-
1
-
-
0026600865
-
Normal development and behavior of mice lacking the neuronal cell-surface PrP protein
-
Büeler H, Fischer M, Lang Y, Fluethmann H, Lipp H-P, et al. (1992) Normal development and behavior of mice lacking the neuronal cell-surface PrP protein. Nature 356: 577-582.
-
(1992)
Nature
, vol.356
, pp. 577-582
-
-
Büeler, H.1
Fischer, M.2
Lang, Y.3
Fluethmann, H.4
Lipp, H.-P.5
-
2
-
-
0028420937
-
129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal
-
Manson JC, Clarke AR, Hooper ML, Aitchison L, McConnell I, et al. (1994) 129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal. Mol Neurobiol 8: 121-127.
-
(1994)
Mol Neurobiol
, vol.8
, pp. 121-127
-
-
Manson, J.C.1
Clarke, A.R.2
Hooper, M.L.3
Aitchison, L.4
McConnell, I.5
-
3
-
-
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
-
4
-
-
21744447704
-
Cellular prion protein inhibits proapoptotic Bax conformational change in human neurons and in breast carcinoma MCF-7 cells
-
Roucou X, Giannopoulos PN, Zhang Y, Jodoin J, Goodyer CG, et al. (2005) Cellular prion protein inhibits proapoptotic Bax conformational change in human neurons and in breast carcinoma MCF-7 cells. Cell Death Differ 12: 783-795.
-
(2005)
Cell Death Differ
, vol.12
, pp. 783-795
-
-
Roucou, X.1
Giannopoulos, P.N.2
Zhang, Y.3
Jodoin, J.4
Goodyer, C.G.5
-
5
-
-
0031194455
-
Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity
-
Brown DR, Schulzschaeffer WJ, Schmidt B, Kretzschmar HA, (1997) Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity. Exp Neurol 146: 104-112.
-
(1997)
Exp Neurol
, vol.146
, pp. 104-112
-
-
Brown, D.R.1
Schulzschaeffer, W.J.2
Schmidt, B.3
Kretzschmar, H.A.4
-
6
-
-
0037080043
-
Lack of prion protein expression results in a neuronal phenotype sensitive to stress
-
Brown DR, Nicholas RS, Canevari L, (2002) Lack of prion protein expression results in a neuronal phenotype sensitive to stress. J Neurosci Res 67: 211-224.
-
(2002)
J Neurosci Res
, vol.67
, pp. 211-224
-
-
Brown, D.R.1
Nicholas, R.S.2
Canevari, L.3
-
7
-
-
0033566067
-
Prions prevent neuronal cell-line death
-
Kuwahara C, Takeuchi AM, Nishimura T, Haraguchi K, Kubosaki A, et al. (1999) Prions prevent neuronal cell-line death. Nature 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
-
8
-
-
9144239220
-
Prion protein prevents human breast carcinoma cell line from tumor necrosis factor alpha-induced cell death
-
Diarra-Mehrpour M, Arrabal S, Jalil A, Pinson X, Gaudin C, et al. (2004) Prion protein prevents human breast carcinoma cell line from tumor necrosis factor alpha-induced cell death. Cancer Res 64: 719-727.
-
(2004)
Cancer Res
, vol.64
, pp. 719-727
-
-
Diarra-Mehrpour, M.1
Arrabal, S.2
Jalil, A.3
Pinson, X.4
Gaudin, C.5
-
9
-
-
52249121412
-
Prion protein lacks robust cytoprotective activity in cultured cells
-
Christensen HM, Harris DA, (2008) Prion protein lacks robust cytoprotective activity in cultured cells. Mol Neurodegener 3: 11.
-
(2008)
Mol Neurodegener
, vol.3
, pp. 11
-
-
Christensen, H.M.1
Harris, D.A.2
-
10
-
-
0001552281
-
Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions
-
Shmerling D, Hegyi I, Fischer M, Blättler T, Brandner S, et al. (1998) Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions. Cell 93: 203-214.
