-
3
-
-
0034625009
-
Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targets
-
Bieschke J, Giese A, Schulz-Schaeffer W, Zerr I, Poser S, Eigen M, Kretzschmar H (2000). Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targets. Proc Natl Acad Sci USA 97: 5468-5473.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 5468-5473
-
-
Bieschke, J.1
Giese, A.2
Schulz-Schaeffer, W.3
Zerr, I.4
Poser, S.5
Eigen, M.6
Kretzschmar, H.7
-
4
-
-
0031444294
-
The cellular prion protein binds copper in vivo
-
Brown DR, Qin K, Herms JW, Madlung A, Manson J, Strome R, Fraser PE, Kruck T, von Bohlen A, 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
Kruck, T.8
von Bohlen, A.9
Schulz-Schaeffer, W.10
Giese, A.11
Westaway, D.12
Kretzschmar, H.13
-
5
-
-
0027319326
-
Mice devoid of PrP are resistant to scrapie
-
Bueler H, Aguzzi A, Sailer A, Greiner RA, 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
-
-
Bueler, H.1
Aguzzi, A.2
Sailer, A.3
Greiner, R.A.4
Autenried, P.5
Aguet, M.6
Weissmann, C.7
-
6
-
-
0031711595
-
Pathologic conformations of prion proteins
-
Cohen FE, Prusiner SB (1998). Pathologic conformations of prion proteins. Annu Rev Biochem 67: 793-819.
-
(1998)
Annu. Rev. Biochem.
, vol.67
, pp. 793-819
-
-
Cohen, F.E.1
Prusiner, S.B.2
-
7
-
-
0029971378
-
Hippocampal slices from prion protein null mice: Disrupted Ca(2+)-activated K+ currents
-
Collinge SB, Collinge J, Jefferys JG (1996). Hippocampal slices from prion protein null mice: disrupted Ca(2+)-activated K+ currents. Neurosci Lett 209: 49-52.
-
(1996)
Neurosci Lett.
, vol.209
, pp. 49-52
-
-
Collinge, S.B.1
Collinge, J.2
Jefferys, J.G.3
-
8
-
-
0027997387
-
Prion protein is necessary for normal synaptic function
-
Collinge J, Whittington MA, Sidle KC, Smith CJ, Palmer MS, Clarke AR, Jefferys JG (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.7
-
9
-
-
0027270578
-
A kinetic model for amyloid formation in the prion diseases: Importance of seeding
-
Come JH, Fraser PE, Lansbury PT Jr (1993). A kinetic model for amyloid formation in the prion diseases: importance of seeding. Proc Natl Acad Sci USA 90: 5959-5963.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 5959-5963
-
-
Come, J.H.1
Fraser, P.E.2
Lansbury P.T., Jr.3
-
10
-
-
33746127253
-
Über eine eigenartige herdförmige Erkrankung des Zentralnervensystems
-
Creutzfeldt HG (1920). Über eine eigenartige herdförmige Erkrankung des Zentralnervensystems. Z Gesamte Neurol Psychiatrie 57: 1-18.
-
(1920)
Z Gesamte Neurol. Psychiatrie
, vol.57
, pp. 1-18
-
-
Creutzfeldt, H.G.1
-
11
-
-
0001907961
-
La tremblante du mounton est bien inoculable
-
Cuillé (1938). La tremblante du mounton est bien inoculable. Acad Sci Paris 206: 78-79.
-
(1938)
Acad Sci. Paris
, vol.206
, pp. 78-79
-
-
Cuillé, A.1
-
13
-
-
0014308027
-
The sequential development of the brain lesion of scrapie in three strains of mice
-
Fraser H, Dickinson AG (1968). The sequential development of the brain lesion of scrapie in three strains of mice. J Comp Pathol 78: 301-311.
-
(1968)
J. Comp. Pathol.
, vol.78
, pp. 301-311
-
-
Fraser, H.1
Dickinson, A.G.2
-
14
-
-
0017643758
-
Unconventional viruses and the origin and disappearance of kuru
-
Gajdusek DC (1977). Unconventional viruses and the origin and disappearance of kuru. Science 197: 943-960.
