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Volumn 247, Issue 1, 2000, Pages 52-55

The monoamine oxidase B gene GT repeat polymorphism and Parkinson's disease in a Chinese population

Author keywords

Genetics; Monoamine oxidase B; Parkinson's disease

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME B; DOPAMINE; NEUROTOXIN;

EID: 0034022516     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150050010     Document Type: Article
Times cited : (35)

References (26)
  • 1
    • 0027464780 scopus 로고
    • Association of monoamine oxidase B allele with Parkinson's disease
    • 1. Kurth JH, Kurth MC, Poduslo SE, Schwankhaus JD (1993) Association of monoamine oxidase B allele with Parkinson's disease. Ann Neurol 33 : 368-372
    • (1993) Ann Neurol , vol.33 , pp. 368-372
    • Kurth, J.H.1    Kurth, M.C.2    Poduslo, S.E.3    Schwankhaus, J.D.4
  • 2
    • 0013642531 scopus 로고
    • Lack of association of CYP2D6 and MAO-B alleles with Parkinson's disease in a Kansas cohort
    • 2. Kurth JH, Hubble JP, Eggers EA, Kurth MC, Koller WC, Lieberman AN (1995) Lack of association of CYP2D6 and MAO-B alleles with Parkinson's disease in a Kansas cohort. Neurology 45 [Suppl 4] : A429
    • (1995) Neurology , vol.45 , Issue.SUPPL. 4
    • Kurth, J.H.1    Hubble, J.P.2    Eggers, E.A.3    Kurth, M.C.4    Koller, W.C.5    Lieberman, A.N.6
  • 3
    • 0028963983 scopus 로고
    • An allelic association study of monoamine oxidase B in Parkinson's disease
    • 3. Ho SL, Kapadi AL, Ramsden DB, Williams AC (1995) An allelic association study of monoamine oxidase B in Parkinson's disease. Ann Neurol 37 : 403-405
    • (1995) Ann Neurol , vol.37 , pp. 403-405
    • Ho, S.L.1    Kapadi, A.L.2    Ramsden, D.B.3    Williams, A.C.4
  • 4
    • 0000797256 scopus 로고    scopus 로고
    • Monoamine oxidase B polymorphism in Parkinson's disease
    • 4. Costa P, Checkoway H, Swanson PD, Costa LG (1996) Monoamine oxidase B polymorphism in Parkinson's disease. Mov Disord 11 [Suppl 1] : 181
    • (1996) Mov Disord , vol.11 , Issue.SUPPL. 1 , pp. 181
    • Costa, P.1    Checkoway, H.2    Swanson, P.D.3    Costa, L.G.4
  • 5
    • 0033407580 scopus 로고    scopus 로고
    • Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease
    • 5. Mellick GD, Buchanan DD, McCann SJ, et al (1999) Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease. Mov Disord 14 : 219-224
    • (1999) Mov Disord , vol.14 , pp. 219-224
    • Mellick, G.D.1    Buchanan, D.D.2    McCann, S.J.3
  • 6
    • 0026506757 scopus 로고
    • Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB gene
    • 6. Konradi C, Ozelius L, Breakefield XO (1992) Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB gene. Genomics 12 : 176-177
    • (1992) Genomics , vol.12 , pp. 176-177
    • Konradi, C.1    Ozelius, L.2    Breakefield, X.O.3
  • 7
    • 0026747176 scopus 로고
    • Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease
    • 7. Smith CAD, Gough AC, Leigh PN, et al (1992) Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease. Lancet 339 : 1375-1377
    • (1992) Lancet , vol.339 , pp. 1375-1377
    • Smith, C.A.D.1    Gough, A.C.2    Leigh, P.N.3
  • 8
    • 0031946127 scopus 로고    scopus 로고
    • Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's disease
    • 8. Pang CP, Zhang J, Woo J, et al (1998) Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's disease. Mov Disord 13 : 529-532
    • (1998) Mov Disord , vol.13 , pp. 529-532
    • Pang, C.P.1    Zhang, J.2    Woo, J.3
  • 9
    • 0029851872 scopus 로고    scopus 로고
    • The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease
    • 9. Gasser T, Muller-Myhsok B, Supala A, et al (1996) The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 61 : 518-519
    • (1996) J Neurol Neurosurg Psychiatry , vol.61 , pp. 518-519
    • Gasser, T.1    Muller-Myhsok, B.2    Supala, A.3
  • 10
  • 12
    • 0030921878 scopus 로고    scopus 로고
    • Association of a polymorphism in the dopamine transporter with Parkinson's disease
    • 12. LeCouteur DG, Leighton PW, McCann SJ, Pond SM (1997) Association of a polymorphism in the dopamine transporter with Parkinson's disease. Mov Disord 12 : 760-763
    • (1997) Mov Disord , vol.12 , pp. 760-763
    • LeCouteur, D.G.1    Leighton, P.W.2    McCann, S.J.3    Pond, S.M.4
  • 13
