-
1
-
-
0027374785
-
Alzheimer's disease and creutzfeldt-jakob disease: Overlap of pathogenic mechanisms
-
PMID:7904883
-
DeArmond SJ. Alzheimer's disease and Creutzfeldt-Jakob disease: overlap of pathogenic mechanisms. Curr Opin Neurol 1993; 6:872-81; PMID:7904883; http://dx.doi.org/10.1097/00019052-199312000-00008.
-
(1993)
Curr Opin Neurol
, vol.6
, pp. 872-881
-
-
DeArmond, S.J.1
-
2
-
-
0021879270
-
Identification of prion amyloid filaments in scrapie-infected brain
-
PMID:3922627
-
DeArmond SJ, McKinley MP, Barry RA, Braunfeld MB, McColloch JR, Prusiner SB. Identification of prion amyloid filaments in scrapie-infected brain. Cell 1985; 41:221-35; PMID:3922627; http://dx.doi.org/10.1016/0092-8674(85)90076-5.
-
(1985)
Cell
, vol.41
, pp. 221-235
-
-
DeArmond, S.J.1
McKinley, M.P.2
Barry, R.A.3
Braunfeld, M.B.4
McColloch, J.R.5
Prusiner, S.B.6
-
3
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
PMID:6801762
-
Prusiner SB. Novel proteinaceous infectious particles cause scrapie. Science 1982; 216:136-44; PMID:6801762; http://dx.doi.org/10.1126/science. 6801762.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
4
-
-
0032506187
-
Prions
-
PMID:9811807
-
Prusiner SB. Prions. Proc Natl Acad Sci U S A 1998; 95:13363-83; PMID:9811807; http://dx.doi.org/10.1073/pnas.95.23.13363.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 13363-13383
-
-
Prusiner, S.B.1
-
5
-
-
0025910229
-
Molecular biology of prion diseases
-
PMID:1675487
-
Prusiner SB. Molecular biology of prion diseases. Science 1991; 252:1515-22; PMID:1675487; http://dx.doi.org/10.1126/science.1675487.
-
(1991)
Science
, vol.252
, pp. 1515-1522
-
-
Prusiner, S.B.1
-
6
-
-
0034916581
-
Prion diseases of humans and animals: Their causes and molecular basis
-
PMID:11283320
-
Collinge J. Prion diseases of humans and animals: their causes and molecular basis. Annu Rev Neurosci 2001; 24:519-50; PMID:11283320; http://dx.doi.org/10.1146/annurev.neuro.24.1.519.
-
(2001)
Annu Rev Neurosci
, vol.24
, pp. 519-550
-
-
Collinge, J.1
-
7
-
-
9444267651
-
The state of the prion
-
PMID:15494743
-
Weissmann C. The state of the prion. Nat Rev Microbiol 2004; 2:861-71; PMID:15494743; http://dx.doi.org/10.1038/nrmicro1025.
-
(2004)
Nat Rev Microbiol
, vol.2
, pp. 861-871
-
-
Weissmann, C.1
-
8
-
-
0842281643
-
Mammalian prion biology: One century of evolving concepts
-
PMID:14744440
-
Aguzzi A, Polymenidou M. Mammalian prion biology: one century of evolving concepts. Cell 2004; 116:313-27; PMID:14744440; http://dx.doi.org/10.1016/ S0092-8674(03)01031-6.
-
(2004)
Cell
, vol.116
, pp. 313-327
-
-
Aguzzi, A.1
Polymenidou, M.2
-
9
-
-
0035312586
-
Interactions between prion protein isoforms: The kiss of death?
-
PMID:11295556
-
Caughey B. Interactions between prion protein isoforms: the kiss of death? Trends Biochem Sci 2001; 26:235-42; PMID:11295556; http://dx.doi.org/10. 1016/S0968-0004(01)01792-3.
-
(2001)
Trends Biochem Sci
, vol.26
, pp. 235-242
-
-
Caughey, B.1
-
10
-
-
0036791019
-
Dominant-negative inhibition of prion replication in transgenic mice
-
PMID:12271119
-
Perrier V, Kaneko K, Safar J, Vergara J, Tremblay P, DeArmond SJ, et al. Dominant-negative inhibition of prion replication in transgenic mice. Proc Natl Acad Sci U S A 2002; 99:13079-84; PMID:12271119; http://dx.doi.org/10.1073/pnas. 182425299.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 13079-13084
-
-
Perrier, V.1
Kaneko, K.2
Safar, J.3
Vergara, J.4
Tremblay, P.5
DeArmond, S.J.6
-
11
-
-
0142184333
-
Rna molecules stimulate prion protein conversion
-
PMID:14562104
-
Deleault NR, Lucassen RW, Supattapone S. RNA molecules stimulate prion protein conversion. Nature 2003; 425:717-20; PMID:14562104; http://dx.doi.org/ 10.1038/nature01979.
-
(2003)
Nature
, vol.425
, pp. 717-720
-
-
Deleault, N.R.1
Lucassen, R.W.2
Supattapone, S.3
-
12
-
-
34547491652
-
Formation of native prions from minimal components in vitro
-
PMID:17535913
-
Deleault NR, Harris BT, Rees JR, Supattapone S. Formation of native prions from minimal components in vitro. Proc Natl Acad Sci U S A 2007; 104:9741-6; PMID:17535913; http://dx.doi.org/10.1073/pnas.0702662104.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 9741-9746
-
-
Deleault, N.R.1
Harris, B.T.2
Rees, J.R.3
Supattapone, S.4
-
13
-
-
84863913395
-
Cofactor molecules maintain infectious conformation and restrict strain properties in purified prions
-
PMID:22711839
-
Deleault NR, Walsh DJ, Piro JR, Wang F, Wang X, Ma J, et al. Cofactor molecules maintain infectious conformation and restrict strain properties in purified prions. Proc Natl Acad Sci U S A 2012; 109:E1938-46; PMID:22711839; http://dx.doi.org/10.1073/pnas.1206999109.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
-
-
Deleault, N.R.1
Walsh, D.J.2
Piro, J.R.3
Wang, F.4
Wang, X.5
Ma, J.6
-
14
-
-
0028338441
-
Structural clues to prion replication
-
PMID:7909169
-
Cohen FE, Pan KM, Huang Z, Baldwin M, Fletterick RJ, Prusiner SB. Structural clues to prion replication. Science 1994; 264:530-1; PMID:7909169; http://dx.doi.org/10.1126/science.7909169.
-
(1994)
Science
, vol.264
, pp. 530-531
-
-
Cohen, F.E.1
Pan, K.M.2
Huang, Z.3
Baldwin, M.4
Fletterick, R.J.5
Prusiner, S.B.6
-
15
-
-
0027332116
-
Conversion of alpha-helices into betasheets features in the formation of the scrapie prion proteins
-
PMID:7902575
-
Pan KM, Baldwin M, Nguyen J, Gasset M, Serban A, Groth D, et al. Conversion of alpha-helices into betasheets features in the formation of the scrapie prion proteins. Proc Natl Acad Sci U S A 1993; 90:10962-6; PMID:7902575; http://dx.doi.org/10.1073/pnas.90.23.10962.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 10962-1096
-
-
Pan, K.M.1
Baldwin, M.2
Nguyen, J.3
Gasset, M.4
Serban, A.5
Groth, D.6
-
16
-
-
0031592937
-
A conformational transition at the n terminus of the prion protein features in formation of the scrapie isoform
-
PMID:9356250
-
Peretz D, Williamson RA, Matsunaga Y, Serban H, Pinilla C, Bastidas RB, et al. A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform. J Mol Biol 1997; 273:614-22; PMID:9356250; http://dx.doi.org/10.1006/jmbi.1997.1328.
