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Volumn 26, Issue 13, 2011, Pages 2415-2417

The PLA2G6 gene in early-onset Parkinson's disease

Author keywords

Genetics; NBIA; PARK14; Parkinson syndrome; SNP

Indexed keywords

LEVODOPA;

EID: 81955160792     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.23851     Document Type: Article
Times cited : (27)

References (19)
  • 1
    • 53749096620 scopus 로고    scopus 로고
    • Genetics of iron regulation and the possible role of iron in Parkinson's disease
    • Rhodes SL, Ritz B. Genetics of iron regulation and the possible role of iron in Parkinson's disease. Neurobiol Dis. 2008; 32: 183-195.
    • (2008) Neurobiol Dis. , vol.32 , pp. 183-195
    • Rhodes, S.L.1    Ritz, B.2
  • 2
    • 68649112842 scopus 로고    scopus 로고
    • Oxidative and nitrosative stress in Parkinson's disease
    • Tsang AH, Chung KK. Oxidative and nitrosative stress in Parkinson's disease. Biochim Biophys Acta. 2009; 1792: 643-650.
    • (2009) Biochim Biophys Acta. , vol.1792 , pp. 643-650
    • Tsang, A.H.1    Chung, K.K.2
  • 3
    • 50949124960 scopus 로고    scopus 로고
    • Phospholipase A(2), reactive oxygen species, and lipid peroxidation in CNS pathologies
    • Adibhatla RM, Hatcher JF. Phospholipase A(2), reactive oxygen species, and lipid peroxidation in CNS pathologies. BMB Rep. 2008; 41: 560-567.
    • (2008) BMB Rep. , vol.41 , pp. 560-567
    • Adibhatla, R.M.1    Hatcher, J.F.2
  • 4
    • 33745553895 scopus 로고    scopus 로고
    • PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron
    • Morgan NV, Westaway SK, Morton JE, et al. PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron. Nat Genet. 2006; 38: 752-754.
    • (2006) Nat Genet. , vol.38 , pp. 752-754
    • Morgan, N.V.1    Westaway, S.K.2    Morton, J.E.3
  • 5
    • 42949158281 scopus 로고    scopus 로고
    • Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)
    • Kurian MA, Morgan NV, MacPherson L, et al. Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN). Neurology. 2008; 70: 1623-1629.
    • (2008) Neurology. , vol.70 , pp. 1623-1629
    • Kurian, M.A.1    Morgan, N.V.2    MacPherson, L.3
  • 6
    • 60849121924 scopus 로고    scopus 로고
    • Characterization of PLA2G6 as a locus for dystonia-parkinsonism
    • Paisan-Ruiz C, Bhatia KP, Li A, et al. Characterization of PLA2G6 as a locus for dystonia-parkinsonism. Ann Neurol. 2009; 65: 19-23.
    • (2009) Ann Neurol. , vol.65 , pp. 19-23
    • Paisan-Ruiz, C.1    Bhatia, K.P.2    Li, A.3
  • 7
    • 77953512439 scopus 로고    scopus 로고
    • Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations
    • Paisan-Ruiz C, Guevara R, Federoff M, et al. Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations. Mov Disord. 2010; 25: 1791-1800.
    • (2010) Mov Disord. , vol.25 , pp. 1791-1800
    • Paisan-Ruiz, C.1    Guevara, R.2    Federoff, M.3
  • 8
    • 57449083599 scopus 로고    scopus 로고
    • R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian family
    • Sina F, Shojaee S, Elahi E, Paisan-Ruiz C. R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian family. Eur J Neurol. 2009; 16: 101-104.
    • (2009) Eur J Neurol. , vol.16 , pp. 101-104
    • Sina, F.1    Shojaee, S.2    Elahi, E.3    Paisan-Ruiz, C.4
  • 9
    • 77958570876 scopus 로고    scopus 로고
    • Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism
    • Yoshino H, Tomiyama H, Tachibana N, et al. Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism. Neurology. 2010; 75: 1356-1361.
    • (2010) Neurology. , vol.75 , pp. 1356-1361
    • Yoshino, H.1    Tomiyama, H.2    Tachibana, N.3
  • 10
    • 77649316334 scopus 로고    scopus 로고
    • PLA2G6 mutations and Parkinson's disease
    • Tan EK, Ho P, Tan L, et al. PLA2G6 mutations and Parkinson's disease. Ann Neurol. 2010; 67: 148.
    • (2010) Ann Neurol. , vol.67 , pp. 148
    • Tan, E.K.1    Ho, P.2    Tan, L.3
  • 11
    • 33644971837 scopus 로고    scopus 로고
    • Epidemiological, clinical, and genetic characteristics of early-onset parkinsonism
    • Schrag A, Schott JM. Epidemiological, clinical, and genetic characteristics of early-onset parkinsonism. Lancet Neurol. 2006; 5: 355-363.
    • (2006) Lancet Neurol. , vol.5 , pp. 355-363
    • Schrag, A.1    Schott, J.M.2
  • 12
    • 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
  • 13
    • 2442668926 scopus 로고    scopus 로고
    • Hereditary early-onset Parkinson's disease caused by mutations in PINK1
    • Valente EM, Abou-Sleiman PM, Caputo V, et al. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science. 2004; 304: 1158-1160.
    • (2004) Science. , vol.304 , pp. 1158-1160
    • Valente, E.M.1    Abou-Sleiman, P.M.2    Caputo, V.3
  • 14
    • 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
  • 15
    • 33750984553 scopus 로고    scopus 로고
    • Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's disease
    • Möller JC, Leinweber B, Rissling I, et al. Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's disease. Mov Disord. 2006; 10: 1789-1792.
    • (2006) Mov Disord. , vol.10 , pp. 1789-1792
    • Möller, J.C.1    Leinweber, B.2    Rissling, I.3
  • 16
    • 0026514953 scopus 로고
    • Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases
    • Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological 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
  • 17
    • 81955165239 scopus 로고    scopus 로고
    • BLAST
    • BLAST. .
  • 19
    • 70350002152 scopus 로고    scopus 로고
    • DJ-1 and prevention of oxidative stress in Parkinson's disease and other age-related disorders
    • Kahle PJ, Waak J, Gasser T. DJ-1 and prevention of oxidative stress in Parkinson's disease and other age-related disorders. Free Radic Biol Med. 2009; 47: 1354-1361.
    • (2009) Free Radic Biol Med. , vol.47 , pp. 1354-1361
    • Kahle, P.J.1    Waak, J.2    Gasser, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.