-
1
-
-
77749265833
-
Cultured cells produce a soluble form of the cellular prion protein
-
Borchelt D. R. & Prusiner, S. B. (1988). Cultured cells produce a soluble form of the cellular prion protein. J Cell Biol 107, 386a.
-
(1988)
J. Cell Biol.
, vol.107
-
-
Borchelt, D.R.1
Prusiner, S.B.2
-
2
-
-
0025304678
-
Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells
-
Borchelt, D. R., Scott M., Taraboulos, A., Stahl, N. & Prusiner, S. B. (1990). Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells. J Cell Biol 110, 743-752.
-
(1990)
J. Cell Biol.
, vol.110
, pp. 743-752
-
-
Borchelt, D.R.1
Scott, M.2
Taraboulos, A.3
Stahl, N.4
Prusiner, S.B.5
-
3
-
-
0028356488
-
Rapid anterograde axonal transport of the cellular prion glycoprotein in the peripheral and central nervous systems
-
Borchelt D. R., Kollatsos, V. E., Guarnieri, M., Pardo, C. A., Sisodia, S. S. & Price, D. L. (1994). Rapid anterograde axonal transport of the cellular prion glycoprotein in the peripheral and central nervous systems. J Biol Chem 269, 14711-14714.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 14711-14714
-
-
Borchelt, D.R.1
Kollatsos, V.E.2
Guarnieri, M.3
Pardo, C.A.4
Sisodia, S.S.5
Price, D.L.6
-
4
-
-
0030054010
-
Normal host prion protein necessary for scrapie-induced neurotoxicity
-
Brandner, S., Isenmann, S., Raeber, A., Fischer, M., Sailer, A., Kobayashi, Y., Marino, S., Weissmann, C. & Aguzzi, A. (1996). Normal host prion protein necessary for scrapie-induced neurotoxicity. Nature 379, 339-343.
-
(1996)
Nature
, vol.379
, pp. 339-343
-
-
Brandner, S.1
Isenmann, S.2
Raeber, A.3
Fischer, M.4
Sailer, A.5
Kobayashi, Y.6
Marino, S.7
Weissmann, C.8
Aguzzi, A.9
-
5
-
-
0020032352
-
Effect of chemicals, heat, and histopathologic processing on high-infectivity hamster-adapted scrapie virus
-
Brown, P., Rohwer, R. G., Green, E. M. & Gajdusek, D. C. (1982). Effect of chemicals, heat, and histopathologic processing on high-infectivity hamster-adapted scrapie virus. J Infect Dis 145, 683-687.
-
(1982)
J. Infect. Dis.
, vol.145
, pp. 683-687
-
-
Brown, P.1
Rohwer, R.G.2
Green, E.M.3
Gajdusek, D.C.4
-
6
-
-
0026600865
-
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
-
Büeler, H., Fisher, M., Lang, Y., Bluethmann, H., Lipp, H.-P., DeArmond, S. J., Prusiner, S. B., Aguet, M. & Weissmann, C. (1992). Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature 356, 577-582.
-
(1992)
Nature
, vol.356
, pp. 577-582
-
-
Büeler, H.1
Fisher, M.2
Lang, Y.3
Bluethmann, H.4
Lipp, H.-P.5
DeArmond, S.J.6
Prusiner, S.B.7
Aguet, M.8
Weissmann, C.9
-
7
-
-
0028276015
-
Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice
-
Carlson, G. A., Ebeling, C., Yang, S.-L., Telling, G., Torchia, M., Groth, D., Westaway, D., DeArmond, S. J. & Prusiner, S. B. (1994). Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice. Proc Natl Acad Sci U S A 91, 5690-5694.
