-
2
-
-
9544238083
-
Transmission dynamics and epidemiology of BSE in British cattle
-
Anderson, R.M.; Donnelly, CA.; Ferguson, N.M.; Woolhouse, M.E.; Watt, C.J.; Udy, HJ.; MaWhinney, S.; Dunstan, S.P.; Southwood, T.R.; Wilesmith, J.W.; Ryan, J.B.; Hoinville, L.J.; Hillerton, J.E.; Austin, A.R.; Wells, G.A. Transmission dynamics and epidemiology of BSE in British cattle. Nature, 1996, 382, 779-788.
-
(1996)
Nature
, vol.382
, pp. 779-788
-
-
Anderson, R.M.1
Donnelly, C.A.2
Ferguson, N.M.3
Woolhouse, M.E.4
Watt, C.J.5
Udy, H.J.6
MaWhinney, S.7
Dunstan, S.P.8
Southwood, T.R.9
Wilesmith, J.W.10
Ryan, J.B.11
Hoinville, L.J.12
Hillerton, J.E.13
Austin, A.R.14
Wells, G.A.15
-
3
-
-
63449094850
-
-
http://www.oie.int/eng/info/en-esbmonde.htm; 2008 [accessed June 2008].
-
http://www.oie.int/eng/info/en-esbmonde.htm; 2008 [accessed June 2008].
-
-
-
-
4
-
-
0030820354
-
The same prion strain causes vCJD and BSE
-
Hill, A.F.; Desbruslais, M.; Joiner, S.; Sidle, K.C.; Gowland, I.; Collinge, J.; Doey, L.J.; Lantos, P. The same prion strain causes vCJD and BSE. Nature, 1997, 389, 448-450.
-
(1997)
Nature
, vol.389
, pp. 448-450
-
-
Hill, A.F.1
Desbruslais, M.2
Joiner, S.3
Sidle, K.C.4
Gowland, I.5
Collinge, J.6
Doey, L.J.7
Lantos, P.8
-
5
-
-
0030775632
-
-
Bruce, M.E.; Will, R.G.; Ironside, J.W.; McConnell, I.; Drummond, D.; Suttie, A.; McCardle, L.; Chree, A.; Hope, J.; Birkett, C; Cousens, S.; Fraser, H.; Bostock, C.J. Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent. Nature, 1997, 389, 498-501.
-
Bruce, M.E.; Will, R.G.; Ironside, J.W.; McConnell, I.; Drummond, D.; Suttie, A.; McCardle, L.; Chree, A.; Hope, J.; Birkett, C; Cousens, S.; Fraser, H.; Bostock, C.J. Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent. Nature, 1997, 389, 498-501.
-
-
-
-
6
-
-
63449128025
-
-
http://www.who.int/zoonoses/diseases/prion-diseases/en/; 2008 [accessed June 2008].
-
http://www.who.int/zoonoses/diseases/prion-diseases/en/; 2008 [accessed June 2008].
-
-
-
-
7
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
Prusiner, S.B. Novel proteinaceous infectious particles cause scrapie. Science, 1982, 216, 136-144.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
8
-
-
0022005315
-
-
Oesch, B.; Westaway, D.; Walchli, M.; McKinley, M.P.: Kent, S.B.; Aebersold, R.; Barry, R.A.; Tempst, P.; Teplow, D.B.; Hood, L.E.; Prusiner, S.B.; Weissmann C. A cellular gene encodes scrapie PrP 27-30 protein. Cell, 1985, 40, 735-746.
-
Oesch, B.; Westaway, D.; Walchli, M.; McKinley, M.P.: Kent, S.B.; Aebersold, R.; Barry, R.A.; Tempst, P.; Teplow, D.B.; Hood, L.E.; Prusiner, S.B.; Weissmann C. A cellular gene encodes scrapie PrP 27-30 protein. Cell, 1985, 40, 735-746.
-
-
-
-
9
-
-
0022476747
-
Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene
-
Basier, K.; Oesch, B.; Scott, M.; Westaway, D.; Walchli, M.; Groth, D.F.; McKinley, M.P.; Prusiner, S.B.; Weissmann, C. Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene. Cell, 1986, 46, 417-428.
-
(1986)
Cell
, vol.46
, pp. 417-428
-
-
Basier, K.1
Oesch, B.2
Scott, M.3
Westaway, D.4
Walchli, M.5
Groth, D.F.6
McKinley, M.P.7
Prusiner, S.B.8
Weissmann, C.9
-
10
-
-
36049020231
-
A general model of prion strains and their pathogenicity
-
Collinge, J.; Clarke, A.R. A general model of prion strains and their pathogenicity. Science, 2007, 318, 930-936.
-
(2007)
Science
, vol.318
, pp. 930-936
-
-
Collinge, J.1
Clarke, A.R.2
-
12
-
-
0026600865
-
-
Bueler, H.; Fischer, M.: Lang, Y.; Bluethmann, H.; Lipp, H.P.; DeArmond, S.J.; Prusiner, S.B.; Aguet, M.; Weissmann, C. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature, 1992, 356, 577-582.
-
Bueler, H.; Fischer, M.: Lang, Y.; Bluethmann, H.; Lipp, H.P.; DeArmond, S.J.; Prusiner, S.B.; Aguet, M.; Weissmann, C. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature, 1992, 356, 577-582.
-
-
-
-
13
-
-
20344394154
-
-
Chesebro, B.; Trifilo, M.; Race, R.; Meade-White, K.; Teng, C; LaCasse, R.; Raymond, L.; Favara, C; Baron, G.; Priola, S.; Caughey, B.; Masliah, E.; Oldstone, M. Anchorless prion protein results in infectious amyloid disease without clinical scrapie. Science, 2005, 308, 1435-1439.
-
Chesebro, B.; Trifilo, M.; Race, R.; Meade-White, K.; Teng, C; LaCasse, R.; Raymond, L.; Favara, C; Baron, G.; Priola, S.; Caughey, B.; Masliah, E.; Oldstone, M. Anchorless prion protein results in infectious amyloid disease without clinical scrapie. Science, 2005, 308, 1435-1439.
-
-
-
-
14
-
-
0035815709
-
In vivo conversion of cellular prion protein to pathogenic isoforms, as monitored by conformation-specific antibodies
-
Yokoyama, T.; Kimura, K.M.; Ushiki, Y.; Yamada, S.; Morooka, A.; Nakashiba, T.; Sassa, T.; Itohara, S. In vivo conversion of cellular prion protein to pathogenic isoforms, as monitored by conformation-specific antibodies. J. Biol. Chem., 2001, 276, 11265-11271.
-
(2001)
J. Biol. Chem
, vol.276
, pp. 11265-11271
-
-
Yokoyama, T.1
Kimura, K.M.2
Ushiki, Y.3
Yamada, S.4
Morooka, A.5
Nakashiba, T.6
Sassa, T.7
Itohara, S.8
-
15
-
-
30944453898
-
Neurodegeneration and oxidative stress: Prion disease results from loss of antioxidant defence
-
Brown, D.R. Neurodegeneration and oxidative stress: prion disease results from loss of antioxidant defence. Folia. Neuropathol., 2005, 43, 229-243.
-
(2005)
Folia. Neuropathol
, vol.43
, pp. 229-243
-
-
Brown, D.R.1
-
16
-
-
0036124813
-
Oxidative stress and the prion protein in transmissible spongiform encephalopathies
-
Milhavet, O.; Lehmann, S. Oxidative stress and the prion protein in transmissible spongiform encephalopathies. Brain Res. Brain Res. Rev., 2002, 38, 328-339.
-
(2002)
Brain Res. Brain Res. Rev
, vol.38
, pp. 328-339
-
-
Milhavet, O.1
Lehmann, S.2
-
17
-
-
1542287942
-
Mitochondrial dysfunction in neurodegenerative diseases associated with copper imbalance
-
Rossi, L.; Lombardo, M.F.; Ciriolo, M.R.; Rotilio, G. Mitochondrial dysfunction in neurodegenerative diseases associated with copper imbalance. Neurochem. Res., 2004, 29, 493-504.
-
(2004)
Neurochem. Res
, vol.29
, pp. 493-504
-
-
Rossi, L.1
Lombardo, M.F.2
Ciriolo, M.R.3
Rotilio, G.4
-
18
-
-
50049132319
-
Cellular pathogenesis in prion diseases
-
Crozet, C; Beranger, F.; Lehmann, S. Cellular pathogenesis in prion diseases. Vet. Res., 2008, 39, 44.
-
(2008)
Vet. Res
, vol.39
, pp. 44
-
-
Crozet, C.1
Beranger, F.2
Lehmann, S.3
-
19
-
-
0036291424
-
Ablation of cellular prion protein expression affects mitochondrial numbers and morphology
-
Miele, G.; Jeffrey, M.; Tumbull, D.; Manson, J.; Clinton, M. Ablation of cellular prion protein expression affects mitochondrial numbers and morphology. Biochem. Biophys. Res. Commun., 2002, 291, 372-377.
-
(2002)
Biochem. Biophys. Res. Commun
, vol.291
, pp. 372-377
-
-
Miele, G.1
Jeffrey, M.2
Tumbull, D.3
Manson, J.4
Clinton, M.5
-
20
-
-
41149107987
-
Complex I specific increase in superoxide formation and respiration rate by PrP-null mouse brain mitochondria
-
Paterson, A.W.; Curtis, J.C.; Macleod, N.K. Complex I specific increase in superoxide formation and respiration rate by PrP-null mouse brain mitochondria. J. Neurochem., 2008, 105, 177-191.
-
(2008)
J. Neurochem
, vol.105
, pp. 177-191
-
-
Paterson, A.W.1
Curtis, J.C.2
Macleod, N.K.3
-
21
-
-
33646571843
-
Recent advances in clarifying prion protein functions using knockout mice and derived cell lines
-
Sakudo, A.; Onodera, T.; Suganuma, Y.; Kobayashi, T.; Saeki, K.; Ikuta, K. Recent advances in clarifying prion protein functions using knockout mice and derived cell lines. Mini Rev. Med. Chem., 2006, 6, 589-601.
-
(2006)
Mini Rev. Med. Chem
, vol.6
, pp. 589-601
-
-
Sakudo, A.1
Onodera, T.2
Suganuma, Y.3
Kobayashi, T.4
Saeki, K.5
Ikuta, K.6
-
22
-
-
34247394797
-
Recent developments in prion disease research: Diagnostic tools and in vitro cell culture models
-
Sakudo, A.; Nakamura, I.; Ikuta, K.; Onodera, T. Recent developments in prion disease research: diagnostic tools and in vitro cell culture models. J. Vet. Med. Sci., 2007, 69, 329-337.
