RNA Western blot Apoptosis Acid Polymerase chain reaction Zygosity Mutation Genome
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MSH2  10 times
Syndrome  8 times
MLH1  8 times
DNA mismatch repair  7 times
Colorectal cancer  6 times
Protein  5 times
Microsatellite instability  5 times
Gene  5 times
Exon  4 times
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Phenotype  2 times
Immunohistochemistry  2 times
Histology  2 times
Genetic disorder  2 times
Adenocarcinoma  2 times
Wireless access point  1 time
Ubiquitin ligase  1 time
TaqMan  1 time
Single-nucleotide polymorphism  1 time
Sebaceous gland  1 time
Sanger sequencing  1 time
Reflex  1 time
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Israel  1 time
Intron  1 time
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DNA replication  1 time
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Publications tagged with this subject: 11

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1. Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel

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

3. The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes

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

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

8. Clinical Impact of Mismatch Repair Protein Testing on Outcome of Early Staged Colorectal Carcinomas

9. A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America

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

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


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