-
(1994)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 5690-5694
-
-
Carlson, G.A.1
Ebeling, C.2
Yang, S.-L.3
Telling, G.4
Torchia, M.5
Groth, D.6
Westaway, D.7
DeArmond, S.J.8
Prusiner, S.B.9
-
8
-
-
0024545093
-
Prion protein biosynthesis in scrapie-infected and uninfected neuroblastoma cells
-
Caughey, B., Race, R. E., Ernst, D., Buchmeier, M. J. & Chesebro, B. (1989). Prion protein biosynthesis in scrapie-infected and uninfected neuroblastoma cells. J Virol 63, 175-181.
-
(1989)
J. Virol.
, vol.63
, pp. 175-181
-
-
Caughey, B.1
Race, R.E.2
Ernst, D.3
Buchmeier, M.J.4
Chesebro, B.5
-
9
-
-
0025193792
-
Normal and scrapie-associated forms of prion protein differ in their sensitivities to phospholipase and proteases in intact neuroblastoma cells
-
Caughey, B., Neary, K., Butler, R., Ernst D., Perry, L., Chesebro, B. & Race, R. E. (1990). Normal and scrapie-associated forms of prion protein differ in their sensitivities to phospholipase and proteases in intact neuroblastoma cells. J Virol 64, 1093-1101.
-
(1990)
J. Virol.
, vol.64
, pp. 1093-1101
-
-
Caughey, B.1
Neary, K.2
Butler, R.3
Ernst, D.4
Perry, L.5
Chesebro, B.6
Race, R.E.7
-
10
-
-
0030896803
-
Identification of intermediate steps in the conversion of a mutant prion protein to a scrapie-like form in cultured cells
-
Daude, N., Lehmann, S. & Harris, D. A. (1997). Identification of intermediate steps in the conversion of a mutant prion protein to a scrapie-like form in cultured cells. J Biol Chem 272, 11604-11612.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 11604-11612
-
-
Daude, N.1
Lehmann, S.2
Harris, D.A.3
-
11
-
-
0031456947
-
Structure of the recombinant full-length hamster prion protein PrP(29-231): The N terminus is highly flexible
-
Donne, D. G., Viles, J. H., Groth, D., Mehlhorn, I., James, T. L., Cohen, F. E., Prusiner, S. B., Wright, P. E. & Dyson, H. J. (1997). Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible. Proc Natl Acad Sci U S A 94, 13452-13457.
-
(1997)
Proc. Natl. Acad. Sci. U. S. A.
, 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
-
12
-
-
0038159514
-
Mutant PrP is delayed in its exit from the endoplasmic reticulum, but neither wild-type nor mutant PrP undergoes retrotranslocation prior to proteasomal degradation
-
Drisaldi, B., Stewart, R. S., Adles, C., Stewart, L. R., Quaglio, E., Biasini, E., Floriti, L., Chiesa, R. & Harris, D. A. (2003). Mutant PrP is delayed in its exit from the endoplasmic reticulum, but neither wild-type nor mutant PrP undergoes retrotranslocation prior to proteasomal degradation. J Biol Chem 278, 21732-21743.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 21732-21743
-
-
Drisaldi, B.1
Stewart, R.S.2
Adles, C.3
Stewart, L.R.4
Quaglio, E.5
Biasini, E.6
Floriti, L.7
Chiesa, R.8
Harris, D.A.9
-
14
-
-
0036956875
-
Studying gene function in eukaryotes by conditional gene inactivation
-
Gossen, M. & Bujard, H. (2002). Studying gene function in eukaryotes by conditional gene inactivation. Annu Rev Genet 36, 153-173.
-
(2002)
Annu. Rev. Genet.
, vol.36
, pp. 153-173
-
-
Gossen, M.1
Bujard, H.2
-
15
-
-
2942616602
-
Evidence for assembly of prions with left-handed β-helices into trimers
-
Govaerts, C., Wille, H., Prusiner, S. B. & Cohen, F. E. (2004). Evidence for assembly of prions with left-handed β-helices into trimers. Proc Natl Acad Sci U S A 101, 8342-8347.
