-
1
-
-
0014211846
-
Does the agent of scrapie replicate without nucleic acid?
-
ALPER, T., CRAMP, W. A., HAIG, D. A. & CLARKE, M. C. (1967). Does the agent of scrapie replicate without nucleic acid? Nature 214, 764-766.
-
(1967)
Nature
, vol.214
, pp. 764-766
-
-
Alper, T.1
Cramp, W.A.2
Haig, D.A.3
Clarke, M.C.4
-
2
-
-
0014004625
-
The exceptionally small size of the scrapie agent
-
ALPER, T., HAIG, D. A. & CLARKE, M. C. (1966). The exceptionally small size of the scrapie agent. Biochem. biophys. Res. Commun. 22, 278-284.
-
(1966)
Biochem. Biophys. Res. Commun.
, vol.22
, pp. 278-284
-
-
Alper, T.1
Haig, D.A.2
Clarke, M.C.3
-
3
-
-
0031692336
-
The caveolae membrane system
-
ANDERSON, R. G. (1998). The caveolae membrane system. A. Rev. Biochem. 67, 199-225.
-
(1998)
A. Rev. Biochem.
, vol.67
, pp. 199-225
-
-
Anderson, R.G.1
-
4
-
-
0026545612
-
Potocytosis: Sequestration and transport of small molecules by caveolae
-
ANDERSON, R. G., KAMEN, B. A., ROTHBERG, K. G. & LACEY, S. W. (1992). Potocytosis: sequestration and transport of small molecules by caveolae. Science 225, 410-411.
-
(1992)
Science
, vol.225
, pp. 410-411
-
-
Anderson, R.G.1
Kamen, B.A.2
Rothberg, K.G.3
Lacey, S.W.4
-
5
-
-
0015859467
-
Principles that govern the folding of protein chains
-
ANFINSEN, C. B. (1973). Principles that govern the folding of protein chains. Science 181, 223-230.
-
(1973)
Science
, vol.181
, pp. 223-230
-
-
Anfinsen, C.B.1
-
6
-
-
0029346911
-
The abnormal isoform of the prion proteins accumulates in late-endosome-like organelles in scrapie-infected mouse brain
-
ARNOLD, J. E., TIPLER, C., LASZLO, L., HOPE, J., LANDON, M. & MAYER, R. J. (1995). The abnormal isoform of the prion proteins accumulates in late-endosome-like organelles in scrapie-infected mouse brain. J. Pathol. 176, 403-411.
-
(1995)
J. Pathol.
, vol.176
, pp. 403-411
-
-
Arnold, J.E.1
Tipler, C.2
Laszlo, L.3
Hope, J.L.M.4
Mayer, R.J.5
-
7
-
-
0021836930
-
Antibodies to the scrapie protein decorate prion rods
-
BARRY, R. A., MCKINLEY, M. P., BENDHEIM, P. E., LEWIS, G. K., DEARMOND, S. J. & PRUSINER, S. B. (1985). Antibodies to the scrapie protein decorate prion rods. J. Immunol. 135, 603-613.
-
(1985)
J. Immunol.
, vol.135
, pp. 603-613
-
-
Barry, R.A.1
Mckinley, M.P.2
Bendheim, P.E.3
Lewis, G.K.4
Dearmond, S.J.5
Prusiner, S.B.6
-
8
-
-
0022476747
-
Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene
-
BASLER, K., OESCH, B., SCOTT, M., WESTAWAY, D., WÄLCHI, M., GROTH, D. F., MCKINLEY, M. P., PRUSINER, S. B. & WEISSMANN, C. (1986). Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene. Cell 46, 417-428.
-
(1986)
Cell
, vol.46
, pp. 417-428
-
-
Basler, K.1
Oesch, B.2
Scott, M.3
Westaway, D.4
Wälchi, M.5
Groth, D.F.6
Mckinley, M.P.7
Prusiner, S.B.8
Weissmann, C.9
-
9
-
-
0023888782
-
Scrapie prion liposomes and rods exhibit target sizes of 55,000 Da
-
BELLINGER-KAWAHARA, C. G., KEMPNER, E., GROTH, D., GABIZON. R. & PRUSINER, S. B. (1988). Scrapie prion liposomes and rods exhibit target sizes of 55,000 Da. Virology 164, 537-541.
-
(1988)
Virology
, vol.164
, pp. 537-541
-
-
Bellinger-Kawahara, C.G.1
Kempner, E.2
Groth, D.3
Gabizon, R.4
Prusiner, S.B.5
-
10
-
-
0021193353
-
Antibodies to a scrapie prion protein
-
BENDHEIM, P. E., BARRY, R. A., DEARMOND, S. J., STITES, D. P. & PRUSINER, S. B. (1984). Antibodies to a scrapie prion protein. Nature 310, 418-421.
-
(1984)
Nature
, vol.310
, pp. 418-421
-
-
Bendheim, P.E.1
Barry, R.A.2
Dearmond, S.J.3
Stites, D.P.4
Prusiner, S.B.5
-
11
-
-
0021907721
-
Scrapie and Creutzfeldt Jakob disease prion proteins share physical properties and antigenic determinant
-
BENDHEIM, P. C., BOCKMAN, J. M., MCKINLEY, M. P., KINGSBURY, D. T. & PRUSINER, S. B. (1985). Scrapie and Creutzfeldt Jakob disease prion proteins share physical properties and antigenic determinant. Proc. natn. Acad. Sci. USA 82, 997-1001.
-
(1985)
Proc. Natn. Acad. Sci. USA
, vol.82
, pp. 997-1001
-
-
Bendheim, P.C.1
Bockman, J.M.2
Mckinley, M.P.3
Kingsbury, D.T.4
Prusiner, S.B.5
-
12
-
-
0032429970
-
Minimal and optimal mechanisms tor GroE-mediated protein folding
-
BEN-ZVI, A. P., CHATELLIER, J., FERSHT, A. R. & GOLOUBINOFF, P. (1998). Minimal and optimal mechanisms tor GroE-mediated protein folding. Proc. natn. Acad. Sci. USA 95, 15275-15280.
-
(1998)
Proc. Natn. Acad. Sci. USA
, vol.95
, pp. 15275-15280
-
-
Ben-Zvi, A.P.1
Chatellier, J.2
Fersht, A.R.3
Goloubinoff, P.4
-
13
-
-
0028043661
-
Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy
-
BESSEN, R. A. & MARSH, R. F. (1994). Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy. J. Virol. 68, 7859-7868.
-
(1994)
J. Virol.
, vol.68
, pp. 7859-7868
-
-
Bessen, R.A.1
Marsh, R.F.2
-
14
-
-
0028997297
-
Non-genetic propagation of strain-specific properties of scrapie prion protein
-
BESSEN, R. A., KOCISKO, D. A., RAYMOND, G. J., NANDAN, S., LANSBURY, P. T. & 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
-
15
-
-
0024311951
-
Comparison of the high-resolution structures of the α-amylase inhibitor Tendamistat determined by nuclear magnetic resonance in solution and by X-ray diffraction in single crystals
-
BILLETER, M., KLINE, A. D., BRAUN, W., HUBER, R. & WÜTHRICH, K. (1989). Comparison of the high-resolution structures of the α-amylase inhibitor Tendamistat determined by nuclear magnetic resonance in solution and by X-ray diffraction in single crystals. J. molec. Biol. 206, 677-687.
-
(1989)
J. Molec. Biol.
, vol.206
, pp. 677-687
-
-
Billeter, M.1
Kline, A.D.2
Braun, W.3
Huber, R.4
Wüthrich, K.5
-
16
-
-
0030790431
-
Prion protein NMR structure and species barrier for prion diseases
-
BILLETER, M., RIEK, R., WIDER, G., HORNEMANN, S., GLOCKSHUBER, R. & WÜTHRICH, K. (1997). Prion protein NMR structure and species barrier for prion diseases, Proc. natn. Acad. Sci USA 94, 7281-7285.
-
(1997)
Proc. Natn. Acad. Sci USA
, vol.94
, pp. 7281-7285
-
-
Billeter, M.1
Riek, R.2
Wider, G.3
Hornemann, S.4
Glockshuber, R.5
Wüthrich, K.6
-
17
-
-
0023160676
-
Immunoblotting of Creutzfeldt-Jakob disease prion proteins: Host species-specific epitopes
-
BOCKMAN, J. M., PRUSINER, S. B., TATEISHI, J. & KINGSBURY, D. T. (1987). Immunoblotting of Creutzfeldt-Jakob disease prion proteins: host species-specific epitopes. Ann. Neurol. 21, 589-595.
-
(1987)
Ann. Neurol.
, vol.21
, pp. 589-595
-
-
Bockman, J.M.1
Prusiner, S.B.2
Tateishi, J.3
Kingsbury, D.T.4
-
18
-
-
0023442502
-
Isolation and structural studies of the intact scrapie agent protein
-
BOLTON, D. C., BENDHEIM, P. K., MARMORSTEIN, A. D. & POTEMPSKA, A. (1987). Isolation and structural studies of the intact scrapie agent protein. Arch. Biochem. Biophys. 258, 579-590.
-
(1987)
Arch. Biochem. Biophys.
, vol.258
, pp. 579-590
-
-
Bolton, D.C.1
Bendheim, P.K.2
Marmorstein, A.D.3
Potempska, A.4
-
19
-
-
0020490156
-
Identification of a protein that purifies with the scrapie prion
-
BOLTON, D. C., MCKINLEY, M. P. & PRUSINER, S. B. (1982). Identification of a protein that purifies with the scrapie prion. Science 218, 1309-1311.
-
(1982)
Science
, vol.218
, pp. 1309-1311
-
-
Bolton, D.C.1
Mckinley, M.P.2
Prusiner, S.B.3
-
20
-
-
0021672620
-
Molecular characteristics of the major scrapie prion protein
-
BOLTON, D. C, MCKINLEY, M. P. & PRUSINER, S. B. (1984). Molecular characteristics of the major scrapie prion protein. Biochemistry 23, 5898-5906.
-
(1984)
Biochemistry
, vol.23
, pp. 5898-5906
-
-
Bolton, D.C.1
Mckinley, M.P.2
Prusiner, S.B.3
-
21
-
-
0027291065
-
Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchor
-
BORCHELT, D. R., ROGERS, M., STAHL, N., TELLING, G. & PRUSINER, S. B. (1993). Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchor. Glycobiology 3, 319-329.
-
(1993)
Glycobiology
, vol.3
, pp. 319-329
-
-
Borchelt, D.R.1
Rogers, M.2
Stahl, N.3
Telling, G.4
Prusiner, S.B.5
-
22
-
-
0025304678
-
Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells
-
BORCHELT, D. R., SCOTT, M., TARABOULOUS, A., STAHL., N. & PRUSINER, S. B. (1990). Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells. J. Cell Biol. 110, 743-752.
-
(1990)
J. Cell Biol.
, vol.110
, pp. 743-752
-
-
Borchelt, D.R.1
Scott, M.2
Taraboulous, A.3
Stahl, N.4
Prusiner, S.B.5
-
23
-
-
0026775909
-
Evidence for synthesis of scrapie prion proteins in the endocytic pathway
-
BORCHELT, D. R., TARABOULOS, A. & PRUSINER, S. B. (1992). Evidence for synthesis of scrapie prion proteins in the endocytic pathway. J. biol. Chem. 267, 16188-161199.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 16188-161199
-
-
Borchelt, D.R.1
Taraboulos, A.2
Prusiner, S.B.3
-
24
-
-
0028885711
-
Conformational variability in the refined structure of the chaperonin GroEL at 2-8 Å resolution
-
BRAIG, K., ADAMS, P. D. & BRÜNGER, A. T. (1995). Conformational variability in the refined structure of the chaperonin GroEL at 2-8 Å resolution. Nat. struct. Biol. 2, 1083-1094.
-
(1995)
Nat. Struct. Biol.
, vol.2
, pp. 1083-1094
-
-
Braig, K.1
Adams, P.D.2
Brünger, A.T.3
-
25
-
-
0027943510
-
The crystal structure of the bacterial chaperonin GroEL at 2-8 Å
-
BRAIG, K., OTWINOWSKI, Z., HEGDE, R., BOISVERT, D. C, JOACHIMIAK, A., HORWICH, A. L. & SIGLER, P. B. (1994). The crystal structure of the bacterial chaperonin GroEL at 2-8 Å. Nature 371, 578-586.
-
(1994)
Nature
, vol.371
, pp. 578-586
-
-
Braig, K.1
Otwinowski, Z.2
Hegde, R.3
Boisvert, D.C.4
Joachimiak, A.5
Horwich, A.L.6
Sigler, P.B.7
-
26
-
-
0032169565
-
Prion protein expression and superoxide dismurase activity
-
BROWN, D. R. & BESINGER, A. (1998). Prion protein expression and superoxide dismurase activity. Biochem. J. 334, 423-429.
-
(1998)
Biochem. J.
, vol.334
, pp. 423-429
-
-
Brown, D.R.1
Besinger, A.2
-
27
-
-
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. (1997a). The cellular prion protein binds copper in vivo. Nature 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
-
28
-
-
18344403931
-
Effects of oxidative stress on prion protein expression in PC12 cells
-
BROWN, D. R., SCHMIDT, B. & KRETZSCHMAR, H. A. (1997b). Effects of oxidative stress on prion protein expression in PC12 cells. Int. J. dev. Neurosci. 15, 961-972.
-
(1997)
Int. J. Dev. Neurosci.
, vol.15
, pp. 961-972
-
-
Brown, D.R.1
Schmidt, B.2
Kretzschmar, H.A.3
-
29
-
-
0031194455
-
Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD- 1 activity
-
BROWN, D. R., SCHULZ-SCHAEFFEK, W. J., SCHMIDT, B. & KRETZSCHMAR, H. A. (1997c). 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
Schulz-Schaeffek, W.J.2
Schmidt, B.3
Kretzschmar, H.A.4
-
30
-
-
0033571055
-
Normal prion protein has an activity like that of superoxide dismutase
-
BROWN, D. R., WONG, B.-S., HAFIZ, F., CLIVE, C., HASWELL, S. J. & JONES, I. M. (1999). Normal prion protein has an activity like that of superoxide dismutase. Biochem. J. 344, 1-5.
-
(1999)
Biochem. J.
, vol.344
, pp. 1-5
-
-
Brown, D.R.1
Wong, B.-S.2
Hafiz, F.3
Clive, C.4
Haswell, S.J.5
Jones, I.M.6
-
31
-
-
0025216783
-
Resistance of scrapie infectivity to steam autoclaving after formaldehyde fixation and limited survival after ashing at 360°C: Practical and theoretical implications
-
BROWN, P., LIBERSKI, P. P., WOLFF, A. & GAJDUSEK, D. C. (1990). Resistance of scrapie infectivity to steam autoclaving after formaldehyde fixation and limited survival after ashing at 360°C: practical and theoretical implications. J. infect. Dis. 161, 467-472.
-
(1990)
J. Infect. Dis.
, vol.161
, pp. 467-472
-
-
Brown, P.1
Liberski, P.P.2
Wolff, A.3
Gajdusek, D.C.4
-
32
-
-
0026523132
-
Immunocytochemical localization of heat-shock protein 60-related protein in β-cell secretory granules and its altered distribution in non-obese diabetic mice
-
BRUDZYNSKI, K., MARTINEZ, V. & GUPTA, R. S. (1992). Immunocytochemical localization of heat-shock protein 60-related protein in β-cell secretory granules and its altered distribution in non-obese diabetic mice. Diabetologia 35, 316-324.
-
(1992)
Diabetologia
, vol.35
, pp. 316-324
-
-
Brudzynski, K.1
Martinez, V.2
Gupta, R.S.3
-
33
-
-
0025727072
-
GroE facilitates refolding of citrate synthase by suppressing aggregation
-
BÜCHNER, J., SCHMIDT, M., FUCHS, M., JAENICKE, R., RUDOLPH, R., SCHMID, F. X. & KIEFHABER, T. (1991). GroE facilitates refolding of citrate synthase by suppressing aggregation. Biochemistry 30, 1586-1591.
-
(1991)
Biochemistry
, vol.30
, pp. 1586-1591
-
-
Büchner, J.1
Schmidt, M.2
Fuchs, M.3
Jaenicke, R.4
Rudolph, R.5
Schmid, F.X.6
Kiefhaber, T.7
-
34
-
-
0030966765
-
A structural model for GroEL-polypeptide recognition
-
BUCKLE, A. M., ZAHN, R. & FERSHT, A. R. (1997). A structural model for GroEL-polypeptide recognition. Proc. natn. Acad. Sci. USA 94, 3571-3575.
-
(1997)
Proc. Natn. Acad. Sci. USA
, vol.94
, pp. 3571-3575
-
-
Buckle, A.M.1
Zahn, R.2
Fersht, A.R.3
-
35
-
-
0027319326
-
Mice devoid of PrP are resistant to scrapie
-
BÜELER, H., AGUZZI, A., SAILER, A., GREINER, R.-A., AUTENRIED, P., AGUET, M. & WEISSMANN, C. (1993). Mice devoid of PrP are resistant to scrapie. Cell 73, 1339-1347.
-
(1993)
Cell
, vol.73
, pp. 1339-1347
-
-
Büeler, H.1
Aguzzi, A.2
Sailer, A.3
Greiner, R.-A.4
Autenried, P.5
Aguet, M.6
Weissmann, C.7
-
36
-
-
0023928927
-
Scrapie-infected murine neuroblastoma cells produce protease-resistant prion proteins
-
BUTLER, D. A., SCOTT, M. R., BOCKMAN, J. M., BORCHELT, D. R., TARABOULOS, A., HSIAO, K. K., KINGSBURY, D. T. & PRUSINER, S. B. (1988). Scrapie-infected murine neuroblastoma cells produce protease-resistant prion proteins. J. Virol. 62, 1558-1564.
-
(1988)
J. Virol.
, vol.62
, pp. 1558-1564
-
-
Butler, D.A.1
Scott, M.R.2
Bockman, J.M.3
Borchelt, D.R.4
Taraboulos, A.5
Hsiao, K.K.6
Kingsbury, D.T.7
Prusiner, S.B.8
-
37
-
-
0030756021
-
Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family
-
CAPELLARI, S., VITAL, C., PARCHI, P., PETERSEN, R. B., FERRER, X., JARNIER, D., PEGORARO, E., GAMBETTI, P. & JULIEN, J. (1997). Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family. Neurology 49, 133-141.
-
(1997)
Neurology
, vol.49
, pp. 133-141
-
-
Capellari, S.1
Vital, C.2
Parchi, P.3
Petersen, R.B.4
Ferrer, X.5
Jarnier, D.6
Pegoraro, E.7
Gambetti, P.8
Julien, J.9
-
38
-
-
0022530549
-
Linkage of prion protein and scrapie incubation time genes
-
CARLSON, G. A., KINGSBURY, D. T., GOODMAN, P. A., COLEMAN, S., MARSHALL, S. T., DEARMOND, S., WESTAWAY, D. & PRUSINER, S. B. (1986). Linkage of prion protein and scrapie incubation time genes. Cell 46, 503-511.
-
(1986)
Cell
, vol.46
, pp. 503-511
-
-
Carlson, G.A.1
Kingsbury, D.T.2
Goodman, P.A.3
Coleman, S.4
Marshall, S.T.5
Dearmond, S.6
Westaway, D.7
Prusiner, S.B.8
-
39
-
-
0025212147
-
Cellular isoform of the scrapie agent protein participates in lymphocyte activation
-
CASHMAN, N. R., LOERTSCHER, R., NALBANTOGLU, J., SHAW, I., KASCSAK, R. J., BOLTON, D. C. & BENDHEIM, P. E. (1990). Cellular isoform of the scrapie agent protein participates in lymphocyte activation. Cell 61, 185-192.
-
(1990)
Cell
, vol.61
, pp. 185-192
-
-
Cashman, N.R.1
Loertscher, R.2
Nalbantoglu, J.3
Shaw, I.4
Kascsak, R.J.5
Bolton, D.C.6
Bendheim, P.E.7
-
40
-
-
0025991466
-
The scrapie-associated form of PrP is made from a cell surface precursor that is both protease- and phospholipase-sensitive
-
CAUGHEY, B. & RAYMOND, G. J. (1991). The scrapie-associated form of PrP is made from a cell surface precursor that is both protease- and phospholipase-sensitive. J. biol. Chem. 266, 18217-18223.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 18217-18223
-
-
Caughey, B.1
Raymond, G.J.2
-
41
-
-
0029583794
-
Aggregates of scrapie-associated prion protein induce the cell-free conversion of protease-sensitive prion protein to the protease-resistant state
-
CAUGHEY, B., KOCISKO, D. A., RAYMOND, G. J. & LANSBURY, P. T., JR. (1995). Aggregates of scrapie-associated prion protein induce the cell-free conversion of protease-sensitive prion protein to the protease-resistant state. Chem. Biol. 2, 807-817.