-
(2007)
J. Vet. Med. Sci
, vol.69
, pp. 329-337
-
-
Sakudo, A.1
Nakamura, I.2
Ikuta, K.3
Onodera, T.4
-
23
-
-
0141849458
-
-
Wadsworth, J.D.; Hill, A.F.; Beck, J.A.; Collinge, J. Molecular and clinical classification of human prion disease. Br. Med. Bull., 2003, 66, 241-254.
-
Wadsworth, J.D.; Hill, A.F.; Beck, J.A.; Collinge, J. Molecular and clinical classification of human prion disease. Br. Med. Bull., 2003, 66, 241-254.
-
-
-
-
24
-
-
0033999635
-
Cultured cell sublines highly susceptible to prion infection
-
Bosque, P.J.; Prusiner, S.B. Cultured cell sublines highly susceptible to prion infection. J. Virol., 2000, 74, 4377-4386.
-
(2000)
J. Virol
, vol.74
, pp. 4377-4386
-
-
Bosque, P.J.1
Prusiner, S.B.2
-
25
-
-
0035979274
-
Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody
-
Enari, M.; Flechsig, E.; Weissmann, C. Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody. Proc. Natl. Acad. Sci. USA, 2001, 98, 9295-9299.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 9295-9299
-
-
Enari, M.1
Flechsig, E.2
Weissmann, C.3
-
26
-
-
0035839080
-
A sensitive filter retention assay for the detection of PrP(Sc) and the screening of anti-prion compounds
-
Winklhofer, K.F.; Hartl, F.U.; Tatzeit, J. A sensitive filter retention assay for the detection of PrP(Sc) and the screening of anti-prion compounds. FEBS Lett., 2001, 503, 41-45.
-
(2001)
FEBS Lett
, vol.503
, pp. 41-45
-
-
Winklhofer, K.F.1
Hartl, F.U.2
Tatzeit, J.3
-
27
-
-
0141891211
-
Characterization of 2′-fluoro-RNA aptamers that bind preferentially to disease-associated conformations of prion protein and inhibit conversion
-
Rhie, A.; Kirby, L.; Sayer, N.; Wellesley, R.; Disterer, P.; Sylvester, I.; Gill, A.; Hope, J.; James, W.; Tahiri-Alaoui, A. Characterization of 2′-fluoro-RNA aptamers that bind preferentially to disease-associated conformations of prion protein and inhibit conversion. J. Biol. Chem., 2003, 278, 39697-39705.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 39697-39705
-
-
Rhie, A.1
Kirby, L.2
Sayer, N.3
Wellesley, R.4
Disterer, P.5
Sylvester, I.6
Gill, A.7
Hope, J.8
James, W.9
Tahiri-Alaoui, A.10
-
28
-
-
1842424691
-
Structural determinants of conformationally selective, prion-binding aptamers
-
Sayer, N.M.; Cubin, M.; Rhie, A.; Bullock, M.; Tahiri-Alaoui, A.; James, W. Structural determinants of conformationally selective, prion-binding aptamers. J. Biol. Chem., 2004, 279, 13102-13109.
-
(2004)
J. Biol. Chem
, vol.279
, pp. 13102-13109
-
-
Sayer, N.M.1
Cubin, M.2
Rhie, A.3
Bullock, M.4
Tahiri-Alaoui, A.5
James, W.6
-
29
-
-
0030843497
-
RNA aptamers specifically interact with the prion protein PrP
-
Weiss, S.; Proske, D.; Neumann, M.; Groschup, M.H.; Kretzschmar, H.A.; Famulok, M.; Winnacker, E.L. RNA aptamers specifically interact with the prion protein PrP. J. Virol., 1997, 71, 8790-8797.
-
(1997)
J. Virol
, vol.71
, pp. 8790-8797
-
-
Weiss, S.1
Proske, D.2
Neumann, M.3
Groschup, M.H.4
Kretzschmar, H.A.5
Famulok, M.6
Winnacker, E.L.7
-
30
-
-
41349117359
-
A sensitive and quantitative assay for normal PrP in plasma
-
Gregori, L.; Gray, B.N.; Rose, E.; Spinner, D.S.; Kascsak, R.J.; Rohwer, R.G. A sensitive and quantitative assay for normal PrP in plasma. J. Virol. Methods, 2008, 149, 251-259.
-
(2008)
J. Virol. Methods
, vol.149
, pp. 251-259
-
-
Gregori, L.1
Gray, B.N.2
Rose, E.3
Spinner, D.S.4
Kascsak, R.J.5
Rohwer, R.G.6
-
31
-
-
0035928432
-
Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay
-
Wadsworth, J.D.; Joiner, S.; Hill, A.F.; Campbell, T.A.; Desbruslais, M.; Luthert, P.J.; Collinge, J. Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay. Lancet, 2001, 358, 171-180.
-
(2001)
Lancet
, vol.358
, pp. 171-180
-
-
Wadsworth, J.D.1
Joiner, S.2
Hill, A.F.3
Campbell, T.A.4
Desbruslais, M.5
Luthert, P.J.6
Collinge, J.7
-
32
-
-
33646175973
-
Distribution of PrP(Sc) in cattle with bovine spongiform encephalopathy slaughtered at abattoirs in Japan
-
Iwata, N.; Sato, Y.; Higuchi, Y.; Nohtomi, K.; Nagata, N.; Hasegawa, H.; Tobiume, M.; Nakamura, Y.; Hagiwara, K.; Furuoka, H.; Horiuchi, M.; Yamakawa, Y.; Sata, T. Distribution of PrP(Sc) in cattle with bovine spongiform encephalopathy slaughtered at abattoirs in Japan. Jpn. J. Infect. Dis., 2006, 59, 100-107.
-
(2006)
Jpn. J. Infect. Dis
, vol.59
, pp. 100-107
-
-
Iwata, N.1
Sato, Y.2
Higuchi, Y.3
Nohtomi, K.4
Nagata, N.5
Hasegawa, H.6
Tobiume, M.7
Nakamura, Y.8
Hagiwara, K.9
Furuoka, H.10
Horiuchi, M.11
Yamakawa, Y.12
Sata, T.13
-
33
-
-
7444263581
-
Identification of putative atypical scrapie in sheep in Portugal
-
Orge, L.; Galo, A.; Machado, C; Lima, C; Ochoa, C.; Silva, J.; Ramos, M.; Simas, J.P. Identification of putative atypical scrapie in sheep in Portugal. J. Gen. Virol., 2004, 85, 3487-3491.
-
(2004)
J. Gen. Virol
, vol.85
, pp. 3487-3491
-
-
Orge, L.1
Galo, A.2
Machado, C.3
Lima, C.4
Ochoa, C.5
Silva, J.6
Ramos, M.7
Simas, J.P.8
-
34
-
-
0026644090
-
Regional mapping of prion proteins in brain
-
Taraboulos, A.; Jendroska, K.; Serban, D.; Yang, S.L.; DeArmond, S.J.; Prusiner, S.B. Regional mapping of prion proteins in brain. Proc. Natl. Acad. Sci. U. S. A., 1992, 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
-
35
-
-
4344684277
-
Advances in the detection of prion protein in peripheral tissues of variant Creutzfeldt-Jakob disease patients using paraffin-embedded tissue blotting
-
Ritchie, D.L.: Head, M.W.; Ironside, J.W. Advances in the detection of prion protein in peripheral tissues of variant Creutzfeldt-Jakob disease patients using paraffin-embedded tissue blotting. Neuropathol. Appl. Neurobiol, 2004, 30, 360-368.
-
(2004)
Neuropathol. Appl. Neurobiol
, vol.30
, pp. 360-368
-
-
Ritchie, D.L.1
Head, M.W.2
Ironside, J.W.3
-
36
-
-
0033874288
-
The paraffin-embedded tissue blot detects PrP(Sc) early in the incubation time in prion diseases
-
Schulz-Schaeffer, W.J.; Tschoke, S.; Kranefuss, N.; Drose, W.; Hause-Reitner, D.; Giese, A.; Groschup, M.H.; Kretzschmar, H.A. The paraffin-embedded tissue blot detects PrP(Sc) early in the incubation time in prion diseases. Am. J. Pathol., 2000, 156, 51-56.
-
(2000)
Am. J. Pathol
, vol.156
, pp. 51-56
-
-
Schulz-Schaeffer, W.J.1
Tschoke, S.2
Kranefuss, N.3
Drose, W.4
Hause-Reitner, D.5
Giese, A.6
Groschup, M.H.7
Kretzschmar, H.A.8
-
37
-
-
0031720905
-
Eight prion strains have PrP(Sc) molecules with different conformations
-
Safar, J.: Wille, H.: Itri, V.; Groth, D.; Serban, H.: Torchia, M.; Cohen, F.E.; Prusiner, S.B. Eight prion strains have PrP(Sc) molecules with different conformations. Nat. Med., 1998, 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
-
38
-
-
33745967590
-
Specific detection of prion antigenic determinants retained in bovine meat and bone meal by flow microbead immunoassay
-
Murayama, Y.; Yoshioka, M.; Horii, H.; Takata, M.; Miura, K.; Shinagawa, M. Specific detection of prion antigenic determinants retained in bovine meat and bone meal by flow microbead immunoassay. J. Appl. Microbiol, 2006, 101, 369-376.
-
(2006)
J. Appl. Microbiol
, vol.101
, pp. 369-376
-
-
Murayama, Y.1
Yoshioka, M.2
Horii, H.3
Takata, M.4
Miura, K.5
Shinagawa, M.6
-
39
-
-
0037352723
-
Analysis of the performance of antibody capture methods using fluorescent peptides with capillary zone electrophoresis with laser-induced fluorescence
-
Jackman, R.; Schmerr, M.J. Analysis of the performance of antibody capture methods using fluorescent peptides with capillary zone electrophoresis with laser-induced fluorescence. Electrophoresis, 2003, 24, 892-896.
-
(2003)
Electrophoresis
, vol.24
, pp. 892-896
-
-
Jackman, R.1
Schmerr, M.J.2
-
40
-
-
0032768236
-
Use of capillary electrophoresis and fluorescent labeled peptides to detect the abnormal prion protein in the blood of animals that are infected with a transmissible spongiform encephalopathy
-
Schmerr, M.J.; Jenny, A.L.; Bulgin, M.S.; Miller, J.M.; Hamir, A.N.; Cutlip, R.C.; Goodwin, K.R. Use of capillary electrophoresis and fluorescent labeled peptides to detect the abnormal prion protein in the blood of animals that are infected with a transmissible spongiform encephalopathy. J. Chromatogr. A, 1999, 853, 207-214.