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 8342-8347
-
-
Govaerts, C.1
Wille, H.2
Prusiner, S.B.3
Cohen, F.E.4
-
16
-
-
0025681138
-
Spontaneous neurodegeneration in transgenic mice with mutant prion protein
-
Hsiao, K. K., Scott, M., Foster, D., Groth, D. F., DeArmond, S. J. & Prusiner, S. B. (1990). Spontaneous neurodegeneration in transgenic mice with mutant prion protein. Science 250, 1587-1590.
-
(1990)
Science
, vol.250
, pp. 1587-1590
-
-
Hsiao, K.K.1
Scott, M.2
Foster, D.3
Groth, D.F.4
DeArmond, S.J.5
Prusiner, S.B.6
-
17
-
-
0028608963
-
Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein
-
& 7 other authors
-
Hsiao, K. K., Groth, D., Scott, M. & 7 other authors (1994). Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein. Proc Natl Acad Sci U S A 91, 9126-9130.
-
(1994)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 9126-9130
-
-
Hsiao, K.K.1
Groth, D.2
Scott, M.3
-
18
-
-
0034723133
-
A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice
-
& 9 other authors
-
Kaneko, K., Ball, H. L., Wille, H. & 9 other authors (2000). A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice. J Mol Biol 295, 997-1007.
-
(2000)
J. Mol. Biol.
, vol.295
, pp. 997-1007
-
-
Kaneko, K.1
Ball, H.L.2
Wille, H.3
-
19
-
-
0037447071
-
Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene
-
& 11 other authors
-
Korth, C., Kaneko, K, Groth, D. & 11 other authors (2003). Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene. Proc Natl Acad Sci U S A 100, 4784-4789.
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 4784-4789
-
-
Korth, C.1
Kaneko, K.2
Groth, D.3
-
20
-
-
3442889359
-
Synthetic mammalian prions
-
Legname, G., Baskakov, I. V., Nguyen, H.-O. B., 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.B.3
Riesner, D.4
Cohen, F.E.5
DeArmond, S.J.6
Prusiner, S.B.7
-
21
-
-
0037188506
-
Amyloid aggregates of the HET-s prion protein are infectious
-
Maddelein, M. L., Dos Reis, S., Duvezin-Caubet, S., Coulary-Salin, B. & Saupe, S. J. (2002). Amyloid aggregates of the HET-s prion protein are infectious. Proc Natl Acad Sci U S A 99, 7402-7407.
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 7402-7407
-
-
Maddelein, M.L.1
Dos Reis, S.2
Duvezin-Caubet, S.3
Coulary-Salin, B.4
Saupe, S.J.5
-
22
-
-
0242363656
-
Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis
-
Mallucci, G., Dickinson, A., Linehan, J., Klohn, P. C., Brandner, S. & Collinge, J. (2003). Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis. Science 302, 871-874.
-
(2003)
Science
, vol.302
, pp. 871-874
-
-
Mallucci, G.1
Dickinson, A.2
Linehan, J.3
Klohn, P.C.4
Brandner, S.5
Collinge, J.6
-
23
-
-
15844419908
-
High-level expression and characterization of a purified 142-residue polypeptide of the prion protein
-
& 10 other authors
-
Mehlhorn, I., Groth, D., Stöckel, J. & 10 other authors (1996). High-level expression and characterization of a purified 142-residue polypeptide of the prion protein. Biochemistry 35, 5528-5537.
-
(1996)
Biochemistry
, vol.35
, pp. 5528-5537
-
-
Mehlhorn, I.1
Groth, D.2
Stöckel, J.3
-
24
-
-
0042855745
-
Cytosolic prion protein in neurons
-
& 7 other authors
-
Mironov, A., Jr, Latawiec, D., Wille, H. & 7 other authors (2003). Cytosolic prion protein in neurons. J Neurosci 23, 7183-7193.