-
(1998)
Cell
, vol.93
, pp. 203-214
-
-
Shmerling, D.1
Hegyi, I.2
Fischer, M.3
Blättler, T.4
Brandner, S.5
-
11
-
-
33846498655
-
Lethal recessive myelin toxicity of prion protein lacking its central domain
-
Baumann F, Tolnay M, Brabeck C, Pahnke J, Kloz U, et al. (2007) Lethal recessive myelin toxicity of prion protein lacking its central domain. EMBO J 26: 538-547.
-
(2007)
EMBO J
, vol.26
, pp. 538-547
-
-
Baumann, F.1
Tolnay, M.2
Brabeck, C.3
Pahnke, J.4
Kloz, U.5
-
12
-
-
33846543360
-
Neonatal lethality in transgenic mice expressing prion protein with a deletion of residues 105-125
-
Li A, Christensen HM, Stewart LR, Roth KA, Chiesa R, et al. (2007) Neonatal lethality in transgenic mice expressing prion protein with a deletion of residues 105-125. EMBO J 26: 548-558.
-
(2007)
EMBO J
, vol.26
, pp. 548-558
-
-
Li, A.1
Christensen, H.M.2
Stewart, L.R.3
Roth, K.A.4
Chiesa, R.5
-
13
-
-
0033215478
-
Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel
-
Moore RC, Lee IY, Silverman GL, Harrison PM, Strome R, et al. (1999) Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel. J Mol Biol 292: 797-817.
-
(1999)
J Mol Biol
, vol.292
, pp. 797-817
-
-
Moore, R.C.1
Lee, I.Y.2
Silverman, G.L.3
Harrison, P.M.4
Strome, R.5
-
14
-
-
0035865398
-
Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain
-
Rossi D, Cozzio A, Flechsig E, Klein MA, Rülicke T, et al. (2001) Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain. EMBO J 20: 694-702.
-
(2001)
EMBO J
, vol.20
, pp. 694-702
-
-
Rossi, D.1
Cozzio, A.2
Flechsig, E.3
Klein, M.A.4
Rülicke, T.5
-
15
-
-
13344282734
-
Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene
-
Sakaguchi S, Katamine S, Nishida N, Moriuchi R, Shigematsu K, et al. (1996) Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene. Nature 380: 528-531.
-
(1996)
Nature
, vol.380
, pp. 528-531
-
-
Sakaguchi, S.1
Katamine, S.2
Nishida, N.3
Moriuchi, R.4
Shigematsu, K.5
-
16
-
-
0035957003
-
Two different neurodegenerative diseases caused by proteins with similar structures
-
Mo H, Moore RC, Cohen FE, Westaway D, Prusiner SB, et al. (2001) Two different neurodegenerative diseases caused by proteins with similar structures. Proc Natl Acad Sci USA 98: 2352-2357.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 2352-2357
-
-
Mo, H.1
Moore, R.C.2
Cohen, F.E.3
Westaway, D.4
Prusiner, S.B.5
-
17
-
-
34249995984
-
Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice
-
Li A, Piccardo P, Barmada SJ, Ghetti B, Harris DA, (2007) Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice. EMBO J 26: 2777-2785.
-
(2007)
EMBO J
, vol.26
, pp. 2777-2785
-
-
Li, A.1
Piccardo, P.2
Barmada, S.J.3
Ghetti, B.4
Harris, D.A.5
-
18
-
-
0043208949
-
Deletion of N-terminal residues 23-88 from prion protein (PrP) abrogates the potential to rescue PrP-deficient mice from PrP-like protein/doppel-induced Neurodegeneration
-
Atarashi R, Nishida N, Shigematsu K, Goto S, Kondo T, et al. (2003) Deletion of N-terminal residues 23-88 from prion protein (PrP) abrogates the potential to rescue PrP-deficient mice from PrP-like protein/doppel-induced Neurodegeneration. J Biol Chem 278: 28944-28949.
