-
1
-
-
0033570204
-
Prion protein interconversions and the transmissible spongiform encephalopathies
-
DOI 10.1016/S0969-2126(00)80049-0
-
Horiuchi, M. & Caughey, B. Prion protein interconversions and the transmissible spongiform encephalopathies. Structure 7, R231-R240 (1999). (Pubitemid 29482978)
-
(1999)
Structure
, vol.7
, Issue.10
-
-
Horiuchi, M.1
Caughey, B.2
-
2
-
-
0025244011
-
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
-
Prusiner, S. B. et al. Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication. Cell 63, 673-686 (1990). (Pubitemid 120035041)
-
(1990)
Cell
, vol.63
, Issue.4
, pp. 673-686
-
-
Prusiner, S.B.1
Scott, M.2
Foster, D.3
Pan, K.-M.4
Groth, D.5
Mirenda, C.6
Torchia, M.7
Yang, S.-L.8
Serban, D.9
Carlson, G.A.10
Hoppe, P.C.11
Westaway, D.12
Dearmond, S.J.13
-
3
-
-
0026600865
-
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
-
Büeler, H. et al. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature 356, 577-582 (1992).
-
(1992)
Nature
, vol.356
, pp. 577-582
-
-
Büeler, H.1
-
4
-
-
0027229676
-
Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes
-
DOI 10.1016/0092-8674(93)90275-U
-
Scott, M. et al. Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes. Cell 73, 979-988 (1993). (Pubitemid 23165612)
-
(1993)
Cell
, vol.73
, Issue.5
, pp. 979-988
-
-
Scott, M.1
Groth, D.2
Foster, D.3
Torchia, M.4
Yang, S.-L.5
DeArmond, S.J.6
Prusiner, S.B.7
-
5
-
-
0027086835
-
Chimeric prion protein expression in cultured cells and transgenic mice
-
Scott, M. R., Köhler, R., Foster, D. & Prusiner, S. B. Chimeric prion protein expression in cultured cells and transgenic mice. Protein Sci. 1, 986-997 (1992). (Pubitemid 23009207)
-
(1992)
Protein Science
, vol.1
, Issue.8
, pp. 986-997
-
-
Scott, M.R.1
Kohler, R.2
Foster, D.3
Prusiner, S.B.4
-
6
-
-
0028364192
-
Heterologous PrP molecules interfere with accumulation of protease-resistant PrP in scrapie-infected murine neuroblastoma cells
-
Priola, S. A., Caughey, B., Race, R. E. & Chesebro, B. Heterologous PrP molecules interfere with accumulation of protease-resistant PrP in scrapie-infected murine neuroblastoma cells. J. Virol. 68, 4873-4878 (1994).
-
(1994)
J. Virol
, vol.68
, pp. 4873-4878
-
-
Priola, S.A.1
Caughey, B.2
Race, R.E.3
Chesebro, B.4
-
7
-
-
0023806142
-
A modified host protein model of scrapie
-
Bolton, D. C. & Bendheim, P. E. A modified host protein model of scrapie. Ciba. Found. Symp. 135, 164-181 (1988).
-
(1988)
Ciba. Found. Symp
, vol.135
, pp. 164-181
-
-
Bolton, D.C.1
Bendheim, P.E.2
-
8
-
-
0022802258
-
The major polypeptide of scrapie-associated fibrils (SAF) has the same size, charge distribution and N-terminal protein sequence as predicted for the normal brain protein (PrP)
-
Hope, J. et al. The major polypeptide of scrapie-associated fibrils (SAF) has the same size, charge distribution and N-terminal protein sequence as predicted for the normal brain protein (PrP). EMBO J. 5, 2591-2597 (1986).
-
(1986)
EMBO J
, vol.5
, pp. 2591-2597
-
-
Hope, J.1
-
9
-
-
0027195933
-
Seeding 'one-dimensional crystallization' of amyloid: A pathogenic mechanism in Alzheimer's disease and scrapie?
