-
2
-
-
0035902194
-
Shattuck lecture-neurodegenerative diseases and prions
-
S.B. Prusiner Shattuck lecture-neurodegenerative diseases and prions N. Engl. J. Med. 344 2001 1516 1526
-
(2001)
N. Engl. J. Med.
, vol.344
, pp. 1516-1526
-
-
Prusiner, S.B.1
-
3
-
-
0033600407
-
Variant creutzfeldt-Jakob disease
-
J. Collinge Variant creutzfeldt-Jakob disease Lancet 354 1999 317 323
-
(1999)
Lancet
, vol.354
, pp. 317-323
-
-
Collinge, J.1
-
4
-
-
0347063992
-
Microtubules-associated intracellular localization of the NH(2)-terminal cellular prion protein fragment
-
N.S. Hachiya, K. Watanabe, Y. Sakasegawa, and K. Kaneko Microtubules-associated intracellular localization of the NH(2)-terminal cellular prion protein fragment Biochem. Biophys. Res. Commun. 313 2004 818 823
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.313
, pp. 818-823
-
-
Hachiya, N.S.1
Watanabe, K.2
Sakasegawa, Y.3
Kaneko, K.4
-
5
-
-
0033566067
-
Prions prevent neuronal cell-line death
-
C. Kuwahara, A.M. Takeuchi, T. Nishimura, K. Haraguchi, A. Kubosaki, Y. Matsumoto, K. Saeki, T. Yokoyama, S. Itohara, and T. Onodera Prions prevent neuronal cell-line death Nature 400 1999 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
-
6
-
-
1342302841
-
Anterograde and retrograde intracellular trafficking of fluorescent cellular prion protein
-
N.S. Hachiya, K. Watanabe, M. Yamada, Y. Sakasegawa, and K. Kaneko Anterograde and retrograde intracellular trafficking of fluorescent cellular prion protein Biochem. Biophys. Res. Commun. 315 2004 802 807
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.315
, pp. 802-807
-
-
Hachiya, N.S.1
Watanabe, K.2
Yamada, M.3
Sakasegawa, Y.4
Kaneko, K.5
-
7
-
-
0034790685
-
Internalization of mammalian fluorescent cellular prion protein and N-terminal deletion mutants in living cells
-
K.S. Lee, A.C. Magalhaes, S.M. Zanata, R.R. Brentani, V.R. Martins, and M.A. Prado Internalization of mammalian fluorescent cellular prion protein and N-terminal deletion mutants in living cells J. Neurochem. 79 2001 79 87
-
(2001)
J. Neurochem.
, vol.79
, pp. 79-87
-
-
Lee, K.S.1
Magalhaes, A.C.2
Zanata, S.M.3
Brentani, R.R.4
Martins, V.R.5
Prado, M.A.6
-
8
-
-
0037031821
-
Endocytic intermediates involved with the intracellular trafficking of a fluorescent cellular prion protein
-
A.C. Magalhaes, J.A. Silva, K.S. Lee, V.R. Martins, V.F. Prado, S.S.G. Ferguson, M.V. Gomez, R.R. Brentani, and M.A.M. Prado Endocytic intermediates involved with the intracellular trafficking of a fluorescent cellular prion protein J. Biol. Chem. 277 2002 33311 33318
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 33311-33318
-
-
Magalhaes, A.C.1
Silva, J.A.2
Lee, K.S.3
Martins, V.R.4
Prado, V.F.5
Ferguson, S.S.G.6
Gomez, M.V.7
Brentani, R.R.8
Prado, M.A.M.9
-
9
-
-
0035069622
-
The metabolism and imaging in live cells of the bovine prion protein in its native form or carrying single amino acid substitutions
-
A. Negro, C. Ballarin, A. Bertoli, M.L. Massimino, and M.C. Sorgato The metabolism and imaging in live cells of the bovine prion protein in its native form or carrying single amino acid substitutions Mol. Cell. Neurosci. 17 2001 521 538
-
(2001)
Mol. Cell. Neurosci.
