-
1
-
-
0842281643
-
Mammalian prion biology: One century of evolving concepts
-
Aguzzi A, Polymenidou M (2004) Mammalian prion biology: one century of evolving concepts. Cell 116:313-327.
-
(2004)
Cell
, vol.116
, pp. 313-327
-
-
Aguzzi, A.1
Polymenidou, M.2
-
2
-
-
14044278145
-
Proteolysis of non-phosphorylated and phosphorylated tau by thrombin
-
Arai T, Guo JP, McGeer PL (2005) Proteolysis of non-phosphorylated and phosphorylated tau by thrombin. J Biol Chem 280:5145-5153.
-
(2005)
J Biol Chem
, vol.280
, pp. 5145-5153
-
-
Arai, T.1
Guo, J.P.2
McGeer, P.L.3
-
3
-
-
34547638271
-
Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein
-
Atarashi R, Moore RA, Sim VL, Hughson AG, Dorward DW, Onwubiko HA, Priola SA, Caughey B (2007) Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein. Nat Methods 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
-
4
-
-
0028997297
-
Non-genetic propagation of strain-specific properties of scrapie prion protein
-
Bessen RA, Kocisko DA, Raymond GJ, Nandan S, Lansbury PT, Caughey B (1995) Non-genetic propagation of strain-specific properties of scrapie prion protein. Nature 375:698-700.
-
(1995)
Nature
, vol.375
, pp. 698-700
-
-
Bessen, R.A.1
Kocisko, D.A.2
Raymond, G.J.3
Nandan, S.4
Lansbury, P.T.5
Caughey, B.6
-
5
-
-
33644858238
-
Annealing prion protein amyloid fibrils at high temperature results in extension of a proteinase K-resistant core
-
Bocharova OV, Makarava N, Breydo L, Anderson M, Salnikov VV, Baskakov IV (2006) Annealing prion protein amyloid fibrils at high temperature results in extension of a proteinase K-resistant core. J Biol Chem 281:2373-2379.
-
(2006)
J Biol Chem
, vol.281
, pp. 2373-2379
-
-
Bocharova, O.V.1
Makarava, N.2
Breydo, L.3
Anderson, M.4
Salnikov, V.V.5
Baskakov, I.V.6
-
6
-
-
0035914410
-
Prion protein protects human neurons against Bax-mediated apoptosis
-
Bounhar Y, Zhang Y, Goodyer CG, LeBlanc A (2001) Prion protein protects human neurons against Bax-mediated apoptosis. J Biol Chem 276:39145-39149.
-
(2001)
J Biol Chem
, vol.276
, pp. 39145-39149
-
-
Bounhar, Y.1
Zhang, Y.2
Goodyer, C.G.3
LeBlanc, A.4
-
7
-
-
28244486826
-
Methionine oxidation interferes with conversion of the prion protein into the fibrillar proteinase K-resistant conformation
-
Breydo L, Bocharova OV, Makarava N, Salnikov VV, Anderson M, Baskakov IV (2005) Methionine oxidation interferes with conversion of the prion protein into the fibrillar proteinase K-resistant conformation. Biochemistry 44:15534-15543.
-
(2005)
Biochemistry
, vol.44
, pp. 15534-15543
-
-
Breydo, L.1
Bocharova, O.V.2
Makarava, N.3
Salnikov, V.V.4
Anderson, M.5
Baskakov, I.V.6
-
8
-
-
0027733637
-
Scrapie associated PrP accumulation and its prevention: Insights from cell culture
-
Caughey B (1993) Scrapie associated PrP accumulation and its prevention: insights from cell culture. Br Med Bull 49:860-872.
-
(1993)
Br Med Bull
, vol.49
, pp. 860-872
-
-
Caughey, B.1
-
9
-
-
0032427904
-
Neurological illness in transgenic mice expressing a prion protein with an insertional mutation
-
Chiesa R, Piccardo P, Ghetti B, Harris DA (1998) Neurological illness in transgenic mice expressing a prion protein with an insertional mutation. Neuron 21:1339-1351.
