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

PUBMED FOR HANDHELDS

Journal Abstract Search

664 related items for PubMed ID: 17276014

  • 1. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship.
    Kraemer KH, Patronas NJ, Schiffmann R, Brooks BP, Tamura D, DiGiovanna JJ.
    Neuroscience; 2007 Apr 14; 145(4):1388-96. PubMed ID: 17276014
    [Abstract] [Full Text] [Related]

  • 2. The case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum.
    Brooks PJ.
    Neuroscience; 2007 Apr 14; 145(4):1407-17. PubMed ID: 17184928
    [Abstract] [Full Text] [Related]

  • 3. DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.
    Lehmann AR.
    Biochimie; 2003 Nov 14; 85(11):1101-11. PubMed ID: 14726016
    [Abstract] [Full Text] [Related]

  • 4. Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition.
    de Boer J, van Steeg H, Berg RJ, Garssen J, de Wit J, van Oostrum CT, Beems RB, van der Horst GT, van Kreijl CF, de Gruijl FR, Bootsma D, Hoeijmakers JH, Weeda G.
    Cancer Res; 1999 Jul 15; 59(14):3489-94. PubMed ID: 10416615
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.
    Itin PH, Sarasin A, Pittelkow MR.
    J Am Acad Dermatol; 2001 Jun 15; 44(6):891-920; quiz 921-4. PubMed ID: 11369901
    [Abstract] [Full Text] [Related]

  • 12. Cockayne syndrome and xeroderma pigmentosum.
    Rapin I, Lindenbaum Y, Dickson DW, Kraemer KH, Robbins JH.
    Neurology; 2000 Nov 28; 55(10):1442-9. PubMed ID: 11185579
    [Abstract] [Full Text] [Related]

  • 13. Bacterial DNA repair genes and their eukaryotic homologues: 4. The role of nucleotide excision DNA repair (NER) system in mammalian cells.
    Maddukuri L, Dudzińska D, Tudek B.
    Acta Biochim Pol; 2007 Nov 28; 54(3):469-82. PubMed ID: 17893751
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Human cancer and DNA repair-deficient diseases.
    Sarasin A, Stary A.
    Cancer Detect Prev; 1997 Nov 28; 21(5):406-11. PubMed ID: 9307843
    [Abstract] [Full Text] [Related]

  • 16. The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect.
    Berneburg M, Clingen PH, Harcourt SA, Lowe JE, Taylor EM, Green MH, Krutmann J, Arlett CF, Lehmann AR.
    Cancer Res; 2000 Jan 15; 60(2):431-8. PubMed ID: 10667598
    [Abstract] [Full Text] [Related]

  • 17. Hot news: temperature-sensitive humans explain hereditary disease.
    Friedberg EC.
    Bioessays; 2001 Aug 15; 23(8):671-3. PubMed ID: 11494313
    [Abstract] [Full Text] [Related]

  • 18. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
    Graham JM, Anyane-Yeboa K, Raams A, Appeldoorn E, Kleijer WJ, Garritsen VH, Busch D, Edersheim TG, Jaspers NG.
    Am J Hum Genet; 2001 Aug 15; 69(2):291-300. PubMed ID: 11443545
    [Abstract] [Full Text] [Related]

  • 19. Restoring DNA repair capacity of cells from three distinct diseases by XPD gene-recombinant adenovirus.
    Armelini MG, Muotri AR, Marchetto MC, de Lima-Bessa KM, Sarasin A, Menck CF.
    Cancer Gene Ther; 2005 Apr 15; 12(4):389-96. PubMed ID: 15650764
    [Abstract] [Full Text] [Related]

  • 20. Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes.
    Carreau M, Eveno E, Quilliet X, Chevalier-Lagente O, Benoit A, Tanganelli B, Stefanini M, Vermeulen W, Hoeijmakers JH, Sarasin A.
    Carcinogenesis; 1995 May 15; 16(5):1003-9. PubMed ID: 7767957
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 34.