-
(1977)
Science
, vol.197
, pp. 943-960
-
-
Gajdusek, D.C.1
-
15
-
-
17944363361
-
The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein
-
Gauczynski S, Peyrin JM, Haik S, Leucht C, Hundt C, Rieger R, Krasemann S, Deslys JP, Dormont D, Lasmezas CI, Weiss S (2001). The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein. EMBO J 20: 5863-5875.
-
(2001)
EMBO J.
, vol.20
, pp. 5863-5875
-
-
Gauczynski, S.1
Peyrin, J.M.2
Haik, S.3
Leucht, C.4
Hundt, C.5
Rieger, R.6
Krasemann, S.7
Deslys, J.P.8
Dormont, D.9
Lasmezas, C.I.10
Weiss, S.11
-
16
-
-
49749220574
-
Scrapie and kuru
-
Hadlow WJ (1959). Scrapie and kuru. Lancet ii: 289-290.
-
(1959)
Lancet
, vol.2
, pp. 289-290
-
-
Hadlow, W.J.1
-
17
-
-
51849177198
-
Über eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswerten anatomischen Befunden (spastische Pseudosklerose-Encephalomyelopathie) mit disseminierten Degenerationsherden)
-
Jakob A (1921). Über eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswerten anatomischen Befunden (spastische Pseudosklerose-Encephalomyelopathie) mit disseminierten Degenerationsherden). Z Gesamte Neurol Psychiatrie 64: 147-228.
-
(1921)
Z Gesamte Neurol. Psychiatrie
, vol.64
, pp. 147-228
-
-
Jakob, A.1
-
18
-
-
17344375337
-
Structural intermediates in the putative pathway from the cellular prion protein to the pathogenic form
-
Jansen K, Schafer O, Birkmann E, Post K, Serban H, Prusiner SB, Riesner D (2001). Structural intermediates in the putative pathway from the cellular prion protein to the pathogenic form. Biol Chem 382: 683-691.
-
(2001)
Biol. Chem.
, vol.382
, pp. 683-691
-
-
Jansen, K.1
Schafer, O.2
Birkmann, E.3
Post, K.4
Serban, H.5
Prusiner, S.B.6
Riesner, D.7
-
19
-
-
0031843985
-
Prion rods contain small amounts of two host sphingolipids as revealed by thin-layer chromatography and mass spectrometry
-
Klein TR, Kirsch D, Kaufmann R, Riesner D (1998). Prion rods contain small amounts of two host sphingolipids as revealed by thin-layer chromatography and mass spectrometry. Biol Chem 379: 655-666.
-
(1998)
Biol. Chem.
, vol.379
, pp. 655-666
-
-
Klein, T.R.1
Kirsch, D.2
Kaufmann, R.3
Riesner, D.4
-
20
-
-
0035859806
-
Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease
-
Korth C, May BC, Cohen FE, Prusiner SB (2001). Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease. Proc Natl Acad Sci USA 98: 9836-9841.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 9836-9841
-
-
Korth, C.1
May, B.C.2
Cohen, F.E.3
Prusiner, S.B.4
-
21
-
-
0027715580
-
Neuropathology of human prion diseases (spongiform encephalopathies)
-
Kretzschmar HA (1993). Neuropathology of human prion diseases (spongiform encephalopathies). Dev Biol Stand 80: 71-90.
-
(1993)
Dev. Biol. Stand.
, vol.80
, pp. 71-90
-
-
Kretzschmar, H.A.1
-
22
-
-
0003699788
-
Nützliche und auf die Erfahrung gegründete Einleitung zur Landwirtschaft
-
Leopoldt JG (1759). Nützliche und auf die Erfahrung gegründete Einleitung zur Landwirtschaft 5: 344-360.
