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Volumn 64, Issue 5, 2005, Pages 905-907

Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

EID: 14644435705     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000152837.82388.DE     Document Type: Article
Times cited : (40)

References (10)
  • 2
  • 3
    • 0029905230 scopus 로고    scopus 로고
    • Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease
    • Mastrianni JA, Iannicola C, Myers RM, DeArmond S, Prusiner SB. Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease. Neurology 1996;47:1305-1312.
    • (1996) Neurology , vol.47 , pp. 1305-1312
    • Mastrianni, J.A.1    Iannicola, C.2    Myers, R.M.3    DeArmond, S.4    Prusiner, S.B.5
  • 4
    • 0032816292 scopus 로고    scopus 로고
    • Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
    • Parchi P, Giese A, Capellari S, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999;6:224-233.
    • (1999) Ann Neurol , vol.6 , pp. 224-233
    • Parchi, P.1    Giese, A.2    Capellari, S.3
  • 5
    • 1942533390 scopus 로고    scopus 로고
    • Sc core generated by protease digestion: Implications for strain typing and molecular classification of CJD
    • Sc core generated by protease digestion: implications for strain typing and molecular classification of CJD. J Biol Chem 2004;279:16797-16804.
    • (2004) J Biol Chem , vol.279 , pp. 16797-16804
    • Notari, S.1    Capellari, S.2    Giese, A.3
  • 6
    • 0030768832 scopus 로고    scopus 로고
    • Allelic origin of the abnormal prion protein isoform in familial prion diseases
    • Chen SG, Parchi P, Brown P, et al. Allelic origin of the abnormal prion protein isoform in familial prion diseases. Nat Med 1997;9:1009-1015.
    • (1997) Nat Med , vol.9 , pp. 1009-1015
    • Chen, S.G.1    Parchi, P.2    Brown, P.3
  • 7
    • 0037317208 scopus 로고    scopus 로고
    • Prion protein allotype profiling by mass spectroscopy
    • Schininà ME, Maras B, Cardone F, et al. Prion protein allotype profiling by mass spectroscopy. Pure Appl Chem 2003;75:317-323.
    • (2003) Pure Appl Chem , vol.75 , pp. 317-323
    • Schininà, M.E.1    Maras, B.2    Cardone, F.3
  • 8
    • 0141577720 scopus 로고    scopus 로고
    • Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease
    • Zou WQ, Capellari S, Parchi P, Sy MS, Gambetti P, Chen SG. Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease. J Biol Chem 2003;278:40429-40436.
    • (2003) J Biol Chem , vol.278 , pp. 40429-40436
    • Zou, W.Q.1    Capellari, S.2    Parchi, P.3    Sy, M.S.4    Gambetti, P.5    Chen, S.G.6
  • 9
    • 0030902421 scopus 로고    scopus 로고
    • Identification of the prion protein allotypes which accumulate in the brain of sporadic and familial Creutzfeldt-Jakob disease patients
    • Silvestrini MC, Cardone F, Maras B, et al. Identification of the prion protein allotypes which accumulate in the brain of sporadic and familial Creutzfeldt-Jakob disease patients. Nat Med 1997;3:521-525.
    • (1997) Nat Med , vol.3 , pp. 521-525
    • Silvestrini, M.C.1    Cardone, F.2    Maras, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.