-
(2003)
J. Neurosci.
, vol.23
, pp. 7183-7193
-
-
Mironov Jr., A.1
Latawiec, D.2
Wille, H.3
-
25
-
-
0342684482
-
Interaction of prion protein mRNA with CBP35 and other cellular proteins: Possible implications for prion replication and age-dependent changes
-
Muller, W. E., Scheffer, U., Perovic, S., Forrest, J. & Schroder, H. C. (1997). Interaction of prion protein mRNA with CBP35 and other cellular proteins: possible implications for prion replication and age-dependent changes. Arch Gerontol Geriatr 25, 41-58.
-
(1997)
Arch. Gerontol. Geriatr.
, vol.25
, pp. 41-58
-
-
Muller, W.E.1
Scheffer, U.2
Perovic, S.3
Forrest, J.4
Schroder, H.C.5
-
26
-
-
0030811015
-
Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix
-
Muramoto, T., DeArmond, S. J., Scott, M., Telling, G. C., Cohen, F. E. & Prusiner, S. B. (1997). Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix. Nat Med 3, 750-755.
-
(1997)
Nat. Med.
, vol.3
, pp. 750-755
-
-
Muramoto, T.1
DeArmond, S.J.2
Scott, M.3
Telling, G.C.4
Cohen, F.E.5
Prusiner, S.B.6
-
27
-
-
0037423296
-
Essential role of the prion protein N terminus in subcellular trafficking and half-life of cellular prion protein
-
Nunziante, M., Gilch, S. & Schätzl, H. M. (2003). Essential role of the prion protein N terminus in subcellular trafficking and half-life of cellular prion protein. J Biol Chem 278, 3726-3734.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 3726-3734
-
-
Nunziante, M.1
Gilch, S.2
Schätzl, H.M.3
-
28
-
-
0022005315
-
A cellular gene encodes scrapie PrP 27-30 protein
-
& 9 other authors
-
Oesch, B., Westaway, D., Wälchli, M. & 9 other authors (1985). A cellular gene encodes scrapie PrP 27-30 protein. Cell 40, 735-746.
-
(1985)
Cell
, vol.40
, pp. 735-746
-
-
Oesch, B.1
Westaway, D.2
Wälchli, M.3
-
29
-
-
0027332116
-
Conversion of α-helices into β-sheets features in the formation of the scrapie prion proteins
-
& 8 other authors
-
Pan, K.-M., Baldwin, M., Nguyen, J. & 8 other authors (1993). Conversion of α-helices into β-sheets features in the formation of the scrapie prion proteins. Proc Natl Acad Sci U S A 90, 10962-10966.
-
(1993)
Proc. Natl. Acad. Sci. U. S. A.
, vol.90
, pp. 10962-10966
-
-
Pan, K.-M.1
Baldwin, M.2
Nguyen, J.3
-
30
-
-
0031592937
-
A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform
-
& 9 other authors
-
Peretz, D., Williamson, R. A., Matsunaga, Y. & 9 other authors (1997). A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform. J Mol Biol 273, 614-622.
-
(1997)
J. Mol. Biol.
, vol.273
, pp. 614-622
-
-
Peretz, D.1
Williamson, R.A.2
Matsunaga, Y.3
-
31
-
-
0035086136
-
Strain-specified relative conformational stability of the scrapie prion protein
-
Peretz, D., Scott, M., Groth, D., Williamson, A., Burton, D., Cohen, F. E. & Prusiner, S. B. (2001a). Strain-specified relative conformational stability of the scrapie prion protein. Protein Sci 10, 854-863.
-
(2001)
Protein Sci.
, vol.10
, pp. 854-863
-
-
Peretz, D.1
Scott, M.2
Groth, D.3
Williamson, A.4
Burton, D.5
Cohen, F.E.6
Prusiner, S.B.7
-
32
-
-
0035899413
-
Antibodies inhibit prion propagation and clear cell cultures of prion infectivity
-
& 10 other authors
-
Peretz, D., Williamson, R. A., Kaneko, K. & 10 other authors (2001b). Antibodies inhibit prion propagation and clear cell cultures of prion infectivity. Nature 412, 739-743.
