-
1
-
-
0030786717
-
Prion research: The next frontiers
-
Aguzzi A, Weissmann C (1997) Prion research: the next frontiers. Nature 389:795-798
-
(1997)
Nature
, vol.389
, pp. 795-798
-
-
Aguzzi, A.1
Weissmann, C.2
-
2
-
-
0022529448
-
Monoclonal antibodies to the cellular and scrapie prion proteins
-
Barry RA, Prusiner SB (1986) Monoclonal antibodies to the cellular and scrapie prion proteins. J Infect Dis 154:518-521
-
(1986)
J Infect Dis
, vol.154
, pp. 518-521
-
-
Barry, R.A.1
Prusiner, S.B.2
-
3
-
-
0031444294
-
The cellular prion protein binds copper in vivo
-
Brown DR, Qin K, Herms JW, Madlung A, Manson J, Strome R, Fraser PE, Knuck T, Bohlen A von, Schulz-Schaeffer W, Giese A, Westaway D, Kretzschmar H (1997) The cellular prion protein binds copper in vivo. Nature 390:684-687
-
(1997)
Nature
, vol.390
, pp. 684-687
-
-
Brown, D.R.1
Qin, K.2
Herms, J.W.3
Madlung, A.4
Manson, J.5
Strome, R.6
Fraser, P.E.7
Knuck, T.8
Bohlen, A.V.9
Schulz-Schaeffer, W.10
Giese, A.11
Westaway, D.12
Kretzschmar, H.13
-
4
-
-
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 SJ, Prusiner SB, 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
-
5
-
-
0027319326
-
Mice devoid of PrP are resistant to scrapie
-
Büeler H, Aguzzi A, Sailer A, Greiner R-A, Autenried P, Aguet M, Weissmann C (1993) Mice devoid of PrP are resistant to scrapie. Cell 73:1339-1347
-
(1993)
Cell
, vol.73
, pp. 1339-1347
-
-
Büeler, H.1
Aguzzi, A.2
Sailer, A.3
Greiner, R.-A.4
Autenried, P.5
Aguet, M.6
Weissmann, C.7
-
6
-
-
0027997387
-
Prion protein is necessary for normal synaptic function
-
Collinge J, Whittington MA, Sidle KC, Smith CJ, Palmer MS, Clarke AR, Jefferys JGR (1994) Prion protein is necessary for normal synaptic function. Nature 370:295-297
-
(1994)
Nature
, vol.370
, pp. 295-297
-
-
Collinge, J.1
Whittington, M.A.2
Sidle, K.C.3
Smith, C.J.4
Palmer, M.S.5
Clarke, A.R.6
Jefferys, J.G.R.7
-
7
-
-
0029112533
-
Ultrastructural localization of cellular prion protein (PrPC) in synaptic boutons of normal hamster hippocampus
-
Fournier J-G, Escaig-Haye F, De Villemeur TB, Robain O (1995) Ultrastructural localization of cellular prion protein (PrPC) in synaptic boutons of normal hamster hippocampus. C R Acad Sci [III] 318:339-344
-
(1995)
C R Acad Sci [III]
, vol.318
, pp. 339-344
-
-
Fournier, J.-G.1
Escaig-Haye, F.2
De Villemeur, T.B.3
Robain, O.4
-
8
-
-
0028793453
-
Patch-clamp analysis of synaptic transmission to cerebellar Purkinje cells of prion protein knockout mice
-
Herms JW, Kretzschmar HA, Titz S, Keller BU (1995) Patch-clamp analysis of synaptic transmission to cerebellar Purkinje cells of prion protein knockout mice. Eur J Neurosci 7:2508-2512
-
(1995)
Eur J Neurosci
, vol.7
, pp. 2508-2512
-
-
Herms, J.W.1
Kretzschmar, H.A.2
Titz, S.3
Keller, B.U.4
-
9
-
-
0033570367
-
Evidence of presynaptic location and function of the prion protein
-
Herms JW, Tings T, Gall S, Madlung A, Giese A, Siebert H, Schurmann P, Windl O, Brose N, Kretzschmar H (1999) Evidence of presynaptic location and function of the prion protein. J Neurosci 19:8866-8875
-
(1999)
J Neurosci
, vol.19
, pp. 8866-8875
-
-
Herms, J.W.1
Tings, T.2
Gall, S.3
Madlung, A.4
Giese, A.5
Siebert, H.6
Schurmann, P.7
Windl, O.8
Brose, N.9
Kretzschmar, H.10
-
10
-
-
0028844207
-
