-
2
-
-
0023860332
-
Detection of prion protein mRNA in normal and scrapie-infected tissues and cell lines
-
Caughey B, Race RE, Chesebro B. Detection of prion protein mRNA in normal and scrapie-infected tissues and cell lines. J Gen Virol 1988 ; 69 : 711-6.
-
(1988)
J Gen Virol
, vol.69
, pp. 711-716
-
-
Caughey, B.1
Race, R.E.2
Chesebro, B.3
-
3
-
-
0040393220
-
Separation and properties of cellular and scrapie prion proteins
-
Meyer RK, McKinley MP, Bowman KA, et al. Separation and properties of cellular and scrapie prion proteins. Proc Natl Acad Sci USA 1986 ; 83 : 2310-4.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 2310-2314
-
-
Meyer, R.K.1
McKinley, M.P.2
Bowman, K.A.3
-
4
-
-
0242300624
-
Games played by rogue proteins in prion disorders and Alzheimer's disease
-
Aguzzi A, Haass C. Games played by rogue proteins in prion disorders and Alzheimer's disease. Science 2003 ; 302 : 814-8.
-
(2003)
Science
, vol.302
, pp. 814-818
-
-
Aguzzi, A.1
Haass, C.2
-
5
-
-
0001289828
-
La maladie dite tremblante du mouton est-elle inoculable ?
-
Cuille J, Chelle P. La maladie dite tremblante du mouton est-elle inoculable ? CR Acad Sci Paris 1936 ; 1552-4.
-
(1936)
CR Acad Sci Paris
, pp. 1552-1554
-
-
Cuille, J.1
Chelle, P.2
-
6
-
-
0036788993
-
PrP(Sc) accumulation in placentas of ewes exposed to natural scrapie: Influence of fetal PrP genotype and effect on ewe-to-lamb transmission
-
Andreoletti O, Lacroux C, Chabert A, et al. PrP(Sc) accumulation in placentas of ewes exposed to natural scrapie: influence of fetal PrP genotype and effect on ewe-to-lamb transmission. J Gen Virol 2002 ; 83 : 2607-16.
-
(2002)
J Gen Virol
, vol.83
, pp. 2607-2616
-
-
Andreoletti, O.1
Lacroux, C.2
Chabert, A.3
-
7
-
-
0028349264
-
PrP genotype and agent effects in scrapie: Change in allelic interaction with different isolates of agent in sheep, a natural host of scrapie
-
Goldmann W, Hunter N, Smith G, et al. PrP genotype and agent effects in scrapie: change in allelic interaction with different isolates of agent in sheep, a natural host of scrapie. J Gen Virol 1994 ; 75 : 989-95.
-
(1994)
J Gen Virol
, vol.75
, pp. 989-995
-
-
Goldmann, W.1
Hunter, N.2
Smith, G.3
-
8
-
-
0028782021
-
An epidemiologist's view of bovine spongiform encephalopathy
-
Wilesmith JW. An epidemiologist's view of bovine spongiform encephalopathy. Philos Trans R Soc Lond B Biol Sci 1994 ; 343 : 357-61.
-
(1994)
Philos Trans R Soc Lond B Biol Sci
, vol.343
, pp. 357-361
-
-
Wilesmith, J.W.1
-
11
-
-
0030754421
-
Spongiform encephalopathy in an imported cheetah in France
-
Baron T, Belli P, Madec JY, et al. Spongiform encephalopathy in an imported cheetah in France. Vet Rec 1997 ; 141 : 270-1.
-
(1997)
Vet Rec
, vol.141
, pp. 270-271
-
-
Baron, T.1
Belli, P.2
Madec, J.Y.3
-
12
-
-
1842457751
-
Comparative molecular analysis of the abnormal prion protein in field scrapie cases and experimental bovine spongiform encephalopathy in sheep by use of Western blotting and immunohistochemical methods
-
Lezmi S, Martin S, Simon S, et al. Comparative molecular analysis of the abnormal prion protein in field scrapie cases and experimental bovine spongiform encephalopathy in sheep by use of Western blotting and immunohistochemical methods. J Virol 2004 ; 78 : 3654-62.