, vol.17
, pp. 521-538
-
-
Negro, A.1
Ballarin, C.2
Bertoli, A.3
Massimino, M.L.4
Sorgato, M.C.5
-
10
-
-
0037041014
-
Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases
-
H. Lorenz, O. Windl, and H.A. Kretzschmar Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases J. Biol. Chem. 277 2002 8508 8516
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 8508-8516
-
-
Lorenz, H.1
Windl, O.2
Kretzschmar, H.A.3
-
11
-
-
0035834680
-
Mutant prion proteins are partially retained in the endoplasmic reticulum
-
L. Ivanova, S. Barmada, T. Kummer, and D.A. Harris Mutant prion proteins are partially retained in the endoplasmic reticulum J. Biol. Chem. 276 2001 42409 42421
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 42409-42421
-
-
Ivanova, L.1
Barmada, S.2
Kummer, T.3
Harris, D.A.4
-
12
-
-
0027236933
-
An amber mutation of prion protein in Gerstmann-Straussler syndrome with mutant PrP plaques
-
T. Kitamoto, R. Iizuka, and J. Tateishi An amber mutation of prion protein in Gerstmann-Straussler syndrome with mutant PrP plaques Biochem. Biophys. Res. Commun. 192 1993 525 531
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.192
, pp. 525-531
-
-
Kitamoto, T.1
Iizuka, R.2
Tateishi, J.3
-
13
-
-
0033551776
-
Proteasomal degradation and N-terminal protease resistance of the codon 145 mutant prion protein
-
G. Zanusso, R.B. Petersen, T. Jin, Y. Jing, R. Kanoush, S. Ferrari, P. Gambetti, and N. Singh Proteasomal degradation and N-terminal protease resistance of the codon 145 mutant prion protein J. Biol. Chem. 274 1999 23396 23404
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 23396-23404
-
-
Zanusso, G.1
Petersen, R.B.2
Jin, T.3
Jing, Y.4
Kanoush, R.5
Ferrari, S.6
Gambetti, P.7
Singh, N.8
-
14
-
-
0027086835
-
Chimeric prion protein expression in cultured cells and transgenic mice
-
M.R. Scott, R. Kohler, D. Foster, and S.B. Prusiner Chimeric prion protein expression in cultured cells and transgenic mice Protein Sci. 1 1992 986 997
-
(1992)
Protein Sci.
, vol.1
, pp. 986-997
-
-
Scott, M.R.1
Kohler, R.2
Foster, D.3
Prusiner, S.B.4
-
15
-
-
19944428175
-
Mitochondrial localization of cellular prion protein (PrPC) invokes neuronal apoptosis in aged transgenic mice overexpressing PrPC
-
in press
-
N.S. Hachiya, M. Yamada, K. Watanabe, A. Jozuka, T. Ohkubo, K. Sano, Y. Takeuchi, Y. Kozuka, Y. Sakasegawa, K. Kaneko, Mitochondrial localization of cellular prion protein (PrPC) invokes neuronal apoptosis in aged transgenic mice overexpressing PrPC, Neurosci. Lett., in press
-
Neurosci. Lett.
-
-
Hachiya, N.S.1
Yamada, M.2
Watanabe, K.3
Jozuka, A.4
Ohkubo, T.5
Sano, K.6
Takeuchi, Y.7
Kozuka, Y.8
Sakasegawa, Y.9
Kaneko, K.10
-
16
-
-
0023928927
-
Scrapie-infected murine neuroblastoma cells produce protease-resistant prion proteins
-
D.A. Butler, M.A. Scott, J.M. Bockman, D.R. Borchelt, A. Taraboulos, K.K. Hsiao, D.T. Kingsbury, and S.B. Prusiner Scrapie-infected murine neuroblastoma cells produce protease-resistant prion proteins J. Virol. 62 1988 1558 1564
-
(1988)
J. Virol.
, vol.62
, pp. 1558-1564
-
-
Butler, D.A.1
Scott, M.A.2
Bockman, J.M.3
Borchelt, D.R.4
Taraboulos, A.5
Hsiao, K.K.6
Kingsbury, D.T.7
Prusiner, S.B.8
-
17
-
-
0028878943
-
Inherited prion diseases and transmission to rodents
-
J. Tateishi, and T. Kitamoto Inherited prion diseases and transmission to rodents Brain Pathol. 5 1995 53 59
-
(1995)
Brain Pathol.
, vol.5
, pp. 53-59
-
-
Tateishi, J.1
Kitamoto, T.2
-
18
-
-
0037195647
-
Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol
-
J. Ma, R. Wollmann, and S. Lindquist Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol Science 298 2002 1781 1785
-
(2002)
Science
, vol.298
, pp. 1781-1785
-
-
Ma, J.1
Wollmann, R.2
Lindquist, S.3
-
19
-
-
0037415754
-
Scrapie-like prion protein accumulates in aggresomes of cyclosporin A-treated cells
-
E. Cohen, and A. Taraboulos Scrapie-like prion protein accumulates in aggresomes of cyclosporin A-treated cells EMBO J. 22 2003 404 417
-
(2003)
EMBO J.
