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Volumn 18, Issue 6, 2003, Pages 631-636

Complex interactions in Parkinson's disease: A two-phases approach

Author keywords

Epistasis; Interactions; Parkinson's disease; Recursive partitioning; Susceptibility genes; Ubiquitin proteasome system

Indexed keywords

ALPHA SYNUCLEIN; HYDROLASE; PARKIN; PROTEASOME; UBIQUITIN; UBIQUITIN CARBOXY TERMINAL HYDROLASE L1; UNCLASSIFIED DRUG;

EID: 0038422898     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/mds.10431     Document Type: Article
Times cited : (28)

References (40)
  • 1
    • 0030744876 scopus 로고    scopus 로고
    • Mutation in the α-synuclein gene identified in families with Parkinson's disease
    • Polymeropoulos MH, Lavedan 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    Lavedan, C.2    Leroy, E.3
  • 2
    • 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
  • 3
    • 0032190090 scopus 로고    scopus 로고
    • The ubiquitin pathway in Parkinson's disease
    • Leroy E, Boyer R, Auburger G, et al. The ubiquitin pathway in Parkinson's disease. Nature 1998;395:451-452.
    • (1998) Nature , vol.395 , pp. 451-452
    • Leroy, E.1    Boyer, R.2    Auburger, G.3
  • 4
    • 0035854437 scopus 로고    scopus 로고
    • Ubiquitination of a new form of α-synuclein by parkin from human brain: Implications for Parkinson's disease
    • Shimura H, Schlossmacher MG, Hattori N, et al. Ubiquitination of a new form of α-synuclein by parkin from human brain: implications for Parkinson's disease. Science 2001;293:263-269.
    • (2001) Science , vol.293 , pp. 263-269
    • Shimura, H.1    Schlossmacher, M.G.2    Hattori, N.3
  • 6
    • 0035880458 scopus 로고    scopus 로고
    • α-synuclein gene haplotypes are associated with Parkinson's disease
    • Farrer M, Maraganore DM, Lockhart P, et al. α-synuclein gene haplotypes are associated with Parkinson's disease. Hum Mol Genet 2001;10:1847-1851.
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 1847-1851
    • Farrer, M.1    Maraganore, D.M.2    Lockhart, P.3
  • 7
    • 0037656778 scopus 로고    scopus 로고
    • Case-control studies of ubiquitin carboxy-terminal hydrolase L1, α-synuclein, and parkin gene polymorphisms in Parkinson's disease
    • [abstract]
    • Maraganore DM, Farrer MJ, Lesnick TG, de Andrade M, Rocca WA, Hardy JA. Case-control studies of ubiquitin carboxy-terminal hydrolase L1, α-synuclein, and parkin gene polymorphisms in Parkinson's disease [abstract]. Neurotoxicology 2001;22:882-883.
    • (2001) Neurotoxicology , vol.22 , pp. 882-883
    • Maraganore, D.M.1    Farrer, M.J.2    Lesnick, T.G.3    de Andrade, M.4    Rocca, W.A.5    Hardy, J.A.6
  • 9
    • 0342950666 scopus 로고    scopus 로고
    • Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype
    • Krüger R, Vieira-Saecker AMM, Kuhn W, et al. Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype. Ann Neurol 1999;45:611-617.
    • (1999) Ann. Neurol. , vol.45 , pp. 611-617
    • Krüger, R.1    Vieira-Saecker, A.M.M.2    Kuhn, W.3
  • 10
    • 0034646346 scopus 로고    scopus 로고
    • Polymorphism of NACP-Rep1 in Parkinson's disease: An etiologic link with essential tremor?
    • Tan EK, Matsuura T, Nagamitsu S, Khajavi M, Jankovic J, Ashizawa T. Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor? Neurology 2000;54:1195-1198.
    • (2000) Neurology , vol.54 , pp. 1195-1198
    • Tan, E.K.1    Matsuura, T.2    Nagamitsu, S.3    Khajavi, M.4    Jankovic, J.5    Ashizawa, T.6
  • 11
    • 0035881339 scopus 로고    scopus 로고