-
(1999)
J. Chromatogr. A
, vol.853
, pp. 207-214
-
-
Schmerr, M.J.1
Jenny, A.L.2
Bulgin, M.S.3
Miller, J.M.4
Hamir, A.N.5
Cutlip, R.C.6
Goodwin, K.R.7
-
41
-
-
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. Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targets. Proc. Natl. Acad. Sci. USA, 2000, 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
-
42
-
-
28444454589
-
Putting prions into focus: Application of single molecule detection to the diagnosis of prion diseases
-
Giese, A.; Bieschke, J.; Eigen, M.; Kretzschmar, H.A. Putting prions into focus: application of single molecule detection to the diagnosis of prion diseases. Arch. Virol. Suppl., 2000, 145, 161-171.
-
(2000)
Arch. Virol. Suppl
, vol.145
, pp. 161-171
-
-
Giese, A.1
Bieschke, J.2
Eigen, M.3
Kretzschmar, H.A.4
-
43
-
-
0036683501
-
Identification of scrapie infection from blood serum by Fourier transform infrared spectroscopy
-
Schmitt, J.; Beekes, M.; Brauer, A.; Udelhoven, T.; Lasch, P.; Naumann, D. Identification of scrapie infection from blood serum by Fourier transform infrared spectroscopy. Anal. Chem., 2002, 74, 3865-3868.
-
(2002)
Anal. Chem
, vol.74
, pp. 3865-3868
-
-
Schmitt, J.1
Beekes, M.2
Brauer, A.3
Udelhoven, T.4
Lasch, P.5
Naumann, D.6
-
44
-
-
0032495875
-
Detection and discrimination of PrPSc by multi-spectral ultraviolet fluorescence
-
Rubenstein, R.; Gray, P.C.; Wehlburg, C.M.; Wagner, J.S.; Tisone, G.C. Detection and discrimination of PrPSc by multi-spectral ultraviolet fluorescence. Biochem. Biophys. Res. Commun., 1998, 246, 100-106.
-
(1998)
Biochem. Biophys. Res. Commun
, vol.246
, pp. 100-106
-
-
Rubenstein, R.1
Gray, P.C.2
Wehlburg, C.M.3
Wagner, J.S.4
Tisone, G.C.5
-
45
-
-
0035859102
-
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding
-
Saborio, O.P.; Permanne, B.; Soto, C. Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature, 2001, 411, 810-813.
-
(2001)
Nature
, vol.411
, pp. 810-813
-
-
Saborio, O.P.1
Permanne, B.2
Soto, C.3
-
46
-
-
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
-
47
-
-
33745879463
-
Presymptomatic detection of prions in blood
-
Saa, P.; Castilla, J.; Soto, C. Presymptomatic detection of prions in blood. Science, 2006, 313, 92-94.
-
(2006)
Science
, vol.313
, pp. 92-94
-
-
Saa, P.1
Castilla, J.2
Soto, C.3
-
48
-
-
24744446203
-
Detection of prions in blood
-
Castilla, J.; Saa, P.; Soto, C. Detection of prions in blood. Nat. Med., 2005, 11, 982-985.
-
(2005)
Nat. Med
, vol.11
, pp. 982-985
-
-
Castilla, J.1
Saa, P.2
Soto, C.3
-
49
-
-
19944430413
-
Pre-symptomatic detection of prions by cyclic amplification of protein misfolding
-
Soto, C.; Anderes, L.; Suardi, S.; Cardone, F.; Castilla, J.; Frossard, M.J.; Peano, S.; Saa, P.; Limido, L.; Carbonatto, M.; Ironside, J.; Torres, J.M.; Pocchiari, M.; Tagliavini, F. Pre-symptomatic detection of prions by cyclic amplification of protein misfolding. FEBS Lett., 2005, 579, 638-642.
-
(2005)
FEBS Lett
, vol.579
, pp. 638-642
-
-
Soto, C.1
Anderes, L.2
Suardi, S.3
Cardone, F.4
Castilla, J.5
Frossard, M.J.6
Peano, S.7
Saa, P.8
Limido, L.9
Carbonatto, M.10
Ironside, J.11
Torres, J.M.12
Pocchiari, M.13
Tagliavini, F.14
-
50
-
-
33749632465
-
Protein misfolding cyclic amplification for diagnosis and prion propagation studies
-
Castilla, J.; Saa, P.; Morales, R.; Abid, K.; Maundrell, K.; Soto, C. Protein misfolding cyclic amplification for diagnosis and prion propagation studies. Methods Enzymol, 2006, 412, 3-21.
-
(2006)
Methods Enzymol
, vol.412
, pp. 3-21
-
-
Castilla, J.1
Saa, P.2
Morales, R.3
Abid, K.4
Maundrell, K.5
Soto, C.6
-
51
-
-
34548394607
-
In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrPSc
-
Jones, M.; Peden, A.H.; Prowse, C.V.; Groner, A.; Manson, J.C.; Turner, M.L.; Ironside, J.W.; MacGregor, I.R.; Head, M.W. In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrPSc. J. Pathol., 2007, 213, 21-26.
-
(2007)
J. Pathol
, vol.213
, pp. 21-26
-
-
Jones, M.1
Peden, A.H.2
Prowse, C.V.3
Groner, A.4
Manson, J.C.5
Turner, M.L.6
Ironside, J.W.7
MacGregor, I.R.8
Head, M.W.9
-
52
-
-
34548175394
-
Efficient in vitro amplification of chronic wasting disease PrPRES
-
Kurt, T.D.; Perrott, M.R.; Wilusz, C.J.; Wilusz, L; Supattapone, S.; Telling, G.C.; Zabel, M.D.; Hoover, E.A. Efficient in vitro amplification of chronic wasting disease PrPRES. J. Virol., 2007, 81, 9605-9608.
-
(2007)
J. Virol
, vol.81
, pp. 9605-9608
-
-
Kurt, T.D.1
Perrott, M.R.2
Wilusz, C.J.3
Wilusz, L.4
Supattapone, S.5
Telling, G.C.6
Zabel, M.D.7
Hoover, E.A.8
-
53
-
-
33846809450
-
Efficient in vitro amplification of a mouse-adapted scrapie prion protein
-
Murayama, Y.; Yoshioka, M.; Yokoyama, T.; Iwamaru, Y.; Imamura, M.; Masujin, K.; Yoshiba, S.; Mohri, S. Efficient in vitro amplification of a mouse-adapted scrapie prion protein. Neurosci. Lett., 2007, 413, 270-273.
-
(2007)
Neurosci. Lett
, vol.413
, pp. 270-273
-
-
Murayama, Y.1
Yoshioka, M.2
Yokoyama, T.3
Iwamaru, Y.4
Imamura, M.5
Masujin, K.6
Yoshiba, S.7
Mohri, S.8
-
54
-
-
34547638271
-
Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein
-
Atarashi, R.; Moore, R.A.; Sim, V.L.; Hughson, A.G.; Dorward, D.W.; Onwubiko, H.A.; Priola, S.A.; Caughey, B. Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein. Nat. Methods, 2007, 4, 645-650.
-
(2007)
Nat. Methods
, vol.4
, pp. 645-650
-
-
Atarashi, R.1
Moore, R.A.2
Sim, V.L.3
Hughson, A.G.4
Dorward, D.W.5
Onwubiko, H.A.6
Priola, S.A.7
Caughey, B.8
-
55
-
-
40149090017
-
Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking
-
Atarashi, R.; Wilham, J.M.; Christensen, L.; Hughson, A.G.; Moore, R.A.; Johnson, L.M.; Onwubiko, H.A.; Priola, S.A.; Caughey, B. Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking. Nat. Methods, 2008, 5, 211-212.
-
(2008)
Nat. Methods
, vol.5
, pp. 211-212
-
-
Atarashi, R.1
Wilham, J.M.2
Christensen, L.3
Hughson, A.G.4
Moore, R.A.5
Johnson, L.M.6
Onwubiko, H.A.7
Priola, S.A.8
Caughey, B.9
-
56
-
-
63449127261
-
Recent advances in cell-free PrPSc amplification technique
-
in press
-
Atarashi, R. Recent advances in cell-free PrPSc amplification technique. Protein Pept. Lett. 2009, in press.
-
(2009)
Protein Pept. Lett
-
-
Atarashi, R.1
-
57
-
-
0842281643
-
Mammalian prion biology: One century of evolving concepts
-
Aguzzi, A.; Polymenidou, M. Mammalian prion biology: one century of evolving concepts. Cell, 2004, 116, 313-327.
-
(2004)
Cell
, vol.116
, pp. 313-327
-
-
Aguzzi, A.1
Polymenidou, M.2
-
58
-
-
15844421385
-
Altered circadian activity rhythms and sleep in mice devoid of prion protein
-
Tobler, L; Gaus, S.E.; Deboer, T.; Achermann, P.; Fischer, M.; Rulicke, T.; Moser, M.; Oesch, B.; McBride, P.A.; Manson, J.C. Altered circadian activity rhythms and sleep in mice devoid of prion protein. Nature, 1996, 380, 639-642.
-
(1996)
Nature
, vol.380
, pp. 639-642
-
-
Tobler, L.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
-
59
-
-
0027997387
-
Prion protein is necessary for normal synaptic function
-
Collinge, L; Whittington, M.A.; Sidle, K.C.; Smith, C.J.; Palmer, M.S.; Clarke, A.R.; Jefferys, J.G. Prion protein is necessary for normal synaptic function. Nature, 1994, 370, 295-297.
-
(1994)
Nature
, vol.370
, pp. 295-297
-
-
Collinge, L.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
-
60
-
-
0035490302
-
Similar target, different effects: Late-onset ataxia and spatial learning in prion protein-deficient mouse lines
-
Valenti, P.; Cozzio, A.; Nishida, N.; Wolfer, D.P.; Sakaguchi, S.; Lipp, H.P. Similar target, different effects: late-onset ataxia and spatial learning in prion protein-deficient mouse lines. Neurogenetics, 2001, 3, 173-184.
