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Summary Expression Gene Literature (18) GO Terms (22) Nucleotides (86) Proteins (26) Interactants (113) Wiki
XB--5828963

Papers associated with dna2

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HELLS and CDCA7 comprise a bipartite nucleosome remodeling complex defective in ICF syndrome., Jenness C, Giunta S, Müller MM, Kimura H, Muir TW, Funabiki H., Proc Natl Acad Sci U S A. January 1, 2018; 115 (5): E876-E885.                                


Dna2 initiates resection at clean DNA double-strand breaks., Paudyal SC, Li S, Yan H, Hunter T, You Z., Nucleic Acids Res. November 16, 2017; 45 (20): 11766-11781.            


Fanconi-Anemia-Associated Mutations Destabilize RAD51 Filaments and Impair Replication Fork Protection., Zadorozhny K, Sannino V, Beláň O, Mlčoušková J, Špírek M, Costanzo V, Krejčí L., Cell Rep. October 10, 2017; 21 (2): 333-340.                


DNA double-strand breaks with 5'' adducts are efficiently channeled to the DNA2-mediated resection pathway., Tammaro M, Liao S, Beeharry N, Yan H., Nucleic Acids Res. January 8, 2016; 44 (1): 221-31.                


The N-terminus of RPA large subunit and its spatial position are important for the 5''->3'' resection of DNA double-strand breaks., Tammaro M, Liao S, McCane J, Yan H., Nucleic Acids Res. October 15, 2015; 43 (18): 8790-800.                  


14-3-3 proteins restrain the Exo1 nuclease to prevent overresection., Chen X, Kim IK, Honaker Y, Paudyal SC, Koh WK, Sparks M, Li S, Piwnica-Worms H, Ellenberger T, You Z., J Biol Chem. May 8, 2015; 290 (19): 12300-12.    


BRCA1 and CtIP promote alternative non-homologous end-joining at uncapped telomeres., Badie S, Carlos AR, Folio C, Okamoto K, Bouwman P, Jonkers J, Tarsounas M., EMBO J. February 3, 2015; 34 (3): 410-24.              


PCNA promotes processive DNA end resection by Exo1., Chen X, Paudyal SC, Chin RI, You Z., Nucleic Acids Res. November 1, 2013; 41 (20): 9325-38.              


DNA2 and EXO1 in replication-coupled, homology-directed repair and in the interplay between HDR and the FA/BRCA network., Karanja KK, Cox SW, Duxin JP, Stewart SA, Campbell JL., Cell Cycle. November 1, 2012; 11 (21): 3983-96.


Analysis of MRE11''s function in the 5''-->3'' processing of DNA double-strand breaks., Liao S, Guay C, Toczylowski T, Yan H., Nucleic Acids Res. May 1, 2012; 40 (10): 4496-506.                


Involvement of DNA ligase III and ribonuclease H1 in mitochondrial DNA replication in cultured human cells., Ruhanen H, Ushakov K, Yasukawa T., Biochim Biophys Acta. December 1, 2011; 1813 (12): 2000-7.          


Cdk1 uncouples CtIP-dependent resection and Rad51 filament formation during M-phase double-strand break repair., Peterson SE, Li Y, Chait BT, Gottesman ME, Baer R, Gautier J., J Cell Biol. September 5, 2011; 194 (5): 705-20.              


Mechanistic analysis of Xenopus EXO1''s function in 5''-strand resection at DNA double-strand breaks., Liao S, Toczylowski T, Yan H., Nucleic Acids Res. August 1, 2011; 39 (14): 5967-77.                


Replication protein A promotes 5''-->3'' end processing during homology-dependent DNA double-strand break repair., Yan H, Toczylowski T, McCane J, Chen C, Liao S., J Cell Biol. January 24, 2011; 192 (2): 251-61.              


Xenopus DNA2 is a helicase/nuclease that is found in complexes with replication proteins And-1/Ctf4 and Mcm10 and DSB response proteins Nbs1 and ATM., Wawrousek KE, Fortini BK, Polaczek P, Chen L, Liu Q, Dunphy WG, Campbell JL., Cell Cycle. March 15, 2010; 9 (6): 1156-66.


Identification of the Xenopus DNA2 protein as a major nuclease for the 5''->3'' strand-specific processing of DNA ends., Liao S, Toczylowski T, Yan H., Nucleic Acids Res. November 1, 2008; 36 (19): 6091-100.              


Identification of the Xenopus laevis homolog of Saccharomyces cerevisiae DNA2 and its role in DNA replication., Liu Q, Choe W, Campbell JL., J Biol Chem. January 21, 2000; 275 (3): 1615-24.


Nucleosome disruption and enhancement of activator binding by a human SW1/SNF complex., Kwon H, Imbalzano AN, Khavari PA, Kingston RE, Green MR., Nature. August 11, 1994; 370 (6489): 477-81.

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