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Journal Abstract Search

231 related items for PubMed ID: 8171034

  • 1. Correction of the DNA repair defect in xeroderma pigmentosum group E by injection of a DNA damage-binding protein.
    Keeney S, Eker AP, Brody T, Vermeulen W, Bootsma D, Hoeijmakers JH, Linn S.
    Proc Natl Acad Sci U S A; 1994 Apr 26; 91(9):4053-6. PubMed ID: 8171034
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  • 2. Relationship of the xeroderma pigmentosum group E DNA repair defect to the chromatin and DNA binding proteins UV-DDB and replication protein A.
    Rapić Otrin V, Kuraoka I, Nardo T, McLenigan M, Eker AP, Stefanini M, Levine AS, Wood RD.
    Mol Cell Biol; 1998 Jun 26; 18(6):3182-90. PubMed ID: 9584159
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  • 4. 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 26; 114(5):1022-9. PubMed ID: 10771487
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  • 7. DNA repair defect in xeroderma pigmentosum group C and complementing factor from HeLa cells.
    Shivji MK, Eker AP, Wood RD.
    J Biol Chem; 1994 Sep 09; 269(36):22749-57. PubMed ID: 8077226
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  • 8. Abnormal regulation of DDB2 gene expression in xeroderma pigmentosum group E strains.
    Itoh T, Nichols A, Linn S.
    Oncogene; 2001 Oct 25; 20(48):7041-50. PubMed ID: 11704828
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  • 9. The DDB1-CUL4ADDB2 ubiquitin ligase is deficient in xeroderma pigmentosum group E and targets histone H2A at UV-damaged DNA sites.
    Kapetanaki MG, Guerrero-Santoro J, Bisi DC, Hsieh CL, Rapić-Otrin V, Levine AS.
    Proc Natl Acad Sci U S A; 2006 Feb 21; 103(8):2588-93. PubMed ID: 16473935
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  • 10. Biochemical heterogeneity in xeroderma pigmentosum complementation group E.
    Keeney S, Wein H, Linn S.
    Mutat Res; 1992 Jan 21; 273(1):49-56. PubMed ID: 1376435
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  • 11. Retroviral-mediated correction of DNA repair defect in xeroderma pigmentosum cells is associated with recovery of catalase activity.
    Quilliet X, Chevallier-Lagente O, Zeng L, Calvayrac R, Mezzina M, Sarasin A, Vuillaume M.
    Mutat Res; 1997 Dec 21; 385(3):235-42. PubMed ID: 9506892
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  • 12. Transient correction of excision repair defects in fibroblasts of 9 xeroderma pigmentosum complementation groups by microinjection of crude human cell extracts.
    Vermeulen W, Osseweijer P, de Jonge AJ, Hoeijmakers JH.
    Mutat Res; 1986 May 21; 165(3):199-206. PubMed ID: 3517635
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  • 14. Xeroderma pigmentosum group E and DDB2, a smaller subunit of damage-specific DNA binding protein: proposed classification of xeroderma pigmentosum, Cockayne syndrome, and ultraviolet-sensitive syndrome.
    Itoh T.
    J Dermatol Sci; 2006 Feb 21; 41(2):87-96. PubMed ID: 16325378
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  • 15. Mutations specific to the xeroderma pigmentosum group E Ddb- phenotype.
    Nichols AF, Ong P, Linn S.
    J Biol Chem; 1996 Oct 04; 271(40):24317-20. PubMed ID: 8798680
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  • 16. The UV-damaged DNA binding protein mediates efficient targeting of the nucleotide excision repair complex to UV-induced photo lesions.
    Moser J, Volker M, Kool H, Alekseev S, Vrieling H, Yasui A, van Zeeland AA, Mullenders LH.
    DNA Repair (Amst); 2005 May 02; 4(5):571-82. PubMed ID: 15811629
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  • 17. Comparative study of nucleotide excision repair defects between XPD-mutated fibroblasts derived from trichothiodystrophy and xeroderma pigmentosum patients.
    Nishiwaki T, Kobayashi N, Iwamoto T, Yamamoto A, Sugiura S, Liu YC, Sarasin A, Okahashi Y, Hirano M, Ueno S, Mori T.
    DNA Repair (Amst); 2008 Dec 01; 7(12):1990-8. PubMed ID: 18817897
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  • 19. [Progress of research on xeroderma pigmentosum].
    Tanaka K.
    Gan To Kagaku Ryoho; 1990 Jun 01; 17(6):1095-103. PubMed ID: 2190536
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