BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 16775218)

  • 1. TDP1-dependent DNA single-strand break repair and neurodegeneration.
    El-Khamisy SF; Caldecott KW
    Mutagenesis; 2006 Jul; 21(4):219-24. PubMed ID: 16775218
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA single-strand break repair and spinocerebellar ataxia with axonal neuropathy-1.
    el-Khamisy SF; Caldecott KW
    Neuroscience; 2007 Apr; 145(4):1260-6. PubMed ID: 17045754
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Defective DNA repair and neurodegenerative disease.
    Rass U; Ahel I; West SC
    Cell; 2007 Sep; 130(6):991-1004. PubMed ID: 17889645
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA single-strand breaks and neurodegeneration.
    Caldecott KW
    DNA Repair (Amst); 2004; 3(8-9):875-82. PubMed ID: 15279772
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy.
    Takashima H; Boerkoel CF; John J; Saifi GM; Salih MA; Armstrong D; Mao Y; Quiocho FA; Roa BB; Nakagawa M; Stockton DW; Lupski JR
    Nat Genet; 2002 Oct; 32(2):267-72. PubMed ID: 12244316
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1.
    El-Khamisy SF; Saifi GM; Weinfeld M; Johansson F; Helleday T; Lupski JR; Caldecott KW
    Nature; 2005 Mar; 434(7029):108-13. PubMed ID: 15744309
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [DNA repair and neurodegeneration].
    Onodera O
    Rinsho Shinkeigaku; 2005 Nov; 45(11):979-81. PubMed ID: 16447779
    [TBL] [Abstract][Full Text] [Related]  

  • 8. In vitro complementation of Tdp1 deficiency indicates a stabilized enzyme-DNA adduct from tyrosyl but not glycolate lesions as a consequence of the SCAN1 mutation.
    Hawkins AJ; Subler MA; Akopiants K; Wiley JL; Taylor SM; Rice AC; Windle JJ; Valerie K; Povirk LF
    DNA Repair (Amst); 2009 May; 8(5):654-63. PubMed ID: 19211312
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary ataxia SCAN1 cells are defective for the repair of transcription-dependent topoisomerase I cleavage complexes.
    Miao ZH; Agama K; Sordet O; Povirk L; Kohn KW; Pommier Y
    DNA Repair (Amst); 2006 Dec; 5(12):1489-94. PubMed ID: 16935573
    [TBL] [Abstract][Full Text] [Related]  

  • 10. TDP1 facilitates repair of ionizing radiation-induced DNA single-strand breaks.
    El-Khamisy SF; Hartsuiker E; Caldecott KW
    DNA Repair (Amst); 2007 Oct; 6(10):1485-95. PubMed ID: 17600775
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deficiency in 3'-phosphoglycolate processing in human cells with a hereditary mutation in tyrosyl-DNA phosphodiesterase (TDP1).
    Zhou T; Lee JW; Tatavarthi H; Lupski JR; Valerie K; Povirk LF
    Nucleic Acids Res; 2005; 33(1):289-97. PubMed ID: 15647511
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tyrosyl-DNA phosphodiesterase (Tdp1) (3'-phosphotyrosyl DNA phosphodiesterase).
    Raymond AC; Burgin AB
    Methods Enzymol; 2006; 409():511-24. PubMed ID: 16793421
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?
    Hirano R; Interthal H; Huang C; Nakamura T; Deguchi K; Choi K; Bhattacharjee MB; Arimura K; Umehara F; Izumo S; Northrop JL; Salih MA; Inoue K; Armstrong DL; Champoux JJ; Takashima H; Boerkoel CF
    EMBO J; 2007 Nov; 26(22):4732-43. PubMed ID: 17948061
    [TBL] [Abstract][Full Text] [Related]  

  • 14. TDP1 mutation causing SCAN1 neurodegenerative syndrome hampers the repair of transcriptional DNA double-strand breaks.
    Geraud M; Cristini A; Salimbeni S; Bery N; Jouffret V; Russo M; Ajello AC; Fernandez Martinez L; Marinello J; Cordelier P; Trouche D; Favre G; Nicolas E; Capranico G; Sordet O
    Cell Rep; 2024 May; 43(5):114214. PubMed ID: 38761375
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA strand break repair and human genetic disease.
    McKinnon PJ; Caldecott KW
    Annu Rev Genomics Hum Genet; 2007; 8():37-55. PubMed ID: 17887919
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Single-strand break repair and genetic disease.
    Caldecott KW
    Nat Rev Genet; 2008 Aug; 9(8):619-31. PubMed ID: 18626472
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Breaks in coordination: DNA repair in inherited ataxia.
    Paulson HL; Miller VM
    Neuron; 2005 Jun; 46(6):845-8. PubMed ID: 15953413
    [TBL] [Abstract][Full Text] [Related]  

  • 18. TDP1 facilitates chromosomal single-strand break repair in neurons and is neuroprotective in vivo.
    Katyal S; el-Khamisy SF; Russell HR; Li Y; Ju L; Caldecott KW; McKinnon PJ
    EMBO J; 2007 Nov; 26(22):4720-31. PubMed ID: 17914460
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spinocerebellar ataxia with axonal neuropathy.
    Walton C; Interthal H; Hirano R; Salih MA; Takashima H; Boerkoel CF
    Adv Exp Med Biol; 2010; 685():75-83. PubMed ID: 20687496
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synergistic decrease of DNA single-strand break repair rates in mouse neural cells lacking both Tdp1 and aprataxin.
    El-Khamisy SF; Katyal S; Patel P; Ju L; McKinnon PJ; Caldecott KW
    DNA Repair (Amst); 2009 Jun; 8(6):760-6. PubMed ID: 19303373
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.