-
(1998)
Neuron
, vol.21
, pp. 1339-1351
-
-
Chiesa, R.1
Piccardo, P.2
Ghetti, B.3
Harris, D.A.4
-
10
-
-
0142184333
-
RNA molecules stimulate prion protein conversion
-
Deleault NR, Lucassen RW, Supattapone S (2003) RNA molecules stimulate prion protein conversion. Nature 425:717-720.
-
(2003)
Nature
, vol.425
, pp. 717-720
-
-
Deleault, N.R.1
Lucassen, R.W.2
Supattapone, S.3
-
11
-
-
22844438894
-
Protease-resistant prion protein amplification reconstituted with partially purified substrates and synthetic polyanions
-
Deleault NR, Geoghegan JC, Nishina K, Kascsak R, Williamson RA, Supattapone S (2005) Protease-resistant prion protein amplification reconstituted with partially purified substrates and synthetic polyanions. J Biol Chem 280:26873-26879.
-
(2005)
J Biol Chem
, vol.280
, pp. 26873-26879
-
-
Deleault, N.R.1
Geoghegan, J.C.2
Nishina, K.3
Kascsak, R.4
Williamson, R.A.5
Supattapone, S.6
-
13
-
-
0031456947
-
Structure of the recombinant full-length hamster prion protein PrP(29-231): The N terminus is highly flexible
-
Donne DG, Viles JH, Groth D, Mehlhorn I, James TL, Cohen FE, Prusiner SB, Wright PE, Dyson HJ (1997) Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible. Proc Natl Acad Sci U S A 94:13452-13457.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 13452-13457
-
-
Donne, D.G.1
Viles, J.H.2
Groth, D.3
Mehlhorn, I.4
James, T.L.5
Cohen, F.E.6
Prusiner, S.B.7
Wright, P.E.8
Dyson, H.J.9
-
14
-
-
0036174010
-
alpha-Synuclein is phosphorylated in synucleinopathy lesions
-
Fujiwara H, Hasegawa M, Dohmae N, Kawashima A, Masliah E, Goldberg MS, Shen J, Takio K, Iwatsubo T (2002) alpha-Synuclein is phosphorylated in synucleinopathy lesions. Nat Cell Biol 4:160-164.
-
(2002)
Nat Cell Biol
, vol.4
, pp. 160-164
-
-
Fujiwara, H.1
Hasegawa, M.2
Dohmae, N.3
Kawashima, A.4
Masliah, E.5
Goldberg, M.S.6
Shen, J.7
Takio, K.8
Iwatsubo, T.9
-
15
-
-
37549068149
-
Selective incorporation of polyanionic molecules into hamster prions
-
Geoghegan JC, Valdes PA, Orem NR, Deleault NR, Williamson RA, Harris BT, Supattapone S (2007) Selective incorporation of polyanionic molecules into hamster prions. J Biol Chem 282:36341-36353.
-
(2007)
J Biol Chem
, vol.282
, pp. 36341-36353
-
-
Geoghegan, J.C.1
Valdes, P.A.2
Orem, N.R.3
Deleault, N.R.4
Williamson, R.A.5
Harris, B.T.6
Supattapone, S.7
-
16
-
-
0037705352
-
Polyclonal anti-PrP auto-antibodies induced with dimeric PrP interfere efficiently with PrPSc propagation in prion-infected cells
-
Gilch S, Wopfner F, Renner-Müller I, Kremmer E, Bauer C, Wolf E, Brem G, Groschup MH, Schätzl HM (2003) Polyclonal anti-PrP auto-antibodies induced with dimeric PrP interfere efficiently with PrPSc propagation in prion-infected cells. J Biol Chem 278:18524-18531.
-
(2003)
J Biol Chem
, vol.278
, pp. 18524-18531
-
-
Gilch, S.1
Wopfner, F.2
Renner-Müller, I.3
Kremmer, E.4
Bauer, C.5
Wolf, E.6
Brem, G.7
Groschup, M.H.8
Schätzl, H.M.9
-
17
-
-
8844254727
-
Loss of glycosylation associated with the T183A mutation in human prion disease
-
Grasbon-Frodl E, Lorenz H, Mann U, Nitsch RM, Windl O, Kretzschmar HA (2004) Loss of glycosylation associated with the T183A mutation in human prion disease. Acta Neuropathol 108:476-484.