-
(1997)
J Mol Biol
, vol.273
, pp. 614-622
-
-
Peretz, D.1
Williamson, R.A.2
Matsunaga, Y.3
Serban, H.4
Pinilla, C.5
Bastidas, R.B.6
-
17
-
-
0343683408
-
Physical studies of conformational plasticity in a recombinant prion protein
-
PMID:9132005
-
Zhang H, Stockel J, Mehlhorn I, Groth D, Baldwin MA, Prusiner SB, et al. Physical studies of conformational plasticity in a recombinant prion protein. Biochemistry 1997; 36:3543-53; PMID:9132005; http://dx.doi.org/10.1021/ bi961965r.
-
(1997)
Biochemistry
, vol.36
, pp. 3543-353
-
-
Zhang, H.1
Stockel, J.2
Mehlhorn, I.3
Groth, D.4
Baldwin, M.A.5
Prusiner, S.B.6
-
18
-
-
3142547067
-
The controversial protein-only hypothesis of prion propagation
-
PMID:15272271
-
Soto C, Castilla J. The controversial protein-only hypothesis of prion propagation. Nat Med 2004; 10(Suppl):S63-7; PMID:15272271; http://dx.doi.org/10. 1038/nm1069.
-
(2004)
Nat Med
, vol.10
, Issue.SUPPL.
-
-
Soto, C.1
Castilla, J.2
-
19
-
-
0029817344
-
Prion diseases and the 'protein only' hypothesis: A theoretical dynamic study
-
PMID8761449
-
Laurent M. Prion diseases and the 'protein only' hypothesis: a theoretical dynamic study. Biochem J 1996; 318:35-9; PMID:8761449.
-
(1996)
Biochem J
, vol.318
, pp. 35-39
-
-
Laurent, M.1
-
20
-
-
1642633056
-
Conformational variations in an infectious protein determine prion strain differences
-
PMID:15029196
-
Tanaka M, Chien P, Naber N, Cooke R, Weissman JS. Conformational variations in an infectious protein determine prion strain differences. Nature 2004; 428:323-8; PMID:15029196; http://dx.doi.org/10.1038/nature02392.
-
(2004)
Nature
, vol.428
, pp. 323-328
-
-
Tanaka, M.1
Chien, P.2
Naber, N.3
Cooke, R.4
Weissman, J.S.5
-
21
-
-
34249993165
-
The prion strain phenomenon: Molecular basis and unprecedented features
-
PMID:17254754
-
Morales R, Abid K, Soto C. The prion strain phenomenon: molecular basis and unprecedented features. Biochim Biophys Acta 2007; 1772:681-91; PMID:17254754; http://dx.doi.org/10.1016/j.bbadis. 2006.12.006.
-
(2007)
Biochim Biophys Acta
, vol.1772
, pp. 681-691
-
-
Morales, R.1
Abid, K.2
Soto, C.3
-
22
-
-
12644272790
-
Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity
-
PMID:8953038
-
Telling GC, Parchi P, DeArmond SJ, Cortelli P, Montagna P, Gabizon R, et al. Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity. Science 1996; 274:2079-82; PMID:8953038; http://dx.doi.org/10.1126/science.274.5295.2079.
-
(1996)
Science
, vol.274
, pp. 2079-2082
-
-
Telling, G.C.1
Parchi, P.2
DeArmond, S.J.3
Cortelli, P.4
Montagna, P.5
Gabizon, R.6
-
23
-
-
0028997297
-
Non-genetic propagation of strain-specific properties of scrapie prion protein
-
PMID:7791905
-
Bessen RA, Kocisko DA, Raymond GJ, Nandan S, Lansbury PT, Caughey B. Non-genetic propagation of strain-specific properties of scrapie prion protein. Nature 1995; 375:698-700; PMID:7791905; http://dx.doi.org/10.1038/375698a0.
-
(1995)
Nature
, vol.375
, pp. 698-700
-
-
Bessen, R.A.1
Kocisko, D.A.2
Raymond, G.J.3
Nandan, S.4
Lansbury, P.T.5
Caughey, B.6
-
24
-
-
0031443433
-
Chaperone-supervised conversion of prion protein to its protease-resistant form
-
PMID:9391131
-
DebBurman SK, Raymond GJ, Caughey B, Lindquist S. Chaperone-supervised conversion of prion protein to its protease-resistant form. Proc Natl Acad Sci U S A 1997; 94:13938-43; PMID:9391131; http://dx.doi.org/10.1073/pnas.94.25. 13938.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 13938-13943
-
-
DebBurman, S.K.1
Raymond, G.J.2
Caughey, B.3
Lindquist, S.4
-
26
-
-
77955298267
-
Human prion strain selection in transgenic mice
-
PMID:20695008
-
Giles K, Glidden DV, Patel S, Korth C, Groth D, Lemus A, et al. Human prion strain selection in transgenic mice. Ann Neurol 2010; 68:151-61; PMID:20695008; http://dx.doi.org/10.1002/ana.22104.
-
(2010)
Ann Neurol
, vol.68
, pp. 151-161
-
-
Giles, K.1
Glidden, D.V.2
Patel, S.3
Korth, C.4
Groth, D.5
Lemus, A.6
-
27
-
-
84961034678
-
Scrapie produced experimentally in goats with special reference to the clinical syndrome
-
PMID:13733383
-
Pattison IH, Millson GC. Scrapie produced experimentally in goats with special reference to the clinical syndrome. J Comp Pathol 1961; 71:101-9; PMID:13733383.
-
(1961)
J Comp Pathol
, vol.71
, pp. 101-109
-
-
Pattison, I.H.1
Millson, G.C.2
-
28
-
-
0032472239
-
Bse and prions: Uncertainties about the agent
-
PMID:9441410
-
Chesebro B. BSE and prions: uncertainties about the agent. Science 1998; 279:42-3; PMID:9441410; http://dx.doi.org/10.1126/science.279.5347.42.
-
(1998)
Science
, vol.279
, pp. 42-43
-
-
Chesebro, B.1
-
29
-
-
0015550206
-
Scrapie in mice. Agent-strain differences in the distribution and intensity of grey matter vacuolation
-
PMID:4199908
-
Fraser H, Dickinson AG. Scrapie in mice. Agent-strain differences in the distribution and intensity of grey matter vacuolation. J Comp Pathol 1973; 83:29-40; PMID:4199908; http://dx.doi.org/10.1016/0021-9975(73)90024-8.
-
(1973)
J Comp Pathol
, vol.83
, pp. 29-40
-
-
Fraser, H.1
Dickinson, A.G.2
-
30
-
-
0021806007
-
Biochemical differences among scrapie-associated fibrils support the biological diversity of scrapie agents
-
PMID:3926951
-
Kascsak RJ, Rubenstein R, Merz PA, Carp RI, Wisniewski HM, Diringer H. Biochemical differences among scrapie-associated fibrils support the biological diversity of scrapie agents. J Gen Virol 1985; 66:1715-22; PMID:3926951; http://dx.doi.org/10.1099/0022-1317-66-8-1715.
