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Research Paper

Evidence that hMLH3 functions primarily in meiosis and in hMSH2-hMSH3 mismatch repair

Pages 1411-1420 | Published online: 15 Jul 2009

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Ufuk Düzenli, Zekiye Altun, Yüksel Olgun, Safiye Aktaş, Ayça Pamukoğlu, Hasan Oğuz Çetinayak, Asuman Feda Bayrak & Levent Olgun. (2019) Role of N-acetyl cysteine and acetyl-l-carnitine combination treatment on DNA-damage-related genes induced by radiation in HEI-OC1 cells. International Journal of Radiation Biology 95:3, pages 298-306.
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Po-Han Lin, Yun-Wen Tien, Wen-Fang Cheng, Ying-Cheng Chiang, Chien-Huei Wu, Karen Yang & Chiun-Sheng Huang. (2023) Diverse genetic spectrum among patients who met the criteria of hereditary breast, ovarian and pancreatic cancer syndrome. Journal of Gynecologic Oncology 34.
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Brooke M. Britton, James A. London, Juana Martin-Lopez, Nathan D. Jones, Jiaquan Liu, Jong-Bong Lee & Richard Fishel. (2022) Exploiting the distinctive properties of the bacterial and human MutS homolog sliding clamps on mismatched DNA. Journal of Biological Chemistry 298:11, pages 102505.
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Jennie C L Roy, Antonia Vitalo, Marissa A Andrew, Eduarda Mota-Silva, Marina Kovalenko, Zoe Burch, Anh M Nhu, Paula E Cohen, Ed Grabczyk, Vanessa C Wheeler & Ricardo Mouro Pinto. (2021) Somatic CAG expansion in Huntington's disease is dependent on the MLH3 endonuclease domain, which can be excluded via splice redirection. Nucleic Acids Research 49:7, pages 3907-3918.
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Marion Dhooge, Stéphanie Baert-Desurmont, Carole Corsini, Olivier Caron, Nadine Andrieu, Pascaline Berthet, Valérie Bonadona, Odile Cohen-Haguenauer, Antoine De Pauw, Capucine Delnatte, Sophie Dussart, Christine Lasset, Dominique Leroux, Christine Maugard, Jessica Moretta-Serra, Cornel Popovici, Bruno Buecher, Chrystelle Colas & Catherine Noguès. (2020) National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tract. European Journal of Medical Genetics 63:12, pages 104080.
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Maya Monakhova, Alexandra Ryazanova, Vladislav Kunetsky, Pingping Li, Evgeniy Shilkin, Olga Kisil, Desirazu N. Rao, Tatiana Oretskaya, Peter Friedhoff & Elena Kubareva. (2020) Probing the DNA-binding center of the MutL protein from the Escherichia coli mismatch repair system via crosslinking and Förster resonance energy transfer. Biochimie 171-172, pages 43-54.
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Xiaonan Zhao, Yongwei Zhang, Kenneth Wilkins, Winfried Edelmann & Karen Usdin. (2018) MutLγ promotes repeat expansion in a Fragile X mouse model while EXO1 is protective. PLOS Genetics 14:10, pages e1007719.
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Anasheh Halabi, Kayla T B Fuselier & Ed Grabczyk. (2018) GAA•TTC repeat expansion in human cells is mediated by mismatch repair complex MutLγ and depends upon the endonuclease domain in MLH3 isoform one. Nucleic Acids Research 46:8, pages 4022-4032.
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Rafael P. de Campos, Iago C. Schultz, Paola de Andrade Mello, Samuel Davies, Manuela S. Gasparin, Ana P. S. Bertoni, Andréia Buffon & Márcia R. Wink. (2018) Cervical cancer stem-like cells: systematic review and identification of reference genes for gene expression. Cell Biology International 42:2, pages 139-152.
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Richard Fishel & Jong-Bong Lee. 2016. DNA Replication, Recombination, and Repair. DNA Replication, Recombination, and Repair 305 339 .
Xiao-Nan Zhao & Karen Usdin. (2015) The Repeat Expansion Diseases: The dark side of DNA repair. DNA Repair 32, pages 96-105.
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Lennart Roesner, Christian Mielke, Silke Faehnrich, Yvonne Merkhoffer, Kurt Dittmar, Hans Drexler & Wilhelm Dirks. (2014) Localization of MLH3 at the Centrosomes. International Journal of Molecular Sciences 15:8, pages 13932-13937.
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Anjana Srivatsan, Nikki Bowen & Richard D. Kolodner. (2014) Mispair-specific Recruitment of the Mlh1-Pms1 Complex Identifies Repair Substrates of the Saccharomyces cerevisiae Msh2-Msh3 Complex. Journal of Biological Chemistry 289:13, pages 9352-9364.
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Ricardo Mouro Pinto, Ella Dragileva, Andrew Kirby, Alejandro Lloret, Edith Lopez, Jason St. Claire, Gagan B. Panigrahi, Caixia Hou, Kim Holloway, Tammy Gillis, Jolene R. Guide, Paula E. Cohen, Guo-Min Li, Christopher E. Pearson, Mark J. Daly & Vanessa C. Wheeler. (2013) Mismatch Repair Genes Mlh1 and Mlh3 Modify CAG Instability in Huntington's Disease Mice: Genome-Wide and Candidate Approaches. PLoS Genetics 9:10, pages e1003930.
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Lennart M. Roesner, Christian Mielke, Silke Fähnrich, Yvonne Merkhoffer, Kurt E.J. Dittmar, Hans G. Drexler & Wilhelm G. Dirks. (2013) Stable expression of MutLγ in human cells reveals no specific response to mismatched DNA, but distinct recruitment to damage sites. Journal of Cellular Biochemistry 114:10, pages 2405-2414.
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Serge Boiteux & Sue Jinks-Robertson. (2013) DNA Repair Mechanisms and the Bypass of DNA Damage in Saccharomyces cerevisiae . Genetics 193:4, pages 1025-1064.
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Stéphanie Tomé, Jodie P. Simard, Meghan M. Slean, Ian Holt, Glenn E. Morris, Kamila Wojciechowicz, Hein te Riele & Christopher E. Pearson. (2013) Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissues. DNA Repair 12:1, pages 46-52.
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Christine Stoehr, Maximilian Burger, Robert Stoehr, Simone Bertz, Petra Ruemmele, Ferdinand Hofstaedter, Stefan Denzinger, Wolf F. Wieland, Arndt Hartmann & Bernhard Walter. (2012) Mismatch Repair Proteins hMLH1 and hMSH2 Are Differently Expressed in the Three Main Subtypes of Sporadic Renal Cell Carcinoma. Pathobiology 79:3, pages 162-168.
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Anna Seriola, Claudia Spits, Jodie P. Simard, Pierre Hilven, Patrick Haentjens, Christopher E. Pearson & Karen Sermon. (2011) Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation. Human Molecular Genetics 20:1, pages 176-185.
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Ravi R. Iyer, Anna Pluciennik, Jochen Genschel, Miaw-Sheue Tsai, Lorena S. Beese & Paul Modrich. (2010) MutLα and Proliferating Cell Nuclear Antigen Share Binding Sites on MutSβ. Journal of Biological Chemistry 285:15, pages 11730-11739.
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