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Volumn 52, Issue 9, 1999, Pages 1899-1901

Molecular genetic analysis of the APEX nuclease gene in amyotrophic lateral sclerosis

Author keywords

[No Author keywords available]

Indexed keywords

DNA (APURINIC OR APYRIMIDINIC SITE) LYASE;

EID: 0033009789     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.52.9.1899     Document Type: Article
Times cited : (79)

References (10)
  • 1
    • 0028916910 scopus 로고
    • Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients
    • Jones CT, Swingler RJ, Simpson SA, Brock DJH. Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients. J Med Genet 1995;32: 290-292.
    • (1995) J Med Genet , vol.32 , pp. 290-292
    • Jones, C.T.1    Swingler, R.J.2    Simpson, S.A.3    Djh, B.4
  • 2
    • 0027401203 scopus 로고
    • Mutations in Cu/Zn Superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
    • Rosen DR, Siddique T, Patterson D, et al. Mutations in Cu/Zn Superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993;362:59-62.
    • (1993) Nature , vol.362 , pp. 59-62
    • Rosen, D.R.1    Siddique, T.2    Patterson, D.3
  • 3
    • 0019935965 scopus 로고
    • A new hypothesis of the etiology of amyotrophic lateral sclerosis: The DNA hypothesis
    • Bradley W, Krasin P. A new hypothesis of the etiology of amyotrophic lateral sclerosis: the DNA hypothesis. Arch Neurol 1982;39:677-680.
    • (1982) Arch Neurol , vol.39 , pp. 677-680
    • Bradley, W.1    Krasin, P.2
  • 4
    • 0030916372 scopus 로고    scopus 로고
    • Evidence of reduced DNA repair in amyotrophic lateral sclerosis brain tissue
    • Kisby GE, Milne J, Sweatt C. Evidence of reduced DNA repair in amyotrophic lateral sclerosis brain tissue. Neuroreport 1997;8:1337-1340.
    • (1997) Neuroreport , vol.8 , pp. 1337-1340
    • Kisby, G.E.1    Milne, J.2    Sweatt, C.3
  • 5
    • 0032567807 scopus 로고    scopus 로고
    • Mutant AP endonuclease in patients with amyotrophic lateral sclerosis
    • Olkowski ZL. Mutant AP endonuclease in patients with amyotrophic lateral sclerosis. Neuroreport 1998;9:239-242.
    • (1998) Neuroreport , vol.9 , pp. 239-242
    • Olkowski, Z.L.1
  • 8
    • 0028220526 scopus 로고
    • Identification of a novel nonsense mutation in the fibrillin gene (FBN1) using nonisotopic techniques
    • Hayward C, Porteous ME, Brock DJH. Identification of a novel nonsense mutation in the fibrillin gene (FBN1) using nonisotopic techniques. Hum Mutât 1994;3:159-162.
    • (1994) Hum Mutât , vol.3 , pp. 159-162
    • Hayward, C.1    Porteous, M.E.2    Djh, B.3
  • 9
    • 0026920775 scopus 로고
    • Rapid and simultaneous detection of multiple mutations by pooled and multiplex single nucleotide primer extension: Application to the study of insulin-responsive glucose transporter and insulin receptor mutations in non-insulin-dependent diabetes
    • Krook A, Stratton IM, O'Rahilly S. Rapid and simultaneous detection of multiple mutations by pooled and multiplex single nucleotide primer extension: application to the study of insulin-responsive glucose transporter and insulin receptor mutations in non-insulin-dependent diabetes. Hum Mol Genet 1992;l:391-395.
    • (1992) Hum Mol Genet , pp. 391-395
    • Krook, A.1    Stratton, I.M.2    O'Rahilly, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.