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PUBMED FOR HANDHELDS

Journal Abstract Search


260 related items for PubMed ID: 3175673

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  • 23. Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient.
    Nouspikel T, Clarkson SG.
    Hum Mol Genet; 1994 Jun; 3(6):963-7. PubMed ID: 7951246
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  • 25. Excision repair in man and the molecular basis of xeroderma pigmentosum syndrome.
    Reardon JT, Thompson LH, Sancar A.
    Cold Spring Harb Symp Quant Biol; 1993 Jun; 58():605-17. PubMed ID: 7956075
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  • 26. p48 Activates a UV-damaged-DNA binding factor and is defective in xeroderma pigmentosum group E cells that lack binding activity.
    Hwang BJ, Toering S, Francke U, Chu G.
    Mol Cell Biol; 1998 Jul; 18(7):4391-9. PubMed ID: 9632823
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  • 27. Xeroderma pigmentosum: recent studies on the DNA repair defects.
    Friedberg EC.
    Arch Pathol Lab Med; 1978 Jan; 102(1):3-7. PubMed ID: 339872
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  • 35. Xeroderma pigmentosum and molecular cloning of DNA repair genes.
    Boulikas T.
    Anticancer Res; 1996 Jan; 16(2):693-708. PubMed ID: 8687116
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  • 37. Xeroderma pigmentosum genes: functions inside and outside DNA repair.
    Sugasawa K.
    Carcinogenesis; 2008 Mar; 29(3):455-65. PubMed ID: 18174245
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  • 38. Purification of a novel UV-damaged-DNA binding protein highly specific for (6-4) photoproduct.
    Wakasugi M, Abe Y, Yoshida Y, Matsunaga T, Nikaido O.
    Nucleic Acids Res; 1996 Mar 15; 24(6):1099-04. PubMed ID: 8604344
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  • 39. True XP group E patients have a defective UV-damaged DNA binding protein complex and mutations in DDB2 which reveal the functional domains of its p48 product.
    Rapić-Otrin V, Navazza V, Nardo T, Botta E, McLenigan M, Bisi DC, Levine AS, Stefanini M.
    Hum Mol Genet; 2003 Jul 01; 12(13):1507-22. PubMed ID: 12812979
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  • 40. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G.
    Cooper PK, Nouspikel T, Clarkson SG, Leadon SA.
    Science; 1997 Feb 14; 275(5302):990-3. PubMed ID: 9020084
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