-
1
-
-
33747570634
-
Magnetically oriented phospholipid bilayered micelles for structural studies of polypeptides. Does the ideal bicelle exist?
-
R.R. Vold, and R.S. Prosser Magnetically oriented phospholipid bilayered micelles for structural studies of polypeptides. Does the ideal bicelle exist? J. Magn. Res. ser. B 113 1996 267 271
-
(1996)
J. Magn. Res. Ser. B
, vol.113
, pp. 267-271
-
-
Vold, R.R.1
Prosser, R.S.2
-
2
-
-
0023046596
-
Spontaneous transmembrane insertion of membrane proteins into lipid vesicles facilitated by short-chain lecithins
-
N.A. Dencher Spontaneous transmembrane insertion of membrane proteins into lipid vesicles facilitated by short-chain lecithins Biochemistry 25 1986 1195 1200
-
(1986)
Biochemistry
, vol.25
, pp. 1195-1200
-
-
Dencher, N.A.1
-
3
-
-
0024317082
-
Gentle and fast transmembrane reconstitution of membrane proteins
-
N.A. Dencher Gentle and fast transmembrane reconstitution of membrane proteins Methods Enzymol. 171 1989 265 274
-
(1989)
Methods Enzymol.
, vol.171
, pp. 265-274
-
-
Dencher, N.A.1
-
4
-
-
0034707098
-
Short-chain phospholipids as detergents
-
H. Hauser Short-chain phospholipids as detergents Biochim. Biophys. Acta 1508 2000 164 181
-
(2000)
Biochim. Biophys. Acta
, vol.1508
, pp. 164-181
-
-
Hauser, H.1
-
5
-
-
12144271772
-
NMR structure of the bovine prion protein isolated from healthy calf brains
-
S. Hornemann, C. Schorn, and K. Wüthrich NMR structure of the bovine prion protein isolated from healthy calf brains EMBO Rep. 5 2004 1159 1164
-
(2004)
EMBO Rep.
, vol.5
, pp. 1159-1164
-
-
Hornemann, S.1
Schorn, C.2
Wüthrich, K.3
-
7
-
-
0020511509
-
Ultrastructural morphology of amyloid fibrils from neuritic and amyloid plaques
-
P.A. Merz, H.M. Wisniewski, R.A. Somerville, S.A. Bobin, C.L. Masters, and K. Iqbal Ultrastructural morphology of amyloid fibrils from neuritic and amyloid plaques Acta Neuropathol. (Berl.) 60 1983 113 124
-
(1983)
Acta Neuropathol. (Berl.)
, vol.60
, pp. 113-124
-
-
Merz, P.A.1
Wisniewski, H.M.2
Somerville, R.A.3
Bobin, S.A.4
Masters, C.L.5
Iqbal, K.6
-
8
-
-
0021019026
-
Scrapie prions aggregate to form amyloid-like birefringent rods
-
S.B. Prusiner, M.P. McKinley, K.A. Bowman, D.C. Bolton, P.E. Bendheim, D.F. Groth, and G.G. Glenner Scrapie prions aggregate to form amyloid-like birefringent rods Cell 35 1983 349 358
-
(1983)
Cell
, vol.35
, pp. 349-358
-
-
Prusiner, S.B.1
McKinley, M.P.2
Bowman, K.A.3
Bolton, D.C.4
Bendheim, P.E.5
Groth, D.F.6
Glenner, G.G.7
-
9
-
-
0021023167
-
A protease-resistant protein is a structural component of the scrapie prion
-