-
DOI 10.1016/0092-8674(93)90635-4
-
Jarrett, J. T. & Lansbury, P. T. Jr. Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie? Cell 73, 1055-1058 (1993). (Pubitemid 23180480)
-
(1993)
Cell
, vol.73
, Issue.6
, pp. 1055-1058
-
-
Jarrett, J.T.1
Lansbury Jr., P.T.2
-
10
-
-
0027733637
-
Scrapie associated PrP accumulation and its prevention: Insights from cell culture
-
Caughey, B. Scrapie associated PrP accumulation and its prevention: insights from cell culture. Br. Med. Bull. 49, 860-872 (1993). (Pubitemid 24025993)
-
(1993)
British Medical Bulletin
, vol.49
, Issue.4
, pp. 860-872
-
-
Caughey, B.1
-
11
-
-
0028882424
-
Prion propagation inmice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
-
Telling, G. C. et al. Prion propagation inmice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein. Cell 83, 79-90 (1995).
-
(1995)
Cell
, vol.83
, pp. 79-90
-
-
Telling, G.C.1
-
12
-
-
0030931519
-
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
-
Kaneko, K. et al. Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation. Proc. Natl. Acad. Sci. USA 94, 10069-10074 (1997).
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 10069-10074
-
-
Kaneko, K.1
-
13
-
-
48849094991
-
Genes contributing to prion pathogenesis
-
Tamgüney, G. et al. Genes contributing to prion pathogenesis. J. Gen. Virol. 89, 1777-1788 (2008).
-
(2008)
J. Gen. Virol
, vol.89
, pp. 1777-1788
-
-
Tamgüney, G.1
-
14
-
-
34748863748
-
The dominant-negative effect of the Q218K variant of the prion protein does not require protein X
-
DOI 10.1110/ps.072954607
-
Lee, C. I., Yang, Q., Perrier, V. & Baskakov, I. V. The dominant-negative effect of the Q218K variant of the prion protein does not require protein X. Protein Sci. 16, 2166-2173 (2007). (Pubitemid 47481651)
-
(2007)
Protein Science
, vol.16
, Issue.10
, pp. 2166-2173
-
-
Lee, C.I.1
Yang, Q.2
Perrier, V.3
Baskakov, I.V.4
-
15
-
-
70049109405
-
Trans-dominant inhibition of prion propagation in vitro is not mediated by an accessory cofactor
-
Geoghegan, J. C. et al. Trans-dominant inhibition of prion propagation in vitro is not mediated by an accessory cofactor. PLoS Pathog 5, e1000535 (2009).
-
(2009)
PLoS Pathog
, vol.5
-
-
Geoghegan, J.C.1
-
16
-
-
84875088471
-
Glycoform-selective prion formation in sporadic and familial forms of prion disease
-
Xiao, X. et al. Glycoform-selective prion formation in sporadic and familial forms of prion disease. PLoS One 8, e58786 (2013).
-
(2013)
PLoS One
, vol.8
-
-
Xiao, X.1
-
17
-
-
33751572491
-
Sc formation in vitro
-
DOI 10.1021/bi061526k
-
Nishina, K. A. et al. The stoichiometry of host PrPC glycoforms modulates the efficiency of PrPSc formation in vitro. Biochemistry 45, 14129-14139 (2006). (Pubitemid 44846202)
-
(2006)
Biochemistry
, vol.45
, Issue.47
, pp. 14129-14139
-
-
Nishina, K.A.1
Deleault, N.R.2
Mahal, S.P.3
Baskakov, I.4
Luhrs, T.5
Riek, R.6
Supattapone, S.7
-
18
-
-
4344593431
-
Autocatalytic self-propagation of misfolded prion protein
-
DOI 10.1073/pnas.0404650101
-
Bieschke, J. et al. Autocatalytic self-propagation of misfolded prion protein. Proc. Natl. Acad. Sci. USA 101, 12207-12211 (2004). (Pubitemid 39145421)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.33
, pp. 12207-12211
-
-
Bieschke, J.1
Weber, P.2
Sarafoff, N.3
Beekes, M.4
Giese, A.5
Kretzschmar, H.6
-
19
-
-
71749087690
-
The role of glycophosphatidylinositol anchor in the amplification of the scrapie isoform of prion protein in vitro
-
Kim, J. I., Surewicz, K., Gambetti, P. & Surewicz, W. K. The role of glycophosphatidylinositol anchor in the amplification of the scrapie isoform of prion protein in vitro. FEBS Lett. 583, 3671-3675 (2009).