-
(2004)
J Virol
, vol.78
, pp. 3654-3662
-
-
Lezmi, S.1
Martin, S.2
Simon, S.3
-
13
-
-
0034749390
-
Molecular analysis of the abnormal prion protein during coinfection of mice by bovine spongiform encephalopathy and a scrapie agent
-
Baron TG, Biacabe AG. Molecular analysis of the abnormal prion protein during coinfection of mice by bovine spongiform encephalopathy and a scrapie agent. J Virol 2001 ; 75 : 107-14.
-
(2001)
J Virol
, vol.75
, pp. 107-114
-
-
Baron, T.G.1
Biacabe, A.G.2
-
14
-
-
18144418908
-
BSE agent signatures in a goat
-
Eloit M, Adjou K, Coulpier M, et al. BSE agent signatures in a goat. Vet Rec 2005 ; 156 : 523-4.
-
(2005)
Vet Rec
, vol.156
, pp. 523-524
-
-
Eloit, M.1
Adjou, K.2
Coulpier, M.3
-
15
-
-
1442286319
-
Atypical scrapie cases in Germany and France are identified by discrepant reaction patterns in BSE rapid tests
-
Buschmann A, Biacabe AG, Ziegler U, et al. Atypical scrapie cases in Germany and France are identified by discrepant reaction patterns in BSE rapid tests. J Virol Methods 2004 ; 117 : 27-36.
-
(2004)
J Virol Methods
, vol.117
, pp. 27-36
-
-
Buschmann, A.1
Biacabe, A.G.2
Ziegler, U.3
-
17
-
-
24344492256
-
Chronic wasting disease of elk: Transmissibility to humans examined by transgenic mouse models
-
Kong Q, Huang S, Zou W, et al. Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. J Neurosci 2005 ; 25 : 7944-9.
-
(2005)
J Neurosci
, vol.25
, pp. 7944-7949
-
-
Kong, Q.1
Huang, S.2
Zou, W.3
-
19
-
-
0000781428
-
Über eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswerten anatomischen Befunde (spastische Pseudosklerose- Encephalomyelopathie mit disseminierten Degenerationsherden)
-
Jakob A. Über eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswerten anatomischen Befunde (spastische Pseudosklerose- Encephalomyelopathie mit disseminierten Degenerationsherden). Deutsche Zeitschrift für Nervenheilkunde 1921 ; 70 : 132-46.
-
(1921)
Deutsche Zeitschrift für Nervenheilkunde
, vol.70
, pp. 132-146
-
-
Jakob, A.1
-
21
-
-
0342951746
-
A new variant of Creutzfeldt-Jakob disease in the UK
-
Will RG, Ironside JW, Zeidler M, et al. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 1996 ; 347 : 921-5.
-
(1996)
Lancet
, vol.347
, pp. 921-925
-
-
Will, R.G.1
Ironside, J.W.2
Zeidler, M.3
-
23
-
-
3242716876
-
Prevalence of lymphoreticular prion protein accumulation in UK tissue samples
-
Hilton DA, Ghani AC, Conyers L, et al. Prevalence of lymphoreticular prion protein accumulation in UK tissue samples. J Pathol 2004 ; 203 : 733-9.
-
(2004)
J Pathol
, vol.203
, pp. 733-739
-
-
Hilton, D.A.1
Ghani, A.C.2
Conyers, L.3
-
24
-
-
33645957674
-
Variant Creutzfeldt-Jakob disease: Risk of transmission by blood transfusion and blood therapies
-
Ironside JW. Variant Creutzfeldt-Jakob disease: risk of transmission by blood transfusion and blood therapies. Haemophilia 2006 ; 12 (suppl 1) : 8-15.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 1
, pp. 8-15
-
-
Ironside, J.W.1
-
25
-
-
33646898809
-
Variant Creutzfeldt-Jakob disease: Prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence study
-
Ironside JW, Bishop MT, Connolly K, et al. Variant Creutzfeldt-Jakob disease: prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence study. Br Med J 2006 ; 332 : 1186-8.