-
(2001)
Neurogenetics
, vol.3
, pp. 173-184
-
-
Valenti, P.1
Cozzio, A.2
Nishida, N.3
Wolfer, D.P.4
Sakaguchi, S.5
Lipp, H.P.6
-
61
-
-
33846549467
-
Prion protein gene-deficient cell lines: Powerful tools for prion biology
-
Sakudo, A.; Onodera, T.; Ikuta, K. Prion protein gene-deficient cell lines: powerful tools for prion biology. Microbiol. Immunol, 2007, 51, 1-13.
-
(2007)
Microbiol. Immunol
, vol.51
, pp. 1-13
-
-
Sakudo, A.1
Onodera, T.2
Ikuta, K.3
-
62
-
-
0027483615
-
Neurotoxicity of a prion protein fragment
-
Forloni, G.; Angeretti, N.; Chiesa, R.; Monzani, E.; Salmona, M.; Bugiani, O.; Tagliavini, F. Neurotoxicity of a prion protein fragment. Nature, 1993, 362, 543-546.
-
(1993)
Nature
, vol.362
, pp. 543-546
-
-
Forloni, G.1
Angeretti, N.2
Chiesa, R.3
Monzani, E.4
Salmona, M.5
Bugiani, O.6
Tagliavini, F.7
-
63
-
-
0033769044
-
A nonfibrillar form of the fusogenic prion protein fragment [118-135] induces apoptotic cell death in rat cortical neurons
-
Pillot, T.; Drouet, B.; Pincon-Raymond, M.; Vandekerckhove, J.; Rosseneu, M.; Chambaz, J. A nonfibrillar form of the fusogenic prion protein fragment [118-135] induces apoptotic cell death in rat cortical neurons. J. Neurochem., 2000, 75, 2298-2308.
-
(2000)
J. Neurochem
, vol.75
, pp. 2298-2308
-
-
Pillot, T.1
Drouet, B.2
Pincon-Raymond, M.3
Vandekerckhove, J.4
Rosseneu, M.5
Chambaz, J.6
-
64
-
-
63449119913
-
Properties and pathogenicity of prion-derived peptides
-
in press
-
Vassallo, N. Properties and pathogenicity of prion-derived peptides. Protein Pept. Lett., 2009, in press.
-
(2009)
Protein Pept. Lett
-
-
Vassallo, N.1
-
65
-
-
0026567814
-
Nearly ubiquitous tissue distribution of the scrapie agent precursor protein
-
Bendheim, P.E.; Brown, H.R.; Rudelli, R.D.; Scala, L.J.; Goller, N.L.; Wen, G.Y.; Kascsak, R.J.; Cashman, N.R.; Bolton, D.C. Nearly ubiquitous tissue distribution of the scrapie agent precursor protein. Neurology, 1992, 42, 149-156.
-
(1992)
Neurology
, vol.42
, pp. 149-156
-
-
Bendheim, P.E.1
Brown, H.R.2
Rudelli, R.D.3
Scala, L.J.4
Goller, N.L.5
Wen, G.Y.6
Kascsak, R.J.7
Cashman, N.R.8
Bolton, D.C.9
-
66
-
-
0034904789
-
Cellular prion protein status in sheep: Tissue-specific biochemical signatures
-
Moudjou, M.; Frobert, Y.; Grassi, J.; La Bonnardiere, C. Cellular prion protein status in sheep: tissue-specific biochemical signatures. J. Gen. Virol., 2001, 82, 2017-2024.
-
(2001)
J. Gen. Virol
, vol.82
, pp. 2017-2024
-
-
Moudjou, M.1
Frobert, Y.2
Grassi, J.3
La Bonnardiere, C.4
-
67
-
-
0031444294
-
The cellular prion protein binds copper in vivo
-
Brown, D.R.; Qin, K.; Herms, J.W.; Madlung, A.; Manson, J.; Strome, R.; Fraser, P.E.; Kruck, T.; von Bohlen, A.; Schulz-Schaeffer, W.; Giese, A.; Westaway, D.; Kretzschmar, H. The cellular prion protein binds copper in vivo. Nature, 1997, 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
-
68
-
-
0033515029
-
Copper binding to the prion protein: Structural implications of four identical cooperative binding sites
-
Viles, J.H.; Cohen, F.E.; Prusiner, S.B.; Goodin, D.B.; Wright, P.E.; Dyson, H.J. Copper binding to the prion protein: structural implications of four identical cooperative binding sites. Proc. Natl. Acad. Sci. U. S. A., 1999, 96, 2042-2047.
-
(1999)
Proc. Natl. Acad. Sci. U. S. A
, vol.96
, pp. 2042-2047
-
-
Viles, J.H.1
Cohen, F.E.2
Prusiner, S.B.3
Goodin, D.B.4
Wright, P.E.5
Dyson, H.J.6
-
69
-
-
0033571055
-
-
Brown, D.R.; Wong, B.S.: Hafiz, F.; Clive, C; Haswell, S.J.; Jones, I.M. Normal prion protein has an activity like that of superoxide dismutase. Biochem. J., 1999, 344, 1-5.
-
Brown, D.R.; Wong, B.S.: Hafiz, F.; Clive, C; Haswell, S.J.; Jones, I.M. Normal prion protein has an activity like that of superoxide dismutase. Biochem. J., 1999, 344, 1-5.
-
-
-
-
70
-
-
0042477520
-
Mapping the functional domain of the prion protein
-
Cui, T.; Daniels, M.; Wong, B.S.; Li, R.; Sy, M.S.; Sassoon, J.; Brown, D.R. Mapping the functional domain of the prion protein. Eur. J. Biochem., 2003, 270, 3368-3376.
-
(2003)
Eur. J. Biochem
, vol.270
, pp. 3368-3376
-
-
Cui, T.1
Daniels, M.2
Wong, B.S.3
Li, R.4
Sy, M.S.5
Sassoon, J.6
Brown, D.R.7
-
71
-
-
29144443530
-
Recombinant prion protein does not possess SOD-1 activity
-
Jones, S.; Batchelor, M.; Bhelt, D.; Clarke, A.R.; Collinge, J.; Jackson, G.S. Recombinant prion protein does not possess SOD-1 activity. Biochem. J., 2005, 392, 309-312.
-
(2005)
Biochem. J
, vol.392
, pp. 309-312
-
-
Jones, S.1
Batchelor, M.2
Bhelt, D.3
Clarke, A.R.4
Collinge, J.5
Jackson, G.S.6
-
72
-
-
38949201989
-
GPI-anchorless human prion protein is secreted and glycosylated but lacks superoxide dismutase activity
-
Sakudo, A.; Nakamura, I.; Tsuji, S.; Ikuta, K. GPI-anchorless human prion protein is secreted and glycosylated but lacks superoxide dismutase activity. Int. J. Mol. Med., 2008, 21, 217-222.
-
(2008)
Int. J. Mol. Med
, vol.21
, pp. 217-222
-
-
Sakudo, A.1
Nakamura, I.2
Tsuji, S.3
Ikuta, K.4
-
73
-
-
0042671502
-
Absence of superoxide dismutase activity in a soluble cellular iso-form of prion protein produced by baculovirus expression system
-
Sakudo, A.; Hamaishi, M.; Hosokawa-Kanai, T.; Tuchiya, K.; Nishimura, T.; Saeki, K.; Matsumoto, Y.: Ueda, S.; Onodera, T. Absence of superoxide dismutase activity in a soluble cellular iso-form of prion protein produced by baculovirus expression system. Biochem. Biophys. Res. Commun., 2003, 307, 678-683.
-
(2003)
Biochem. Biophys. Res. Commun
, vol.307
, pp. 678-683
-
-
Sakudo, A.1
Hamaishi, M.2
Hosokawa-Kanai, T.3
Tuchiya, K.4
Nishimura, T.5
Saeki, K.6
Matsumoto, Y.7
Ueda, S.8
Onodera, T.9
-
74
-
-
1642410070
-
Alpha- and beta- cleavages of the amino-terminus of the cellular prion protein
-
Mange, A.; Beranger, F.; Peoc'h, K.; Onodera, T.; Frobert, Y.; Lehmann, S. Alpha- and beta- cleavages of the amino-terminus of the cellular prion protein. Biol. Cell, 2004, 96, 125-132.
-
(2004)
Biol. Cell
, vol.96
, pp. 125-132
-
-
Mange, A.1
Beranger, F.2
Peoc'h, K.3
Onodera, T.4
Frobert, Y.5
Lehmann, S.6
-
75
-
-
0032488777
-
A transmembrane form of the prion protein in neurodegenerative disease
-
Hegde, R.S.; Mastrianni, J.A.; Scott, M.R.; DeFea, K.A.; Tremblay, P.; Torchia, M.; DeArmond, S.J.; Prusiner, S.B.; Lingappa, V.R. A transmembrane form of the prion protein in neurodegenerative disease. Science, 1998, 279, 827-834.
-
(1998)
Science
, vol.279
, pp. 827-834
-
-
Hegde, R.S.1
Mastrianni, J.A.2
Scott, M.R.3
DeFea, K.A.4
Tremblay, P.5
Torchia, M.6
DeArmond, S.J.7
Prusiner, S.B.8
Lingappa, V.R.9
-
76
-
-
18444397736
-
Stress-inducible protein 1 is a cell surface ligand for cellular prion that triggers neuroprotection
-
Zanata, S.M.; Lopes, M.H.; Mercadante, A.F.; Hajj, G.N.: Chiarini, L.B.: Nomizo, R.; Freitas, A.R.: Cabrai, A.L.: Lee, K.S.: Juliano, M.A.; de Oliveira, E.; Jachieri, S.G.; Burlingame, A.; Huang, L.; Linden, R.; Brentani, R.R.; Martins, V.R. Stress-inducible protein 1 is a cell surface ligand for cellular prion that triggers neuroprotection. EMBO J., 2002, 21, 3307-3316.
-
(2002)
EMBO J
, vol.21
, pp. 3307-3316
-
-
Zanata, S.M.1
Lopes, M.H.2
Mercadante, A.F.3
Hajj, G.N.4
Chiarini, L.B.5
Nomizo, R.6
Freitas, A.R.7
Cabrai, A.L.8
Lee, K.S.9
Juliano, M.A.10
de Oliveira, E.11
Jachieri, S.G.12
Burlingame, A.13
Huang, L.14
Linden, R.15
Brentani, R.R.16
Martins, V.R.17
-
77
-
-
0029997484
-
Role of microglia and host prion protein in neurotoxicity of a prion protein fragment
-
Brown, D.R.; Schmidt, B.; Kretzschmar, H.A. Role of microglia and host prion protein in neurotoxicity of a prion protein fragment. Nature, 1996, 380, 345-347.
