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Items: 1 to 20 of 133

1.

Dissection of the molecular defects caused by pathogenic mutations in the DNA repair factor XPC.

Bernardes de Jesus BM, Bjørås M, Coin F, Egly JM.

Mol Cell Biol. 2008 Dec;28(23):7225-35. doi: 10.1128/MCB.00781-08. Epub 2008 Sep 22.

2.
3.

The xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA.

Yokoi M, Masutani C, Maekawa T, Sugasawa K, Ohkuma Y, Hanaoka F.

J Biol Chem. 2000 Mar 31;275(13):9870-5.

4.

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.

5.

XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase.

Fuss JO, Tainer JA.

DNA Repair (Amst). 2011 Jul 15;10(7):697-713. doi: 10.1016/j.dnarep.2011.04.028. Epub 2011 May 14. Review.

6.
7.

The carboxy-terminal domain of the XPC protein plays a crucial role in nucleotide excision repair through interactions with transcription factor IIH.

Uchida A, Sugasawa K, Masutani C, Dohmae N, Araki M, Yokoi M, Ohkuma Y, Hanaoka F.

DNA Repair (Amst). 2002 Jun 21;1(6):449-61.

PMID:
12509233
8.

Comparative study of nucleotide excision repair defects between XPD-mutated fibroblasts derived from trichothiodystrophy and xeroderma pigmentosum patients.

Nishiwaki T, Kobayashi N, Iwamoto T, Yamamoto A, Sugiura S, Liu YC, Sarasin A, Okahashi Y, Hirano M, Ueno S, Mori T.

DNA Repair (Amst). 2008 Dec 1;7(12):1990-8. doi: 10.1016/j.dnarep.2008.08.009. Epub 2008 Oct 10.

PMID:
18817897
9.

A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.

Weeda G, Eveno E, Donker I, Vermeulen W, Chevallier-Lagente O, Taïeb A, Stary A, Hoeijmakers JH, Mezzina M, Sarasin A.

Am J Hum Genet. 1997 Feb;60(2):320-9.

10.
11.

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.

12.

Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.

Vermeulen W, Scott RJ, Rodgers S, Müller HJ, Cole J, Arlett CF, Kleijer WJ, Bootsma D, Hoeijmakers JH, Weeda G.

Am J Hum Genet. 1994 Feb;54(2):191-200.

13.

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.

14.
15.

Mechanism of open complex and dual incision formation by human nucleotide excision repair factors.

Evans E, Moggs JG, Hwang JR, Egly JM, Wood RD.

EMBO J. 1997 Nov 3;16(21):6559-73.

16.

A 3' --> 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription.

Hwang JR, Moncollin V, Vermeulen W, Seroz T, van Vuuren H, Hoeijmakers JH, Egly JM.

J Biol Chem. 1996 Jul 5;271(27):15898-904.

17.

New functions of XPC in the protection of human skin cells from oxidative damage.

D'Errico M, Parlanti E, Teson M, de Jesus BM, Degan P, Calcagnile A, Jaruga P, Bjørås M, Crescenzi M, Pedrini AM, Egly JM, Zambruno G, Stefanini M, Dizdaroglu M, Dogliotti E.

EMBO J. 2006 Sep 20;25(18):4305-15. Epub 2006 Sep 7.

18.

Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels.

Chavanne F, Broughton BC, Pietra D, Nardo T, Browitt A, Lehmann AR, Stefanini M.

Cancer Res. 2000 Apr 1;60(7):1974-82.

20.

Xeroderma pigmentosum and molecular cloning of DNA repair genes.

Boulikas T.

Anticancer Res. 1996 Mar-Apr;16(2):693-708. Review.

PMID:
8687116

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