Latest papers

How old is this mutation? - a study of three Ashkenazi Jewish founder mutations.

A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory.

Mutational screening of hMLH1 and hMSH2 that confer inherited colorectal cancer susceptibility using denature gradient gel electrophoresis (DGGE).

Immunohistochemistry staining for the mismatch repair proteins in the clinical care of patients with colorectal cancer.

Mechanism of cadmium-mediated inhibition of Msh2-Msh6 function in DNA mismatch repair.

[Expression and clinical significance of CDC6 and hMSH2 in cervical carcinoma]

Mismatch recognition protein MutSbeta does not hijack (CAG)n hairpin repair in vitro.

Identifying Muir-Torre syndrome in a patient with glioblastoma multiforme.

[Expression of cyclooxygenase-2 and relationship with mismatch repair gene and microsatellite instability in hereditary non-polyposis colorectal cancer].

Histopathologic features and microsatellite instability of cancers of the papilla of vater and their precursor lesions.

The nucleotide binding dynamics of human MSH2–MSH3 are lesion dependent

Disruption of a mitochondrial MutS DNA repair enzyme homologue confers drug resistance in the parasite Toxoplasma gondii.

[Our experience with the incidence of hereditary non-polyposis colorectal cancer].

Genetic testing for hereditary nonpolyposis colorectal cancer (HNPCC).

Intraductal papillary mucinous neoplasm of the pancreas with loss of mismatch repair in a patient with Lynch syndrome.

Colorectal cancer in South Africa: a heritable cause suspected in many young black patients.

Human MutL-complexes monitor homologous recombination independently of mismatch repair

Molecular analysis: microsatellity instability and loss of heterozygosity of tumor suppressor gene in hereditary non-polyposis colorectal cancers (HNPCC).

Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer.

Solitary subungual keratoacanthoma arising in an MSH2 germline mutation carrier: confirmation of a relationship by immunohistochemical analysis.