    • A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population
    • Satoh J, Kuroda Y. A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population. J Neurol Sci 2001;189:113-117.
    • (2001) J. Neurol. Sci. , vol.189 , pp. 113-117
    • Satoh, J.1    Kuroda, Y.2
  • 12
    • 0032937416 scopus 로고    scopus 로고
    • Polymorphism in the parkin gene in sporadic Parkinson's disease
    • Wang M, Hattori N, Matsumine H, et al. Polymorphism in the parkin gene in sporadic Parkinson's disease. Ann Neurol 1999;45: 655-658.
    • (1999) Ann. Neurol. , vol.45 , pp. 655-658
    • Wang, M.1    Hattori, N.2    Matsumine, H.3
  • 13
    • 0033946025 scopus 로고    scopus 로고
    • Association studies of Parkinson's disease and parkin polymorphisms
    • Klein C, Schumacher K, Jacobs H, et al. Association studies of Parkinson's disease and parkin polymorphisms. Ann Neurol 2000; 48:126-127.
    • (2000) Ann. Neurol. , vol.48 , pp. 126-127
    • Klein, C.1    Schumacher, K.2    Jacobs, H.3
  • 14
    • 0035126379 scopus 로고    scopus 로고
    • The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls
    • Mellick GD, Buchanan DD, Hattori N, et al. The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls. Parkinsonism Rel Disord 2001;7:89-91.
    • (2001) Parkinsonism Rel. Disord. , vol.7 , pp. 89-91
    • Mellick, G.D.1    Buchanan, D.D.2    Hattori, N.3
  • 15
    • 0004185387 scopus 로고    scopus 로고
    • Ubiquitin C-terminal hydrolase L1 in sporadic Parkinson's disease
    • (Abstract)
    • Gasser T, Pilz P, Omasmeier D, Müller-Myhsok B. Ubiquitin C-terminal hydrolase L1 in sporadic Parkinson's disease (Abstract). Mov Disord 2000;15:A201.
    • (2000) Mov. Disord. , vol.15
    • Gasser, T.1    Pilz, P.2    Omasmeier, D.3    Müller-Myhsok, B.4
  • 16
    • 0034647948 scopus 로고    scopus 로고
    • Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients
    • Wintermeyer P, Krüger R, Kuhn W, et al. Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients. Neuroreport 2000;11:2079-2082.
    • (2000) Neuroreport , vol.11 , pp. 2079-2082
    • Wintermeyer, P.1    Krüger, R.2    Kuhn, W.3
  • 17
    • 0033947504 scopus 로고    scopus 로고
    • Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease
    • Zhang J, Hattori N, Leroy E, et al. Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease. Parkinsonism Rel Disord 2000;6:195-197.
    • (2000) Parkinsonism Rel. Disord. , vol.6 , pp. 195-197
    • Zhang, J.1    Hattori, N.2    Leroy, E.3
  • 18
    • 0035881339 scopus 로고    scopus 로고
    • A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population
    • Satoh J, Kuroda Y. A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population. J Neurol Sci 2001;189:113-117.
    • (2001) J. Neurol. Sci. , vol.189 , pp. 113-117
    • Satoh, J.1    Kuroda, Y.2
  • 19
    • 0036135090 scopus 로고    scopus 로고
    • Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms
    • Momose Y, Murata M, Kobayashi K, et al. Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms. Ann Neurol 2002;51:133-136.
    • (2002) Ann. Neurol. , vol.51 , pp. 133-136
    • Momose, Y.1    Murata, M.2    Kobayashi, K.3
  • 20
    • 0034722106 scopus 로고    scopus 로고
    • The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease
    • Mellick GD, Silburn PA. The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease. Neurosci Lett 2000;293; 127-130.
    • (2000) Neurosci. Lett. , vol.293 , pp. 127-130
    • Mellick, G.D.1    Silburn, P.A.2
  • 21
    • 0035859766 scopus 로고    scopus 로고
    • Lack of association between ubiquitin carboxy-terminal hydrolase L1 gene polymorphism and PD