-
(1985)
J Gen Virol
, vol.66
, pp. 1715-1722
-
-
Kascsak, R.J.1
Rubenstein, R.2
Merz, P.A.3
Carp, R.I.4
Wisniewski, H.M.5
Diringer, H.6
-
31
-
-
0026583834
-
Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent
-
PMID:1347795
-
Bessen RA, Marsh RF. Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent. J Virol 1992; 66:2096-101; PMID:1347795.
-
(1992)
J Virol
, vol.66
, pp. 2096-2101
-
-
Bessen, R.A.1
Marsh, R.F.2
-
32
-
-
0026552043
-
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
-
PMID:1346338
-
Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, et al. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. N Engl J Med 1992; 326:444-9; PMID:1346338; http://dx.doi.org/10.1056/NEJM199202133260704.
-
(1992)
N Engl J Med
, vol.326
, pp. 444-449
-
-
Medori, R.1
Tritschler, H.J.2
LeBlanc, A.3
Villare, F.4
Manetto, V.5
Chen, H.Y.6
-
33
-
-
0023004230
-
Familial insomnia with a malignant course: A new thalamic disease
-
PMID:3823713
-
Lugaresi E, Montagna P, Baruzzi A, Cortelli P, Tinuper P, Zucconi M, et al. Familial insomnia with a malignant course: a new thalamic disease. Rev Neurol (Paris) 1986; 142:791-2; PMID:3823713.
-
(1986)
Rev Neurol (Paris)
, vol.142
, pp. 791-792
-
-
Lugaresi, E.1
Montagna, P.2
Baruzzi, A.3
Cortelli, P.4
Tinuper, P.5
Zucconi, M.6
-
34
-
-
0026496257
-
Fatal familial insomnia and familial creutzfeldt-jakob disease: Disease phenotype determined by a dna polymorphism
-
PMID:1439789
-
Goldfarb LG, Petersen RB, Tabaton M, Brown P, LeBlanc AC, Montagna P, et al. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Science 1992; 258:806-8; PMID:1439789; http://dx.doi.org/10.1126/science.1439789.
-
(1992)
Science
, vol.258
, pp. 806-808
-
-
Goldfarb, L.G.1
Petersen, R.B.2
Tabaton, M.3
Brown, P.4
LeBlanc, A.C.5
Montagna, P.6
-
35
-
-
0028351904
-
Fatal familial insomnia and familial creutzfeldt-jakob disease: Different prion proteins determined by a dna polymorphism
-
PMID:7908444
-
Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, et al. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Proc Natl Acad Sci U S A 1994; 91:2839-42; PMID:7908444; http://dx.doi.org/10.1073/pnas.91.7.2839.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 2839-2842
-
-
Monari, L.1
Chen, S.G.2
Brown, P.3
Parchi, P.4
Petersen, R.B.5
Mikol, J.6
-
36
-
-
0026558780
-
Identification of two biologically distinct strains of transmissible mink encephalopathy in hamsters
-
PMID:1531675
-
Bessen RA, Marsh RF. Identification of two biologically distinct strains of transmissible mink encephalopathy in hamsters. J Gen Virol 1992; 73:329-34; PMID:1531675; http://dx.doi.org/10.1099/0022-1317-73-2-329.
-
(1992)
J Gen Virol
, vol.73
, pp. 329-334
-
-
Bessen, R.A.1
Marsh, R.F.2
-
37
-
-
0027740178
-
Scrapie strain variation and mutation
-
PMID:8137131
-
Bruce ME. Scrapie strain variation and mutation. Br Med Bull 1993; 49:822-38; PMID:8137131.
-
(1993)
Br Med Bull
, vol.49
, pp. 822-838
-
-
Bruce, M.E.1
-
38
-
-
0027741445
-
Diversity in the neuropathology of scrapielike diseases in animals
-
PMID:8137129
-
Fraser H. Diversity in the neuropathology of scrapielike diseases in animals. Br Med Bull 1993; 49:792-809; PMID:8137129.
-
(1993)
Br Med Bull
, vol.49
, pp. 792-809
-
-
Fraser, H.1
-
39
-
-
0029831213
-
Molecular analysis of prion strain variation and the aetiology of 'new variant'
-
PMID:8878476
-
Collinge J, Sidle KC, Meads J, Ironside J, Hill AF. Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. Nature 1996; 383:685-90; PMID:8878476; http://dx.doi.org/10.1038/383685a0.
-
(1996)
CJD. Nature
, vol.383
, pp. 685-690
-
-
Collinge, J.1
Sidle, K.C.2
Meads, J.3
Ironside, J.4
Hill, A.F.5
-
40
-
-
8944259890
-
Molecular basis of phenotypic variability in sporadic creutzfeldt-jakob disease
-
PMID:8651649
-
Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, et al. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 1996; 39:767-78; PMID:8651649; http://dx.doi.org/10.1002/ana. 410390613.
-
(1996)
Ann Neurol
, vol.39
, pp. 767-778
-
-
Parchi, P.1
Castellani, R.2
Capellari, S.3
Ghetti, B.4
Young, K.5
Chen, S.G.6
-
41
-
-
23844544189
-
Prp glycoforms are associated in a strain-specific ratio in native prpsc
-
PMID:16099923
-
Khalili-Shirazi A, Summers L, Linehan J, Mallinson G, Anstee D, Hawke S, et al. PrP glycoforms are associated in a strain-specific ratio in native PrPSc. J Gen Virol 2005; 86:2635-44; PMID:16099923; http://dx.doi.org/10.1099/vir.0. 80375-0.
-
(2005)
J Gen Virol
, vol.86
, pp. 2635-2644
-
-
Khalili-Shirazi, A.1
Summers, L.2
Linehan, J.3
Mallinson, G.4
Anstee, D.5
Hawke, S.6
-
42
-
-
0031720905
-
Eight prion strains have prp(sc) molecules with different conformations
-
PMID:9771749
-
Safar J, Wille H, Itri V, Groth D, Serban H, Torchia M, et al. Eight prion strains have PrP(Sc) molecules with different conformations. Nat Med 1998; 4:1157-65; PMID:9771749; http://dx.doi.org/10.1038/2654.
-
(1998)
Nat Med
, vol.4
, pp. 1157-1165
-
-
Safar, J.1
Wille, H.2
Itri, V.3
Groth, D.4
Serban, H.5
Torchia, M.6
-
43
-
-
0033130083
-
Strain-specific prion-protein conformation determined by metal ions
-
PMID:10559865
-
Wadsworth JD, Hill AF, Joiner S, Jackson GS, Clarke AR, Collinge J. Strain-specific prion-protein conformation determined by metal ions. Nat Cell Biol 1999; 1:55-9; PMID:10559865; http://dx.doi.org/10.1038/9030.
