메뉴 건너뛰기




Volumn 15, Issue 8, 2008, Pages 827-830

M129V polymorphism in the prion protein gene is not associated with mesial temporal lobe epilepsy in a Han Chinese population

Author keywords

Association; Han chinese; M129V; Mesial temporal lobe epilepsy; Prion protein

Indexed keywords

PRION PROTEIN; PRNP PROTEIN, HUMAN;

EID: 54549092066     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2008.02191.x     Document Type: Article
Times cited : (6)

References (21)
  • 2
    • 0030786717 scopus 로고    scopus 로고
    • Prion research: The next frontiers
    • Aguzzi A, Weissmann C. Prion research: the next frontiers. Nature 1997; 389: 795-798.
    • (1997) Nature , vol.389 , pp. 795-798
    • Aguzzi, A.1    Weissmann, C.2
  • 4
    • 0033570367 scopus 로고    scopus 로고
    • Evidence of presynaptic localization and function of the prion protein
    • Herms J, Tings T, Gall S, et al. Evidence of presynaptic localization and function of the prion protein. Journal of Neuroscience 1999; 19: 8866-8875.
    • (1999) Journal of Neuroscience , vol.19 , pp. 8866-8875
    • Herms, J.1    Tings, T.2    Gall, S.3
  • 6
    • 0036625255 scopus 로고    scopus 로고
    • Cellular priron protein: Implication in seizures and epilepsy
    • Walz R, Castro RMRPS, Velasco TR, et al. Cellular priron protein: implication in seizures and epilepsy. Cellular and Molecular Neurobiology 2002; 22: 249-257.
    • (2002) Cellular and Molecular Neurobiology , vol.22 , pp. 249-257
    • Walz, R.1    RMRPS, C.2    Velasco, T.R.3
  • 7
    • 0032806450 scopus 로고    scopus 로고
    • Increased sensitivity to seizures in mice lacking cellular prion protein
    • Walz R, Amaral OB, Rockenbach IC, et al. Increased sensitivity to seizures in mice lacking cellular prion protein. Epilepsia 1999; 40: 1679-1682.
    • (1999) Epilepsia , vol.40 , pp. 1679-1682
    • Walz, R.1    Amaral, O.B.2    Rockenbach, I.C.3
  • 8
    • 34548331735 scopus 로고    scopus 로고
    • Enhanced susceptibility of Prnp-deficient mice to kainate-induced seizures, neuronal apoptosis, and death: Role of AMPA/kainate receptors
    • Rangel A, Burgaya F, Gavin R, Soriano E, Aguzzi A, Del Rio JA. Enhanced susceptibility of Prnp-deficient mice to kainate-induced seizures, neuronal apoptosis, and death: role of AMPA/kainate receptors. Journal of Neuroscience Research 2007; 85: 2741-2755.
    • (2007) Journal of Neuroscience Research , vol.85 , pp. 2741-2755
    • Rangel, A.1    Burgaya, F.2    Gavin, R.3    Soriano, E.4    Aguzzi, A.5    Del Rio, J.A.6
  • 9
    • 3543054070 scopus 로고    scopus 로고
    • Cortical malformations are associated with a rare polymorphism of cellular prion protein
    • Walz R, Castro RM, Landemberger MC, et al. Cortical malformations are associated with a rare polymorphism of cellular prion protein. Neurology 2004; 63: 557-560.
    • (2004) Neurology , vol.63 , pp. 557-560
    • Walz, R.1    Castro, R.M.2    Landemberger, M.C.3
  • 10
    • 34547636490 scopus 로고    scopus 로고
    • Correction: Cortical malformations are associated with a rare polymorphism of cellular prion protein
    • Walz R, Castro RM, Landemberger MC, et al. Correction: cortical malformations are associated with a rare polymorphism of cellular prion protein. Neurology 2007; 69: 414-416.
    • (2007) Neurology , vol.69 , pp. 414-416
    • Walz, R.1    Castro, R.M.2    Landemberger, M.C.3
  • 11
    • 85205850447 scopus 로고    scopus 로고
    • Voluntary retraction of: Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant
    • Walz R, Castro RM, Velasco TR, et al. Voluntary retraction of: surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant. Neurology 2007; 69: 405.
    • (2007) Neurology , vol.69 , pp. 405
    • Walz, R.1    Castro, R.M.2    Velasco, T.R.3
  • 12
    • 3843131903 scopus 로고    scopus 로고
    • Methionine 129 variant of human prion protein oligomerizes more rapidly than the valine 129 variant: Implications for disease susceptibility to Creutzfeldt-Jakob disease