    • Savettieri G, De Marco EV, Civitelli D, et al. Lack of association between ubiquitin carboxy-terminal hydrolase L1 gene polymorphism and PD. Neurology 2001;57:560-561.
    • (2001) Neurology , vol.57 , pp. 560-561
    • Savettieri, G.1    De Marco, E.V.2    Civitelli, D.3
  • 22
    • 0034864346 scopus 로고    scopus 로고
    • No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease
    • Levecque C, Destée A, Mouroux V, et al. No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease. J Neural Transm 2001;108:979-984.
    • (2001) J. Neural. Transm. , vol.108 , pp. 979-984
    • Levecque, C.1    Destée, A.2    Mouroux, V.3
  • 23
    • 0036869217 scopus 로고    scopus 로고
    • Case-control study of doparmine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease
    • Goudreau JL, Maraganore DM, Farrer MJ, et al. Case-control study of doparmine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease. Mov Disord 2002;17:1305-1311.
    • (2002) Mov. Disord. , vol.17 , pp. 1305-1311
    • Goudreau, J.L.1    Maraganore, D.M.2    Farrer, M.J.3
  • 24
    • 0032946784 scopus 로고    scopus 로고
    • Incidence and distribution of parkinsonism in Olmsted County, Minnesota, 1976-1990
    • Bower JH, Maraganore DM, McDonnell SK, Rocca WA. Incidence and distribution of parkinsonism in Olmsted County, Minnesota, 1976-1990. Neurology 1999;52:1214-1220.
    • (1999) Neurology , vol.52 , pp. 1214-1220
    • Bower, J.H.1    Maraganore, D.M.2    McDonnell, S.K.3    Rocca, W.A.4
  • 25
    • 0003516711 scopus 로고    scopus 로고
    • An introduction to recursive partitioning using the RPART routines
    • Technical Report 61, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota
    • Therneau TM, Atkinson EJ. An introduction to recursive partitioning using the RPART routines. Technical Report 61, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, 1997.
    • (1997)
    • Therneau, T.M.1    Atkinson, E.J.2
  • 26
    • 0033680875 scopus 로고    scopus 로고
    • Use of classification trees for association studies
    • Zhang H, Bonney G. Use of classification trees for association studies. Genet Epidemiol 2000;19:323-332.
    • (2000) Genet. Epidemiol. , vol.19 , pp. 323-332
    • Zhang, H.1    Bonney, G.2
  • 27
    • 0036589892 scopus 로고    scopus 로고
    • Case-control study of estrogen receptor gene polymorphisms in Parkinson's disease
    • Maraganore DM, Farrer MJ, McDonnell SK, et al. Case-control study of estrogen receptor gene polymorphisms in Parkinson's disease. Mov Disord 2002;17:509-512.
    • (2002) Mov. Disord. , vol.17 , pp. 509-512
    • Maraganore, D.M.1    Farrer, M.J.2    McDonnell, S.K.3
  • 29
    • 0031889945 scopus 로고    scopus 로고
    • Recursive partitioning for the identification of disease risk subgroups: A case-control study of subarachnoid hemorrhage
    • Nelson LM, Bloch DA, Longstreth WT Jr, Shi H. Recursive partitioning for the identification of disease risk subgroups: a case-control study of subarachnoid hemorrhage. J Clin Epidemiol 1998;51:199-209.
    • (1998) J. Clin. Epidemiol. , vol.51 , pp. 199-209
    • Nelson, L.M.1    Bloch, D.A.2    Longstreth W.T., Jr.3    Shi, H.4
  • 31
    • 0032736005 scopus 로고    scopus 로고
    • Using recursive partitioning for exploration and follow-up of linkage and association analyses
    • Wilcox MA, Smoller JW, Lunetta KL, Neuberg D. Using recursive partitioning for exploration and follow-up of linkage and association analyses. Genet Epidemiol 1999;17(Suppl. 1):S391-S396.
