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Results: 1 to 20 of 382

Similar articles for PubMed (Select 9426063)

1.

Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality.

de Boer J, Donker I, de Wit J, Hoeijmakers JH, Weeda G.

Cancer Res. 1998 Jan 1;58(1):89-94.

2.

Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition.

de Boer J, van Steeg H, Berg RJ, Garssen J, de Wit J, van Oostrum CT, Beems RB, van der Horst GT, van Kreijl CF, de Gruijl FR, Bootsma D, Hoeijmakers JH, Weeda G.

Cancer Res. 1999 Jul 15;59(14):3489-94.

4.

Mutations in the XPD gene in xeroderma pigmentosum group D cell strains: confirmation of genotype-phenotype correlation.

Kobayashi T, Uchiyama M, Fukuro S, Tanaka K.

Am J Med Genet. 2002 Jul 1;110(3):248-52.

PMID:
12116233
5.

Mutations in the XPD gene leading to xeroderma pigmentosum symptoms.

Kobayashi T, Kuraoka I, Saijo M, Nakatsu Y, Tanaka A, Someda Y, Fukuro S, Tanaka K.

Hum Mutat. 1997;9(4):322-31.

PMID:
9101292
6.

TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair.

Winkler GS, Araújo SJ, Fiedler U, Vermeulen W, Coin F, Egly JM, Hoeijmakers JH, Wood RD, Timmers HT, Weeda G.

J Biol Chem. 2000 Feb 11;275(6):4258-66.

8.

Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.

Takayama K, Salazar EP, Lehmann A, Stefanini M, Thompson LH, Weber CA.

Cancer Res. 1995 Dec 1;55(23):5656-63.

9.

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.

Taylor EM, Broughton BC, Botta E, Stefanini M, Sarasin A, Jaspers NG, Fawcett H, Harcourt SA, Arlett CF, Lehmann AR.

Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8658-63.

10.

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.

11.

Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.

Broughton BC, Thompson AF, Harcourt SA, Vermeulen W, Hoeijmakers JH, Botta E, Stefanini M, King MD, Weber CA, Cole J, et al.

Am J Hum Genet. 1995 Jan;56(1):167-74. Review.

12.

Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.

Graham JM Jr, Anyane-Yeboa K, Raams A, Appeldoorn E, Kleijer WJ, Garritsen VH, Busch D, Edersheim TG, Jaspers NG.

Am J Hum Genet. 2001 Aug;69(2):291-300. Epub 2001 Jul 3.

13.

A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy.

de Boer J, de Wit J, van Steeg H, Berg RJ, Morreau H, Visser P, Lehmann AR, Duran M, Hoeijmakers JH, Weeda G.

Mol Cell. 1998 Jun;1(7):981-90.

14.

Human xeroderma pigmentosum group D gene encodes a DNA helicase.

Sung P, Bailly V, Weber C, Thompson LH, Prakash L, Prakash S.

Nature. 1993 Oct 28;365(6449):852-5.

PMID:
8413672
15.

Effects of XPD mutations on ultraviolet-induced apoptosis in relation to skin cancer-proneness in repair-deficient syndromes.

Queille S, Drougard C, Sarasin A, Daya-Grosjean L.

J Invest Dermatol. 2001 Nov;117(5):1162-70.

16.

Codominance associated with overexpression of certain XPD mutations.

Kadkhodayan S, Coin F, Salazar EP, George JW, Egly JM, Thompson LH.

Mutat Res. 2001 Mar 7;485(2):153-68.

PMID:
11182546
17.

Restoring DNA repair capacity of cells from three distinct diseases by XPD gene-recombinant adenovirus.

Armelini MG, Muotri AR, Marchetto MC, de Lima-Bessa KM, Sarasin A, Menck CF.

Cancer Gene Ther. 2005 Apr;12(4):389-96.

PMID:
15650764
18.

Structural and mutational analysis of the xeroderma pigmentosum group D (XPD) gene.

Frederick GD, Amirkhan RH, Schultz RA, Friedberg EC.

Hum Mol Genet. 1994 Oct;3(10):1783-8.

PMID:
7849702
19.

Basal transcription defect discriminates between xeroderma pigmentosum and trichothiodystrophy in XPD patients.

Dubaele S, Proietti De Santis L, Bienstock RJ, Keriel A, Stefanini M, Van Houten B, Egly JM.

Mol Cell. 2003 Jun;11(6):1635-46.

PMID:
12820975
20.

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
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