Copper binding to the N-terminal tandem repeat region of mammalian and avian prion protein: Structural studies using synthetic peptides
-
Hornshaw MP, McDermott JR, Candy JM, Lakey JH (1995) Copper binding to the N-terminal tandem repeat region of mammalian and avian prion protein: structural studies using synthetic peptides. Biochem Biophys Res Commun 214:993-999
-
(1995)
Biochem Biophys Res Commun
, vol.214
, pp. 993-999
-
-
Hornshaw, M.P.1
McDermott, J.R.2
Candy, J.M.3
Lakey, J.H.4
-
11
-
-
0030956658
-
Scrapie infection alters the membrane and synaptic properties of mouse hippocampal CA1 pyramidal neurones
-
Johnston AR, Black C, Fraser J, MacLeod N (1997) Scrapie infection alters the membrane and synaptic properties of mouse hippocampal CA1 pyramidal neurones. J Physiol (Lond) 500:1-15
-
(1997)
J Physiol (Lond)
, vol.500
, pp. 1-15
-
-
Johnston, A.R.1
Black, C.2
Fraser, J.3
MacLeod, N.4
-
12
-
-
0029916617
-
Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus
-
Lledo P-M, Tremblay P, DeArmond SJ, Prusiner SB, Nicoll RA (1996) Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus. Proc Natl Acad Sci USA 93:2403-2407
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 2403-2407
-
-
Lledo, P.-M.1
Tremblay, P.2
DeArmond, S.J.3
Prusiner, S.B.4
Nicoll, R.A.5
-
13
-
-
0028420937
-
129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal
-
Manson JC, Clarke AR, Hooper ML, Aitchison L, McConnell I, Hope J (1994) 129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal. Mol Neurobiol 8:121-127
-
(1994)
Mol Neurobiol
, vol.8
, pp. 121-127
-
-
Manson, J.C.1
Clarke, A.R.2
Hooper, M.L.3
Aitchison, L.4
McConnell, I.5
Hope, J.6
-
14
-
-
0029265461
-
PrP gene dosage and long term potentiation
-
Manson JC, Hope J, Clarke AR, Johnston A, Black C, MacLeod N (1995) PrP gene dosage and long term potentiation (letter). Neurodegeneration 4:113-114
-
(1995)
Neurodegeneration
, vol.4
, pp. 113-114
-
-
Manson, J.C.1
Hope, J.2
Clarke, A.R.3
Johnston, A.4
Black, C.5
MacLeod, N.6
-
16
-
-
0029092955
-
Double replacement gene targeting for the production of a series of mouse strains with different prion protein gene alterations
-
Moore RC, Redhead NJ, Selfridge J, Hope J, Manson JC, Melton DW (1995) Double replacement gene targeting for the production of a series of mouse strains with different prion protein gene alterations. Biotechnology 13:999-1004
-
(1995)
Biotechnology
, vol.13
, pp. 999-1004
-
-
Moore, R.C.1
Redhead, N.J.2
Selfridge, J.3
Hope, J.4
Manson, J.C.5
Melton, D.W.6
-
17
-
-
0033215478
-
Ataxia in prion protein (PrP) deficient mice is associated with upregulation of the novel PrP-like protein doppel
-
Moore RC, Lee IY, Silverman GL, Harrison PM, Strome R, Heinrich C, Karunaratne A, Pasternak SH, Chishti MA, Liang Y, Mastrangelo P, Wang K, Smit AFA, Katamine S, Carlson GA, Cohen FE, Prusiner SB, Melton DW, Tremblay P, Hood LE, Westaway D (1999) Ataxia in prion protein (PrP) deficient mice is associated with upregulation of the novel PrP-like protein doppel. J Mol Biol 292:797-817
-
(1999)
J Mol Biol
, vol.292
, pp. 797-817
-
-
Moore, R.C.1
Lee, I.Y.2
Silverman, G.L.3
Harrison, P.M.4
Strome, R.5
Heinrich, C.6
Karunaratne, A.7
Pasternak, S.H.8
Chishti, M.A.9
Liang, Y.10
Mastrangelo, P.11
Wang, K.12
Smit, A.F.A.13
Katamine, S.14
Carlson, G.A.15
Cohen, F.E.16
Prusiner, S.B.17
Melton, D.W.18
Tremblay, P.19
Hood, L.E.20
Westaway, D.21
more..