-
(1996)
Nature
, vol.380
, pp. 345-347
-
-
Brown, D.R.1
Schmidt, B.2
Kretzschmar, H.A.3
-
78
-
-
33846027136
-
Neurotoxic prion protein (PrP) fragment 106-126 requires the N-terminal half of the hydrophobic region of PrP in the PrP-deficient neuronal cell line
-
Sakudo, A.; Nakamura, I.; Lee, D.C; Saeki, K.; Ikuta, K.; Onodera, T. Neurotoxic prion protein (PrP) fragment 106-126 requires the N-terminal half of the hydrophobic region of PrP in the PrP-deficient neuronal cell line. Protein Pept. Lett., 2007, 14, 1-6.
-
(2007)
Protein Pept. Lett
, vol.14
, pp. 1-6
-
-
Sakudo, A.1
Nakamura, I.2
Lee, D.C.3
Saeki, K.4
Ikuta, K.5
Onodera, T.6
-
79
-
-
0030469956
-
Neurotoxicity of beta-amyloid and prion peptides
-
Forloni, G. Neurotoxicity of beta-amyloid and prion peptides. Curr. Opin. Neurol., 1996, 9, 492-500.
-
(1996)
Curr. Opin. Neurol
, vol.9
, pp. 492-500
-
-
Forloni, G.1
-
80
-
-
0035066332
-
Alzheimer's disease: Genes, proteins, and therapy
-
Selkoe, D.J. Alzheimer's disease: genes, proteins, and therapy. Physiol. Rev., 2001, 81, 741-766.
-
(2001)
Physiol. Rev
, vol.81
, pp. 741-766
-
-
Selkoe, D.J.1
-
81
-
-
1442264828
-
Take five - BACE and the gamma-secretase quartet conduct Alzheimer's amyloid beta-peptide generation
-
Haass, C. Take five - BACE and the gamma-secretase quartet conduct Alzheimer's amyloid beta-peptide generation. EMBO J., 2004, 23, 483-488.
-
(2004)
EMBO J
, vol.23
, pp. 483-488
-
-
Haass, C.1
-
82
-
-
0242330374
-
ADAMs family members as amyloid precursor protein alpha-secretases
-
Allinson, T.M.; Parkin, E.T.; Turner, A.J.; Hooper, N.M. ADAMs family members as amyloid precursor protein alpha-secretases. J. Neurosci. Res., 2003, 74, 342-352.
-
(2003)
J. Neurosci. Res
, vol.74
, pp. 342-352
-
-
Allinson, T.M.1
Parkin, E.T.2
Turner, A.J.3
Hooper, N.M.4
-
83
-
-
0035851151
-
The disintegrins ADAM10 and TACE contribute to the constitutive and phorbol ester-regulated normal cleavage of the cellular prion protein
-
Vincent, B.; Paitel, E.; Saftig, P.; Frobert, Y.; Hartmann, D.; De Strooper, B.; Grassi, J.; Lopez-Perez, E.; Checler, F. The disintegrins ADAM10 and TACE contribute to the constitutive and phorbol ester-regulated normal cleavage of the cellular prion protein. J. Biol. Chem., 2001, 276, 37743-37746.
-
(2001)
J. Biol. Chem
, vol.276
, pp. 37743-37746
-
-
Vincent, B.1
Paitel, E.2
Saftig, P.3
Frobert, Y.4
Hartmann, D.5
De Strooper, B.6
Grassi, J.7
Lopez-Perez, E.8
Checler, F.9
-
84
-
-
28844433559
-
The disintegrin ADAM9 indirectly contributes to the physiological processing of cellular prion by modulating ADAM10 activity
-
Cisse, M.A.; Sunyach, C; Lefranc-Jullien, S.; Postina, R.; Vincent, B.; Checler, F. The disintegrin ADAM9 indirectly contributes to the physiological processing of cellular prion by modulating ADAM10 activity. J. Biol. Chem., 2005, 280, 40624-40631.
-
(2005)
J. Biol. Chem
, vol.280
, pp. 40624-40631
-
-
Cisse, M.A.1
Sunyach, C.2
Lefranc-Jullien, S.3
Postina, R.4
Vincent, B.5
Checler, F.6
-
85
-
-
42149140619
-
Regulation of betaAPP and PrPc cleavage by alphasecretase: Mechanistic and therapeutic perspectives
-
Vincent, B.: Cisse, M.A.: Sunyach, C.; Guillot-Sestier, M.V.; Checler, F. Regulation of betaAPP and PrPc cleavage by alphasecretase: mechanistic and therapeutic perspectives. Curr. Alzheimer Res., 2008, 5, 202-211.
-
(2008)
Curr. Alzheimer Res
, vol.5
, pp. 202-211
-
-
Vincent, B.1
Cisse, M.A.2
Sunyach, C.3
Guillot-Sestier, M.V.4
Checler, F.5
-
86
-
-
34547400403
-
Cellular prion protein regulates beta-secretase cleavage of the Alzheimer's amyloid precursor protein
-
Parkin, E.T.; Watt, N.T.; Hussain, I.; Eckman, E.A.; Eckman, C.B.; Manson, J.C.; Baybutt, H.N.; Turner, A.J.; Hooper, N.M. Cellular prion protein regulates beta-secretase cleavage of the Alzheimer's amyloid precursor protein. Proc. Natl. Acad. Sci. U. S. A., 2007, 104, 11062-11067.
-
(2007)
Proc. Natl. Acad. Sci. U. S. A
, vol.104
, pp. 11062-11067
-
-
Parkin, E.T.1
Watt, N.T.2
Hussain, I.3
Eckman, E.A.4
Eckman, C.B.5
Manson, J.C.6
Baybutt, H.N.7
Turner, A.J.8
Hooper, N.M.9
-
87
-
-
0031847332
-
Coexistence of Alzheimer-type neuropathology in Creutzfeldt-Jakob disease
-
Hainfellner, J.A.; Wanschitz, J.; Jellinger, K.; Liberski, P.P.; Gullotta, F.; Budka, H. Coexistence of Alzheimer-type neuropathology in Creutzfeldt-Jakob disease. Acta Neuropathol., 1998, 96, 116-122.
-
(1998)
Acta Neuropathol
, vol.96
, pp. 116-122
-
-
Hainfellner, J.A.1
Wanschitz, J.2
Jellinger, K.3
Liberski, P.P.4
Gullotta, F.5
Budka, H.6
-
88
-
-
0034963098
-
Marked increase of neuronal prion protein immunoreactivity in Alzheimer's disease and human prion diseases
-
Voigtlander, T.; Kloppel, S.; Birner, P.; Jarius, C.; Flicker, H.; Verghese-Nikolakaki, S.; Sklaviadis, T.; Guentchev, M.; Budka, H. Marked increase of neuronal prion protein immunoreactivity in Alzheimer's disease and human prion diseases. Acta Neuropathol., 2001, 101, 417-423.
-
(2001)
Acta Neuropathol
, vol.101
, pp. 417-423
-
-
Voigtlander, T.1
Kloppel, S.2
Birner, P.3
Jarius, C.4
Flicker, H.5
Verghese-Nikolakaki, S.6
Sklaviadis, T.7
Guentchev, M.8
Budka, H.9
-
89
-
-
33646472022
-
-
Del Bo, R.; Scarlato, M.; Ghezzi, S.; Martinelli-Boneschi, F.; Fenoglio, C; Galimberti, G.; Galbiati, S.; Virgilio, R.; Galimberti, D.; Ferrarese, C; Scarpini, E.; Bresolin, N.; Comi, G.P. Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis. Neurobiol. Aging, 2006, 27, 770.
-
Del Bo, R.; Scarlato, M.; Ghezzi, S.; Martinelli-Boneschi, F.; Fenoglio, C; Galimberti, G.; Galbiati, S.; Virgilio, R.; Galimberti, D.; Ferrarese, C; Scarpini, E.; Bresolin, N.; Comi, G.P. Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis. Neurobiol. Aging, 2006, 27, 770.
-
-
-
-
90
-
-
2542583141
-
Time-controlled transcardiac perfusion cross-linking for the study of protein interactions in complex tissues
-
Schmitt-Ulms, G.; Hansen, K.; Liu, J.; Cowdrey, C; Yang, J.; DeArmond, S.J.; Cohen, F.E.; Prusiner, S.B.; Baldwin, M.A. Time-controlled transcardiac perfusion cross-linking for the study of protein interactions in complex tissues. Nat. Biotechnol., 2004, 22, 724-731.
-
(2004)
Nat. Biotechnol
, vol.22
, pp. 724-731
-
-
Schmitt-Ulms, G.1
Hansen, K.2
Liu, J.3
Cowdrey, C.4
Yang, J.5
DeArmond, S.J.6
Cohen, F.E.7
Prusiner, S.B.8
Baldwin, M.A.9
-
91
-
-
35648990044
-
Role of lipid rafts in the processing of the pathogenic prion and Alzheimer's amyloid-beta proteins
-
Taylor, D.R.; Hooper, N.M. Role of lipid rafts in the processing of the pathogenic prion and Alzheimer's amyloid-beta proteins. Semin. Cell. Dev. Biol., 2007, 18, 638-648.
-
(2007)
Semin. Cell. Dev. Biol
, vol.18
, pp. 638-648
-
-
Taylor, D.R.1
Hooper, N.M.2
-
92
-
-
0035880007
-
Brain protein oxidation in age-related neurodegenerative disorders that are associated with aggregated proteins
-
Butterfield, D.A.; Kanski, J. Brain protein oxidation in age-related neurodegenerative disorders that are associated with aggregated proteins. Mech. Ageing Dev., 2001, 122, 945-962.
-
(2001)
Mech. Ageing Dev
, vol.122
, pp. 945-962
-
-
Butterfield, D.A.1
Kanski, J.2
-
93
-
-
9144257861
-
Prion protein suppresses perturbation of cellular copper homeostasis under oxidative conditions
-
Sakudo, A.; Lee, D.C.; Yoshimura, E.; Nagasaka, S.; Nitta, K.; Saeki, K.; Matsumoto, Y.; Lehmann, S.; Itohara, S.; Sakaguchi, S.; Onodera, T. Prion protein suppresses perturbation of cellular copper homeostasis under oxidative conditions. Biochem. Biophys. Res. Commun., 2004, 313, 850-855.