M.P. McKinley, D.C. Bolton, and S.B. Prusiner A protease-resistant protein is a structural component of the scrapie prion Cell 35 1983 57 62
-
(1983)
Cell
, vol.35
, pp. 57-62
-
-
McKinley, M.P.1
Bolton, D.C.2
Prusiner, S.B.3
-
10
-
-
0022619528
-
Partial copurification of scrapie-associated fibrils and scrapie infectivity
-
R.A. Somerville, P.A. Merz, and R.I. Carp Partial copurification of scrapie-associated fibrils and scrapie infectivity Intervirology 25 1986 48 55
-
(1986)
Intervirology
, vol.25
, pp. 48-55
-
-
Somerville, R.A.1
Merz, P.A.2
Carp, R.I.3
-
11
-
-
0014190760
-
Self-replication and scrapie
-
J.S. Griffith Self-replication and scrapie Nature 215 1967 1043 1044
-
(1967)
Nature
, vol.215
, pp. 1043-1044
-
-
Griffith, J.S.1
-
12
-
-
0025910229
-
Molecular biology of prion diseases
-
S.B. Prusiner Molecular biology of prion diseases Science 252 1991 1515 1522
-
(1991)
Science
, vol.252
, pp. 1515-1522
-
-
Prusiner, S.B.1
-
13
-
-
0026008203
-
Search for a putative scrapie genome in purified prion fractions reveals a paucity of nucleic acids
-
N. Meyer, V. Rosenbaum, B. Schmidt, K. Gilles, C. Mirenda, and D. Groth Search for a putative scrapie genome in purified prion fractions reveals a paucity of nucleic acids J. Gen. Virol. 72 1991 37 49
-
(1991)
J. Gen. Virol.
, vol.72
, pp. 37-49
-
-
Meyer, N.1
Rosenbaum, V.2
Schmidt, B.3
Gilles, K.4
Mirenda, C.5
Groth, D.6
-
14
-
-
0345716276
-
Highly infectious purified preparations of disease-specific amyloid of transmissible spongiform encephalopathies are not devoid of nucleic acids of viral size
-
H. Diringer, M. Beekes, M. Ozel, D. Simon, I. Queck, and F. Cardone Highly infectious purified preparations of disease-specific amyloid of transmissible spongiform encephalopathies are not devoid of nucleic acids of viral size Intervirology 40 1997 238 246
-
(1997)
Intervirology
, vol.40
, pp. 238-246
-
-
Diringer, H.1
Beekes, M.2
Ozel, M.3
Simon, D.4
Queck, I.5
Cardone, F.6
-
15
-
-
0031843985
-
Prion rods contain small amounts of two host sphingolipids as revealed by thin-layer chromatography and mass spectrometry
-
T.R. Klein, D. Kirsch, R. Kaufmann, and D. Riesner Prion rods contain small amounts of two host sphingolipids as revealed by thin-layer chromatography and mass spectrometry Biol. Chem. 379 1998 655 666
-
(1998)
Biol. Chem.
, vol.379
, pp. 655-666
-
-
Klein, T.R.1
Kirsch, D.2
Kaufmann, R.3
Riesner, D.4
-
17
-
-
0035753222
-
The prion theory: Background and basic information
-
D. Riesner The prion theory: background and basic information Contrib. Microbiol. 7 2001 7 20
-
(2001)
Contrib. Microbiol.
