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Items: 14

1.

The BioGRID interaction database: 2017 update.

Chatr-Aryamontri A, Oughtred R, Boucher L, Rust J, Chang C, Kolas NK, O'Donnell L, Oster S, Theesfeld C, Sellam A, Stark C, Breitkreutz BJ, Dolinski K, Tyers M.

Nucleic Acids Res. 2017 Jan 4;45(D1):D369-D379. doi: 10.1093/nar/gkw1102. Epub 2016 Dec 14.

2.

NEK1 Facilitates Cohesin Removal during Mammalian Spermatogenesis.

Holloway K, Roberson EC, Corbett KL, Kolas NK, Nieves E, Cohen PE.

Genes (Basel). 2011 Mar 7;2(1):260-79. doi: 10.3390/genes2010260.

3.

The MMS22L-TONSL complex mediates recovery from replication stress and homologous recombination.

O'Donnell L, Panier S, Wildenhain J, Tkach JM, Al-Hakim A, Landry MC, Escribano-Diaz C, Szilard RK, Young JT, Munro M, Canny MD, Kolas NK, Zhang W, Harding SM, Ylanko J, Mendez M, Mullin M, Sun T, Habermann B, Datti A, Bristow RG, Gingras AC, Tyers MD, Brown GW, Durocher D.

Mol Cell. 2010 Nov 24;40(4):619-31. doi: 10.1016/j.molcel.2010.10.024. Epub 2010 Nov 4.

4.

The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage.

Stewart GS, Panier S, Townsend K, Al-Hakim AK, Kolas NK, Miller ES, Nakada S, Ylanko J, Olivarius S, Mendez M, Oldreive C, Wildenhain J, Tagliaferro A, Pelletier L, Taubenheim N, Durandy A, Byrd PJ, Stankovic T, Taylor AM, Durocher D.

Cell. 2009 Feb 6;136(3):420-34. doi: 10.1016/j.cell.2008.12.042.

5.

Comparative analysis of meiotic progression in female mice bearing mutations in genes of the DNA mismatch repair pathway.

Kan R, Sun X, Kolas NK, Avdievich E, Kneitz B, Edelmann W, Cohen PE.

Biol Reprod. 2008 Mar;78(3):462-71. Epub 2007 Dec 5.

PMID:
18057311
6.

Orchestration of the DNA-damage response by the RNF8 ubiquitin ligase.

Kolas NK, Chapman JR, Nakada S, Ylanko J, Chahwan R, Sweeney FD, Panier S, Mendez M, Wildenhain J, Thomson TM, Pelletier L, Jackson SP, Durocher D.

Science. 2007 Dec 7;318(5856):1637-40. Epub 2007 Nov 15.

7.

DNA repair: DNA polymerase zeta and Rev1 break in.

Kolas NK, Durocher D.

Curr Biol. 2006 Apr 18;16(8):R296-9.

8.

Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I.

Kolas NK, Svetlanov A, Lenzi ML, Macaluso FP, Lipkin SM, Liskay RM, Greally J, Edelmann W, Cohen PE.

J Cell Biol. 2005 Nov 7;171(3):447-58. Epub 2005 Oct 31.

9.

Mutant meiotic chromosome core components in mice can cause apparent sexual dimorphic endpoints at prophase or X-Y defective male-specific sterility.

Kolas NK, Marcon E, Crackower MA, Höög C, Penninger JM, Spyropoulos B, Moens PB.

Chromosoma. 2005 Jul;114(2):92-102. Epub 2005 Jun 28.

PMID:
15983832
10.

Novel and diverse functions of the DNA mismatch repair family in mammalian meiosis and recombination.

Kolas NK, Cohen PE.

Cytogenet Genome Res. 2004;107(3-4):216-31. Review.

PMID:
15467367
12.

Essential role of Fkbp6 in male fertility and homologous chromosome pairing in meiosis.

Crackower MA, Kolas NK, Noguchi J, Sarao R, Kikuchi K, Kaneko H, Kobayashi E, Kawai Y, Kozieradzki I, Landers R, Mo R, Hui CC, Nieves E, Cohen PE, Osborne LR, Wada T, Kunieda T, Moens PB, Penninger JM.

Science. 2003 May 23;300(5623):1291-5.

13.

Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility.

Wei K, Clark AB, Wong E, Kane MF, Mazur DJ, Parris T, Kolas NK, Russell R, Hou H Jr, Kneitz B, Yang G, Kunkel TA, Kolodner RD, Cohen PE, Edelmann W.

Genes Dev. 2003 Mar 1;17(5):603-14.

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