-
(2004)
Biochem. Biophys. Res. Commun
, vol.313
, pp. 850-855
-
-
Sakudo, A.1
Lee, D.C.2
Yoshimura, E.3
Nagasaka, S.4
Nitta, K.5
Saeki, K.6
Matsumoto, Y.7
Lehmann, S.8
Itohara, S.9
Sakaguchi, S.10
Onodera, T.11
-
94
-
-
0035961173
-
Neurodegeneration in the animal model of Menkes' disease involves Bcl-2-linked apoptosis
-
Rossi, L.; De Martino, A.; Marchese, E.; Piccirilli, S.; Rotilio, G.; Ciriolo, M.R. Neurodegeneration in the animal model of Menkes' disease involves Bcl-2-linked apoptosis. Neuroscience, 2001, 103, 181-188.
-
(2001)
Neuroscience
, vol.103
, pp. 181-188
-
-
Rossi, L.1
De Martino, A.2
Marchese, E.3
Piccirilli, S.4
Rotilio, G.5
Ciriolo, M.R.6
-
95
-
-
0042830827
-
Prolonged copper depletion induces expression of antioxidants and triggers apoptosis in SH-SY5Y neuroblastoma cells
-
Lombardo, M.F.; Ciriolo, M.R.; Rotilio, G.; Rossi, L. Prolonged copper depletion induces expression of antioxidants and triggers apoptosis in SH-SY5Y neuroblastoma cells. Cell. Mol. Life Sci., 2003, 60, 1733-1743.
-
(2003)
Cell. Mol. Life Sci
, vol.60
, pp. 1733-1743
-
-
Lombardo, M.F.1
Ciriolo, M.R.2
Rotilio, G.3
Rossi, L.4
-
96
-
-
33847065138
-
Copper imbalance and oxidative stress in neurodegeneration
-
Rossi, L.; Arciello, M.; Capo, C.; Rotilio, G. Copper imbalance and oxidative stress in neurodegeneration. Ital. J. Biochem., 2006, 55, 212-221.
-
(2006)
Ital. J. Biochem
, vol.55
, pp. 212-221
-
-
Rossi, L.1
Arciello, M.2
Capo, C.3
Rotilio, G.4
-
97
-
-
0031723519
-
Energy-dependent redox state of heme a + a3 and copper of cytochrome oxidase in perfused rat brain in situ
-
Matsunaga, A.; Nomura, Y.; Kuroda, S.; Tamura, M.; Nishihira, J.; Yoshimura, N. Energy-dependent redox state of heme a + a3 and copper of cytochrome oxidase in perfused rat brain in situ. Am. J. Physiol., 1998, 275, C1022-1030.
-
(1998)
Am. J. Physiol
, vol.275
-
-
Matsunaga, A.1
Nomura, Y.2
Kuroda, S.3
Tamura, M.4
Nishihira, J.5
Yoshimura, N.6
-
98
-
-
0035937654
-
Changes in cortical and hippocampal ectonucleotidase activities in mice lacking cellular prion protein
-
Pereira, G.S.; Walz, R.; Bonan, C.D.; Battastini, A.M.; Izquierdo, I.; Martins, V.R.; Brentani, R.R.; Sarkis, J.J. Changes in cortical and hippocampal ectonucleotidase activities in mice lacking cellular prion protein. Neurosci. Lett., 2001, 301, 72-14.
-
(2001)
Neurosci. Lett
, vol.301
, pp. 72-14
-
-
Pereira, G.S.1
Walz, R.2
Bonan, C.D.3
Battastini, A.M.4
Izquierdo, I.5
Martins, V.R.6
Brentani, R.R.7
Sarkis, J.J.8
-
99
-
-
0035145614
-
Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein
-
Wong, B.S.; Liu, T.; Li, R.; Pan, T.; Petersen, R.B.; Smith, M.A.; Gambetti, P.; Perry, G.; Manson, J.C.; Brown, D.R.; Sy, M.S. Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein. J. Neurochem., 2001, 76, 565-572.
-
(2001)
J. Neurochem
, vol.76
, pp. 565-572
-
-
Wong, B.S.1
Liu, T.2
Li, R.3
Pan, T.4
Petersen, R.B.5
Smith, M.A.6
Gambetti, P.7
Perry, G.8
Manson, J.C.9
Brown, D.R.10
Sy, M.S.11
-
100
-
-
41449101209
-
Normal cytochrome C oxidase activity in prion protein genedeficient mice
-
Sakudo, A.; Taniuchi, Y.; Kobayashi, T.; Onodera, T.; Ikuta, K. Normal cytochrome C oxidase activity in prion protein genedeficient mice. Protein Pept. Lett., 2008, 15, 250-254.
-
(2008)
Protein Pept. Lett
, vol.15
, pp. 250-254
-
-
Sakudo, A.1
Taniuchi, Y.2
Kobayashi, T.3
Onodera, T.4
Ikuta, K.5
-
101
-
-
0031710192
-
Mitochondrial dysfunction induced by oxidative stress in the brains of hamsters infected with the 263 K scrapie agent
-
Choi, S.I.; Ju, W.K.; Choi, E.K.; Kim, J.; Lea, H.Z.; Carp, R.I.; Wisniewski, H.M.; Kim, Y.S. Mitochondrial dysfunction induced by oxidative stress in the brains of hamsters infected with the 263 K scrapie agent. Acta Neuropathol., 1998, 96, 279-286.
-
(1998)
Acta Neuropathol
, vol.96
, pp. 279-286
-
-
Choi, S.I.1
Ju, W.K.2
Choi, E.K.3
Kim, J.4
Lea, H.Z.5
Carp, R.I.6
Wisniewski, H.M.7
Kim, Y.S.8
-
102
-
-
0033566067
-
Prions prevent neuronal cell-line death
-
Kuwahara, C; Takeuchi, A.M.; Nishimura, T.; Haraguchi, K.; Kubosaki, A.; Matsumoto, Y.; Saeki, K.; Yokoyama, T.; Itohara, S.; Onodera, T. Prions prevent neuronal cell-line death. Nature, 1999, 400, 225-226.
-
(1999)
Nature
, vol.400
, pp. 225-226
-
-
Kuwahara, C.1
Takeuchi, A.M.2
Nishimura, T.3
Haraguchi, K.4
Kubosaki, A.5
Matsumoto, Y.6
Saeki, K.7
Yokoyama, T.8
Itohara, S.9
Onodera, T.10
-
103
-
-
0041664024
-
Impairment of superoxide dismutase activation by N-terminally truncated prion protein (PrP) in PrP-deficient neuronal cell line
-
Sakudo, A.; Lee, D.C.; Saeki, K.; Nakamura, Y.; Inoue, K.; Matsumoto, Y.; Itohara, S.; Onodera, T. Impairment of superoxide dismutase activation by N-terminally truncated prion protein (PrP) in PrP-deficient neuronal cell line. Biochem. Biophys. Res. Commun., 2003, 308, 660-667.
-
(2003)
Biochem. Biophys. Res. Commun
, vol.308
, pp. 660-667
-
-
Sakudo, A.1
Lee, D.C.2
Saeki, K.3
Nakamura, Y.4
Inoue, K.5
Matsumoto, Y.6
Itohara, S.7
Onodera, T.8
-
104
-
-
34247364609
-
Serum withdrawal-induced apoptosis in ZrchI prion protein (PrP) gene-deficient neuronal cell line is suppressed by PrP, independent of Doppel
-
Nishimura, T.; Sakudo, A.; Hashiyama, Y.; Yachi, A.; Saeki, K.; Matsumoto, Y.; Ogawa, M.; Sakaguchi, S.; Itohara, S.; Onodera, T. Serum withdrawal-induced apoptosis in ZrchI prion protein (PrP) gene-deficient neuronal cell line is suppressed by PrP, independent of Doppel. Microbiol. Immunol., 2007, 51, 457-466.
-
(2007)
Microbiol. Immunol
, vol.51
, pp. 457-466
-
-
Nishimura, T.1
Sakudo, A.2
Hashiyama, Y.3
Yachi, A.4
Saeki, K.5
Matsumoto, Y.6
Ogawa, M.7
Sakaguchi, S.8
Itohara, S.9
Onodera, T.10
-
105
-
-
1942485480
-
The cellular prion protein (PrPC) prevents apoptotic neuronal cell death and mitochondrial dysfunction induced by serum deprivation
-
Kim, B.H.; Lee, H.G.; Choi, J.K.; Kim, J.I.; Choi, E.K.; Carp, R.I.; Kim, Y.S. The cellular prion protein (PrPC) prevents apoptotic neuronal cell death and mitochondrial dysfunction induced by serum deprivation. Brain Res. Mol. Brain Res., 2004, 124, 40-50.
-
(2004)
Brain Res. Mol. Brain Res
, vol.124
, pp. 40-50
-
-
Kim, B.H.1
Lee, H.G.2
Choi, J.K.3
Kim, J.I.4
Choi, E.K.5
Carp, R.I.6
Kim, Y.S.7
-
106
-
-
19344370943
-
Activation of phosphatidy-linositol 3-kinase by cellular prion protein and its role in cell survival
-
Vassallo, N.; Herms, J.; Behrens, C: Krebs, B.; Saeki, K.; Onodera, T.; Windl, O.; Kretzschmar, H.A. Activation of phosphatidy-linositol 3-kinase by cellular prion protein and its role in cell survival. Biochem. Biophys. Res. Commun., 2005, 332, 75-82.
-
(2005)
Biochem. Biophys. Res. Commun
, vol.332
, pp. 75-82
-
-
Vassallo, N.1
Herms, J.2
Behrens, C.3
Krebs, B.4
Saeki, K.5
Onodera, T.6
Windl, O.7
Kretzschmar, H.A.8
-
107
-
-
16444374116
-
A neuronal cell line that does not express either prion or doppel proteins
-
Kim, B.H.; Kim, J.I.; Choi, E.K.; Carp, R.I.; Kim, Y.S. A neuronal cell line that does not express either prion or doppel proteins. Neuroreport, 2005, 16, 425-429.
-
(2005)
Neuroreport
, vol.16
, pp. 425-429
-
-
Kim, B.H.1
Kim, J.I.2
Choi, E.K.3
Carp, R.I.4
Kim, Y.S.5
-
108
-
-
0032079515
-
Cultured skin fibroblasts isolated from mice devoid of the prion protein gene express major heat shock proteins in response to heat stress
-
Satoh, J.; Yukitake, M.; Kurohara, K.; Nishida, N.; Katamine, S.; Miyamoto, T.; Kuroda, Y. Cultured skin fibroblasts isolated from mice devoid of the prion protein gene express major heat shock proteins in response to heat stress. Exp. Neurol., 1998, 151, 105-115.