-
(2004)
Acta Neuropathol
, vol.108
, pp. 476-484
-
-
Grasbon-Frodl, E.1
Lorenz, H.2
Mann, U.3
Nitsch, R.M.4
Windl, O.5
Kretzschmar, H.A.6
-
18
-
-
0025681138
-
Spontaneous neurodegeneration in transgenic mice with mutant prion protein
-
Hsiao KK, Scott M, Foster D, Groth DF, DeArmond SJ, Prusiner SB (1990) Spontaneous neurodegeneration in transgenic mice with mutant prion protein. Science 250:1587-1590.
-
(1990)
Science
, vol.250
, pp. 1587-1590
-
-
Hsiao, K.K.1
Scott, M.2
Foster, D.3
Groth, D.F.4
DeArmond, S.J.5
Prusiner, S.B.6
-
19
-
-
0033583190
-
Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations
-
Jackson GS, Hosszu LL, Power A, Hill AF, Kenney J, Saibil H, Craven CJ, Waltho JP, Clarke AR, Collinge J (1999) Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations. Science 283:1935-1937.
-
(1999)
Science
, vol.283
, pp. 1935-1937
-
-
Jackson, G.S.1
Hosszu, L.L.2
Power, A.3
Hill, A.F.4
Kenney, J.5
Saibil, H.6
Craven, C.J.7
Waltho, J.P.8
Clarke, A.R.9
Collinge, J.10
-
20
-
-
34248351522
-
Defective retrotranslocation causes loss of anti-Bax function in human familial prion protein mutants
-
Jodoin J, Laroche-Pierre S, Goodyer CG, LeBlanc AC (2007) Defective retrotranslocation causes loss of anti-Bax function in human familial prion protein mutants. J Neurosci 27:5081-5091.
-
(2007)
J Neurosci
, vol.27
, pp. 5081-5091
-
-
Jodoin, J.1
Laroche-Pierre, S.2
Goodyer, C.G.3
LeBlanc, A.C.4
-
21
-
-
0023499868
-
Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins
-
Kascsak RJ, Rubenstein R, Merz PA, Tonna-DeMasi M, Fersko R, Carp RI, Wisniewski HM, Diringer H (1987) Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins. J Virol 61:3688-3693.
-
(1987)
J Virol
, vol.61
, pp. 3688-3693
-
-
Kascsak, R.J.1
Rubenstein, R.2
Merz, P.A.3
Tonna-DeMasi, M.4
Fersko, R.5
Carp, R.I.6
Wisniewski, H.M.7
Diringer, H.8
-
22
-
-
0027956109
-
Cell-free formation of protease-resistant prion protein
-
Kocisko DA, Come JH, Priola SA, Chesebro B, Raymond GJ, Lansbury PT, Caughey B (1994) Cell-free formation of protease-resistant prion protein. Nature 370:471-474.
-
(1994)
Nature
, vol.370
, pp. 471-474
-
-
Kocisko, D.A.1
Come, J.H.2
Priola, S.A.3
Chesebro, B.4
Raymond, G.J.5
Lansbury, P.T.6
Caughey, B.7
-
23
-
-
3442889359
-
Synthetic mammalian prions
-
Legname G, Baskakov IV, Nguyen HO, Riesner D, Cohen FE, DeArmond SJ, Prusiner SB (2004) Synthetic mammalian prions. Science 305:673-676.
-
(2004)
Science
, vol.305
, pp. 673-676
-
-
Legname, G.1
Baskakov, I.V.2
Nguyen, H.O.3
Riesner, D.4
Cohen, F.E.5
DeArmond, S.J.6
Prusiner, S.B.7
-
24
-
-
34250312098
-
Phosphorylation of protein phosphatase 1 by cyclin-dependent protein kinase 5 during nerve growth factor-induced PC12 cell differentiation
-
Li T, Chalifour LE, Paudel HK (2007) Phosphorylation of protein phosphatase 1 by cyclin-dependent protein kinase 5 during nerve growth factor-induced PC12 cell differentiation. J Biol Chem 282:6619-6628.