-
(2001)
Nature
, vol.412
, pp. 739-743
-
-
Peretz, D.1
Williamson, R.A.2
Kaneko, K.3
-
33
-
-
0041888516
-
Trafficking of prion proteins through a caveolae-mediated endosomal pathway
-
& 8 other authors
-
Peters, P. J., Mironov, A., Jr, Peretz, D. & 8 other authors (2003). Trafficking of prion proteins through a caveolae-mediated endosomal pathway. J Cell Biol 162, 703-717.
-
(2003)
J. Cell Biol.
, vol.162
, pp. 703-717
-
-
Peters, P.J.1
Mironov Jr., A.2
Peretz, D.3
-
34
-
-
0021019026
-
Scrapie prions aggregate to form amyloid-like birefringent rods
-
Prusiner, S. B., McKinley, M. P., Bowman, K. A., Bolton, D. C., Bendheim, P. E., Groth, D. F. & Glenner, G. G. (1983). Scrapie prions aggregate to form amyloid-like birefringent rods. Cell 35, 349-358.
-
(1983)
Cell
, vol.35
, pp. 349-358
-
-
Prusiner, S.B.1
McKinley, M.P.2
Bowman, K.A.3
Bolton, D.C.4
Bendheim, P.E.5
Groth, D.F.6
Glenner, G.G.7
-
35
-
-
0025244011
-
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
-
& 10 other authors
-
Prusiner, S. B., Scott, M., Foster, D. & 10 other authors (1990). Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication. Cell 63, 673-686.
-
(1990)
Cell
, vol.63
, pp. 673-686
-
-
Prusiner, S.B.1
Scott, M.2
Foster, D.3
-
36
-
-
0030836511
-
NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231)
-
Riek, R., Hornemann, S., Wider, G., Glockshuber, R. & Wüthrich, K. (1997). NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231). FEBS Lett 413, 282-288.
-
(1997)
FEBS Lett.
, vol.413
, pp. 282-288
-
-
Riek, R.1
Hornemann, S.2
Wider, G.3
Glockshuber, R.4
Wüthrich, K.5
-
37
-
-
0029978989
-
Spectroscopic conformational studies of prion protein isoforms and the mechanism of transformation
-
Safar, J. (1996). Spectroscopic conformational studies of prion protein isoforms and the mechanism of transformation. Semin Virol 7, 207-214.
-
(1996)
Semin. Virol.
, vol.7
, pp. 207-214
-
-
Safar, J.1
-
38
-
-
0031720905
-
Sc molecules with different conformations
-
Sc molecules with different conformations. Nat Med 4, 1157-1165.
-
(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
Cohen, F.E.7
Prusiner, S.B.8
-
39
-
-
0036843448
-
Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice
-
& 12 other authors
-
Safar, J. G., Scott, M., Monaghan, J. & 12 other authors (2002). Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice. Nat Biotechnol 20, 1147-1150.
-
(2002)
Nat. Biotechnol.
, vol.20
, pp. 1147-1150
-
-
Safar, J.G.1
Scott, M.2
Monaghan, J.3
-
40
-
-
0037611374
-
A hypothalamic neuronal cell line persistently infected with scrapie prions exhibits apoptosis
-
Schätzl, H. M., Laszlo, L., Holtzman, D. M., Tatzelt, J., DeArmond, S. J., Weiner, R. I., Mobley, W. C. & Prusiner, S. B. (1997). A hypothalamic neuronal cell line persistently infected with scrapie prions exhibits apoptosis. J Virol 71, 8821-8831.
