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Items: 1 to 20 of 184

1.

The role of XPC: implications in cancer and oxidative DNA damage.

Melis JP, Luijten M, Mullenders LH, van Steeg H.

Mutat Res. 2011 Nov-Dec;728(3):107-17. doi: 10.1016/j.mrrev.2011.07.001. Epub 2011 Jul 7.

2.

Slow accumulation of mutations in Xpc-/- mice upon induction of oxidative stress.

Melis JP, Kuiper RV, Zwart E, Robinson J, Pennings JL, van Oostrom CT, Luijten M, van Steeg H.

DNA Repair (Amst). 2013 Dec;12(12):1081-6. doi: 10.1016/j.dnarep.2013.08.019. Epub 2013 Sep 29.

3.

Mouse models for xeroderma pigmentosum group A and group C show divergent cancer phenotypes.

Melis JP, Wijnhoven SW, Beems RB, Roodbergen M, van den Berg J, Moon H, Friedberg E, van der Horst GT, Hoeijmakers JH, Vijg J, van Steeg H.

Cancer Res. 2008 Mar 1;68(5):1347-53. doi: 10.1158/0008-5472.CAN-07-6067.

4.

Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair.

Sugasawa K, Ng JM, Masutani C, Iwai S, van der Spek PJ, Eker AP, Hanaoka F, Bootsma D, Hoeijmakers JH.

Mol Cell. 1998 Aug;2(2):223-32.

5.

Oxidative DNA damage and nucleotide excision repair.

Melis JP, van Steeg H, Luijten M.

Antioxid Redox Signal. 2013 Jun 20;18(18):2409-19. doi: 10.1089/ars.2012.5036. Epub 2012 Dec 7. Review.

6.

Cell-type-specific consequences of nucleotide excision repair deficiencies: Embryonic stem cells versus fibroblasts.

de Waard H, Sonneveld E, de Wit J, Esveldt-van Lange R, Hoeijmakers JH, Vrieling H, van der Horst GT.

DNA Repair (Amst). 2008 Oct 1;7(10):1659-69. doi: 10.1016/j.dnarep.2008.06.009. Epub 2008 Jul 26.

PMID:
18634906
7.

Centrin 2 stimulates nucleotide excision repair by interacting with xeroderma pigmentosum group C protein.

Nishi R, Okuda Y, Watanabe E, Mori T, Iwai S, Masutani C, Sugasawa K, Hanaoka F.

Mol Cell Biol. 2005 Jul;25(13):5664-74.

8.

Tissue specific mutagenic and carcinogenic responses in NER defective mouse models.

Wijnhoven SW, Hoogervorst EM, de Waard H, van der Horst GT, van Steeg H.

Mutat Res. 2007 Jan 3;614(1-2):77-94. Review.

PMID:
16769089
10.

In vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutation.

Yasuda G, Nishi R, Watanabe E, Mori T, Iwai S, Orioli D, Stefanini M, Hanaoka F, Sugasawa K.

Mol Cell Biol. 2007 Oct;27(19):6606-14. Epub 2007 Aug 6.

11.

Cancer predisposition in mutant mice defective in multiple genetic pathways: uncovering important genetic interactions.

Meira LB, Reis AM, Cheo DL, Nahari D, Burns DK, Friedberg EC.

Mutat Res. 2001 Jun 2;477(1-2):51-8. Review.

PMID:
11376686
12.

Nucleotide excision repair activity on DNA damage induced by photoactivated methylene blue.

Berra CM, de Oliveira CS, Garcia CC, Rocha CR, Lerner LK, Lima LC, Baptista Mda S, Menck CF.

Free Radic Biol Med. 2013 Aug;61:343-56. doi: 10.1016/j.freeradbiomed.2013.03.026. Epub 2013 Apr 6.

PMID:
23567189
13.

DMBA-induced toxic and mutagenic responses vary dramatically between NER-deficient Xpa, Xpc and Csb mice.

Wijnhoven SW, Kool HJ, Mullenders LH, Slater R, van Zeeland AA, Vrieling H.

Carcinogenesis. 2001 Jul;22(7):1099-106.

PMID:
11408355
14.

Ubiquitin-specific protease 7 regulates nucleotide excision repair through deubiquitinating XPC protein and preventing XPC protein from undergoing ultraviolet light-induced and VCP/p97 protein-regulated proteolysis.

He J, Zhu Q, Wani G, Sharma N, Han C, Qian J, Pentz K, Wang QE, Wani AA.

J Biol Chem. 2014 Sep 26;289(39):27278-89. doi: 10.1074/jbc.M114.589812. Epub 2014 Aug 12.

15.

XPC is essential for nucleotide excision repair of zidovudine-induced DNA damage in human hepatoma cells.

Wu Q, Beland FA, Chang CW, Fang JL.

Toxicol Appl Pharmacol. 2011 Mar 1;251(2):155-62. doi: 10.1016/j.taap.2010.12.009. Epub 2010 Dec 28.

PMID:
21192964
16.

Age-related neuronal degeneration: complementary roles of nucleotide excision repair and transcription-coupled repair in preventing neuropathology.

Jaarsma D, van der Pluijm I, de Waard MC, Haasdijk ED, Brandt R, Vermeij M, Rijksen Y, Maas A, van Steeg H, Hoeijmakers JH, van der Horst GT.

PLoS Genet. 2011 Dec;7(12):e1002405. doi: 10.1371/journal.pgen.1002405. Epub 2011 Dec 8.

17.

Differential ultraviolet-B-induced immunomodulation in XPA, XPC, and CSB DNA repair-deficient mice.

Boonstra A, van Oudenaren A, Baert M, van Steeg H, Leenen PJ, van der Horst GT, Hoeijmakers JH, Savelkoul HF, Garssen J.

J Invest Dermatol. 2001 Jul;117(1):141-6.

18.

Complementation of the DNA repair deficiency in human xeroderma pigmentosum group a and C cells by recombinant adenovirus-mediated gene transfer.

Muotri AR, Marchetto MC, Zerbini LF, Libermann TA, Ventura AM, Sarasin A, Menck CF.

Hum Gene Ther. 2002 Oct 10;13(15):1833-44.

PMID:
12396616
19.

XPC deficiency is related to APE1 and OGG1 expression and function.

de Melo JT, de Souza Timoteo AR, Lajus TB, Brandão JA, de Souza-Pinto NC, Menck CF, Campalans A, Radicella JP, Vessoni AT, Muotri AR, Agnez-Lima LF.

Mutat Res. 2016 Feb-Mar;784-785:25-33. doi: 10.1016/j.mrfmmm.2016.01.004. Epub 2016 Jan 16.

PMID:
26811994
20.

XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients.

Khan SG, Yamanegi K, Zheng ZM, Boyle J, Imoto K, Oh KS, Baker CC, Gozukara E, Metin A, Kraemer KH.

Hum Mutat. 2010 Feb;31(2):167-75. doi: 10.1002/humu.21166.

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