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119 related items for PubMed ID: 2474861

  • 1. Ethyl methane sulfonate- and bleomycin-generated deletion mutations at HPRT locus in xeroderma pigmentosum complementation group D fibroblasts.
    Wood CM, Moses RE.
    Somat Cell Mol Genet; 1989 Jul; 15(4):345-57. PubMed ID: 2474861
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  • 3. Mutation screening of bleomycin-induced V79 Chinese hamster hprt mutants using multiplex polymerase chain reaction.
    Köberle B, Haupter S, Just W, Speit G.
    Mutagenesis; 1991 Nov; 6(6):527-31. PubMed ID: 1724791
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  • 10. PCR-directed DNA sequencing of "nondeletion" HPRT-mutants induced by bleomycin in CHO K1-BH4 cells.
    An J, Trieff NM, Hsie AW.
    Environ Mol Mutagen; 1998 Nov; 32(3):244-50. PubMed ID: 9814439
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  • 12. Molecular analysis of mutation at the hprt locus of Chinese hamster V79 cells induced by ethyl methanesulphonate and mitomycin C.
    Davies MJ, Phillips BJ, Anderson D, Rumbsy PC.
    Mutat Res; 1993 Apr; 291(2):117-24. PubMed ID: 7680415
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  • 14. Characterization of HAT- and HAsT-resistant HPRT mutant clones of V79 Chinese hamster cells.
    Zhang LH, Jenssen D.
    Mutat Res; 1991 Jul; 263(3):151-8. PubMed ID: 1712425
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  • 15. Molecular analysis of hypoxanthine phosphoribosyltransferase gene deletions induced by alpha- and X-radiation in human lymphoblastoid cells.
    Bao CY, Ma AH, Evans HH, Horng MF, Mencl J, Hui TE, Sedwick WD.
    Mutat Res; 1995 Jan; 326(1):1-15. PubMed ID: 7528877
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  • 18. Elevated hprt mutant frequency in circulating T-lymphocytes of xeroderma pigmentosum patients.
    Cole J, Arlett CF, Norris PG, Stephens G, Waugh AP, Beare DM, Green MH.
    Mutat Res; 1992 Mar; 273(2):171-8. PubMed ID: 1372100
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  • 19. Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletions.
    Monnat RJ, Hackmann AF, Chiaverotti TA.
    Genomics; 1992 Jul; 13(3):777-87. PubMed ID: 1639404
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  • 20. Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndrome.
    Tvrdik T, Marcus S, Hou SM, Fält S, Noori P, Podlutskaja N, Hanefeld F, Strømme P, Lambert B.
    Hum Genet; 1998 Sep; 103(3):311-8. PubMed ID: 9799086
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