-
(2003)
J Biol Chem
, vol.278
, pp. 28944-28949
-
-
Atarashi, R.1
Nishida, N.2
Shigematsu, K.3
Goto, S.4
Kondo, T.5
-
19
-
-
0029054937
-
The N-terminal domain of a glycolipid-anchored prion protein is essential for its endocytosis via clathrin-coated pits
-
Shyng SL, Moulder KL, Lesko A, Harris DA, (1995) The N-terminal domain of a glycolipid-anchored prion protein is essential for its endocytosis via clathrin-coated pits. J Biol Chem 270: 14793-14800.
-
(1995)
J Biol Chem
, vol.270
, pp. 14793-14800
-
-
Shyng, S.L.1
Moulder, K.L.2
Lesko, A.3
Harris, D.A.4
-
20
-
-
0042313964
-
The mechanism of internalization of glycosylphosphatidylinositol-anchored prion protein
-
Sunyach C, Jen A, Deng J, Fitzgerald KT, Frobert Y, et al. (2003) The mechanism of internalization of glycosylphosphatidylinositol-anchored prion protein. EMBO J 22: 3591-3601.
-
(2003)
EMBO J
, vol.22
, pp. 3591-3601
-
-
Sunyach, C.1
Jen, A.2
Deng, J.3
Fitzgerald, K.T.4
Frobert, Y.5
-
21
-
-
27944486535
-
Assigning functions to distinct regions of the N-terminus of the prion protein that are involved in its copper-stimulated, clathrin-dependent endocytosis
-
Taylor DR, Watt NT, Perera WS, Hooper NM, (2005) Assigning functions to distinct regions of the N-terminus of the prion protein that are involved in its copper-stimulated, clathrin-dependent endocytosis. J Cell Sci 118: 5141-5153.
-
(2005)
J Cell Sci
, vol.118
, pp. 5141-5153
-
-
Taylor, D.R.1
Watt, N.T.2
Perera, W.S.3
Hooper, N.M.4
-
22
-
-
0037113169
-
Cell-surface prion protein interacts with glycosaminoglycans
-
Pan T, Wong BS, Liu T, Li R, Petersen RB, et al. (2002) Cell-surface prion protein interacts with glycosaminoglycans. Biochem J 368: 81-90.
-
(2002)
Biochem J
, vol.368
, pp. 81-90
-
-
Pan, T.1
Wong, B.S.2
Liu, T.3
Li, R.4
Petersen, R.B.5
-
23
-
-
0037166240
-
Identification of the Heparan Sulfate Binding Sites in the Cellular Prion Protein
-
Warner RG, Hundt C, Weiss S, Turnbull JE, (2002) Identification of the Heparan Sulfate Binding Sites in the Cellular Prion Protein. Journal of Biological Chemistry 277: 18421-18430.
-
(2002)
Journal of Biological Chemistry
, vol.277
, pp. 18421-18430
-
-
Warner, R.G.1
Hundt, C.2
Weiss, S.3
Turnbull, J.E.4
-
24
-
-
73249135395
-
Structure of the Flexible Amino-Terminal Domain of Prion Protein Bound to a Sulfated Glycan
-
Taubner LM, Bienkiewicz EA, Copié V, Caughey B, (2010) Structure of the Flexible Amino-Terminal Domain of Prion Protein Bound to a Sulfated Glycan. Journal of Molecular Biology 395: 475-490.
-
(2010)
Journal of Molecular Biology
, vol.395
, pp. 475-490
-
-
Taubner, L.M.1
Bienkiewicz, E.A.2
Copié, V.3
Caughey, B.4
-
25
-
-
53749088102
-
Pathologic Prion Protein Infects Cells by Lipid-Raft Dependent Macropinocytosis
-
Wadia JS, Schaller M, Williamson RA, Dowdy SF, (2008) Pathologic Prion Protein Infects Cells by Lipid-Raft Dependent Macropinocytosis. PLoS ONE 3: e3314.
-
(2008)
PLoS ONE
, vol.3
-
-
Wadia, J.S.1
Schaller, M.2
Williamson, R.A.3
Dowdy, S.F.4
-
26
-
-
20444454586
-
Mammalian prion protein suppresses Bax-induced cell death in yeast
-
Li A, Harris DA, (2005) Mammalian prion protein suppresses Bax-induced cell death in yeast. J Biol Chem 280: 17430-17434.
