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Items: 1 to 20 of 163

1.

The genetic basis of xeroderma pigmentosum and trichothiodystrophy syndromes.

Stary A, Sarasin A.

Cancer Surv. 1996;26:155-71. Review. No abstract available.

PMID:
8783572
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.

3.

DNA repair and cancer: speculations based on studies with xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophy.

Lehmann AR, Norris PG.

Carcinogenesis. 1989 Aug;10(8):1353-6. No abstract available.

PMID:
2752510
4.
5.

UV-induced mutations and skin cancer: how important is the link?

Bridges BA.

Mutat Res. 1998 Nov 9;422(1):23-30. Review.

PMID:
9920425
6.

[Xeroderma pigmentosum and related syndromes].

Berneburg M, Krutmann J.

Hautarzt. 2003 Jan;54(1):33-40. Epub 2002 Dec 20. German.

PMID:
12567255
7.

A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy.

Cleaver JE, Thompson LH, Richardson AS, States JC.

Hum Mutat. 1999;14(1):9-22. Review.

PMID:
10447254
8.

The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect.

Berneburg M, Clingen PH, Harcourt SA, Lowe JE, Taylor EM, Green MH, Krutmann J, Arlett CF, Lehmann AR.

Cancer Res. 2000 Jan 15;60(2):431-8.

9.
10.

Trichothiodystrophy and the relationship between DNA repair and cancer.

Lehmann AR.

Bioessays. 1989 Dec;11(6):168-70. Review.

PMID:
2695082
11.
12.

[Xeroderma pigmentosum: children of the moon].

Herouy Y, Krutmann J, Norgauer J, Schöpf E.

J Dtsch Dermatol Ges. 2003 Mar;1(3):191-8. Review. German.

PMID:
16285494
13.

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.

14.

Xeroderma pigmentosum: genetic and environmental influences in skin carcinogenesis.

Cleaver JE.

Int J Dermatol. 1978 Jul-Aug;17(6):435-44. Review. No abstract available.

PMID:
355163
15.

[Endonuclease deficiency in xeroderma pigmentosum].

Feinstein A.

Harefuah. 1973 May 1;84(9):488-90. Hebrew. No abstract available.

PMID:
4719222
16.

Human diseases associated with defective DNA excision repair.

Wood RD.

J R Coll Physicians Lond. 1991 Oct;25(4):300-3. Review.

PMID:
1960684
17.

The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.

Riou L, Zeng L, Chevallier-Lagente O, Stary A, Nikaido O, Taïeb A, Weeda G, Mezzina M, Sarasin A.

Hum Mol Genet. 1999 Jun;8(6):1125-33.

PMID:
10332046
18.

Relationship between posttranslational modification of transaldolase and catalase deficiency in UV-sensitive repair-deficient xeroderma pigmentosum fibroblasts and SV40-transformed human cells.

Lachaise F, Martin G, Drougard C, Perl A, Vuillaume M, Wegnez M, Sarasin A, Daya-Grosjean L.

Free Radic Biol Med. 2001 Jun 15;30(12):1365-73.

PMID:
11390181
19.

What's new in photoimmunology?

Norval M.

Photodermatol Photoimmunol Photomed. 2002 Aug;18(4):209-11. No abstract available.

PMID:
12390679
20.

Trichothiodystrophy, xeroderma pigmentosum and PIBI(D)S syndrome.

Rebora A, Crovato F.

Hum Genet. 1988 Jan;78(1):106-8. No abstract available.

PMID:
3338790

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