-
(1997)
J. Virol.
, vol.71
, pp. 8821-8831
-
-
Schätzl, H.M.1
Laszlo, L.2
Holtzman, D.M.3
Tatzelt, J.4
DeArmond, S.J.5
Weiner, R.I.6
Mobley, W.C.7
Prusiner, S.B.8
-
41
-
-
0024820814
-
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
-
& 9 other authors
-
Scott, M., Foster, D., Miranda, C. & 9 other authors (1989). Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques. Cell 59, 847-857.
-
(1989)
Cell
, vol.59
, pp. 847-857
-
-
Scott, M.1
Foster, D.2
Miranda, C.3
-
42
-
-
0033592877
-
Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans
-
Scott, M. R., Will, R., Ironside, J., Nguyen, H.-O. B., Tremblay, P., DeArmond, S. J. & Prusiner, S. B. (1999). Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans. Proc Natl Acad Sci U S A 96, 15137-15142.
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 15137-15142
-
-
Scott, M.R.1
Will, R.2
Ironside, J.3
Nguyen, H.-O.B.4
Tremblay, P.5
DeArmond, S.J.6
Prusiner, S.B.7
-
43
-
-
17444393595
-
Transmission barriers for bovine, ovine, and human prions in transgenic mice
-
Scott M. R., Peretz, D., Nguyen, H.-O. B., DeArmond, S. J. & Prusiner, S. B. (2005). Transmission barriers for bovine, ovine, and human prions in transgenic mice. J Virol 79, 5259-5271.
-
(2005)
J. Virol.
, vol.79
, pp. 5259-5271
-
-
Scott, M.R.1
Peretz, D.2
Nguyen, H.-O.B.3
DeArmond, S.J.4
Prusiner, S.B.5
-
45
-
-
0033460187
-
Elimination of prions by branched polyamines and implications for therapeutics
-
Supattapone, S., Nguyen, H.-O. B., Cohen, F. E., Prusiner, S. B. & Scott, M. R. (1999). Elimination of prions by branched polyamines and implications for therapeutics. Proc Natl Acad Sci U S A 96, 14529-14534.
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 14529-14534
-
-
Supattapone, S.1
Nguyen, H.-O.B.2
Cohen, F.E.3
Prusiner, S.B.4
Scott, M.R.5
-
46
-
-
0035152345
-
Identification of two prion protein regions that modify scrapie incubation time
-
Supattapone, S., Muramoto, T., Legname, G., Mehlhorn, I., Cohen, F. E., DeArmond, S. J., Prusiner, S. B. & Scott, M. R. (2001a). Identification of two prion protein regions that modify scrapie incubation time. J Virol 75, 1408-1413.
-
(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
-
47
-
-
0035108195
-
Branched polyamines cure prion-infected neuroblastoma cells
-
Supattapone, S., Wille, H., Uyechi, L., Safar, J., Tremblay, P., Szoka, F. C., Cohen, F. E., Prusiner, S. B. & Scott, M. R. (2001b). Branched polyamines cure prion-infected neuroblastoma cells. J Virol 75, 3453-3461.
-
(2001)
J. Virol.
, vol.75
, pp. 3453-3461
-
-
Supattapone, S.1
Wille, H.2
Uyechi, L.3
Safar, J.4
Tremblay, P.5
Szoka, F.C.6
Cohen, F.E.7
Prusiner, S.B.8
Scott, M.R.9
-
48
-
-
0026644090
-
Regional mapping of prion proteins in brains
-
Taraboulos, A., Jendroska, K., Serban, D., Yang, S.-L., DeArmond, S. J. & Prusiner, S. B. (1992a). Regional mapping of prion proteins in brains. Proc Natl Acad Sci U S A 89, 7620-7624.
-
(1992)
Proc. Natl. Acad. Sci. U. S. A.
, vol.89
, pp. 7620-7624
-
-
Taraboulos, A.1
Jendroska, K.2
Serban, D.3
Yang, S.-L.4
DeArmond, S.J.5
Prusiner, S.B.6
-
49
-
-
0027096137
-
Synthesis and trafficking of prion proteins in cultured cells
-
Taraboulos, A., Raeber, A. J., Borchelt, D. R., Serban, D. & Prusiner, S. B. (1992b). Synthesis and trafficking of prion proteins in cultured cells. Mol Biol Cell 3, 851-863.
