DNA mismatch repair: functions and mechanisms.

By R. Iyer, A. Pluciennik, V. Burdett, P. Modrich. Chemical Reviews, 2006

911 citations recorded by the source corpus.

Subfields: Molecular Biology, Pathology and Forensic Medicine, Plant Science

View Paper: https://www.semanticscholar.org/paper/b8e5ae49167dd894b23aa087bd73f03f3444560a

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In Molecular Biology

1. Gregory A. Newby
2. Britt Adamson
3. Mustafa Sahin
4. M. Marinus
5. David R. Liu
6. Jonathan S. Weissman
7. Jennifer A. Doudna
8. Lei S. Qi

In Pathology and Forensic Medicine

1. M. Marinus

Citations in the corpus

• Endonucleolytic Function of MutLα in Human Mismatch Repair (2006, neutral): “... and is the primary cause of hereditary nonpolyposis colon cancer(HNPCC).Genetic stabilizationaffordedbythissystem has been attributed to its function in the correction of DNA biosynthetic errors, its role in ensuring the fidelity of genetic recombination, and its participation in the checkpoint ”
• DNA Mismatch Repair (2012, background): “Although the initial reconstitution of mismatch repair in vitro included only ExoI (88), subsequent work showed that other nucleases can participate in mismatch repair (72,142).”
• Enhanced prime editing systems by manipulating cellular determinants of editing outcomes (2021, background): “Across all screen conditions, CRISPRi targeting of MSH2, MSH6, MLH1, and PMS2, components of the MutSa–MutLa MMR complex (Iyer et al., 2006; Kunkel and Erie, 2005; Li, 2008), substantially increased editing efficiency by up to 5.”