-
(2005)
J Biol Chem
, vol.280
, pp. 17430-17434
-
-
Li, A.1
Harris, D.A.2
-
27
-
-
0030499678
-
A vector for expressing foreign genes in the brains and hearts of transgenic mice
-
Borchelt DR, Davis J, Fischer M, Lee MK, Slunt HH, et al. (1996) A vector for expressing foreign genes in the brains and hearts of transgenic mice. Genet Anal Biomol Eng 13: 159-163.
-
(1996)
Genet Anal Biomol Eng
, vol.13
, pp. 159-163
-
-
Borchelt, D.R.1
Davis, J.2
Fischer, M.3
Lee, M.K.4
Slunt, H.H.5
-
28
-
-
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
-
29
-
-
80053228890
-
A Nine Amino Acid Domain is Essential for Mutant Prion Protein Toxicity
-
DOI:10.1523/JNEUROSCI.1243-11.2011
-
Westergard L, Turnbaugh JA, Harris DA, (2011) A Nine Amino Acid Domain is Essential for Mutant Prion Protein Toxicity. J Neurosci DOI:10.1523/JNEUROSCI.1243-11.2011.
-
(2011)
J Neurosci
-
-
Westergard, L.1
Turnbaugh, J.A.2
Harris, D.A.3
-
30
-
-
67649963292
-
Dominant roles of the polybasic proline motif and copper in the PrP23-89-mediated stress protection response
-
Haigh CL, Drew SC, Boland MP, Masters CL, Barnham KJ, et al. (2009) Dominant roles of the polybasic proline motif and copper in the PrP23-89-mediated stress protection response. J Cell Sci 122: 1518-1528.
-
(2009)
J Cell Sci
, vol.122
, pp. 1518-1528
-
-
Haigh, C.L.1
Drew, S.C.2
Boland, M.P.3
Masters, C.L.4
Barnham, K.J.5
-
31
-
-
53049087145
-
Dominant-negative Effects of the N-terminal Half of Prion Protein on Neurotoxicity of Prion Protein-like Protein/Doppel in Mice
-
Yoshikawa D, Yamaguchi N, Ishibashi D, Yamanaka H, Okimura N, et al. (2008) Dominant-negative Effects of the N-terminal Half of Prion Protein on Neurotoxicity of Prion Protein-like Protein/Doppel in Mice. Journal of Biological Chemistry 283: 24202-24211.
-
(2008)
Journal of Biological Chemistry
, vol.283
, pp. 24202-24211
-
-
Yoshikawa, D.1
Yamaguchi, N.2
Ishibashi, D.3
Yamanaka, H.4
Okimura, N.5
-
32
-
-
79954607779
-
An N-terminal polybasic domain and cell surface localization are required for mutant prion protein toxicity
-
Solomon IH, Khatri N, Biasini E, Massignan T, Huettner JE, et al. (2011) An N-terminal polybasic domain and cell surface localization are required for mutant prion protein toxicity. J Biol Chem.
-
(2011)
J Biol Chem
-
-
Solomon, I.H.1
Khatri, N.2
Biasini, E.3
Massignan, T.4
Huettner, J.E.5
-
33
-
-
18644383026
-
Truncated prion protein and Doppel are myelinotoxic in the absence of oligodendrocytic PrPC
-
Radovanovic I, Braun N, Giger OT, Mertz K, Miele G, et al. (2005) Truncated prion protein and Doppel are myelinotoxic in the absence of oligodendrocytic PrPC. J Neurosci 25: 4879-4888.
-
(2005)
J Neurosci
, vol.25
, pp. 4879-4888
-
-
Radovanovic, I.1
Braun, N.2
Giger, O.T.3
Mertz, K.4
Miele, G.5
-
34
-
-
77649091387
-
Axonal prion protein is required for peripheral myelin maintenance
-
Bremer J, Baumann F, Tiberi C, Wessig C, Fischer H, et al. (2010) Axonal prion protein is required for peripheral myelin maintenance. Nat Neurosci 13: 310-318.
