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Literature citations Results

Citation
HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes.

Jaeger A.C., Rasmussen M., Bisgaard H.C., Singh K.K., Nielsen F.C., Rasmussen L.J.

Oncogene 20:3590-3595(2001) · UniProtKB (3)

Hereditary non-polyposis colorectal cancer (HNPCC): phenotype-genotype correlation between patients with and without identified mutation.

Bisgaard M.L., Jaeger A.C., Myrhoej T., Bernstein I., Nielsen F.C.

Hum. Mutat. 20:20-27(2002) · UniProtKB (1)

Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.

Andersen S.D., Liberti S.E., Luetzen A., Drost M., Bernstein I., Nilbert M., Dominguez M., Nystroem M., Hansen T.V., Christoffersen J.W. et al.

Hum. Mutat. 33:1647-1655(2012) · UniProtKB (1) · Mapped (33)

Characterization of human exonuclease 1 in complex with mismatch repair proteins, subcellular localization and association with PCNA.

Nielsen F.C., Jaeger A.C., Luetzen A., Bundgaard J.R., Rasmussen L.J.

Oncogene 23:1457-1468(2004) · UniProtKB (3) · Mapped (4)

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