-
18
-
-
0033049539
-
A mouse prion protein transgene rescues mice deficient for the prion protein gene from Purkinje cell degeneration and demyelination
-
Nishida N, Tremblay P, Sugimoto T, Shigematsu K, Shirabe S, Petromilli C, Erpel SP, Nakaoke R, Atarashi R, Houtani T, Torchia M, Sakaguchi S, DeArmond SJ, Prusiner SB, Katamine S (1999) A mouse prion protein transgene rescues mice deficient for the prion protein gene from Purkinje cell degeneration and demyelination. Lab Invest 79:689-697
-
(1999)
Lab Invest
, vol.79
, pp. 689-697
-
-
Nishida, N.1
Tremblay, P.2
Sugimoto, T.3
Shigematsu, K.4
Shirabe, S.5
Petromilli, C.6
Erpel, S.P.7
Nakaoke, R.8
Atarashi, R.9
Houtani, T.10
Torchia, M.11
Sakaguchi, S.12
DeArmond, S.J.13
Prusiner, S.B.14
Katamine, S.15
-
19
-
-
0030822582
-
Prion diseases and the BSE crisis
-
Prusiner SB (1997) Prion diseases and the BSE crisis. Science 278:245-251
-
(1997)
Science
, vol.278
, pp. 245-251
-
-
Prusiner, S.B.1
-
20
-
-
0027491308
-
Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies
-
Prusiner SB, Groth D, Serban A, Koehler R, Foster D, Torchia M, Burton D, Yang S-L, DeArmond SJ (1993) Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies. Proc Natl Acad Sci USA 90:10608-10612
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 10608-10612
-
-
Prusiner, S.B.1
Groth, D.2
Serban, A.3
Koehler, R.4
Foster, D.5
Torchia, M.6
Burton, D.7
Yang, S.-L.8
DeArmond, S.J.9
-
22
-
-
0028820122
-
Accumulation of proteinase K-resistant prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob disease agent
-
Sakaguchi S, Katamine S, Shigematsu K, Nakatani A, Moriuchi R, Nishida N, Kurokawa K, Nakaoke R, Sato H, Jishage K, Kuno J, Noda T, Miyamoto T (1995) Accumulation of proteinase K-resistant prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob disease agent. J Virol 69:7586-7592
-
(1995)
J Virol
, vol.69
, pp. 7586-7592
-
-
Sakaguchi, S.1
Katamine, S.2
Shigematsu, K.3
Nakatani, A.4
Moriuchi, R.5
Nishida, N.6
Kurokawa, K.7
Nakaoke, R.8
Sato, H.9
Jishage, K.10
Kuno, J.11
Noda, T.12
Miyamoto, T.13
-
23
-
-
13344282734
-
Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene
-
Sakaguchi S, Katamine S, Nishida N, Moriuchi R, Shigematsu K, Sugimoto T, Nakatani A, Kataoka Y, Houtani T, Shirabe S, Okada H, Hasegawa S, Miyamoto T, Noda T (1996) Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene. Nature 380:528-531
-
(1996)
Nature
, vol.380
, pp. 528-531
-
-
Sakaguchi, S.1
Katamine, S.2
Nishida, N.3
Moriuchi, R.4
Shigematsu, K.5
Sugimoto, T.6
Nakatani, A.7
Kataoka, Y.8
Houtani, T.9
Shirabe, S.10
Okada, H.11
Hasegawa, S.12
Miyamoto, T.13
Noda, T.14
-
24
-
-
0037965529
-
Prion protein selectively binds copper (II) ions
