-
1
-
-
0026583834
-
Biochemical and physical properties of the prion protein from 2 strains of the transmissible mink encephalopathy agent
-
(1992)
J. Virol.
, vol.66
, pp. 2096-2101
-
-
Bessen, R.A.1
Marsh, R.F.2
-
5
-
-
0033231290
-
Prion protein and the transmissible spongiform encephalopathy diseases
-
(1999)
Neuron
, vol.24
, pp. 503-506
-
-
Chesebro, B.1
-
12
-
-
0031456947
-
Structure of the recombinant full-length hamster prion protein PrP(29-231): The N-terminus is highly flexible
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 13452-13457
-
-
Donne, D.G.1
Viles, J.H.2
Groth, D.3
Mehlhorn, I.4
James, T.L.5
Cohen, F.E.6
Prusiner, S.B.7
Wright, P.E.8
Dyson, H.J.9
-
13
-
-
0033695126
-
Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice
-
(2000)
Neuron
, vol.27
, pp. 399-408
-
-
Flechsig, E.1
Shmerling, D.2
Hegyi, I.3
Raeber, A.J.4
Fischer, M.5
Cozzio, A.6
Von Mering, C.7
Aguzzi, A.8
Weissmann, C.9
-
15
-
-
0026496257
-
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Disease phenotype determined by a DNA polymorphism
-
(1992)
Science
, vol.258
, pp. 806-808
-
-
Goldfarb, L.G.1
-
18
-
-
0030820354
-
The same prion strain causes vCJD and BSE
-
(1997)
Nature
, vol.389
, pp. 448-450
-
-
Hill, A.F.1
Desbruslais, M.2
Joiner, S.3
Sidle, K.C.L.4
Gowland, I.5
Collinge, J.6
Doey, L.J.7
Lantos, P.8
-
20
-
-
0030878056
-
Recombinant full-length murine prion protein, mPrP(23-231): Purification and spectroscopic characterization
-
(1997)
FEBS Lett.
, vol.413
, pp. 277-281
-
-
Hornemann, S.1
Korth, C.2
Oesch, B.3
Riek, R.4
Wider, G.5
Wuthrich, K.6
Glockshuber, R.7
-
21
-
-
0024519771
-
Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome
-
(1989)
Nature
, vol.338
, pp. 342-345
-
-
Hsiao, K.1
Baker, H.F.2
Crow, T.J.3
Poulter, M.4
Owen, F.5
Terwilliger, J.D.6
Westaway, D.7
Ott, J.8
Prusiner, S.B.9
-
23
-
-
0028608963
-
Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 9126-9130
-
-
Hsiao, K.K.1
-
25
-
-
0027195933
-
Seeding 'one-dimensional crystallization' of amyloid: A pathogenic mechanism in Alzheimer's disease and scrapie?
-
(1993)
Cell
, vol.73
, pp. 1055-1058
-
-
Jarrett, J.T.1
Lansbury P.T., Jr.2
-
26
-
-
0030931519
-
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 10069-10074
-
-
Kaneko, K.1
Zulianello, L.2
Scott, M.3
Cooper, C.M.4
Wallace, A.C.5
James, T.L.6
Cohen, F.E.7
Prusiner, S.B.8
-
28
-
-
0023499868
-
Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins
-
(1987)
J. Virol.
, vol.61
, pp. 3688-3693
-
-
Kascsak, R.J.1
Rubenstein, R.2
Merz, P.A.3
Tonnademasi, M.4
Fersko, R.5
Carp, R.I.6
Wisniewski, H.M.7
Diringer, H.8
-
34
-
-
0033485260
-
A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy
-
(1999)
EMBO J.
, vol.18
, pp. 6855-6864
-
-
Manson, J.C.1
-
35
-
-
0031942579
-
Mice with gene targetted prion protein alterations show that Prnp, Sinc and Prni are congruent
-
(1998)
Nature Genet.
, vol.18
, pp. 118-125
-
-
Moore, R.C.1
Hope, J.2
McBride, P.A.3
McConnell, I.4
Selfridge, J.5
Melton, D.W.6
Manson, J.C.7
-
38
-
-
0015240315
-
Molecular weight determination of protein-dodecyl sulfate complexes by gel electrophoresis in a discontinuous buffer system
-
(1971)
J. Biol. Chem.
, vol.246
, pp. 6328-6334
-
-
Neville, D.M.1
-
40
-
-
0031592937
-
A conformational transition at the N-terminus of the prion protein features in formation of the scrapie isoform
-
(1997)
J. Mol. Biol.
, vol.273
, pp. 614-622
-
-
Peretz, D.1
-
41
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
45
-
-
0025244011
-
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
-
(1990)
Cell
, vol.63
, pp. 673-686
-
-
Prusiner, S.B.1
-
46
-
-
0034282971
-
Evidence of a molecular barrier limiting susceptibility of humans, cattle and sheep to chronic wasting disease
-
(2000)
EMBO J.
, vol.19
, pp. 4425-4430
-
-
Raymond, G.J.1
-
48
-
-
0031720905
-
Eight prion strains have PrPSc molecules with different conformations
-
(1998)
Nature Med.
, vol.4
, pp. 1157-1165
-
-
Safar, J.1
Wille, H.2
Itrri, V.3
Groth, D.4
Serban, H.5
Torchia, M.6
Cohen, F.E.7
Prusiner, S.B.8
-
49
-
-
0024820814
-
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
-
(1989)
Cell
, vol.59
, pp. 847-857
-
-
Scott, M.1
-
53
-
-
0035152345
-
Identification of two prion protein regions that modify scrapie incubation time
-
(2001)
J. Virol.
, vol.75
, pp. 1408-1413
-
-
Supattapone, S.1
Muramoto, T.2
Legname, G.3
Mehlhorn, I.4
Cohen, F.E.5
DeArmond, S.J.6
Prusiner, S.B.7
Scott, M.R.8
-
54
-
-
0028882424
-
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
-
(1995)
Cell
, vol.83
, pp. 79-90
-
-
Telling, G.C.1
Scott, M.2
Mastrianni, J.3
Gabizon, R.4
Torchia, M.5
Cohen, F.E.6
Dearmond, S.J.7
Prusiner, S.B.8
-
56
-
-
12644272790
-
Evidence for the conformation of the pathological isoform of the prion protein enciphering and propagating prion diversity
-
(1996)
Science
, vol.274
, pp. 2079-2082
-
-
Telling, G.C.1
-
57
-
-
0030600139
-
Molecular biology of transmissible spongiform encephalopathies
-
(1996)
FEBS Lett.
, vol.389
, pp. 3-11
-
-
Weissmann, C.1
-
58
-
-
0025850771
-
Paradoxical shortening of scrapie incubation times by expression of prion protein transgenes derived from long incubation period mice
-
(1991)
Neuron
, vol.7
, pp. 59-68
-
-
Westaway, D.1
|