-
(1995)
Chem. Biol.
, vol.2
, pp. 807-817
-
-
Caughey, B.1
Kocisko, D.A.2
Raymond, G.J.3
Lansbury P.T., Jr.4
-
42
-
-
0025193792
-
Normal and scrapie-associated forms of prion protein differ in their sensitivies to phospholipase and proteases in intact neuroblastoma cells
-
CAUGHEY, B., NEARY, K., BULLER, R., ERNST, D., PERRY, L. L., CHESEBRO, B. & RACE, R. E. (1990). Normal and scrapie-associated forms of prion protein differ in their sensitivies to phospholipase and proteases in intact neuroblastoma cells. J. Virol. 64, 1093-1101.
-
(1990)
J. Virol.
, vol.64
, pp. 1093-1101
-
-
Caughey, B.1
Neary, K.2
Buller, R.3
Ernst, D.4
Perry, L.L.5
Chesebro, B.6
Race, R.E.7
-
43
-
-
0024545093
-
Prion protein biosynthesis in scrapie-infected and unintected neuroblastoma cells
-
CAUGHEY, B., RACE, R. E., ERNST, D., BUCHMEIER, M. J. & CHESEBRO, B. (1989). Prion protein biosynthesis in scrapie-infected and unintected neuroblastoma cells. J. Virol. 63, 175-181.
-
(1989)
J. Virol.
, vol.63
, pp. 175-181
-
-
Caughey, B.1
Race, R.E.2
Ernst, D.3
Buchmeier, M.J.4
Chesebro, B.5
-
44
-
-
0025876226
-
N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): Implications regarding the site of conversion ot PrP to the protease-resistant state
-
CAUGHEY, B., RAYMOND, G. J., ERNST, D. & RACE, R. E. (1991b). N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion ot PrP to the protease-resistant state. J. Virol. 65, 6597-6603.
-
(1991)
J. Virol.
, vol.65
, pp. 6597-6603
-
-
Caughey, B.1
Raymond, G.J.2
Ernst, D.3
Race, R.E.4
-
45
-
-
0025944507
-
Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared specrroscopy
-
CAUGHEY, B. W., DONG, A., BHAT, K. S., ERNST, D., HAYES, S. F. & CAUGHEY, W. S. (1991a). Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared specrroscopy. Biochemistry 30, 7672-7680.
-
(1991)
Biochemistry
, vol.30
, pp. 7672-7680
-
-
Caughey, B.W.1
Dong, A.2
Bhat, K.S.3
Ernst, D.4
Hayes, S.F.5
Caughey, W.S.6
-
46
-
-
0028276107
-
The purification of early-pregnancy factor to homogeneity from human platelets and identification as chaperonin 10
-
CAVANAGH, A. C. & MORTON, H. (1994). The purification of early-pregnancy factor to homogeneity from human platelets and identification as chaperonin 10. Eur. J. Biochem. 222, 551-560.
-
(1994)
Eur. J. Biochem.
, vol.222
, pp. 551-560
-
-
Cavanagh, A.C.1
Morton, H.2
-
47
-
-
0032557457
-
Specific inhibition of in vitro formation of protease-resistant prion protein by synthetic peptides
-
CHABKY, J., CAUGHEY, B. & CHESEBRO, B. (1998). Specific inhibition of in vitro formation of protease-resistant prion protein by synthetic peptides. J. biol. Chem. 273, 13203-13207.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 13203-13207
-
-
Chabky, J.1
Caughey, B.2
Chesebro, B.3
-
48
-
-
0000048085
-
Experimental scrapie in mouse
-
CHANDLER, R. L. (1963). Experimental scrapie in mouse. Res. vet. Sci. 4, 276-285.
-
(1963)
Res. Vet. Sci.
, vol.4
, pp. 276-285
-
-
Chandler, R.L.1
-
49
-
-
0033543656
-
GroEL, recognises sequential and non-sequential linear structural motifs compatible with extended β-strands and α-helices
-
CHATELLIER, J., BUCKLE, A. M. & FERSHT, A. R. (1999). GroEL, recognises sequential and non-sequential linear structural motifs compatible with extended β-strands and α-helices. J. molec. Biol. 292, 163-172.
-
(1999)
J. Molec. Biol.
, vol.292
, pp. 163-172
-
-
Chatellier, J.1
Buckle, A.M.2
Fersht, A.R.3
-
50
-
-
0032544101
-
In vitro activities of GroEL minichaperones
-
CHATELLIER, J., HILL, F., LUND, P. A. & FERSHT, A. R. (1998). In vitro activities of GroEL minichaperones. Proc. natn. Acad. Sci. USA 95, 9861-9866
-
(1998)
Proc. Natn. Acad. Sci. USA
, vol.95
, pp. 9861-9866
-
-
Chatellier, J.1
Hill, F.2
Lund, P.A.3
Fersht, A.R.4
-
51
-
-
0028338441
-
Structural clues to prion replication
-
COHEN, F. E., PAN, K.-M., HUANG, Z., BALDWIN, M., FLETTERICK, R. J. & PRUSINER, S. B. (1994). Structural clues to prion replication. Science 264, 530-531.
-
(1994)
Science
, vol.264
, pp. 530-531
-
-
Cohen, F.E.1
Pan, K.-M.2
Huang, Z.3
Baldwin, M.4
Fletterick, R.J.5
Prusiner, S.B.6
-
52
-
-
0029831213
-
Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD
-
COLLINGE, J., SIDLE, K. C. L., MEADS, J., IRONSIDE, J. & HILL, A. F. (1996). Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. Nature 383, 685-690.
-
(1996)
Nature
, vol.383
, pp. 685-690
-
-
Collinge, J.1
Sidle, K.C.L.2
Meads, J.3
Ironside, J.4
Hill, A.F.5
-
53
-
-
0027997387
-
Prion protein is necessary for normal synaptic function
-
COLLINGE, J., WHITTINGTON, M. A., SIDLE, K. C., SMETH, C. J., PALMER, M. S., CLARKE, A. R. & JEFFERYS, J. G. (1994). Prion protein is necessary for normal synaptic function. Nature 370, 295-297.
-
(1994)
Nature
, vol.370
, pp. 295-297
-
-
Collinge, J.1
Whittington, M.A.2
Sidle, K.C.3
Smeth, C.J.4
Palmer, M.S.5
Clarke, A.R.6
Jefferys, J.G.7
-
54
-
-
0027270578
-
A kinetic model for amyloid formation in the prion diseases: Importance of seedling
-
COME, J. H., FRÄSER, P. E. & LANSBURY, P. T., JR. (1993). A kinetic model for amyloid formation in the prion diseases: importance of seedling. Proc. natn. Acad. Sci. USA 90, 5959-5963.
-
(1993)
Proc. Natn. Acad. Sci. USA
, vol.90
, pp. 5959-5963
-
-
Come, J.H.1
Fräser, P.E.2
Lansbury P.T., Jr.3
-
55
-
-
0030334841
-
2 complexes in molecular chaperone activity
-
2 complexes in molecular chaperone activity. Fold. Des. 1, 265-273.
-
(1996)
Fold. Des.
, vol.1
, pp. 265-273
-
-
Corrales, F.J.1
Fersht, A.R.2
-
56
-
-
0029664316
-
Toward a mechanism for GroEL GroES chaperone activity : An ATPase-gated and -pulsed folding and annealing cage
-
CORRALES, F. J. & FERSHT, A. R. (1996b). Toward a mechanism for GroEL GroES chaperone activity : an ATPase-gated and -pulsed folding and annealing cage. I'roc. natn. Acad. Sci. USA 93, 4509-4512.
-
(1996)
I'roc. Natn. Acad. Sci. USA
, vol.93
, pp. 4509-4512
-
-
Corrales, F.J.1
Fersht, A.R.2
-
57
-
-
0000229130
-
Membrane continuities involving chloroplasts and other organelles in plant cells
-
CROTTY, W. J. & LEDBETTER, M. C. (1973). Membrane continuities involving chloroplasts and other organelles in plant cells. Science 182, 839-841.
-
(1973)
Science
, vol.182
, pp. 839-841
-
-
Crotty, W.J.1
Ledbetter, M.C.2
-
58
-
-
0030896803
-
Identification of intermediate steps in the conversion of a mutant prion protein to a scrapie-like form in cultured cells
-
DAUDE, N., LEHMANN, S. & HARRIS, D. A. (1997). Identification of intermediate steps in the conversion of a mutant prion protein to a scrapie-like form in cultured cells. J. biol. Chem. 272, 11604-11612.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 11604-11612
-
-
Daude, N.1
Lehmann, S.2
Harris, D.A.3
-
59
-
-
0021879270
-
Identification of prion amyloid filaments in scrapie-infected brain
-
DEARMOND, S. J., MCKINLEY, M. P., BARRY, R. A., BRAUNFELD, M. B., MCCOLLOCH, J. R. & PRUSINER, S. B. (1985). Identification of prion amyloid filaments in scrapie-infected brain. Cell 41, 221-235.
-
(1985)
Cell
, vol.41
, pp. 221-235
-
-
Dearmond, S.J.1
Mckinley, M.P.2
Barry, R.A.3
Braunfeld, M.B.4
Mccolloch, J.R.5
Prusiner, S.B.6
-
60
-
-
0344222186
-
Selective neuronal targeting in prion disease
-
DEARMOND, S. J., SÁNCHEZ, H., YEHIELY, F., QIU, Y., NINCHAK-CASEY, A., DAGGETT, V., CAMERINO, A. P., CAYETANO, J., ROGERS, M., GROTH, D., TORCHIA, M., TREMBLAY, P., SCOTT, M. R., COHEN, F. F. & PRUSINER, S. B. (1997). Selective neuronal targeting in prion disease. Neuron 19, 1337-1348.
-
(1997)
Neuron
, vol.19
, pp. 1337-1348
-
-
Dearmond, S.J.1
Sánchez, H.2
Yehiely, F.3
Qiu, Y.4
Ninchak-Casey, A.5
Daggett, V.6
Camerino, A.P.7
Cayetano, J.8
Rogers, M.9
Groth, D.10
Torchia, M.11
Tremblay, P.12
Scott, M.R.13
Cohen, F.F.14
Prusiner, S.B.15
-
61
-
-
0031443433
-
Chaperone-supervised conversion of prion protein to its protease-resistant form
-
DEBBURMAN, S. K., RAYMOND, G. J., CAUGHEY, B. & LINDQUIST, S. (1997). Chaperone-supervised conversion of prion protein to its protease-resistant form. Proc. natn. Acad. Sci. USA 94, 13938-13943.
-
(1997)
Proc. Natn. Acad. Sci. USA
, vol.94
, pp. 13938-13943
-
-
Debburman, S.K.1
Raymond, G.J.2
Caughey, B.3
Lindquist, S.4
-
62
-
-
0028301577
-
Conformational polymorphism ot the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein
-
DE GIOLA, L., SELVAGGINI, C., GHIBAUDI, E., DIOMEDE, L., BUGIANI, O., FORLONI, G., TAGLIAVINI, F. & SALMONA, M. (1994). Conformational polymorphism ot the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein. J. biol. Cliem. 269, 7859-7862.
-
(1994)
J. Biol. Cliem.
, vol.269
, pp. 7859-7862
-
-
De Giola, L.1
Selvaggini, C.2
Ghibaudi, E.3
Diomede, L.4
Bugiani, O.5
Forloni, G.6
Tagliavini, F.7
Salmona, M.8
-
63
-
-
0021036329
-
Scrapie infectivity, fibrils and low molecular weight protein
-
DIRINGER, H., GELDERBLOM, H., HILMERT, H., ÖZEL, M., EDELBLUTH, C. & KIMBERLIN, R. H. (1983). Scrapie infectivity, fibrils and low molecular weight protein. Nature 306, 476-478.
-
(1983)
Nature
, vol.306
, pp. 476-478
-
-
Diringer, H.1
Gelderblom, H.2
Hilmert, H.3
Özel, M.4
Edelbluth, C.5
Kimberlin, R.H.6
-
64
-
-
0024473899
-
Pro-leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann Sträussler syndrome
-
DOH-URA, K., TATEISHI, J., SASAKI, H., KITAMOTO, T. & SAKAKI, Y. (1989). Pro-leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann Sträussler syndrome. Biochem. biophys. Res. Commun. 163, 974-979.
-
(1989)
Biochem. Biophys. Res. Commun.
, vol.163
, pp. 974-979
-
-
Doh-Ura, K.1
Tateishi, J.2
Sasaki, H.3
Kitamoto, T.4
Sakaki, Y.5
-
65
-
-
0031456947
-
Structure of the recombinant full-length hamster prion protein PrP(29-231): The N terminus is highly flexible
-
DONNE, D. G., VILES, J. H., GROTH, D., MEHLHORN, I., JAMES, T. L., COHEN, F. E., PRUSINER, S. B., WRIGHT, P. H. & DYSON, H. J. (1997). Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible. Proc. natn. Acad. Sci. USA 94, 13452-13457.
-
(1997)
Proc. Natn. Acad. Sci. USA
, 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.H.8
Dyson, H.J.9
-
66
-
-
0023062990
-
Protein serine/threonine kinases
-
EDELMAN, A. M., BLUMENTHAL, D. K. & KREBS, E. G. (1987). Protein serine/threonine kinases. A. Rev. Biochem. 56, 567-613.
-
(1987)
A. Rev. Biochem.
, vol.56
, pp. 567-613
-
-
Edelman, A.M.1
Blumenthal, D.K.2
Krebs, E.G.3
-
68
-
-
0030579560
-
Prionics or the kinetic basis of prion diseases
-
EIGEN, M. (1996). Prionics or the kinetic basis of prion diseases. Biophys. Chem. 63, A1-18.
-
(1996)
Biophys. Chem.
, vol.63
-
-
Eigen, M.1
-
69
-
-
0004167360
-
-
San Diego: Academic Press
-
ELLIS, R. J. (1996). The chaperonins. San Diego: Academic Press.
-
(1996)
The Chaperonins
-
-
Ellis, R.J.1
-
70
-
-
0024506867
-
The molecular chaperone concept
-
ELLIS, R. J., VAN DER VIES, S. M. & HEMMINGSEN, S. M. (1989). The molecular chaperone concept. Biochem. Soc. Symp. 55, 145-153.
-
(1989)
Biochem. Soc. Symp.
, vol.55
, pp. 145-153
-
-
Ellis, R.J.1
Van Der Vies, S.M.2
Hemmingsen, S.M.3
-
71
-
-
0024434503
-
Diversity of oligosaccharide structures linked to asparagines of the scrapie priori protein
-
ENDO, T., GROTH, D., PRUSINER, S. B. & KOBATA, A. (1989). Diversity of oligosaccharide structures linked to asparagines of the scrapie priori protein. Biochemistry 28, 8380-8388.
-
(1989)
Biochemistry
, vol.28
, pp. 8380-8388
-
-
Endo, T.1
Groth, D.2
Prusiner, S.B.3
Kobata, A.4
-
72
-
-
0030910349
-
GroEL-mediated protein folding
-
FENTON, W. A. & HORNWICH, A. L. (1997). GroEL-mediated protein folding. Protein Sci. 6, 743-760.
-
(1997)
Protein Sci.
, vol.6
, pp. 743-760
-
-
Fenton, W.A.1
Hornwich, A.L.2
-
73
-
-
0028113299
-
Residues in chaperonin GroEL required for polypeptide binding and release
-
FENTON, W. A., KASHI, Y., FURTAK, K. & HORWICH, A. L. (1994). Residues in chaperonin GroEL required for polypeptide binding and release. Nature 371, 614-619.
-
(1994)
Nature
, vol.371
, pp. 614-619
-
-
Fenton, W.A.1
Kashi, Y.2
Furtak, K.3
Horwich, A.L.4
-
74
-
-
0030790687
-
Common themes in microbial pathogenicity revisited
-
FINLAY, B. B. & FALKOW, S. (1997). Common themes in microbial pathogenicity revisited. Microbiol. mol. Biol. Rev. 61, 136-169.
-
(1997)
Microbiol. Mol. Biol. Rev.
, vol.61
, pp. 136-169
-
-
Finlay, B.B.1
Falkow, S.2
-
75
-
-
0029863648
-
Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie
-
FISCHER, M., RÜLICKE, T., RAEBER, A., SAILER, A., MOSER, M., OESCH, B., BRANDNER, S., AGUZZI, A. & WEISSMANN, C. (1996). Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. EMBO J. 15, 1255-1264.
-
(1996)
EMBO J.
, vol.15
, pp. 1255-1264
-
-
Fischer, M.1
Rülicke, T.2
Raeber, A.3
Sailer, A.4
Moser, M.5
Oesch, B.6
Brandner, S.7
Aguzzi, A.8
Weissmann, C.9
-
76
-
-
0027483615
-
Neurotoxicity of a prion protein fragment
-
FORLONI, G., ANGERETTI, N., CHIESA, R., MONZANI, E., SALMONA, M., BUGLANI, O. & TAGLIAVINI, F. (1993). Neurotoxicity of a prion protein fragment. Nature 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
Buglani, O.6
Tagliavini, F.7
-
77
-
-
0014308027
-
The sequential development of the brain lesion of scrapie in three strains of mice
-
FRASER, H. & DICKINSON, A. G. (1968). The sequential development of the brain lesion of scrapie in three strains of mice. J. comp. Pathol. 78, 301-311.
-
(1968)
J. Comp. Pathol.
, vol.78
, pp. 301-311
-
-
Fraser, H.1
Dickinson, A.G.2
-
78
-
-
0343364948
-
Purified prion proteins and scrapie infectivity copartition into liposomes
-
GABIZON, R., MCKINLEY, M. P., PRUSINER, S. B. (1987). Purified prion proteins and scrapie infectivity copartition into liposomes. Proc. natn. Acad. Sci. USA 84, 4017-4021.
-
(1987)
Proc. Natn. Acad. Sci. USA
, vol.84
, pp. 4017-4021
-
-
Gabizon, R.1
Mckinley, M.P.2
Prusiner, S.B.3
-
79
-
-
0030069023
-
Insoluble wild-type and protease-resisrant mutant prion protein in brains of patients with inherited prion disease
-
GABIZON, R., TELLING, G., MEINER, Z., HALIMI, M., KAHANA, I. & PRUSINER, S. B. (1996). Insoluble wild-type and protease-resisrant mutant prion protein in brains of patients with inherited prion disease. Nat. Med. 2, 59-64.
-
(1996)
Nat. Med.
, vol.2
, pp. 59-64
-
-
Gabizon, R.1
Telling, G.2
Meiner, Z.3
Halimi, M.4
Kahana, I.5
Prusiner, S.B.6
-
80
-
-
0027388993
-
Perturbation of the secondary structure of the srapie prion protein under conditions that alter infectivity
-
GASSET, M., BALDWIN, M. A., FLETTERICK, R. J. & PRUSINER, S. B. (1993). Perturbation of the secondary structure of the srapie prion protein under conditions that alter infectivity. Proc. natn. Acad. Sci. USA 90, 1-5.
-
(1993)
Proc. Natn. Acad. Sci. USA
, vol.90
, pp. 1-5
-
-
Gasset, M.1
Baldwin, M.A.2
Fletterick, R.J.3
Prusiner, S.B.4
-
81
-
-
0026442278
-
Predicted α-helical regions of the prion protein when synthesized as peptides trom amyloid
-
GASSET, M., BALDWIN, M. A., LLOYD, D. H., GABRIEL, J.-M., HOLTZMAN, D. M., COHEN, F., FLETTERICK, R. & PRUSINER, S. B. (1992). Predicted α-helical regions of the prion protein when synthesized as peptides trom amyloid. Proc. natn. Acad. Sci. USA 89, 10940-10944.