-
(1998)
Exp. Neurol
, vol.151
, pp. 105-115
-
-
Satoh, J.1
Yukitake, M.2
Kurohara, K.3
Nishida, N.4
Katamine, S.5
Miyamoto, T.6
Kuroda, Y.7
-
109
-
-
0033900833
-
Gene expression profile in prion protein-deficient fibroblasts in culture
-
Satoh, J.; Kuroda, Y.; Katamine, S. Gene expression profile in prion protein-deficient fibroblasts in culture. Am. J. Pathol., 2000, 157, 59-68.
-
(2000)
Am. J. Pathol
, vol.157
, pp. 59-68
-
-
Satoh, J.1
Kuroda, Y.2
Katamine, S.3
-
110
-
-
34547839621
-
Normal cellular prion protein protects against manganese-induced oxidative stress and apoptotic cell death
-
Choi, C.J.; Anantharam, V.; Saetveit, N.J.; Houk, R.S.; Kanthasamy, A.; Kanthasamy, A.G. Normal cellular prion protein protects against manganese-induced oxidative stress and apoptotic cell death. Toxicol. Sci., 2007, 98, 495-509.
-
(2007)
Toxicol. Sci
, vol.98
, pp. 495-509
-
-
Choi, C.J.1
Anantharam, V.2
Saetveit, N.J.3
Houk, R.S.4
Kanthasamy, A.5
Kanthasamy, A.G.6
-
111
-
-
0028962532
-
Prion protein gene variation among primates
-
Schatzl, H.M.; Da Costa, M.; Taylor, L.; Cohen, F.E.; Prusiner, S.B. Prion protein gene variation among primates. J. Mol. Biol., 1995, 245, 362-374.
-
(1995)
J. Mol. Biol
, vol.245
, pp. 362-374
-
-
Schatzl, H.M.1
Da Costa, M.2
Taylor, L.3
Cohen, F.E.4
Prusiner, S.B.5
-
112
-
-
0344326239
-
Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions ofthe prion protein
-
Wopfner, F.; Weidenhofer, G.; Schneider, R.; von Brunn, A.; Gilch, S.; Schwarz, T.F.; Werner, T.; Schatzl, H.M. Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions ofthe prion protein. J. Mol. Biol., 1999, 289, 1163-1178.
-
(1999)
J. Mol. Biol
, vol.289
, pp. 1163-1178
-
-
Wopfner, F.1
Weidenhofer, G.2
Schneider, R.3
von Brunn, A.4
Gilch, S.5
Schwarz, T.F.6
Werner, T.7
Schatzl, H.M.8
-
113
-
-
0033988236
-
Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein
-
Nishida, N.; Harris, D.A.; Vilette, D.; Laude, H.; Frobert, Y.; Grassi, J.; Casanova, D.; Milhavet, O.; Lehmann, S. Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein. J. Virol., 2000, 74, 320-325.
-
(2000)
J. Virol
, vol.74
, pp. 320-325
-
-
Nishida, N.1
Harris, D.A.2
Vilette, D.3
Laude, H.4
Frobert, Y.5
Grassi, J.6
Casanova, D.7
Milhavet, O.8
Lehmann, S.9
-
114
-
-
0021745705
-
In vitro replication of scrapie agent in a neuronal model: Infection of PC12 cells
-
Rubenstein, R.; Carp, R.I.; Callahan, S.M. In vitro replication of scrapie agent in a neuronal model: infection of PC12 cells. J. Gen. Virol., 1984, 65, 2191-2198.
-
(1984)
J. Gen. Virol
, vol.65
, pp. 2191-2198
-
-
Rubenstein, R.1
Carp, R.I.2
Callahan, S.M.3
-
115
-
-
35748956812
-
CpG and LPS can interfere negatively with prion clearance in macrophage and microglial cells
-
Gilch, S.; Schmitz, F.; Aguib, Y.; Kehler, C.; Bulow, S.; Bauer, S.; Kremmer, E.; Schatzl, H.M. CpG and LPS can interfere negatively with prion clearance in macrophage and microglial cells. FEBS J., 2007, 274, 5834-5844.
-
(2007)
FEBS J
, vol.274
, pp. 5834-5844
-
-
Gilch, S.1
Schmitz, F.2
Aguib, Y.3
Kehler, C.4
Bulow, S.5
Bauer, S.6
Kremmer, E.7
Schatzl, H.M.8
-
116
-
-
43049102451
-
CRBL cells: Establishment, characterization and susceptibility to prion infection
-
Mays, C.E.; Kang, H.E.; Kim, Y.; Shim, S.H.; Bang, J.E.; Woo, H.J.; Cho, Y.H.; Kim, J.B.; Ryou, C. CRBL cells: Establishment, characterization and susceptibility to prion infection. Brain Res., 2008, 1208, 170-180.
-
(2008)
Brain Res
, vol.1208
, pp. 170-180
-
-
Mays, C.E.1
Kang, H.E.2
Kim, Y.3
Shim, S.H.4
Bang, J.E.5
Woo, H.J.6
Cho, Y.H.7
Kim, J.B.8
Ryou, C.9
-
117
-
-
1142285202
-
Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents
-
Vorberg, I.; Raines, A.; Story, B.; Priola, S.A. Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents. J. Infect. Dis., 2004, 189, 431-439.
-
(2004)
J. Infect. Dis
, vol.189
, pp. 431-439
-
-
Vorberg, I.1
Raines, A.2
Story, B.3
Priola, S.A.4
-
118
-
-
0028967732
-
Proteinase-resistant protein in human neuroblastoma cells infected with brain material from Creutzfeldt-Jakob patient
-
Ladogana, A.; Liu, Q.: Xi, Y.G.: Pocchiari, M. Proteinase-resistant protein in human neuroblastoma cells infected with brain material from Creutzfeldt-Jakob patient. Lancet, 1995, 345, 594-595.
-
(1995)
Lancet
, vol.345
, pp. 594-595
-
-
Ladogana, A.1
Liu, Q.2
Xi, Y.G.3
Pocchiari, M.4
-
119
-
-
0023091197
-
Characterization of scrapie infection in mouse neuroblastoma cells
-
Race, R.E.; Fadness, L.H.: Chesebro, B. Characterization of scrapie infection in mouse neuroblastoma cells. J. Gen. Virol., 1987, 68, 1391-1399.
-
(1987)
J. Gen. Virol
, vol.68
, pp. 1391-1399
-
-
Race, R.E.1
Fadness, L.H.2
Chesebro, B.3
-
120
-
-
7444246851
-
Propagation of a protease-resistant form of prion protein in long-term cultured human glioblastoma cell line T98G
-
Kikuchi, Y.; Kakeya, T.; Sakai, A.; Takatori, K.; Nakamura, N.; Matsuda, H.; Yamazaki, T.; Tanamoto, K.; Sawada, J. Propagation of a protease-resistant form of prion protein in long-term cultured human glioblastoma cell line T98G. J. Gen. Virol., 2004, 85, 3449-3457.
-
(2004)
J. Gen. Virol
, vol.85
, pp. 3449-3457
-
-
Kikuchi, Y.1
Kakeya, T.2
Sakai, A.3
Takatori, K.4
Nakamura, N.5
Matsuda, H.6
Yamazaki, T.7
Tanamoto, K.8
Sawada, J.9
-
121
-
-
33846530529
-
Microglial cell line established from prion protein-overexpressing mice is susceptible to various murine prion strains
-
Iwamaru, Y.; Takenouchi, T.; Ogihara, K.; Hoshino, M.; Takata, M.; Imamura, M.; Tagawa, Y.; Hayashi-Kato, H.; Ushiki-Kaku, Y.; Shimizu, Y.; Okada, H,; Shinagawa, M.; Kitani, H,; Yokoyama, T, Microglial cell line established from prion protein-overexpressing mice is susceptible to various murine prion strains. J. Virol., 2007, 81, 1524-1527.
-
(2007)
J. Virol
, vol.81
, pp. 1524-1527
-
-
Iwamaru, Y.1
Takenouchi, T.2
Ogihara, K.3
Hoshino, M.4
Takata, M.5
Imamura, M.6
Tagawa, Y.7
Hayashi-Kato, H.8
Ushiki-Kaku, Y.9
Shimizu, Y.10
Okada, H.11
Shinagawa, M.12
Kitani, H.13
Yokoyama, T.14
-
122
-
-
0035957345
-
Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein
-
Vilette, D.; Andreoletti, O.; Archer, F.; Madelaine, M.F.; Vilotte, J.L.; Lehmann, S.; Laude, H. Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein. Proc. Natl. Acad. Sci. U. S. A., 2001, 98, 4055-4059.
-
(2001)
Proc. Natl. Acad. Sci. U. S. A
, vol.98
, pp. 4055-4059
-
-
Vilette, D.1
Andreoletti, O.2
Archer, F.3
Madelaine, M.F.4
Vilotte, J.L.5
Lehmann, S.6
Laude, H.7
-
123
-
-
0023785139
-
Analyses of frequency of infection, specific infectivity, and prion protein biosynthesis in scrapie-infected neuroblastoma cell clones
-
Race, R.E.; Caughey, B.; Graham, K.; Ernst, D.; Chesebro, B. Analyses of frequency of infection, specific infectivity, and prion protein biosynthesis in scrapie-infected neuroblastoma cell clones. J. Virol., 1988, 62, 2845-2849.
-
(1988)
J. Virol
, vol.62
, pp. 2845-2849
-
-
Race, R.E.1
Caughey, B.2
Graham, K.3
Ernst, D.4
Chesebro, B.5
-
124
-
-
26944462341
-
Aggravation of ischemic brain injury by prion protein deficiency: Role of ERK-1/-2 and STAT-1
-
Spudich, A.; Frigg, R.; Kilic, E.; Kilic, U.; Oesch, B.; Raeber, A.; Bassetti, C.L.; Hermann, D.M. Aggravation of ischemic brain injury by prion protein deficiency: role of ERK-1/-2 and STAT-1. Neurobiol. Dis., 2005, 20, 442-449.
-
(2005)
Neurobiol. Dis
, vol.20
, pp. 442-449
-
-
Spudich, A.1
Frigg, R.2
Kilic, E.3
Kilic, U.4
Oesch, B.5
Raeber, A.6
Bassetti, C.L.7
Hermann, D.M.8
-
125
-
-
0028876414
-
Neuron-specific expression of a hamster prion protein minigene in transgenic mice induces susceptibility to hamster scrapie agent
-
Race, R.E.; Priola, S.A.; Bessen, R.A.; Ernst, D.; Dockter, J.; Rall, G.F.; Mucke, L.: Chesebro, B.; Oldstone, M.B. Neuron-specific expression of a hamster prion protein minigene in transgenic mice induces susceptibility to hamster scrapie agent. Neuron, 1995, 15, 1183-1191.
