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Journal Abstract Search

205 related items for PubMed ID: 1372469

  • 41. High sensitivity of the ultraviolet-induced p53 response in ultraviolet-sensitive syndrome, a photosensitive disorder with a putative defect in deoxyribonucleic acid repair of actively transcribed genes.
    Ohta M, Nitta M, Yamaizumi M.
    Mutat Res; 1999 Jan 26; 433(1):23-32. PubMed ID: 10047776
    [Abstract] [Full Text] [Related]

  • 42. Ocular manifestations of xeroderma pigmentosum: long-term follow-up highlights the role of DNA repair in protection from sun damage.
    Brooks BP, Thompson AH, Bishop RJ, Clayton JA, Chan CC, Tsilou ET, Zein WM, Tamura D, Khan SG, Ueda T, Boyle J, Oh KS, Imoto K, Inui H, Moriwaki S, Emmert S, Iliff NT, Bradford P, Digiovanna JJ, Kraemer KH.
    Ophthalmology; 2013 Jul 26; 120(7):1324-36. PubMed ID: 23601806
    [Abstract] [Full Text] [Related]

  • 43. Ultraviolet-sensitive syndrome cells are defective in transcription-coupled repair of cyclobutane pyrimidine dimers.
    Spivak G, Itoh T, Matsunaga T, Nikaido O, Hanawalt P, Yamaizumi M.
    DNA Repair (Amst); 2002 Aug 06; 1(8):629-43. PubMed ID: 12509286
    [Abstract] [Full Text] [Related]

  • 44. Xeroderma pigmentosum and related disorders: defects in DNA repair and transcription.
    Berneburg M, Lehmann AR.
    Adv Genet; 2001 Aug 06; 43():71-102. PubMed ID: 11037299
    [Abstract] [Full Text] [Related]

  • 45. 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 06; 118(6):972-82. PubMed ID: 12060391
    [Abstract] [Full Text] [Related]

  • 46. DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.
    Lehmann AR.
    Biochimie; 2003 Nov 06; 85(11):1101-11. PubMed ID: 14726016
    [Abstract] [Full Text] [Related]

  • 47. Xeroderma pigmentosum and related disorders: examining the linkage between defective DNA repair and cancer.
    Kraemer KH, Levy DD, Parris CN, Gozukara EM, Moriwaki S, Adelberg S, Seidman MM.
    J Invest Dermatol; 1994 Nov 06; 103(5 Suppl):96S-101S. PubMed ID: 7963692
    [Abstract] [Full Text] [Related]

  • 48. A simple method for diagnosing xeroderma pigmentosum variant.
    Itoh T, Ono T, Yamaizumi M.
    J Invest Dermatol; 1996 Sep 06; 107(3):349-53. PubMed ID: 8751969
    [Abstract] [Full Text] [Related]

  • 49. Cross-sensitivity of certain xeroderma pigmentosum and Cockayne syndrome fibroblast strains to both ionizing radiation and ultraviolet light.
    Chan GL, Little JB.
    Mol Gen Genet; 1981 Sep 06; 181(4):562-3. PubMed ID: 6943407
    [No Abstract] [Full Text] [Related]

  • 50. Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy: do the genes explain the diseases?
    Chu G, Mayne L.
    Trends Genet; 1996 May 06; 12(5):187-92. PubMed ID: 8984734
    [Abstract] [Full Text] [Related]

  • 51. [Xeroderma pigmentosum. What may be expected from biological studies?].
    Robert C, Sarasin A.
    Ann Dermatol Venereol; 1994 May 06; 121(5):434-9. PubMed ID: 7702274
    [No Abstract] [Full Text] [Related]

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  • 53. The versatile DNA nucleotide excision repair (NER) and its medical significance.
    Falik-Zaccai TC, Keren Z, Slor H.
    Pediatr Endocrinol Rev; 2009 Dec 06; 7(2):37-42. PubMed ID: 20118892
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  • 56. Xeroderma pigmentosum-Cockayne syndrome complex in two patients: absence of skin tumors despite severe deficiency of DNA excision repair.
    Scott RJ, Itin P, Kleijer WJ, Kolb K, Arlett C, Muller H.
    J Am Acad Dermatol; 1993 Nov 06; 29(5 Pt 2):883-9. PubMed ID: 8408834
    [Abstract] [Full Text] [Related]

  • 57. Xeroderma pigmentosum-Cockayne syndrome complex.
    Dev N, Aggarwal P.
    Indian J Med Res; 2020 Nov 06; 152(Suppl 1):S74-S75. PubMed ID: 35345132
    [No Abstract] [Full Text] [Related]

  • 58. Functional and molecular genetic analyses of nine newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes.
    Schäfer A, Gratchev A, Seebode C, Hofmann L, Schubert S, Laspe P, Apel A, Ohlenbusch A, Tzvetkov M, Weishaupt C, Oji V, Schön MP, Emmert S.
    Exp Dermatol; 2013 Jul 06; 22(7):486-9. PubMed ID: 23800062
    [Abstract] [Full Text] [Related]

  • 59. Cockayne syndrome without typical clinical manifestations including neurologic abnormalities.
    Miyauchi-Hashimoto H, Akaeda T, Maihara T, Ikenaga M, Horio T.
    J Am Acad Dermatol; 1998 Oct 06; 39(4 Pt 1):565-70. PubMed ID: 9777763
    [Abstract] [Full Text] [Related]

  • 60. Roles of poly(ADP-ribose) synthesis in repair and replication in normal human, Cockayne syndrome, and xeroderma pigmentosum fibroblasts after UV irradiation.
    Fujiwara Y, Goto K, Yamamoto K, Ichihashi M.
    Princess Takamatsu Symp; 1983 Oct 06; 13():209-18. PubMed ID: 6418714
    [Abstract] [Full Text] [Related]

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