PubMed=4778857; DOI=10.1016/0027-5107(73)90062-6 Kleijer W.J., de Weerd-Kastelein E.A., Sluyter M.L., Keijzer W., de Wit J., Bootsma D. UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes. Mutat. Res. 20:417-428(1973) PubMed=4842087; DOI=10.1016/0027-5107(74)90013-x de Weerd-Kastelein E.A., Keijzer W., Bootsma D. A third complementation group in xeroderma pigmentosum. Mutat. Res. 22:87-91(1974) DOI=10.5962/bhl.title.4090 Coriell L.L., Greene A.E. The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977. (In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977) PubMed=837385 Lehmann A.R., Kirk-Bell S., Arlett C.F., Harcourt S.A., de Weerd-Kastelein E.A., Keijzer W., Hall-Smith P. Repair of ultraviolet light damage in a variety of human fibroblast cell strains. Cancer Res. 37:904-910(1977) PubMed=273925; DOI=10.1073/pnas.75.4.1984 Andrews A.D., Barrett S.F., Robbins J.H. Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation. Proc. Natl. Acad. Sci. U.S.A. 75:1984-1988(1978) PubMed=3922833; DOI=10.20772/cancersci1985.76.3_162 Fujiwara Y., Satoh Y. Assignment of two Japanese xeroderma pigmentosum patients to complementation group D and their characteristics. Jpn. J. Cancer Res. 76:162-166(1985) PubMed=4066782; DOI=10.1242/jcs.76.1.115 Johnson R.T., Squires S., Elliott G.C., Koch G.L.E., Rainbow A.J. Xeroderma pigmentosum D-HeLa hybrids with low and high ultraviolet sensitivity associated with normal and diminished DNA repair ability, respectively. J. Cell Sci. 76:115-133(1985) PubMed=3010096; DOI=10.1016/0167-8817(86)90052-0 Barbis D.P., Schultz R.A., Friedberg E.C. Isolation and partial characterization of virus-transformed cell lines representing the A, G and variant complementation groups of xeroderma pigmentosum. Mutat. Res. 165:175-184(1986) PubMed=3030788; DOI=10.1016/0014-4827(87)90214-X Wood C.M., Timme T.L., Hurt M.M., Brinkley B.R., Ledbetter D.H., Moses R.E. Transformation of DNA repair-deficient human diploid fibroblasts with a simian virus 40 plasmid. Exp. Cell Res. 169:543-553(1987) DOI=10.1007/978-1-4757-5016-4_9 Jaspers N.G.J., Roza L., Vermeulen W., Eker A.P.M., Taalman R.D.F.M., Hoeijmakers J.H.J., Bootsma D. In vitro correction of cells from patients with mutagen hypersensitivity. (In) DNA damage and repair; Castellani A. (eds.); pp.73-82; Springer; Boston (1989) CLPUB00447 Mulivor R.A., Suchy S.F. 1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992. (In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992) PubMed=1376435; DOI=10.1016/0921-8777(92)90049-9 Keeney S.N., Wein H., Linn S.M. Biochemical heterogeneity in xeroderma pigmentosum complementation group E. Mutat. Res. 273:49-56(1992) PubMed=8798680; DOI=10.1074/jbc.271.40.24317 Nichols A.F., Ong P., Linn S.M. Mutations specific to the xeroderma pigmentosum group E Ddb- phenotype. J. Biol. Chem. 271:24317-24320(1996) PubMed=8823375; DOI=10.1111/1523-1747.ep12584287 Moriwaki S.-i., Stefanini M., Lehmann A.R., Hoeijmakers J.H.J., Robbins J.H., Rapin I., Botta E., Tanganelli B., Vermeulen W., Broughton B.C., Kraemer K.H. DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and Cockayne syndrome resemble xeroderma pigmentosum cells. J. Invest. Dermatol. 107:647-653(1996) PubMed=9584159; DOI=10.1128/mcb.18.6.3182 Rapic-Otrin V., Kuraoka I., Nardo T., McLenigan M., Eker A.P.M., Stefanini M., Levine A.S., Wood R.D. Relationship of the xeroderma pigmentosum group E DNA repair defect to the chromatin and DNA binding proteins UV-DDB and replication protein A. Mol. Cell. Biol. 18:3182-3190(1998) PubMed=10771487; DOI=10.1046/j.1523-1747.2000.00952.x Itoh T., Linn S.M., Ono T., Yamaizumi M. Reinvestigation of the classification of five cell strains of xeroderma pigmentosum group E with reclassification of three of them. J. Invest. Dermatol. 114:1022-1029(2000) PubMed=10777490; DOI=10.1074/jbc.M000960200 Nichols A.F., Itoh T., Graham J.A., Liu W., Yamaizumi M., Linn S.M. Human damage-specific DNA-binding protein p48. Characterization of XPE mutations and regulation following UV irradiation. J. Biol. Chem. 275:21422-21428(2000) |