-
(2009)
FEBS Lett
, vol.583
, pp. 3671-3675
-
-
Kim, J.I.1
Surewicz, K.2
Gambetti, P.3
Surewicz, W.K.4
-
20
-
-
73349140865
-
Interactome analyses identify ties of PrP and its mammalian paralogs to oligomannosidic N-glycans and endoplasmic reticulum-derived chaperones
-
Watts, J. C. et al. Interactome analyses identify ties of PrP and its mammalian paralogs to oligomannosidic N-glycans and endoplasmic reticulum-derived chaperones. PLoS Pathog. 5, e1000608 (2009).
-
(2009)
PLoS Pathog
, vol.5
-
-
Watts, J.C.1
-
21
-
-
81255152420
-
Alkylating antitumor drug mechlorethamine conceals a structured PrP domain and inhibits in vitro prion amplification
-
Zhou, X. et al. Alkylating antitumor drug mechlorethamine conceals a structured PrP domain and inhibits in vitro prion amplification. J. Toxicol. Environ. Health A. 74, 1493-1503 (2011).
-
(2011)
J. Toxicol. Environ. Health A
, vol.74
, pp. 1493-1503
-
-
Zhou, X.1
-
22
-
-
0842277807
-
Antibody to DNA detects scrapie but not normal prion protein
-
Zou, W. Q. et al. Antibody to DNA detects scrapie but not normal prion protein. Proc. Natl. Acad. Sci. USA 101, 1380-1385 (2004).
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 1380-1385
-
-
Zou, W.Q.1
-
23
-
-
0033601248
-
Membrane environment alters the conformational structure of the recombinant human prion protein
-
Morillas, M., Swietnicki, W., Gambetti, P. & Surewicz, W. K. Membrane environment alters the conformational structure of the recombinant human prion protein. J. Biol. Chem. 274, 36859-36865 (1999).
-
(1999)
J. Biol. Chem
, vol.274
, pp. 36859-36865
-
-
Morillas, M.1
Swietnicki, W.2
Gambetti, P.3
Surewicz, W.K.4
-
24
-
-
0024545093
-
Prion protein biosynthesis in scrapie-infected and uninfected neuroblastoma cells
-
Caughey, B. et al. Prion protein biosynthesis in scrapie-infected and uninfected neuroblastoma cells. J. Virol. 63, 175-181 (1989). (Pubitemid 19028095)
-
(1989)
Journal of Virology
, vol.63
, Issue.1
, pp. 175-181
-
-
Caughey, B.1
Race, R.E.2
Ernst, D.3
Buchmeier, M.J.4
Chesebro, B.5
-
25
-
-
0034001444
-
Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie- associated prion protein accumulation
-
DOI 10.1128/JVI.74.10.4894-4897.2000
-
Doh-Ura, K., Iwaki, T. & Caughey, B. Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie-associated prion protein accumulation. J Virol. 74, 4894-4897 (2000). (Pubitemid 30237920)
-
(2000)
Journal of Virology
, vol.74
, Issue.10
, pp. 4894-4897
-
-
Doh-Ura, K.1
Iwaki, T.2
Caughey, B.3
-
26
-
-
24644450571
-
Increased susceptibility to oxidative stress in scrapie-infected neuroblastoma cells is associated with intracellular iron status
-
DOI 10.1016/j.neulet.2005.07.032, PII S0304394005008414
