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482 related items for PubMed ID: 20157511

  • 1. WRN helicase defective in the premature aging disorder Werner syndrome genetically interacts with topoisomerase 3 and restores the top3 slow growth phenotype of sgs1 top3.
    Aggarwal M, Brosh RM.
    Aging (Albany NY); 2009 Feb 05; 1(2):219-33. PubMed ID: 20157511
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  • 2. Premature aging syndrome gene WRN genetically interacts with a topoisomerase.
    Aggarwal M, Brosh RM.
    Cell Cycle; 2009 Jul 15; 8(14):2143. PubMed ID: 19587535
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  • 4. Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases.
    Yamagata K, Kato J, Shimamoto A, Goto M, Furuichi Y, Ikeda H.
    Proc Natl Acad Sci U S A; 1998 Jul 21; 95(15):8733-8. PubMed ID: 9671747
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  • 7. In vivo function of the conserved non-catalytic domain of Werner syndrome helicase in DNA replication.
    Sharma S, Sommers JA, Brosh RM.
    Hum Mol Genet; 2004 Oct 01; 13(19):2247-61. PubMed ID: 15282207
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  • 9. Association of yeast DNA topoisomerase III and Sgs1 DNA helicase: studies of fusion proteins.
    Bennett RJ, Wang JC.
    Proc Natl Acad Sci U S A; 2001 Sep 25; 98(20):11108-13. PubMed ID: 11553789
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  • 14. WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.
    Chen L, Huang S, Lee L, Davalos A, Schiestl RH, Campisi J, Oshima J.
    Aging Cell; 2003 Aug 25; 2(4):191-9. PubMed ID: 12934712
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