-
(2006)
Br Med J
, vol.332
, pp. 1186-1188
-
-
Ironside, J.W.1
Bishop, M.T.2
Connolly, K.3
-
26
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
Prusiner SB. Novel proteinaceous infectious particles cause scrapie. Science 1982 ; 216 : 136-44.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
27
-
-
0344030333
-
Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein
-
Lasmezas CI, Deslys JP, Robain O, et al. Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein. Science 1997 ; 275 : 402-5.
-
(1997)
Science
, vol.275
, pp. 402-405
-
-
Lasmezas, C.I.1
Deslys, J.P.2
Robain, O.3
-
28
-
-
0033485260
-
A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy
-
Manson JC, Jamieson E, Baybutt H, et al. A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy. EMBO J 1999 ; 18 : 6855-64.
-
(1999)
EMBO J
, vol.18
, pp. 6855-6864
-
-
Manson, J.C.1
Jamieson, E.2
Baybutt, H.3
-
29
-
-
0028608963
-
Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein
-
Hsiao KK, Groth D, Scott M, et al. Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein. Proc Natl Acad Sci USA 1994 ; 91 : 9126-30.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 9126-9130
-
-
Hsiao, K.K.1
Groth, D.2
Scott, M.3
-
31
-
-
17444413067
-
In vitro generation of infectious scrapie prions
-
Castilla J, Saa P, Hetz C, Soto C. In vitro generation of infectious scrapie prions. Cell 2005 ; 121 : 195-206.
-
(2005)
Cell
, vol.121
, pp. 195-206
-
-
Castilla, J.1
Saa, P.2
Hetz, C.3
Soto, C.4
-
32
-
-
33847079282
-
25 nm virion is the likely cause of transmissible spongiform encephalopathies
-
Manuelidis L. A 25 nm virion is the likely cause of transmissible spongiform encephalopathies. J Cell Biochem 2007 ; 100 : 897-915.
-
(2007)
J Cell Biochem
, vol.100
, pp. 897-915
-
-
Manuelidis, L.A.1
-
33
-
-
0028235039
-
Dementias, neurodegeneration, and viral mechanisms of disease from the perspective of human transmissible encephalopathies
-
Manuelidis L. Dementias, neurodegeneration, and viral mechanisms of disease from the perspective of human transmissible encephalopathies. Ann NY Acad Sci 1994 ; 724 : 259-81.
-
(1994)
Ann NY Acad Sci
, vol.724
, pp. 259-281
-
-
Manuelidis, L.1
-
34
-
-
33745565356
-
Retrovirus infection strongly enhances scrapie infectivity release in cell culture
-
Leblanc P, Alais S, Porto-Carreiro I, et al. Retrovirus infection strongly enhances scrapie infectivity release in cell culture. EMBO J 2006 ; 25 : 2674-85.
-
(2006)
EMBO J
, vol.25
, pp. 2674-2685
-
-
Leblanc, P.1
Alais, S.2
Porto-Carreiro, I.3
-
35
-
-
0033534610
-
Prions of yeast and fungi. Proteins as genetic material
-
Wickner RB, Edskes HK, Maddelein ML, et al. Prions of yeast and fungi. Proteins as genetic material. J Biol Chem 1999 ; 274 : 555-8.
-
(1999)
J Biol Chem
, vol.274
, pp. 555-558
-
-
Wickner, R.B.1
Edskes, H.K.2
Maddelein, M.L.3
-
37
-
-
0026600865
-
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
-
Bueler H, Fischer M, Lang Y, et al. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature 1992 ; 356 : 577-82.
-
(1992)
Nature
, vol.356
, pp. 577-582
-
-
Bueler, H.1
Fischer, M.2
Lang, Y.3
-
39
-
-
0036525729
-
Metal ions and prion diseases
-
Lehmann S. Metal ions and prion diseases. Curr Opin Chem Biol 2002 ; 6 : 187-92.
