Associated Papers
Functions of PMS2 and MLH1 important for regulation of divergent repeat-mediated deletions.
Trost H et al.
Biorxiv : the Preprint Server for Biology, 2024
WRN helicase and mismatch repair complexes independently and synergistically disrupt cruciform DNA structures.
Mengoli V et al.
The Embo Journal, 2023
Optimized prime editing efficiently generates glyphosate-resistant rice plants carrying homozygous TAP-IVS mutation in EPSPS.
Jiang Y et al.
Molecular Plant, 2022
The MLH1 ATPase domain is needed for suppressing aberrant formation of interstitial telomeric sequences.
Jia P et al.
Dna Repair, 2018
Residues in the N-terminal domain of MutL required for mismatch repair in Bacillus subtilis.
Bolz NJ et al.
Journal of Bacteriology, 2012
Conservation of functional asymmetry in the mammalian MutLα ATPase.
Johnson JR et al.
Dna Repair, 2010
Mutations in the MutSalpha interaction interface of MLH1 can abolish DNA mismatch repair.
Plotz G et al.
Nucleic Acids Research, 2006
Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair.
Tomer G et al.
The Journal of Biological Chemistry, 2002
Mutations within the hMLH1 and hPMS2 subunits of the human MutLalpha mismatch repair factor affect its ATPase activity, but not its ability to interact with hMutSalpha.
Räschle M et al.
The Journal of Biological Chemistry, 2002
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