, vol.22
, pp. 404-417
-
-
Cohen, E.1
Taraboulos, A.2
-
20
-
-
0036882127
-
Overexpression of PrPc triggers caspase 3 activation: Potentiation by proteasome inhibitors and blockade by anti-PrP antibodies
-
E. Paitel, C. Alves da Costa, D. Vilette, J. Grassi, and F. Checler Overexpression of PrPc triggers caspase 3 activation: potentiation by proteasome inhibitors and blockade by anti-PrP antibodies J. Neurochem. 83 2002 1208 1214
-
(2002)
J. Neurochem.
, vol.83
, pp. 1208-1214
-
-
Paitel, E.1
Alves Da Costa, C.2
Vilette, D.3
Grassi, J.4
Checler, F.5
-
21
-
-
0028052363
-
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
-
D. Westaway, J. Cayetano-Canlas, D. Groth, D. Foster, S.-L. Yang, M. Torchia, G.A. Carlson, and S.B. Prusiner Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins Cell 76 1994 117 129
-
(1994)
Cell
, vol.76
, pp. 117-129
-
-
Westaway, D.1
Cayetano-Canlas, J.2
Groth, D.3
Foster, D.4
Yang, S.-L.5
Torchia, M.6
Carlson, G.A.7
Prusiner, S.B.8
-
22
-
-
0036791019
-
Dominant-negative inhibition of prion replication in transgenic mice
-
V. Perrier, K. Kaneko, J. Safar, J. Vergara, P. Tremblay, S.J. DeArmond, F.E. Cohen, S.B. Prusiner, and A.C. Wallace Dominant-negative inhibition of prion replication in transgenic mice Proc. Natl. Acad. Sci. USA 99 2002 13079 13084
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 13079-13084
-
-
Perrier, V.1
Kaneko, K.2
Safar, J.3
Vergara, J.4
Tremblay, P.5
Dearmond, S.J.6
Cohen, F.E.7
Prusiner, S.B.8
Wallace, A.C.9
-
23
-
-
0026326210
-
Ultrastructural localization of scrapie prion proteins in cytoplasmic vesicles of infected cultured cells
-
M.P. McKinley, A. Taraboulos, L. Kenaga, D. Serban, A. Stieber, S.J. DeArmond, S.B. Prusiner, and N. Gonatas Ultrastructural localization of scrapie prion proteins in cytoplasmic vesicles of infected cultured cells Lab. Invest. 65 1991 622 630
-
(1991)
Lab. Invest.
, vol.65
, pp. 622-630
-
-
McKinley, M.P.1
Taraboulos, A.2
Kenaga, L.3
Serban, D.4
Stieber, A.5
Dearmond, S.J.6
Prusiner, S.B.7
Gonatas, N.8
-
24
-
-
0028867086
-
Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform
-
K. Kaneko, D. Peretz, K.M. Pan, T.C. Blochberger, H. Wille, R. Gabizon, O.H. Griffith, F.E. Cohen, M.A. Baldwin, and S.B. Prusiner Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform Proc. Natl. Acad. Sci. USA 92 1995 11160 11164
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 11160-11164
-
-
Kaneko, K.1
Peretz, D.2
Pan, K.M.3
Blochberger, T.C.4
Wille, H.5
Gabizon, R.6
Griffith, O.H.7
Cohen, F.E.8
Baldwin, M.A.9
Prusiner, S.B.10
-
25
-
-
0031586212
-
Molecular properties of complexes formed between the prion protein and synthetic peptides
-
K. Kaneko, H. Wille, I. Mehlhorn, H. Zhang, H. Ball, F.E. Cohen, M.A. Baldwin, and S.B. Prusiner Molecular properties of complexes formed between the prion protein and synthetic peptides J. Mol. Biol. 270 1997 574 586
-
(1997)
J. Mol. Biol.
, vol.270
, pp. 574-586
-
-
Kaneko, K.1
Wille, H.2
Mehlhorn, I.3
Zhang, H.4
Ball, H.5
Cohen, F.E.6
Baldwin, M.A.7
Prusiner, S.B.8
-
26
-
-
0142091396
-
Nucleation-dependent conformational conversion of the Y145Stop variant of human prion protein: Structural clues for prion propagation
-
B. Kundu, N.R. Maiti, E.M. Jones, K.A. Surewicz, D.L. Vanik, and W.K. Surewicz Nucleation-dependent conformational conversion of the Y145Stop variant of human prion protein: structural clues for prion propagation Proc. Natl. Acad. Sci. USA 100 2003 12069 12074
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 12069-12074
-
-
Kundu, B.1
Maiti, N.R.2
Jones, E.M.3
Surewicz, K.A.4
Vanik, D.L.5
Surewicz, W.K.6
-
27
-
-
0038128629
-
Molecular distinction between pathogenic and infectious properties of the prion protein
-
R. Chiesa, P. Piccardo, E. Quaglio, B. Drisaldi, S.L. Si-Hoe, M. Takao, B. Ghetti, and D.A. Harris Molecular distinction between pathogenic and infectious properties of the prion protein J. Virol. 77 2003 7611 7622
-
(2003)
J. Virol.
, vol.77
, pp. 7611-7622
-
-
Chiesa, R.1
Piccardo, P.2
Quaglio, E.3
Drisaldi, B.4
Si-Hoe, S.L.5
Takao, M.6
Ghetti, B.7
Harris, D.A.8
|