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Volumn 17, Issue 12, 2010, Pages 1479-1481

Genetic analysis of LRRK2 functional domains in Brazilian patients with Parkinson's disease

Author keywords

LRRK2; MAPKKK; Parkinson's disease; ROC

Indexed keywords

LEUCINE RICH REPEAT KINASE 2;

EID: 78649610022     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2010.03039.x     Document Type: Article
Times cited : (15)

References (9)
  • 2
    • 33745034020 scopus 로고    scopus 로고
    • Parkinson's disease: the genetics of a heterogeneous disorder
    • Gosal D, Ross OA, Toft M. Parkinson's disease: the genetics of a heterogeneous disorder. Eur J Neurol 2006; 13: 616-627.
    • (2006) Eur J Neurol , vol.13 , pp. 616-627
    • Gosal, D.1    Ross, O.A.2    Toft, M.3
  • 3
    • 39149100952 scopus 로고    scopus 로고
    • A study of LRRK2 mutations and Parkinson's disease in Brazil
    • Pimentel MM, Moura KC, Abdalla CB, et al. A study of LRRK2 mutations and Parkinson's disease in Brazil. Neurosci Lett 2008; 433: 17-21.
    • (2008) Neurosci Lett , vol.433 , pp. 17-21
    • Pimentel, M.M.1    Moura, K.C.2    Abdalla, C.B.3
  • 4
    • 19944431081 scopus 로고    scopus 로고
    • Italian Parkinson Genetics Network, A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
    • Di Fonzo A, Rohé CF, Ferreira J, et al. Italian Parkinson Genetics Network, A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet 2005; 365: 412-415.
    • (2005) Lancet , vol.365 , pp. 412-415
    • Di Fonzo, A.1    Rohé, C.F.2    Ferreira, J.3
  • 5
    • 33750941013 scopus 로고    scopus 로고
    • LRRK2 mutations in a clinic-based cohort of Parkinson's disease
    • Scholz S, Mandel RJ, Fernandez HH, et al. LRRK2 mutations in a clinic-based cohort of Parkinson's disease. Eur J Neurol 2006; 13: 1298-1301.
    • (2006) Eur J Neurol , vol.13 , pp. 1298-1301
    • Scholz, S.1    Mandel, R.J.2    Fernandez, H.H.3
  • 6
    • 67650501546 scopus 로고    scopus 로고
    • French Parkinson's Disease Genetics Study Group, Molecular analyses of the LRRK2 gene in European and North-African autosomal dominant Parkinson's disease
    • Lesage S, Condroyer C, Lannuzel A, et al. French Parkinson's Disease Genetics Study Group, Molecular analyses of the LRRK2 gene in European and North-African autosomal dominant Parkinson's disease. J Med Genet 2009; 46: 458-464.
    • (2009) J Med Genet , vol.46 , pp. 458-464
    • Lesage, S.1    Condroyer, C.2    Lannuzel, A.3
  • 7
    • 40349101849 scopus 로고    scopus 로고
    • Structure of the ROC domain from the Parkinson's disease-associated leucine-rich repeat kinase 2 reveals a dimeric GTPase
    • Deng J, Lewis PA, Greggio E, Sluch E, Beilina A, Cookson MR. Structure of the ROC domain from the Parkinson's disease-associated leucine-rich repeat kinase 2 reveals a dimeric GTPase. Proc Natl Acad Sci USA 2008; 105: 1499-1504.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 1499-1504
    • Deng, J.1    Lewis, P.A.2    Greggio, E.3    Sluch, E.4    Beilina, A.5    Cookson, M.R.6
  • 8
    • 72749105819 scopus 로고    scopus 로고
    • Identification of the Autophosphorylation Sites of LRRK2
    • Kamikawaji S, Ito G, Iwatsubo T. Identification of the Autophosphorylation Sites of LRRK2. Biochemistry 2009; 48: 10963-10975.
    • (2009) Biochemistry , vol.48 , pp. 10963-10975
    • Kamikawaji, S.1    Ito, G.2    Iwatsubo, T.3
  • 9
    • 41049086705 scopus 로고    scopus 로고
    • Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients
    • Nuytemans K, Rademakers R, Theuns J, et al. Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients. Eur J Hum Genet 2008; 16: 471-479.
    • (2008) Eur J Hum Genet , vol.16 , pp. 471-479
    • Nuytemans, K.1    Rademakers, R.2    Theuns, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.