-
1
-
-
33748342540
-
Early intermediate in human prion protein folding as evidenced by ultrarapid mixing experiments
-
Apetri A. C., Maki K., Roder H. Surewicz W. K. (2006) Early intermediate in human prion protein folding as evidenced by ultrarapid mixing experiments. J. Am. Chem. Soc. 128, 11673 11678.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 11673-11678
-
-
Apetri, A.C.1
Maki, K.2
Roder, H.3
Surewicz, W.K.4
-
2
-
-
20544459159
-
Visualization of prion infection in transgenic mice expressing green fluorescent protein-tagged prion protein
-
Barmada S. J. Harris D. A. (2005) Visualization of prion infection in transgenic mice expressing green fluorescent protein-tagged prion protein. J. Neurosci. 25, 5824 5832.
-
(2005)
J. Neurosci.
, vol.25
, pp. 5824-5832
-
-
Barmada, S.J.1
Harris, D.A.2
-
3
-
-
3242661985
-
GFP-tagged prion protein is correctly localized and functionally active in the brains of transgenic mice
-
Barmada S., Piccardo P., Yamaguchi K., Ghetti B. Harris D. A. (2004) GFP-tagged prion protein is correctly localized and functionally active in the brains of transgenic mice. Neurobiol. Dis. 16, 527 537.
-
(2004)
Neurobiol. Dis.
, vol.16
, pp. 527-537
-
-
Barmada, S.1
Piccardo, P.2
Yamaguchi, K.3
Ghetti, B.4
Harris, D.A.5
-
4
-
-
1542379868
-
Autocatalytic conversion of recombinant prion proteins displays a species barrier
-
Baskakov I. V. (2004) Autocatalytic conversion of recombinant prion proteins displays a species barrier. J. Biol. Chem. 279, 7671 7677.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 7671-7677
-
-
Baskakov, I.V.1
-
5
-
-
34249947345
-
Converting the prion protein: What makes the protein infectious
-
Baskakov I. V. Breydo L. (2007) Converting the prion protein: what makes the protein infectious. Biochim. Biophys. Acta 1772, 692 703.
-
(2007)
Biochim. Biophys. Acta
, vol.1772
, pp. 692-703
-
-
Baskakov, I.V.1
Breydo, L.2
-
6
-
-
0037077234
-
Pathway complexity of prion protein assembly into amyloid
-
Baskakov I. V., Legname G., Baldwin M. A., Prusiner S. B. Cohen F. E. (2002) Pathway complexity of prion protein assembly into amyloid. J. Biol. Chem. 277, 21140 21148.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 21140-21148
-
-
Baskakov, I.V.1
Legname, G.2
Baldwin, M.A.3
Prusiner, S.B.4
Cohen, F.E.5
-
7
-
-
33646728858
-
Analysis of the cerebellar proteome in a transgenic mouse model of inherited prion disease reveals preclinical alteration of calcineurin activity
-
Biasini E., Massignan T., Fioriti L., Rossi V., Dossena S., Salmona M., Forloni G., Bonetto V. Chiesa R. (2006) Analysis of the cerebellar proteome in a transgenic mouse model of inherited prion disease reveals preclinical alteration of calcineurin activity. Proteomics 6, 2823 2834.
-
(2006)
Proteomics
, vol.6
, pp. 2823-2834
-
-
Biasini, E.1
Massignan, T.2
Fioriti, L.3
Rossi, V.4
Dossena, S.5
Salmona, M.6
Forloni, G.7
Bonetto, V.8
Chiesa, R.9
-
8
-
-
33644858238
-
Annealing prion protein amyloid fibrils at high temperature results in extension of a proteinase K-resistant core
-
Bocharova O. V., Makarava N., Breydo L., Anderson M., Salnikov V. V. Baskakov I. V. (2006) Annealing prion protein amyloid fibrils at high temperature results in extension of a proteinase K-resistant core. J. Biol. Chem. 281, 2373 2379.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 2373-2379
-
-
Bocharova, O.V.1
Makarava, N.2
Breydo, L.3
Anderson, M.4
Salnikov, V.V.5
Baskakov, I.V.6
-
9
-
-
0025740570
-
Molecular location of a species-specific epitope on the hamster scrapie agent protein
-
Bolton D. C., Seligman S. J., Bablanian G., Windsor D., Scala L. J., Kim K. S., Chen C. M., Kascsak R. J. Bendheim P. E. (1991) Molecular location of a species-specific epitope on the hamster scrapie agent protein. J. Virol. 65, 3667 3675.
