Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 93

1.

Rad50 is dispensable for the maintenance and viability of postmitotic tissues.

Adelman CA, De S, Petrini JH.

Mol Cell Biol. 2009 Jan;29(2):483-92. doi: 10.1128/MCB.01525-08. Epub 2008 Nov 10.

2.

The Rad50S allele promotes ATM-dependent DNA damage responses and suppresses ATM deficiency: implications for the Mre11 complex as a DNA damage sensor.

Morales M, Theunissen JW, Kim CF, Kitagawa R, Kastan MB, Petrini JH.

Genes Dev. 2005 Dec 15;19(24):3043-54.

3.

DNA damage signaling in hematopoietic cells: a role for Mre11 complex repair of topoisomerase lesions.

Morales M, Liu Y, Laiakis EC, Morgan WF, Nimer SD, Petrini JH.

Cancer Res. 2008 Apr 1;68(7):2186-93. doi: 10.1158/0008-5472.CAN-07-2355.

4.

Division of labor: DNA repair and the cell cycle specific functions of the Mre11 complex.

Adelman CA, Petrini JH.

Cell Cycle. 2009 May 15;8(10):1510-4. Epub 2009 May 10.

5.

The Drosophila Mre11/Rad50 complex is required to prevent both telomeric fusion and chromosome breakage.

Ciapponi L, Cenci G, Ducau J, Flores C, Johnson-Schlitz D, Gorski MM, Engels WR, Gatti M.

Curr Biol. 2004 Aug 10;14(15):1360-6.

7.

Disruption of telomere maintenance by depletion of the MRE11/RAD50/NBS1 complex in cells that use alternative lengthening of telomeres.

Zhong ZH, Jiang WQ, Cesare AJ, Neumann AA, Wadhwa R, Reddel RR.

J Biol Chem. 2007 Oct 5;282(40):29314-22. Epub 2007 Aug 9.

8.
9.
10.

The Drosophila Nbs protein functions in multiple pathways for the maintenance of genome stability.

Ciapponi L, Cenci G, Gatti M.

Genetics. 2006 Jul;173(3):1447-54. Epub 2006 Apr 30.

11.

Mre11-Rad50 promotes rapid repair of DNA damage in the polyploid archaeon Haloferax volcanii by restraining homologous recombination.

Delmas S, Shunburne L, Ngo HP, Allers T.

PLoS Genet. 2009 Jul;5(7):e1000552. doi: 10.1371/journal.pgen.1000552. Epub 2009 Jul 10.

12.

MRE11/RAD50/NBS1: complex activities.

Assenmacher N, Hopfner KP.

Chromosoma. 2004 Oct;113(4):157-66. Epub 2004 Aug 10. Review.

PMID:
15309560
13.
14.

Rad50 zinc hook is important for the Mre11 complex to bind chromosomal DNA double-stranded breaks and initiate various DNA damage responses.

He J, Shi LZ, Truong LN, Lu CS, Razavian N, Li Y, Negrete A, Shiloach J, Berns MW, Wu X.

J Biol Chem. 2012 Sep 14;287(38):31747-56. doi: 10.1074/jbc.M112.384750. Epub 2012 Jul 25.

15.

Yeast xrs2 binds DNA and helps target rad50 and mre11 to DNA ends.

Trujillo KM, Roh DH, Chen L, Van Komen S, Tomkinson A, Sung P.

J Biol Chem. 2003 Dec 5;278(49):48957-64. Epub 2003 Sep 30.

16.

The Aspergillus nidulans sldI(RAD50) gene interacts with bimE(APC1), a homologue of an anaphase-promoting complex subunit.

Malavazi I, Lima JF, von Zeska Kress Fagundes MR, Efimov VP, de Souza Goldman MH, Goldman GH.

Mol Microbiol. 2005 Jul;57(1):222-37.

17.

Mammalian Ku86 protein prevents telomeric fusions independently of the length of TTAGGG repeats and the G-strand overhang.

Samper E, Goytisolo FA, Slijepcevic P, van Buul PP, Blasco MA.

EMBO Rep. 2000 Sep;1(3):244-52.

18.

The Rad50 hook domain is a critical determinant of Mre11 complex functions.

Wiltzius JJ, Hohl M, Fleming JC, Petrini JH.

Nat Struct Mol Biol. 2005 May;12(5):403-7. Epub 2005 Apr 24.

PMID:
15852023
19.

Coordination and processing of DNA ends during double-strand break repair: the role of the bacteriophage T4 Mre11/Rad50 (MR) complex.

Almond JR, Stohr BA, Panigrahi AK, Albrecht DW, Nelson SW, Kreuzer KN.

Genetics. 2013 Nov;195(3):739-55. doi: 10.1534/genetics.113.154872. Epub 2013 Aug 26.

20.

Fission yeast Rad50 stimulates sister chromatid recombination and links cohesion with repair.

Hartsuiker E, Vaessen E, Carr AM, Kohli J.

EMBO J. 2001 Dec 3;20(23):6660-71.

Items per page

Supplemental Content

Write to the Help Desk