-
(1992)
Proc. Natn. Acad. Sci. USA
, vol.89
, pp. 10940-10944
-
-
Gasset, M.1
Baldwin, M.A.2
Lloyd, D.H.3
Gabriel, J.-M.4
Holtzman, D.M.5
Cohen, F.6
Fletterick, R.7
Prusiner, S.B.8
-
82
-
-
0023109951
-
Deamidation, isomerization, and racemization at asparaginyl and aspartyl residues in peptides. Succinimide-linked reactions that contribute to protein degradation
-
GEIGER, T. & CLARKE, S. (1987). Deamidation, isomerization, and racemization at asparaginyl and aspartyl residues in peptides. Succinimide-linked reactions that contribute to protein degradation. J. biol. Chem. 262, 785-794.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 785-794
-
-
Geiger, T.1
Clarke, S.2
-
83
-
-
15844415943
-
Prion protein amyloidosis
-
GHETTI, B., PICCARDO, P., FRANGIONE, B., BUGIANI, O., GIACCONE, G., YOUNG, K., PRELLI, F., FARLOW, M. R., DLOUHY, S. R. & TAGLIAVINI, F. (1996). Prion protein amyloidosis. Brain Pathol. 6, 127-145.
-
(1996)
Brain Pathol.
, vol.6
, pp. 127-145
-
-
Ghetti, B.1
Piccardo, P.2
Frangione, B.3
Bugiani, O.4
Giaccone, G.5
Young, K.6
Prelli, F.7
Farlow, M.R.8
Dlouhy, S.R.9
Tagliavini, F.10
-
84
-
-
0018215610
-
Unusual resistance to ionizing radiation of the viruses of kuru, Creutzfeldt-Jakob disease, and scrapie
-
GIBBS, C. J., JR., GAJDUSEK, D. C. & LATARJET, R. (1978). Unusual resistance to ionizing radiation of the viruses of kuru, Creutzfeldt-Jakob disease, and scrapie. Proc. natn. Acad. Sci USA 75, 6268-6270.
-
(1978)
Proc. Natn. Acad. Sci USA
, vol.75
, pp. 6268-6270
-
-
Gibbs C.J., Jr.1
Gajdusek, D.C.2
Latarjet, R.3
-
85
-
-
0031183651
-
Three-dimensional NMR structure of a self-folding domain of the prion protein PrP(121 231)
-
GLOCKSHUBER, R., HORNEMANX, S., RIEK, R., WIDER, G., BILLETER, M. & WÜTHRICH, K. (1997). Three-dimensional NMR structure of a self-folding domain of the prion protein PrP(121 231). Trends biochem. Sci. 22, 241-242.
-
(1997)
Trends Biochem. Sci.
, vol.22
, pp. 241-242
-
-
Glockshuber, R.1
Hornemanx, S.2
Riek, R.3
Wider, G.4
Billeter, M.5
Wüthrich, K.6
-
86
-
-
0032548994
-
Thermodynamic stability and folding of GroEL minichaperones
-
GOLBIK, R., ZAHN, R., HARDING, S. E. & FERSHT, A. R. (1998). Thermodynamic stability and folding of GroEL minichaperones. J. molec. Biol. 276, 505-515.
-
(1998)
J. Molec. Biol.
, vol.276
, pp. 505-515
-
-
Golbik, R.1
Zahn, R.2
Harding, S.E.3
Fersht, A.R.4
-
87
-
-
0027159497
-
Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils
-
GOLDFARB, L. G., BROWN, P., HALTIA, M., GHISO, J., FRANGIONE, B. & GAJDUSEK, D. C. (1993). Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils. Proc. natn. Acad. Sci. USA 90, 4451-4454.
-
(1993)
Proc. Natn. Acad. Sci. USA
, vol.90
, pp. 4451-4454
-
-
Goldfarb, L.G.1
Brown, P.2
Haltia, M.3
Ghiso, J.4
Frangione, B.5
Gajdusek, D.C.6
-
88
-
-
0024467653
-
Mutations in familial Creutzfeldt-Jakob disease and Gerstmann Sträussler Scheinker's syndrome
-
GOLDGABER, D., GOLDFARB, L. G., BROWN, P., ASHER, D. M., BROWN, W. T., LIN, S., TEENER, J. W., FEINSTONE, S. M., RUBENSTEIN, R., KASCSAK, R. J., BOELLAARD J. W. & GAJDUSEK, D. C (1989). Mutations in familial Creutzfeldt-Jakob disease and Gerstmann Sträussler Scheinker's syndrome. Exp. Neurol. 106, 204-206.
-
(1989)
Exp. Neurol.
, vol.106
, pp. 204-206
-
-
Goldgaber, D.1
Goldfarb, L.G.2
Brown, P.3
Asher, D.M.4
Brown, W.T.5
Lin, S.6
Teener, J.W.7
Feinstone, S.M.8
Rubenstein, R.9
Kascsak, R.J.10
Boellaard, J.W.11
Gajdusek, D.C.12
-
89
-
-
0024820705
-
Reconstitution of active dimeric ribulose biphosphate carboxylase from an unfolded state depends on two chaperonin proteins and Mg-ATP
-
GOLOUBINOFF, P., CHRISTELLER, J. T., GATENBY, A. A. & LORIMER, G. H. (1989). Reconstitution of active dimeric ribulose biphosphate carboxylase from an unfolded state depends on two chaperonin proteins and Mg-ATP. Nature 342, 884-889.
-
(1989)
Nature
, vol.342
, pp. 884-889
-
-
Goloubinoff, P.1
Christeller, J.T.2
Gatenby, A.A.3
Lorimer, G.H.4
-
90
-
-
0025005940
-
Secondary structure and dosage of soluble and membrane proteins by attenuated total reflection Fourier-transform infrared spectroscopy on hydrated films
-
GOORMAGHTIGH, E., CABIAUX, V. & RUYSSCHAERT, J. M. (1990). Secondary structure and dosage of soluble and membrane proteins by attenuated total reflection Fourier-transform infrared spectroscopy on hydrated films. Eur. J. Biocbem. 193, 409-420.
-
(1990)
Eur. J. Biocbem.
, vol.193
, pp. 409-420
-
-
Goormaghtigh, E.1
Cabiaux, V.2
Ruysschaert, J.M.3
-
91
-
-
0028926204
-
Glycolipid-anchored proteins in neuroblastoma cells form detergent-resistant complexes without caveolin
-
GORODINSKY, A. & HARRIS, D. A. (1995). Glycolipid-anchored proteins in neuroblastoma cells form detergent-resistant complexes without caveolin. J. Cell Biol. 129, 619-627.
-
(1995)
J. Cell Biol.
, vol.129
, pp. 619-627
-
-
Gorodinsky, A.1
Harris, D.A.2
-
92
-
-
0014190760
-
Self-replication and scrapie
-
GRIFFITTH, J. S. (1967). Self-replication and scrapie. Nature 215, 1043-1044.
-
(1967)
Nature
, vol.215
, pp. 1043-1044
-
-
Griffitth, J.S.1
-
94
-
-
0024744915
-
Asparagine-linked glycosylation of the scrapie and cellular prion proteins
-
HARAGUCHI, T., FISHER, S., OLOFSSON, S., ENDO, T., GROTH, D., TARENTINO, A., BORCHELT, D. R., TEPLOW, D., HOOD, L., BURLINGAME, A., LYCKE, E., KOBATA, A. & PRUSINER, S. B. (1989). Asparagine-linked glycosylation of the scrapie and cellular prion proteins. Archs. Biochem. Biophys. 274, 1-13.
-
(1989)
Archs. Biochem. Biophys.
, vol.274
, pp. 1-13
-
-
Haraguchi, T.1
Fisher, S.2
Olofsson, S.3
Endo, T.4
Groth, D.5
Tarentino, A.6
Borchelt, D.R.7
Teplow, D.8
Hood, L.9
Burlingame, A.10
Lycke, E.11
Kobata, A.12
Prusiner, S.B.13
-
96
-
-
0029655950
-
Cell biology of the prion protein
-
HARRIS, D. A., GORODINSKY, A., LEHMANN, S., MOULDER, K. & SHYNG, S. L. (1996). Cell biology of the prion protein. Curr. Top. microbiol. Immunol. 207, 77-93.
-
(1996)
Curr. Top. Microbiol. Immunol.
, vol.207
, pp. 77-93
-
-
Harris, D.A.1
Gorodinsky, A.2
Lehmann, S.3
Moulder, K.4
Shyng, S.L.5
-
97
-
-
0029992278
-
Molecular chaperones in cellular protein folding
-
HARTL, F. U. (1996). Molecular chaperones in cellular protein folding. Nature 381, 571-580.
-
(1996)
Nature
, vol.381
, pp. 571-580
-
-
Hartl, F.U.1
-
98
-
-
0023830814
-
67Copper by two ligand-dependent saturable processes. A high affinity, low capacity and a low affinity, high capacity process
-
67Copper by two ligand-dependent saturable processes. A high affinity, low capacity and a low affinity, high capacity process. J. biol. Chem. 263, 799-805.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 799-805
-
-
Hartter, D.E.1
Barnea, A.2
-
99
-
-
0023098327
-
Biogenesis and transmembrane orientation of the cellular isoform of the scrapie prion protein
-
HAY, B., BARRY, R. A., LIEBERBURG, I., PRUSINER, S. B. & LINGAPPA, V. R. (1987a). Biogenesis and transmembrane orientation of the cellular isoform of the scrapie prion protein. Mol. Cell Biol. 7, 914-920.
-
(1987)
Mol. Cell Biol.
, vol.7
, pp. 914-920
-
-
Hay, B.1
Barry, R.A.2
Lieberburg, I.3
Prusiner, S.B.4
Lingappa, V.R.5
-
100
-
-
0023566948
-
Evidence for a secretory form of the cellular prion protein
-
HAY, B., PRUSINER, S. B. & LINGAPPA, V. R. (1987b). Evidence for a secretory form of the cellular prion protein. Biochemistry 26, 8110-8115.
-
(1987)
Biochemistry
, vol.26
, pp. 8110-8115
-
-
Hay, B.1
Prusiner, S.B.2
Lingappa, V.R.3
-
101
-
-
0028334547
-
Conformational specificity of the chaperonin GroEL for the compact folding intermediates of α-lactalbumin
-
HAYER-HARTL, M. K., EWBANK, J. J., CREIGHTON, T. E. & HARTL, F. U. (1994). Conformational specificity of the chaperonin GroEL for the compact folding intermediates of α-lactalbumin. EMBO J. 13, 3192-3202.
-
(1994)
EMBO J.
, vol.13
, pp. 3192-3202
-
-
Hayer-Hartl, M.K.1
Ewbank, J.J.2
Creighton, T.E.3
Hartl, F.U.4
-
102
-
-
0026729945
-
Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters
-
HECKER, R., TARABOULOS, A., SCOTT, M., PAN, K.-M., YANG, S.-L., TORCHIA, M., JENDROSKA, K., DEARMOND, S. J. & PRUSINER, S. B. (1992). Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters. Genes Dev: 6, 1213-1228.
-
(1992)
Genes Dev
, vol.6
, pp. 1213-1228
-
-
Hecker, R.1
Taraboulos, A.2
Scott, M.3
Pan, K.-M.Y.S.-L.4
Torchia, M.5
Jendroska, K.6
Dearmond, S.J.7
Prusiner, S.B.8
-
103
-
-
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. (1998). A transmembrane form of the prion protein in neurodegenerative disease. Science 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
-
104
-
-
0033576323
-
Transmissible and genetic prion diseases share a common pathway of neurodegeneration
-
HEGDE, R. S., TREMBLAY, P., GROTH, D., DEARMOND, S. J., PRUSINER, S. B. & LINGAPPA, V. R. (1999). Transmissible and genetic prion diseases share a common pathway of neurodegeneration. Nature 402, 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
-
105
-
-
0030035952
-
Solid-state NMR studies of the prion protein 111 fragment
-
HELLER, J., KOLBERT, A. C., LARSEN, R., ERNST, M., BEKKER, T., BALDWIN, M., PRUSINER, S. B., PINES, A. & WEMMER, D. E. (1996). Solid-state NMR studies of the prion protein 111 fragment. Protein Sci. 5, 1655-1661.
-
(1996)
Protein Sci.
, vol.5
, pp. 1655-1661
-
-
Heller, J.1
Kolbert, A.C.2
Larsen, R.3
Ernst, M.4
Bekker, T.5
Baldwin, M.6
Prusiner, S.B.7
Pines, A.8
Wemmer, D.E.9
-
106
-
-
0032479890
-
The importance of the disulfide bond in prion protein conversion
-
HERRMANN, L. M. & CAUGHEY, B. (1998). The importance of the disulfide bond in prion protein conversion. Neuroreport 9, 2457-2461.
-
(1998)
Neuroreport
, vol.9
, pp. 2457-2461
-
-
Herrmann, L.M.1
Caughey, B.2
-
107
-
-
0032892306
-
Protease-resistant prion protein produced in vitro lacks detectable infectivity
-
HILL, A. F., ANTONIOU, M. & COLLINGE, J. (1999). Protease-resistant prion protein produced in vitro lacks detectable infectivity. J. gen. Virol. 80, 11-14.
-
(1999)
J. Gen. Virol.
, vol.80
, pp. 11-14
-
-
Hill, A.F.1
Antoniou, M.2
Collinge, J.3
-
108
-
-
0022802258
-
The major polypeptide of scrapie-associated fibrils (SAF) has the same size, charge distribution and N-terminal protein sequence as predicted for the normal brain protein (PrP)
-
HOPE, J., MORTON, L. J. D., FARQUHAR, C. F., MULTHAUP, G., BEYREUTHER, K. & KIMBERLIN, R. H. (1986). The major polypeptide of scrapie-associated fibrils (SAF) has the same size, charge distribution and N-terminal protein sequence as predicted for the normal brain protein (PrP). EMBO J. 5, 2591-2597.
-
(1986)
EMBO J.
, vol.5
, pp. 2591-2597
-
-
Hope, J.1
Morton, L.J.D.2
Farquhar, C.F.3
Multhaup, G.4
Beyreuther, K.5
Kimberlin, R.H.6
-
109
-
-
0023975851
-
Molecular pathology of scrapic-associated fibril protein (PrP) in mouse brain affected by the ME7 strain of scrapie
-
HOPE, J., MULTHAUP, G., REEKIE, L. J. D., KIMBERLIN, R. H. & BEYREUTHER, K. (1988). Molecular pathology of scrapic-associated fibril protein (PrP) in mouse brain affected by the ME7 strain of scrapie. Eur: J. Biochem. 172, 271-277.
-
(1988)
Eur: J. Biochem.
, vol.172
, pp. 271-277
-
-
Hope, J.1
Multhaup, G.2
Reekie, L.J.D.3
Kimberlin, R.H.4
Beyreuther, K.5
-
110
-
-
0033564204
-
Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state
-
HORIUCHI, M. & CAUGHEY, B. (1999a). Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state. EMBO J. 18, 3193-3203.
-
(1999)
EMBO J.
, vol.18
, pp. 3193-3203
-
-
Horiuchi, M.1
Caughey, B.2
-
111
-
-
0033570204
-
Prion protein interconversions and the transmissible spongiform encephalopathies
-
HORIUCHI, M. & CAUGHEY, B. (1999b). Prion protein interconversions and the transmissible spongiform encephalopathies. Structure Fold. Des. 7, R231-R240.
-
(1999)
Structure Fold. Des.
, vol.7
-
-
Horiuchi, M.1
Caughey, B.2
-
112
-
-
0030572627
-
Autonomous and reversible folding ot a soluble amino-terminally truncated segment of the mouse prion protein
-
HORNEMANN, S. & GLOCKSHUBER, R. (1996). Autonomous and reversible folding ot a soluble amino-terminally truncated segment of the mouse prion protein. J. molec. Biol. 261, 614-619.
-
(1996)
J. Molec. Biol.
, vol.261
, pp. 614-619
-
-
Hornemann, S.1
Glockshuber, R.2
-
113
-
-
0032568592
-
A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH
-
HORNEMANN, S. & GLOCKSHUBER, R. (1998). A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH. Proc. natn. Acad. Sci. USA 95, 6010-6014.
-
(1998)
Proc. Natn. Acad. Sci. USA
, vol.95
, pp. 6010-6014
-
-
Hornemann, S.1
Glockshuber, R.2
-
114
-
-
0028883341
-
Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein
-
HORNSHAW, M. P., MCDERMOTT, J. R. & CANDY, J. M. (1995). Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein. Biochem. biopbys. Res. Commun. 207, 621-629.
-
(1995)
Biochem. Biopbys. Res. Commun.
, vol.207
, pp. 621-629
-
-
Hornshaw, M.P.1
Mcdermott, J.R.2
Candy, J.M.3
-
115
-
-
0024519771
-
Linkage of a prion protein missense variant to Gerstmann Sträussler syndrome
-
HSIAO, K., BAKER, H. P., CROW, T. J., POULTER, M., OWEN, F., TERWILLIGER, J. D., WESTAWAY, D., OTT, J. & PRUSINER, S. B. (1989). Linkage of a prion protein missense variant to Gerstmann Sträussler syndrome. Nature 338, 342-345.
-
(1989)
Nature
, vol.338
, pp. 342-345
-
-
Hsiao, K.1
Baker, H.P.2
Crow, T.J.3
Poulter, M.4
Owen, F.5
Terwilliger, J.D.6
Westaway, D.7
Ott, J.8
Prusiner, S.B.9
-
116
-
-
0025847141
-
A prion protein variant in a family with the telencephalic form of Gerstmann Sträussler Scheinker syndrome
-
HSIAO, K. K., CASS, C., SCHELLENBERG, G. D., BIRD, T., DEVINE-GAGE, E., WISNIEWSKI, H. & PRUSINER, S. B. (1991). A prion protein variant in a family with the telencephalic form of Gerstmann Sträussler Scheinker syndrome, Neurology 41, 681-684.
-
(1991)
Neurology
, vol.41
, pp. 681-684
-
-
Hsiao, K.K.1
Cass, C.2
Schellenberg, G.D.3
Bird, T.4
Devine-Gage, E.5
Wisniewski, H.6
Prusiner, S.B.7
-
117
-
-
0028608963
-
Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein
-
HSIAO, K. K., GROTH, D., SCOTT, M., YANG, S.-L., SERBAN, H., RAPP, D., FOSTER, D., TORCHIA, M., DEARMOND, S. J. & PRUSINER, S. B. (1994). Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein. Proc. natn. Acad. Sci. USA 91, 9126-9130.
-
(1994)
Proc. Natn. Acad. Sci. USA
, vol.91
, pp. 9126-9130
-
-
Hsiao, K.K.1
Groth, D.2
Scott, M.3
Yang, S.-L.4
Serban, H.5
Rapp, D.6
Foster, D.7
Torchia, M.8
Dearmond, S.J.9
Prusiner, S.B.10
-
118
-
-
0025681138
-
Spontaneous neurodegeneration in transgenic mice with mutant prion protein
-
HSIAO, K. K., SCOTT, M., FOSTER, D., GROTH, D. F., DEARMOND, S. J. & PRUSINER, S. B. (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
-
119
-
-
0028339962
-
Proposed three-dimensional structure for the cellular prion protein
-
HUANG, Z., GABRIEL, J.-M., BALDWIN, M. A., FLETTERICK, R. J., PRUSINER, S. B. & COHEN, F. E. (1994). Proposed three-dimensional structure for the cellular prion protein. Proc. natn. Acad. Sci. USA 91, 7139-7143.
-
(1994)
Proc. Natn. Acad. Sci. USA
, vol.91
, pp. 7139-7143
-
-
Huang, Z.1
Gabriel, J.-M.2
Baldwin, M.A.3
Fletterick, R.J.4
Prusiner, S.B.5
Cohen, F.E.6
-
120
-
-
0030342679
-
Scrapie prions: A three-dimensional model of an infectious fragment
-
HUANG, Z., PRUSINER, S. B. & COHEN, F. E. (1995). Scrapie prions: a three-dimensional model of an infectious fragment. Fold. Des. 1, 13-19.
-
(1995)
Fold. Des.
, vol.1
, pp. 13-19
-
-
Huang, Z.1
Prusiner, S.B.2
Cohen, F.E.3
-
121
-
-
0030067634
-
The crystal structure of the GroES co-chaperonin at 2-8 Å resolution
-
HUNT, J. F., WEAVER, A. J., LANDRY, S. J., GIERASCH, L. & DEISENHOFER, J. (1996). The crystal structure of the GroES co-chaperonin at 2-8 Å resolution. Nature 379, 37-45.
-
(1996)
Nature
, vol.379
, pp. 37-45
-
-
Hunt, J.F.1
Weaver, A.J.2
Landry, S.J.3
Gierasch, L.4
Deisenhofer, J.5
-
123
-
-
0031547975
-
X-ray diffraction analysis of scrapie prion : Intermediate and folded structures in a peptide containing two putative α-helices
-
INOUYE, H. & KIRSCHNER, D. A. (1997). X-ray diffraction analysis of scrapie prion : intermediate and folded structures in a peptide containing two putative α-helices. J. molec. Biol. 268, 375-389.