-
(2007)
J Biol Chem
, vol.282
, pp. 6619-6628
-
-
Li, T.1
Chalifour, L.E.2
Paudel, H.K.3
-
25
-
-
0026597280
-
Phosphorylation by cAMP-dependent protein kinase inhibits the degradation of tau by calpain
-
Litersky JM, Johnson GV (1992) Phosphorylation by cAMP-dependent protein kinase inhibits the degradation of tau by calpain. J Biol Chem 267:1563-1568.
-
(1992)
J Biol Chem
, vol.267
, pp. 1563-1568
-
-
Litersky, J.M.1
Johnson, G.V.2
-
26
-
-
33644958800
-
Amyloid formation by recombinant full-length prion proteins in phospholipid bicelle solutions
-
Lührs T, Zahn R, Wüthrich K (2006) Amyloid formation by recombinant full-length prion proteins in phospholipid bicelle solutions. J Mol Biol 357:833-841.
-
(2006)
J Mol Biol
, vol.357
, pp. 833-841
-
-
Lührs, T.1
Zahn, R.2
Wüthrich, K.3
-
27
-
-
0037195617
-
Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol
-
Ma J, Lindquist S (2002) Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol. Science 298:1785-1788.
-
(2002)
Science
, vol.298
, pp. 1785-1788
-
-
Ma, J.1
Lindquist, S.2
-
28
-
-
0037195647
-
Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol
-
Ma J, Wollmann R, Lindquist S (2002) Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol. Science 298:1781-1785.
-
(2002)
Science
, vol.298
, pp. 1781-1785
-
-
Ma, J.1
Wollmann, R.2
Lindquist, S.3
-
29
-
-
0035956518
-
Inherited prion disease caused by the V210I mutation: Transmission to transgenic mice
-
Mastrianni JA, Capellari S, Telling GC, Han D, Bosque P, Prusiner SB, DeArmond SJ (2001) Inherited prion disease caused by the V210I mutation: transmission to transgenic mice. Neurology 57:2198-2205.
-
(2001)
Neurology
, vol.57
, pp. 2198-2205
-
-
Mastrianni, J.A.1
Capellari, S.2
Telling, G.C.3
Han, D.4
Bosque, P.5
Prusiner, S.B.6
DeArmond, S.J.7
-
30
-
-
0028351904
-
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Different prion proteins determined by a DNA polymorphism
-
Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B, et al (1994) Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Proc Natl Acad Sci U S A 91:2839-2842.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 2839-2842
-
-
Monari, L.1
Chen, S.G.2
Brown, P.3
Parchi, P.4
Petersen, R.B.5
Mikol, J.6
Gray, F.7
Cortelli, P.8
Montagna, P.9
Ghetti, B.10
-
31
-
-
0026069414
-
Protease sensitivity and nuclease resistance of the scrapie agent propagated in vitro in neuroblastoma cells
-
Neary K, Caughey B, Ernst D, Race RE, Chesebro B (1991) Protease sensitivity and nuclease resistance of the scrapie agent propagated in vitro in neuroblastoma cells. J Virol 65:1031-1034.
-
(1991)
J Virol
, vol.65
, pp. 1031-1034
-
-
Neary, K.1
Caughey, B.2
Ernst, D.3
Race, R.E.4
Chesebro, B.5
-
32
-
-
0034630734
-
Susceptibility of the prion protein to enzymic phosphorylation
-
Negro A, Meggio F, Bertoli A, Battistutta R, Sorgato MC, Pinna LA (2000) Susceptibility of the prion protein to enzymic phosphorylation. Biochem Biophys Res Commun 271:337-341.