-
(1991)
J. Virol.
, vol.65
, pp. 3667-3675
-
-
Bolton, D.C.1
Seligman, S.J.2
Bablanian, G.3
Windsor, D.4
Scala, L.J.5
Kim, K.S.6
Chen, C.M.7
Kascsak, R.J.8
Bendheim, P.E.9
-
10
-
-
0028235176
-
Human spongiform encephalopathy: The National Institutes of Health series of 300 cases of experimentally transmitted disease
-
Brown P., Gibbs C. J., Rodgers-Johnson P., Asher D. M., Sulima M. P., Bacote A., Goldfarb L. G. Gajdusek D. C. (1994) Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann. Neurol. 35, 513 529.
-
(1994)
Ann. Neurol.
, vol.35
, pp. 513-529
-
-
Brown, P.1
Gibbs, C.J.2
Rodgers-Johnson, P.3
Asher, D.M.4
Sulima, M.P.5
Bacote, A.6
Goldfarb, L.G.7
Gajdusek, D.C.8
-
11
-
-
0026600865
-
Normal development and behavior of mice lacking the neuronal cell-surface PrP protein
-
Büeler H., Fischer M., Lang Y., Fluethmann H., Lipp H.-P., DeArmond S. J., Prusiner S. B., Aguet M. Weissmann C. (1992) Normal development and behavior of mice lacking the neuronal cell-surface PrP protein. Nature 356, 577 582.
-
(1992)
Nature
, vol.356
, pp. 577-582
-
-
Büeler, H.1
Fischer, M.2
Lang, Y.3
Fluethmann, H.4
Lipp, H.-P.5
Dearmond, S.J.6
Prusiner, S.B.7
Aguet, M.8
Weissmann, C.9
-
12
-
-
17444413067
-
In vitro generation of infectious scrapie prions
-
Castilla J., Saa P., Hetz C. Soto C. (2005) In vitro generation of infectious scrapie prions. Cell 121, 195 206.
-
(2005)
Cell
, vol.121
, pp. 195-206
-
-
Castilla, J.1
Saa, P.2
Hetz, C.3
Soto, C.4
-
13
-
-
0035312586
-
Interactions between prion protein isoforms: The kiss of death?
-
Caughey B. (2001) Interactions between prion protein isoforms: the kiss of death? Trends Biochem. Sci. 26, 235 242.
-
(2001)
Trends Biochem. Sci.
, vol.26
, pp. 235-242
-
-
Caughey, B.1
-
14
-
-
0029027854
-
Truncated forms of the human prion protein in normal brain and in prion diseases
-
Chen S. G., Teplow D. B., Parchi P., Teller J. K., Gambetti P. Autilio-Gambetti L. (1995) Truncated forms of the human prion protein in normal brain and in prion diseases. J. Biol. Chem. 270, 19173 19180.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 19173-19180
-
-
Chen, S.G.1
Teplow, D.B.2
Parchi, P.3
Teller, J.K.4
Gambetti, P.5
Autilio-Gambetti, L.6
-
15
-
-
0035168351
-
Prion diseases: What is the neurotoxic molecule?
-
Chiesa R. Harris D. A. (2001) Prion diseases: what is the neurotoxic molecule? Neurobiol. Dis. 8, 743 763.
-
(2001)
Neurobiol. Dis.
, vol.8
, pp. 743-763
-
-
Chiesa, R.1
Harris, D.A.2
-
16
-
-
0032427904
-
Neurological illness in transgenic mice expressing a prion protein with an insertional mutation
-
Chiesa R., Piccardo P., Ghetti B. Harris D. A. (1998) Neurological illness in transgenic mice expressing a prion protein with an insertional mutation. Neuron 21, 1339 1351.
-
(1998)
Neuron
, vol.21
, pp. 1339-1351
-
-
Chiesa, R.1
Piccardo, P.2
Ghetti, B.3
Harris, D.A.4
-
17
-
-
0034625069
-
Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation
-
Chiesa R., Drisaldi B., Quaglio E., Migheli A., Piccardo P., Ghetti B. Harris D. A. (2000) Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation. Proc. Natl Acad. Sci. USA 97, 5574 5579.