-
(1997)
J. Molec. Biol.
, vol.268
, pp. 375-389
-
-
Inouye, H.1
Kirschner, D.A.2
-
124
-
-
0031707767
-
Polypeptide chain folding in the Hydrophobic core of hamster scrapie prion: Analysis by X-ray diffraction
-
INOUYE, H. & KIRSCHNER, D. A. (1998). Polypeptide chain folding in the Hydrophobic core of hamster scrapie prion: analysis by X-ray diffraction. J. struct. Biol. 122, 247-255.
-
(1998)
J. Struct. Biol.
, vol.122
, pp. 247-255
-
-
Inouye, H.1
Kirschner, D.A.2
-
125
-
-
0028792612
-
Nature and consequences ot GroEL protein interactions
-
ITZHAKI, L. S., OTZEN, D. E. & FERSHT, A. R. (1995). Nature and consequences ot GroEL protein interactions. Biochemistry 34, 14581-14587.
-
(1995)
Biochemistry
, vol.34
, pp. 14581-14587
-
-
Itzhaki, L.S.1
Otzen, D.E.2
Fersht, A.R.3
-
126
-
-
0032933448
-
Multiple folding pathways for heterologously expressed human prion protein
-
JACKSON, G. S., HILL, A. F., IOSEPH, C., HOSSZU, L., POWER, A., WALTHO, J. P., CLARKE, A. R. & COLLINGE, J. (1999a). Multiple folding pathways for heterologously expressed human prion protein. Biochem. biophys. Acta 1431, 1-13.
-
(1999)
Biochem. Biophys. Acta
, vol.1431
, pp. 1-13
-
-
Jackson, G.S.1
Hill, A.F.2
Ioseph, C.3
Hosszu, L.4
Power, A.5
Waltho, J.P.6
Clarke, A.R.7
Collinge, J.8
-
127
-
-
0033583190
-
Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations
-
199b
-
JACKSON, G. S., HOSSZU, L. L., POWER, A., HILL, A. F., KENNEY, J., SAIBIL, H., CRAVEN, C. J., WALTHO, J. P., CLARKE, A. R. & COLLINGE, J. (199b). Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations. Science 283, 1935-1937.
-
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
-
128
-
-
0022555883
-
Refolding and association of oligomeric proteins
-
JAENICKE, R. & RUDOLPH, R. (1986). Refolding and association of oligomeric proteins. Methods Enzymol. 131, 218-250.
-
(1986)
Methods Enzymol.
, vol.131
, pp. 218-250
-
-
Jaenicke, R.1
Rudolph, R.2
-
129
-
-
0030967895
-
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
-
JAMES, T. L., LIU, H., ULYANOV, N. B., FARR-JONES, S., ZHANG, H., DONNE, D. G., KANEKO, K., GROTH, D., MEHLHORN, J., PRUSINER, S. B. & COHEN, F. E. (1997). Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform. Proc. natn. Acad. Sci. USA 94, 10086-10091.
-
(1997)
Proc. Natn. 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
Kaneko, K.7
Groth, D.8
Mehlhorn, J.9
Prusiner, S.B.10
Cohen, F.E.11
-
130
-
-
0027195933
-
Seeding 'one-dimensional crystallization' of amyloid: A pathogenic mechanism in Alzheimer's disease and scrapie?
-
JARRETT, J. T. & LANSBURY, P. T., JR. (1993). Seeding 'one-dimensional crystallization' of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie? Ceil 73, 1055-1058.
-
(1993)
Ceil
, vol.73
, pp. 1055-1058
-
-
Jarrett, J.T.1
Lansbury P.T., Jr.2
-
131
-
-
0028158395
-
Enhancement in amount ot P1 (hsp60) in mutants of Chinese hamster ovary (CHO K1) cells exhibiting increases in the A system of amino acid transport
-
JONES, M., GUPTA, R. S. & EAGLESBERG, E. (1994). Enhancement in amount ot P1 (hsp60) in mutants of Chinese hamster ovary (CHO K1) cells exhibiting increases in the A system of amino acid transport. Proc. natn. Acad. Sci. USA 91, 858-862.
-
(1994)
Proc. Natn. Acad. Sci. USA
, vol.91
, pp. 858-862
-
-
Jones, M.1
Gupta, R.S.2
Eaglesberg, E.3
-
132
-
-
0028278214
-
Deficient type 1 protein kinase A isozyme activity in systemic lupus erythematosus T lymphocytes
-
KAMMER, G. M., KHAN, I. U. & MALEMUD, C. J. (1994). Deficient type 1 protein kinase A isozyme activity in systemic lupus erythematosus T lymphocytes. J. clin. Invest. 94, 422-430.
-
(1994)
J. Clin. Invest.
, vol.94
, pp. 422-430
-
-
Kammer, G.M.1
Khan, I.U.2
Malemud, C.J.3
-
133
-
-
0028867086
-
Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform
-
KANEKO, K., PERETZ, D., PAN, K.-M., BLOCHBERGER, T. C., WILLE, H., GABIZON, R., GRIFFITH, O. H., COHEN, F. E., BALDWIN, M. A. & PRUSINER, S. B. (1995). Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform. Proc. natn. Acad. Sci USA 92, 11160-11164.
-
(1995)
Proc. Natn. 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
-
134
-
-
0030964917
-
COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform
-
KANEKO, K., VEY, M., SCOTT, M., PILKUHN, S., COHEN, F. E. & PRUSINER, S. B. (1997a). COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform, Proc. natn. Acad. Sci. USA 94, 2333-2338.
-
(1997)
Proc. Natn. Acad. Sci. USA
, vol.94
, pp. 2333-2338
-
-
Kaneko, K.1
Vey, M.2
Scott, M.3
Pilkuhn, S.4
Cohen, F.E.5
Prusiner, S.B.6
-
135
-
-
0031586212
-
Molecular properties of complexes formed between the prion protein and synthetic peptides
-
KANEKO, K., WILLE, H., MEHLHORN, I., ZHANG, H., BALL, H., COHEN, F. E., BALDWIN, M. A. & PRUSINER, S. B. (1997b). Molecular properties of complexes formed between the prion protein and synthetic peptides. J. molec. Biol. 270, 574-586.
-
(1997)
J. Molec. 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
-
136
-
-
0030931519
-
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
-
KANEKO, K., ZULIANELLO, L., SCOTT, M., COOPER, C. M., WALLACE, A. C., JAMES, T. L., COHEN, F. E. & PRUSINER, S. B. (1997c). Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation. Proc. natn. Acad. Sci. USA 94, 10069-10074.
-
(1997)
Proc. Natn. Acad. Sci. USA
, vol.94
, pp. 10069-10074
-
-
Kaneko, K.1
Zulianello, L.2
Scott, M.3
Cooper, C.M.4
Wallace, A.C.5
James, T.L.6
Cohen, F.E.7
Prusiner, S.B.8
-
137
-
-
0022447893
-
Immunological comparison of scrapic-associated fibrils isolated from animals infected with four different scrapie strains
-
KASCSAK, R. J., RUBENSTEIN, R., MERZ, P. A., CARP, R. I., ROBAKIS, N. K., WISNIEWSKI, H. M. & DIRINGER, H. (1986). Immunological comparison of scrapic-associated fibrils isolated from animals infected with four different scrapie strains. J. Virol. 59, 676-683.
-
(1986)
J. Virol.
, vol.59
, pp. 676-683
-
-
Kascsak, R.J.1
Rubenstein, R.2
Merz, P.A.3
Carp, R.I.4
Robakis, N.K.5
Wisniewski, H.M.6
Diringer, H.7
-
138
-
-
0023499868
-
Mouse polyclonal and monoclonal antibody to scrapic-associated fibril proteins
-
KASCSAK, R. J., RUBENSTEIN, R., MERZ, P. A., TONNA-DEMASI, M., FERSKO, R., CARP, R. I., WISNIEWSKI, H. M. & DIRINGER, H. J. (1987). Mouse polyclonal and monoclonal antibody to scrapic-associated fibril proteins. Virol. 61, 3688-3693.
-
(1987)
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.J.8
-
139
-
-
0026604959
-
Further analysis of nucleic acids in purified scrapie prion preparations by improved return refocusing gel electrophoresis
-
KELLINGS, K., MEYER, N., MIRENDA, C., PRUSINER, S. B. & RIESNER, D. (1992). Further analysis of nucleic acids in purified scrapie prion preparations by improved return refocusing gel electrophoresis. J. gen. Virol. 73, 1025-1029.
-
(1992)
J. Gen. Virol.
, vol.73
, pp. 1025-1029
-
-
Kellings, K.1
Meyer, N.2
Mirenda, C.3
Prusiner, S.B.4
Riesner, D.5
-
140
-
-
0028782011
-
Nucleic acids m prion preparations : Unspecific background or essential component?
-
KELLINGS, K., PRUSINER, S. B. & RIESNER, D. (1994). Nucleic acids m prion preparations : unspecific background or essential component? Phil. Trans. R. Soc. Lond. B 343, 425-430.
-
(1994)
Phil. Trans. R. Soc. Lond. B
, vol.343
, pp. 425-430
-
-
Kellings, K.1
Prusiner, S.B.2
Riesner, D.3
-
141
-
-
0026781044
-
Glycosylation inhibits the interaction of invertase with the chaperone GroEL
-
KERN, G., SCHMIDT, M., BUCHNER, J. & JAENICKE, R. (1992). Glycosylation inhibits the interaction of invertase with the chaperone GroEL. FEBS Lett. 305, 203-205.
-
(1992)
FEBS Lett.
, vol.305
, pp. 203-205
-
-
Kern, G.1
Schmidt, M.2
Buchner, J.3
Jaenicke, R.4
-
142
-
-
0032168039
-
Protein kinase A-catalyzed phosphorylation of heat shock protein 60 chaperone regulates its attachment to histone 2B in the T lymphocyte plasma membrane
-
KHAN, I. U., WALLIN, R., GUPTA, R. S. & KAMMER, G. M. (1998). Protein kinase A-catalyzed phosphorylation of heat shock protein 60 chaperone regulates its attachment to histone 2B in the T lymphocyte plasma membrane. Proc. natn. Acad. Sci. USA 95, 10425-10430.
-
(1998)
Proc. Natn. Acad. Sci. USA
, vol.95
, pp. 10425-10430
-
-
Khan, I.U.1
Wallin, R.2
Gupta, R.S.3
Kammer, G.M.4
-
143
-
-
0017866857
-
Evidence that the transmission of one source of scrapie agent to hamsters involves separation of agent strains from a mixture
-
KIMBERLIN, R. H. & WALKER, C. A. (1978). Evidence that the transmission of one source of scrapie agent to hamsters involves separation of agent strains from a mixture. J. gen. Virol. 39, 487-496.
-
(1978)
J. Gen. Virol.
, vol.39
, pp. 487-496
-
-
Kimberlin, R.H.1
Walker, C.A.2
-
144
-
-
0023265523
-
Temporary and permanent modifications to a single strain of mouse scrapie on transmission to rats and hamsters
-
KIMBERLIN, R. H., COLE, S. & WALKER, C. A. (1987). Temporary and permanent modifications to a single strain of mouse scrapie on transmission to rats and hamsters. J. gen. Virol. 68, 1875-1881.
-
(1987)
J. Gen. Virol.
, vol.68
, pp. 1875-1881
-
-
Kimberlin, R.H.1
Cole, S.2
Walker, C.A.3
-
145
-
-
0024325787
-
The genome identity of different strains of mouse scrapie is expressed in hamsters and preserved on reisolation in mice
-
KIMBERLIN, R. H., WALKER, C. A. & FRASER, H. (1989). The genome identity of different strains of mouse scrapie is expressed in hamsters and preserved on reisolation in mice. J. gen. Virol. 70, 2017-2025.
-
(1989)
J. Gen. Virol.
, vol.70
, pp. 2017-2025
-
-
Kimberlin, R.H.1
Walker, C.A.2
Fraser, H.3
-
146
-
-
0027236933
-
An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques
-
KITAMOTO, T., IIZUKA, R. & TATEISHI, J. (1993). An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques. Biochem. biophys. Res. Commun. 192, 525-531.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.192
, pp. 525-531
-
-
Kitamoto, T.1
Iizuka, R.2
Tateishi, J.3
-
147
-
-
0033543736
-
NMR analysis of the binding of a rhodanese peptide to a minichaperone in solution
-
KOBAYASHI, N., FREUND, S. M. V., CHATELLIER, J., ZAHN, R. & FERSHT, A. R. (1999). NMR analysis of the binding of a rhodanese peptide to a minichaperone in solution. J. molec. Biol. 292, 181-190.
-
(1999)
J. Molec. Biol.
, vol.292
, pp. 181-190
-
-
Kobayashi, N.1
Freund, S.M.V.2
Chatellier, J.3
Zahn, R.4
Fersht, A.R.5
-
148
-
-
0027956109
-
Cell-free formation of protease-resistam prion protein
-
KOCISKO, D. A., COME, J. H., PRIOLA, S. A., CHESEBRO, B., RAYMOND, G. J., LANSBURY, P. T. & CAUGHEY, B. (1994). Cell-free formation of protease-resistam 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
-
149
-
-
0029066886
-
Species specificity in the cell-free conversion ot prion protein to protease-resistant forms: A model for the scrapie species barrier
-
KOCISKO, D. A., PRIOLA, S. A., RAYMOND, G. J., CHESEBRO, B., LANSBURY, P. T., JR. & CAUGHEY, B. (1995). Species specificity in the cell-free conversion ot prion protein to protease-resistant forms: a model for the scrapie species barrier. Proc. natn. Acad. Sci. USA 92, 3923-3927.
-
(1995)
Proc. Natn. Acad. Sci. USA
, vol.92
, pp. 3923-3927
-
-
Kocisko, D.A.1
Priola, S.A.2
Raymond, G.J.3
Chesebro, B.4
Lansbury P.T., Jr.5
Caughey, B.6
-
150
-
-
0029881007
-
MOLMOL: A program for display and analysis of macromolecular structures
-
KORADI, R., BILLETER, M. & WÜTHRICH, K. (1996). MOLMOL: a program for display and analysis of macromolecular structures. J. molec. Graph. 14, 51-55.
-
(1996)
J. Molec. Graph.
, vol.14
, pp. 51-55
-
-
Koradi, R.1
Billeter, M.2
Wüthrich, K.3
-
151
-
-
0030613755
-
Sc)-specific epitope defined by a monoclonal antibody
-
Sc)-specific epitope defined by a monoclonal antibody. Nature 390, 74-77.
-
(1997)
Nature
, vol.390
, pp. 74-77
-
-
Korth, C.1
Stierli, B.2
Streit, P.3
Moser, M.4
Schaller, O.5
Fischer, R.6
Schulz-Schaeffer, W.7
Kretzschmar, H.8
Raeber, A.9
Braun, U.10
Ehrensperger, F.11
Hornemann, S.12
Glockshuber, R.13
Riek, R.14
Billeter, M.15
Wüthrich, K.16
Oesch, B.17
-
152
-
-
0032847543
-
Monoclonal antibodies specific for the native, disease-associated isoform of the prion protein
-
KORTH, C., STREIT, P. & OESCH, B. (1999). Monoclonal antibodies specific for the native, disease-associated isoform of the prion protein. Methods Enzymol. 309, 106-122.
-
(1999)
Methods Enzymol.
, vol.309
, pp. 106-122
-
-
Korth, C.1
Streit, P.2
Oesch, B.3
-
153
-
-
0025906297
-
Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker
-
KRETZSCHMAR, H. A., HONOLD, G., SETTELBERGER, F., FEUCHT, M., WESSELY, P., MEHRAEIN, P. & BUDKA, H. (1991). Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker. Lancet 337, 1160.
-
(1991)
Lancet
, vol.337
, pp. 1160
-
-
Kretzschmar, H.A.1
Honold, G.2
Settelberger, F.3
Feucht, M.4
Wessely, P.5
Mehraein, P.6
Budka, H.7
-
154
-
-
0022569404
-
Scrapie prion proteins are synthesixed in neurons
-
KRETZSCHMAR, H. A., PRUSINER, S. B., STOWRING, L. E. & DEARMOND, S. J. (1986). Scrapie prion proteins are synthesixed in neurons. Am. J. Pathol. 122, 1-5.
-
(1986)
Am. J. Pathol.
, vol.122
, pp. 1-5
-
-
Kretzschmar, H.A.1
Prusiner, S.B.2
Stowring, L.E.3
Dearmond, S.J.4
-
155
-
-
0032859326
-
Neurotoxicity of prion peptide 106 126 not confirmed
-
KUNZ, B., SANDMEIER, E. & CHRISTEN, P. (1999). Neurotoxicity of prion peptide 106 126 not confirmed. FEBS Lett. 458, 65-68.
-
(1999)
FEBS Lett.
, vol.458
, pp. 65-68
-
-
Kunz, B.1
Sandmeier, E.2
Christen, P.3
-
156
-
-
0024417964
-
The molten globule state as a clue for understanding the folding and cooperativity of globular-protein structure
-
KUWAJIMA, K. (1989). The molten globule state as a clue for understanding the folding and cooperativity of globular-protein structure. Proteins 6, 87-103.
-
(1989)
Proteins
, vol.6
, pp. 87-103
-
-
Kuwajima, K.1
-
157
-
-
0025291463
-
The Escherichia coli heat shock proteins GroEL, and GroES modulate the folding of the β-lactamase precursor
-
LAMINET, A. A., ZIEGELHOFFER, T., GEORGOPOULOS, C. & PLÜCKTHUN, A. (1990). The Escherichia coli heat shock proteins GroEL, and GroES modulate the folding of the β-lactamase precursor. EMBO J. 9, 2315-2319.
-
(1990)
EMBO J.
, vol.9
, pp. 2315-2319
-
-
Laminet, A.A.1
Ziegelhoffer, T.2
Georgopoulos, C.3
Plückthun, A.4
-
158
-
-
0027165388
-
Characterization ot a functionally important mobile domain of GroES
-
LANDRY, S. J., ZEILSTRA-RYALLS, J., FAYET, O., GEORGOPOULOS, C. & GIERASCH, L. M. (1993). Characterization ot a functionally important mobile domain of GroES. Nature 364, 255-258.
-
(1993)
Nature
, vol.364
, pp. 255-258
-
-
Landry, S.J.1
Zeilstra-Ryalls, J.2
Fayet, O.3
Georgopoulos, C.4
Gierasch, L.M.5
-
159
-
-
0014963710
-
Inactivation of the scrapie agent by near monochromatic ultraviolet light
-
LATARJET, R., MUEL, B., HAIG, D. A., CLARKE, M. C. & ALPER, T. (1970). Inactivation of the scrapie agent by near monochromatic ultraviolet light. Nature 227, 1341-1343.
-
(1970)
Nature
, vol.227
, pp. 1341-1343
-
-
Latarjet, R.1
Muel, B.2
Haig, D.A.3
Clarke, M.C.4
Alper, T.5
-
160
-
-
0027517117
-
Early events of human T lymphocyte activation are associated with type I protein kinase A activity
-
LAXMINARAYANA, D., BERRADA, A. & KAMMER, G. M. (1993). Early events of human T lymphocyte activation are associated with type I protein kinase A activity. J. clin. Invest. 92, 2207-2214.
-
(1993)
J. Clin. Invest.
, vol.92
, pp. 2207-2214
-
-
Laxminarayana, D.1
Berrada, A.2
Kammer, G.M.3
-
161
-
-
0030600223
-
Measurement of endosome pH following folate receptor-mediated endocytosis
-
LEE, R. J., WANG, S. & LOW, P. S. (1996). Measurement of endosome pH following folate receptor-mediated endocytosis. Biochem. biophys. Acta 1312, 237-242.
-
(1996)
Biochem. Biophys. Acta
, vol.1312
, pp. 237-242
-
-
Lee, R.J.1
Wang, S.2
Low, P.S.3
-
162
-
-
0028866917
-
A mutant prion protein displays an aberrant membrane association when expressed in cultured cells
-
LEHMANN, S. & HARRIS, D. A. (1995). A mutant prion protein displays an aberrant membrane association when expressed in cultured cells. J. biol. Chem. 270, 24589-24597.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 24589-24597
-
-
Lehmann, S.1
Harris, D.A.2
-
163
-
-
0030050733
-
Mutant and infectious prion proteins display common biochemical properties in cultured cells
-
LEHMANN, S. & HARRIS, D. A. (1996a). Mutant and infectious prion proteins display common biochemical properties in cultured cells. J. biol. Chem. 271, 1633-1637.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 1633-1637
-
-
Lehmann, S.1
Harris, D.A.2
-
164
-
-
0030006902
-
Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform
-
LEHMANN, S. & HARRIS, D. A. (1996b). Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform, Proc. natn. Acad. Sci. USA 93, 5610-5614.
