These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


114 related items for PubMed ID: 7163956

  • 41. The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet-light irradiation.
    Arlett CF, Harcourt SA, Broughton BC.
    Mutat Res; 1975 Dec; 33(2-3):341-6. PubMed ID: 1214825
    [Abstract] [Full Text] [Related]

  • 42. Clinical and photobiological characteristics of xeroderma pigmentosum complementation group F: a review of cases from Japan.
    Yamamura K, Ichihashi M, Hiramoto T, Ogoshi M, Nishioka K, Fujiwara Y.
    Br J Dermatol; 1989 Oct; 121(4):471-80. PubMed ID: 2696553
    [Abstract] [Full Text] [Related]

  • 43. Xeroderma pigmentosum variant heterozygotes show reduced levels of recovery of replicative DNA synthesis in the presence of caffeine after ultraviolet irradiation.
    Itoh T, Linn S, Kamide R, Tokushige H, Katori N, Hosaka Y, Yamaizumi M.
    J Invest Dermatol; 2000 Dec; 115(6):981-5. PubMed ID: 11121129
    [Abstract] [Full Text] [Related]

  • 44. Studies on repair of adenovirus 2 by human fibroblasts using normal, xeroderma pigmentosum, and xeroderma pigmentosum heterozygous strains.
    Day RS.
    Cancer Res; 1974 Aug; 34(8):1965-70. PubMed ID: 4842250
    [No Abstract] [Full Text] [Related]

  • 45. Xeroderma pigmentosum group E cells lack a nuclear factor that binds to damaged DNA.
    Chu G, Chang E.
    Science; 1988 Oct 28; 242(4878):564-7. PubMed ID: 3175673
    [Abstract] [Full Text] [Related]

  • 46. Complement analysis of xeroderma pigmentosum variants.
    Jaspers NG, Jansen-van de Kuilen G, Bootsma D.
    Exp Cell Res; 1981 Nov 28; 136(1):81-90. PubMed ID: 7297615
    [No Abstract] [Full Text] [Related]

  • 47. Xeroderma pigmentosum D-HeLa hybrids with low and high ultraviolet sensitivity associated with normal and diminished DNA repair ability, respectively.
    Johnson RT, Squires S, Elliott GC, Koch GL, Rainbow AJ.
    J Cell Sci; 1985 Jun 28; 76():115-33. PubMed ID: 4066782
    [Abstract] [Full Text] [Related]

  • 48. Ultraviolet light-resistant primary transfectants of xeroderma pigmentosum cells are also DNA repair-proficient.
    Stark M, Naiman T, Canaani D.
    Biochem Biophys Res Commun; 1989 Aug 15; 162(3):1351-6. PubMed ID: 2764936
    [Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 52. Complementation of DNA repair defect in xeroderma pigmentosum cells of group C by the transfer of human chromosome 5.
    Kaur GP, Athwal RS.
    Somat Cell Mol Genet; 1993 Jan 15; 19(1):83-93. PubMed ID: 8460401
    [Abstract] [Full Text] [Related]

  • 53. Correction of excision repair in xeroderma pigmentosum by hamster chromosome fragments involves both classes of pyrimidine dimers.
    Karentz D, Mitchell D, Cleaver JE.
    Somat Cell Mol Genet; 1987 Nov 15; 13(6):621-5. PubMed ID: 3478816
    [Abstract] [Full Text] [Related]

  • 54. Studies on a new case of xeroderma pigmentosum (XP3BR) from complementation group G with cellular sensitivity to ionizing radiation.
    Arlett CF, Harcourt SA, Lehmann AR, Stevens S, Ferguson-Smith MA, Morley WN.
    Carcinogenesis; 1980 Sep 15; 1(9):745-51. PubMed ID: 11219864
    [Abstract] [Full Text] [Related]

  • 55. Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.
    Flejter WL, McDaniel LD, Johns D, Friedberg EC, Schultz RA.
    Proc Natl Acad Sci U S A; 1992 Jan 01; 89(1):261-5. PubMed ID: 1729695
    [Abstract] [Full Text] [Related]

  • 56. Assignment of three patients with xeroderma pigmentosum to complementation group E and their characteristics.
    Kondo S, Fukuro S, Mamada A, Kawada A, Satoh Y, Fujiwara Y.
    J Invest Dermatol; 1988 Feb 01; 90(2):152-7. PubMed ID: 3339259
    [Abstract] [Full Text] [Related]

  • 57. DNA repair characteristics and skin cancers of xeroderma pigmentosum patients in Japan.
    Takebe H, Miki Y, Kozuka T, Furuyama JI, Tanaka K.
    Cancer Res; 1977 Feb 01; 37(2):490-5. PubMed ID: 832273
    [Abstract] [Full Text] [Related]

  • 58. Complementation of the DNA repair deficiency in human xeroderma pigmentosum group a and C cells by recombinant adenovirus-mediated gene transfer.
    Muotri AR, Marchetto MC, Zerbini LF, Libermann TA, Ventura AM, Sarasin A, Menck CF.
    Hum Gene Ther; 2002 Oct 10; 13(15):1833-44. PubMed ID: 12396616
    [Abstract] [Full Text] [Related]

  • 59. Interspecies complementation analysis of xeroderma pigmentosum and UV-sensitive Chinese hamster cells.
    Stefanini M, Keijzer W, Westerveld A, Bootsma D.
    Exp Cell Res; 1985 Dec 10; 161(2):373-80. PubMed ID: 4065224
    [Abstract] [Full Text] [Related]

  • 60. A case of xeroderma pigmentosum complementation group F with neurological abnormalities.
    Moriwaki S, Nishigori C, Imamura S, Yagi T, Takahashi C, Fujimoto N, Takebe H.
    Br J Dermatol; 1993 Jan 10; 128(1):91-4. PubMed ID: 8427828
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 6.