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 5574-5579
-
-
Chiesa, R.1
Drisaldi, B.2
Quaglio, E.3
Migheli, A.4
Piccardo, P.5
Ghetti, B.6
Harris, D.A.7
-
18
-
-
0038128629
-
Molecular distinction between pathogenic and infectious properties of the prion protein
-
Chiesa R., Piccardo P., Quaglio E., Drisaldi B., Si-Hoe S. L., Takao M., Ghetti B. Harris D. A. (2003) Molecular distinction between pathogenic and infectious properties of the prion protein. J. Virol. 77, 7611 7622.
-
(2003)
J. Virol.
, vol.77
, pp. 7611-7622
-
-
Chiesa, R.1
Piccardo, P.2
Quaglio, E.3
Drisaldi, B.4
Si-Hoe, S.L.5
Takao, M.6
Ghetti, B.7
Harris, D.A.8
-
19
-
-
11844296730
-
Bax deletion prevents neuronal loss but not neurological symptoms in a transgenic model of inherited prion disease
-
Chiesa R., Piccardo P., Dossena S., Nowoslawski L., Roth K. A., Ghetti B. Harris D. A. (2005) Bax deletion prevents neuronal loss but not neurological symptoms in a transgenic model of inherited prion disease. Proc. Natl Acad. Sci. USA 102, 238 243.
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 238-243
-
-
Chiesa, R.1
Piccardo, P.2
Dossena, S.3
Nowoslawski, L.4
Roth, K.A.5
Ghetti, B.6
Harris, D.A.7
-
20
-
-
22844438894
-
Protease-resistant prion protein amplification reconstituted with partially purified substrates and synthetic polyanions
-
Deleault N. R., Geoghegan J. C., Nishina K., Kascsak R., Williamson R. A. Supattapone S. (2005) Protease-resistant prion protein amplification reconstituted with partially purified substrates and synthetic polyanions. J. Biol. Chem. 280, 26873 26879.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 26873-26879
-
-
Deleault, N.R.1
Geoghegan, J.C.2
Nishina, K.3
Kascsak, R.4
Williamson, R.A.5
Supattapone, S.6
-
21
-
-
0027258807
-
Dementia associated with a 216 base pair insertion in the prion protein gene: Clinical and neuropathological features
-
Duchen L. W., Poulter M. Harding A. E. (1993) Dementia associated with a 216 base pair insertion in the prion protein gene: clinical and neuropathological features. Brain 116, 555 567.
-
(1993)
Brain
, vol.116
, pp. 555-567
-
-
Duchen, L.W.1
Poulter, M.2
Harding, A.E.3
-
22
-
-
33847662852
-
Soluble protein oligomers in neurodegeneration: Lessons from the Alzheimer's amyloid beta-peptide
-
Haass C. Selkoe D. J. (2007) Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid beta-peptide. Nat. Rev. Mol. Cell. Biol. 8, 101 112.
-
(2007)
Nat. Rev. Mol. Cell. Biol.
, vol.8
, pp. 101-112
-
-
Haass, C.1
Selkoe, D.J.2
-
23
-
-
33646126278
-
New insights into prion structure and toxicity
-
Harris D. A. True H. L. (2006) New insights into prion structure and toxicity. Neuron 50, 353 357.
-
(2006)
Neuron
, vol.50
, pp. 353-357
-
-
Harris, D.A.1
True, H.L.2
-
24
-
-
1842644947
-
Inherited prion diseases
-
in. Prusiner, S. B., ed. pp. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
Kong Q., Surewicz W. K., Petersen R. B. et al. (2004) Inherited prion diseases, in Prion Biology and Diseases (Prusiner S. B., ed pp. 673 775. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(2004)
Prion Biology and Diseases
, pp. 673-775
-
-
Kong, Q.1
Surewicz, W.K.2
Petersen, R.B.3
-
25
-
-
0030613755
-
Sc)-specific epitope defined by a monoclonal antibody
-
Sc)-specific epitope defined by a monoclonal antibody. Nature 390, 74 77.
