Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 96

1.

Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4.

Kim Y, Spitz GS, Veturi U, Lach FP, Auerbach AD, Smogorzewska A.

Blood. 2013 Jan 3;121(1):54-63. doi: 10.1182/blood-2012-07-441212. Epub 2012 Oct 23.

2.

Disruption of SLX4-MUS81 Function Increases the Relative Biological Effectiveness of Proton Radiation.

Liu Q, Underwood TS, Kung J, Wang M, Lu HM, Paganetti H, Held KD, Hong TS, Efstathiou JA, Willers H.

Int J Radiat Oncol Biol Phys. 2016 May 1;95(1):78-85. doi: 10.1016/j.ijrobp.2016.01.046. Epub 2016 Feb 1.

3.

Involvement of SLX4 in interstrand cross-link repair is regulated by the Fanconi anemia pathway.

Yamamoto KN, Kobayashi S, Tsuda M, Kurumizaka H, Takata M, Kono K, Jiricny J, Takeda S, Hirota K.

Proc Natl Acad Sci U S A. 2011 Apr 19;108(16):6492-6. doi: 10.1073/pnas.1018487108. Epub 2011 Apr 4.

4.

Orchestrating the nucleases involved in DNA interstrand cross-link (ICL) repair.

Sengerová B, Wang AT, McHugh PJ.

Cell Cycle. 2011 Dec 1;10(23):3999-4008. doi: 10.4161/cc.10.23.18385. Epub 2011 Dec 1. Review.

5.

Nuclease delivery: versatile functions of SLX4/FANCP in genome maintenance.

Kim Y.

Mol Cells. 2014 Aug;37(8):569-74. doi: 10.14348/molcells.2014.0118. Epub 2014 Jun 18. Review.

6.

Mouse SLX4 is a tumor suppressor that stimulates the activity of the nuclease XPF-ERCC1 in DNA crosslink repair.

Hodskinson MR, Silhan J, Crossan GP, Garaycoechea JI, Mukherjee S, Johnson CM, Schärer OD, Patel KJ.

Mol Cell. 2014 May 8;54(3):472-84. doi: 10.1016/j.molcel.2014.03.014. Epub 2014 Apr 10.

7.

Coordination of structure-specific nucleases by human SLX4/BTBD12 is required for DNA repair.

Muñoz IM, Hain K, Déclais AC, Gardiner M, Toh GW, Sanchez-Pulido L, Heuckmann JM, Toth R, Macartney T, Eppink B, Kanaar R, Ponting CP, Lilley DM, Rouse J.

Mol Cell. 2009 Jul 10;35(1):116-27. doi: 10.1016/j.molcel.2009.06.020.

8.

Mutations of the SLX4 gene in Fanconi anemia.

Kim Y, Lach FP, Desetty R, Hanenberg H, Auerbach AD, Smogorzewska A.

Nat Genet. 2011 Feb;43(2):142-6. doi: 10.1038/ng.750. Epub 2011 Jan 16.

9.

The nuclease hSNM1B/Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP/SLX4.

Salewsky B, Schmiester M, Schindler D, Digweed M, Demuth I.

Hum Mol Genet. 2012 Nov 15;21(22):4948-56. doi: 10.1093/hmg/dds338. Epub 2012 Aug 19.

PMID:
22907656
10.

Physical interaction between SLX4 (FANCP) and XPF (FANCQ) proteins and biological consequences of interaction-defective missense mutations.

Hashimoto K, Wada K, Matsumoto K, Moriya M.

DNA Repair (Amst). 2015 Nov;35:48-54. doi: 10.1016/j.dnarep.2015.09.022. Epub 2015 Sep 30.

11.

Distinct functional roles for the two SLX4 ubiquitin-binding UBZ domains mutated in Fanconi anemia.

Lachaud C, Castor D, Hain K, Muñoz I, Wilson J, MacArtney TJ, Schindler D, Rouse J.

J Cell Sci. 2014 Jul 1;127(Pt 13):2811-7. doi: 10.1242/jcs.146167. Epub 2014 May 2.

12.

Human SLX4 is a Holliday junction resolvase subunit that binds multiple DNA repair/recombination endonucleases.

Fekairi S, Scaglione S, Chahwan C, Taylor ER, Tissier A, Coulon S, Dong MQ, Ruse C, Yates JR 3rd, Russell P, Fuchs RP, McGowan CH, Gaillard PH.

Cell. 2009 Jul 10;138(1):78-89. doi: 10.1016/j.cell.2009.06.029.

13.

Mammalian BTBD12/SLX4 assembles a Holliday junction resolvase and is required for DNA repair.

Svendsen JM, Smogorzewska A, Sowa ME, O'Connell BC, Gygi SP, Elledge SJ, Harper JW.

Cell. 2009 Jul 10;138(1):63-77. doi: 10.1016/j.cell.2009.06.030.

14.

Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia.

Crossan GP, van der Weyden L, Rosado IV, Langevin F, Gaillard PH, McIntyre RE; Sanger Mouse Genetics Project, Gallagher F, Kettunen MI, Lewis DY, Brindle K, Arends MJ, Adams DJ, Patel KJ.

Nat Genet. 2011 Feb;43(2):147-52. doi: 10.1038/ng.752. Epub 2011 Jan 16.

15.

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype.

Stoepker C, Hain K, Schuster B, Hilhorst-Hofstee Y, Rooimans MA, Steltenpool J, Oostra AB, Eirich K, Korthof ET, Nieuwint AW, Jaspers NG, Bettecken T, Joenje H, Schindler D, Rouse J, de Winter JP.

Nat Genet. 2011 Feb;43(2):138-41. doi: 10.1038/ng.751. Epub 2011 Jan 16.

PMID:
21240277
16.

Identification and characterization of MUS81 point mutations that abolish interaction with the SLX4 scaffold protein.

Nair N, Castor D, Macartney T, Rouse J.

DNA Repair (Amst). 2014 Dec;24:131-7. doi: 10.1016/j.dnarep.2014.08.004. Epub 2014 Sep 16.

17.

XPF-ERCC1 participates in the Fanconi anemia pathway of cross-link repair.

Bhagwat N, Olsen AL, Wang AT, Hanada K, Stuckert P, Kanaar R, D'Andrea A, Niedernhofer LJ, McHugh PJ.

Mol Cell Biol. 2009 Dec;29(24):6427-37. doi: 10.1128/MCB.00086-09. Epub 2009 Oct 5.

18.

Mechanism and regulation of incisions during DNA interstrand cross-link repair.

Zhang J, Walter JC.

DNA Repair (Amst). 2014 Jul;19:135-42. doi: 10.1016/j.dnarep.2014.03.018. Epub 2014 Apr 24. Review.

19.

XPF-ERCC1 acts in Unhooking DNA interstrand crosslinks in cooperation with FANCD2 and FANCP/SLX4.

Klein Douwel D, Boonen RA, Long DT, Szypowska AA, Räschle M, Walter JC, Knipscheer P.

Mol Cell. 2014 May 8;54(3):460-71. doi: 10.1016/j.molcel.2014.03.015. Epub 2014 Apr 10.

20.

Supplemental Content

Support Center