, vol.7
, pp. 7-20
-
-
Riesner, D.1
-
18
-
-
0037077234
-
Pathway complexity of prion protein assembly into amyloid
-
I.V. Baskakov, G. Legname, M.A. Baldwin, S.B. Prusiner, and F.E. Cohen Pathway complexity of prion protein assembly into amyloid J. Biol. Chem. 277 2002 21140 21148
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 21140-21148
-
-
Baskakov, I.V.1
Legname, G.2
Baldwin, M.A.3
Prusiner, S.B.4
Cohen, F.E.5
-
19
-
-
3442889359
-
Synthetic mammalian prions
-
G. Legname, I.V. Baskakov, H.O. Nguyen, D. Riesner, F.E. Cohen, S.J. DeArmond, and S.B. Prusiner Synthetic mammalian prions Science 305 2004 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
-
20
-
-
0029937271
-
NMR structure of the mouse prion protein domain PrP(121-321)
-
R. Riek, S. Hornemann, G. Wider, M. Billeter, R. Glockshuber, and K. Wüthrich NMR structure of the mouse prion protein domain PrP(121-321) Nature 382 1996 180 182
-
(1996)
Nature
, vol.382
, pp. 180-182
-
-
Riek, R.1
Hornemann, S.2
Wider, G.3
Billeter, M.4
Glockshuber, R.5
Wüthrich, K.6
-
21
-
-
0030967895
-
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
-
T.L. James, H. Liu, N.B. Ulyanov, S. Farr-Jones, H. Zhang, and D.G. Donne Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform Proc. Natl Acad. Sci. USA 94 1997 10086 10091
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 10086-10091
-
-
James, T.L.1
Liu, H.2
Ulyanov, N.B.3
Farr-Jones, S.4
Zhang, H.5
Donne, D.G.6
-
22
-
-
0033609035
-
Solution structure of Syrian hamster prion protein rPrP(90-231)
-
H. Liu, S. Farr-Jones, N.B. Ulyanov, M. Llinas, S. Marqusee, and D. Groth Solution structure of Syrian hamster prion protein rPrP(90-231) Biochemistry 38 1999 5362 5377
-
(1999)
Biochemistry
, vol.38
, pp. 5362-5377
-
-
Liu, H.1
Farr-Jones, S.2
Ulyanov, N.B.3
Llinas, M.4
Marqusee, S.5
Groth, D.6
-
23
-
-
0012710491
-
NMR solution structure of the human prion protein
-
R. Zahn, A. Liu, T. Lührs, R. Riek, C. von Schroetter, and F. Lopez Garcia NMR solution structure of the human prion protein Proc. Natl Acad. Sci. USA 97 2000 145 150
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 145-150
-
-
Zahn, R.1
Liu, A.2
Lührs, T.3
Riek, R.4
Von Schroetter, C.5
Lopez Garcia, F.6
-
25
-
-
0344326239
-
Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein
-
F. Wopfner, G. Weidenhofer, R. Schneider, A. von Brunn, S. Gilch, and T.F. Schwarz Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein J. Mol. Biol. 289 1999 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
-
26
-
-
0021752457
-
Purification and structural studies of a major scrapie prion protein
-
S.B. Prusiner, D.F. Groth, D.C. Bolton, S.B. Kent, and L.E. Hood Purification and structural studies of a major scrapie prion protein Cell 38 1984 127 134
-
(1984)
Cell
, vol.38
, pp. 127-134
-
-
Prusiner, S.B.1
Groth, D.F.2
Bolton, D.C.3
Kent, S.B.4
Hood, L.E.5
-
27
-
-
0027332116
-
Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins
-
K.M. Pan, M. Baldwin, J. Nguyen, M. Gasset, A. Serban, and D. Groth Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins Proc. Natl Acad. Sci. USA 90 1993 10962 10966
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 10962-10966
-
-
Pan, K.M.1
Baldwin, M.2
Nguyen, J.3
Gasset, M.4
Serban, A.5
Groth, D.6
-
28
-
-
0023663071
-
Scrapie prion protein contains a phosphatidylinositol glycolipid
-
N. Stahl, D.R. Borchelt, K. Hsiao, and S.B. Prusiner Scrapie prion protein contains a phosphatidylinositol glycolipid Cell 51 1987 229 240
-
(1987)
Cell
, vol.51
, pp. 229-240
-
-
Stahl, N.1
Borchelt, D.R.2
Hsiao, K.3
Prusiner, S.B.4
-
29
-