-
(1997)
Nature
, vol.390
, pp. 74-77
-
-
Korth, C.1
Stierli, B.2
Streit, P.3
-
26
-
-
0035907363
-
Prion protein binds copper within the physiological concentration range
-
Kramer M. L., Kratzin H. D., Schmidt B., Romer A., Windl O., Liemann S., Hornemann S. Kretzschmar H. (2001) Prion protein binds copper within the physiological concentration range. J. Biol. Chem. 276, 16711 16719.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 16711-16719
-
-
Kramer, M.L.1
Kratzin, H.D.2
Schmidt, B.3
Romer, A.4
Windl, O.5
Liemann, S.6
Hornemann, S.7
Kretzschmar, H.8
-
27
-
-
0028820863
-
Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene
-
Krasemann S., Zerr I., Weber T., Poser S., Kretzschmar H., Hunsmann G. Bodemer W. (1995) Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene. Mol. Brain Res. 34, 173 176.
-
(1995)
Mol. Brain Res.
, vol.34
, pp. 173-176
-
-
Krasemann, S.1
Zerr, I.2
Weber, T.3
Poser, S.4
Kretzschmar, H.5
Hunsmann, G.6
Bodemer, W.7
-
28
-
-
26444434251
-
Selective precipitation of prions by polyoxometalate complexes
-
Lee I. S., Long J. R., Prusiner S. B. Safar J. G. (2005) Selective precipitation of prions by polyoxometalate complexes. J. Am. Chem. Soc. 127, 13802 13803.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 13802-13803
-
-
Lee, I.S.1
Long, J.R.2
Prusiner, S.B.3
Safar, J.G.4
-
29
-
-
3442889359
-
Synthetic mammalian prions
-
Legname G., Baskakov I. V., Nguyen H. O., Riesner D., Cohen F. E., DeArmond S. J. Prusiner S. B. (2004) Synthetic mammalian prions. Science 305, 673 676.
-
(2004)
Science
, vol.305
, pp. 673-676
-
-
Legname, G.1
Baskakov, I.V.2
Nguyen, H.O.3
Riesner, D.4
Cohen, F.E.5
Dearmond, S.J.6
Prusiner, S.B.7
-
30
-
-
34447639732
-
Continuum of prion protein structures enciphers a multitude of prion isolate-specified phenotypes
-
Legname G., Nguyen H. O., Peretz D., Cohen F. E., DeArmond S. J. Prusiner S. B. (2006) Continuum of prion protein structures enciphers a multitude of prion isolate-specified phenotypes. Proc. Natl Acad. Sci. USA 103, 19105 19110.
-
(2006)
Proc. Natl Acad. Sci. USA
, 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
-
31
-
-
34249995984
-
Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice
-
Li A., Piccardo P., Barmada S. J., Ghetti B. Harris D. A. (2007) Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice. EMBO J. 26, 2777 2785.
-
(2007)
EMBO J.
, vol.26
, pp. 2777-2785
-
-
Li, A.1
Piccardo, P.2
Barmada, S.J.3
Ghetti, B.4
Harris, D.A.5
-
32
-
-
0029909560
-
Metabolic and genetic analyses of apoptosis in potassium/serum-deprived rat cerebellar granule cells
-
Miller T. M. Johnson E. M. Jr. (1996) Metabolic and genetic analyses of apoptosis in potassium/serum-deprived rat cerebellar granule cells. J. Neurosci. 16, 7487 7495.
-
(1996)
J. Neurosci.
, vol.16
, pp. 7487-7495
-
-
Miller, T.M.1
Johnson Jr., E.M.2
-
33
-
-
34249941302
-
Copper and the prion protein: Methods, structures, function, and disease
-
Millhauser G. L. (2007) Copper and the prion protein: methods, structures, function, and disease. Annu. Rev. Phys. Chem. 58, 299 320.
-
(2007)
Annu. Rev. Phys. Chem.
, vol.58
, pp. 299-320
-
-
Millhauser, G.L.1
-
35
-
-
22744448690
-
Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice
-
Nazor K. E., Kuhn F., Seward T. et al. (2005) Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice. EMBO J. 24, 2472 2480.
-
(2005)
EMBO J.
, vol.24
, pp. 2472-2480
-
-
Nazor, K.E.1
Kuhn, F.2
Seward, T.3
-
36
-
-
33744961169
-
Amyloid fibrils of mammalian prion protein are highly toxic to cultured cells and primary neurons
-
Novitskaya V., Bocharova O. V., Bronstein I. Baskakov I. V. (2006) Amyloid fibrils of mammalian prion protein are highly toxic to cultured cells and primary neurons. J. Biol. Chem. 281, 13828 13836.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 13828-13836
-
-
Novitskaya, V.1
Bocharova, O.V.2
Bronstein, I.3
Baskakov, I.V.4
-
37
-
-
0026513044
-
A dementing illness associated with a novel insertion in the prion protein gene
-
Owen F., Poulter M., Collinge J., Leach M., Lofthouse R., Crow T. J. Harding A. E. (1992) A dementing illness associated with a novel insertion in the prion protein gene. Mol. Brain Res. 13, 155 157.
