PubMed for id: 1677530627

Year	Number of Results
1993	1
1995	1
2000	1
2001	2
2004	1
2020	3
2021	3
2024	0

1

Exonic sequencing and MLH3 gene expression analysis of breast cancer patients.

Khailany RA, Ozaslan M. Khailany RA, et al. Cell Mol Biol (Noisy-le-grand). 2021 Nov 25;67(3):35-43. doi: 10.14715/cmb/2021.67.3.5. Cell Mol Biol (Noisy-le-grand). 2021. PMID: 34933735

2

A loss-of-function variant in DNA mismatch repair gene MLH3 underlies severe oligozoospermia.

Nawaz S, Ullah MI, Hamid BS, Nargis J, Nawaz M, Hussain S, Ahmad W. Nawaz S, et al. J Hum Genet. 2021 Jul;66(7):725-730. doi: 10.1038/s10038-021-00907-z. Epub 2021 Jan 30. J Hum Genet. 2021. PMID: 33517345

3

Genetic evidence for the involvement of mismatch repair proteins, PMS2 and MLH3, in a late step of homologous recombination.

Rahman MM, Mohiuddin M, Shamima Keka I, Yamada K, Tsuda M, Sasanuma H, Andreani J, Guerois R, Borde V, Charbonnier JB, Takeda S. Rahman MM, et al. J Biol Chem. 2020 Dec 18;295(51):17460-17475. doi: 10.1074/jbc.RA120.013521. J Biol Chem. 2020. PMID: 33453991 Free PMC article.

4

Regulation of the MLH1-MLH3 endonuclease in meiosis.

Cannavo E, Sanchez A, Anand R, Ranjha L, Hugener J, Adam C, Acharya A, Weyland N, Aran-Guiu X, Charbonnier JB, Hoffmann ER, Borde V, Matos J, Cejka P. Cannavo E, et al. Nature. 2020 Oct;586(7830):618-622. doi: 10.1038/s41586-020-2592-2. Epub 2020 Aug 19. Nature. 2020. PMID: 32814904 Free article.

5

Human MutLγ, the MLH1-MLH3 heterodimer, is an endonuclease that promotes DNA expansion.

Kadyrova LY, Gujar V, Burdett V, Modrich PL, Kadyrov FA. Kadyrova LY, et al. Proc Natl Acad Sci U S A. 2020 Feb 18;117(7):3535-3542. doi: 10.1073/pnas.1914718117. Epub 2020 Feb 3. Proc Natl Acad Sci U S A. 2020. PMID: 32015124 Free PMC article.

6

Lynch Syndrome.

Idos G, Valle L. Idos G, et al. 2004 Feb 5 [updated 2021 Feb 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2004 Feb 5 [updated 2021 Feb 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301390 Free Books & Documents. Review.

7

Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers.

Lipkin SM, Wang V, Stoler DL, Anderson GR, Kirsch I, Hadley D, Lynch HT, Collins FS. Lipkin SM, et al. Hum Mutat. 2001 May;17(5):389-96. doi: 10.1002/humu.1114. Hum Mutat. 2001. PMID: 11317354

8

The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2.

Kondo E, Horii A, Fukushige S. Kondo E, et al. Nucleic Acids Res. 2001 Apr 15;29(8):1695-702. doi: 10.1093/nar/29.8.1695. Nucleic Acids Res. 2001. PMID: 11292842 Free PMC article.

9

MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability.

Lipkin SM, Wang V, Jacoby R, Banerjee-Basu S, Baxevanis AD, Lynch HT, Elliott RM, Collins FS. Lipkin SM, et al. Nat Genet. 2000 Jan;24(1):27-35. doi: 10.1038/71643. Nat Genet. 2000. PMID: 10615123

10

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.

Sherrington R, Rogaev EI, Liang Y, Rogaeva EA, Levesque G, Ikeda M, Chi H, Lin C, Li G, Holman K, Tsuda T, Mar L, Foncin JF, Bruni AC, Montesi MP, Sorbi S, Rainero I, Pinessi L, Nee L, Chumakov I, Pollen D, Brookes A, Sanseau P, Polinsky RJ, Wasco W, Da Silva HA, Haines JL, Perkicak-Vance MA, Tanzi RE, Roses AD, Fraser PE, Rommens JM, St George-Hyslop PH. Sherrington R, et al. Nature. 1995 Jun 29;375(6534):754-60. doi: 10.1038/375754a0. Nature. 1995. PMID: 7596406

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