-
(2000)
Biochem Biophys Res Commun
, vol.271
, pp. 337-341
-
-
Negro, A.1
Meggio, F.2
Bertoli, A.3
Battistutta, R.4
Sorgato, M.C.5
Pinna, L.A.6
-
33
-
-
0036855635
-
Misfolded proteinase K-resistant hyperphosphorylated alpha-synuclein in aged transgenic mice with locomotor deterioration and in human alpha-synucleinopathies
-
Neumann M, Kahle PJ, Giasson BI, Ozmen L, Borroni E, Spooren W, Müller V, Odoy S, Fujiwara H, Hasegawa M, Iwatsubo T, Trojanowski JQ, Kretzschmar HA, Haass C (2002) Misfolded proteinase K-resistant hyperphosphorylated alpha-synuclein in aged transgenic mice with locomotor deterioration and in human alpha-synucleinopathies. J Clin Invest 110:1429-1439.
-
(2002)
J Clin Invest
, vol.110
, pp. 1429-1439
-
-
Neumann, M.1
Kahle, P.J.2
Giasson, B.I.3
Ozmen, L.4
Borroni, E.5
Spooren, W.6
Müller, V.7
Odoy, S.8
Fujiwara, H.9
Hasegawa, M.10
Iwatsubo, T.11
Trojanowski, J.Q.12
Kretzschmar, H.A.13
Haass, C.14
-
34
-
-
0034614415
-
Constitutive phosphorylation of the Parkinson's disease associated alphasynuclein
-
Okochi M, Walter J, Koyama A, Nakajo S, Baba M, Iwatsubo T, Meijer L, Kahle PJ, Haass C (2000) Constitutive phosphorylation of the Parkinson's disease associated alphasynuclein. J Biol Chem 275:390-397.
-
(2000)
J Biol Chem
, vol.275
, pp. 390-397
-
-
Okochi, M.1
Walter, J.2
Koyama, A.3
Nakajo, S.4
Baba, M.5
Iwatsubo, T.6
Meijer, L.7
Kahle, P.J.8
Haass, C.9
-
35
-
-
0027421625
-
Brain proline-directed protein kinase phosphorylates tau on sites that are abnormally phosphorylated in tau associated with Alzheimer's paired helical filaments
-
Paudel HK, Lew J, Ali Z, Wang JH (1993) Brain proline-directed protein kinase phosphorylates tau on sites that are abnormally phosphorylated in tau associated with Alzheimer's paired helical filaments. J Biol Chem 268:23512-23518.
-
(1993)
J Biol Chem
, vol.268
, pp. 23512-23518
-
-
Paudel, H.K.1
Lew, J.2
Ali, Z.3
Wang, J.H.4
-
36
-
-
0034974318
-
Prion proteins with different conformations accumulate in Gerstmann-Straussler-Scheinker disease caused by A117V and F198S mutations
-
Piccardo P, Liepnieks JJ, William A, Dlouhy SR, Farlow MR, Young K, Nochlin D, Bird TD, Nixon RR, Ball MJ, DeCarli C, Bugiani O, Tagliavini F, Benson MD, Ghetti B (2001) Prion proteins with different conformations accumulate in Gerstmann-Straussler-Scheinker disease caused by A117V and F198S mutations. Am J Pathol 158:2201-2207.
-
(2001)
Am J Pathol
, vol.158
, pp. 2201-2207
-
-
Piccardo, P.1
Liepnieks, J.J.2
William, A.3
Dlouhy, S.R.4
Farlow, M.R.5
Young, K.6
Nochlin, D.7
Bird, T.D.8
Nixon, R.R.9
Ball, M.J.10
DeCarli, C.11
Bugiani, O.12
Tagliavini, F.13
Benson, M.D.14
Ghetti, B.15
-
37
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
Prusiner SB (1982) Novel proteinaceous infectious particles cause scrapie. Science 216:136-144.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
38
-
-
0023091197
-
Characterization of scrapie infection in mouse neuroblastoma cells
-
Race RE, Fadness LH, Chesebro B (1987) Characterization of scrapie infection in mouse neuroblastoma cells. J Gen Virol 68:1391-1399.