-
0029962468
-
Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains
-
M. Vey, S. Pilkuhn, H. Wille, R. Nixon, S.J. DeArmond, and E.J. Smart Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains Proc. Natl Acad. Sci. USA 93 1996 14945 14949
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 14945-14949
-
-
Vey, M.1
Pilkuhn, S.2
Wille, H.3
Nixon, R.4
Dearmond, S.J.5
Smart, E.J.6
-
30
-
-
0030894380
-
Characterization of detergent-insoluble complexes containing the cellular prion protein and its scrapie isoform
-
N. Naslavsky, R. Stein, A. Yanai, G. Friedlander, and A. Taraboulos Characterization of detergent-insoluble complexes containing the cellular prion protein and its scrapie isoform J. Biol. Chem. 272 1997 6324 6331
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 6324-6331
-
-
Naslavsky, N.1
Stein, R.2
Yanai, A.3
Friedlander, G.4
Taraboulos, A.5
-
31
-
-
0030949124
-
Functional rafts in cell membranes
-
K. Simons, and E. Ikonen Functional rafts in cell membranes Nature 387 1997 569 572
-
(1997)
Nature
, vol.387
, pp. 569-572
-
-
Simons, K.1
Ikonen, E.2
-
32
-
-
0032488777
-
A transmembrane form of the prion protein in neurodegenerative disease
-
R.S. Hegde, J.A. Mastrianni, M.R. Scott, K.A. DeFea, P. Tremblay, and M. Torchia A transmembrane form of the prion protein in neurodegenerative disease Science 279 1998 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
-
33
-
-
0033576323
-
Transmissible and genetic prion diseases share a common pathway of neurodegeneration
-
R.S. Hegde, P. Tremblay, D. Groth, S.J. DeArmond, S.B. Prusiner, and V.R. Lingappa Transmissible and genetic prion diseases share a common pathway of neurodegeneration Nature 402 1999 822 826
-
(1999)
Nature
, vol.402
, pp. 822-826
-
-
Hegde, R.S.1
Tremblay, P.2
Groth, D.3
Dearmond, S.J.4
Prusiner, S.B.5
Lingappa, V.R.6
-
34
-
-
20344394154
-
Anchorless prion protein results in infectious amyloid disease without clinical scrapie
-
B. Chesebro, M. Trifilo, R. Race, K. Meade-White, C. Teng, and R. LaCasse Anchorless prion protein results in infectious amyloid disease without clinical scrapie Science 308 2005 1435 1439
-
(2005)
Science
, vol.308
, pp. 1435-1439
-
-
Chesebro, B.1
Trifilo, M.2
Race, R.3
Meade-White, K.4
Teng, C.5
Lacasse, R.6
-
35
-
-
0035818453
-
Conformational dimorphism and transmembrane orientation of prion protein residues 110-136 in bicelles
-
K.J. Glover, J.A. Whiles, M.J. Wood, G. Melacini, E.A. Komives, and R.R. Vold Conformational dimorphism and transmembrane orientation of prion protein residues 110-136 in bicelles Biochemistry 40 2001 13137 13142
-
(2001)
Biochemistry
, vol.40
, pp. 13137-13142
-
-
Glover, K.J.1
Whiles, J.A.2
Wood, M.J.3
Melacini, G.4
Komives, E.A.5
Vold, R.R.6
-
36
-
-
0031555486
-
The 118-135 peptide of the human prion protein forms amyloid fibrils and induces liposome fusion
-
T. Pillot, L. Lins, M. Goethals, B. Vanloo, J. Baert, and J. Vandekerckhove The 118-135 peptide of the human prion protein forms amyloid fibrils and induces liposome fusion J. Mol. Biol. 274 1997 381 393
-
(1997)
J. Mol. Biol.
, vol.274
, pp. 381-393
-
-
Pillot, T.1
Lins, L.2
Goethals, M.3
Vanloo, B.4
Baert, J.5
Vandekerckhove, J.6
-
37
-
-
0033769044
-
A nonfibrillar form of the fusogenic prion protein fragment [118-135] induces apoptotic cell death in rat cortical neurons
-
T. Pillot, B. Drouet, R.L. Pincon-Raymond, J. Vandekerckhove, T. Rosseneu, and J. Chambaz A nonfibrillar form of the fusogenic prion protein fragment [118-135] induces apoptotic cell death in rat cortical neurons J. Neurochem. 75 2000 2298 2308
-
(2000)
