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Wim J. Kleijer, Elizabeth A. de Weerd-Kastelein, Milou L. Sluyter, Wilma Keijzer, Jan de Wit, Dirk Bootsma;
UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes.
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Vazken Movses Der Kaloustian, Elizabeth A. de Weerd-Kastelein, Wim J. Kleijer, Wilma Keijzer, Dirk Bootsma;
The genetic defect in the de Sanctis-Cacchione syndrome.
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Elizabeth A. de Weerd-Kastelein, Wilma Keijzer, Dirk Bootsma;
A third complementation group in xeroderma pigmentosum.
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Elizabeth A. de Weerd-Kastelein, Wilma Keijzer, M. Sabour, Jennifer M. Parrington, Dirk Bootsma;
A xeroderma pigmentosum patient having a high residual activity of unscheduled DNA synthesis after UV is assigned to complementation group A.
Mutat. Res. 37:307-312(1976) DOI=10.5962/bhl.title.4090
Lewis Lemon Coriell, Arthur E. Greene;
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(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977) PubMed=837385
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Repair of ultraviolet light damage in a variety of human fibroblast cell strains.
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Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation.
Proc. Natl. Acad. Sci. U.S.A. 75:1984-1988(1978) PubMed=643622; DOI=10.1093/nar/5.3.951; PMCID=PMC342035
Urs Kuhnlein, Betty Lee, Edward E. Penhoet, Stuart M. Linn;
Xeroderma pigmentosum fibroblasts of the D group lack an apurinic DNA endonuclease species with a low apparent Km.
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Human tumor cell strains defective in the repair of alkylation damage.
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Heinz Walter Thielmann, Odilia Popanda, Lutz Edler;
XP patients from Germany: correlation of colony-forming ability, unscheduled DNA synthesis and single-strand breaks after UV damage in xeroderma pigmentosum fibroblasts.
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Action spectra (254-302 nm) for four human photosensitive cell lines.
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Enhanced reactivation and enhanced mutagenesis of herpes simplex virus in normal human and xeroderma pigmentosum cells.
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Ichiro Satokata, Kiyoji Tanaka, Naoyuki Miura, Iwai Miyamoto, Yoshiaki Satoh, Seiji Kondo, Yoshio Okada;
Characterization of a splicing mutation in group A xeroderma pigmentosum.
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Richard A. Mulivor, Sharon F. Suchy;
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Ichiro Satokata, Kiyoji Tanaka, Naoyuki Miura, Masashi Narita, Takashi Mimaki, Yoshiaki Satoh, Seiji Kondo, Yoshio Okada;
Three nonsense mutations responsible for group A xeroderma pigmentosum.
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Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.
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Ram Parshad, Katherine Koontz Sanford, Floyd M. Price, Lynn K. Melnick, Linda E. Nee, Mark B. Schapiro, Robert E. Tarone, Jay H. Robbins;
Fluorescent light-induced chromatid breaks distinguish Alzheimer disease cells from normal cells in tissue culture.
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Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein.
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DNA repair in human fibroblasts, as reflected by host-cell reactivation of a transfected UV-irradiated luciferase gene, is not related to donor age.
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Mariangela Sabatella, Arjan F. Theil, Cristina Ribeiro-Silva, Jana Slyskova, Karen Thijssen, Chantal Voskamp, Hannes Lans, Wim Vermeulen;
Repair protein persistence at DNA lesions characterizes XPF defect with Cockayne syndrome features.
Nucleic Acids Res. 46:9563-9577(2018) | 