-
(1992)
Mol. Brain Res.
, vol.13
, pp. 155-157
-
-
Owen, F.1
Poulter, M.2
Collinge, J.3
Leach, M.4
Lofthouse, R.5
Crow, T.J.6
Harding, A.E.7
-
38
-
-
4444356433
-
Epitope scanning reveals gain and loss of strain specific antibody binding epitopes associated with the conversion of normal cellular prion to scrapie prion
-
Pan T., Li R., Kang S. C., Wong B. S., Wisniewski T. Sy M. S. (2004) Epitope scanning reveals gain and loss of strain specific antibody binding epitopes associated with the conversion of normal cellular prion to scrapie prion. J. Neurochem. 90, 1205 1217.
-
(2004)
J. Neurochem.
, vol.90
, pp. 1205-1217
-
-
Pan, T.1
Li, R.2
Kang, S.C.3
Wong, B.S.4
Wisniewski, T.5
Sy, M.S.6
-
39
-
-
33845915792
-
Sc fraction
-
Sc fraction. Biochemistry 45, 15710 15717.
-
(2006)
Biochemistry
, vol.45
, pp. 15710-15717
-
-
Pastrana, M.A.1
Sajnani, G.2
Onisko, B.3
Castilla, J.4
Morales, R.5
Soto, C.6
Requena, J.R.7
-
40
-
-
32944457929
-
Amyloidosis
-
Pepys M. B. (2006) Amyloidosis. Annu. Rev. Med. 57, 223 241.
-
(2006)
Annu. Rev. Med.
, vol.57
, pp. 223-241
-
-
Pepys, M.B.1
-
41
-
-
34248396416
-
Accumulation of prion protein in the brain that is not associated with transmissible disease
-
Piccardo P., Manson J. C., King D., Ghetti B. Barron R. M. (2007) Accumulation of prion protein in the brain that is not associated with transmissible disease. Proc. Natl Acad. Sci. USA 104, 4712 4717.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 4712-4717
-
-
Piccardo, P.1
Manson, J.C.2
King, D.3
Ghetti, B.4
Barron, R.M.5
-
43
-
-
33845944898
-
Ultra-efficient replication of infectious prions by automated protein misfolding cyclic amplification
-
Saa P., Castilla J. Soto C. (2006) Ultra-efficient replication of infectious prions by automated protein misfolding cyclic amplification. J. Biol. Chem. 281, 35245 35252.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 35245-35252
-
-
Saa, P.1
Castilla, J.2
Soto, C.3
-
44
-
-
0035859102
-
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding
-
Saborio G. P., Permanne B. Soto C. (2001) Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature 411, 810 813.
-
(2001)
Nature
, vol.411
, pp. 810-813
-
-
Saborio, G.P.1
Permanne, B.2
Soto, C.3
-
45
-
-
0031720905
-
Sc molecules with different conformations
-
Sc molecules with different conformations. Nature Med. 4, 1157 1165.
-
(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
-
46
-
-
0034869272
-
Copper binding to the prp isoforms: A putative marker of their conformation and function
-
Shaked Y., Rosenmann H., Hijazi N., Halimi M. Gabizon R. (2001) Copper binding to the prp isoforms: a putative marker of their conformation and function. J. Virol. 75, 7872 7874.
-
(2001)
J. Virol.
, vol.75
, pp. 7872-7874
-
-
Shaked, Y.1
Rosenmann, H.2
Hijazi, N.3
Halimi, M.4
Gabizon, R.5
-
47
-
-
24644448839
-
The most infectious prion protein particles
-
Silveira J. R., Raymond G. J., Hughson A. G., Race R. E., Sim V. L., Hayes S. F. Caughey B. (2005) The most infectious prion protein particles. Nature 437, 257 261.
-
(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
Caughey, B.7
-
49
-
-
4844220510
-
Diagnosing prion diseases: Needs, challenges and hopes
-
Soto C. (2004) Diagnosing prion diseases: needs, challenges and hopes. Nat. Rev. Microbiol. 2, 809 819.
-
(2004)
Nat. Rev. Microbiol.