-
Stöckel J, Safar J, Wallace AC, Cohen FE, Prusiner SB (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
-
25
-
-
0026644090
-
Regional mapping of prion proteins in brains
-
Taraboulos A, Jendroska K, Serban D, Yang SL, DeArmond SJ, Prusiner SB (1992) Regional mapping of prion proteins in brains. Proc Natl Acad Sci USA 89:7620-7624
-
(1992)
Proc Natl Acad Sci USA
, 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
-
26
-
-
0029740354
-
Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice
-
Telling GC. Haga T, Torchia M, Tremblay P, DeArmond SJ, Prusiner SB (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
-
27
-
-
15844421385
-
Altered circadian activity rhythms and sleep in mice devoid of prion protein
-
Tobler I, Gaus SE, Deboer T, Achermann P, Fischer M, Rülicke T, Moser M, Oesch B, McBride PA, Manson JC (1996) Altered circadian activity rhythms and sleep in mice devoid of prion protein. Nature 380:639-642
-
(1996)
Nature
, vol.380
, pp. 639-642
-
-
Tobler, I.1
Gaus, S.E.2
Deboer, T.3
Achermann, P.4
Fischer, M.5
Rülicke, T.6
Moser, M.7
Oesch, B.8
McBride, P.A.9
Manson, J.C.10
-
28
-
-
0032514707
-
Doxycyline control of prion protein transgene expression modulates prion disease in mice
-
Tremblay P, Meiner Z, Galou M, Heinrich C, Petromilli C, Lisse T, Cayetano J, Torchia M, Mobley W, Bujard H, DeArmond SJ, Prusiner SB (1998) Doxycyline control of prion protein transgene expression modulates prion disease in mice. Proc Natl Acad Sci USA 95:12580-12585
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 12580-12585
-
-
Tremblay, P.1
Meiner, Z.2
Galou, M.3
Heinrich, C.4
Petromilli, C.5
Lisse, T.6
Cayetano, J.7
Torchia, M.8
Mobley, W.9
Bujard, H.10
DeArmond, S.J.11
Prusiner, S.B.12
-
29
-
-
0033135312
-
Homeostatic plasticity in neuronal networks: The more things change, the more they stay the same
-
Turrigiano GG (1999) Homeostatic plasticity in neuronal networks: the more things change, the more they stay the same. Trends Neurosci 22:221-227
-
(1999)
Trends Neurosci
, vol.22
, pp. 221-227
-
-
Turrigiano, G.G.1
-
30
-
-
0028802150
-
Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein
-
Whittington MA, Sidle KC, Gowland I, Meads J, Hill AF, Palmer MS, Jefferys JG Collinge J (1995) Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein. Nat Genet 9:197-201
-
(1995)
Nat Genet
, vol.9
, pp. 197-201
-
-
Whittington, M.A.1
Sidle, K.C.2
Gowland, I.3
Meads, J.4
Hill, A.F.5
Palmer, M.S.6
Jefferys, J.G.7
Collinge, J.8
-
31
-
-
0024600340
-
Short-term plasticity
-
Zucker RS (1989) Short-term plasticity. Annu Rev Neurosci 12:13-31
-
(1989)
Annu Rev Neurosci
, vol.12
, pp. 13-31
-
-
Zucker, R.S.1
|