-
(1996)
Proc. Natn. Acad. Sci. USA
, vol.93
, pp. 5610-5614
-
-
Lehmann, S.1
Harris, D.A.2
-
165
-
-
0030799062
-
Blockade of glycosylation promotes acquisition ot scrapie-like properties by the prion protein in cultured cells
-
LEHMANN, S. & HARRIS, D. A. (1997). Blockade of glycosylation promotes acquisition ot scrapie-like properties by the prion protein in cultured cells. J. biol. Chem. 272, 21479-21487.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 21479-21487
-
-
Lehmann, S.1
Harris, D.A.2
-
166
-
-
0033574161
-
Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein
-
LIEMANN, S. & GLOCKSHUBER, R. (1999). Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein. Biochemistry 36, 3258-3267.
-
(1999)
Biochemistry
, vol.36
, pp. 3258-3267
-
-
Liemann, S.1
Glockshuber, R.2
-
168
-
-
0031663159
-
Gram-negative bacteria produce membrane vesicles which are capable of killing other bacteria
-
LI, Z., CLARKE, A. J. & BEVERIDGE, T. J. (1998). Gram-negative bacteria produce membrane vesicles which are capable of killing other bacteria. J. Bacteriol. 180, 5478-5483.
-
(1998)
J. Bacteriol.
, vol.180
, pp. 5478-5483
-
-
Li, Z.1
Clarke, A.J.2
Beveridge, T.J.3
-
169
-
-
0033609035
-
Solution structure of Syrian hamster prion protein rPrP(90-231)
-
LIU, H., FARR-JONES, S., ULYANOV, N. B., LLINAS, M., MARQUSEE, S., GROTH, D., COHEN, F. E., PRUSINER, S. B. & JAMES, T. L. (1999a). Solution structure of Syrian hamster prion protein rPrP(90-231). Biochemistry 38, 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
Cohen, F.E.7
Prusiner, S.B.8
T, L.9
-
170
-
-
0032781345
-
Peptides and proteins in neurodegenerative disease: Helix propensity of a polypeptide containing helix 1 of the mouse prion protein studied by NMR and CD spectrosocpy
-
LIU, A., RIEK, R., ZAHN, R., HORNEMANN, S., GLOCKSHUBER, R. & WÜTHRICH, K. (1999b). Peptides and proteins in neurodegenerative disease:
-
(1999)
Biopolymers
, vol.51
, pp. 145-152
-
-
Liu, A.1
Riek, R.2
Zahn, R.3
Hornemann, S.4
Glockshuber, R.5
Wüthrich, K.6
-
171
-
-
0029916617
-
Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus
-
LLEDO, P. M., TREMBLAY, P., DEARMOND, S. J., PRUSINER, S. B., PRUSINER, S. B. & NICOLL, R. A. (1996). Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus. Proc. natn. Acad. Sci. USA 93, 2403-2407.
-
(1996)
Proc. Natn. Acad. Sci. USA
, vol.93
, pp. 2403-2407
-
-
Lledo, P.M.1
Tremblay, P.2
Dearmond, S.J.3
Prusiner, S.B.4
Prusiner, S.B.5
Nicoll, R.A.6
-
172
-
-
0025239839
-
Unusual topogenic sequence directs prion protein biogenesis
-
LOPEZ, C. D., YOST, C. S., PRUSINER, S. B., MYERS, R. M. & LINGAPPA, V. R. (1990). Unusual topogenic sequence directs prion protein biogenesis. Science 248, 226-229.
-
(1990)
Science
, vol.248
, pp. 226-229
-
-
Lopez, C.D.1
Yost, C.S.2
Prusiner, S.B.3
Myers, R.M.4
Lingappa, V.R.5
-
173
-
-
0027231702
-
2-terminal helix by proline but not by glutamine
-
2-terminal helix by proline but not by glutamine. J. biol. Chem. 268, 10246-10251.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 10246-10251
-
-
Luo, G.X.1
Horowitz, P.M.2
-
174
-
-
0026637514
-
The prion protein gene: A role in mouse embryogenesis?
-
MANSON, J., WEST, J. D., THOMSON, V., MCBRIDE, P., KAUFMAN, M. H. & HOPE, J. (1992). The prion protein gene: a role in mouse embryogenesis? Development 115, 117-122.
-
(1992)
Development
, vol.115
, pp. 117-122
-
-
Manson, J.1
West, J.D.2
Thomson, V.3
Mcbride, P.4
Kaufman, M.H.5
Hope, J.6
-
175
-
-
0026416043
-
Chaperonin-mediated protein folding at the surface of groEL through a 'molten globule'-like intermediate
-
MARTIN, J., LANGER, T., BOTEVA, R., SCHRAMEL, A., HORNWICH, A. L. & HARTL, F.-U. (1991). Chaperonin-mediated protein folding at the surface of groEL through a 'molten globule'-like intermediate. Nature 352, 36-42.
-
(1991)
Nature
, vol.352
, pp. 36-42
-
-
Martin, J.1
Langer, T.2
Boteva, R.3
Schramel, A.4
Hornwich, A.L.5
Hartl, F.-U.6
-
176
-
-
0031466157
-
Complementary hydropathy identifies a cellular prion protein receptor
-
MARTINS, V. R., GRANER, E., GARCIA-ABREU, J., DE SOUZA, S. J., MERCADANTE, A. F., VEIGA, S. S., ZANATA, S. M., NETO, V. M. & BRENTANI, R. R. (1997). Complementary hydropathy identifies a cellular prion protein receptor. Nat. Med. 3, 1376-1382.
-
(1997)
Nat. Med.
, vol.3
, pp. 1376-1382
-
-
Martins, V.R.1
Graner, E.2
Garcia-Abreu, J.3
De Souza, S.J.4
Mercadante, A.F.5
Veiga, S.S.6
Zanata, S.M.7
Neto, V.M.8
Brentani, R.R.9
-
177
-
-
0030045870
-
Protein folding in the central cavity of the GroEL-GroES chaperonin complex
-
MAYHEW, M., DA SILVA, A. C. R., MARTIN, J., ERDJUMENT-BROMAGE, H., TEMPST, P. & HARTL, F. U. (1996). Protein folding in the central cavity of the GroEL-GroES chaperonin complex. Nature 379, 420-426.
-
(1996)
Nature
, vol.379
, pp. 420-426
-
-
Mayhew, M.1
Da Silva, A.C.R.2
Martin, J.3
Erdjument-Bromage, H.4
Tempst, P.5
Hartl, F.U.6
-
178
-
-
0021023167
-
A protease-resistant protein is a structural component of the scrapie prion
-
MCKINLEY, M. P., BOLTON, D. C. & PRUSINER, S. B. (1983). A protease-resistant protein is a structural component of the scrapie prion. Cell 35, 57-62.
-
(1983)
Cell
, vol.35
, pp. 57-62
-
-
Mckinley, M.P.1
Bolton, D.C.2
Prusiner, S.B.3
-
179
-
-
0019864625
-
Reversible chemical modification of the scrapie agent
-
MCKINLEY, M. P., MASIARZ, F. R. & PRUSINER, S. B. (1981). Reversible chemical modification of the scrapie agent. Science 214, 1259-1261.
-
(1981)
Science
, vol.214
, pp. 1259-1261
-
-
Mckinley, M.P.1
Masiarz, F.R.2
Prusiner, S.B.3
-
180
-
-
0026062496
-
Scrapie prion rod formation in vitro requires both detergent extraction and limited proteolysis
-
MCKINLEY, M. P., MEYER, R. K., KENAGA, L., RAHBAR, F., COTTER, R., SERBAN, A. & PRUSINER, S. B. (1991a). Scrapie prion rod formation in vitro requires both detergent extraction and limited proteolysis. J. Virol. 65, 1340-1351.
-
(1991)
J. Virol.
, vol.65
, pp. 1340-1351
-
-
Mckinley, M.P.1
Meyer, R.K.2
Kenaga, L.3
Rahbar, F.4
Cotter, R.5
Serban, A.6
Prusiner, S.B.7
-
181
-
-
0026326210
-
Ultrastructural localization ot scrapie prion proteins in cytoplasmic vesicles of infected cultured cells
-
MCKINLEY, M. P., TARABOULOS, A., KENAGA, L., SERBAN, D., STIEBER, A., DEARMOND, S. J., PRUSINER, S. B. & GONATAS, N. (1991b). Ultrastructural localization ot scrapie prion proteins in cytoplasmic vesicles of infected cultured cells. Lab. Invest. 65, 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
-
182
-
-
15844419908
-
High-level expression and characterization of a purified 142-residue polypeptide of the prion protein
-
MEHLHORN, I., GROTH, D., STÖCKEL, J., MOFFAT, B., REILLY, D., YANSURA, D., WILLETT, W. S., BALDWIN, M., FLETTERICK, R., COHEN, F. E., VANDLEN, R., HENNER, D. & PRUSINER, S. B. (1996). High-level expression and characterization of a purified 142-residue polypeptide of the prion protein. Biochemistry 35, 5528-5537.
-
(1996)
Biochemistry
, vol.35
, pp. 5528-5537
-
-
Mehlhorn, I.1
Groth, D.2
Stöckel, J.3
Moffat, B.4
Reilly, D.5
Yansura, D.6
Willett, W.S.7
Baldwin, M.8
Fletterick, R.9
Cohen, F.E.10
Vandlen, R.11
Henner, D.12
Prusiner, S.B.13
-
183
-
-
0026489533
-
Characterization of a stable, reactivatable complex between chaperonin 60 and mitochondrial rhodanese
-
MENDOZA, J. A., BUTLER, M. C. & HOROWITZ, P. M. (1992). Characterization of a stable, reactivatable complex between chaperonin 60 and mitochondrial rhodanese. J. biol. Chem. 267, 24648-24654.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 24648-24654
-
-
Mendoza, J.A.1
Butler, M.C.2
Horowitz, P.M.3
-
184
-
-
0026095524
-
Intermediates in the chaperonin-assisted refolding of rhodanese are trapped at low temperature and show a small stoichiometry
-
MENDOZA, J. A., LORIMER, G. H. & HOROWITZ, P. M. (1991). Intermediates in the chaperonin-assisted refolding of rhodanese are trapped at low temperature and show a small stoichiometry. J. biol. Chem. 266, 16973-16976.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 16973-16976
-
-
Mendoza, J.A.1
Lorimer, G.H.2
Horowitz, P.M.3
-
185
-
-
0023226378
-
Antisera to scrapie-associated fibril protein and prion protein decorate scrapie-associated fibrils
-
MERZ, P. A., KASCSAK, R. J., RUBENSTEIN, R., CARP, R. I. & WISNIEWSKI, H. M. (1987). Antisera to scrapie-associated fibril protein and prion protein decorate scrapie-associated fibrils. J. Virol. 61, 42-49.
-
(1987)
J. Virol.
, vol.61
, pp. 42-49
-
-
Merz, P.A.1
Kascsak, R.J.2
Rubenstein, R.3
Carp, R.I.4
Wisniewski, H.M.5
-
186
-
-
0021176718
-
Infection-specific particle from the unconventional slow virus diseases
-
MERZ, P. A., ROHWER, R. G., KASCSAK, R., WISNIEWSKI, H. M., SOMERVILLE, R. A., GIBBS, C. J., JR. & GAJDUSEK, D. C. (1984). Infection-specific particle from the unconventional slow virus diseases. Science 225, 437-440.
-
(1984)
Science
, vol.225
, pp. 437-440
-
-
Merz, P.A.1
Rohwer, R.G.2
Kascsak, R.3
Wisniewski, H.M.4
Somerville, R.A.5
Gibbs C.J., Jr.6
Gajdusek, D.C.7
-
187
-
-
0019402779
-
Abnormal fibrils from scrapie-infected brain
-
MERZ, P. A., SOMERVILLE, R. A., WISNIEWSKI, H. M. & IQBAL, K. (1981). Abnormal fibrils from scrapie-infected brain. Acta Neuropathol. 54, 63-74.
-
(1981)
Acta Neuropathol.
, vol.54
, pp. 63-74
-
-
Merz, P.A.1
Somerville, R.A.2
Wisniewski, H.M.3
Iqbal, K.4
-
188
-
-
0021036327
-
Scrapie-associated fibrils in Creutzfeldt Jakob disease
-
MERZ, P. A., SOMERVILLE, R. A., WISNIEWSKI, M. M., MANUELIDIS, L. & MANUELIDIS, E. E. (1983). Scrapie-associated fibrils in Creutzfeldt Jakob disease. Nature 306, 474-476.
-
(1983)
Nature
, vol.306
, pp. 474-476
-
-
Merz, P.A.1
Somerville, R.A.2
Wisniewski, M.M.3
Manuelidis, L.4
Manuelidis, E.E.5
-
189
-
-
0040393220
-
Separation and properties of cellular and scrapie prion proteins
-
MEYER, R. K., MCKINLEY, M. P., BOWMAN, K. A., BRAUNFELD, M. B., BARRY, R. A. & PRUSINER, S. B. (1986). Separation and properties of cellular and scrapie prion proteins. Proc. natn. Acad. Sci. USA 83, 2310-2314.
-
(1986)
Proc. Natn. Acad. Sci. USA
, vol.83
, pp. 2310-2314
-
-
Meyer, R.K.1
Mckinley, M.P.2
Bowman, K.A.3
Braunfeld, M.B.4
Barry, R.A.5
Prusiner, S.B.6
-
190
-
-
0030569412
-
Metal-dependent α-helix formation promoted by the glycinerich octapeptide region of prion protein
-
MIURA, T., HORI-I, A. & TAKEUCHI, H. (1996). Metal-dependent α-helix formation promoted by the glycinerich octapeptide region of prion protein. FEBS Lett. 396, 248-252.
-
(1996)
FEBS Lett.
, vol.396
, pp. 248-252
-
-
Miura, T.1
Hori-I, A.2
Takeuchi, H.3
-
191
-
-
0001585073
-
Nerve growth factor increases mRNA levels for the prion protein and the β-amyloid protein precursor in developing hamster brain
-
MOBLEY, W. C., NEVE, R. L., PRUSINER, S. B. & MCKINLEY, M. P. (1988). Nerve growth factor increases mRNA levels for the prion protein and the β-amyloid protein precursor in developing hamster brain. Proc. natn. Acad. Sci. USA 85, 9811-9815.
-
(1988)
Proc. Natn. Acad. Sci. USA
, vol.85
, pp. 9811-9815
-
-
Mobley, W.C.1
Neve, R.L.2
Prusiner, S.B.3
Mckinley, M.P.4
-
192
-
-
0023841448
-
Two membrane-bound proteins associated with alanine resistance and increased A-system amino acid transport in mutants of CHO K1
-
MOFFETT, J., MENDIAZ, E., JONES, M. & ENGLESBERG, E. (1988). Two membrane-bound proteins associated with alanine resistance and increased A-system amino acid transport in mutants of CHO K1. Somat. Cell mol. Genet. 14, 1-12.
-
(1988)
Somat. Cell Mol. Genet.
, vol.14
, pp. 1-12
-
-
Moffett, J.1
Mendiaz, E.2
Jones, M.3
Englesberg, E.4
-
193
-
-
0028351904
-
Fatal familial insomnia and familial Creutzfeldt Jakob disease : Different prion proteins determined by a DNA polymorphism
-
MONARI, L., CHEN, S. G., BROWN, P., PARCHI, P., PETERSEN, R. B., MIKOL, J., GRAY, F., CORTELLI, P., MONTAGNA, P., GHETTI, B., GOLDFARB, L. G., GAJDUSEK, D. C., LUGARESI, E., GAMBETTI, P. & AUTILIO-GAMBETTI, L. (1994). Fatal familial insomnia and familial Creutzfeldt Jakob disease : different prion proteins determined by a DNA polymorphism. Proc. natn. Acad. Sci. USA 91, 2839-2842.
-
(1994)
Proc. Natn. Acad. Sci. USA
, 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
Goldfarb, L.G.11
Gajdusek, D.C.12
Lugaresi, E.13
Gambetti, P.14
Autilio-Gambetti, L.15
-
195
-
-
0033215478
-
Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel
-
MOORE, R. C., LEE, I. Y., SILVERMAN, G. L., HARRISON, P. M., STROME, R., HEINRICH, C., KARUNARATNE, A., PASTERNAK, S. H., CHISHTI, M. A., LIANG, Y., MASTRANGELO, P., WANG, K., SMIT, A. F. A., KATAMINE, S., CARLSON, G. A., COHEN, F. E., PRUSINER, S. B., MELTON, D. W., TREMBLAY, P., HOOD, L. E. & WESTAWAY, D. (1999). Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel. J. molec. Biol. 292, 797-817.
-
(1999)
J. Molec. 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
Heinrich, C.6
Karunaratne, A.7
Pasternak, S.H.8
Chishti, M.A.9
Liang, Y.10
Mastrangelo, P.11
Wang, K.12
Smit, A.F.A.13
Katamine, S.14
Carlson, G.A.15
Cohen, F.E.16
Prusiner, S.B.17
Melton, D.W.18
Tremblay, P.19
Hood, L.E.20
Westaway, D.21
more..
-
196
-
-
0030811015
-
Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix
-
MURAMOTO, T., DEARMOND, S. J., SCOTT, M., TELLING, G. C., COHEN, F. E. & PRUSINER, S. B. (1997). Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix. Nat. Med. 3, 750-755.
-
(1997)
Nat. Med.
, vol.3
, pp. 750-755
-
-
Muramoto, T.1
Dearmond, S.J.2
Scott, M.3
Telling, G.C.4
Cohen, F.E.5
Prusiner, S.B.6
-
197
-
-
0030480271
-
Recombinant scrapie-like prion protein of 106 amino acids is soluble
-
MURAMOTO, T., SCOTT, M., COHEN, F. E. & PRUSINER, S. B. (1996). Recombinant scrapie-like prion protein of 106 amino acids is soluble. Proc. natn. Acad. Sci. USA 93, 15457-15462.
-
(1996)
Proc. Natn. Acad. Sci. USA
, vol.93
, pp. 15457-15462
-
-
Muramoto, T.1
Scott, M.2
Cohen, F.E.3
Prusiner, S.B.4
-
198
-
-
0001767436
-
The rubisco large subunit binding protein. Phil
-
MUSGROVE, J. E. & ELLIS, R. J. (1986). The rubisco large subunit binding protein. Phil. Trans. R. Soc. Lond. B 313, 419-428.
-
(1986)
Trans. R. Soc. Lond. B
, vol.313
, pp. 419-428
-
-
Musgrove, J.E.1
Ellis, R.J.2
-
199
-
-
0033529289
-
Prion proteins carrying pathogenic mutations are resistant to phospholipase cleavage of their glycolipid anchors
-
NARWA, R. & HARRIS, D. A. (1999). Prion proteins carrying pathogenic mutations are resistant to phospholipase cleavage of their glycolipid anchors. Biochemistry 38, 8770-8777.
-
(1999)
Biochemistry
, vol.38
, pp. 8770-8777
-
-
D, A.1
-
200
-
-
0033597931
-
Sphingolipid depletion increases formation of the scrapic prion protein in neuroblastoma cells infected with prions
-
NASLAVASKY, N., SHMEEDA, H., FRIEDLANDER, G., YANAI, A., FUTERMAN, A. H., BARENHOLZ, Y. & TARABOULOS, A. (1999). Sphingolipid depletion increases formation of the scrapic prion protein in neuroblastoma cells infected with prions. J. biol. Chem. 274, 20763-20771.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 20763-20771
-
-
Naslavasky, N.1
Shmeeda, H.2
Friedlander, G.3
Yanai, A.4
Futerman, A.H.5
Barenholz, Y.6
Taraboulos, A.7
-
201
-
-
0030894380
-
Characterization of detergent-insoluble complexes containing the cellular prion protein and its scrapic isotorm
-
NASLAVSKY, N., STEIN, R., YANAI, A., FRIEDLANDER, G. & TARABOULOS, A. (1997). Characterization of detergent-insoluble complexes containing the cellular prion protein and its scrapic isotorm. J. biol. Chem. 272, 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
-
202
-
-
0032005026
-
Protein folding in the cytosol: Chaperonin-dependent and -independent mechanisms
-
NETZER, W. J. & HARTL, F. U. (1998). Protein folding in the cytosol: chaperonin-dependent and -independent mechanisms. Trends biochem. Sci. 23, 68-73.
