메뉴 건너뛰기




Volumn 19, Issue 5, 2002, Pages 409-411

A new point mutation on exon 2 of parkin gene in Parkinson's disease

Author keywords

Parkin gene; Parkinson's disease; Point mutation; Polymerase chain reaction

Indexed keywords

DISEASES; DNA; ELECTROPHORESIS; ENZYMES; GENES;

EID: 0036800165     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (8)
  • 1
    • 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
  • 2
    • 0345490853 scopus 로고    scopus 로고
    • A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe
    • Abbas N, Lucking CB, Ricard S, et al. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. Hum Mol Genet, 1999,8: 567-574.
    • (1999) Hum Mol Genet , vol.8 , pp. 567-574
    • Abbas, N.1    Lucking, C.B.2    Ricard, S.3
  • 4
    • 0026515731 scopus 로고
    • Core assessment program for intracerebral transplantations (CAPIT)
    • Langston JW, Widner H, Goetz CG, et al. Core assessment program for intracerebral transplantations (CAPIT). Mov Dis, 1992,7: 2-13.
    • (1992) Mov Dis , vol.7 , pp. 2-13
    • Langston, J.W.1    Widner, H.2    Goetz, C.G.3
  • 5
    • 0033787310 scopus 로고    scopus 로고
    • Preliminary studies on parkin gene deletion at exons 1 to 6 in Chinese patients with praecox Parkinson's disease
    • Bai H, Shao M, Dong XM, et al. Preliminary studies on parkin gene deletion at exons 1 to 6 in Chinese patients with praecox Parkinson's disease. Chin J Med Genet, 2000,17: 323-325.
    • (2000) Chin J Med Genet , vol.17 , pp. 323-325
    • Bai, H.1    Shao, M.2    Dong, X.M.3
  • 7
    • 0033933048 scopus 로고    scopus 로고
    • Familial Parkinson's disease gene product, parkin, is a ubiquitin-protein ligase
    • Shimura H, Hattori N, Kubo S, et al. Familial Parkinson's disease gene product, parkin, is a ubiquitin-protein ligase. Nat Genet, 2000,25: 302-305.
    • (2000) Nat Genet , vol.25 , pp. 302-305
    • Shimura, H.1    Hattori, N.2    Kubo, S.3
  • 8
    • 0034700158 scopus 로고    scopus 로고
    • Parkin functions as an E2-dependent ubiquitin-protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1 Parkin functions as an E2-dependent ubiquitin-protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1
    • Zhang Y, Gao J, Chung KK, et al. Parkin functions as an E2-dependent ubiquitin-protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1 Parkin functions as an E2-dependent ubiquitin-protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1. Proc Natl Acad Sci U S A. 2000,97: 13354-13359.
    • (2000) Proc Natl Acad Sci U S A , vol.97 , pp. 13354-13359
    • Zhang, Y.1    Gao, J.2    Chung, K.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.