    • Tahiri AA, Gill AC, Disterer P, James W. Methionine 129 variant of human prion protein oligomerizes more rapidly than the valine 129 variant: implications for disease susceptibility to Creutzfeldt-Jakob disease. Journal of Biological Chemistry 2004; 279: 31390-31397.
    • (2004) Journal of Biological Chemistry , vol.279 , pp. 31390-31397
    • Tahiri, A.A.1    Gill, A.C.2    Disterer, P.3    James, W.4
  • 13
    • 0025820942 scopus 로고
    • Homo-zygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease
    • Palmer MS, Dryden AJ, Hughes JT, Collinge J. Homo-zygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature 1991; 352: 340-342.
    • (1991) Nature , vol.352 , pp. 340-342
    • Palmer, M.S.1    Dryden, A.J.2    Hughes, J.T.3    Collinge, J.4
  • 14
    • 34250182052 scopus 로고    scopus 로고
    • Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women
    • Labate A, Manna I, Gambardella A, et al. Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women. Neuroscience Letters 2007; 421: 1-4.
    • (2007) Neuroscience Letters , vol.421 , pp. 1-4
    • Labate, A.1    Manna, I.2    Gambardella, A.3
  • 15
    • 0024317220 scopus 로고
    • Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy
    • ILAE, International League Against Epilepsy
    • ILAE, International League Against Epilepsy. Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy. Epilepsia 1989; 30: 389-399.
    • (1989) Epilepsia , vol.30 , pp. 389-399
  • 16
    • 0000497985 scopus 로고    scopus 로고
    • PS power and sample size program available for free on the Internet
    • Dupont WD, Plummer WD. PS power and sample size program available for free on the Internet. Controlled Clinical Trials 1997; 18: 274.
    • (1997) Controlled Clinical Trials , vol.18 , pp. 274
    • Dupont, W.D.1    Plummer, W.D.2
  • 17
    • 7944233055 scopus 로고    scopus 로고
    • Genetic association studies in epilepsy: ''the truth is out there''
    • Tan NCK, Mulley JC, Berkovic SF. Genetic association studies in epilepsy: ''the truth is out there''. Epilepsia 2004; 45: 1429-1442.
    • (2004) Epilepsia , vol.45 , pp. 1429-1442
    • Tan, N.C.K.1    Mulley, J.C.2    Berkovic, S.F.3
  • 18
    • 6444241321 scopus 로고    scopus 로고
    • Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation
    • Yu SL, Jin L, Sy MS, et al. Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation. European Journal of Human Genetics 2004; 12: 867-870.
    • (2004) European Journal of Human Genetics , vol.12 , pp. 867-870
    • Yu, S.L.1    Jin, L.2    Sy, M.S.3
  • 19
    • 0035137101 scopus 로고    scopus 로고
    • Lack of evidence to support the association of the human prion gene with schizophrenia
    • Tsai MT, Su YC, Chen YH, Chen CH. Lack of evidence to support the association of the human prion gene with schizophrenia. Molecular Psychiatry 2001; 6: 74-78.
    • (2001) Molecular Psychiatry , vol.6 , pp. 74-78
    • Tsai, M.T.1    Su, Y.C.2    Chen, Y.H.3    Chen, C.H.4
  • 20
    • 0035209184 scopus 로고    scopus 로고
    • Sporadic - but not variant - Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon1
    • Mead S, Mahal SP, Beck J, et al. Sporadic - but not variant - Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon1. The American Journal ofHuman Genetics 2001; 69: 1225-1235.
    • (2001) The American Journal ofHuman Genetics , vol.69 , pp. 1225-1235
    • Mead, S.1    Mahal, S.P.2    Beck, J.3
  • 21
    • 33947116652 scopus 로고    scopus 로고
    • Significant association of a M129V independent polymorphism in the 5́ UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study
    • Vollmert C, Windl O, Xiang W, et al. Significant association of a M129V independent polymorphism in the 5́ UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study. Journal of Medical Genetics 2006; 43: e53.
    • (2006) Journal of Medical Genetics , vol.43
    • Vollmert, C.1    Windl, O.2    Xiang, W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.