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A novel splice variant of the DNA- PKcs gene is associated with clinical and cellular radiosensitivity in a patient with xeroderma pigmentosum Abbaszadeh, Fatemeh; Clingen, Peter H.; Arlett, Colin F.; Plowman, Piers N.; Bourton, Emma C.; Themis, Matthew; Makarov, Evgeny M.; Newbold, Robert F.; Green, Michael H. L.; Parris, Christopher N. 分享 收藏
Neurological symptoms and natural course of xeroderma pigmentosum 着色性干皮病的神经系统症状和自然病程 Anttinen, Anu; Koulu, Leena; Nikoskelainen, Eeva; Portin, Raija; Kurki, Timo; Erkinjuntti, Matti; Jaspers, Nicolaas G. J.; Raams, Anja; Green, Michael H. L.; Lehmann, Alan R.; Wing, Jonathan F.; Arlett, Colin F.; Marttila, Reijo J. 分享 收藏
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Short tandem repeat profiling provides an international reference standard for human cell lines Masters, JR; Thomson, JA; Daly-Burns, B; Reid, YA; Dirks, WG; Packer, P; Toji, LH; Ohno, T; Tanabe, H; Arlett, CF; Kelland, LR; Harrison, M; Virmani, A; Ward, TH; Ayres, KL; Debenham, PG 分享 收藏
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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 分享 收藏
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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, NGJ; Fawcett, H; Harcourt, SA; Arlett, CF; Lehmann, AR 分享 收藏
Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individuals Ahrens, C; Grewe, M; Berneburg, M; GretherBeck, S; Quilliet, X; Mezzina, M; Sarasin, A; Lehmann, AR; Arlett, CF; Krutmann, J 分享 收藏
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