-
(1998)
Trends Biochem. Sci.
, vol.23
, pp. 68-73
-
-
Netzer, W.J.1
Hartl, F.U.2
-
203
-
-
0028925377
-
Prion protein peptides induce α-helix to β-sheet conformational transitions
-
NGUYEN, J., BALDWIN, M. A., COHEN, F. E. & PRUSINER, S. B. (1995a). Prion protein peptides induce α-helix to β-sheet conformational transitions. Biochemistry 34, 4186-4192.
-
(1995)
Biochemistry
, vol.34
, pp. 4186-4192
-
-
Nguyen, J.1
Baldwin, M.A.2
Cohen, F.E.3
Prusiner, S.B.4
-
204
-
-
0029149975
-
X-ray diffraction of scrapie prion rods and PrP peptides
-
NGUYGEN, J. T., INOUYE, H., BALDWIN, M. A., FLETTERICK, R. J., COHEN, F. E., PRUSINER, S. B. & KIRSCHNEK, D. A. (1995b). X-ray diffraction of scrapie prion rods and PrP peptides. J. molec. Biol. 252, 412-422.
-
(1995)
J. Molec. Biol.
, vol.252
, pp. 412-422
-
-
Nguygen, J.T.1
Inouye, H.2
Baldwin, M.A.3
Fletterick, R.J.4
Cohen, F.E.5
Prusiner, S.B.6
Kirschnek, D.A.7
-
205
-
-
15644366144
-
Familial spongiform encephalopathy associated with a novel prion protein gene mutation
-
NITRINI, R., ROSEMBERG, S., PASSOS-BUENO, M. R., DA SILVA, L. S., IUGHETTI, P., PAPADOPOULOS, M., CARRILHO, P. M., CARAMELLI, P., ALBRECHT, S., ZATZ, M. & LEBLANC, A. (1997). Familial spongiform encephalopathy associated with a novel prion protein gene mutation. Ann. Neurol. 42, 138-146.
-
(1997)
Ann. Neurol.
, vol.42
, pp. 138-146
-
-
Nitrini, R.1
Rosemberg, S.2
Passos-Bueno, M.R.3
Da Silva, L.S.4
Iughetti, P.5
Papadopoulos, M.6
Carrilho, P.M.7
Caramelli, P.8
Albrecht, S.9
Zatz, M.10
Leblanc, A.11
-
206
-
-
0022005315
-
A cellular gene encodes scrapie PrP 27-30 protein
-
OESCH, B., WESTAWAY, D., WÄLCHLI, M., MCKINLEY, M. P., KENT, S. B. H., AEBERSOLD, R., BARRY, R. A., TEMPST, P., TEPLOW, D. B., HOOD, L. E., PRUSINER, S. B. & WEISSMANN, C. (1985). A cellular gene encodes scrapie PrP 27-30 protein. Cell 40, 735-746.
-
(1985)
Cell
, vol.40
, pp. 735-746
-
-
Oesch, B.1
Westaway, D.2
Wälchli, M.3
Mckinley, M.P.4
Kent, S.B.H.5
Aebersold, R.6
Barry, R.A.7
Tempst, P.8
Teplow, D.B.9
Hood, L.E.10
Prusiner, S.B.11
Weissmann, C.12
-
207
-
-
0027332116
-
Conversion of α-helices into β-sheets features in the formation of the scrapie prion proteins
-
PAN, K.-M., BALDWIN, M., NGUYEN, J., GASSET, M., SERBAN, A., GROTH, D., MEHLHORN, I., HUANG, Z., FLETTERICK, R. J., COHEN, F. E. & PRUSINER, S. B. (1993). Conversion of α-helices into β-sheets features in the formation of the scrapie prion proteins. Proc. natn. Acad. Sci. USA 90, 10962-10966.
-
(1993)
Proc. Natn. 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
Mehlhorn, I.7
Huang, Z.8
Fletterick, R.J.9
Cohen, F.E.10
Prusiner, S.B.11
-
208
-
-
0027074458
-
Purification and properties of the cellular prion protein from Syrian hamster brain
-
PAN, K.-M., STAHL, N. & PRUSINER, S. B. (1992). Purification and properties of the cellular prion protein from Syrian hamster brain. Protein Sci. 1, 1343-1352.
-
(1992)
Protein Sci.
, vol.1
, pp. 1343-1352
-
-
Pan, K.-M.1
Stahl, N.2
Prusiner, S.B.3
-
210
-
-
8944259890
-
Molecular basis of phenotypic variability in sporadic Creutzfeldt- Jakob disease
-
PARCHI, P., CASTELLANI, R., CAPELLARI, S., GHETTI, B., YOUNG, K., CHEN, S. G., FARLOW, M., DICKSON, D. W., SIMA, A. A., TROJANOWSKI, J. Q., PETERSEN, R. B. & GAMBETTI, P. (1996). Molecular basis of phenotypic variability in sporadic Creutzfeldt- Jakob disease. Ann. Neurol. 39, 767-778.
-
(1996)
Ann. Neurol.
, vol.39
, pp. 767-778
-
-
Parchi, P.1
Castellani, R.2
Capellari, S.3
Ghetti, B.4
Young, K.5
Chen, S.G.6
Farlow, M.7
Dickson, D.W.8
Sima, A.A.9
Trojanowski, J.Q.10
Petersen, R.B.11
Gambetti, P.12
-
211
-
-
0026711256
-
Atomic structures of wild-type and thermostable mutant recombinant human Cu, Zn superoxide dismutase
-
PARGE, H. E., HALLEWELL, R. A. & TAINER, J. A. (1992). Atomic structures of wild-type and thermostable mutant recombinant human Cu, Zn superoxide dismutase. Proc. natn. Acad. Sci. USA 89, 6109-6113.
-
(1992)
Proc. Natn. Acad. Sci. USA
, vol.89
, pp. 6109-6113
-
-
Parge, H.E.1
Hallewell, R.A.2
Tainer, J.A.3
-
212
-
-
0013851909
-
Scrapie in the welsh mountain breed of sheep and its experimental transmission to goats
-
PATTISON, I. H. (1965). Scrapie in the welsh mountain breed of sheep and its experimental transmission to goats. Vet. Rec. 77, 1388-1390.
-
(1965)
Vet. Rec.
, vol.77
, pp. 1388-1390
-
-
Pattison, I.H.1
-
213
-
-
0014336086
-
Modification of a strain of mouse-adapted scrapie by passage through rats
-
PATTISON, I. H. & JONES, K. M. (1968). Modification of a strain of mouse-adapted scrapie by passage through rats. Res. vet. Sci. 9, 408-410.
-
(1968)
Res. Vet. Sci.
, vol.9
, pp. 408-410
-
-
Pattison, I.H.1
Jones, K.M.2
-
214
-
-
84961034678
-
Scrapie produced experimentally in goats with special reference to the clinical syndrome
-
PATTISON, I. H. & MILLSON, G. C. (1961). Scrapie produced experimentally in goats with special reference to the clinical syndrome. J. comp. Pathol. 71, 101-108.
-
(1961)
J. Comp. Pathol.
, vol.71
, pp. 101-108
-
-
Pattison, I.H.1
Millson, G.C.2
-
215
-
-
0032509499
-
Copper stimulates endocytosis ot the prion protein
-
PAULY, P. C. & HARRIS, D. A. (1998). Copper stimulates endocytosis ot the prion protein. J. biol. Chem. 273, 33107-33110.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 33107-33110
-
-
Pauly, P.C.1
Harris, D.A.2
-
216
-
-
0031592937
-
A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform
-
PERETZ, D., WILLIAMSON, R. A., MATSUNAGA, Y., SERBAN, H., PINILLA, C., BASTIDAS, R. B., ROZENSHTEYN, R., JAMES, T. L., HOUGHTEN, R. A., COHEN, F. E., PRUSINER, S. B. & BURTON, D. R. (1997). A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform. J. molec. biol. 273, 614-622.
-
(1997)
J. Molec. Biol.
, vol.273
, pp. 614-622
-
-
Peretz, D.1
Williamson, R.A.2
Matsunaga, Y.3
Serban, H.4
Pinilla, C.5
Bastidas, R.B.6
Rozenshteyn, R.7
James, T.L.8
Houghten, R.A.9
Cohen, F.E.10
Prusiner, S.B.11
Burton, D.R.12
-
217
-
-
0031588017
-
Importance of electrostatic interactions in the rapid binding of polypeptides to GroEL
-
PERRETT, S., ZAHN, R., STENBERG, G. & FERSHT, A. R. (1997). Importance of electrostatic interactions in the rapid binding of polypeptides to GroEL. J. molec. Biol. 269, 892-901.
-
(1997)
J. Molec. Biol.
, vol.269
, pp. 892-901
-
-
Perrett, S.1
Zahn, R.2
Stenberg, G.3
Fersht, A.R.4
-
218
-
-
17544366508
-
Effect of the D178N mutation and the codon 129 polymorphism on the metabolism of the prion protein
-
PETERSEN, R. B., PARCHI, P., RICHARDSON, S. L., URIG, C. B. & GAMBETTI, P. (1996). Effect of the D178N mutation and the codon 129 polymorphism on the metabolism of the prion protein. J. biol. Chem. 271, 12661-12668.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 12661-12668
-
-
Petersen, R.B.1
Parchi, P.2
Richardson, S.L.3
Urig, C.B.4
Gambetti, P.5
-
219
-
-
0024311503
-
Molecular cloning of a Chinese hamster mitochondrial protein related to the 'chaperonin' family of bacterial and plant proteins
-
PICKETTS, D. J., MAYANIL, C. S. & GUPTA, R. S. (1989). Molecular cloning of a Chinese hamster mitochondrial protein related to the 'chaperonin' family of bacterial and plant proteins. J. biol. Chem. 264, 12001-12008.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 12001-12008
-
-
Picketts, D.J.1
Mayanil, C.S.2
Gupta, R.S.3
-
220
-
-
0031555486
-
The 118-135 peptide of the human prion protein forms amyloid fibrils and induces liposome fusion
-
PILLOT, T., LINS, L., GOETHALS, M., VANLOO, B., BAERT, J., VANDEKERCKHOVE, J., ROSSENEU, M. & BRASSEUR, R. (1997). The 118-135 peptide of the human prion protein forms amyloid fibrils and induces liposome fusion. J. molec. Biol. 274, 381-393.
-
(1997)
J. Molec. Biol.
, vol.274
, pp. 381-393
-
-
Pillot, T.1
Lins, L.2
Goethals, M.3
Vanloo, B.4
Baert, J.5
Vandekerckhove, J.6
Rosseneu, M.7
Brasseur, R.8
-
221
-
-
0028822204
-
A single hamster PrP amino acid blocks conversion to protease-resistant PrP in scrapie-infected mouse neuroblastoma cells
-
PRIOLA, S. A. & CHESEBRO, B. (1995). A single hamster PrP amino acid blocks conversion to protease-resistant PrP in scrapie-infected mouse neuroblastoma cells. J. Virol. 69, 7754-7758.
-
(1995)
J. Virol.
, vol.69
, pp. 7754-7758
-
-
Priola, S.A.1
Chesebro, B.2
-
222
-
-
0032496218
-
Abnormal properties of prion protein with insertional mutations in different cell types
-
PRIOLA, S. A. & CHESEBRO, B. (1998). Abnormal properties of prion protein with insertional mutations in different cell types. J. biol. Chem. 273, 11980-11985.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 11980-11985
-
-
Priola, S.A.1
Chesebro, B.2
-
223
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
PRUSINER, S. B. (1982). Novel proteinaceous infectious particles cause scrapie. Science 216, 136-144.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
224
-
-
0023583026
-
Prions and neurodegenerative diseases
-
PRUSINER, S. B. (1987). Prions and neurodegenerative diseases. New Engl. J. Med. 317, 1571-1581.
-
(1987)
New Engl. J. Med.
, vol.317
, pp. 1571-1581
-
-
Prusiner, S.B.1
-
225
-
-
0025910229
-
Molecular biology of prion diseases
-
PRUSINER, S. B. (1991). Molecular biology of prion diseases. Science 252, 1515-1522.
-
(1991)
Science
, vol.252
, pp. 1515-1522
-
-
Prusiner, S.B.1
-
226
-
-
0030822582
-
Prion diseases and the BSE crisis
-
PRUSINER, S. B. (1997). Prion diseases and the BSE crisis. Science 278, 245-251.
-
(1997)
Science
, vol.278
, pp. 245-251
-
-
Prusiner, S.B.1
-
229
-
-
0020285570
-
Further purification and characterization of scrapie prions
-
PRUSINER, S. B., BOLTON, D. C., GROTH, D. F., BOWMAN, K. A., COCHRAN, S. P. & MCKINLEY, M. P. (1982). Further purification and characterization of scrapie prions. Biochemistry 21, 6942-6950.
-
(1982)
Biochemistry
, vol.21
, pp. 6942-6950
-
-
Prusiner, S.B.1
Bolton, D.C.2
Groth, D.F.3
Bowman, K.A.4
Cochran, S.P.5
Mckinley, M.P.6
-
230
-
-
0019479696
-
Determination of scrapie agent titer from incubation period measurements in hamsters
-
PRUSINER, S. B., COCHRAN, S. P., DOWNEY, D. E. & GROTH, D. F. (1981a). Determination of scrapie agent titer from incubation period measurements in hamsters. Adv. Exp. Med. Biol. 134, 385-399.
-
(1981)
Adv. Exp. Med. Biol.
, vol.134
, pp. 385-399
-
-
Prusiner, S.B.1
Cochran, S.P.2
Downey, D.E.3
Groth, D.F.4
-
231
-
-
0021752457
-
Purification and structural studies of a major scrapie prion protein
-
PRUSINER, S. B., GROTH, D. F., BOLTON, D. C., KENT, S. B. & HOOD, L. E. (1984). Purification and structural studies of a major scrapie prion protein. Cell 38, 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
-
232
-
-
0019324430
-
Molecular properties, partial purification, and assay by incubation period measurements of the hamster scrapie agent
-
PRUSINER, S. B., GROTH, D. F., COCHRAN, S. P., MASIARZ, F. R., MCKINLEY, M. P. & MARTINEZ, H. M. (1980). Molecular properties, partial purification, and assay by incubation period measurements of the hamster scrapie agent, Biochemistry 19, 4883-4891.
-
(1980)
Biochemistry
, vol.19
, pp. 4883-4891
-
-
Prusiner, S.B.1
Groth, D.F.2
Cochran, S.P.3
Masiarz, F.R.4
Mckinley, M.P.5
Martinez, H.M.6
-
233
-
-
0348169164
-
Sedimentation properties of the scrapic agent
-
PRUSINER, S. B., HADLOW, W. J., EKLUND, C. M. & RACE, R. E. (1977). Sedimentation properties of the scrapic agent. Proc. natn. Acad. Sci. USA 74, 4656-4660.
-
(1977)
Proc. Natn. Acad. Sci. USA
, vol.74
, pp. 4656-4660
-
-
Prusiner, S.B.1
Hadlow, W.J.2
Eklund, C.M.3
Race, R.E.4
-
234
-
-
0021019026
-
Scrapie prions aggregate to form amyloid-like birefringent rods
-
PRUSINER, S. B., MCKINLEY, M. P., BOWMAN, K. A., BOLTON, D. C., BENDHEIM, P. K., GROTH, D. F. & GLENNER, G. G. (1983). Scrapie prions aggregate to form amyloid-like birefringent rods. Cell 35, 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.K.5
Groth, D.F.6
Glenner, G.G.7
-
235
-
-
2442490085
-
Scrapie agent contains a hydrophobic protein
-
PRUSINER, S. B., MCKINLEY, M. P., GROTH, D. F., BOWMAN, K. A., MOCK, N. I., COCHRAN, S. P. & MASIARZ, F. R. (1981b). Scrapie agent contains a hydrophobic protein. Proc. natn. Acad. Sci. USA 78, 6675-6679.
-
(1981)
Proc. Natn. Acad. Sci. USA
, vol.78
, pp. 6675-6679
-
-
Prusiner, S.B.1
Mckinley, M.P.2
Groth, D.F.3
Bowman, K.A.4
Mock, N.I.5
Cochran, S.P.6
Masiarz, F.R.7
-
236
-
-
0025244011
-
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
-
PRUSINER, S. B., SCOTT, M., FOSTER, D., PAN, K.-M., GROTH, D., MIRENDA, C., TORCHIA, M., YANG, S.-L., SERBAN, D., CARLSON, G. A., HOPPE, P. C., WESTAWAY, D. & DEARMOND, S. J. (1990). Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication. Cell 63, 673-686.
-
(1990)
Cell
, vol.63
, pp. 673-686
-
-
Prusiner, S.B.1
Scott, M.2
Foster, D.3
Pan, K.-M.4
Groth, D.5
Mirenda, C.6
Torchia, M.7
Yang, S.-L.8
Serban, D.9
Carlson, G.A.10
Hoppe, P.C.11
Westaway, D.12
Dearmond, S.J.13
-
237
-
-
0032076463
-
Prion protein biology
-
PRUSINER, S. B., SCOTT, M. R., DEARMOND, S. J. & COHEN, F. E. (1998). Prion protein biology. Cell 93, 337-348.
-
(1998)
Cell
, vol.93
, pp. 337-348
-
-
Prusiner, S.B.1
Scott, M.R.2
Dearmond, S.J.3
Cohen, F.E.4
-
238
-
-
0030802361
-
Molecular assessment of the potential transmissibilities of BSE and scrapie to humans
-
RAYMOND, G. J., HOPE, J., KOCISKO, D. A., PRIOLA, S. A., RAYMOND, L. D., BOSSERS, A., IRONSIDE, J., WILL, R. G., CHEN, S. G., PETERSEN, R. B., GAMBETTI, P., RUBENSTEIN, R., SMITS, M. A., LANSBURY, P. T., JR. & CAUGHEY, B. (1997). Molecular assessment of the potential transmissibilities of BSE and scrapie to humans. Nature 388, 285-288.
-
(1997)
Nature
, vol.388
, pp. 285-288
-
-
Raymond, G.J.1
Hope, J.2
Kocisko, D.A.3
Priola, S.A.4
Raymond, L.D.5
Bossers, A.6
Ironside, J.7
Will, R.G.8
Chen, S.G.9
Petersen, R.B.10
Gambetti, P.11
Rubenstein, R.12
Smits, M.A.13
Lansbury P.T., Jr.14
Caughey, B.15
-
239
-
-
0031436335
-
The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells
-
RIEGER, R., EDENHOFER, F., LASMÉZAS, C. I. & WEISS, S. (1997). The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells. Nat. Med. 3, 1383-1388.
-
(1997)
Nat. Med.
, vol.3
, pp. 1383-1388
-
-
Rieger, R.1
Edenhofer, F.2
Lasmézas, C.I.3
Weiss, S.4
-
240
-
-
0029937271
-
NMR structure of the mouse prion protein domain PrP(121-231)
-
RIEK, R., HORNEMANN, S., WIDER, G., BILLETER, M., GLOCKSHUBER, R. & WUTHRICH, K. (1996). NMR structure of the mouse prion protein domain PrP(121-231). Nature 382, 180-182.
-
(1996)
Nature
, vol.382
, pp. 180-182
-
-
Riek, R.1
Hornemann, S.2
Wider, G.3
Billeter, M.4
Glockshuber, R.5
Wuthrich, K.6
-
241
-
-
0030836511
-
NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231)
-
RIEK, R., HORNEMANN, S., WIDER, G., GLOCKSHUBER, R. & WÜTHRICH, K. (1997). NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231). FEBS Lett. 4123, 282-288.
-
(1997)
FEBS Lett.
, vol.4123
, pp. 282-288
-
-
Riek, R.1
Hornemann, S.2
Wider, G.3
Glockshuber, R.4
Wüthrich, K.5
-
242
-
-
0032578451
-
Prion protein NMR structure and familial human spongiform encephalopathies
-
RIEK, R., WIDER, G., BILLETER, M., HORNEMANN, S., GLOCKSHUBER, R. & WUTHRICH, K. (1998). Prion protein NMR structure and familial human spongiform encephalopathies. Proc. natn. Acad. Sci. USA 95, 11667-11672.
