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Volumn 20, Issue 3, 2013, Pages 584-587

Genetic analysis of NR4A2 gene in a large population of Han Chinese patients with Parkinson's disease

Author keywords

Genetic analysis; NR4A2 gene; Parkinson's disease

Indexed keywords

NUCLEAR RECEPTOR RELATED FACTOR 1;

EID: 84874000386     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2012.03824.x     Document Type: Article
Times cited : (15)

References (11)
  • 1
    • 63049089544 scopus 로고    scopus 로고
    • A Nurr1 pathway for neuroprotection
    • Bensinger SJ, Tontonoz P. A Nurr1 pathway for neuroprotection. Cell 2009; 137: 26-28.
    • (2009) Cell , vol.137 , pp. 26-28
    • Bensinger, S.J.1    Tontonoz, P.2
  • 2
    • 0032874648 scopus 로고    scopus 로고
    • Nurr1, an orphan nuclear receptor, is a transcriptional activator of endogenous tyrosine hydroxylase in neural progenitor cells derived from the adult brain
    • Sakurada K, Ohshima-Sakurada M, Palmer TD, Gage FH. Nurr1, an orphan nuclear receptor, is a transcriptional activator of endogenous tyrosine hydroxylase in neural progenitor cells derived from the adult brain. Development 1999; 126: 4017-4026.
    • (1999) Development , vol.126 , pp. 4017-4026
    • Sakurada, K.1    Ohshima-Sakurada, M.2    Palmer, T.D.3    Gage, F.H.4
  • 3
    • 0037177097 scopus 로고    scopus 로고
    • Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson's disease
    • Xu PY, Liang R, Jankovic J, et al. Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson's disease. Neurology 2002; 58: 881-884.
    • (2002) Neurology , vol.58 , pp. 881-884
    • Xu, P.Y.1    Liang, R.2    Jankovic, J.3
  • 4
    • 0037226797 scopus 로고    scopus 로고
    • Mutations in NR4A2 associated with familial Parkinson disease
    • Le WD, Xu P, Jankovic J, et al. Mutations in NR4A2 associated with familial Parkinson disease. Nat Genet 2003; 33: 85-89.
    • (2003) Nat Genet , vol.33 , pp. 85-89
    • Le, W.D.1    Xu, P.2    Jankovic, J.3
  • 5
    • 0038326633 scopus 로고    scopus 로고
    • A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease
    • Zheng K, Heydari B, Simon DK, Zheng K, Heydari B, Simon DK. A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease. Arch Neurol 2003; 60: 722-725.
    • (2003) Arch Neurol , vol.60 , pp. 722-725
    • Zheng, K.1    Heydari, B.2    Simon, D.K.3    Zheng, K.4    Heydari, B.5    Simon, D.K.6
  • 6
    • 33746916754 scopus 로고    scopus 로고
    • Translated mutation in the Nurr1 gene as a cause for Parkinson's disease
    • Grimes DA, Han F, Panisset M, et al. Translated mutation in the Nurr1 gene as a cause for Parkinson's disease. Mov Disord 2006; 21: 906-909.
    • (2006) Mov Disord , vol.21 , pp. 906-909
    • Grimes, D.A.1    Han, F.2    Panisset, M.3
  • 7
    • 34547145165 scopus 로고    scopus 로고
    • G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences
    • Faul F, Erdfelder E, Lang AG, Buchner A. G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods 2007; 39: 175-191.
    • (2007) Behav Res Methods , vol.39 , pp. 175-191
    • Faul, F.1    Erdfelder, E.2    Lang, A.G.3    Buchner, A.4
  • 9
    • 11144354907 scopus 로고    scopus 로고
    • Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease
    • Hering R, Petrovic S, Mietz EM, et al. Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease. Neurology 2004; 62: 1231-1232.
    • (2004) Neurology , vol.62 , pp. 1231-1232
    • Hering, R.1    Petrovic, S.2    Mietz, E.M.3
  • 10
    • 33845205797 scopus 로고    scopus 로고
    • NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach
    • Healy DG, Abou-Sleiman PM, Ahmadi KR, et al. NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach. Mov Disord 2006; 21: 1960-1963.
    • (2006) Mov Disord , vol.21 , pp. 1960-1963
    • Healy, D.G.1    Abou-Sleiman, P.M.2    Ahmadi, K.R.3
  • 11
    • 0042336994 scopus 로고    scopus 로고
    • NR4A2 mutations are rare among European patients with familial Parkinson's disease [1]
    • Wellenbrock C, Hedrich K, Schafer N, et al. NR4A2 mutations are rare among European patients with familial Parkinson's disease [1]. Annals of Neurology 2003; 54: 415.
    • (2003) Annals of Neurology , vol.54 , pp. 415
    • Wellenbrock, C.1    Hedrich, K.2    Schafer, N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.