-
(1987)
J Gen Virol
, vol.68
, pp. 1391-1399
-
-
Race, R.E.1
Fadness, L.H.2
Chesebro, B.3
-
39
-
-
33744748011
-
Aggregation/fibrillogenesis of recombinant human prion protein and Gerstmann-Straussler-Scheinker disease peptides in the presence of metal ions
-
Ricchelli F, Buggio R, Drago D, Salmona M, Forloni G, Negro A, Tognon G, Zatta P (2006) Aggregation/fibrillogenesis of recombinant human prion protein and Gerstmann-Straussler-Scheinker disease peptides in the presence of metal ions. Biochemistry 45:6724-6732.
-
(2006)
Biochemistry
, vol.45
, pp. 6724-6732
-
-
Ricchelli, F.1
Buggio, R.2
Drago, D.3
Salmona, M.4
Forloni, G.5
Negro, A.6
Tognon, G.7
Zatta, P.8
-
40
-
-
0142135128
-
Cytosolic prion protein is not toxic and protects against Bax-mediated cell death in human primary neurons
-
Roucou X, Guo Q, Zhang Y, Goodyer CG, LeBlanc AC (2003) Cytosolic prion protein is not toxic and protects against Bax-mediated cell death in human primary neurons. J Biol Chem 278:40877-40881.
-
(2003)
J Biol Chem
, vol.278
, pp. 40877-40881
-
-
Roucou, X.1
Guo, Q.2
Zhang, Y.3
Goodyer, C.G.4
LeBlanc, A.C.5
-
41
-
-
0035859102
-
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding
-
Saborio GP, Permanne B, Soto C (2001) Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature 411:810-813.
-
(2001)
Nature
, vol.411
, pp. 810-813
-
-
Saborio, G.P.1
Permanne, B.2
Soto, C.3
-
42
-
-
0142040121
-
Formation of critical oligomers is a key event during conformational transition of recombinant syrian hamster prion protein
-
Sokolowski F, Modler AJ, Masuch R, Zirwer D, Baier M, Lutsch G, Moss DA, Gast K, Naumann D (2003) Formation of critical oligomers is a key event during conformational transition of recombinant syrian hamster prion protein. J Biol Chem 278:40481-40492.
-
(2003)
J Biol Chem
, vol.278
, pp. 40481-40492
-
-
Sokolowski, F.1
Modler, A.J.2
Masuch, R.3
Zirwer, D.4
Baier, M.5
Lutsch, G.6
Moss, D.A.7
Gast, K.8
Naumann, D.9
-
43
-
-
3042760011
-
Prion protein conversion in vitro
-
Supattapone S (2004) Prion protein conversion in vitro. J Mol Med 82:348-356.
-
(2004)
J Mol Med
, vol.82
, pp. 348-356
-
-
Supattapone, S.1
-
44
-
-
0030781922
-
pH-dependent stability and conformation of the recombinant human prion protein PrP(90-231)
-
Swietnicki W, Petersen R, Gambetti P, Surewicz WK (1997) pH-dependent stability and conformation of the recombinant human prion protein PrP(90-231). J Biol Chem 272:27517-27520.
-
(1997)
J Biol Chem
, vol.272
, pp. 27517-27520
-
-
Swietnicki, W.1
Petersen, R.2
Gambetti, P.3
Surewicz, W.K.4
-
45
-
-
0034681173
-
Aggregation and fibrillization of the recombinant human prion protein hu-PrP90-231
-
Swietnicki W, Morillas M, Chen SG, Gambetti P, Surewicz WK (2000) Aggregation and fibrillization of the recombinant human prion protein hu-PrP90-231. Biochemistry 39:424-431.
-
(2000)
Biochemistry
, vol.39
, pp. 424-431
-
-
Swietnicki, W.1
Morillas, M.2
Chen, S.G.3
Gambetti, P.4
Surewicz, W.K.5
-
46
-
-
0028878943
-
Inherited prion diseases and transmission to rodents
-
Tateishi J, Kitamoto T (1995) Inherited prion diseases and transmission to rodents. Brain Pathol 5:53-59.
