메뉴 건너뛰기




Volumn 45, Issue 5, 1999, Pages 611-617

Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; APOLIPOPROTEIN E;

EID: 0342950666     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(199905)45:5<611::AID-ANA9>3.0.CO;2-X     Document Type: Article
Times cited : (253)

References (38)
  • 1
    • 0026514953 scopus 로고
    • Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinicopathologic study of 100 cases
    • Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinicopathologic study of 100 cases. J Neurol Neurosurg Psychiatry 1992;55: 181-184
    • (1992) J Neurol Neurosurg Psychiatry , vol.55 , pp. 181-184
    • Hughes, A.J.1    Daniel, S.E.2    Kilford, L.3    Lees, A.J.4
  • 2
    • 10544234193 scopus 로고    scopus 로고
    • Mapping of a gene for Parkinson's disease to chromosome 4q12-q23
    • Polymeropoulos MH, Higgins JJ, Golbe LI, et al. Mapping of a gene for Parkinson's disease to chromosome 4q12-q23. Science 1997;274:1197-1199
    • (1997) Science , vol.274 , pp. 1197-1199
    • Polymeropoulos, M.H.1    Higgins, J.J.2    Golbe, L.I.3
  • 3
    • 0030744876 scopus 로고    scopus 로고
    • Mutation in the α-synuclein gene identified in families with Parkinson's disease
    • Polymeropoulos MH, Laavedan C, Leroy E, et al. Mutation in the α-synuclein gene identified in families with Parkinson's disease. Science 1997;276:2045-2047
    • (1997) Science , vol.276 , pp. 2045-2047
    • Polymeropoulos, M.H.1    Laavedan, C.2    Leroy, E.3
  • 4
    • 0031990490 scopus 로고    scopus 로고
    • Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease
    • Krüger R, Kuhn W, Müller T, et al. Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease. Nat Genet 1998;18:106-108
    • (1998) Nat Genet , vol.18 , pp. 106-108
    • Krüger, R.1    Kuhn, W.2    Müller, T.3
  • 5
    • 0031951197 scopus 로고    scopus 로고
    • A susceptibility locus for Parkinson's disease maps to chromosome 2p13
    • Gasser T, Muller-Myhsok B, Wszolek ZK, et al. A susceptibility locus for Parkinson's disease maps to chromosome 2p13. Nat Genet 1998;18:262-265
    • (1998) Nat Genet , vol.18 , pp. 262-265
    • Gasser, T.1    Muller-Myhsok, B.2    Wszolek, Z.K.3
  • 6
    • 0032499264 scopus 로고    scopus 로고
    • Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
    • Kitada T, Asakawa S, Hattori N, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998;392:605-608
    • (1998) Nature , vol.392 , pp. 605-608
    • Kitada, T.1    Asakawa, S.2    Hattori, N.3
  • 7
    • 0023097950 scopus 로고
    • Ecogenetics of Parkinson's disease: Prevalence and environmental aspects in rural areas
    • Barbeau A, Roy M, Bernier G, et al. Ecogenetics of Parkinson's disease: prevalence and environmental aspects in rural areas. Can J Neurol Sci 1987;14:36-41
    • (1987) Can J Neurol Sci , vol.14 , pp. 36-41
    • Barbeau, A.1    Roy, M.2    Bernier, G.3
  • 9
    • 0029396761 scopus 로고
    • The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part IX. A prospective cliniconeuropathologic study of Parkinson's disease features in Alzheimer's disease
    • Hulette C, Mirra S, Wilkinson W, et al. The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part IX. A prospective cliniconeuropathologic study of Parkinson's disease features in Alzheimer's disease. Neurology 1995;45:1991-1995
    • (1995) Neurology , vol.45 , pp. 1991-1995
    • Hulette, C.1    Mirra, S.2    Wilkinson, W.3
  • 10
    • 84936613596 scopus 로고
    • History of dementia and Parkinson's disease in 1st degree relatives of patients with Alzheimer's disease
    • Hofman A, Schulte W, Tanja TA, et al. History of dementia and Parkinson's disease in 1st degree relatives of patients with Alzheimer's disease. Neurology 1989;39:1589-1592
    • (1989) Neurology , vol.39 , pp. 1589-1592
    • Hofman, A.1    Schulte, W.2    Tanja, T.A.3
  • 11
    • 0032485258 scopus 로고    scopus 로고
    • Chaperoning brain diseases
    • Welch WJ, Gambetti P. Chaperoning brain diseases. Nature 1998;392:23-24
    • (1998) Nature , vol.392 , pp. 23-24
    • Welch, W.J.1    Gambetti, P.2
  • 12
    • 0029073383 scopus 로고
    • Genetic dissection of Alzheimer's disease, a heterogenous disorder