-
(1999)
Nat Cell Biol
, vol.1
, pp. 55-59
-
-
Wadsworth, J.D.1
Hill, A.F.2
Joiner, S.3
Jackson, G.S.4
Clarke, A.R.5
Collinge, J.6
-
44
-
-
4644259154
-
Identification of distinct n-terminal truncated forms of prion protein in different creutzfeldt-jakob disease subtypes
-
PMID:15247220
-
Zanusso G, Farinazzo A, Prelli F, Fiorini M, Gelati M, Ferrari S, et al. Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes. J Biol Chem 2004; 279:38936-42; PMID:15247220; http://dx.doi.org/10.1074/jbc.M405468200.
-
(2004)
J Biol Chem
, vol.279
, pp. 38936-3842
-
-
Zanusso, G.1
Farinazzo, A.2
Prelli, F.3
Fiorini, M.4
Gelati, M.5
Ferrari, S.6
-
45
-
-
0141577720
-
Identification of novel proteinase k-resistant c-terminal fragments of prp in creutzfeldt-jakob disease
-
PMID:12917418
-
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; 278:40429-36; PMID:12917418; http://dx.doi.org/10.1074/jbc. M308550200.
-
(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
-
46
-
-
0033610870
-
Strain-dependent differences in beta-sheet conformations of abnormal prion protein
-
PMID:9822701
-
Caughey B, Raymond GJ, Bessen RA. Strain-dependent differences in beta-sheet conformations of abnormal prion protein. J Biol Chem 1998; 273:32230-5; PMID:9822701; http://dx.doi.org/10.1074/jbc.273.48.32230.
-
(1998)
J Biol Chem
, vol.273
, pp. 32230-32235
-
-
Caughey, B.1
Raymond, G.J.2
Bessen, R.A.3
-
47
-
-
33746698975
-
The physical basis of how prion conformations determine strain phenotypes
-
PMID:16810177
-
Tanaka M, Collins SR, Toyama BH, Weissman JS. The physical basis of how prion conformations determine strain phenotypes. Nature 2006; 442:585-9; PMID:16810177; http://dx.doi.org/10.1038/nature04922.
-
(2006)
Nature
, vol.442
, pp. 585-589
-
-
Tanaka, M.1
Collins, S.R.2
Toyama, B.H.3
Weissman, J.S.4
-
48
-
-
34247216627
-
In vitro analysis of spure2p, a prionrelated protein, exemplifies the relationship between amyloid and prion
-
PMID:17234629
-
Immel F, Jiang Y, Wang YQ, Marchal C, Maillet L, Perrett S, et al. In vitro analysis of SpUre2p, a prionrelated protein, exemplifies the relationship between amyloid and prion. J Biol Chem 2007; 282:7912-20; PMID:17234629; http://dx.doi.org/10.1074/jbc. M608652200.
-
(2007)
J Biol Chem
, vol.282
, pp. 7912-7920
-
-
Immel, F.1
Jiang, Y.2
Wang, Y.Q.3
Marchal, C.4
Maillet, L.5
Perrett, S.6
-
49
-
-
34447639732
-
Continuum of prion protein structures enciphers a multitude of prion isolate-specified phenotypes
-
PMID:17142317
-
Legname G, Nguyen HO, Peretz D, Cohen FE, DeArmond SJ, Prusiner SB. Continuum of prion protein structures enciphers a multitude of prion isolate-specified phenotypes. Proc Natl Acad Sci U S A 2006; 103:19105-10; PMID:17142317; http://dx.doi.org/10.1073/pnas.0608970103.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 19105-19110
-
-
Legname, G.1
Nguyen, H.O.2
Peretz, D.3
Cohen, F.E.4
DeArmond, S.J.5
Prusiner, S.B.6
-
50
-
-
68249110632
-
Investigating the conformational stability of prion strains through a kinetic replication model
-
PMID:19578427
-
Zampieri M, Legname G, Altafini C. Investigating the conformational stability of prion strains through a kinetic replication model. PLoS Comput Biol 2009; 5:e1000420; PMID:19578427; http://dx.doi.org/10.1371/journal.pcbi. 1000420.
-
(2009)
PLoS Comput Biol
, vol.5
-
-
Zampieri, M.1
Legname, G.2
Altafini, C.3
-
51
-
-
79953286302
-
The strain-encoded relationship between prp replication, stability and processing in neurons is predictive of the incubation period of disease
-
PMID:21437239
-
Ayers JI, Schutt CR, Shikiya RA, Aguzzi A, Kincaid AE, Bartz JC. The strain-encoded relationship between PrP replication, stability and processing in neurons is predictive of the incubation period of disease. PLoS Pathog 2011; 7:e1001317; PMID:21437239; http://dx.doi.org/10.1371/journal.ppat.1001317.
-
(2011)
PLoS Pathog
, vol.7
-
-
Ayers, J.I.1
Schutt, C.R.2
Shikiya, R.A.3
Aguzzi, A.4
Kincaid, A.E.5
Bartz, J.C.6
-
52
-
-
84860903170
-
Biochemical properties of highly neuroinvasive prion strains
-
PMID:22319450
-
Bett C, Joshi-Barr S, Lucero M, Trejo M, Liberski P, Kelly JW, et al. Biochemical properties of highly neuroinvasive prion strains. PLoS Pathog 2012; 8:e1002522; PMID:22319450; http://dx.doi.org/10.1371/journal.ppat.1002522.
-
(2012)
PLoS Pathog
, vol.8
-
-
Bett, C.1
Joshi-Barr, S.2
Lucero, M.3
Trejo, M.4
Liberski, P.5
Kelly, J.W.6
-
53
-
-
24644448839
-
The most infectious prion protein particles
-
PMID:16148934
-
Silveira JR, Raymond GJ, Hughson AG, Race RE, Sim VL, Hayes SF, et al. The most infectious prion protein particles. Nature 2005; 437:257-61; PMID:16148934; http://dx.doi.org/10.1038/nature03989.
-
(2005)
Nature
, vol.437
, pp. 257-261
-
-
Silveira, J.R.1
Raymond, G.J.2
Hughson, A.G.3
Race, R.E.4
Sim, V.L.5
Hayes, S.F.6
-
54
-
-
76749109480
-
Darwinian evolution of prions in cell culture
-
PMID:20044542
-
Li J, Browning S, Mahal SP, Oelschlegel AM, Weissmann C. Darwinian evolution of prions in cell culture. Science 2010; 327:869-72; PMID:20044542; http://dx.doi.org/10.1126/science.1183218.
-
(2010)
Science
, vol.327
, pp. 869-872
-
-
Li, J.1
Browning, S.2
Mahal, S.P.3
Oelschlegel, A.M.4
Weissmann, C.5
-
55
-
-
0023205075
-
Biological evidence that scrapie agent has an independent genome
-
PMID:3100717
-
Bruce ME, Dickinson AG. Biological evidence that scrapie agent has an independent genome. J Gen Virol 1987; 68:79-89; PMID:3100717; http://dx.doi.org/10.1099/0022-1317-68-1-79.
-
(1987)
J Gen Virol
, vol.68
, pp. 79-89
-
-
Bruce, M.E.1
Dickinson, A.G.2
-
56
-
-
0032567088
-
The host range of chronic wasting disease is altered on passage in ferrets
-
PMID:9837794
-
Bartz JC, Marsh RF, McKenzie DI, Aiken JM. The host range of chronic wasting disease is altered on passage in ferrets. Virology 1998; 251:297-301; PMID:9837794; http://dx.doi.org/10.1006/viro.1998.9427.