-
(1759)
, vol.5
, pp. 344-360
-
-
Leopoldt, J.G.1
-
23
-
-
0026008203
-
Search for a putative scrapie genome in purified prion fractions reveals a paucity of nucleic acids
-
Meyer N, Rosenbaum V, Schmidt B, Gilles K, Mirenda C, Groth D, Prusiner SB, Riesner D (1991). Search for a putative scrapie genome in purified prion fractions reveals a paucity of nucleic acids. J Gen Virol 72(Pt 1): 37-49.
-
(1991)
J. Gen. Virol.
, vol.72
, Issue.PART 1
, pp. 37-49
-
-
Meyer, N.1
Rosenbaum, V.2
Schmidt, B.3
Gilles, K.4
Mirenda, C.5
Groth, D.6
Prusiner, S.B.7
Riesner, D.8
-
24
-
-
0034665847
-
Signal transduction through prion protein
-
Mouillet-Richard S, Ermonval M, Chebassier C, Laplanche JL, Lehmann S, Launay JM, Kellermann O (2000). Signal transduction through prion protein. Science 289: 1925-1928.
-
(2000)
Science
, vol.289
, pp. 1925-1928
-
-
Mouillet-Richard, S.1
Ermonval, M.2
Chebassier, C.3
Laplanche, J.L.4
Lehmann, S.5
Launay, J.M.6
Kellermann, O.7
-
25
-
-
0022005315
-
A cellular gene encodes scrapie PrP 27-30 protein
-
Oesch B, Westaway D, Walchli M, McKinley MP, Kent SB, Aebersold R, Barry RA, Tempst P, Teplow DB, Hood LE (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
Walchli, M.3
McKinley, M.P.4
Kent, S.B.5
Aebersold, R.6
Barry, R.A.7
Tempst, P.8
Teplow, D.B.9
Hood, L.E.10
-
26
-
-
0031871740
-
Detection of single amyloid beta-protein aggregates in the cerebrospinal fluid of Alzheimer's patients by fluorescence correlation spectroscopy
-
Pitschke M, Prior R, Haupt M, Riesner D (1998). Detection of single amyloid beta-protein aggregates in the cerebrospinal fluid of Alzheimer's patients by fluorescence correlation spectroscopy. Nat Med 4: 832-834.
-
(1998)
Nat. Med.
, vol.4
, pp. 832-834
-
-
Pitschke, M.1
Prior, R.2
Haupt, M.3
Riesner, D.4
-
27
-
-
0031789527
-
Rapid acquisition of beta-sheet structure in the prion protein prior to multimer formation
-
Post K, Pitschke M, Schafer O, Wille H, Appel TR, Kirsch D, Mehlhorn I, Serban H, Prusiner SB, Riesner D (1998). Rapid acquisition of beta-sheet structure in the prion protein prior to multimer formation. Biol Chem 379: 1307-1317.
-
(1998)
Biol. Chem.
, vol.379
, pp. 1307-1317
-
-
Post, K.1
Pitschke, M.2
Schafer, O.3
Wille, H.4
Appel, T.R.5
Kirsch, D.6
Mehlhorn, I.7
Serban, H.8
Prusiner, S.B.9
Riesner, D.10
-
28
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
Prusiner SB (1982). Novel proteinaceous infectious particles cause scrapie. Science 216: 136-144.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
29
-
-
0027421540
-
Genetic and infectious prion diseases
-
Prusiner SB (1993). Genetic and infectious prion diseases. Arch Neurol 50: 1129-1153.
-
(1993)
Arch. Neurol.
, vol.50
, pp. 1129-1153
-
-
Prusiner, S.B.1
-
30
-
-
0029937271
-
NMR structure of the mouse prion protein domain PrP(121-321)
-
Riek R, Hornemann S, Wider G, Billeter M, Glockshuber R, Wuthrich K (1996). NMR structure of the mouse prion protein domain PrP(121-321). Nature 382: 180-182.
-
(1996)
Nature
, vol.382
, pp. 180-182
-
-
Riek, R.1
Hornemann, S.2
Wider, G.3
Billeter, M.4
Glockshuber, R.5
Wuthrich, K.6
-
31
-
-
0000522861
-
The search for a nucleic acid component to scrapie infectivity
-
Riesner D (1992). The search for a nucleic acid component to scrapie infectivity. SemiVirol 2: 215-226.
