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Volumn 16, Issue 8, 2009, Pages 909-911

GRN 3′UTR+78 C>T is not associated with risk for Parkinson's disease

Author keywords

Genetics; GRN; MiRNA; Parkinson's disease; Rs5848; SNP

Indexed keywords

MICRORNA; PROGRANULIN; GRN PROTEIN, HUMAN; SIGNAL PEPTIDE;

EID: 67651250941     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2009.02621.x     Document Type: Article
Times cited : (9)

References (18)
  • 1
    • 0021219372 scopus 로고
    • Epidemiology of parkinsonism: Incidence, classification, and mortality
    • Rajput AH, Offord KP, Beard CM, Kurland LT. Epidemiology of parkinsonism: incidence, classification, and mortality. Ann Neurol 1984 16 : 278 282.
    • (1984) Ann Neurol , vol.16 , pp. 278-282
    • Rajput, A.H.1    Offord, K.P.2    Beard, C.M.3    Kurland, L.T.4
  • 2
    • 0037058799 scopus 로고    scopus 로고
    • Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)
    • Tsuboi Y, Baker M, Hutton ML, et al. Clinical and genetic studies of families with the tau N279K mutation (FTDP-17). Neurology 2002 59 : 1791 1793.
    • (2002) Neurology , vol.59 , pp. 1791-1793
    • Tsuboi, Y.1    Baker, M.2    Hutton, M.L.3
  • 3
    • 39749153296 scopus 로고    scopus 로고
    • Prominent phenotypic variability associated with mutations in progranulin
    • Oct 18. [Epub ahead of print].
    • Kelley BJ, Haidar W, Boeve BF, et al. Prominent phenotypic variability associated with mutations in progranulin. Neurobiol Aging 2007. Oct 18. [Epub ahead of print].
    • (2007) Neurobiol Aging
    • Kelley, B.J.1    Haidar, W.2    Boeve, B.F.3
  • 4
    • 48249102700 scopus 로고    scopus 로고
    • Haplotypes and gene expression implicate the MAPT region for Parkinson disease: The GenePD Study
    • Tobin JE, Latourelle JC, Lew MF, et al. Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology 2008 71 : 28 34.
    • (2008) Neurology , vol.71 , pp. 28-34
    • Tobin, J.E.1    Latourelle, J.C.2    Lew, M.F.3
  • 5
    • 4544297675 scopus 로고    scopus 로고
    • Linkage disequilibrium and association of MAPT H1 in Parkinson disease
    • Skipper L, Wilkes K, Toft M, et al. Linkage disequilibrium and association of MAPT H1 in Parkinson disease. Am J Hum Genet 2004 75 : 669 677.
    • (2004) Am J Hum Genet , vol.75 , pp. 669-677
    • Skipper, L.1    Wilkes, K.2    Toft, M.3
  • 7
    • 45049084534 scopus 로고    scopus 로고
    • Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease
    • Rovelet-Lecrux A, Deramecourt V, Legallic S, et al. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease. Neurobiology Dis 2008 31 : 41 45.
    • (2008) Neurobiology Dis , vol.31 , pp. 41-45
    • Rovelet-Lecrux, A.1    Deramecourt, V.2    Legallic, S.3
  • 8
    • 35348872039 scopus 로고    scopus 로고
    • Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
    • Brouwers N, Nuytemans K, van der Zee J, et al. Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family. Arch Neurol 2007 64 : 1436 1446.
    • (2007) Arch Neurol , vol.64 , pp. 1436-1446
    • Brouwers, N.1    Nuytemans, K.2    Van Der Zee, J.3
  • 9
    • 56049083010 scopus 로고    scopus 로고
    • Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
    • Rademakers R, Eriksen JL, Baker M, et al. Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia. Hum Mol Genet 2008 17 : 3631 3642.
    • (2008) Hum Mol Genet , vol.17 , pp. 3631-3642
    • Rademakers, R.1    Eriksen, J.L.2    Baker, M.3
  • 10
    • 37349008891 scopus 로고    scopus 로고
    • Progranulin: Normal function and role in neurodegeneration
    • Eriksen JL, Mackenzie IR. Progranulin: normal function and role in neurodegeneration. J Neurochem 2008 104 : 287 297.
    • (2008) J Neurochem , vol.104 , pp. 287-297
    • Eriksen, J.L.1    MacKenzie, I.R.2
  • 11
    • 0032937059 scopus 로고    scopus 로고
    • Diagnostic criteria for Parkinson disease
    • Gelb DJ, Oliver E, Gilman S. Diagnostic criteria for Parkinson disease. Arch Neurol 1999 56 : 33 39.
    • (1999) Arch Neurol , vol.56 , pp. 33-39
    • Gelb, D.J.1    Oliver, E.2    Gilman, S.3
  • 12
    • 55249086715 scopus 로고    scopus 로고
    • Progranulin variability has no major role in Parkinson disease genetic etiology
    • Nuytemans K, Pals P, Sleegers K, et al. Progranulin variability has no major role in Parkinson disease genetic etiology. Neurology 2008 71 : 1147 1151.
    • (2008) Neurology , vol.71 , pp. 1147-1151
    • Nuytemans, K.1    Pals, P.2    Sleegers, K.3
  • 13
    • 42049120518 scopus 로고    scopus 로고
    • Progranulin genetic variability contributes to amyotrophic lateral sclerosis
    • Sleegers K, Brouwers N, Maurer-Stroh S, et al. Progranulin genetic variability contributes to amyotrophic lateral sclerosis. Neurology 2008 71 : 253 259.
    • (2008) Neurology , vol.71 , pp. 253-259
    • Sleegers, K.1    Brouwers, N.2    Maurer-Stroh, S.3
  • 15
    • 38349186896 scopus 로고    scopus 로고
    • MicroRNAs (miRNAs) in neurodegenerative diseases
    • Nelson PT, Wang WX, Rajeev BW. MicroRNAs (miRNAs) in neurodegenerative diseases. Brain Pathol 2008 18 : 130 138.
    • (2008) Brain Pathol , vol.18 , pp. 130-138
    • Nelson, P.T.1    Wang, W.X.2    Rajeev, B.W.3
  • 16
    • 48949092066 scopus 로고    scopus 로고
    • Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
    • Ross OA, Wu YR, Lee MC, et al. Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease. Ann Neurol 2008 64 : 88 92.
    • (2008) Ann Neurol , vol.64 , pp. 88-92
    • Ross, O.A.1    Wu, Y.R.2    Lee, M.C.3
  • 17
    • 33746869343 scopus 로고    scopus 로고
    • Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease
    • Maraganore DM, de Andrade M, Elbaz A, et al. Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. J Am Med Assoc 2006 296 : 661 670.
    • (2006) J Am Med Assoc , vol.296 , pp. 661-670
    • Maraganore, D.M.1    De Andrade, M.2    Elbaz, A.3
  • 18
    • 33746079596 scopus 로고    scopus 로고
    • A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan
    • Di Fonzo A, Wu-Chou YH, Lu CS, et al. A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. Neurogenetics 2006 7 : 133 138.
    • (2006) Neurogenetics , vol.7 , pp. 133-138
    • Di Fonzo, A.1    Wu-Chou, Y.H.2    Lu, C.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.