-
(1998)
Virology
, vol.251
, pp. 297-301
-
-
Bartz, J.C.1
Marsh, R.F.2
McKenzie, D.I.3
Aiken, J.M.4
-
57
-
-
0034758487
-
The role of conformational flexibility in prion propagation and maintenance for sup35p
-
PMID:11685242
-
Scheibel T, Lindquist SL. The role of conformational flexibility in prion propagation and maintenance for Sup35p. Nat Struct Biol 2001; 8:958-62; PMID:11685242; http://dx.doi.org/10.1038/nsb1101-958.
-
(2001)
Nat Struct Biol
, vol.8
, pp. 958-962
-
-
Scheibel, T.1
Lindquist, S.L.2
-
58
-
-
0034714351
-
Nucleated conformational conversion and the replication of conformational information by a prion determinant
-
PMID:10958771
-
Serio TR, Cashikar AG, Kowal AS, Sawicki GJ, Moslehi JJ, Serpell L, et al. Nucleated conformational conversion and the replication of conformational information by a prion determinant. Science 2000; 289:1317-21; PMID:10958771; http://dx.doi.org/10.1126/science.289.5483.1317.
-
(2000)
Science
, vol.289
, pp. 1317-1321
-
-
Serio, T.R.1
Cashikar, A.G.2
Kowal, A.S.3
Sawicki, G.J.4
Moslehi, J.J.5
Serpell, L.6
-
59
-
-
0028043661
-
Distinct prp properties suggest the molecular basis of strain variation in transmissible mink encephalopathy
-
PMID:7966576
-
Bessen RA, Marsh RF. Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy. J Virol 1994; 68:7859-68; PMID:7966576.
-
(1994)
J Virol
, vol.68
, pp. 7859-768
-
-
Bessen, R.A.1
Marsh, R.F.2
-
60
-
-
33845433794
-
Strain fidelity of chronic wasting disease upon murine adaptation
-
PMID:17020952
-
Sigurdson CJ, Manco G, Schwarz P, Liberski P, Hoover EA, Hornemann S, et al. Strain fidelity of chronic wasting disease upon murine adaptation. J Virol 2006; 80:12303-11; PMID:17020952; http://dx.doi.org/10.1128/JVI.01120-06.
-
(2006)
J Virol
, vol.80
, pp. 12303-12311
-
-
Sigurdson, C.J.1
Manco, G.2
Schwarz, P.3
Liberski, P.4
Hoover, E.A.5
Hornemann, S.6
-
61
-
-
36749074412
-
Prion strain discrimination using luminescent conjugated polymers
-
PMID:18026110
-
Sigurdson CJ, Nilsson KP, Hornemann S, Manco G, Polymenidou M, Schwarz P, et al. Prion strain discrimination using luminescent conjugated polymers. Nat Methods 2007; 4:1023-30; PMID:18026110; http://dx.doi.org/10.1038/nmeth1131.
-
(2007)
Nat Methods
, vol.4
, pp. 1023-1030
-
-
Sigurdson, C.J.1
Nilsson, K.P.2
Hornemann, S.3
Manco, G.4
Polymenidou, M.5
Schwarz, P.6
-
62
-
-
3343003514
-
Techniques to study amyloid fibril formation in vitro
-
PMID:15283924
-
Nilsson MR. Techniques to study amyloid fibril formation in vitro. Methods 2004; 34:151-60; PMID:15283924; http://dx.doi.org/10.1016/j.ymeth.2004. 03.012.
-
(2004)
Methods
, vol.34
, pp. 151-160
-
-
Nilsson, M.R.1
-
63
-
-
0017866857
-
Evidence that the transmission of one source of scrapie agent to hamsters involves separation of agent strains from a mixture
-
PMID:96212
-
Kimberlin RH, Walker CA. Evidence that the transmission of one source of scrapie agent to hamsters involves separation of agent strains from a mixture. J Gen Virol 1978; 39:487-96; PMID:96212; http://dx.doi.org/10.1099/0022-1317-39- 3-487.
-
(1978)
J Gen Virol
, vol.39
, pp. 487-496
-
-
Kimberlin, R.H.1
Walker, C.A.2
-
64
-
-
27744459883
-
Coexistence of multiple prpsc types in individuals with creutzfeldt-jakob disease
-
PMID:16297838
-
Polymenidou M, Stoeck K, Glatzel M, Vey M, Bellon A, Aguzzi A. Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease. Lancet Neurol 2005; 4:805-14; PMID:16297838; http://dx.doi.org/10.1016/ S1474-4422(05)70225-8.
-
(2005)
Lancet Neurol
, vol.4
, pp. 805-814
-
-
Polymenidou, M.1
Stoeck, K.2
Glatzel, M.3
Vey, M.4
Bellon, A.5
Aguzzi, A.6
-
65
-
-
0031765497
-
Observations on thermostable subpopulations of the unconventional agents that cause transmissible degenerative encephalopathies
-
PMID:9874101
-
Taylor DM, Fernie K, McConnell I, Steele PJ. Observations on thermostable subpopulations of the unconventional agents that cause transmissible degenerative encephalopathies. Vet Microbiol 1998; 64:33-8; PMID:9874101; http://dx.doi.org/10.1016/S0378-1135(98)00257-0.
-
(1998)
Vet Microbiol
, vol.64
, pp. 33-38
-
-
Taylor, D.M.1
Fernie, K.2
McConnell, I.3
Steele, P.J.4
-
66
-
-
26244461742
-
Prion clearance in bigenic mice
-
PMID:16186247
-
Safar JG, DeArmond SJ, Kociuba K, Deering C, Didorenko S, Bouzamondo-Bernstein E, et al. Prion clearance in bigenic mice. J Gen Virol 2005; 86:2913-23; PMID:16186247; http://dx.doi.org/10.1099/vir.0.80947-0.
-
(2005)
J Gen Virol
, vol.86
, pp. 2913-2923
-
-
Safar, J.G.1
DeArmond, S.J.2
Kociuba, K.3
Deering, C.4
Didorenko, S.5
Bouzamondo-Bernstein, E.6
-
67
-
-
79952585579
-
Integration of clearance mechanisms: The proteasome and autophagy
-
PMID:21068151
-
Wong E, Cuervo AM. Integration of clearance mechanisms: the proteasome and autophagy. Cold Spring Harb Perspect Biol 2010; 2:a006734; PMID:21068151; http://dx.doi.org/10.1101/cshperspect.a006734.
-
(2010)
Cold Spring Harb Perspect Biol
, vol.2
-
-
Wong, E.1
Cuervo, A.M.2
-
68
-
-
34247323549
-
Prion protein resides in membrane microclusters of the immunological synapse during lymphocyte activation
-
PMID:17449139
-
Paar C, Wurm S, Pfarr W, Sonnleitner A, Wechselberger C. Prion protein resides in membrane microclusters of the immunological synapse during lymphocyte activation. Eur J Cell Biol 2007; 86:253-64; PMID:17449139; http://dx.doi.org/10.1016/j.ejcb.2007.03.001.