-
(2010)
Nat Neurosci
, vol.13
, pp. 310-318
-
-
Bremer, J.1
Baumann, F.2
Tiberi, C.3
Wessig, C.4
Fischer, H.5
-
35
-
-
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, et al. (2001) The disintegrins ADAM10 and TACE contribute to the constitutive and phorbol ester-regulated normal cleavage of the cellular prion protein. J Biol Chem 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
-
36
-
-
72149127389
-
The α-Secretase-derived N-terminal Product of Cellular Prion, N1, Displays Neuroprotective Function in Vitro and in Vivo
-
Guillot-Sestier M-V, Sunyach C, Druon C, Scarzello S, Checler F, (2009) The α-Secretase-derived N-terminal Product of Cellular Prion, N1, Displays Neuroprotective Function in Vitro and in Vivo. Journal of Biological Chemistry 284: 35973-35986.
-
(2009)
Journal of Biological Chemistry
, vol.284
, pp. 35973-35986
-
-
Guillot-Sestier, M.-V.1
Sunyach, C.2
Druon, C.3
Scarzello, S.4
Checler, F.5
-
37
-
-
0028874320
-
A 60 kDa prion protein (PrP) with properties of both the normal and scrapie-associated forms of PrP
-
Priola SA, Caughey B, Wehrly K, Chesebro B, (1995) A 60 kDa prion protein (PrP) with properties of both the normal and scrapie-associated forms of PrP. J Biol Chem 270: 3299-3305.
-
(1995)
J Biol Chem
, vol.270
, pp. 3299-3305
-
-
Priola, S.A.1
Caughey, B.2
Wehrly, K.3
Chesebro, B.4
-
38
-
-
0034537674
-
A monomer-dimer equilibrium of a cellular prion protein (PrPC) not observed with recombinant PrP
-
Meyer RK, Lustig A, Oesch B, Fatzer R, Zurbriggen A, et al. (2000) A monomer-dimer equilibrium of a cellular prion protein (PrPC) not observed with recombinant PrP. J Biol Chem 275: 38081-38087.
-
(2000)
J Biol Chem
, vol.275
, pp. 38081-38087
-
-
Meyer, R.K.1
Lustig, A.2
Oesch, B.3
Fatzer, R.4
Zurbriggen, A.5
-
39
-
-
47949104726
-
Stress-protective signalling of prion protein is corrupted by scrapie prions
-
Rambold AS, Muller V, Ron U, Ben-Tal N, Winklhofer KF, et al. (2008) Stress-protective signalling of prion protein is corrupted by scrapie prions. Embo J 27: 1974-1984.
-
(2008)
Embo J
, vol.27
, pp. 1974-1984
-
-
Rambold, A.S.1
Muller, V.2
Ron, U.3
Ben-Tal, N.4
Winklhofer, K.F.5
-
40
-
-
33846953615
-
The low-density lipoprotein receptor-related protein 1 (LRP1) mediates the endocytosis of the cellular prion protein
-
Taylor DR, Hooper NM, (2007) The low-density lipoprotein receptor-related protein 1 (LRP1) mediates the endocytosis of the cellular prion protein. Biochem J 402: 17-23.
-
(2007)
Biochem J
, vol.402
, pp. 17-23
-
-
Taylor, D.R.1
Hooper, N.M.2
-
41
-
-
0037423296
-
Essential role of the prion protein N terminus in subcellular trafficking and half-life of cellular prion protein
-
Nunziante M, Gilch S, Schatzl HM, (2003) Essential role of the prion protein N terminus in subcellular trafficking and half-life of cellular prion protein. J Biol Chem 278: 3726-3734.
-
(2003)
J Biol Chem
, vol.278
, pp. 3726-3734
-
-
Nunziante, M.1
Gilch, S.2
Schatzl, H.M.3
-
42
-
-
17944377091
-
Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor
-
Hundt C, Peyrin JM, Haik S, Gauczynski S, Leucht C, et al. (2001) Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor. EMBO J 20: 5876-5886.
