Arlett CF - Search Results

1

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. Taylor EM, et al. Among authors: arlett cf. Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8658-63. doi: 10.1073/pnas.94.16.8658. Proc Natl Acad Sci U S A. 1997. PMID: 9238033 Free PMC article.

2

A comparison of the response of unstimulated and stimulated T-lymphocytes and fibroblasts from normal, xeroderma pigmentosum and trichothiodystrophy donors to the lethal action of UV-C.

Arlett CF, Harcourt SA, Cole J, Green MH, Anstey AV. Arlett CF, et al. Mutat Res. 1992 Mar;273(2):127-35. doi: 10.1016/0921-8777(92)90074-d. Mutat Res. 1992. PMID: 1372096

3

Molecular analysis of ultraviolet-induced mutations in a xeroderma pigmentosum cell line.

Dorado G, Steingrimsdottir H, Arlett CF, Lehmann AR. Dorado G, et al. Among authors: arlett cf. J Mol Biol. 1991 Jan 20;217(2):217-22. doi: 10.1016/0022-2836(91)90533-c. J Mol Biol. 1991. PMID: 1992158

4

Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: studies using cells from patients with trichothiodystrophy.

Broughton BC, Lehmann AR, Harcourt SA, Arlett CF, Sarasin A, Kleijer WJ, Beemer FA, Nairn R, Mitchell DL. Broughton BC, et al. Among authors: arlett cf. Mutat Res. 1990 Jan;235(1):33-40. doi: 10.1016/0921-8777(90)90020-6. Mutat Res. 1990. PMID: 2300071

5

Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light.

Lehmann AR, Arlett CF, Broughton BC, Harcourt SA, Steingrimsdottir H, Stefanini M, Malcolm A, Taylor R, Natarajan AT, Green S, et al. Lehmann AR, et al. Among authors: arlett cf. Cancer Res. 1988 Nov 1;48(21):6090-6. Cancer Res. 1988. PMID: 2458832

6

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. Berneburg M, et al. Among authors: arlett cf. Cancer Res. 2000 Jan 15;60(2):431-8. Cancer Res. 2000. PMID: 10667598

7

Studies on a new case of xeroderma pigmentosum (XP3BR) from complementation group G with cellular sensitivity to ionizing radiation.

Arlett CF, Harcourt SA, Lehmann AR, Stevens S, Ferguson-Smith MA, Morley WN. Arlett CF, et al. Carcinogenesis. 1980 Sep;1(9):745-51. doi: 10.1093/carcin/1.9.745. Carcinogenesis. 1980. PMID: 11219864

8

Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene.

Broughton BC, Berneburg M, Fawcett H, Taylor EM, Arlett CF, Nardo T, Stefanini M, Menefee E, Price VH, Queille S, Sarasin A, Bohnert E, Krutmann J, Davidson R, Kraemer KH, Lehmann AR. Broughton BC, et al. Among authors: arlett cf. Hum Mol Genet. 2001 Oct 15;10(22):2539-47. doi: 10.1093/hmg/10.22.2539. Hum Mol Genet. 2001. PMID: 11709541

9

Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts.

Arlett CF, Green MH, Rogers PB, Lehmann AR, Plowman PN. Arlett CF, et al. Br J Radiol. 2008 Jan;81(961):51-8. doi: 10.1259/bjr/27072321. Br J Radiol. 2008. PMID: 18079351

10

Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair.

Sarasin A, Blanchet-Bardon C, Renault G, Lehmann A, Arlett C, Dumez Y. Sarasin A, et al. Br J Dermatol. 1992 Nov;127(5):485-91. doi: 10.1111/j.1365-2133.1992.tb14845.x. Br J Dermatol. 1992. PMID: 1281671

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