    • 0031467513 scopus 로고    scopus 로고
    • The dopamine transporter gene and Parkinson's disease in a chinese population
    • 13. Leighton PW, LeCouteur DG, Pang CCP, et al (1997) The dopamine transporter gene and Parkinson's disease in a Chinese population. Neurology 49 : 1577-1579
    • (1997) Neurology , vol.49 , pp. 1577-1579
    • Leighton, P.W.1    LeCouteur, D.G.2    Pang, C.C.P.3
  • 14
    • 0026651968 scopus 로고
    • Multiple dopamine D4 receptor variants in the human population
    • 14. Tol HHM van, Wu CM, Guan HC, et al (1992) Multiple dopamine D4 receptor variants in the human population. Nature 358 : 149-152
    • (1992) Nature , vol.358 , pp. 149-152
    • Van Tol, H.H.M.1    Wu, C.M.2    Guan, H.C.3
  • 15
    • 0027250606 scopus 로고
    • Low density of dopamine D4 receptors in Parkinson's, schizophrenia and control brain striata
    • 15. Seaman P, Guan HC, van Tol HHM, Niznik HB (1993) Low density of dopamine D4 receptors in Parkinson's, schizophrenia and control brain striata. Synapse 14 : 247-253
    • (1993) Synapse , vol.14 , pp. 247-253
    • Seaman, P.1    Guan, H.C.2    Van Tol, H.H.M.3    Niznik, H.B.4
  • 16
    • 0033429665 scopus 로고    scopus 로고
    • Lack of allelic association of dopamine D4 receptor gene polymorphism with Parkinson's disease in Chinese population
    • 16. Wan DCC, Law LK, Ip DTM, et al (1999) Lack of allelic association of dopamine D4 receptor gene polymorphism with Parkinson's disease in Chinese population. Mov Disord 14: 225-229
    • (1999) Mov Disord , vol.14 , pp. 225-229
    • Wan, D.C.C.1    Law, L.K.2    Ip, D.T.M.3
  • 17
    • 0031472072 scopus 로고    scopus 로고
    • Association between polymorphisms in the cytochrome P-450 2D6 gene and Parkinson's disease: A case-control study and meta-analysis
    • 17. McCann SJ, Pond SM, James KM, LeCouteur DG (1997) Association between polymorphisms in the cytochrome P-450 2D6 gene and Parkinson's disease: a case-control study and meta-analysis. J Neurol Sci 153 : 50-53
    • (1997) J Neurol Sci , vol.153 , pp. 50-53
    • McCann, S.J.1    Pond, S.M.2    James, K.M.3    LeCouteur, D.G.4
  • 18
  • 19
    • 18844469020 scopus 로고    scopus 로고
    • Genetic and environmental risk factors for Parkinson's disease in a Chinese population
    • 19. Chan DKY, Woo J, Ho SC, et al (1998) Genetic and environmental risk factors for Parkinson's disease in a Chinese population. J Neurol Neurosurg Psychiatry 65: 781-784
    • (1998) J Neurol Neurosurg Psychiatry , vol.65 , pp. 781-784
    • Chan, D.K.Y.1    Woo, J.2    Ho, S.C.3
  • 20
    • 0013684669 scopus 로고    scopus 로고
    • Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease
    • 20. Bordet R, Broly F, Destee A, Libersa C (1996) Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease. Adv Neurol 36 : 387-396
    • (1996) Adv Neurol , vol.36 , pp. 387-396
    • Bordet, R.1    Broly, F.2    Destee, A.3    Libersa, C.4
  • 23
    • 0029751103 scopus 로고    scopus 로고
    • The etiology of Parkinson's disease with emphasis on the MPTP story
    • 23. Langston JW (1996) The etiology of Parkinson's disease with emphasis on the MPTP story. Neurology 47 [Suppl 3] : S153-S160
    • (1996) Neurology , vol.47 , Issue.SUPPL. 3
    • Langston, J.W.1
  • 24
    • 0032543684 scopus 로고    scopus 로고
    • Association of missense and 5′-splice-site mutations in tau with the inherited demetia FTDP-17
    • 24. Hutton M, Lendon CL, Rizzu P, et al (1998) Association of missense and 5′-splice-site mutations in tau with the inherited demetia FTDP-17. Nature 393 : 702-705
    • (1998) Nature , vol.393 , pp. 702-705
    • Hutton, M.1    Lendon, C.L.2    Rizzu, P.3
  • 25
    • 0029157488 scopus 로고
    • Minisatellites and human disease
    • 25. Krontiris TG (1995) Minisatellites and human disease. Science 269 : 1682-1683
    • (1995) Science , vol.269 , pp. 1682-1683
    • Krontiris, T.G.1
  • 26
    • 0030600144 scopus 로고    scopus 로고
    • Genomic simple repetitive DNAs are targets for differential binding of nuclear proteins
    • 26. Epplen JT, Kyas A, Maueler W (1996) Genomic simple repetitive DNAs are targets for differential binding of nuclear proteins. FEBS Lett 389 : 92-95
    • (1996) FEBS Lett , vol.389 , pp. 92-95
    • Epplen, J.T.1    Kyas, A.2    Maueler, W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.