-
1
-
-
0023837236
-
Characterisation of prion protein with monospecific antisera to synthetic peptides
-
Barry RA, Vincent, MT, Kent SB, Hood LE, Prusiner SB (1988) Characterisation of prion protein with monospecific antisera to synthetic peptides. J Immunol 140:1188-1193
-
(1988)
J Immunol
, vol.140
, pp. 1188-1193
-
-
Barry, R.A.1
Vincent, M.T.2
Kent, S.B.3
Hood, L.E.4
Prusiner, S.B.5
-
2
-
-
0024366602
-
Precise targeting of the pathology of the sialoglycoprotein PrP, and vacuolar degeneration in mouse scrapie
-
Bruce ME, McBride PA, Farquhar CF (1989) Precise targeting of the pathology of the sialoglycoprotein PrP, and vacuolar degeneration in mouse scrapie. Neurosci Lett 102:1-6
-
(1989)
Neurosci Lett
, vol.102
, pp. 1-6
-
-
Bruce, M.E.1
McBride, P.A.2
Farquhar, C.F.3
-
3
-
-
0025876226
-
N-terminal truncation of the scrapie associated form of PrP by lysosomal protease (s): Implications regarding the site of conversion of PrP to the protease-resistant state
-
Caughey B, Raymond GJ, Ernst D, Race RE (1991) N-terminal truncation of the scrapie associated form of PrP by lysosomal protease (s): implications regarding the site of conversion of PrP to the protease-resistant state. J Virol 65:6597-6603
-
(1991)
J Virol
, vol.65
, pp. 6597-6603
-
-
Caughey, B.1
Raymond, G.J.2
Ernst, D.3
Race, R.E.4
-
4
-
-
0027724075
-
Overview of the transmissible spongiform encephalopathies: Prion protein disorders
-
DeArmond SJ (1993) Overview of the transmissible spongiform encephalopathies: Prion protein disorders. Brit Med Bull 49:725-737
-
(1993)
Brit Med Bull
, vol.49
, pp. 725-737
-
-
DeArmond, S.J.1
-
5
-
-
0027482868
-
The neurochemistry of prion diseases
-
DeArmond SJ, Prusiner SB (1993) The neurochemistry of prion diseases. J Neurochem 61:1589-1601
-
(1993)
J Neurochem
, vol.61
, pp. 1589-1601
-
-
DeArmond, S.J.1
Prusiner, S.B.2
-
6
-
-
0343202801
-
A review of the detection of PrPsc
-
Farquhar CF, Somerville RA, Dornan J, Armstrong D, Birkett C, Hope J (1993) A review of the detection of PrPsc. Proceedings of a consultation on BSE with the Scientific Veterinary Committee of the CEC: 301-313
-
(1993)
Proceedings of a Consultation on BSE with the Scientific Veterinary Committee of the CEC
, pp. 301-313
-
-
Farquhar, C.F.1
Somerville, R.A.2
Dornan, J.3
Armstrong, D.4
Birkett, C.5
Hope, J.6
-
7
-
-
0026705377
-
Prion protein preamyloid and amyloid deposits in Gerstmann-StrausslerScheinker disease, Indiana kindred
-
USA
-
Giaccone GG, Verga L, Bugiani O, Frangione B, Serban D, Prusiner SB, Farlow MR, Ghetti B and Tagliavini F (1992) Prion protein preamyloid and amyloid deposits in Gerstmann-StrausslerScheinker disease, Indiana kindred. PNAS (USA) 89:9349-9353
-
(1992)
PNAS
, vol.89
, pp. 9349-9353
-
-
Giaccone, G.G.1
Verga, L.2
Bugiani, O.3
Frangione, B.4
Serban, D.5
Prusiner, S.B.6
Farlow, M.R.7
Ghetti, B.8
Tagliavini, F.9
-
8
-
-
0026539090
-
Processing of the amyloid protein precursor to potentially amyloidogenic derivatives
-
Golde TE, Estus S, Younkin LH, Selkoe DJ, Younkin SG (1992) Processing of the amyloid protein precursor to potentially amyloidogenic derivatives. Science 255:728-730
-
(1992)
Science
, vol.255
, pp. 728-730