-
(1992)
Mol. Biol. Cell
, vol.3
, pp. 851-863
-
-
Taraboulos, A.1
Raeber, A.J.2
Borchelt, D.R.3
Serban, D.4
Prusiner, S.B.5
-
50
-
-
0029832863
-
Chemical chaperones interfere with the formation of scrapie prion protein
-
Tatzelt, J., Prusiner, S. B. & Welch, W. J. (1996). Chemical chaperones interfere with the formation of scrapie prion protein. EMBO J 15, 6363-6373.
-
(1996)
EMBO J.
, vol.15
, pp. 6363-6373
-
-
Tatzelt, J.1
Prusiner, S.B.2
Welch, W.J.3
-
51
-
-
0028882424
-
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
-
Telling, G. C., Scott, M., Mastrianni, J., Gabizon, R., Torchia, M., Cohen, F. E., DeArmond, S. J. & Prusiner, S. B. (1995). Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein. Cell 83, 79-90.
-
(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
-
52
-
-
0029740354
-
Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice
-
Telling, G. C., Haga, T., Torchia, M., Tremblay, P., DeArmond, S. J. & Prusiner, S. B. (1996). Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice. Genes Dev 10, 1736-1750.
-
(1996)
Genes Dev.
, vol.10
, pp. 1736-1750
-
-
Telling, G.C.1
Haga, T.2
Torchia, M.3
Tremblay, P.4
DeArmond, S.J.5
Prusiner, S.B.6
-
53
-
-
0032514707
-
Doxycyline control of prion protein transgene expression modulates prion disease in mice
-
& 9 other authors
-
Tremblay, P., Meiner, Z., Galou, M. & 9 other authors (1998). Doxycyline control of prion protein transgene expression modulates prion disease in mice. Proc Natl Acad Sci U S A 95, 12580-12585.
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, pp. 12580-12585
-
-
Tremblay, P.1
Meiner, Z.2
Galou, M.3
-
54
-
-
0842304471
-
Sc conformers induced by a synthetic peptide and several prion strains
-
Sc conformers induced by a synthetic peptide and several prion strains. J Virol 78, 2088-2099.
-
(2004)
J. Virol.
, vol.78
, pp. 2088-2099
-
-
Tremblay, P.1
Ball, H.L.2
Kaneko, K.3
Groth, D.4
Hegde, R.S.5
Cohen, F.E.6
DeArmond, S.J.7
Prusiner, S.B.8
Safer, J.G.9
-
55
-
-
0023467393
-
Distinct prion proteins in short and long scrapie incubation period mice
-
Westaway, D., Goodman, P. A., Miranda, C. A., McKinley, M. P., Carlson, G. A. & Prusiner, S. B. (1987). Distinct prion proteins in short and long scrapie incubation period mice. Cell 51, 651-662.
-
(1987)
Cell
, vol.51
, pp. 651-662
-
-
Westaway, D.1
Goodman, P.A.2
Miranda, C.A.3
McKinley, M.P.4
Carlson, G.A.5
Prusiner, S.B.6
-
56
-
-
0037133587
-
Structural studies of the scrapie prion protein by electron crystallography
-
Wille, H., Michelitsch, M. D., Guénebaut V., Supattapone, S., Serban, A., Cohen, F. E., Agard, D. A. & Prusiner, S. B. (2002). Structural studies of the scrapie prion protein by electron crystallography. Proc Natl Acad Sci U S A 99, 3563-3568.
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 3563-3568
-
-
Wille, H.1
Michelitsch, M.D.2
Guénebaut, V.3
Supattapone, S.4
Serban, A.5
Cohen, F.E.6
Agard, D.A.7
Prusiner, S.B.8
|