-
(1995)
Neuron
, vol.15
, pp. 1183-1191
-
-
Race, R.E.1
Priola, S.A.2
Bessen, R.A.3
Ernst, D.4
Dockter, J.5
Rall, G.F.6
Mucke, L.7
Chesebro, B.8
Oldstone, M.B.9
-
126
-
-
0030684056
-
Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie
-
Raeber, A.J.: Race, R.E.; Brandner, S.: Priola, S.A.; Sailer, A.; Bessen, R.A.; Mucke, L.; Manson, J.; Aguzzi, A.; Oldstone, M.B.; Weissmann, C; Chesebro, B. Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie. EMBO J., 1997, 16, 6057-6065.
-
(1997)
EMBO J
, vol.16
, pp. 6057-6065
-
-
Raeber, A.J.1
Race, R.E.2
Brandner, S.3
Priola, S.A.4
Sailer, A.5
Bessen, R.A.6
Mucke, L.7
Manson, J.8
Aguzzi, A.9
Oldstone, M.B.10
Weissmann, C.11
Chesebro, B.12
-
127
-
-
0024820814
-
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
-
Scott, M.; Foster, D.; Mirenda, C; Serban, D.; Coufal, F.; Walchli, M.; Torchia, M.; Groth, D.; Carlson, G.; DeArmond, S.J.; West-away, D.; Prusiner, S.B. Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques. Cell, 1989, 59, 847-857.
-
(1989)
Cell
, vol.59
, pp. 847-857
-
-
Scott, M.1
Foster, D.2
Mirenda, C.3
Serban, D.4
Coufal, F.5
Walchli, M.6
Torchia, M.7
Groth, D.8
Carlson, G.9
DeArmond, S.J.10
West-away, D.11
Prusiner, S.B.12
-
128
-
-
0029740354
-
Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice
-
Telling, G.G.; Haga, T.; Torchia, M.; Tremblay, P.; DeArmond, S.J.; Prusiner, S.B. Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice. Genes Dev., 1996, 10, 1736-1750.
-
(1996)
Genes Dev
, vol.10
, pp. 1736-1750
-
-
Telling, G.G.1
Haga, T.2
Torchia, M.3
Tremblay, P.4
DeArmond, S.J.5
Prusiner, S.B.6
-
129
-
-
36048993416
-
Octapeptide repeat region of prion protein (PrP) is required at an early stage for production of abnormal prion protein in PrP-deficient neuronal cell line
-
Sakudo, A.; Wu, G.; Onodera, T.; Ikuta, K. Octapeptide repeat region of prion protein (PrP) is required at an early stage for production of abnormal prion protein in PrP-deficient neuronal cell line. Biochem. Biophys. Res. Commun., 2008, 365, 164-169.
-
(2008)
Biochem. Biophys. Res. Commun
, vol.365
, pp. 164-169
-
-
Sakudo, A.1
Wu, G.2
Onodera, T.3
Ikuta, K.4
-
130
-
-
0001552281
-
Expression of aminoterminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions
-
Shmerling, D.; Hegyi, I.; Fischer, M.; Blattler, T.; Brandner, S.; Gotz, J.; Rulicke, T.; Flechsig, E.; Cozzio, A.; von Mering, C.; Hangartner, C; Aguzzi, A.; Weissmann, C. Expression of aminoterminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions. Cell, 1998, 93, 203-214.
-
(1998)
Cell
, vol.93
, pp. 203-214
-
-
Shmerling, D.1
Hegyi, I.2
Fischer, M.3
Blattler, T.4
Brandner, S.5
Gotz, J.6
Rulicke, T.7
Flechsig, E.8
Cozzio, A.9
von Mering, C.10
Hangartner, C.11
Aguzzi, A.12
Weissmann, C.13
-
131
-
-
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. Identification of two prion protein regions that modify scrapie incubation time. J. Virol., 2001, 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
-
132
-
-
0033582935
-
Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice
-
Supattapone, S.; Bosque, P.; Muramoto, T.; Wille, H.; Aagaard, C; Peretz, D.; Nguyen, H.O.; Heinrich, C; Torchia, M.; Safar, J.; Cohen, F.E.; DeArmond, S.I.; Prusiner, S.B.; Scott, M. Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice. Cell, 1999, 96, 869-878.
-
(1999)
Cell
, vol.96
, pp. 869-878
-
-
Supattapone, S.1
Bosque, P.2
Muramoto, T.3
Wille, H.4
Aagaard, C.5
Peretz, D.6
Nguyen, H.O.7
Heinrich, C.8
Torchia, M.9
Safar, J.10
Cohen, F.E.11
DeArmond, S.I.12
Prusiner, S.B.13
Scott, M.14
-
133
-
-
0035929635
-
N-terminal truncation of prion protein affects both formation and conformation of abnormal protease-resistant prion protein generated in vitro
-
Lawson, V.A.; Priola, S.A.; Wehrly, K.; Chesebro, B. N-terminal truncation of prion protein affects both formation and conformation of abnormal protease-resistant prion protein generated in vitro. J. Biol. Chem., 2001, 276, 35265-35271.
-
(2001)
J. Biol. Chem
, vol.276
, pp. 35265-35271
-
-
Lawson, V.A.1
Priola, S.A.2
Wehrly, K.3
Chesebro, B.4
-
134
-
-
1842791529
-
Flexible N-terminal region of prion protein influences conformation of protease-resistant prion protein isoforms associated with cross-species scrapie infection in vivo and in vitro
-
Lawson, V.A.; Priola, S.A.; Meade-White, K.; Lawson, M.; Chesebro, B. Flexible N-terminal region of prion protein influences conformation of protease-resistant prion protein isoforms associated with cross-species scrapie infection in vivo and in vitro. J. Biol. Chem., 2004, 279, 13689-13695.
-
(2004)
J. Biol. Chem
, vol.279
, pp. 13689-13695
-
-
Lawson, V.A.1
Priola, S.A.2
Meade-White, K.3
Lawson, M.4
Chesebro, B.5
-
135
-
-
34547118602
-
Scrapie infection of prion protein-deficient cell line upon ectopic expression of mutant prion proteins
-
Maas, E.; Geissen, M.; Groschup, M.H.; Rost, R.; Onodera, T.; Schatzl, H.; Vorberg, I.M. Scrapie infection of prion protein-deficient cell line upon ectopic expression of mutant prion proteins. J. Biol. Chem., 2007, 282, 18702-18710.
-
(2007)
J. Biol. Chem
, vol.282
, pp. 18702-18710
-
-
Maas, E.1
Geissen, M.2
Groschup, M.H.3
Rost, R.4
Onodera, T.5
Schatzl, H.6
Vorberg, I.M.7
-
136
-
-
1442328250
-
Prions prevent brain damage after experimental brain injury: A preliminary report
-
Hoshino, S.; Inoue, K.; Yokoyama, T.; Kobayashi, S.; Asakura, T.; Teramoto, A.; Itohara, S. Prions prevent brain damage after experimental brain injury: a preliminary report. Acta Neurochir. Suppl., 2003, 86, 297-299.
-
(2003)
Acta Neurochir. Suppl
, vol.86
, pp. 297-299
-
-
Hoshino, S.1
Inoue, K.2
Yokoyama, T.3
Kobayashi, S.4
Asakura, T.5
Teramoto, A.6
Itohara, S.7
-
137
-
-
26944460813
-
Female-specific neuroprotection against transient brain ischemia observed in mice devoid of prion protein is abolished by ectopic expression of prion proteinlike protein
-
Sakurai-Yamashita, Y.; Sakaguchi, S.; Yoshikawa, D.; Okimura, N.; Masuda, Y.; Katamine, S.; Niwa, M. Female-specific neuroprotection against transient brain ischemia observed in mice devoid of prion protein is abolished by ectopic expression of prion proteinlike protein. Neuroscience, 2005, 136, 281-287.
-
(2005)
Neuroscience
, vol.136
, pp. 281-287
-
-
Sakurai-Yamashita, Y.1
Sakaguchi, S.2
Yoshikawa, D.3
Okimura, N.4
Masuda, Y.5
Katamine, S.6
Niwa, M.7
-
138
-
-
0032806450
-
Increased sensitivity to seizures in mice lacking cellular prion protein
-
Walz, R.; Amaral, O.B.; Rockenbach, I.C.: Roesler, R.: Izquierdo, I.; Cavalheiro, E.A.; Martins, V.R.; Brentani, R.R. Increased sensitivity to seizures in mice lacking cellular prion protein. Epilepsia, 1999, 40, 1679-1682.
-
(1999)
Epilepsia
, vol.40
, pp. 1679-1682
-
-
Walz, R.1
Amaral, O.B.2
Rockenbach, I.C.3
Roesler, R.4
Izquierdo, I.5
Cavalheiro, E.A.6
Martins, V.R.7
Brentani, R.R.8
-
139
-
-
0034675211
-
Transmission of BSE by blood transfusion in sheep
-
Houston, F.; Foster, J.D.; Chong, A.; Hunter, N.; Bostock, C.J. Transmission of BSE by blood transfusion in sheep. Lancet, 2000, 356, 999-1000.
-
(2000)
Lancet
, vol.356
, pp. 999-1000
-
-
Houston, F.1
Foster, J.D.2
Chong, A.3
Hunter, N.4
Bostock, C.J.5
-
140
-
-
19944415286
-
Infection route-independent accumulation of splenic abnormal prion protein
-
Inoue, Y.; Yamakawa, Y.: Sakudo, A.; Kinumi, T.; Nakamura, Y.; Matsumoto, Y.; Saeki, K.; Kamiyama, T.; Onodera, T.; Nishijima, M. Infection route-independent accumulation of splenic abnormal prion protein. Jpn. J. Infect. Dis., 2005, 58, 78-82.
-
(2005)
Jpn. J. Infect. Dis
, vol.58
, pp. 78-82
-
-
Inoue, Y.1
Yamakawa, Y.2
Sakudo, A.3
Kinumi, T.4
Nakamura, Y.5
Matsumoto, Y.6
Saeki, K.7
Kamiyama, T.8
Onodera, T.9
Nishijima, M.10
|