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TY  - JOUR
AU  - Caughey, B.
AU  - Chesebro, B.
TI  - Prion protein and the transmissible spongiform encephalopathies
JO  - Trends Biol. Sci.
PY  - 1997///
VL  - 7
SP  - 56
EP  - 62
M3  - 10.1016/S0962-8924(96)10054-4
N1  - 10.1016/S0962-8924(96)10054-4
UR  - http://dx.doi.org/10.1016/S0962-8924(96)10054-4
ER  - 

TY  - JOUR
AU  - Griffith, J.S.
TI  - Self-replication and scrapie
JO  - Nature
PY  - 1967///
VL  - 215
SP  - 1043
EP  - 1044
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TY  - JOUR
AU  - Prusiner, S.B.
TI  - Novel proteinaceous infectious particles cause scrapie
JO  - Science
PY  - 1982///
VL  - 216
SP  - 136
EP  - 144
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TY  - JOUR
AU  - Gajdusek, D.C.
TI  - Transmissible and nontransmissible amyloidoses: Autocatalytic post-translational conversion of host precursor proteins to beta-pleated configurations
JO  - J. Neuroimmunol.
PY  - 1988///
VL  - 20
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M3  - 10.1016/0165-5728(88)90140-3
N1  - 10.1016/0165-5728(88)90140-3
UR  - http://dx.doi.org/10.1016/0165-5728(88)90140-3
ER  - 

TY  - JOUR
AU  - Hsiao, K.K.
TI  - Spontaneous neurodegeneration in transgenic mice with mutant prion protein
JO  - Science
PY  - 1990///
VL  - 250
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EP  - 1590
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TY  - JOUR
AU  - Westaway, D.
TI  - Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
JO  - Cell
PY  - 1994///
VL  - 76
SP  - 117
EP  - 129
M3  - 10.1016/0092-8674(94)90177-5
N1  - 10.1016/0092-8674(94)90177-5
UR  - http://dx.doi.org/10.1016/0092-8674(94)90177-5
ER  - 

TY  - JOUR
AU  - Hsiao, K.K.
TI  - Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein
JO  - Proc. Natl. Acad. Sci. USA
PY  - 1994///
VL  - 91
SP  - 9126
EP  - 9130
ER  - 

TY  - JOUR
AU  - Brown, P.
TI  - Human spongiform encephalopathy: The National Institutes of Health series of 300 cases of experimentally transmitted disease
JO  - Ann. Neurol.
PY  - 1994///
VL  - 35
SP  - 513
EP  - 529
ER  - 

TY  - JOUR
AU  - Silvestrini, M.C.
TI  - Identification of the prion protein allotypes that accumulate in the brain of sporadic and familial Creutzfeldt-jakob disease patients
JO  - Nature Med.
PY  - 1997///
VL  - 3
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EP  - 525
M3  - 10.1038/nm0597-521
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UR  - http://dx.doi.org/10.1038/nm0597-521
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TY  - JOUR
AU  - Tagliavini, F.
TI  - Amyloid fibrils in Gerstmann-Straussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele
JO  - Cell
PY  - 1994///
VL  - 79
SP  - 695
EP  - 703
ER  - 

TY  - JOUR
AU  - Barbanti, P.
TI  - Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Straussler-Scheinker disease (PrP-P102L mutation)
JO  - Neurology
PY  - 1996///
VL  - 47
SP  - 734
EP  - 741
ER  - 

TY  - JOUR
AU  - Gabizon, R.
TI  - Insoluble wild-type and protease-resistant mutant protein in brains of patients with inherited prion disease
JO  - Nature Med.
PY  - 1996///
VL  - 2
SP  - 59
EP  - 64
M3  - 10.1038/nm0196-59
N1  - 10.1038/nm0196-59
UR  - http://dx.doi.org/10.1038/nm0196-59
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TY  - JOUR
AU  - Kitamoto, T.
AU  - Yamaguchi, K.
AU  - Doh-ura, K.
AU  - Tateishi, J.
TI  - A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann-Straussler syndrome
JO  - Neurology
PY  - 1991///
VL  - 41
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EP  - 310
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TY  - GEN
AU  - Young, N.S.
TI  - Fields Virology
PY  - 1996///
ER  - 

TY  - JOUR
AU  - Goldfarb, L.G.
TI  - Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families
JO  - Eur. J. Epidemiol.
PY  - 1991///
VL  - 7
SP  - 477
EP  - 486
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TY  - JOUR
AU  - Pocchiari, M.
TI  - A new point mutation of the prion protein gene in Creutzfeldt-jakob disease
JO  - Ann. Neural.
PY  - 1993///
VL  - 34
SP  - 802
EP  - 807
ER  - 