-
(2001)
EMBO J
, vol.20
, pp. 5876-5886
-
-
Hundt, C.1
Peyrin, J.M.2
Haik, S.3
Gauczynski, S.4
Leucht, C.5
-
43
-
-
70350215545
-
Antimicrobial Activity of Human Prion Protein Is Mediated by Its N-Terminal Region
-
Pasupuleti M, Roupe M, Rydengård V, Surewicz K, Surewicz WK, et al. (2009) Antimicrobial Activity of Human Prion Protein Is Mediated by Its N-Terminal Region. PLoS ONE 4: e7358.
-
(2009)
PLoS ONE
, vol.4
-
-
Pasupuleti, M.1
Roupe, M.2
Rydengård, V.3
Surewicz, K.4
Surewicz, W.K.5
-
44
-
-
38149114599
-
Relevance of the N-terminal NLS-like sequence of the prion protein for membrane perturbation effects
-
Oglecka K, Lundberg P, Magzoub M, Goran Eriksson LE, Langel U, et al. (2008) Relevance of the N-terminal NLS-like sequence of the prion protein for membrane perturbation effects. Biochim Biophys Acta 1778: 206-213.
-
(2008)
Biochim Biophys Acta
, vol.1778
, pp. 206-213
-
-
Oglecka, K.1
Lundberg, P.2
Magzoub, M.3
Goran Eriksson, L.E.4
Langel, U.5
-
45
-
-
77957797498
-
Anionic phospholipid interactions of the prion protein N terminus are minimally perturbing and not driven solely by the octapeptide repeat domain
-
Boland MP, Hatty CR, Separovic F, Hill AF, Tew DJ, et al. (2010) Anionic phospholipid interactions of the prion protein N terminus are minimally perturbing and not driven solely by the octapeptide repeat domain. J Biol Chem 285: 32282-32292.
-
(2010)
J Biol Chem
, vol.285
, pp. 32282-32292
-
-
Boland, M.P.1
Hatty, C.R.2
Separovic, F.3
Hill, A.F.4
Tew, D.J.5
-
46
-
-
0037343746
-
Identification of cryptic nuclear localization signals in the prion protein
-
Gu Y, Hinnerwisch J, Fredricks R, Kalepu S, Mishra RS, et al. (2003) Identification of cryptic nuclear localization signals in the prion protein. Neurobiol Dis 12: 133-149.
-
(2003)
Neurobiol Dis
, vol.12
, pp. 133-149
-
-
Gu, Y.1
Hinnerwisch, J.2
Fredricks, R.3
Kalepu, S.4
Mishra, R.S.5
-
47
-
-
70349448466
-
Prion protein region 23-32 interacts with tubulin and inhibits microtubule assembly
-
Osiecka KM, Nieznanska H, Skowronek KJ, Karolczak J, Schneider G, et al. (2009) Prion protein region 23-32 interacts with tubulin and inhibits microtubule assembly. Proteins 77: 279-296.
-
(2009)
Proteins
, vol.77
, pp. 279-296
-
-
Osiecka, K.M.1
Nieznanska, H.2
Skowronek, K.J.3
Karolczak, J.4
Schneider, G.5
-
48
-
-
77956197815
-
Interaction between Human Prion Protein and Amyloid-β (Aβ) Oligomers
-
Chen S, Yadav SP, Surewicz WK, (2010) Interaction between Human Prion Protein and Amyloid-β (Aβ) Oligomers. Journal of Biological Chemistry 285: 26377-26383.
-
(2010)
Journal of Biological Chemistry
, vol.285
, pp. 26377-26383
-
-
Chen, S.1
Yadav, S.P.2
Surewicz, W.K.3
-
49
-
-
79956110918
-
The cellular prion protein mediates neurotoxic signalling of [beta]-sheet-rich conformers independent of prion replication
-
Resenberger UK, Harmeier A, Woerner AC, Goodman JL, Muller V, et al. (2011) The cellular prion protein mediates neurotoxic signalling of [beta]-sheet-rich conformers independent of prion replication. EMBO J advance online publication.
-
(2011)
EMBO J Advance Online Publication
-
-
Resenberger, U.K.1
Harmeier, A.2
Woerner, A.C.3
Goodman, J.L.4
Muller, V.5
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