-
Fernaeus, S., Reis, K., Bedecs, K. & Land, T. Increased susceptibility to oxidative stress in scrapie-infected neuroblastoma cells is associated with intracellular iron status. Neurosci Lett. 389, 133-136 (2005). (Pubitemid 41267213)
-
(2005)
Neuroscience Letters
, vol.389
, Issue.3
, pp. 133-136
-
-
Fernaeus, S.1
Reis, K.2
Bedecs, K.3
Land, T.4
-
27
-
-
33845925066
-
Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains
-
DOI 10.1074/jbc.M602238200
-
Yuan, J. et al. Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains. J. Biol. Chem. 281, 34848-34858 (2006). (Pubitemid 46036524)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.46
, pp. 34848-34858
-
-
Yuan, J.1
Xiao, X.2
McGeehan, J.3
Dong, Z.4
Cali, I.5
Fujioka, H.6
Kong, Q.7
Kneale, G.8
Gambetti, P.9
Zou, W.-Q.10
-
28
-
-
0034705020
-
Interactions between heterologous forms of prion protein: Binding, inhibition of conversion, and species barriers
-
DOI 10.1073/pnas.110523897
-
Horiuchi, M., Priola, S. A., Chabry, J. & Caughey, B. Interactions between heterologous forms of prion protein: binding, inhibition of conversion, and species barriers. Proc. Natl. Acad. Sci. USA 97, 5836-5841 (2000). (Pubitemid 30367485)
-
(2000)
Proceedings of the National Academy of Sciences of the United States of America
, vol.97
, Issue.11
, pp. 5836-5841
-
-
Horiuchi, M.1
Priola, S.A.2
Chabry, J.3
Caughey, B.4
-
29
-
-
0024744915
-
Asparagine-linked glycosylation of the scrapie and cellular prion proteins
-
Haraguchi, T. et al. Asparagine-linked glycosylation of the scrapie and cellular prion proteins. Arch Biochem Biophys. 274, 1-13 (1989).
-
(1989)
Arch Biochem Biophys
, vol.274
, pp. 1-13
-
-
Haraguchi, T.1
-
30
-
-
0023663071
-
Scrapie prion protein contains a phosphatidylinositol glycolipid
-
Stahl, N., Borchelt, D. R.,Hsiao, K.&Prusiner, S. B. Scrapie prion protein contains a phosphatidylinositol glycolipid. Cell 51, 229-240 (1987).
-
(1987)
Cell
, vol.51
, pp. 229-240
-
-
Stahl, N.1
Borchelt, D.R.2
Hsiao D, K.3
Prusiner, S.B.4
-
31
-
-
0035803405
-
Glycosylation influences cross-species formation of protease-resistant prion protein
-
DOI 10.1093/emboj/20.23.6692
-
Priola, S. A. & Lawson, V. A. Glycosylation influences cross-species formation of protease-resistant prion protein. EMBO J. 20, 6692-6699 (2001). (Pubitemid 33134199)
-
(2001)
EMBO Journal
, vol.20
, Issue.23
, pp. 6692-6699
-
-
Priola, S.A.1
Lawson, V.A.2
-
32
-
-
84883776249
-
Species barriers in prion disease
-
Zou, W. Q. & Gambetti, P. (eds.) Springer Science, New York
-
Priola, S. A. Species barriers in prion disease. Prions and Diseases. Zou, W. Q. & Gambetti, P. (eds.), 139-154 (Springer Science, New York, 2013).