-
(1995)
Brain Pathol
, vol.5
, pp. 53-59
-
-
Tateishi, J.1
Kitamoto, T.2
-
47
-
-
0032906903
-
Direct effects of phosphorylation on the preferred backbone conformation of peptides: A nuclear magnetic resonance study
-
Tholey A, Lindemann A, Kinzel V, Reed J (1999) Direct effects of phosphorylation on the preferred backbone conformation of peptides: a nuclear magnetic resonance study. Biophys J 76:76-87.
-
(1999)
Biophys J
, vol.76
, pp. 76-87
-
-
Tholey, A.1
Lindemann, A.2
Kinzel, V.3
Reed, J.4
-
48
-
-
21644489193
-
High pressure, an alternative approach to understand protein misfolding diseases
-
Torrent J, Marchal S, Tortora P, Lange R, Balny C (2004) High pressure, an alternative approach to understand protein misfolding diseases. Cell Mol Biol (Noisy-le-grand) 50:377-385.
-
(2004)
Cell Mol Biol (Noisy-le-grand)
, vol.50
, pp. 377-385
-
-
Torrent, J.1
Marchal, S.2
Tortora, P.3
Lange, R.4
Balny, C.5
-
49
-
-
34250158426
-
Lipid interaction converts prion protein to a PrPSc-like proteinase K-resistant conformation under physiological conditions
-
Wang F, Yang F, Hu Y, Wang X, Wang X, Jin C, Ma J (2007) Lipid interaction converts prion protein to a PrPSc-like proteinase K-resistant conformation under physiological conditions. Biochemistry 46:7045-7053.
-
(2007)
Biochemistry
, vol.46
, pp. 7045-7053
-
-
Wang, F.1
Yang, F.2
Hu, Y.3
Wang, X.4
Wang, X.5
Jin, C.6
Ma, J.7
-
50
-
-
0034758223
-
Conformational change, aggregation and fibril formation induced by detergent treatments of cellular prion protein
-
Xiong LW, Raymond LD, Hayes SF, Raymond GJ, Caughey B (2001) Conformational change, aggregation and fibril formation induced by detergent treatments of cellular prion protein. J Neurochem 79:669-678.
-
(2001)
J Neurochem
, vol.79
, pp. 669-678
-
-
Xiong, L.W.1
Raymond, L.D.2
Hayes, S.F.3
Raymond, G.J.4
Caughey, B.5
-
51
-
-
0012710491
-
NMR solution structure of the human prion protein
-
Zahn R, Liu A, Lührs T, Riek R, von Schroetter C, López García F, Billeter M, Calzolai L, Wider G, Wüthrich K (2000) NMR solution structure of the human prion protein. Proc Natl Acad Sci U S A 97:145-150.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 145-150
-
-
Zahn, R.1
Liu, A.2
Lührs, T.3
Riek, R.4
von Schroetter, C.5
López García, F.6
Billeter, M.7
Calzolai, L.8
Wider, G.9
Wüthrich, K.10
-
52
-
-
47249085094
-
Nuclear localization of Cdk5 is a key determinant in the postmitotic state of neurons
-
Zhang J, Cicero SA, Wang L, Romito-Digiacomo RR, Yang Y, Herrup K (2008) Nuclear localization of Cdk5 is a key determinant in the postmitotic state of neurons. Proc Natl Acad Sci U S A 105:8772-8777.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 8772-8777
-
-
Zhang, J.1
Cicero, S.A.2
Wang, L.3
Romito-Digiacomo, R.R.4
Yang, Y.5
Herrup, K.6
-
53
-
-
0037017399
-
Selective cytotoxicity of intracellular amyloid beta peptide1-42 through p53 and Bax in cultured primary human neurons
-
Zhang Y, McLaughlin R, Goodyer C, LeBlanc A (2002) Selective cytotoxicity of intracellular amyloid beta peptide1-42 through p53 and Bax in cultured primary human neurons. J Cell Biol 156:519-529.
-
(2002)
J Cell Biol
, vol.156
, pp. 519-529
-
-
Zhang, Y.1
McLaughlin, R.2
Goodyer, C.3
LeBlanc, A.4
|