-
(1998)
Proc. Natn. Acad. Sci. USA
, vol.95
, pp. 11667-11672
-
-
Riek, R.1
Wider, G.2
Billeter, M.3
Hornemann, S.4
Glockshuber, R.5
Wuthrich, K.6
-
243
-
-
0030026759
-
Disruption of prion rods generates 10-nm spherical particles having high α-helical content and lacking scrapie infectivity
-
RIESNEK, D., KELLINGS, K., POST, K., WILLE, H., SERBAN, H., GROTH, D., BALDWIN, M. A. & PRUSINER, S. B. (1996). Disruption of prion rods generates 10-nm spherical particles having high α-helical content and lacking scrapie infectivity. J. Virol. 70, 1714-1722.
-
(1996)
J. Virol.
, vol.70
, pp. 1714-1722
-
-
Riesnek, D.1
Kellings, K.2
Post, K.3
Wille, H.4
Serban, H.5
Groth, D.6
Baldwin, M.A.7
Prusiner, S.B.8
-
244
-
-
0025643347
-
Intracellular accumulation of the cellular prion protein after mutagenesis of its Asn-linked glycosylation sites
-
ROGERS, M., TARABOULOS, A., SCOTT, M., GROTH, D. & PRUSINER, S. B. (1990). Intracellular accumulation of the cellular prion protein after mutagenesis of its Asn-linked glycosylation sites. Glycobiology 1, 101-109.
-
(1990)
Glycobiology
, vol.1
, pp. 101-109
-
-
Rogers, M.1
Taraboulos, A.2
Scott, M.3
Groth, D.4
Prusiner, S.B.5
-
245
-
-
0027520888
-
Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells
-
ROGERS, M., YEHIELY, P., SCOTT, M. & PRUSINER, S. B. (1993). Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells. Proc. natn. Acad. Sci. USA 90, 3182-3186.
-
(1993)
Proc. Natn. Acad. Sci. USA
, vol.90
, pp. 3182-3186
-
-
Rogers, M.1
Yehiely, P.2
Scott, M.3
Prusiner, S.B.4
-
246
-
-
0027477463
-
Structural alterations in the peptide backbone of β-amyloid core protein may account tor its deposition and stability in Alzheimer's disease
-
ROHER, A. E., LOWENSON, J. D., CLARKE, S., WOLKOW, C., WANG, R., COTTER, R. J., REARDON, I. M., ZURCHER-NEELY, H. A., HEINRIKSON, R. L., BALL, M. J. & GREENBERG, B. D. (1993a). Structural alterations in the peptide backbone of β-amyloid core protein may account tor its deposition and stability in Alzheimer's disease. J. Biol. Chem. 268, 3072-3083.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 3072-3083
-
-
Roher, A.E.1
Lowenson, J.D.2
Clarke, S.3
Wolkow, C.4
Wang, R.5
Cotter, R.J.6
Reardon, I.M.7
Zurcher-Neely, H.A.8
Heinrikson, R.L.9
Ball, M.J.10
Greenberg, B.D.11
-
247
-
-
0027332081
-
β-Amyloid-(1-42) is a major component of cerebrovascular amyloid deposits : Implications for the pathology of Alzheimer disease
-
ROHER, A. E., LOWENSON, J. D., CLARKE, S., WOODS, A. S., COTTER, R. J., GOWING, E. & BALL, M. J. (1993b). β-Amyloid-(1-42) is a major component of cerebrovascular amyloid deposits : implications for the pathology of Alzheimer disease. Proc. natn. Acad. Sci. USA 90, 10836-10840.
-
(1993)
Proc. Natn. Acad. Sci. USA
, vol.90
, pp. 10836-10840
-
-
Roher, A.E.1
Lowenson, J.D.2
Clarke, S.3
Woods, A.S.4
Cotter, R.J.5
Gowing, E.6
Ball, M.J.7
-
248
-
-
0033542142
-
Cell-lysate conversion of prion protein into its protease-resistant isoform suggests the participation of a cellular chaperone
-
SABORÍO, G. P., SOTO, C., KASCSAK, R. J., LEVY, E., KASCSAK, R., HARRIS, D. A. & FRANGIONE, B. (1999). Cell-lysate conversion of prion protein into its protease-resistant isoform suggests the participation of a cellular chaperone. Biochem. biophys. Res. Commun. 258, 470-475.
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.258
, pp. 470-475
-
-
Saborío, G.P.1
Soto, C.2
Kascsak, R.J.3
Levy, E.4
Kascsak, R.5
Harris, D.A.6
Frangione, B.7
-
249
-
-
0027182522
-
Conformational transitions, dissociation, and unfolding of scrapie amyloid (prion) protein
-
SAFAR, J., ROLLER, P. P., GAJDUSEK, D. C., GIBBS, C. J., JR. (1993a). Conformational transitions, dissociation, and unfolding of scrapie amyloid (prion) protein. J. biol. Chem. 268, 20276-20284.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 20276-20284
-
-
Safar, J.1
Roller, P.P.2
Gajdusek, D.C.3
Gibbs C.J., Jr.4
-
250
-
-
0027363495
-
Thermal stability and conformational transitions ot scrapie amyloid (prion) protein correlate with infectivity
-
SAFAR, J., ROLLER, P. P., GAJDUSEK, D. C. & GIBBS, C. J., JR. (1993b). Thermal stability and conformational transitions ot scrapie amyloid (prion) protein correlate with infectivity. Protein Sci. 2, 2206-2216.
-
(1993)
Protein Sci.
, vol.2
, pp. 2206-2216
-
-
Safar, J.1
Roller, P.P.2
Gajdusek, D.C.3
Gibbs C.J., Jr.4
-
251
-
-
0028120343
-
Scrapie amyloid (prion) protein has the conformational characteristics ot an aggregated molten globule folding intermediate
-
SAFAR, J., ROLLER, P. P., GAJDUSEK, D. C. & GIBBS, C. J., JR. (1994). Scrapie amyloid (prion) protein has the conformational characteristics ot an aggregated molten globule folding intermediate. Biochemistry 33, 8375-8383.
-
(1994)
Biochemistry
, vol.33
, pp. 8375-8383
-
-
Safar, J.1
Roller, P.P.2
Gajdusek, D.C.3
Gibbs C.J., Jr.4
-
252
-
-
0031720905
-
Sc molecules with different conformations
-
Sc molecules with different conformations. Nat. Med. 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
-
253
-
-
0028343093
-
No propagation ot prions in mice devoid of PrP
-
SAILER, A., BÜELER, H., FISCHER, M., AGUZZI, A. & WEISSMANN, C. (1994). No propagation ot prions in mice devoid of PrP. Cell 77, 967-968.
-
(1994)
Cell
, vol.77
, pp. 967-968
-
-
Sailer, A.1
Büeler, H.2
Fischer, M.3
Aguzzi, A.4
Weissmann, C.5
-
254
-
-
13344282734
-
Loss of cerebellar Purkinje cells in aged mice homoxygous for a disrupted PrP gene
-
SAKAGUCHI, S., KATAMINE, S., NISHIDA, N., MORIUCHI, R., SHIGEMATSU, K., SUGIMOTO, T., NAKATANI, A., KATAOKA, Y., HOUTANI, T., SHIRABE, S., OKADA, H., HASEGAWA, S., MIYAMOTO, T. & NODA, T. (1996). Loss of cerebellar Purkinje cells in aged mice homoxygous 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
Sugimoto, T.6
Nakatani, A.7
Kataoka, Y.8
Houtani, T.9
Shirabe, S.10
Okada, H.11
Hasegawa, S.12
Miyamoto, T.13
Noda, T.14
-
255
-
-
0033567401
-
Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106-126
-
SALMONA, M., MALESANI, P., DE GIOLA, L., GORLA, S., BRUSCHI, M., MOLINARI, A., DELLA VEDOVA, F., PEDROTTI, B., MARRARI, M. A., AWAN, T., BUGIANI, O., FORLONI, G. & TAGLIAVINI, F. (1999). Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106-126. Biochem J. 342, 207-214.
-
(1999)
Biochem J.
, vol.342
, pp. 207-214
-
-
Salmona, M.1
Malesani, P.2
De Giola, L.3
Gorla, S.4
Bruschi, M.5
Molinari, A.6
Della Vedova, F.7
Pedrotti, B.8
Marrari, M.A.9
Awan, T.10
Bugiani, O.11
Forloni, G.12
Tagliavini, F.13
-
256
-
-
0028962532
-
Prion protein gene variation among primates
-
SCHÄTZL, H. M., DA COSTA, M., TAYLOR, L., COHEN, F. E. & PRUSINER, S. B. (1995). Prion protein gene variation among primates. J. molec. Biol. 245, 362-374.
-
(1995)
J. Molec. Biol.
, vol.245
, pp. 362-374
-
-
Schätzl, H.M.1
Da Costa, M.2
Taylor, L.3
Cohen, F.E.4
Prusiner, S.B.5
-
257
-
-
0024820814
-
Transgenic mice expressing hamster prion protein produce species-species scrapie infectivity and amyloid plaques
-
SCOTT, M., FOSTER, D., MIRENDA, C., SERBAN, D., COUFAL, F., WÄLCHLI, M., TORCHIA, M., GROTH, D., CARLSON, G., DEARMOND, S. J., WESTAWAY, D. & PRUSINER, S. B. (1989). Transgenic mice expressing hamster prion protein produce species-species scrapie infectivity and amyloid plaques. Cell 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
Wälchli, M.6
Torchia, M.7
Groth, D.8
Carlson, G.9
Dearmond, S.J.10
Westaway, D.11
Prusiner, S.B.12
-
258
-
-
0027229676
-
Propagation of prions with artiricial properties in transgenic mice expressing chimeric PrP genes
-
SCOTT, M., GROTH, D., FOSTER, D., TORCHIA, M., YANG, S.-L., DEARMOND, S. J. & PRUSINER, S. B. (1993). Propagation of prions with artiricial properties in transgenic mice expressing chimeric PrP genes. Cell 73, 979-988.
-
(1993)
Cell
, vol.73
, pp. 979-988
-
-
Scott, M.1
Groth, D.2
Foster, D.3
Torchia, M.4
Yang, S.-L.5
Dearmond, S.J.6
Prusiner, S.B.7
-
259
-
-
0030731124
-
Propagation of prion strains through specific conformers of the prion protein
-
SCOTT, M. R., GROTH, D., TATZELT, J., TORCHIA, M., TREMBLAY, P., DEARMOND, S. J. & PRUSINER, S. B. (1997a). Propagation of prion strains through specific conformers of the prion protein. J. Virol. 71, 9032-9044.
-
(1997)
J. Virol.
, vol.71
, pp. 9032-9044
-
-
Scott, M.R.1
Groth, D.2
Tatzelt, J.3
Torchia, M.4
Tremblay, P.5
Dearmond, S.J.6
Prusiner, S.B.7
-
260
-
-
0027086835
-
Chimeric prion protein expression in cultured cells and transgenic mice
-
SCOTT, M. R., KOHLER, R., FOSTER, D. & PRUSINER, S. B. (1992). Chimeric prion protein expression in cultured cells and transgenic mice. Protein Sci. 1, 986-997.
-
(1992)
Protein Sci.
, vol.1
, pp. 986-997
-
-
Scott, M.R.1
Kohler, R.2
Foster, D.3
Prusiner, S.B.4
-
261
-
-
13144275223
-
Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice
-
SCOTT, M. R., SAFAR, J., TELLING, G., NGUYEN, O., GROTH, D., TORCHIA, M., KOEHLER, R., TREMBLAY, P., WALTHER, D., COHEN, F. E., DEARMOND, S. J. & PRUSINER, S. B. (1997b). Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice. Proc. natn. Acad. Sci. USA 94, 14279-14284.
-
(1997)
Proc. Natn. Acad. Sci. USA
, vol.94
, pp. 14279-14284
-
-
Scott, M.R.1
Safar, J.2
Telling, G.3
Nguyen, O.4
Groth, D.5
Torchia, M.6
Koehler, R.7
Tremblay, P.8
Walther, D.9
Cohen, F.E.10
Dearmond, S.J.11
Prusiner, S.B.12
-
262
-
-
0033592877
-
Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans
-
SCOTT, M. R., WILL, R., IRONSIDE, J., NGUYEN, H.-O. B., TREMBLAY, P., DEARMOND, S. J. & PRUSINER, S. B. (1999). Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans. Proc. natn. Acad. Sci. USA 96, 15137-15142.
-
(1999)
Proc. Natn. Acad. Sci. USA
, vol.96
, pp. 15137-15142
-
-
Scott, M.R.1
Will, R.2
Ironside, J.3
Nguyen, H.-O.B.4
Tremblay, P.5
Dearmond, S.J.6
Prusiner, S.B.7
-
263
-
-
0027259274
-
Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein
-
SELVAGGINI, C., DE GIOLA, L., CANTÚ, L., GHIBAUDI, E., DIOMEDE, L., PASSERINI, F., FORLONI, G., BUGIANI, O., TAGLIAVINI, F. & SALMONA, M. (1993). Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein. Biochem. biophys. Res. Commun. 194, 1380-1386.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.194
, pp. 1380-1386
-
-
Selvaggini, C.1
De Giola, L.2
Cantú, L.3
Ghibaudi, E.4
Diomede, L.5
Passerini, F.6
Forloni, G.7
Bugiani, O.8
Tagliavini, F.9
Salmona, M.10
-
264
-
-
0033580818
-
Protease-resistant and detergent-insoluble prion protein is not necessarily associated with prion infectivity
-
SHAKED, G. M., FRIDLANDER, G., MEINER, Z., TARABOULOS, A. & GABIZON, R. (1999). Protease-resistant and detergent-insoluble prion protein is not necessarily associated with prion infectivity. J. biol. Chem. 274, 17981-17986.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 17981-17986
-
-
Shaked, G.M.1
Fridlander, G.2
Meiner, Z.3
Taraboulos, A.4
Gabizon, R.5
-
265
-
-
0031787736
-
Prion protein fragments spanning helix 1 and both strands of β sheet (residues 125-170) show evidence for predominantly helical propensity by CD and NMR
-
SHARMAN, G. J., KENWARD, N., WILLIAMS, H. E., LANDON, M., MAYER, R. J. & SHARLE, M. S. (1998). Prion protein fragments spanning helix 1 and both strands of β sheet (residues 125-170) show evidence for predominantly helical propensity by CD and NMR. Fold. Des. 3, 313-320.
-
(1998)
Fold. Des.
, vol.3
, pp. 313-320
-
-
Sharman, G.J.1
Kenward, N.2
Williams, H.E.3
Landon, M.4
Mayer, R.J.5
Sharle, M.S.6
-
266
-
-
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., GÖTZ, J., RÜLICKE, T., FLECHSIG, E., COZZIO, A., VON MERING, C., HANGARTNER, C., AGUZZI, A. & WEISSMANN, C. (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
Götz, J.6
Rülicke, T.7
Flechsig, E.8
Cozzio, A.9
Von Mering, C.10
Hangartner, C.11
Aguzzi, A.12
Weissmann, C.13
-
267
-
-
0033617534
-
Chaperonin function: Folding by forced unfolding
-
SHTILERMAN, M., LORIMER, G. H. & ENGLANDER, S. W. (1999). Chaperonin function: folding by forced unfolding. Science 284, 822-825.
-
(1999)
Science
, vol.284
, pp. 822-825
-
-
Shtilerman, M.1
Lorimer, G.H.2
Englander, S.W.3
-
268
-
-
0028305135
-
A glycolipid-anchored prion protein is endocytosed via clathrin-coated pits
-
SHYNG, S.-L., HEUSER, J. E. & HARRIS, D. A. (1994). A glycolipid-anchored prion protein is endocytosed via clathrin-coated pits. J. Cell Biol. 125, 1239-1250.
-
(1994)
J. Cell Biol.
, vol.125
, pp. 1239-1250
-
-
Shyng, S.-L.1
Heuser, J.E.2
Harris, D.A.3
-
269
-
-
0027204276
-
A prion protein cycle between the cell surface and an endocyric compartment in cultured neuroblastoma cell
-
SHYNG, S.-L., HUBER, M. T. & HARRIS, D. A. (1993). A prion protein cycle between the cell surface and an endocyric compartment in cultured neuroblastoma cell. J. biol. Chem. 268, 15922-15928.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 15922-15928
-
-
Shyng, S.-L.1
Huber, M.T.2
Harris, D.A.3
-
270
-
-
0029054937
-
The N-terminal domain of a glycolipid-anchored priori protein is essential for its endocytosis via clathrin-coated pits
-
SHYNG, S.-L., MOULDER, K. L., LESKO, A. & HARRIS, D. A. (1995). The N-terminal domain of a glycolipid-anchored priori 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
-
271
-
-
0031684079
-
Structure and function in GroEL-mediated protein folding
-
SIGLER, P. B., XU, Z., RYE, H. S., BURSTON, S. G., FENTON, W. A. & HORWICH, A. L. (1998). Structure and function in GroEL-mediated protein folding. A. Rev. Biochem. 67, 581-608.
-
(1998)
A. Rev. Biochem.
, vol.67
, pp. 581-608
-
-
Sigler, P.B.1
Xu, Z.2
Rye, H.S.3
Burston, S.G.4
Fenton, W.A.5
Horwich, A.L.6
-
272
-
-
0030023858
-
Immunoelectron microscopic localization ot the 60-kDa heat shock chaperonin protein (Hsp60) in mammalian cells
-
SOLTYS, B. J. & GUPTA, R. S. (1996). Immunoelectron microscopic localization ot the 60-kDa heat shock chaperonin protein (Hsp60) in mammalian cells. Exp. Cell. Res. 222, 16-27.
-
(1996)
Exp. Cell. Res.
, vol.222
, pp. 16-27
-
-
Soltys, B.J.1
Gupta, R.S.2
-
273
-
-
0031147756
-
Cell surface localization of the 60 kDa heat shock chaperonin protein (Hsp60) in mammalian cells
-
SOLTYS, B. J. & GUPTA, R. S. (1997). Cell surface localization of the 60 kDa heat shock chaperonin protein (Hsp60) in mammalian cells. Cell. Biol. Int. 21, 315-320.
-
(1997)
Cell. Biol. Int.
, vol.21
, pp. 315-320
-
-
Soltys, B.J.1
Gupta, R.S.2
-
274
-
-
0033133729
-
Mitochondrial-matrix proteins at unexpected locations: Are they exported?
-
SOLTYS, B. J. & GUPTA, R. S. (1999). Mitochondrial-matrix proteins at unexpected locations: are they exported? Trends biochem. Sci. 24, 174-177.
-
(1999)
Trends Biochem. Sci.
, vol.24
, pp. 174-177
-
-
Soltys, B.J.1
Gupta, R.S.2
-
275
-
-
0025091084
-
Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein
-
STAHL, N., BALDWIN, M. A., BURLINGAME, A. L. & PRUSINER, S. B. (1990a). Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein. Biochemistry 29, 8879-8884.
-
(1990)
Biochemistry
, vol.29
, pp. 8879-8884
-
-
Stahl, N.1
Baldwin, M.A.2
Burlingame, A.L.3
Prusiner, S.B.4
-
276
-
-
0027534612
-
Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing
-
STAHL, N., BALDWIN, M. A., TEPLOW, D. B., HOOD, L., GIBSON, B. W., BURLINGAME, A. L. & PRUSINER, S. B. (1993). Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing. Biochemistry 32, 1991-2002.
-
(1993)
Biochemistry
, vol.32
, pp. 1991-2002
-
-
Stahl, N.1
Baldwin, M.A.2
Teplow, D.B.3
Hood, L.4
Gibson, B.W.5
Burlingame, A.L.6
Prusiner, S.B.7
-
277
-
-
0023663071
-
Scrapie prion protein contains a phosphatidylinositol glycolipid
-
STAHL, N., BORCHELT, D. R., HSIAO, K. & PRUSINER, S. B. (1987). Scrapie prion protein contains a phosphatidylinositol glycolipid. Cell 51, 229-240.
-
(1987)
Cell
, vol.51
, pp. 229-240
-
-
Stahl, N.1
Borchelt, D.R.2
Hsiao, K.3
Prusiner, S.B.4
-
278
-
-
0025339439
-
Differential release of cellular and scrapie prion proteins from cellular membranes by phosphatidylinositol-specific phospholipase: C
-
STAHL, N., BORCHELT, D. R. & PRUSINER, S. B. (1990b). Differential release of cellular and scrapie prion proteins from cellular membranes by phosphatidylinositol-specific phospholipase: C. Biochemistry 29, 5405-5412.