-
-
Golde, T.E.1
Estus, S.2
Younkin, L.H.3
Selkoe, D.J.4
Younkin, S.G.5
-
9
-
-
0026735070
-
Targeting of cell -surface, β Amyloid precursor protein to lysosomes: Alternative processing into amyloid-bearing fragments
-
Haass C, Koo EH, Mellon A, Hung AY, Selkoe DJ (1992) Targeting of cell -surface, β Amyloid precursor protein to lysosomes: alternative processing into amyloid-bearing fragments. Nature 357:500-503
-
(1992)
Nature
, vol.357
, pp. 500-503
-
-
Haass, C.1
Koo, E.H.2
Mellon, A.3
Hung, A.Y.4
Selkoe, D.J.5
-
10
-
-
0026692758
-
Immunohistochemical study of kuru plaques using antibodies against synthetic prion protein peptides
-
Hashimoto K, Mannen T, Nukina N (1992) Immunohistochemical study of kuru plaques using antibodies against synthetic prion protein peptides. Acta Neuropathol 83:613-617
-
(1992)
Acta Neuropathol
, vol.83
, pp. 613-617
-
-
Hashimoto, K.1
Mannen, T.2
Nukina, N.3
-
11
-
-
0023975851
-
Molecular pathology of scrapie associated fibril protein (PrP) in mouse brain affected by the ME7 strain of scrapie
-
Hope J, Multhaup G, Reekie LJD, Kimberlin RH, Beyreuther K (1988) Molecular pathology of scrapie associated fibril protein (PrP) in mouse brain affected by the ME7 strain of scrapie. Eur J Biochem 172:271-277
-
(1988)
Eur J Biochem
, vol.172
, pp. 271-277
-
-
Hope, J.1
Multhaup, G.2
Reekie, L.J.D.3
Kimberlin, R.H.4
Beyreuther, K.5
-
12
-
-
0022802258
-
The major protein 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, Morton LJD, Farquhar CF, Multhaup G, Beyreuther K, Kimberlin RH (1986) The major protein 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 5:2591-2597
-
(1986)
EMBO
, vol.5
, pp. 2591-2597
-
-
Hope, J.1
Morton, L.J.D.2
Farquhar, C.F.3
Multhaup, G.4
Beyreuther, K.5
Kimberlin, R.H.6
-
13
-
-
0026849947
-
Mutant prion proteins in Gerstmann-Straussler-Scheinker disease with neurofibrillary tangles
-
Hsiao K, Dlouhy SR, Farlow MR, Ghetti B, Cass C, Da Costa M, Coneally PM, Hodes ME, Prusiner S B (1992) Mutant prion proteins in Gerstmann-Straussler-Scheinker disease with neurofibrillary tangles. Nature Genetics 1:68-71
-
(1992)
Nature Genetics
, vol.1
, pp. 68-71
-
-
Hsiao, K.1
Dlouhy, S.R.2
Farlow, M.R.3
Ghetti, B.4
Cass, C.5
Da Costa, M.6
Coneally, P.M.7
Hodes, M.E.8
Prusiner, S.B.9
-
14
-
-
0027982241
-
Correlative light and electron microscopy studies of PrP localisation in 87V scrapie
-
Jeffrey M, Goodsir CM, Bruce ME, McBride PA, Scott JR, Halliday WG (1994a) Correlative light and electron microscopy studies of PrP localisation in 87V scrapie. Brain Res 656:329-343
-
(1994)
Brain Res
, vol.656
, pp. 329-343
-
-
Jeffrey, M.1
Goodsir, C.M.2
Bruce, M.E.3
McBride, P.A.4
Scott, J.R.5
Halliday, W.G.6
-
15
-
-
0028593861
-
Morphogenesis of amyloid plaques in 87V murine scrapie
-
Jeffrey M, Goodsir CM, Bruce ME, McBride PA, Farquhar C (1994b) Morphogenesis of amyloid plaques in 87V murine scrapie. Neuropath and Appl Neurobiol 20:535-542
-
(1994)
Neuropath and Appl Neurobiol
, vol.20
, pp. 535-542
-
-
Jeffrey, M.1
Goodsir, C.M.2
Bruce, M.E.3
McBride, P.A.4
Farquhar, C.5
-
16
-
-
0028263412
-
Murine scrapie-infected neurons in vivo release excess PrP into the extracellular space
