Skip Header

You are using a version of browser that may not display all the features of this website. Please consider upgrading your browser.
1 to 4 of 4  Show

Literature citations Results

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)

1 to 4 of 4  Show
UniProt is an ELIXIR core data resource
Main funding by: National Institutes of Health

We'd like to inform you that we have updated our Privacy Notice to comply with Europe’s new General Data Protection Regulation (GDPR) that applies since 25 May 2018.

Do not show this banner again