J. Neurochem.
, vol.75
, pp. 2298-2308
-
-
Pillot, T.1
Drouet, B.2
Pincon-Raymond, R.L.3
Vandekerckhove, J.4
Rosseneu, T.5
Chambaz, J.6
-
38
-
-
0031594587
-
Overexpression of non-convertible PrPc delta114-121 in scrapie-infected mouse neuroblastoma cells leads to trans-dominant inhibition of wild-type PrP(Sc) accumulation
-
C. Holscher, H. Delius, and A. Burkle Overexpression of non-convertible PrPc delta114-121 in scrapie-infected mouse neuroblastoma cells leads to trans-dominant inhibition of wild-type PrP(Sc) accumulation J. Virol. 72 1998 1153 1159
-
(1998)
J. Virol.
, vol.72
, pp. 1153-1159
-
-
Holscher, C.1
Delius, H.2
Burkle, A.3
-
39
-
-
0036257318
-
Mutant prion protein acquires resistance to protease in mouse neuroblastoma cells
-
C. Wegner, A. Romer, R. Schmalzbauer, H. Lorenz, O. Windl, and H.A. Kretzschmar Mutant prion protein acquires resistance to protease in mouse neuroblastoma cells J. Gen. Virol. 83 2002 1237 1245
-
(2002)
J. Gen. Virol.
, vol.83
, pp. 1237-1245
-
-
Wegner, C.1
Romer, A.2
Schmalzbauer, R.3
Lorenz, H.4
Windl, O.5
Kretzschmar, H.A.6
-
40
-
-
0028966735
-
Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform
-
A. Taraboulos, M. Scott, A. Semenov, D. Avrahami, L. Laszlo, S.B. Prusiner, and D. Avraham Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform J. Cell. Biol. 129 1995 121 132
-
(1995)
J. Cell. Biol.
, vol.129
, pp. 121-132
-
-
Taraboulos, A.1
Scott, M.2
Semenov, A.3
Avrahami, D.4
Laszlo, L.5
Prusiner, S.B.6
Avraham, D.7
-
41
-
-
0033597931
-
Sphingolipid depletion increases formation of the scrapie prion protein in neuroblastoma cells infected with prions
-
N. Naslavsky, H. Shmeeda, G. Friedlander, A. Yanai, A.H. Futerman, Y. Barenholz, and A. Taraboulos Sphingolipid depletion increases formation of the scrapie prion protein in neuroblastoma cells infected with prions J. Biol. Chem. 274 1999 20763 20771
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 20763-20771
-
-
Naslavsky, N.1
Shmeeda, H.2
Friedlander, G.3
Yanai, A.4
Futerman, A.H.5
Barenholz, Y.6
Taraboulos, A.7
-
42
-
-
0036500554
-
Conversion of raft associated prion protein to the protease-resistant state requires insertion of PrP-res (PrP(Sc)) into contiguous membranes
-
G.S. Baron, K. Wehrly, D.W. Dorward, B. Chesebro, and B. Caughey Conversion of raft associated prion protein to the protease-resistant state requires insertion of PrP-res (PrP(Sc)) into contiguous membranes EMBO J. 21 2002 1031 1040
-
(2002)
EMBO J.
