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Journal Abstract Search

109 related items for PubMed ID: 8765158

  • 1. Splice site mutations in a xeroderma pigmentosum group A patient with delayed onset of neurological disease.
    States JC, Myrand SP.
    Mutat Res; 1996 Aug 08; 363(3):171-7. PubMed ID: 8765158
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  • 2. Aberrant splicing and truncated-protein expression due to a newly identified XPA gene mutation.
    Sato M, Nishigori C, Yagi T, Takebe H.
    Mutat Res; 1996 Feb 15; 362(2):199-208. PubMed ID: 8596539
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  • 3. Stable transformation of xeroderma pigmentosum group A cells with an XPA minigene restores normal DNA repair and mutagenesis of UV-treated plasmids.
    Myrand SP, Topping RS, States JC.
    Carcinogenesis; 1996 Sep 15; 17(9):1909-17. PubMed ID: 8824513
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  • 4. Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein.
    States JC, McDuffie ER, Myrand SP, McDowell M, Cleaver JE.
    Hum Mutat; 1998 Sep 15; 12(2):103-13. PubMed ID: 9671271
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  • 5. A novel XPA gene mutation and its functional analysis in a Japanese patient with xeroderma pigmentosum group A.
    Tanioka M, Budiyant A, Ueda T, Nagano T, Ichihashi M, Miyachi Y, Nishigori C.
    J Invest Dermatol; 2005 Aug 15; 125(2):244-6. PubMed ID: 16098033
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  • 7. Expression of a transfected DNA repair gene (XPA) in xeroderma pigmentosum group A cells restores normal DNA repair and mutagenesis of UV-treated plasmids.
    Levy DD, Saijo M, Tanaka K, Kraemer KH.
    Carcinogenesis; 1995 Jul 15; 16(7):1557-63. PubMed ID: 7614689
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  • 8. Analysis of cells harboring a putative DNA repair gene reveals a lack of evidence for a second independent xeroderma pigmentosum group A correcting gene.
    Jones CJ, Lloyd RS, Wood RD.
    Mutat Res; 1994 Aug 15; 324(4):159-64. PubMed ID: 7519740
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  • 9. Characterization of a splicing mutation in group A xeroderma pigmentosum.
    Satokata I, Tanaka K, Miura N, Miyamoto I, Satoh Y, Kondo S, Okada Y.
    Proc Natl Acad Sci U S A; 1990 Dec 15; 87(24):9908-12. PubMed ID: 1702221
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  • 11. Severe neurological abnormalities associated with a mutation in the zinc-finger domain in a group A xeroderma pigmentosum patient.
    Maeda T, Sato K, Minami H, Taguchi H, Yoshikawa K.
    Br J Dermatol; 1994 Oct 15; 131(4):566-70. PubMed ID: 7947212
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  • 16. Structural and mutational analysis of the xeroderma pigmentosum group D (XPD) gene.
    Frederick GD, Amirkhan RH, Schultz RA, Friedberg EC.
    Hum Mol Genet; 1994 Oct 15; 3(10):1783-8. PubMed ID: 7849702
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  • 17. High prevalence of the point mutation in exon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients in Tunisia.
    Nishigori C, Zghal M, Yagi T, Imamura S, Komoun MR, Takebe H.
    Am J Hum Genet; 1993 Nov 15; 53(5):1001-6. PubMed ID: 8105686
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  • 18. Ultraviolet mutational spectrum in a shuttle vector propagated in xeroderma pigmentosum lymphoblastoid cells and fibroblasts.
    Seetharam S, Kraemer KH, Waters HL, Seidman MM.
    Mutat Res; 1991 Jan 15; 254(1):97-105. PubMed ID: 1986277
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