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Journal Abstract Search

126 related items for PubMed ID: 4066782

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  • 3. Lack of complementation between xeroderma pigmentosum complementation groups D and H.
    Johnson RT, Elliott GC, Squires S, Joysey VC.
    Hum Genet; 1989 Feb; 81(3):203-10. PubMed ID: 2921028
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  • 4. Phenotypic correction of the defect in xeroderma pigmentosum cells after fusion with isolated cytoplasts.
    Keijzer W, Verkerk A, Bootsma D.
    Exp Cell Res; 1982 Jul; 140(1):119-25. PubMed ID: 7106197
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  • 8. Kinetic analysis of UV-induced incision discriminates between fibroblasts from different xeroderma pigmentosum complementation groups, XPA heterozygotes and normal individuals.
    Squires S, Johnson RT.
    Mutat Res; 1988 Mar; 193(2):181-92. PubMed ID: 3347209
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  • 9. Effects of XPD mutations on ultraviolet-induced apoptosis in relation to skin cancer-proneness in repair-deficient syndromes.
    Queille S, Drougard C, Sarasin A, Daya-Grosjean L.
    J Invest Dermatol; 2001 Nov; 117(5):1162-70. PubMed ID: 11710928
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  • 15. Reinvestigation of the classification of five cell strains of xeroderma pigmentosum group E with reclassification of three of them.
    Itoh T, Linn S, Ono T, Yamaizumi M.
    J Invest Dermatol; 2000 May; 114(5):1022-9. PubMed ID: 10771487
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  • 18. Abnormal mutation frequencies in human repair-defective hybrid cell lines.
    Johnson RT, Rasko I, Collins AR.
    Mutat Res; 1987 Sep; 184(2):113-20. PubMed ID: 3627140
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