-
(2007)
Eur J Cell Biol
, vol.86
, pp. 253-64
-
-
Paar, C.1
Wurm, S.2
Pfarr, W.3
Sonnleitner, A.4
Wechselberger, C.5
-
69
-
-
84864515731
-
Molecular mechanisms used by chaperones to reduce the toxicity of aberrant protein oligomers
-
PMID:22802614
-
Mannini B, Cascella R, Zampagni M, van Waarde-Verhagen M, Meehan S, Roodveldt C, et al. Molecular mechanisms used by chaperones to reduce the toxicity of aberrant protein oligomers. Proc Natl Acad Sci U S A 2012; 109:12479-84; PMID:22802614; http://dx.doi.org/10.1073/pnas.1117799109.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 12479-84
-
-
Mannini, B.1
Cascella, R.2
Zampagni, M.3
Van Waarde-Verhagen, M.4
Meehan, S.5
Roodveldt, C.6
-
70
-
-
80255140360
-
Prions on the move
-
PMID:21997298
-
Weissmann C, Li J, Mahal SP, Browning S. Prions on the move. EMBO Rep 2011; 12:1109-17; PMID:21997298; http://dx.doi.org/10.1038/embor.2011.192.
-
(2011)
EMBO Rep
, vol.12
, pp. 1109-17
-
-
Weissmann, C.1
Li, J.2
Mahal, S.P.3
Browning, S.4
-
71
-
-
0036184403
-
Strain characterization of natural sheep scrapie and comparison with bse
-
PMID:11842264
-
Bruce ME, Boyle A, Cousens S, McConnell I, Foster J, Goldmann W, et al. Strain characterization of natural sheep scrapie and comparison with BSE. J Gen Virol 2002; 83:695-704; PMID:11842264.
-
(2002)
J Gen Virol
, vol.83
, pp. 695-704
-
-
Bruce, M.E.1
Boyle, A.2
Cousens, S.3
McConnell, I.4
Foster, J.5
Goldmann, W.6
-
72
-
-
0028782015
-
Transmission of bovine spongiform encephalopathy and scrapie to mice: Strain variation and the species barrier
-
PMID:7913758
-
Bruce M, Chree A, McConnell I, Foster J, Pearson G, Fraser H. Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier. Philos Trans R Soc Lond B Biol Sci 1994; 343:405-11; PMID:7913758; http://dx.doi.org/10.1098/rstb.1994.0036.
-
(1994)
Philos Trans R Soc Lond B Biol Sci
, vol.343
, pp. 405-11
-
-
Bruce, M.1
Chree, A.2
McConnell, I.3
Foster, J.4
Pearson, G.5
Fraser, H.6
-
73
-
-
3042742406
-
Prion strains and species barriers
-
PMID:15077403
-
Hill AF, Collinge J. Prion strains and species barriers. Contrib Microbiol 2004; 11:33-49; PMID:15077403; http://dx.doi.org/10.1159/000077061.
-
(2004)
Contrib Microbiol
, vol.11
, pp. 33-49
-
-
Hill, A.F.1
Collinge, J.2
-
74
-
-
36049020231
-
A general model of prion strains and their pathogenicity
-
PMID:17991853
-
Collinge J, Clarke AR. A general model of prion strains and their pathogenicity. Science 2007; 318:930-6; PMID:17991853; http://dx.doi.org/10. 1126/science. 1138718.
-
(2007)
Science
, vol.318
, pp. 930-6
-
-
Collinge, J.1
Clarke, A.R.2
-
75
-
-
0034079165
-
Adaptation and selection of prion protein strain conformations following interspecies transmission of transmissible mink encephalopathy
-
PMID:10823860
-
Bartz JC, Bessen RA, McKenzie D, Marsh RF, Aiken JM. Adaptation and selection of prion protein strain conformations following interspecies transmission of transmissible mink encephalopathy. J Virol 2000; 74:5542-7; PMID:10823860; http://dx.doi.org/10.1128/JVI.74.12.5542-5547.2000.
-
(2000)
J Virol
, vol.74
, pp. 5542-5547
-
-
Bartz, J.C.1
Bessen, R.A.2
McKenzie, D.3
Marsh, R.F.4
Aiken, J.M.5
-
76
-
-
77957198527
-
Chemical and biophysical insights into the propagation of prion strains
-
PMID:19436493
-
Falsig J, Nilsson KP, Knowles TP, Aguzzi A. Chemical and biophysical insights into the propagation of prion strains. HFSP J 2008; 2:332-41; PMID:19436493; http://dx.doi.org/10.2976/1.2990786.
-
(2008)
HFSP J
, vol.2
, pp. 332-41
-
-
Falsig, J.1
Nilsson, K.P.2
Knowles, T.P.3
Aguzzi, A.4
-
77
-
-
18744362997
-
Bse prions propagate as either variant cjd-like or sporadic cjd-like prion strains in transgenic mice expressing human prion protein
-
PMID:12456643
-
Asante EA, Linehan JM, Desbruslais M, Joiner S, Gowland I, Wood AL, et al. BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein. EMBO J 2002; 21:6358-66; PMID:12456643; http://dx.doi.org/10.1093/emboj/cdf653.
-
(2002)
EMBO J
, vol.21
, pp. 6358-66
-
-
Asante, E.A.1
Linehan, J.M.2
Desbruslais, M.3
Joiner, S.4
Gowland, I.5
Wood, A.L.6
-
78
-
-
4043154915
-
Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice
-
PMID:15269389
-
Lloyd SE, Linehan JM, Desbruslais M, Joiner S, Buckell J, Brandner S, et al. Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice. J Gen Virol 2004; 85:2471-8; PMID:15269389; http://dx.doi.org/10.1099/vir.0.79889-0.
-
(2004)
J Gen Virol
, vol.85
, pp. 2471-8
-
-
Lloyd, S.E.1
Linehan, J.M.2
Desbruslais, M.3
Joiner, S.4
Buckell, J.5
Brandner, S.6
-
79
-
-
37549068149
-
Selective incorporation of polyanionic molecules into hamster prions
-
PMID:17940287
-
Geoghegan JC, Valdes PA, Orem NR, Deleault NR, Williamson RA, Harris BT, et al. Selective incorporation of polyanionic molecules into hamster prions. J Biol Chem 2007; 282:36341-53; PMID:17940287; http://dx.doi.org/10.1074/jbc. M704447200.
-
(2007)
J Biol Chem
, vol.282
, pp. 36341-53
-
-
Geoghegan, J.C.1
Valdes, P.A.2
Orem, N.R.3
Deleault, N.R.4
Williamson, R.A.5
Harris, B.T.6
-
80
-
-
77951923337
-
Species-dependent differences in cofactor utilization for formation of the protease-resistant prion protein in vitro
-
PMID:20377181
-
Deleault NR, Kascsak R, Geoghegan JC, Supattapone S. Species-dependent differences in cofactor utilization for formation of the protease-resistant prion protein in vitro. Biochemistry 2010; 49:3928-34; PMID:20377181; http://dx.doi.org/10.1021/bi100370b.