, vol.21
, pp. 1031-1040
-
-
Baron, G.S.1
Wehrly, K.2
Dorward, D.W.3
Chesebro, B.4
Caughey, B.5
-
43
-
-
0030878056
-
Recombinant full-length murine prion protein, mPrP(23-231): Purification and spectroscopic characterization
-
S. Hornemann, C. Korth, B. Oesch, R. Riek, G. Wider, K. Wüthrich, and R. Glockshuber Recombinant full-length murine prion protein, mPrP(23-231): purification and spectroscopic characterization FEBS Letters 413 1997 277 281
-
(1997)
FEBS Letters
, vol.413
, pp. 277-281
-
-
Hornemann, S.1
Korth, C.2
Oesch, B.3
Riek, R.4
Wider, G.5
Wüthrich, K.6
Glockshuber, R.7
-
44
-
-
0032568592
-
A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH
-
S. Hornemann, and R. Glockshuber A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH Proc. Natl Acad. Sci. USA 95 1998 6010 6014
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 6010-6014
-
-
Hornemann, S.1
Glockshuber, R.2
-
45
-
-
0034681173
-
Aggregation and fibrillization of the recombinant human prion protein huPrP90-231
-
W. Swietnicki, M. Morillas, S.G. Chen, P. Gambetti, and W.K. Surewicz Aggregation and fibrillization of the recombinant human prion protein huPrP90-231 Biochemistry 39 2000 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
-
-
0033583190
-
Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations
-
G.S. Jackson, L.L. Hosszu, A. Power, A.F. Hill, J. Kenney, and H. Saibil Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations Science 283 1999 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
-
47
-
-
0036306046
-
Binding of prion protein to lipid membranes and implications for prion conversion
-
N. Sanghera, and T.J. Pinheiro Binding of prion protein to lipid membranes and implications for prion conversion J. Mol. Biol. 315 2002 1241 1256
-
(2002)
J. Mol. Biol.
, vol.315
, pp. 1241-1256
-
-
Sanghera, N.1
Pinheiro, T.J.2
-
48
-
-
0037465821
-
Structural changes of the prion protein in lipid membranes leading to aggregation and fibrillization
-
J. Kazlauskaite, N. Sanghera, I. Sylvester, C. Venien-Bryan, and T.J. Pinheiro Structural changes of the prion protein in lipid membranes leading to aggregation and fibrillization Biochemistry 42 2003 3295 3304
-
(2003)
Biochemistry
, vol.42
, pp. 3295-3304
-
-
Kazlauskaite, J.1
Sanghera, N.2
Sylvester, I.3
Venien-Bryan, C.4
Pinheiro, T.J.5
-
49
-
-
14044250915
-
In vitro conversion of mammalian prion protein into amyloid fibrils displays unusual features
-
I.V. Baskakov, and O.V. Bocharova In vitro conversion of mammalian prion protein into amyloid fibrils displays unusual features Biochemistry 44 2005 2339 2348
-
(2005)
Biochemistry
, vol.44
, pp. 2339-2348
-
-
Baskakov, I.V.1
Bocharova, O.V.2
-
50
-
-
0031575333
-
Prion protein gene variation among primates
-
H.M. Schätzel, M. Da Costa, L. Taylor, F.E. Cohen, and S.B. Prusiner Prion protein gene variation among primates J. Mol. Biol. 265 1997 257
-
(1997)
J. Mol. Biol.
, vol.265
, pp. 257
-
-
Schätzel, H.M.1
Da Costa, M.2
Taylor, L.3
Cohen, F.E.4
Prusiner, S.B.5
-
51
-
-
0029066886
-
Species specificity in the cell-free conversion of prion protein to protease-resistant forms: A model for the scrapie species barrier
-
D.A. Kocisko, S.A. Priola, G.J. Raymond, B. Chesebro, P.T. Lansbury Jr, and B. Caughey Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier Proc. Natl Acad. Sci. USA 92 1995 3923 3927
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 3923-3927
-
-
Kocisko, D.A.1
Priola, S.A.2
Raymond, G.J.3
Chesebro, B.4
Lansbury Jr., P.T.5
Caughey, B.6
-
52
-
-
0030810150
-
Human prion proteins expressed in Escherichia coli and purified by high-affinity column refolding
-
R. Zahn, C. von Schroetter, and K. Wüthrich Human prion proteins expressed in Escherichia coli and purified by high-affinity column refolding FEBS Letters 417 1997 400 404
-
(1997)
FEBS Letters
, vol.417
, pp. 400-404
-
-
Zahn, R.1
Von Schroetter, C.2
Wüthrich, K.3
-
53
-
-
0023472472
-
Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa
-
H. Schagger, and G. von Jagow Tricine-sodium dodecyl sulfate- polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa Anal. Biochem. 166 1987 368 379
-
(1987)
Anal. Biochem.
, vol.166
, pp. 368-379
-
-
Schagger, H.1
Von Jagow, G.2
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