, vol.2
, pp. 809-819
-
-
Soto, C.1
-
50
-
-
0037965529
-
Prion protein selectively binds copper(II) ions
-
Stöckel J., Safar J., Wallace A. C., Cohen F. E. Prusiner S. B. (1998) Prion protein selectively binds copper(II) ions. Biochemistry 37, 7185 7193.
-
(1998)
Biochemistry
, vol.37
, pp. 7185-7193
-
-
Stöckel, J.1
Safar, J.2
Wallace, A.C.3
Cohen, F.E.4
Prusiner, S.B.5
-
51
-
-
33749822624
-
The emerging principles of mammalian prion propagation and transmissibility barriers: Insight from studies in vitro
-
Surewicz W. K., Jones E. M. Apetri A. C. (2006) The emerging principles of mammalian prion propagation and transmissibility barriers: insight from studies in vitro. Acc. Chem. Res. 39, 654 662.
-
(2006)
Acc. Chem. Res.
, vol.39
, pp. 654-662
-
-
Surewicz, W.K.1
Jones, E.M.2
Apetri, A.C.3
-
52
-
-
0034681173
-
Aggregation and fibrillization of the recombinant human prion protein huPrP90-231
-
Swietnicki W., Morillas M., Chen S. G., Gambetti P. Surewicz W. K. (2000) Aggregation and fibrillization of the recombinant human prion protein huPrP90-231. Biochemistry 39, 424 431.
-
(2000)
Biochemistry
, vol.39
, pp. 424-431
-
-
Swietnicki, W.1
Morillas, M.2
Chen, S.G.3
Gambetti, P.4
Surewicz, W.K.5
-
53
-
-
33746698975
-
The physical basis of how prion conformations determine strain phenotypes
-
Tanaka M., Collins S. R., Toyama B. H. Weissman J. S. (2006) The physical basis of how prion conformations determine strain phenotypes. Nature 442, 585 589.
-
(2006)
Nature
, vol.442
, pp. 585-589
-
-
Tanaka, M.1
Collins, S.R.2
Toyama, B.H.3
Weissman, J.S.4
-
54
-
-
0028878943
-
Inherited prion diseases and transmission to rodents
-
Tateishi J. Kitamoto T. (1995) Inherited prion diseases and transmission to rodents. Brain Pathol. 5, 53 59.
-
(1995)
Brain Pathol.
, vol.5
, pp. 53-59
-
-
Tateishi, J.1
Kitamoto, T.2
-
55
-
-
0037159185
-
Protease-sensitive scrapie prion protein in aggregates of heterogeneous sizes
-
Tzaban S., Friedlander G., Schonberger O., Horonchik L., Yedidia Y., Shaked G., Gabizon R. Taraboulos A. (2002) Protease-sensitive scrapie prion protein in aggregates of heterogeneous sizes. Biochemistry 41, 12868 12875.
-
(2002)
Biochemistry
, vol.41
, pp. 12868-12875
-
-
Tzaban, S.1
Friedlander, G.2
Schonberger, O.3
Horonchik, L.4
Yedidia, Y.5
Shaked, G.6
Gabizon, R.7
Taraboulos, A.8
-
56
-
-
0035928432
-
Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay
-
Wadsworth J. D., Joiner S., Hill A. F., Campbell T. A., Desbruslais M., Luthert P. J. Collinge J. (2001) Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay. Lancet 358, 171 180.
-
(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
Collinge, J.7
-
57
-
-
9444267651
-
The state of the prion
-
Weissmann C. (2004) The state of the prion. Nat. Rev. Microbiol. 2, 861 871.
-
(2004)
Nat. Rev. Microbiol.
, vol.2
, pp. 861-871
-
-
Weissmann, C.1
-
59
-
-
33845925066
-
Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains
-
Yuan J., Xiao X., McGeehan J. et al. (2006) Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains. J. Biol. Chem. 281, 34848 34858.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 34848-34858
-
-
Yuan, J.1
Xiao, X.2
McGeehan, J.3
-
60
-
-
13144256747
-
Prion protein expression in different species: Analysis with a panel of new mAbs
-
Zanusso G., Liu D., Ferrari S. et al. (1998) Prion protein expression in different species: analysis with a panel of new mAbs. Proc. Natl Acad. Sci. USA 95, 8812 8816.
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 8812-8816
-
-
Zanusso, G.1
Liu, D.2
Ferrari, S.3
|