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Journal Abstract Search

135 related items for PubMed ID: 3372781

  • 41. Xeroderma pigmentosum and squamous cell carcinoma of the tongue. Identification of two black patients as members of complementation group C.
    Wade MH, Plotnick H.
    J Am Acad Dermatol; 1985 Mar; 12(3):515-21. PubMed ID: 3989010
    [Abstract] [Full Text] [Related]

  • 42. DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells.
    Moriwaki S, Stefanini M, Lehmann AR, Hoeijmakers JH, Robbins JH, Rapin I, Botta E, Tanganelli B, Vermeulen W, Broughton BC, Kraemer KH.
    J Invest Dermatol; 1996 Oct; 107(4):647-53. PubMed ID: 8823375
    [Abstract] [Full Text] [Related]

  • 43. Sodium butyrate stimulates cellular recovery from UV damage in xeroderma pigmentosum cells belonging to complementation group F.
    Nishigori C, Takebe H.
    Jpn J Cancer Res; 1987 Sep; 78(9):932-6. PubMed ID: 3117749
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  • 44. Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.
    Broughton BC, Thompson AF, Harcourt SA, Vermeulen W, Hoeijmakers JH, Botta E, Stefanini M, King MD, Weber CA, Cole J.
    Am J Hum Genet; 1995 Jan; 56(1):167-74. PubMed ID: 7825573
    [Abstract] [Full Text] [Related]

  • 45. A novel mutation in the XPA gene associated with unusually mild clinical features in a patient who developed a spindle cell melanoma.
    Sidwell RU, Sandison A, Wing J, Fawcett HD, Seet JE, Fisher C, Nardo T, Stefanini M, Lehmann AR, Cream JJ.
    Br J Dermatol; 2006 Jul; 155(1):81-8. PubMed ID: 16792756
    [Abstract] [Full Text] [Related]

  • 46. Whole-exome sequencing and host cell reactivation assay lead to a diagnosis of xeroderma pigmentosum group D with mild ultraviolet radiation sensitivity.
    Sugaya M, Funamizu K, Kono M, Okuno Y, Kondo T, Ono R, Akiyama M, Nishigori C, Sato S.
    J Dermatol; 2021 Jan; 48(1):96-100. PubMed ID: 32974964
    [Abstract] [Full Text] [Related]

  • 47. 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]

  • 48. A 10-year follow-up of a child with mild case of xeroderma pigmentosum complementation group D diagnosed by whole-genome sequencing.
    Ono R, Masaki T, Mayca Pozo F, Nakazawa Y, Swagemakers SM, Nakano E, Sakai W, Takeuchi S, Kanda F, Ogi T, van der Spek PJ, Sugasawa K, Nishigori C.
    Photodermatol Photoimmunol Photomed; 2016 Jul; 32(4):174-80. PubMed ID: 26993158
    [Abstract] [Full Text] [Related]

  • 49. Repair of DNA damage after exposure to 4-nitroquinoline-1-oxide in heterokaryons derived from xeroderma pigmentosum cells.
    Zelle B, Bootsma D.
    Mutat Res; 1980 May; 70(3):373-81. PubMed ID: 6770261
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  • 52. Diagnosis of eight groups of xeroderma pigmentosum by genetic complementation using recombinant adenovirus vectors.
    Yamashita T, Okura M, Ishii-Osai Y, Hida T.
    J Dermatol; 2016 Oct; 43(10):1167-1173. PubMed ID: 26971583
    [Abstract] [Full Text] [Related]

  • 53. Regulation of DNA repair in serum-stimulated xeroderma pigmentosum cells.
    Gupta PK, Sirover MA.
    J Cell Biol; 1984 Oct; 99(4 Pt 1):1275-81. PubMed ID: 6480691
    [Abstract] [Full Text] [Related]

  • 54. Clinical symptoms and DNA repair characteristics of xeroderma pigmentosum patients from Germany.
    Thielmann HW, Popanda O, Edler L, Jung EG.
    Cancer Res; 1991 Jul 01; 51(13):3456-70. PubMed ID: 2054785
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  • 55. 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 01; 114(5):1022-9. PubMed ID: 10771487
    [Abstract] [Full Text] [Related]

  • 56. Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.
    Emmert S, Slor H, Busch DB, Batko S, Albert RB, Coleman D, Khan SG, Abu-Libdeh B, DiGiovanna JJ, Cunningham BB, Lee MM, Crollick J, Inui H, Ueda T, Hedayati M, Grossman L, Shahlavi T, Cleaver JE, Kraemer KH.
    J Invest Dermatol; 2002 Jun 01; 118(6):972-82. PubMed ID: 12060391
    [Abstract] [Full Text] [Related]

  • 57. Clonal chromosome rearrangements in a fibroblast strain from a patient affected by xeroderma pigmentosum (complementation group C).
    Nuzzo F, Lagomarsini P, Casati A, Giorgi R, Berardesca E, Stefanini M.
    Mutat Res; 1989 Jul 01; 219(4):209-15. PubMed ID: 2770768
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  • 58. A mild form of xeroderma pigmentosum assigned to complementation group G and its repair heterogeneity.
    Ichihashi M, Fujiwara Y, Uehara Y, Matsumoto A.
    J Invest Dermatol; 1985 Sep 01; 85(3):284-7. PubMed ID: 4031543
    [Abstract] [Full Text] [Related]

  • 59. The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I.
    van Duin M, Vredeveldt G, Mayne LV, Odijk H, Vermeulen W, Klein B, Weeda G, Hoeijmakers JH, Bootsma D, Westerveld A.
    Mutat Res; 1989 Mar 01; 217(2):83-92. PubMed ID: 2918869
    [Abstract] [Full Text] [Related]

  • 60. [Disorders of DNA repair--xeroderma pigmentosum, and other hereditary diseases with abnormal DNA repair].
    Sugano T, Yamaizumi M.
    Tanpakushitsu Kakusan Koso; 1988 Apr 01; 33(5):619-24. PubMed ID: 3270873
    [No Abstract] [Full Text] [Related]

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