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Volumn 8, Issue 1, 2013, Pages

Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MARKER; PRION PROTEIN; PROTEIN 14 3 3; TAU PROTEIN;

EID: 84872851444     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0054915     Document Type: Article
Times cited : (127)

References (7)
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  • 2
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    • Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion
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    • Atarashi, R.1    Satoh, K.2    Sano, K.3    Fuse, T.4    Yamaguchi, N.5
  • 3
    • 77957711945 scopus 로고    scopus 로고
    • Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt-Jakob disease
    • Satoh K, Tobiume M, Matsui Y, Mutsukura K, Nishida N, et al. (2010) Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt-Jakob disease. Lab Invest 90: 1637-1644.
    • (2010) Lab Invest , vol.90 , pp. 1637-1644
    • Satoh, K.1    Tobiume, M.2    Matsui, Y.3    Mutsukura, K.4    Nishida, N.5
  • 4
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    • Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies
    • Ladogana A, Sanchez-Juan P, Mitrová E, Green A, Cuadrado-Corrales N, et al. (2009) Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies. J Neurol 256: 1620-1628.
    • (2009) J Neurol , vol.256 , pp. 1620-1628
    • Ladogana, A.1    Sanchez-Juan, P.2    Mitrová, E.3    Green, A.4    Cuadrado-Corrales, N.5
  • 5
    • 54949126830 scopus 로고    scopus 로고
    • Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series
    • Webb TE, Poulter M, Beck J, Uphill J, Adamson G, et al. (2008) Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series. Brain 131 (Pt 10): 2632-2646.
    • (2008) Brain , vol.131 , Issue.Pt 10 , pp. 2632-2646
    • Webb, T.E.1    Poulter, M.2    Beck, J.3    Uphill, J.4    Adamson, G.5
  • 6
    • 78651246462 scopus 로고    scopus 로고
    • Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis
    • Capellari S, Strammiello R, Saverioni D, Kretzschmar H, Parchi P, (2011) Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis. Acta Neuropathol 121(1): 21-37.
    • (2011) Acta Neuropathol , vol.121 , Issue.1 , pp. 21-37
    • Capellari, S.1    Strammiello, R.2    Saverioni, D.3    Kretzschmar, H.4    Parchi, P.5
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    • Phenotypic variability of Gerstmann-Straussler-Scheinker disease is associated with prion protein heterogeneity
    • Piccardo P, Dlouhy SR, Lievens PM, Young K, Bird TD, et al. (1998) Phenotypic variability of Gerstmann-Straussler-Scheinker disease is associated with prion protein heterogeneity. J Neuropathol Exp Neuro 57(10): 979-988.
    • (1998) J Neuropathol Exp Neuro , vol.57 , Issue.10 , pp. 979-988
    • Piccardo, P.1    Dlouhy, S.R.2    Lievens, P.M.3    Young, K.4    Bird, T.D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.