-
(2002)
Curr Opin Chem Biol
, vol.6
, pp. 187-192
-
-
Lehmann, S.1
-
40
-
-
0345505687
-
Different signal transduction pathways are involved in neurite outgrowth and neuronal survival mediated by the prion protein
-
Chen S, Mange A, Dong L, Schachner M. Different signal transduction pathways are involved in neurite outgrowth and neuronal survival mediated by the prion protein. Mol Cell Neurosci 2003 ; 2 : 227-33.
-
(2003)
Mol Cell Neurosci
, vol.2
, pp. 227-233
-
-
Chen, S.1
Mange, A.2
Dong, L.3
Schachner, M.4
-
41
-
-
0037299870
-
Different isoforms of the non-integrin laminin receptor are present in mouse brain and bind PrP
-
Simoneau S, Haik S, Leucht C, et al. Different isoforms of the non-integrin laminin receptor are present in mouse brain and bind PrP. Biol Chem 2003 ; 384 : 243-6.
-
(2003)
Biol Chem
, vol.384
, pp. 243-246
-
-
Simoneau, S.1
Haik, S.2
Leucht, C.3
-
43
-
-
33644766915
-
Prion protein (PrPc) positively regulates neural precursor proliferation during developmental and adult mammalian neurogenesis
-
Steele AD, Emsley JG, Ozdinler PH, et al. Prion protein (PrPc) positively regulates neural precursor proliferation during developmental and adult mammalian neurogenesis. Proc Natl Acad Sci USA 2006 ; 103 : 3416-21.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 3416-3421
-
-
Steele, A.D.1
Emsley, J.G.2
Ozdinler, P.H.3
-
44
-
-
33144456321
-
Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their self-renewal
-
Zhang CC, Steele AD, Lindquist S, Lodish HF. Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their self-renewal. Proc Natl Acad Sci USA 2006 ; 103 : 2184-9.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 2184-2189
-
-
Zhang, C.C.1
Steele, A.D.2
Lindquist, S.3
Lodish, H.F.4
-
45
-
-
0000561330
-
The 14-3-3 brain protein and transmissible spongiform encephalopathy
-
Zerr I, Bodemer M, Weber T. The 14-3-3 brain protein and transmissible spongiform encephalopathy. N Engl J Med 1997 ; 336 : 875.
-
(1997)
N Engl J Med
, vol.336
, pp. 875
-
-
Zerr, I.1
Bodemer, M.2
Weber, T.3
-
46
-
-
23844471279
-
Blood infectivity, processing and screening tests in transmissible spongiform encephalopathy
-
Brown P. Blood infectivity, processing and screening tests in transmissible spongiform encephalopathy. Vox Sang 2005 ; 89 : 63-70.
-
(2005)
Vox Sang
, vol.89
, pp. 63-70
-
-
Brown, P.1
-
47
-
-
0037172849
-
Drug therapy in human and experimental transmissible spongiform encephalopathy
-
Brown P. Drug therapy in human and experimental transmissible spongiform encephalopathy. Neurology 2002 ; 58 : 1720-5.
-
(2002)
Neurology
, vol.58
, pp. 1720-1725
-
-
Brown, P.1
-
48
-
-
18844434701
-
Cerebroventricular infusion of pentosan polysulphate in human variant Creutzfeldt-Jakob disease
-
Todd NV, Morrow J, Doh-Ura K, et al. Cerebroventricular infusion of pentosan polysulphate in human variant Creutzfeldt-Jakob disease. J Infect 2005 ; 50 : 394-6.
-
(2005)
J Infect
, vol.50
, pp. 394-396
-
-
Todd, N.V.1
Morrow, J.2
Doh-Ura, K.3
-
49
-
-
0035487106
-
Interventional strategies against prion diseases
-
Aguzzi A, Glatzel M, Montrasio F, et al. Interventional strategies against prion diseases. Nat Rev Neurosci 2001 ; 2 : 745-9.