-
(1992)
Semi Virol.
, vol.2
, pp. 215-226
-
-
Riesner, D.1
-
32
-
-
0012564204
-
C
-
Hörnliman B, Riesner D (eds). De Gruyter: Berlin
-
C. In: Prionen and Prionkrankheiten, Hörnliman B, Riesner D (eds). De Gruyter: Berlin, pp 81-91.
-
(2001)
Prionen and Prionkrankheiten
, pp. 81-91
-
-
Riesner, D.1
-
33
-
-
0030026759
-
Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity
-
Riesner D, Kellings K, Post K, Wille H, Serban H, Groth D, Baldwin MA, Prusiner SB (1996). Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity. J Virol 70: 1714-1722.
-
(1996)
J. Virol.
, vol.70
, pp. 1714-1722
-
-
Riesner, D.1
Kellings, K.2
Post, K.3
Wille, H.4
Serban, H.5
Groth, D.6
Baldwin, M.A.7
Prusiner, S.B.8
-
34
-
-
0035859102
-
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding
-
Saborio GP, 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
-
35
-
-
0031720905
-
Eight prion strains have PrP(Sc) molecules with different conformations
-
Safar J, Wille H, Itri V, Groth D, Serban H, Torchia M, Cohen FE, Prusiner SB (1998). Eight prion strains have PrP(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
-
36
-
-
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
-
37
-
-
0035861987
-
Prusiner SB Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein
-
Schmitt-Ulms G, Legname G, Baldwin MA, Ball HL, Bradon N, Bosque PJ, Crossin KL, Edelman GM, DeArmond SJ, Cohen FE, Prusiner SB (2001). Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein. J Mol Biol 314: 1209-1225.
-
(2001)
J. Mol. Biol.
, vol.314
, pp. 1209-1225
-
-
Schmitt-Ulms, G.1
Legname, G.2
Baldwin, M.A.3
Ball, H.L.4
Bradon, N.5
Bosque, P.J.6
Crossin, K.L.7
Edelman, G.M.8
DeArmond, S.J.9
Cohen, F.E.10
-
38
-
-
28444439297
-
Transgenic models of prion disease
-
Scott MR, Supattapone S, Nguyen HO, DeArmond SJ, Prusiner SB (2000). Transgenic models of prion disease. Arch Virol Suppl 113-124.
-
(2000)
Arch. Virol. Suppl.
, pp. 113-124
-
-
Scott, M.R.1
Supattapone, S.2
Nguyen, H.O.3
DeArmond, S.J.4
Prusiner, S.B.5
-
39
-
-
0028882424
-
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
-
Telling GC, Scott M, Mastrianni J, Gabizon R, Torchia M, Cohen FE, DeArmond SJ, Prusiner SB (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
-
40
-
-
15844421385
-
Altered circadian activity rhythms and sleep in mice devoid of prion protein
-
Tobler I, Gaus SE, Deboer T, Achermann P, Fischer M, Rulicke 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
Rulicke, T.6
Moser, M.7
Oesch, B.8
McBride, P.A.9
Manson, J.C.10
-
41
-
-
0023669586
-
A novel progressive spongiform encephalopathy in cattle
-
Wells GA, Scott AC, Johnson CT, Gunning RF, Hancock RD, Jeffrey M, Dawson M, Bradley R (1987). A novel progressive spongiform encephalopathy in cattle. Vet Rec 121: 419-420.
-
(1987)
Vet. Rec.
, vol.121
, pp. 419-420
-
-
Wells, G.A.1
Scott, A.C.2
Johnson, C.T.3
Gunning, R.F.4
Hancock, R.D.5
Jeffrey, M.6
Dawson, M.7
Bradley, R.8
-
42
-
-
0003721038
-
Laughing death-the untold story of kuru
-
Human Press: Clifton, NJ
-
Zigas V (1990). Laughing death-the untold story of kuru. Human Press: Clifton, NJ.
-
(1990)
-
-
Zigas, V.1
|