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Volumn 382, Issue 4, 2009, Pages 715-719

The number of octapeptide repeat affects the expression and conversion of prion protein

Author keywords

Conversion; Creutzfeldt Jakob disease; Insertional mutation; Octapeptide repeat; Prion protein

Indexed keywords

MUTANT PROTEIN; OCTAPEPTIDE; PRION PROTEIN;

EID: 64549145015     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.03.093     Document Type: Article
Times cited : (3)

References (23)
  • 3
    • 0026730281 scopus 로고
    • The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system
    • Kitamoto T., Doh-ura K., Muramoto T., Miyazono M., and Tateishi J. The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system. Am. J. Pathol. 141 (1992) 271-277
    • (1992) Am. J. Pathol. , vol.141 , pp. 271-277
    • Kitamoto, T.1    Doh-ura, K.2    Muramoto, T.3    Miyazono, M.4    Tateishi, J.5
  • 5
    • 0027258807 scopus 로고
    • Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features
    • Duchen L.W., Poulter M., and Harding A.E. Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features. Brain 116 (1993) 555-567
    • (1993) Brain , vol.116 , pp. 555-567
    • Duchen, L.W.1    Poulter, M.2    Harding, A.E.3
  • 9
    • 8844228940 scopus 로고    scopus 로고
    • Creutzfeldt-Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNP
    • Nishida Y., Sodeyama N., Toru Y., Toru S., Kitamoto T., and Mizusawa H. Creutzfeldt-Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNP. Neurology 63 (2004) 1978-1979
    • (2004) Neurology , vol.63 , pp. 1978-1979
    • Nishida, Y.1    Sodeyama, N.2    Toru, Y.3    Toru, S.4    Kitamoto, T.5    Mizusawa, H.6
  • 11
    • 0027520888 scopus 로고
    • Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells
    • Rogers M., Yehiely F., Scott M., and Prusiner S.B. Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells. Proc. Natl. Acad. Sci. USA 90 (1993) 3182-3186
    • (1993) Proc. Natl. Acad. Sci. USA , vol.90 , pp. 3182-3186
    • Rogers, M.1    Yehiely, F.2    Scott, M.3    Prusiner, S.B.4
  • 12
    • 0032496218 scopus 로고    scopus 로고
    • Abnormal properties of prion protein with insertional mutations in different cell types
    • Priola S.A., and Chesebro B. Abnormal properties of prion protein with insertional mutations in different cell types. J. Biol. Chem. 273 (1998) 11980-11985
    • (1998) J. Biol. Chem. , vol.273 , pp. 11980-11985
    • Priola, S.A.1    Chesebro, B.2
  • 16
    • 0027086835 scopus 로고
    • Chimeric prion protein expression in cultured cells and transgenic mice
    • Scott M.R., Kohler R., Foster D., and Prusiner S.B. Chimeric prion protein expression in cultured cells and transgenic mice. Protein Sci. 1 (1992) 986-997
    • (1992) Protein Sci. , vol.1 , pp. 986-997
    • Scott, M.R.1    Kohler, R.2    Foster, D.3    Prusiner, S.B.4
  • 18
    • 0028883341 scopus 로고
    • Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein
    • Hornshaw M.P., McDermott J.R., and Candy J.M. Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein. Biochem. Biophys. Res. Commun. 207 (1995) 621-629
    • (1995) Biochem. Biophys. Res. Commun. , vol.207 , pp. 621-629
    • Hornshaw, M.P.1    McDermott, J.R.2    Candy, J.M.3
  • 19
    • 0030006902 scopus 로고    scopus 로고
    • Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform
    • Lehmann S., and Harris D.A. Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform. Proc. Natl. Acad. Sci. USA 93 (1996) 5610-5614
    • (1996) Proc. Natl. Acad. Sci. USA , vol.93 , pp. 5610-5614
    • Lehmann, S.1    Harris, D.A.2
  • 20
    • 0032427904 scopus 로고    scopus 로고
    • Neurological illness in transgenic mice expressing a prion protein with an insertional mutation
    • Chiesa R., Piccardo P., Ghetti B., and Harris D.A. Neurological illness in transgenic mice expressing a prion protein with an insertional mutation. Neuron 21 (1998) 1339-1351
    • (1998) Neuron , vol.21 , pp. 1339-1351
    • Chiesa, R.1    Piccardo, P.2    Ghetti, B.3    Harris, D.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.