-
Prions and Diseases
, vol.2013
, pp. 139-154
-
-
Priola, S.A.1
-
33
-
-
33749665082
-
Sc glycosylation
-
DOI 10.1016/j.neulet.2006.08.008, PII S0304394006008007
-
Chasseigneaux, S. et al. V180I mutation of the prion protein gene associated with atypical PrPSc glycosylation. Neurosci. Lett. 408, 165-169 (2006). (Pubitemid 44550155)
-
(2006)
Neuroscience Letters
, vol.408
, Issue.3
, pp. 165-169
-
-
Chasseigneaux, S.1
Haik, S.2
Laffont-Proust, I.3
De Marco, O.4
Lenne, M.5
Brandel, J.-P.6
Hauw, J.-J.7
Laplanche, J.-L.8
Peoc'h, K.9
-
34
-
-
80855133151
-
Characterization of spontaneously generated prion-like conformers in cultured cells
-
Zou, R. S. et al. Characterization of spontaneously generated prion-like conformers in cultured cells. Aging 3, 968-984 (2011).
-
(2011)
Aging
, vol.3
, pp. 968-984
-
-
Zou, R.S.1
-
35
-
-
34547638271
-
Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein
-
DOI 10.1038/nmeth1066, PII NMETH1066
-
Atarashi, R. et al. Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein. Nat Methods. 4, 645-650 (2007). (Pubitemid 47202476)
-
(2007)
Nature Methods
, vol.4
, Issue.8
, pp. 645-650
-
-
Atarashi, R.1
Moore, R.A.2
Sim, V.L.3
Hughson, A.G.4
Dorward, D.W.5
Onwubiko, H.A.6
Priola, S.A.7
Caughey, B.8
-
36
-
-
40149090017
-
Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking [1]
-
DOI 10.1038/nmeth0308-211, PII NMETH0308-211
-
Atarashi, R. et al. Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking. Nat Methods. 5, 211-212 (2008). (Pubitemid 351325633)
-
(2008)
Nature Methods
, vol.5
, Issue.3
, pp. 211-212
-
-
Atarashi, R.1
Wilham, J.M.2
Christensen, L.3
Hughson, A.G.4
Moore, R.A.5
Johnson, L.M.6
Onwubiko, H.A.7
Priola, S.A.8
Suzette, A.9
Caughey, B.10
-
37
-
-
77951979579
-
Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors
-
Kim, J. I. et al. Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors. J Biol Chem. 285, 14083-14087 (2010).
-
(2010)
J Biol Chem
, vol.285
, pp. 14083-14087
-
-
Kim, J.I.1
-
38
-
-
77649213673
-
Generating a prion with bacterially expressed recombinant prion protein
-
Wang, F., Wang, X., Yuan, C. G. & Ma, J. Generating a prion with bacterially expressed recombinant prion protein. Science 327, 1132-5 (2010).
-
(2010)
Science
, vol.327
, pp. 1132-1135
-
-
Wang, F.1
Wang, X.2
Yuan, C.G.3
Ma, J.4
-
39
-
-
84861848298
-
Isolation of phosphatidylethanolamine as a solitary cofactor for prion formation in the absence of nucleic acids
-
Deleault, N. R. et al. Isolation of phosphatidylethanolamine as a solitary cofactor for prion formation in the absence of nucleic acids. Proc Natl Acad Sci USA. 109, 8546-8551 (2012).
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, pp. 8546-8551
-
-
Deleault, N.R.1
-
40
-
-
77449142074
-
Recombinant prion protein induces a new transmissible prion disease in wild-type animals
-
Makarava, N. et al. Recombinant prion protein induces a new transmissible prion disease in wild-type animals. Acta Neuropathol. 119, 177-187 (2010).
