This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

. 2008 Jun 15;6(2):103-4.

doi: 10.1186/1897-4287-6-2-103.

MSH6 syndrome

Janina Suchy¹, Jan Lubinski

Affiliations

PMID: 19804606
PMCID: PMC2735474
DOI: 10.1186/1897-4287-6-2-103

MSH6 syndrome

Janina Suchy et al. Hered Cancer Clin Pract. 2008.

. 2008 Jun 15;6(2):103-4.

doi: 10.1186/1897-4287-6-2-103.

Authors

Janina Suchy¹, Jan Lubinski

Affiliation

¹ International Hereditary Cancer Centre, Department of Genetics and Pathology, Szczecin, Poland. jsuchy@sci.pam.szczecin.pl

PMID: 19804606
PMCID: PMC2735474
DOI: 10.1186/1897-4287-6-2-103

No abstract available

PubMed Disclaimer

Similar articles

MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer.
Talseth-Palmer BA, McPhillips M, Groombridge C, Spigelman A, Scott RJ. Talseth-Palmer BA, et al. Hered Cancer Clin Pract. 2010 May 21;8(1):5. doi: 10.1186/1897-4287-8-5. Hered Cancer Clin Pract. 2010. PMID: 20487569 Free PMC article.
Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome.
Cederquist K, Emanuelsson M, Wiklund F, Golovleva I, Palmqvist R, Grönberg H. Cederquist K, et al. Clin Genet. 2005 Dec;68(6):533-41. doi: 10.1111/j.1399-0004.2005.00537.x. Clin Genet. 2005. PMID: 16283884
Role of microsatellite instability-low as a diagnostic biomarker of Lynch syndrome in colorectal cancer.
Vilar E, Mork ME, Cuddy A, Borras E, Bannon SA, Taggart MW, Ying J, Broaddus RR, Luthra R, Rodriguez-Bigas MA, Lynch PM, You YQ. Vilar E, et al. Cancer Genet. 2014 Oct-Dec;207(10-12):495-502. doi: 10.1016/j.cancergen.2014.10.002. Epub 2014 Oct 13. Cancer Genet. 2014. PMID: 25432668 Free PMC article.
MSH6, Past and Present and Muir-Torre Syndrome-Connecting the Dots.
Mahalingam M. Mahalingam M. Am J Dermatopathol. 2017 Apr;39(4):239-249. doi: 10.1097/DAD.0000000000000633. Am J Dermatopathol. 2017. PMID: 28323777 Review.
Meta-analysis of MSH6 gene mutation frequency in colorectal and endometrial cancers.
Zhao YS, Hu FL, Wang F, Han B, Li DD, Li XW, Zhu S. Zhao YS, et al. J Toxicol Environ Health A. 2009;72(11-12):690-7. doi: 10.1080/15287390902841003. J Toxicol Environ Health A. 2009. PMID: 19492230

See all similar articles

References

1. Fleck O, Nielsen O. DNA repair. J Cell Sci. 2004;117:515–517. doi: 10.1242/jcs.00952. - DOI - PubMed
1. Pinto LA, Regis da Silva CG, Lopes D, Machado-Silva A, Machado CR. Escherichia coli as a model system to study DNA repair genes of eukaryotic organisms. Genetics Mol Res. 2003;2:77–91. - PubMed
1. Marti T, Kunz C, Fleck O. DNA mismatch repair and mutation avoidance pathways. J Cell Physiol. 2002;191:28–41. doi: 10.1002/jcp.10077. - DOI - PubMed
1. Abdel-Rahman WM, Mecklin JP, Peltomäki P. The genetics of HNPCC: application to diagnosis and screening. Crit Rev Oncol Hematol. 2006;58:208–220. doi: 10.1016/j.critrevonc.2005.11.001. - DOI - PubMed
1. Lagerstedt Robinson K, Liu T, Vandrovcova J, Halvarsson B, Clendenning M, Frebourg T, Papadopoulos N, Kinzler KW, Vogelstein B, Peltomäki P, Kolodner RD, Nilbert M, Lindblom A. Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics. J Natl Cancer Inst. 2007;99:291–299. doi: 10.1093/jnci/djk051. - DOI - PubMed

LinkOut - more resources

Full Text Sources
- Europe PubMed Central
- PubMed Central
Miscellaneous
- NCI CPTAC Assay Portal