    • (1999) Genet. Epidemiol. , vol.17 , Issue.SUPPL. 1
    • Wilcox, M.A.1    Smoller, J.W.2    Lunetta, K.L.3    Neuberg, D.4
  • 32
    • 0025094785 scopus 로고
    • An epidemiologic approach to gene-environment interaction
    • Ottman R. An epidemiologic approach to gene-environment interaction. Genet Epidemiol 1990;7:177-185.
    • (1990) Genet. Epidemiol. , vol.7 , pp. 177-185
    • Ottman, R.1
  • 33
    • 0031868194 scopus 로고    scopus 로고
    • The impact of gender and estrogen on striatal dopaminergic neurotoxicity
    • Miller DB, Ali SF, O'Callaghan JP, Laws SC. The impact of gender and estrogen on striatal dopaminergic neurotoxicity. Ann NY Acad Sci 1998;844:153-165.
    • (1998) Ann. NY Acad. Sci. , vol.844 , pp. 153-165
    • Miller, D.B.1    Ali, S.F.2    O'Callaghan, J.P.3    Laws, S.C.4
  • 34
    • 0031678048 scopus 로고    scopus 로고
    • Mutation, sequence analysis, and association studies of α-synuclein in Parkinson's disease
    • Parsian A, Racette B, Zhang ZH, et al. Mutation, sequence analysis, and association studies of α-synuclein in Parkinson's disease. Neurology 1998;51:1757-1759.
    • (1998) Neurology , vol.51 , pp. 1757-1759
    • Parsian, A.1    Racette, B.2    Zhang, Z.H.3
  • 35
    • 0035831303 scopus 로고    scopus 로고
    • Genetic studies in Parkinson's disease with an α-synuclein/NACP gene polymorphism in Japan
    • Izumi Y, Morino H, Oda M, et al. Genetic studies in Parkinson's disease with an α-synuclein/NACP gene polymorphism in Japan. Neurosci Lett 2001;300:125-127.
    • (2001) Neurosci. Lett. , vol.300 , pp. 125-127
    • Izumi, Y.1    Morino, H.2    Oda, M.3
  • 36
    • 18544406092 scopus 로고    scopus 로고
    • Parkinson's disease is not associated with the combined α-synuclein/apolipoprotein E susceptibility genotype
    • Khan N, Graham E, Dixon P, et al. Parkinson's disease is not associated with the combined α-synuclein/apolipoprotein E susceptibility genotype. Ann Neurol 2001;49:665-668.
    • (2001) Ann. Neurol. , vol.49 , pp. 665-668
    • Khan, N.1    Graham, E.2    Dixon, P.3
  • 37
    • 0035084663 scopus 로고    scopus 로고
    • A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation
    • Nelson MR, Kardia SLR, Ferrell RE, Sing CF. A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation. Genome Res 2001;11:458-470.
    • (2001) Genome Res. , vol.11 , pp. 458-470
    • Nelson, M.R.1    Kardia, S.L.R.2    Ferrell, R.E.3    Sing, C.F.4
  • 38
    • 0033854953 scopus 로고    scopus 로고
    • Combinations of variations in multiple genes are associated with hypertension
    • Williams SM, Addy JH, Phillips JA III, et al. Combinations of variations in multiple genes are associated with hypertension. Hypertension 2000;36:2-6.
    • (2000) Hypertension , vol.36 , pp. 2-6
    • Williams, S.M.1    Addy, J.H.2    Phillips J.A. III3
  • 39
    • 0034973569 scopus 로고    scopus 로고
    • Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer
    • Ritchie MD, Hahn LW, Roodi N, et al. Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. Am J Hum Genet 2001;69: 138-147.
    • (2001) Am. J. Hum. Genet. , vol.69 , pp. 138-147
    • Ritchie, M.D.1    Hahn, L.W.2    Roodi, N.3
  • 40
    • 0037428241 scopus 로고    scopus 로고
    • Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
    • Bonifati V, Rizzu P, van Baren MJ, et al. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science 2003;299:256-259.
    • (2003) Science , vol.299 , pp. 256-259
    • Bonifati, V.1    Rizzu, P.2    van Baren, M.J.3


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