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Cell Growth and Development

Dimerization of MLH1 and PMS2 Limits Nuclear Localization of MutLα

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Pages 3320-3328 | Received 04 Nov 2002, Accepted 31 Jan 2003, Published online: 27 Mar 2023

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Peggy Hsieh & Kazuhiko Yamane. (2008) DNA mismatch repair: Molecular mechanism, cancer, and ageing. Mechanisms of Ageing and Development 129:7-8, pages 391-407.
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Yimei Fan, Wei Wang, Ming Zhu, Jiji Zhou, Jingyuan Peng, Lizhi Xu, Zichun Hua, Xiang Gao & Yaping Wang. (2007) Analysis of hMLH1 Missense Mutations in East Asian Patients with Suspected Hereditary Nonpolyposis Colorectal Cancer. Clinical Cancer Research 13:24, pages 7515-7521.
Crossref
Angela Brieger, Guido Plotz, Stefan Zeuzem & Joerg Trojan. (2007) Thymosin beta 4 expression and nuclear transport are regulated by hMLH1. Biochemical and Biophysical Research Communications 364:4, pages 731-736.
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Wan-Ju Kim, Baskaran Rajasekaran & Kevin D. Brown. (2007) MLH1- and ATM-dependent MAPK Signaling Is Activated through c-Abl in Response to the Alkylator N-Methyl-N′-nitro-N′-nitrosoguanidine. Journal of Biological Chemistry 282:44, pages 32021-32031.
Crossref
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Suzanne M. Deschênes, Guy Tomer, Megan Nguyen, Naz Erdeniz, Nicole C. Juba, Natalia Sepúlveda, Jenna E. Pisani & R. Michael Liskay. (2007) The E705K mutation in hPMS2 exerts recessive, not dominant, effects on mismatch repair. Cancer Letters 249:2, pages 148-156.
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Nina Østergaard Knudsen, Finn Cilius Nielsen, Lena Vinther, Ronni Bertelsen, Steen Holten-Andersen, Sascha Emilie Liberti, Robert Hofstra, Krista Kooi & Lene Juel Rasmussen. (2007) Nuclear localization of human DNA mismatch repair protein exonuclease 1 (hEXO1). Nucleic Acids Research 35:8, pages 2609-2619.
Crossref
Elda Cannavo, Bertran Gerrits, Giancarlo Marra, Ralph Schlapbach & Josef Jiricny. (2007) Characterization of the Interactome of the Human MutL Homologues MLH1, PMS1, and PMS2. Journal of Biological Chemistry 282:5, pages 2976-2986.
Crossref
Thomas Jascur & C. Richard Boland. (2006) Structure and function of the components of the human DNA mismatch repair system. International Journal of Cancer 119:9, pages 2030-2035.
Crossref
Vincent O'Brien & Robert Brown. (2006) Signalling cell cycle arrest and cell death through the MMR System. Carcinogenesis 27:4, pages 682-692.
Crossref
Azizah B. Mohd, Brett Palama, Scott E. Nelson, Guy Tomer, Megan Nguyen, Xin Huo & Andrew B. Buermeyer. (2006) Truncation of the C-terminus of human MLH1 blocks intracellular stabilization of PMS2 and disrupts DNA mismatch repair. DNA Repair 5:3, pages 347-361.
Crossref
Nimesh Joseph, Viswanadham Duppatla & Desirazu N. Rao. 2006. 1 49 .
A. Brieger, G. Plotz, J. Raedle, N. Weber, W. Baum, W.F. Caspary, S. Zeuzem & J. Trojan. (2005) Characterization of the nuclear import of human MutL?. Molecular Carcinogenesis 43:1, pages 51-58.
Crossref
Xiaosheng Wu, Pedro Geraldes, Jeffrey L. Platt & Marilia Cascalho. (2005) The Double-Edged Sword of Activation-Induced Cytidine Deaminase. The Journal of Immunology 174:2, pages 934-941.
Crossref
Annegret Müller, Giuseppe Giuffre, Tina Bocker Edmonston, Micaela Mathiak, Beate Roggendorf, Ernst Heinmöller, Thomas Brodegger, Giovanni Tuccari, Elisabeth Mangold, Reinhard Buettner & Josef Rüschoff. (2004) Challenges and Pitfalls in HNPCC Screening by Microsatellite Analysis and Immunohistochemistry. The Journal of Molecular Diagnostics 6:4, pages 308-315.
Crossref
Alba Guarné, Santiago Ramon-Maiques, Erika M Wolff, Rodolfo Ghirlando, Xiaojian Hu, Jeffrey H Miller & Wei Yang. (2004) Structure of the MutL C-terminal domain: a model of intact MutL and its roles in mismatch repair. The EMBO Journal 23:21, pages 4134-4145.
Crossref
Marilia Cascalho. (2004) Advantages and Disadvantages of Cytidine Deamination. The Journal of Immunology 172:11, pages 6513-6518.
Crossref

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