Arlett CF - Search Results

1

Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient.

Riballo E, Critchlow SE, Teo SH, Doherty AJ, Priestley A, Broughton B, Kysela B, Beamish H, Plowman N, Arlett CF, Lehmann AR, Jackson SP, Jeggo PA. Riballo E, et al. Among authors: arlett cf. Curr Biol. 1999 Jul 1;9(13):699-702. doi: 10.1016/s0960-9822(99)80311-x. Curr Biol. 1999. PMID: 10395545 Free article.

2

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

3

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

4

Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome.

Lehmann AR, Willis AE, Broughton BC, James MR, Steingrimsdottir H, Harcourt SA, Arlett CF, Lindahl T. Lehmann AR, et al. Among authors: arlett cf. Cancer Res. 1988 Nov 15;48(22):6343-7. Cancer Res. 1988. PMID: 3180052

5

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.

6

Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects.

Girard PM, Foray N, Stumm M, Waugh A, Riballo E, Maser RS, Phillips WP, Petrini J, Arlett CF, Jeggo PA. Girard PM, et al. Among authors: arlett cf. Cancer Res. 2000 Sep 1;60(17):4881-8. Cancer Res. 2000. PMID: 10987302

7

Growth retardation and immunodeficiency in a patient with mutations in the DNA ligase I gene.

Webster AD, Barnes DE, Arlett CF, Lehmann AR, Lindahl T. Webster AD, et al. Among authors: arlett cf. Lancet. 1992 Jun 20;339(8808):1508-9. doi: 10.1016/0140-6736(92)91266-b. Lancet. 1992. PMID: 1351188

8

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

9

Comparative human cellular radiosensitivity: I. The effect of SV40 transformation and immortalisation on the gamma-irradiation survival of skin derived fibroblasts from normal individuals and from ataxia-telangiectasia patients and heterozygotes.

Arlett CF, Green MH, Priestley A, Harcourt SA, Mayne LV. Arlett CF, et al. Int J Radiat Biol. 1988 Dec;54(6):911-28. doi: 10.1080/09553008814552321. Int J Radiat Biol. 1988. PMID: 2903889

10

Cells from an immunodeficient patient (46BR) with a defect in DNA ligation are hypomutable but hypersensitive to the induction of sister chromatid exchanges.

Henderson LM, Arlett CF, Harcourt SA, Lehmann AR, Broughton BC. Henderson LM, et al. Among authors: arlett cf. Proc Natl Acad Sci U S A. 1985 Apr;82(7):2044-8. doi: 10.1073/pnas.82.7.2044. Proc Natl Acad Sci U S A. 1985. PMID: 3856882 Free PMC article.

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