-
(2010)
Biochemistry
, vol.49
, pp. 3928-34
-
-
Deleault, N.R.1
Kascsak, R.2
Geoghegan, J.C.3
Supattapone, S.4
-
81
-
-
84861848298
-
Isolation of phosphatidylethanolamine as a solitary cofactor for prion formation in the absence of nucleic acids
-
PMID:22586108
-
Deleault NR, Piro JR, Walsh DJ, Wang F, Ma J, Geoghegan JC, et al. Isolation of phosphatidylethanolamine as a solitary cofactor for prion formation in the absence of nucleic acids. Proc Natl Acad Sci U S A 2012; 109:8546-51; PMID:22586108; http://dx.doi.org/10.1073/pnas.1204498109.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 8546-51
-
-
Deleault, N.R.1
Piro, J.R.2
Walsh, D.J.3
Wang, F.4
Ma, J.5
Geoghegan, J.C.6
-
82
-
-
0027135501
-
The function of heat-shock proteins in stress tolerance: Degradation and reactivation of damaged proteins
-
PMID:8122909
-
Parsell DA, Lindquist S. The function of heat-shock proteins in stress tolerance: degradation and reactivation of damaged proteins. Annu Rev Genet 1993; 27:437-96; PMID:8122909; http://dx.doi.org/10.1146/annurev.ge.27.120193. 002253.
-
(1993)
Annu Rev Genet
, vol.27
, pp. 437-96
-
-
Parsell, D.A.1
Lindquist, S.2
-
83
-
-
0035859102
-
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding
-
PMID:11459061
-
Saborio GP, Permanne B, Soto C. Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature 2001; 411:810-3; PMID:11459061; http://dx.doi.org/10.1038/35081095.
-
(2001)
Nature
, vol.411
, pp. 810-3
-
-
Saborio, G.P.1
Permanne, B.2
Soto, C.3
-
84
-
-
38049170555
-
Prion strain discrimination in cell culture: The cell panel assay
-
PMID:18077360
-
Mahal SP, Baker CA, Demczyk CA, Smith EW, Julius C, Weissmann C. Prion strain discrimination in cell culture: the cell panel assay. Proc Natl Acad Sci U S A 2007; 104:20908-13; PMID:18077360; http://dx.doi.org/10.1073/pnas. 0710054104.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 20908-13
-
-
Mahal, S.P.1
Baker, C.A.2
Demczyk, C.A.3
Smith, E.W.4
Julius, C.5
Weissmann, C.6
-
85
-
-
0842304471
-
Mutant prpsc conformers induced by a synthetic peptide and several prion strains
-
PMID:14747574
-
Tremblay P, Ball HL, Kaneko K, Groth D, Hegde RS, Cohen FE, et al. Mutant PrPSc conformers induced by a synthetic peptide and several prion strains. J Virol 2004; 78:2088-99; PMID:14747574; http://dx.doi.org/10.1128/JVI.78.4.2088- 2099.2004.
-
(2004)
J Virol
, vol.78
, pp. 2088-99
-
-
Tremblay, P.1
Ball, H.L.2
Kaneko, K.3
Groth, D.4
Hegde, R.S.5
Cohen, F.E.6
-
87
-
-
0032578283
-
Prion immunoreactivity in appendix before clinical onset of variant creutzfeldt-jakob disease
-
PMID:9728989
-
Hilton DA, Fathers E, Edwards P, Ironside JW, Zajicek J. Prion immunoreactivity in appendix before clinical onset of variant Creutzfeldt-Jakob disease. Lancet 1998; 352:703-4; PMID:9728989; http://dx.doi.org/10.1016/S0140- 6736(98)24035-9.
-
(1998)
Lancet
, vol.352
, pp. 703-4
-
-
Hilton, D.A.1
Fathers, E.2
Edwards, P.3
Ironside, J.W.4
Zajicek, J.5
-
88
-
-
0035928432
-
Tissue distribution of protease resistant prion protein in variant creutzfeldt-jakob disease using a highly sensitive immunoblotting assay
-
PMID:11476832
-
Wadsworth JD, Joiner S, Hill AF, Campbell TA, Desbruslais M, Luthert PJ, et al. Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay. Lancet 2001; 358:171-80; PMID:11476832; http://dx.doi.org/10.1016/S0140-6736(01)05403- 4.
-
(2001)
Lancet
, vol.358
, pp. 171-180
-
-
Wadsworth, J.D.1
Joiner, S.2
Hill, A.F.3
Campbell, T.A.4
Desbruslais, M.5
Luthert, P.J.6
-
89
-
-
78651082619
-
Transfer of a prion strain to different hosts leads to emergence of strain variants
-
PMID:21156827
-
Mahal SP, Browning S, Li J, Suponitsky-Kroyter I, Weissmann C. Transfer of a prion strain to different hosts leads to emergence of strain variants. Proc Natl Acad Sci U S A 2010; 107:22653-8; PMID:21156827; http://dx.doi.org/10. 1073/pnas.1013014108.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 22653-8
-
-
Mahal, S.P.1
Browning, S.2
Li, J.3
Suponitsky-Kroyter, I.4
Weissmann, C.5
-
90
-
-
0032816292
-
Classification of sporadic creutzfeldt-jakob disease based on molecular and phenotypic analysis of 300 subjects
-
PMID:10443888
-
Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999; 46:224-33; PMID:10443888; http://dx.doi.org/10.1002/1531-8249(199908)46:2;224::AIDANA12; 3.0.CO;2-W.
-
(1999)
Ann Neurol
, vol.46
, pp. 224-33
-
-
Parchi, P.1
Giese, A.2
Capellari, S.3
Brown, P.4
Schulz-Schaeffer, W.5
Windl, O.6
-
91
-
-
0141514771
-
Sporadic and familial cjd: Classification and characterisation
-
PMID:14522861
-
Gambetti P, Kong Q, Zou W, Parchi P, Chen SG. Sporadic and familial CJD: classification and characterisation. Br Med Bull 2003; 66:213-39; PMID:14522861; http://dx.doi.org/10.1093/bmb/66.1.213.
-
(2003)
Br Med Bull
, vol.66
, pp. 213-39
-
-
Gambetti, P.1
Kong, Q.2
Zou, W.3
Parchi, P.4
Chen, S.G.5
-
92
-
-
79960231821
-
Quantification of surviving cerebellar granule neurones and abnormal prion protein (prpsc) deposition in sporadic creutzfeldt-jakob disease supports a pathogenic role for small prpsc deposits common to the various molecular subtypes
-
PMID:21450052
-
Faucheux BA, Morain E, Diouron V, Brandel JP, Salomon D, Sazdovitch V, et al. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes. Neuropathol Appl Neurobiol 2011; 37:500-12; PMID:21450052; http://dx.doi.org/10.1111/j.1365-2990.2011.01179.x.
-
(2011)
Neuropathol Appl Neurobiol
, vol.37
, pp. 500-12
-
-
Faucheux, B.A.1
Morain, E.2
Diouron, V.3
Brandel, J.P.4
Salomon, D.5
Sazdovitch, V.6
-
93
-
-
33644845779
-
Analysis of prion strains by prpsc profiling in sporadic creutzfeldt-jakob disease
-
PMID:16354106
-
Schoch G, Seeger H, Bogousslavsky J, Tolnay M, Janzer RC, Aguzzi A, et al. Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease. PLoS Med 2006; 3:e14; PMID:16354106; http://dx.doi.org/10.1371/journal. pmed.0030014.