-
(2010)
Acta Neuropathol
, vol.119
, pp. 177-187
-
-
Makarava, N.1
-
41
-
-
0027956109
-
Cell-free formation of protease-resistant prion protein
-
DOI 10.1038/370471a0
-
Kocisko, D. A. et al. Cell-free formation of protease-resistant prion protein. Nature 370, 471-474 (1994). (Pubitemid 24263553)
-
(1994)
Nature
, vol.370
, Issue.6489
, pp. 471-474
-
-
Kocisko, D.A.1
Come, J.H.2
Priola, S.A.3
Chesebro, B.4
Raymond, G.J.5
Lansbury, P.T.6
Caughey, B.7
-
42
-
-
0035961323
-
Prion protein interconversions
-
DOI 10.1098/rstb.2000.0765
-
Caughey, B. Prion protein interconversions. Philos. Trans. R. Soc. Lond. B Biol. Sci. 356, 197-202 (2001). (Pubitemid 32241468)
-
(2001)
Philosophical Transactions of the Royal Society B: Biological Sciences
, vol.356
, Issue.1406
, pp. 197-202
-
-
Caughey, B.1
Pepys, M.B.2
Kelly, J.W.3
Ellis, R.J.4
Collinge, J.5
Perutz, M.F.6
Masel, J.7
-
43
-
-
0036500554
-
Sc) into contiguous membranes
-
DOI 10.1093/emboj/21.5.1031
-
Baron, G. S. et al. Conversion of raft associated prion protein to the proteaseresistant state requires insertion of PrP-res (PrP(Sc)) into contiguous membranes. EMBO J. 21, 1031-1040 (2002). (Pubitemid 34206176)
-
(2002)
EMBO Journal
, vol.21
, Issue.5
, pp. 1031-1040
-
-
Baron, G.S.1
Wehrly, K.2
Dorward, D.W.3
Chesebro, B.4
Caughey, B.5
-
44
-
-
0037385673
-
res as a model for conversion
-
DOI 10.1099/vir.0.18903-0
-
Kirby, L. et al. In vitro cell-free conversion of bacterial recombinant PrP to PrPres as a model for conversion. J. Gen. Virol. 84, 1013-1020 (2003). (Pubitemid 36432234)
-
(2003)
Journal of General Virology
, vol.84
, Issue.4
, pp. 1013-1020
-
-
Kirby, L.1
Birkett, C.R.2
Rudyk, H.3
Gilbert, I.H.4
Hope, J.5
-
45
-
-
20344394154
-
Medicine: Anchorless prion protein results in infectious amyloid disease without clinical scrapie
-
DOI 10.1126/science.1110837
-
Chesebro, B. et al. Anchorless prion protein results in infectious amyloid disease without clinical scrapie. Science 308, 1435-1439 (2005). (Pubitemid 40791292)
-
(2005)
Science
, vol.308
, Issue.5727
, pp. 1435-1439
-
-
Chesebro, B.1
Trifilo, M.2
Race, R.3
Meade-White, K.4
Teng, C.5
LaCasse, R.6
Raymond, L.7
Favara, C.8
Baron, G.9
Priola, S.10
Caughey, B.11
Masliah, E.12
Oldstone, M.13
-
46
-
-
0030613755
-
Prion (PrP(Sc))-specific epitope defined by a monoclonal antibody
-
DOI 10.1038/36337
-
Korth, C. et al. Prion (PrPSc)-specific epitope defined by a monoclonal antibody. Nature 390, 74-77 (1997). (Pubitemid 27494758)
-
(1997)
Nature
, vol.390
, Issue.6655
, pp. 74-77
-
-
Korth, C.1
Stierli, B.2
Streit, P.3
Moser, M.4
Schaller, O.5
Fischer, R.6
Schulz-Schaeffer, W.7
Kretzschmar, H.8
Raeber, A.9
Braun, U.10
Ehrensperger, F.11
Hornemann, S.12
Glockshuber, R.13
Riek, R.14
Billeter, M.15
Wuthrich, K.16
Oesch, B.17
-
47
-
-
0037113898
-
Sc-like form
-
DOI 10.1074/jbc.M203611200
-
Zou, W. Q. & Cashman, N. R. Acidic pH and detergents enhance in vitro conversion of human brain PrPC to a PrPSc-like form. J. Biol. Chem. 277, 43942-43947 (2002). (Pubitemid 36157818)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.46