-
Jeffrey M, Goodsir CM, Bruce ME, McBride PA, Fowler N, Scott JR (1994c) Murine scrapie-infected neurons in vivo release excess PrP into the extracellular space. Neurosci Lett 174:39-42
-
(1994)
Neurosci Lett
, vol.174
, pp. 39-42
-
-
Jeffrey, M.1
Goodsir, C.M.2
Bruce, M.E.3
McBride, P.A.4
Fowler, N.5
Scott, J.R.6
-
17
-
-
0023105114
-
The precursor of Alzheimer's disease amyloid A4 protein re-sembles a cell surface receptor
-
Kang J., Lemaire H-G, Unterbeck A, Salbaum JM, Masters CL, Grzeschik K-H, Multhaup G, Beyreuther K, Muller-Hill B (1987) The precursor of Alzheimer's disease amyloid A4 protein re-sembles a cell surface receptor. Nature Gen 325:733-736
-
(1987)
Nature Gen
, vol.325
, pp. 733-736
-
-
Kang, J.1
Lemaire, H.-G.2
Unterbeck, A.3
Salbaum, J.M.4
Masters, C.L.5
Grzeschik, K.-H.6
Multhaup, G.7
Beyreuther, K.8
Muller-Hill, B.9
-
18
-
-
0025794115
-
N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Straussler-syndrome
-
Kitamoto T, Muramoto T, Hilbich C, Beyreuther K, Tateishi J (1991) N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Straussler-syndrome. Brain Res 545:319-321
-
(1991)
Brain Res
, vol.545
, pp. 319-321
-
-
Kitamoto, T.1
Muramoto, T.2
Hilbich, C.3
Beyreuther, K.4
Tateishi, J.5
-
19
-
-
85030189991
-
Antigenic sites of bovine prion protein
-
Bradley R, Marchant B (eds) Transmissible Spongiform Encephalopathies. Commission of the European Communities, Brussels, 14-15 September 1993
-
Langeveld JPM, Farquhar CF, Pocchiari M, Birkett C, Bostock C, Meloen RH (1993) Antigenic sites of bovine prion protein. In Bradley R, Marchant B (eds) Transmissible Spongiform Encephalopathies. Proceedings of a Consultation on BSE. Commission of the European Communities, Brussels, 14-15 September 1993
-
(1993)
Proceedings of a Consultation on BSE
-
-
Langeveld, J.P.M.1
Farquhar, C.F.2
Pocchiari, M.3
Birkett, C.4
Bostock, C.5
Meloen, R.H.6
-
20
-
-
0022005315
-
A cellular gene encodes scrapie PrP 27-30 protein
-
Oesch B, Westaway D, Walchi M, McKinley MP, Kent SBH, Aebersold R, Barry RA, Teplow DB, Tempst DB, Hood LE, Prusiner S B, Weissmann C (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
Walchi, M.3
McKinley, M.P.4
Kent, S.B.H.5
Aebersold, R.6
Barry, R.A.7
Teplow, D.B.8
Tempst, D.B.9
Hood, L.E.10
Prusiner, S.B.11
Weissmann, C.12
-
21
-
-
0009267732
-
Prion Biology
-
Prusiner SB, Collinge J, Powell J, Anderton B (eds). Ellis Horwood, New York
-
Prusiner SB (1992) Prion Biology. In Prusiner SB, Collinge J, Powell J, Anderton B (eds). Prion Diseases of Humans and Animals. Ellis Horwood, New York, pp 533-567
-
(1992)
Prion Diseases of Humans and Animals
, pp. 533-567
-
-
Prusiner, S.B.1
-
22
-
-
0028004290
-
Amyloid fibrils in Gerstmann-Straussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele
-
Tagliavini F, Prelli F, Porro M, Rossi G, Giaccone G, Farlow MR, Dlouhy SR, Ghetti B, Bugiani O, Frangione B (1994) Amyloid fibrils in Gerstmann-Straussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele. Cell 79:695-703
-
(1994)
Cell
, vol.79
, pp. 695-703
-
-
Tagliavini, F.1
Prelli, F.2
Porro, M.3
Rossi, G.4
Giaccone, G.5
Farlow, M.R.6
Dlouhy, S.R.7
Ghetti, B.8
Bugiani, O.9
Frangione, B.10
|