Reinvestigation of the classification of five cell strains of xeroderma pigmentosum group E with reclassification of three of them.
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M. Yamaizumi | S. Linn | T. Ono | T. Itoh
[1] M. Yamaizumi,et al. A newly identified patient with clinical xeroderma pigmentosum phenotype has a non-sense mutation in the DDB2 gene and incomplete repair in (6-4) photoproducts. , 1999, The Journal of investigative dermatology.
[2] Robert E. Johnson,et al. hRAD30 mutations in the variant form of xeroderma pigmentosum. , 1999, Science.
[3] Chikahide Masutani,et al. The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η , 1999, Nature.
[4] R. Wood,et al. Relationship of the Xeroderma Pigmentosum Group E DNA Repair Defect to the Chromatin and DNA Binding Proteins UV-DDB and Replication Protein A , 1998, Molecular and Cellular Biology.
[5] P. Raychaudhuri,et al. DDB, a Putative DNA Repair Protein, Can Function as a Transcriptional Partner of E2F1 , 1998, Molecular and Cellular Biology.
[6] Richard D. Wood,et al. Nucleotide Excision Repair in Mammalian Cells* , 1997, The Journal of Biological Chemistry.
[7] S. Linn,et al. Mutations Specific to the Xeroderma Pigmentosum Group E Ddb− Phenotype* , 1996, The Journal of Biological Chemistry.
[8] R. Wood,et al. Xeroderma Pigmentosum Group F Caused by a Defect in a Structure-Specific DNA Repair Endonuclease , 1996, Cell.
[9] M. Yamaizumi,et al. A simple method for diagnosing xeroderma pigmentosum variant. , 1996, The Journal of investigative dermatology.
[10] M. Yamaizumi,et al. Clinical characteristics of three patients with UVS syndrome, a photosensitive disorder with defective DNA repair , 1996, The British journal of dermatology.
[11] E. Friedberg,et al. Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A. , 1996, Mutation research.
[12] S. Keeney,et al. Chromosomal localization and cDNA cloning of the genes (DDB1 and DDB2) for the p127 and p48 subunits of a human damage-specific DNA binding protein. , 1995, Genomics.
[13] M. Yamaizumi,et al. UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I. , 1995, American journal of human genetics.
[14] M. Yamaizumi,et al. A young woman with xeroderma pigmentosum complementation group F and a morphoeic basal cell carcinoma , 1995, The British journal of dermatology.
[15] T. Sugano,et al. U.v.-induced nuclear accumulation of p53 is evoked through DNA damage of actively transcribed genes independent of the cell cycle. , 1994, Oncogene.
[16] M. Yamaizumi,et al. A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations , 1994 .
[17] M. Yamaizumi,et al. Complementation of xeroderma pigmentosum cells by microinjection of mRNA fractionated under denaturing conditions: an estimation of sizes of XP-E and XP-G mRNA. , 1994, Mutation research.
[18] S. Keeney,et al. Characterization of a human DNA damage binding protein implicated in xeroderma pigmentosum E. , 1993, The Journal of biological chemistry.
[19] J. Hecht,et al. Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes. , 1992, American journal of human genetics.
[20] S. Keeney,et al. Biochemical heterogeneity in xeroderma pigmentosum complementation group E. , 1992, Mutation research.
[21] Y. Fujiwara,et al. UV damage-specific DNA-binding protein in xeroderma pigmentosum complementation group E. , 1991, Biochemical and biophysical research communications.
[22] Y. Satoh,et al. Late onset of skin cancers in 2 xeroderma pigmentosum group F siblings and a review of 30 Japanese xeroderma pigmentosum patients in groups D, E and F. , 1989, Photo-dermatology.
[23] G. Chu,et al. Xeroderma pigmentosum group E cells lack a nuclear factor that binds to damaged DNA. , 1988, Science.
[24] Y. Satoh,et al. Assignment of three patients with xeroderma pigmentosum to complementation group E and their characteristics. , 1988, The Journal of investigative dermatology.
[25] M. Ichihashi,et al. Assignment of 2 patients with xeroderma pigmentosum to complementation group E. , 1985, Mutation research.
[26] A. Lehmann,et al. Repair of ultraviolet light damage in a variety of human fibroblast cell strains. , 1977, Cancer research.
[27] E. Friedberg,et al. Semi-conservative deoxyribonucleic acid synthesis in unirradiated and ultraviolet-irradiated xeroderma pigmentosum and normal human skin fibroblasts. , 1977, Mutation research.
[28] D. Bootsma,et al. Five complementation groups in xeroderma pigmentosum. , 1975, Mutation research.
[29] M. Paterson,et al. Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[30] K. Kraemer,et al. Genetic heterogeneity in xeroderma pigmentosum: complementation groups and their relationship to DNA repair rates. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[31] D. Bootsma,et al. A third complementation group in xeroderma pigmentosum. , 1974, Mutation research.
[32] D. Bootsma,et al. UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes. , 1973, Mutation research.
[33] J. Cohen,et al. Different inherited levels of DNA repair replication in xeroderma pigmentosum cell strains after exposure to ultraviolet irradiation. , 1970, Mutation research.