, pp. 43942-43947
-
-
Zou, W.-Q.1
Cashman, N.R.2
-
48
-
-
33744941586
-
Intracerebroventricular delivery of dominant negative prion protein in a mouse model of iatrogenic Creutzfeldt-Jakob disease after dura graft transplantation
-
DOI 10.1016/j.neulet.2006.03.062, PII S0304394006003417
-
Furuya, K. et al. Intracerebroventricular delivery of dominant negative prion protein in a mouse model of iatrogenic Creutzfeldt-Jakob disease after dura graft transplantation. Neurosci. Lett. 402, 222-226 (2006). (Pubitemid 43850152)
-
(2006)
Neuroscience Letters
, vol.402
, Issue.3
, pp. 222-226
-
-
Furuya, K.1
Kawahara, N.2
Yamakawa, Y.3
Kishida, H.4
Hachiya, N.S.5
Nishijima, M.6
Kirino, T.7
Kaneko, K.8
-
49
-
-
84855508163
-
A novel expression system for production of soluble prion proteins in E. Coli
-
Abskharon, R. N. et al. A novel expression system for production of soluble prion proteins in E. coli. Microb. Cell Fact. 11, 6 (2012).
-
(2012)
Microb. Cell Fact
, vol.11
, pp. 6
-
-
Abskharon, R.N.1
-
50
-
-
56249094492
-
Oxidative protein folding in vitro: A study of the cooperation between quiescin-sulfhydryl oxidase and protein disulfide isomerase
-
Rancy, P. C. & Thorpe, C. Oxidative protein folding in vitro: a study of the cooperation between quiescin-sulfhydryl oxidase and protein disulfide isomerase. Biochemistry 47, 12047-12056 (2008).
-
(2008)
Biochemistry
, vol.47
, pp. 12047-12056
-
-
Rancy, P.C.1
Thorpe, C.2
-
51
-
-
0029863648
-
Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie
-
Fischer, M. et al. Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. EMBO J. 15, 1255-1264 (1996). (Pubitemid 26093461)
-
(1996)
EMBO Journal
, vol.15
, Issue.6
, pp. 1255-1264
-
-
Fischer, M.1
Rulicke, T.2
Raeber, A.3
Sailer, A.4
Moser, M.5
Oesch, B.6
Brandner, S.7
Aguzzi, A.8
Weissmann, C.9
-
52
-
-
84863999188
-
Creutzfeldt-Jakob disease with unusually extensive neuropathology in a child treated by native human growth hormone
-
Mikol, J. et al. Creutzfeldt-Jakob disease with unusually extensive neuropathology in a child treated by native human growth hormone. Clin. Neuropath. 31, 127-134 (2012).
-
(2012)
Clin. Neuropath
, vol.31
, pp. 127-134
-
-
Mikol, J.1
-
53
-
-
0033988236
-
Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein
-
Nishida, N. et al. Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein. J Virol. 74, 320-325 (2000). (Pubitemid 30002912)
-
(2000)
Journal of Virology
, vol.74
, Issue.1
, pp. 320-325
-
-
Nishida, N.1
Harris, D.A.2
Vilette, D.3
Laude, H.4
Frobert, Y.5
Grassi, J.6
Casanova, D.7
Milhavet, O.8
Lehmann, S.9
-
54
-
-
17444413067
-
In vitro generation of infectious scrapie prions
-
DOI 10.1016/j.cell.2005.02.011
-
Castilla, J., Saá, P., Hetz, C. & Soto, C. In vitro generation of infectious scrapie prions. Cell 121, 195-206 (2005). (Pubitemid 40546388)
-
(2005)
Cell
, vol.121
, Issue.2
, pp. 195-206
-
-
Castilla, J.1
Saa, P.2
Hetz, C.3
Soto, C.4
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