-
(2001)
Nat Rev Neurosci
, vol.2
, pp. 745-749
-
-
Aguzzi, A.1
Glatzel, M.2
Montrasio, F.3
-
50
-
-
0242363656
-
Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis. Post-natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration
-
Mallucci G, Dickinson A, Linehan J, et al. Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis. Post-natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration. Science 2003 ; 302 : 871-4.
-
(2003)
Science
, vol.302
, pp. 871-874
-
-
Mallucci, G.1
Dickinson, A.2
Linehan, J.3
-
51
-
-
10944262733
-
Inhibition of PrPSc formation by lentiviral gene transfer of PrP containing dominant negative mutations
-
Crozet C, Lin YL, Mettling C, et al. Inhibition of PrPSc formation by lentiviral gene transfer of PrP containing dominant negative mutations. J Cell Sci 2004 ; 117 : 5591-7.
-
(2004)
J Cell Sci
, vol.117
, pp. 5591-5597
-
-
Crozet, C.1
Lin, Y.L.2
Mettling, C.3
-
52
-
-
0036168788
-
The URE3 phenotype: Evidence for a soluble prion in yeast
-
Fernandez-Bellot E, Guillemet E, Ness F, et al. The URE3 phenotype: evidence for a soluble prion in yeast. EMBO Rep 2002 ; 3 : 76-81.
-
(2002)
EMBO Rep
, vol.3
, pp. 76-81
-
-
Fernandez-Bellot, E.1
Guillemet, E.2
Ness, F.3
-
53
-
-
0033661670
-
Vegetative incompatibility in filamentous fungi: Podospora and Neurospora provide some clues
-
Saupe SJ, Clave C Begueret J. Vegetative incompatibility in filamentous fungi: Podospora and Neurospora provide some clues. Curr Opin Microbiol 2000 ; 3 : 608-12.
-
(2000)
Curr Opin Microbiol
, vol.3
, pp. 608-612
-
-
Saupe, S.J.1
Clave, C.2
Begueret, J.3
-
54
-
-
0348077417
-
A neuronal isoform of the aplysia CPEB has prion-like properties
-
Si K, Lindquist S, Kandel ER. A neuronal isoform of the aplysia CPEB has prion-like properties. Cell 2003 ; 115 : 879-91.
-
(2003)
Cell
, vol.115
, pp. 879-891
-
-
Si, K.1
Lindquist, S.2
Kandel, E.R.3
-
55
-
-
19544363062
-
Prions as adaptive conduits of memory and inheritance
-
Shorter J, Lindquist S. Prions as adaptive conduits of memory and inheritance. Nat Rev Genet 2005 ; 6 : 435-50.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 435-450
-
-
Shorter, J.1
Lindquist, S.2
-
57
-
-
22144467370
-
Protéines prions : Propriétés de repliement et d'agrégation
-
Bousset L, Melki R. Protéines prions : propriétés de repliement et d'agrégation. Med Sci (Paris) 2005 ; 21 : 634-40.
-
(2005)
Med Sci (Paris)
, vol.21
, pp. 634-640
-
-
Bousset, L.1
Melki, R.2
-
58
-
-
27144434140
-
La structure de la protéine prion et la relation avec son infectiosité
-
Madly B, Chrétien F. La structure de la protéine prion et la relation avec son infectiosité. Med Sci (Paris) 2005 ; 21 : 806-7.
-
(2005)
Med Sci (Paris)
, vol.21
, pp. 806-807
-
-
Madly, B.1
Chrétien, F.2
-
60
-
-
36049046084
-
La protéine prion ne se fait pas prier pour faire des agrégats moléculaires
-
Goggin K, Roucou X. La protéine prion ne se fait pas prier pour faire des agrégats moléculaires. Med Sci (Paris) 2006 ; 22 : 1013-4.
-
(2006)
Med Sci (Paris)
, vol.22
, pp. 1013-1014
-
-
Goggin, K.1
Roucou, X.2
-
61
-
-
37849010634
-
-
TIRÉS À PART S. Lehmann
-
TIRÉS À PART S. Lehmann
-
-
-
|