-
(2006)
PLoS Med
, vol.3
-
-
Schoch, G.1
Seeger, H.2
Bogousslavsky, J.3
Tolnay, M.4
Janzer, R.C.5
Aguzzi, A.6
-
94
-
-
0032763817
-
Sporadic creutzfeldt-jakob disease: Co-occurrence of different types of prp(sc) in the same brain
-
PMID:10599800
-
Puoti G, Giaccone G, Rossi G, Canciani B, Bugiani O, Tagliavini F. Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain. Neurology 1999; 53:2173-6; PMID:10599800; http://dx.doi.org/10.1212/WNL.53.9.2173.
-
(1999)
Neurology
, vol.53
, pp. 2173-6
-
-
Puoti, G.1
Giaccone, G.2
Rossi, G.3
Canciani, B.4
Bugiani, O.5
Tagliavini, F.6
-
95
-
-
70349937836
-
Co-existence of scrapie prion protein types 1 and 2 in sporadic creutzfeldt-jakob disease: Its effect on the phenotype and prion-type characteristics
-
PMID:19734292
-
Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, et al. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. Brain 2009; 132:2643-58; PMID:19734292; http://dx.doi.org/10. 1093/brain/awp196.
-
(2009)
Brain
, vol.132
, pp. 2643-58
-
-
Cali, I.1
Castellani, R.2
Alshekhlee, A.3
Cohen, Y.4
Blevins, J.5
Yuan, J.6
-
96
-
-
33645778583
-
Efficient transmission and characterization of creutzfeldt-jakob disease strains in bank voles
-
PMID:16518470
-
Nonno R, Di Bari MA, Cardone F, Vaccari G, Fazzi P, Dell'Omo G, et al. Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles. PLoS Pathog 2006; 2:e12; PMID:16518470; http://dx.doi.org/10. 1371/journal.ppat.0020012.
-
(2006)
PLoS Pathog
, vol.2
-
-
Nonno, R.1
Di Bari, M.A.2
Cardone, F.3
Vaccari, G.4
Fazzi, P.5
Dell'Omo, G.6
-
97
-
-
77955344991
-
Defining sporadic creutzfeldt-jakob disease strains and their transmission properties
-
PMID:20547859
-
Bishop MT, Will RG, Manson JC. Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties. Proc Natl Acad Sci U S A 2010; 107:12005-10; PMID:20547859; http://dx.doi.org/10.1073/pnas.1004688107.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 12005-10
-
-
Bishop, M.T.1
Will, R.G.2
Manson, J.C.3
-
98
-
-
30344438495
-
Detection of type 1 prion protein in variant creutzfeldt-jakob disease
-
PMID:16400018
-
Yull HM, Ritchie DL, Langeveld JP, van Zijderveld FG, Bruce ME, Ironside JW, et al. Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease. Am J Pathol 2006; 168:151-7; PMID:16400018; http://dx.doi.org/10.2353/ ajpath.2006.050766.
-
(2006)
Am J Pathol
, vol.168
, pp. 151-157
-
-
Yull, H.M.1
Ritchie, D.L.2
Langeveld, J.P.3
Van Zijderveld, F.G.4
Bruce, M.E.5
Ironside, J.W.6
-
99
-
-
0030820354
-
The same prion strain causes vcjd and bse
-
526 PMID:9333232
-
Hill AF, Desbruslais M, Joiner S, Sidle KC, Gowland I, Collinge J, et al. The same prion strain causes vCJD and BSE. Nature 1997; 389:448-50, 526; PMID:9333232; http://dx.doi.org/10.1038/38925
-
(1997)
Nature
, vol.389
, pp. 448-50
-
-
Hill, A.F.1
Desbruslais, M.2
Joiner, S.3
Sidle, K.C.4
Gowland, I.5
Collinge, J.6
-
100
-
-
65249149613
-
Variant creutzfeldt-jakob disease in france and the united kingdom: Evidence for the same agent strain
-
PMID:19334063
-
Brandel JP, Heath CA, Head MW, Levavasseur E, Knight R, Laplanche JL, et al. Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain. Ann Neurol 2009; 65:249-56; PMID:19334063; http://dx.doi.org/10.1002/ana.21583.
-
(2009)
Ann Neurol
, vol.65
, pp. 249-56
-
-
Brandel, J.P.1
Heath, C.A.2
Head, M.W.3
Levavasseur, E.4
Knight, R.5
Laplanche, J.L.6
-
101
-
-
2942694110
-
Standards for the assay of creutzfeldt-jakob disease specimens
-
WHO Working Group on International Reference Materials for the Diagnosis and Study of Transmissible Spongiform Encephalopathies PMID:15166463
-
Minor P, Newham J, Jones N, Bergeron C, Gregori L, Asher D, et al.; WHO Working Group on International Reference Materials for the Diagnosis and Study of Transmissible Spongiform Encephalopathies. Standards for the assay of Creutzfeldt-Jakob disease specimens. J Gen Virol 2004; 85:1777-84; PMID:15166463; http://dx.doi.org/10.1099/vir.0.79959-0.
-
(2004)
J Gen Virol
, vol.85
, pp. 1777-84
-
-
Minor, P.1
Newham, J.2
Jones, N.3
Bergeron, C.4
Gregori, L.5
Asher, D.6
-
102
-
-
56949108846
-
Transmission of atypical bovine prions to mice transgenic for human prion protein
-
PMID:19046515
-
Béringue V, Herzog L, Reine F, Le Dur A, Casalone C, Vilotte JL, et al. Transmission of atypical bovine prions to mice transgenic for human prion protein. Emerg Infect Dis 2008; 14:1898-901; PMID:19046515; http://dx.doi.org/10.3201/eid1412.080941.
-
(2008)
Emerg Infect Dis
, vol.14
, pp. 1898-901
-
-
Béringue, V.1
Herzog, L.2
Reine, F.3
Le Dur, A.4
Casalone, C.5
Vilotte, J.L.6
-
103
-
-
38949108662
-
Prominent and persistent extraneural infection in human prp transgenic mice infected with variant cjd
-
PMID:18183299
-
Béringue V, Le Dur A, Tixador P, Reine F, Lepourry L, Perret-Liaudet A, et al. Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD. PLoS One 2008; 3:e1419; PMID:18183299; http://dx.doi.org/10.1371/journal.pone.0001419.
-
(2008)
PLoS One
, vol.3
-
-
Béringue, V.1
Le Dur, A.2
Tixador, P.3
Reine, F.4
Lepourry, L.5
Perret-Liaudet, A.6
-
104
-
-
3142514201
-
Protein aggregation and neurodegenerative disease
-
PMID:15272267
-
Ross CA, Poirier MA. Protein aggregation and neurodegenerative disease. Nat Med 2004; 10(Suppl):S10-7; PMID:15272267; http://dx.doi.org/10.1038/nm1066.
-
(2004)
Nat Med
, vol.10
, Issue.SUPPL.
-
-
Ross, C.A.1
Poirier, M.A.2
-
105
-
-
70349705441
-
Prions: Protein aggregation and infectious diseases
-
PMID:19789378
-
Aguzzi A, Calella AM. Prions: protein aggregation and infectious diseases. Physiol Rev 2009; 89:1105-52; PMID:19789378; http://dx.doi.org/10. 1152/physrev. 00006.2009.
-
(2009)
Physiol Rev
, vol.89
, pp. 1105-1152
-
-
Aguzzi, A.1
Calella, A.M.2
|