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Results: 1 to 20 of 104

Similar articles for PubMed (Select 24001775)

1.

Inactivation of Uaf1 causes defective homologous recombination and early embryonic lethality in mice.

Park E, Kim JM, Primack B, Weinstock DM, Moreau LA, Parmar K, D'Andrea AD.

Mol Cell Biol. 2013 Nov;33(22):4360-70. doi: 10.1128/MCB.00870-13. Epub 2013 Sep 3.

2.

The USP1/UAF1 complex promotes double-strand break repair through homologous recombination.

Murai J, Yang K, Dejsuphong D, Hirota K, Takeda S, D'Andrea AD.

Mol Cell Biol. 2011 Jun;31(12):2462-9. doi: 10.1128/MCB.05058-11. Epub 2011 Apr 11.

3.

Inactivation of murine Usp1 results in genomic instability and a Fanconi anemia phenotype.

Kim JM, Parmar K, Huang M, Weinstock DM, Ruit CA, Kutok JL, D'Andrea AD.

Dev Cell. 2009 Feb;16(2):314-20. doi: 10.1016/j.devcel.2009.01.001.

4.

Regulation of the Fanconi anemia pathway by a SUMO-like delivery network.

Yang K, Moldovan GL, Vinciguerra P, Murai J, Takeda S, D'Andrea AD.

Genes Dev. 2011 Sep 1;25(17):1847-58. doi: 10.1101/gad.17020911.

5.

A UAF1-containing multisubunit protein complex regulates the Fanconi anemia pathway.

Cohn MA, Kowal P, Yang K, Haas W, Huang TT, Gygi SP, D'Andrea AD.

Mol Cell. 2007 Dec 14;28(5):786-97.

6.

Human ELG1 regulates the level of ubiquitinated proliferating cell nuclear antigen (PCNA) through Its interactions with PCNA and USP1.

Lee KY, Yang K, Cohn MA, Sikdar N, D'Andrea AD, Myung K.

J Biol Chem. 2010 Apr 2;285(14):10362-9. doi: 10.1074/jbc.M109.092544. Epub 2010 Feb 9.

7.

The deubiquitinating enzyme USP1 regulates the Fanconi anemia pathway.

Nijman SM, Huang TT, Dirac AM, Brummelkamp TR, Kerkhoven RM, D'Andrea AD, Bernards R.

Mol Cell. 2005 Feb 4;17(3):331-9.

PMID:
15694335
8.

Embryonic lethality after combined inactivation of Fancd2 and Mlh1 in mice.

van de Vrugt HJ, Eaton L, Hanlon Newell A, Al-Dhalimy M, Liskay RM, Olson SB, Grompe M.

Cancer Res. 2009 Dec 15;69(24):9431-8. doi: 10.1158/0008-5472.CAN-09-2452. Epub .

9.

UAF1 is a subunit of multiple deubiquitinating enzyme complexes.

Cohn MA, Kee Y, Haas W, Gygi SP, D'Andrea AD.

J Biol Chem. 2009 Feb 20;284(8):5343-51. doi: 10.1074/jbc.M808430200. Epub 2008 Dec 15.

10.

Deubiquitination of FANCD2 is required for DNA crosslink repair.

Oestergaard VH, Langevin F, Kuiken HJ, Pace P, Niedzwiedz W, Simpson LJ, Ohzeki M, Takata M, Sale JE, Patel KJ.

Mol Cell. 2007 Dec 14;28(5):798-809.

11.

Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice.

Houghtaling S, Timmers C, Noll M, Finegold MJ, Jones SN, Meyn MS, Grompe M.

Genes Dev. 2003 Aug 15;17(16):2021-35. Epub 2003 Jul 31.

12.

Functional interaction between the Fanconi Anemia D2 protein and proliferating cell nuclear antigen (PCNA) via a conserved putative PCNA interaction motif.

Howlett NG, Harney JA, Rego MA, Kolling FW 4th, Glover TW.

J Biol Chem. 2009 Oct 16;284(42):28935-42. doi: 10.1074/jbc.M109.016352. Epub 2009 Aug 24.

13.

The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability.

Howlett NG, Taniguchi T, Durkin SG, D'Andrea AD, Glover TW.

Hum Mol Genet. 2005 Mar 1;14(5):693-701. Epub 2005 Jan 20.

14.

Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1.

Parmar K, Kim J, Sykes SM, Shimamura A, Stuckert P, Zhu K, Hamilton A, Deloach MK, Kutok JL, Akashi K, Gilliland DG, D'andrea A.

Stem Cells. 2010 Jul;28(7):1186-95. doi: 10.1002/stem.437.

15.

The Fanconi anemia ID2 complex: dueling saxes at the crossroads.

Boisvert RA, Howlett NG.

Cell Cycle. 2014;13(19):2999-3015. doi: 10.4161/15384101.2014.956475.

PMID:
25486561
16.

Genomic instability in mice is greater in Fanconi anemia caused by deficiency of Fancd2 than Fancg.

Reliene R, Yamamoto ML, Rao PN, Schiestl RH.

Cancer Res. 2010 Dec 1;70(23):9703-10. doi: 10.1158/0008-5472.CAN-09-1022. Epub 2010 Nov 30.

17.

Synthesis and structure-activity relationship studies of N-benzyl-2-phenylpyrimidin-4-amine derivatives as potent USP1/UAF1 deubiquitinase inhibitors with anticancer activity against nonsmall cell lung cancer.

Dexheimer TS, Rosenthal AS, Luci DK, Liang Q, Villamil MA, Chen J, Sun H, Kerns EH, Simeonov A, Jadhav A, Zhuang Z, Maloney DJ.

J Med Chem. 2014 Oct 9;57(19):8099-110. doi: 10.1021/jm5010495. Epub 2014 Sep 17.

PMID:
25229643
18.

Rad18-mediated translesion synthesis of bulky DNA adducts is coupled to activation of the Fanconi anemia DNA repair pathway.

Song IY, Palle K, Gurkar A, Tateishi S, Kupfer GM, Vaziri C.

J Biol Chem. 2010 Oct 8;285(41):31525-36. doi: 10.1074/jbc.M110.138206. Epub 2010 Jul 30.

19.

Deficient regulation of DNA double-strand break repair in Fanconi anemia fibroblasts.

Donahue SL, Lundberg R, Saplis R, Campbell C.

J Biol Chem. 2003 Aug 8;278(32):29487-95. Epub 2003 May 14.

20.

FANCD2 activates transcription of TAp63 and suppresses tumorigenesis.

Park E, Kim H, Kim JM, Primack B, Vidal-Cardenas S, Xu Y, Price BD, Mills AA, D'Andrea AD.

Mol Cell. 2013 Jun 27;50(6):908-18. doi: 10.1016/j.molcel.2013.05.017.

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