    • Schellenberg GD. Genetic dissection of Alzheimer's disease, a heterogenous disorder. Proc Natl Acad Sci USA 1995;92:8552-8559
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 8552-8559
    • Schellenberg, G.D.1
  • 13
    • 0028798254 scopus 로고
    • Apolipoprotein E genotypes in Parkinson's disease with and without dementia
    • Koller WC, Glatt SL, Hubble JP, et al. Apolipoprotein E genotypes in Parkinson's disease with and without dementia. Ann Neurol 1995;37:242-245
    • (1995) Ann Neurol , vol.37 , pp. 242-245
    • Koller, W.C.1    Glatt, S.L.2    Hubble, J.P.3
  • 15
    • 0030881644 scopus 로고    scopus 로고
    • Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes
    • Zareparsi S, Kaye J, Camicioli R, et al. Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes. Ann Neurol 1997;42:655-658
    • (1997) Ann Neurol , vol.42 , pp. 655-658
    • Zareparsi, S.1    Kaye, J.2    Camicioli, R.3
  • 16
    • 0030798577 scopus 로고    scopus 로고
    • Apolipoprotein E genotype in familial Parkinson's disease
    • The French Parkinson's Disease Genetics Study Group. Apolipoprotein E genotype in familial Parkinson's disease. J Neurol Neurosurg Psychiatry 1997;63:394-395
    • (1997) J Neurol Neurosurg Psychiatry , vol.63 , pp. 394-395
  • 17
  • 18
    • 0030590067 scopus 로고    scopus 로고
    • The apolipoprotein E epsilon 4 allele in Parkinson's disease with Alzheimer lesions
    • Egensperger R, Bancher C, Kosel S, et al. The apolipoprotein E epsilon 4 allele in Parkinson's disease with Alzheimer lesions. Biochem Biophys Res Commun 1996;224:484-486
    • (1996) Biochem Biophys Res Commun , vol.224 , pp. 484-486
    • Egensperger, R.1    Bancher, C.2    Kosel, S.3
  • 19
    • 1842410720 scopus 로고    scopus 로고
    • Genetic predisposition to multiple sclerosis as revealed by immunoprinting
    • Epplen C, Jackel S, Santos EJ, et al. Genetic predisposition to multiple sclerosis as revealed by immunoprinting. Ann Neurol 1997;41:341-352
    • (1997) Ann Neurol , vol.41 , pp. 341-352
    • Epplen, C.1    Jackel, S.2    Santos, E.J.3
  • 20
    • 0031911596 scopus 로고    scopus 로고
    • A new polymorphism in the APOE promoter associated with risk of developing Alzheimer's disease
    • Lambert JC, Pasquier F, Cottel D, et al. A new polymorphism in the APOE promoter associated with risk of developing Alzheimer's disease. Hum Mol Genet 1998;7:533-540
    • (1998) Hum Mol Genet , vol.7 , pp. 533-540
    • Lambert, J.C.1    Pasquier, F.2    Cottel, D.3
  • 21
    • 0020643052 scopus 로고
    • HLA and disease 1982: A survey
    • Svejgard A, Ryder LP. HLA and disease 1982: a survey. Immunol Rev 1983;70:193-218
    • (1983) Immunol Rev , vol.70 , pp. 193-218
    • Svejgard, A.1    Ryder, L.P.2
  • 22
    • 0028084548 scopus 로고
    • HLA and disease associations: Detecting the strongest association
    • Svejgard A, Rydet LP. HLA and disease associations: detecting the strongest association. Tissue Antigens 1994;43:18-27
    • (1994) Tissue Antigens , vol.43 , pp. 18-27
    • Svejgard, A.1    Rydet, L.P.2
  • 23
    • 0021707651 scopus 로고
    • Enhanced gene expression by poly(dT-dG)•poly(dC-dA) sequence
    • Hamada H, Seidman M, Howard BH, Gorman CM. Enhanced gene expression by poly(dT-dG)•poly(dC-dA) sequence. Mol Cell Biol 1984;4:2622-2630
    • (1984) Mol Cell Biol , vol.4 , pp. 2622-2630
    • Hamada, H.1    Seidman, M.2    Howard, B.H.3    Gorman, C.M.4
  • 24
    • 0024428644 scopus 로고
    • E1A-induced enhancer activity of the poly(dG-dT)•poly(dA-dC) element (GT element) and interactions with a GT-specific nuclear factor
    • Berg DT, Walls JD, Reifel-Miller AE, Grinnell BW. E1A-induced enhancer activity of the poly(dG-dT)•poly(dA-dC) element (GT element) and interactions with a GT-specific nuclear factor. Mol Cell Biol 1989;9:5248-5253
    • (1989) Mol Cell Biol , vol.9 , pp. 5248-5253
    • Berg, D.T.1    Walls, J.D.2    Reifel-Miller, A.E.3    Grinnell, B.W.4
  • 25
    • 0026636898 scopus 로고
    • Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3
    • Andrew S, Theilmann J, Hedrick A, et al. Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3. Genomics 1992;13:301-311
    • (1992) Genomics , vol.13 , pp. 301-311
    • Andrew, S.1    Theilmann, J.2    Hedrick, A.3
  • 27
    • 0030723043 scopus 로고    scopus 로고
    • Distortion of allelic expression of apolipoprotein E in Alzheimer's disease
    • Lambert JC, Perez-Tur J, Dupire MJ, et al. Distortion of allelic expression of apolipoprotein E in Alzheimer's disease. Hum Mol Genet 1997;12:2151-2154
    • (1997) Hum Mol Genet , vol.12 , pp. 2151-2154
    • Lambert, J.C.1    Perez-Tur, J.2    Dupire, M.J.3
  • 28
    • 0032102455 scopus 로고    scopus 로고
    • The synucleins: A family of proteins involved in synaptic function, plasticity, neurodegeneration and disease
    • Clayton DF, George JM. The synucleins: a family of proteins involved in synaptic function, plasticity, neurodegeneration and disease. Trends Neurosci 1998;21:249-254
    • (1998) Trends Neurosci , vol.21 , pp. 249-254
    • Clayton, D.F.1    George, J.M.2
  • 29
    • 0031668101 scopus 로고    scopus 로고
    • Genetic dissection of familial Parkinson's disease
    • Riess O, Jakes R, Krüger R. Genetic dissection of familial Parkinson's disease. Mol Med Today 1998;4:438-444
    • (1998) Mol Med Today , vol.4 , pp. 438-444
    • Riess, O.1    Jakes, R.2    Krüger, R.3
  • 30
    • 0027464780 scopus 로고
    • Association of a monoamine oxidase B allele with Parkinson's disease
    • Kurth JH, Kurth MC, Poduslo SE, Schwankhaus JD. Association of a monoamine oxidase B allele with Parkinson's disease. Ann Neurol 1993;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
  • 31
    • 0028260282 scopus 로고
    • Hereditary variations in monoamine oxidase as a risk factor for Parkinsons's disease
    • Hotamisligil GS, Girmen S, Fink S, et al. Hereditary variations in monoamine oxidase as a risk factor for Parkinsons's disease. Mov Disord 1994;9:305-310
    • (1994) Mov Disord , vol.9 , pp. 305-310
    • Hotamisligil, G.S.1    Girmen, S.2    Fink, S.3
  • 32
    • 0030895917 scopus 로고    scopus 로고
    • Association of a polymorphism in intron 13 of the monoamine oxidase B gene with Parkinson disease
    • Costa P, Checkoway H, Levy D, et al. Association of a polymorphism in intron 13 of the monoamine oxidase B gene with Parkinson disease. Am J Med Genet 1997;74:154-156
    • (1997) Am J Med Genet , vol.74 , pp. 154-156
    • Costa, P.1    Checkoway, H.2    Levy, D.3
  • 33
    • 0030692086 scopus 로고    scopus 로고
    • Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease
    • Bandmann O, Vaughan J, Holmans P, et al. Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease. Lancet 1997;350:1136-1139
    • (1997) Lancet , vol.350 , pp. 1136-1139
    • Bandmann, O.1    Vaughan, J.2    Holmans, P.3
  • 35
    • 0026747176 scopus 로고
    • Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease
    • Smith CAD, Gough AC, Leigh PN, et al. Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease. Lancet 1992;339:1375-1377
    • (1992) Lancet , vol.339 , pp. 1375-1377
    • Smith, C.A.D.1    Gough, A.C.2    Leigh, P.N.3
  • 36
    • 15644367326 scopus 로고    scopus 로고
    • Is there a genetic susceptibility locus for Parkinson's disease on chromosome 22q13
    • Wilhelmsen K, Mirel D, Marder K, et al. Is there a genetic susceptibility locus for Parkinson's disease on chromosome 22q13. Ann Neurol 1997;41:813-817
    • (1997) Ann Neurol , vol.41 , pp. 813-817
    • Wilhelmsen, K.1    Mirel, D.2    Marder, K.3
  • 37
    • 2542507783 scopus 로고    scopus 로고
    • Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: Evidence for association of a DRD2 allele
    • Planté-Bordeneuve V, Taussig D, Thomas F, et al. Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele. Neurology 1997;48:1589-1593
    • (1997) Neurology , vol.48 , pp. 1589-1593
    • Planté-Bordeneuve, V.1    Taussig, D.2    Thomas, F.3
  • 38
    • 0031891886 scopus 로고    scopus 로고
    • Association between the gene encoding the E2 subunit of the α-ketoglutarate dehydrogenase complex and Parkinson's disease
    • Kobayashi T, Matsumine H, Matuda S, Mizuno Y. Association between the gene encoding the E2 subunit of the α-ketoglutarate dehydrogenase complex and Parkinson's disease. Ann Neurol 1998;43:120-123
    • (1998) Ann Neurol , vol.43 , pp. 120-123
    • Kobayashi, T.1    Matsumine, H.2    Matuda, S.3    Mizuno, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.