-
(1990)
Biochemistry
, vol.29
, pp. 5405-5412
-
-
Stahl, N.1
Borchelt, D.R.2
Prusiner, S.B.3
-
279
-
-
0037965529
-
Prion protein selectively binds copper(II) ions
-
STÖCKEL, J., SAFAR, J., WALLACE, A. C., COHEN, F. E. & PRUSINER, S. B. (1998). Prion protein selectively binds copper(II) ions. Biochemistry 37, 7185-7193.
-
(1998)
Biochemistry
, vol.37
, pp. 7185-7193
-
-
Stöckel, J.1
Safar, J.2
Wallace, A.C.3
Cohen, F.E.4
Prusiner, S.B.5
-
281
-
-
0031825554
-
From the globular to the fibrous state: Protein structure and structural conversion in amyloid formation
-
SUNDE, M. & BLAKE, C. C. (1998). From the globular to the fibrous state: protein structure and structural conversion in amyloid formation. Q. Rev. Biophys. 31, 1-39.
-
(1998)
Q. Rev. Biophys.
, vol.31
, pp. 1-39
-
-
Sunde, M.1
Blake, C.C.2
-
282
-
-
0033582935
-
Prion protein of 106 residues creates an artificial transmission barrier for prion replication in transgenic mice
-
SUPATTAPONE, S., BOSQUE, P., MURAMOTO, T., WILLE, H., AAGAARD, C., PERETZ, D., NGUYEN, H.-O. B., HEINRICH, C., TORCHIA, M., SAFAR, J., COHEN, F. E., DEARMOND, S. J., PRUSINER, S. B. & SCOTT, M. (1999). Prion protein of 106 residues creates an artificial transmission barrier for prion replication in transgenic mice. Cell 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.B.7
Heinrich, C.8
Torchia, M.9
Safar, J.10
Cohen, F.E.11
Dearmond, S.J.12
Prusiner, S.B.13
Scott, M.14
-
283
-
-
0034681173
-
Aggregation and fibrillization of the recombinant human prion protein huPrP90 231
-
SWIFTNICKI, W., MORILLAS, M., CHEN, S. G., GAMBETTI, P. & SUREWICZ, W. K. (2000). Aggregation and fibrillization of the recombinant human prion protein huPrP90 231. Biochemistry 39, 424-431.
-
(2000)
Biochemistry
, vol.39
, pp. 424-431
-
-
Swiftnicki, W.1
Morillas, M.2
Chen, S.G.3
Gambetti, P.4
W, K.5
-
284
-
-
0030781922
-
pH-dependent stability and conformation of the recombinant human prion protein PrP(90-231)
-
SWIETNICKI, W., PETERSEN, R., GAMBETTI, P. & SUREWICZ, W. K. (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
-
285
-
-
0032553530
-
Familial mutations and the thermodynamic stability of the recombinant human prion protein
-
SWIETNICKI, W., PETERSEN, R. B., GAMBETTI, P. & SUREWICZ, W. K. (1998). Familial mutations and the thermodynamic stability of the recombinant human prion protein. J. biol. Chem. 273, 31048-31052.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 31048-31052
-
-
Swietnicki, W.1
Petersen, R.B.2
Gambetti, P.3
Surewicz, W.K.4
-
286
-
-
0026033998
-
Amyloid protein of Gerstmann Stäussler Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58
-
TAGLIAVINI, F., PRELLI, F., GHISO, J., BUGIANI, O., SERBAN, D., PRUSINER, S. B., FARLOW, M. R., GHETTI, B. & FRANGIONE, B. (1991). Amyloid protein of Gerstmann Stäussler Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58. EMBO J. 10, 513-519.
-
(1991)
EMBO J.
, vol.10
, pp. 513-519
-
-
Tagliavini, F.1
Prelli, F.2
Ghiso, J.3
Bugiani, O.4
Serban, D.5
Prusiner, S.B.6
Farlow, M.R.7
Ghetti, B.8
Frangione, B.9
-
287
-
-
0027367506
-
Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro
-
TAGLIAVINI, F., PRELLI, F., VERGA, L., GIACCONE, G., SARMA, R., GOREVIC, P., GHETTI, B., PASSERINI, F., GHIBAUDI, K., FORLONI, G., SALMONA, M., BUGIANI, O. & FRANGIONE, B. (1993). Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro. Proc. natn. Acad. Sci. USA 90, 9678-9682.
-
(1993)
Proc. Natn. Acad. Sci. USA
, vol.90
, pp. 9678-9682
-
-
Tagliavini, F.1
Prelli, F.2
Verga, L.3
Giaccone, G.4
Sarma, R.5
Gorevic, P.6
Ghetti, B.7
Passerini, F.8
Ghibaudi, K.9
Forloni, G.10
Salmona, M.11
Bugiani, O.12
Frangione, B.13
-
288
-
-
0033543671
-
Identification of substrate binding site of GroEL minichaperone in solution
-
TANAKA, N. & FERSHT, A. R. (1999). Identification of substrate binding site of GroEL minichaperone in solution. J. molec. Biol. 292, 173-180.
-
(1999)
J. Molec. Biol.
, vol.292
, pp. 173-180
-
-
Tanaka, N.1
Fersht, A.R.2
-
289
-
-
0025087141
-
Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation
-
TARABOULOS, A., ROGERS, M., BORCHELT, D. R., MCKINLEY, M. P., SCOTT, M., SERBAN, D. & PRUSINER, S. B. (1990a). Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation. Proc. natn. Acad. Sci. USA 87, 8262-8266.
-
(1990)
Proc. Natn. Acad. Sci. USA
, vol.87
, pp. 8262-8266
-
-
Taraboulos, A.1
Rogers, M.2
Borchelt, D.R.3
Mckinley, M.P.4
Scott, M.5
Serban, D.6
Prusiner, S.B.7
-
290
-
-
0028966735
-
Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isotorm
-
TARABOULOS, A., SCOTT, M., SEMENOV, A., AVRAHAMI, D., LASZLO, L. & PRUSINER, S. B. (1995). Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isotorm. J. Cell biol. 129, 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
-
291
-
-
0025373111
-
Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells
-
TARABOULOS, A., SERBAN, D. & PRUSINER, S. B. (1990b). Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells. J. Cell biol. 110, 2117-2132.
-
(1990)
J. Cell Biol.
, vol.110
, pp. 2117-2132
-
-
Taraboulos, A.1
Serban, D.2
Prusiner, S.B.3
-
292
-
-
0029832863
-
Chemical chaperones interfere with the formation of scrapie prion protein
-
TATZELT, J., PRUSINER, S. B. & WELCH, W. J. (1996). Chemical chaperones interfere with the formation of scrapie prion protein. EMBO J. 15, 6363-6373.
-
(1996)
EMBO J.
, vol.15
, pp. 6363-6373
-
-
Tatzelt, J.1
Prusiner, S.B.2
Welch, W.J.3
-
293
-
-
0029740354
-
Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice
-
TELLING, G. C., HAGA, T., TORCHIA, M., TREMBLAY, P., DEARMOND, S. J. & PRUSINER, S. B. (1996a). Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice. Genes Dev. 10, 1736-1750.
-
(1996)
Genes Dev.
, vol.10
, pp. 1736-1750
-
-
Telling, G.C.1
Haga, T.2
Torchia, M.3
Tremblay, P.4
Dearmond, S.J.5
Prusiner, S.B.6
-
294
-
-
12644272790
-
Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity
-
TELLING, G. C., PARCHI, P., DEARMOND, S. J., CORTELLI, P., MONTAGNA, P., GABIZON, R., MASTRIANNI, J., LUGARESI, K., GAMBETTI, P. & PRUSINER, S. B. (1996b). Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity. Science 274, 2079-2082.
-
(1996)
Science
, vol.274
, pp. 2079-2082
-
-
Telling, G.C.1
Parchi, P.2
Dearmond, S.J.3
Cortelli, P.4
Montagna, P.5
Gabizon, R.6
Mastrianni, J.7
Lugaresi, K.8
Gambetti, P.9
Prusiner, S.B.10
-
295
-
-
0028102794
-
Transmission ot Creutzfeldt Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein
-
TELLING, G. C., SCOTT, M., HSIAO, K. K., FOSTER, D., YANG, S.-L., TORCHIA, M., SIDLE, K. C. L., COLLINGE, J., DEARMOND, S. J. & PRUSINER, S. B. (1994). Transmission ot Creutzfeldt Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein. Proc. natn Acad. Sci. 91, 9936-9940.
-
(1994)
Proc. Natn Acad. Sci.
, vol.91
, pp. 9936-9940
-
-
Telling, G.C.1
Scott, M.2
Hsiao, K.K.3
Foster, D.4
Yang, S.-L.5
Torchia, M.6
Sidle, K.C.L.7
Collinge, J.8
Dearmond, S.J.9
Prusiner, S.B.10
-
296
-
-
0028882424
-
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction ot cellular PrP with another protein
-
TELLING, G. C., SCOTT, M., MASTRIANNI, J., GABIZON, R., TORCHIA, M., COHEN, F. E., DEARMOND, S. J. & PRUSINER, S. B. (1995). Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction ot cellular PrP with another protein. Cell 83, 79-90.
-
(1995)
Cell
, vol.83
, pp. 79-90
-
-
Telling, G.C.1
Scott, M.2
Mastrianni, J.3
Gabizon, R.4
Torchia, M.5
Cohen, F.E.6
Dearmond, S.J.7
Prusiner, S.B.8
-
297
-
-
15844421385
-
Altered circadian activity rhythms and sleep in mice devoid of prion protein
-
TOBLER, I., GAUS, S. E., DEBOER, T., ACHERMANN, P., FISCHER, M., RÜLICKE, T., MOSER, M., OESCH, B., MCBRIDE, P. A. & MANSON, J. C. (1996). Altered circadian activity rhythms and sleep in mice devoid of prion protein. Nature 380, 639-642.
-
(1996)
Nature
, vol.380
, pp. 639-642
-
-
Tobler, I.1
Gaus, S.E.2
Deboer, T.3
Achermann, P.4
Fischer, M.5
Rülicke, T.6
Moser, M.7
Oesch, B.8
Mcbride, P.A.9
Manson, J.C.10
-
298
-
-
0023676109
-
Purification and properties of the cellular and scrapie hamster prion proteins
-
TURK, E., TEPLOW, D. B., HOOD, L. E. & PRUSINER, S. B. (1988). Purification and properties of the cellular and scrapie hamster prion proteins. Eur. J. biochem. 176, 21-20.
-
(1988)
Eur. J. Biochem.
, vol.176
, pp. 21-120
-
-
Turk, E.1
Teplow, D.B.2
Hood, L.E.3
Prusiner, S.B.4
-
299
-
-
0028345717
-
Molecular chaperones in pancreatic tissue: The presence of cpn10, cpn60 and hsp70 in distinct compartments along the secretory pathway of the acinar cells
-
VÉLEZ-GRANELL, C. S., ARIAS, A. E., TORRES-RUÍZ, J. A. & BENDAYAN, M. (1994). Molecular chaperones in pancreatic tissue: the presence of cpn10, cpn60 and hsp70 in distinct compartments along the secretory pathway of the acinar cells. J. Cell Sci. 107, 539-549.
-
(1994)
J. Cell Sci.
, vol.107
, pp. 539-549
-
-
Vélez-Granell, C.S.1
Arias, A.E.2
Torres-Ruíz, J.A.3
Bendayan, M.4
-
300
-
-
0029962468
-
Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains
-
VEY, M., PILKUHN, S., WILLE, H., NIXON, R., DEARMOND, S. J., SMART, E. J., ANDERSON, R. G., TARABOULOS, A. & PRUSINER, S. B. (1996). Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains. Proc. natn. Acad. Sci. USA 93, 14945-14949.
-
(1996)
Proc. Natn. 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
Anderson, R.G.7
Taraboulos, A.8
Prusiner, S.B.9
-
301
-
-
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. (1999). Copper binding to the prion protein: structural implications of four identical cooperative binding sites. Proc. natn. Acad. Sci. USA 96, 2042-2047.
-
(1999)
Proc. Natn. Acad. Sci. USA
, 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
-
302
-
-
0029837424
-
A thermodynamic coupling mechanism tor GroEL-mediated unfolding
-
WALTER, S., LORIMER, G. H. & SCHMID, F. X. (1996). A thermodynamic coupling mechanism tor GroEL-mediated unfolding. Proc. natn. Acad. Sci. USA 93, 9425-9430.
-
(1996)
Proc. Natn. Acad. Sci. USA
, vol.93
, pp. 9425-9430
-
-
Walter, S.1
Lorimer, G.H.2
Schmid, F.X.3
-
303
-
-
0032577248
-
Measurement of altered aspartyl residues in the scrapie associated form of prion protein
-
WEBER, D. J., MCFADDEN, P. N. & CAUGHEY, B. (1998). Measurement of altered aspartyl residues in the scrapie associated form of prion protein. Biochem. biophys. Res. Commun. 246, 606-608.
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.246
, pp. 606-608
-
-
Weber, D.J.1
Mcfadden, P.N.2
Caughey, B.3
-
304
-
-
0030056969
-
Characterization of the active intermediate of a GroEL GroES-mediated protein folding reaction
-
WEISSMAN, J. S., RYE, H. S., FENTON, W. A., BEECHEM, J. M. & HORWICH, A. L. (1996). Characterization of the active intermediate of a GroEL GroES-mediated protein folding reaction. Cell 84, 481-490.
-
(1996)
Cell
, vol.84
, pp. 481-490
-
-
Weissman, J.S.1
Rye, H.S.2
Fenton, W.A.3
Beechem, J.M.4
Horwich, A.L.5
-
305
-
-
0032923522
-
Molecular genetics of transmissible spongiform encephalopathies
-
WEISSMANN, C. (1999). Molecular genetics of transmissible spongiform encephalopathies. J. biol. Chem. 274, 3-6.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 3-6
-
-
Weissmann, C.1
-
306
-
-
0032979289
-
Extremely rapid folding of the C-terminal domain of the priori protein without kinetic intermediates
-
WILDEGGER, G., LIEMANN, S. & GLOCKSHUBER, R. (1999). Extremely rapid folding of the C-terminal domain of the priori protein without kinetic intermediates. Nat. struct. Biol. 6, 550-553.
-
(1999)
Nat. Struct. Biol.
, vol.6
, pp. 550-553
-
-
Wildegger, G.1
Liemann, S.2
Glockshuber, R.3
-
307
-
-
0033030954
-
Ultrastructural studies on scrapie prion protein crystals obtained from reverse micellar solutions
-
WILLE, H. & PRUSINER, S. B. (1999). Ultrastructural studies on scrapie prion protein crystals obtained from reverse micellar solutions, Biophys. J. 76, 1048-1062.
-
(1999)
Biophys. J.
, vol.76
, pp. 1048-1062
-
-
Wille, H.1
Prusiner, S.B.2
-
308
-
-
0031034679
-
Tyrosine kinase receptors concentrated in caveolae-like domains from neuronal plasma membrane
-
WU, C., BUTZ, S., YING, Y. & ANDERSON, R. G. (1997). Tyrosine kinase receptors concentrated in caveolae-like domains from neuronal plasma membrane. J. biol. Chem. 272, 3554-3559.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 3554-3559
-
-
Wu, C.1
Butz, S.2
Ying, Y.3
Anderson, R.G.4
-
310
-
-
0030870719
-
The crystal structure of the asymmetric GroEL GroES (ADP), chaperonin complex
-
XU, Z., HORWICH, A. L. & SIGLER, P. B. (1997). The crystal structure of the asymmetric GroEL GroES (ADP), chaperonin complex. Nature 388, 741-750.
-
(1997)
Nature
, vol.388
, pp. 741-750
-
-
Xu, Z.1
Horwich, A.L.2
Sigler, P.B.3
-
311
-
-
0026979978
-
-
YING, Y.-S., ANDERSON, R. G. W. & ROTHBERG, K. G. (1992). Cold Spring Harbor Symp. quant. Biol. 57, 593-604.
-
(1992)
Cold Spring Harbor Symp. Quant. Biol.
, vol.57
, pp. 593-604
-
-
Ying, Y.-S.1
Anderson, R.G.W.2
Rothberg, K.G.3
-
312
-
-
0025120245
-
Non-hydrophobic extracytoplasmic determination of stop transfer in the prion protein
-
YOST, C. S., LOPEZ, C. D., PRUSINER, S. B., MYERS, R. M. & LINGAPPA, V. R. (1990). Non-hydrophobic extracytoplasmic determination of stop transfer in the prion protein. Nature 343, 669-672.
-
(1990)
Nature
, vol.343
, pp. 669-672
-
-
Yost, C.S.1
Lopez, C.D.2
Prusiner, S.B.3
Myers, R.M.4
Lingappa, V.R.5
-
313
-
-
0001612412
-
The human genetic prion diseases
-
ed. D. A. Harris, Wymondham: Horizon Scientific Press
-
YOUNG, K., PICCARDO, P., DLOUHY, S., BUGIANI, O., TAGLIAVINI, F. & GHETTI, B. (1999). The human genetic prion diseases. In Prions: Molecular and Cellular Biology (ed. D. A. Harris), pp. 139-175. Wymondham: Horizon Scientific Press.
-
(1999)
Prions: Molecular and Cellular Biology
, pp. 139-175
-
-
Young, K.1
Piccardo, P.2
Dlouhy, S.3
Bugiani, O.4
Tagliavini, F.5
Ghetti, B.6
-
314
-
-
0026689459
-
GroE prevents the accumulation of early folding intermediates of pre-β-lactamase without changing the folding pathway
-
ZAHN, R. & PLÜCKTHUN, A. (1992). GroE prevents the accumulation of early folding intermediates of pre-β-lactamase without changing the folding pathway. Biochemistry 31, 3249-3255.
-
(1992)
Biochemistry
, vol.31
, pp. 3249-3255
-
-
Zahn, R.1
Plückthun, A.2
-
315
-
-
0028025404
-
Thermodynamic partitioning model for Hydrophobic binding of polypeptides by GroEL. II. GroEL recognizes thermally unfolded mature β-lactamase
-
ZAHN, R. & PLÜCKTHUN, A. (1994). Thermodynamic partitioning model for Hydrophobic binding of polypeptides by GroEL. II. GroEL recognizes thermally unfolded mature β-lactamase. J. molec. Biol. 242, 165-174.
-
(1994)
J. Molec. Biol.
, vol.242
, pp. 165-174
-
-
Zahn, R.1
Plückthun, A.2
-
316
-
-
0028075011
-
Thermodynamic partitioning model for hydrophobic binding of polypeptides by GroEL. I. GroEL recognizes the signal sequences of β-lactamase precursor
-
ZAHN, R., AXMANN, S. E., RÜCKNAGEL, K.-P., JAEGER, E., LAMINET, A. A. & PLÜCKTHUN, A. (1994a). Thermodynamic partitioning model for hydrophobic binding of polypeptides by GroEL. I. GroEL recognizes the signal sequences of β-lactamase precursor. J. molec. Biol. 242, 150-164.
-
(1994)
J. Molec. Biol.
, vol.242
, pp. 150-164
-
-
Zahn, R.1
Axmann, S.E.2
Rücknagel, K.-P.3
Jaeger, E.4
Laminet, A.A.5
Plückthun, A.6
-
317
-
-
0030461621
-
Chaperone activity and structure of monomeric polypeptide binding domains of GroEL
-
ZAHN, R., BUCKLE, A. M., PERRETT, S., JOHNSON, C. M., CORRALES, F. J., GOLBIK, R. & FERSHT, A. R. (1996a). Chaperone activity and structure of monomeric polypeptide binding domains of GroEL. Proc. natn. Acad. Sci. USA 93, 15024-15029.
-
(1996)
Proc. Natn. Acad. Sci. USA
, vol.93
, pp. 15024-15029
-
-
Zahn, R.1
Buckle, A.M.2
Perrett, S.3
Johnson, C.M.4
Corrales, F.J.5
Golbik, R.6
Fersht, A.R.7
-
318
-
-
0027404951
-
Two-dimensional crystals of the molecular chaperone GroEL reveal structural plasticity
-
ZAHN, R., HARRIS, J. R., PFEIFER, G., PLÜCKTHUN, A. & BAUMEISTER, W. (1993). Two-dimensional crystals of the molecular chaperone GroEL reveal structural plasticity. J. molec. Biol. 229, 579-584.
-
(1993)
J. Molec. Biol.
, vol.229
, pp. 579-584
-
-
Zahn, R.1
Harris, J.R.2
Pfeifer, G.3
Plückthun, A.4
Baumeister, W.5
-
319
-
-
0030024588
-
Effect of single point mutations in citrate synthase on binding to GroEL
-
ZAHN, R., LINDNER, P., AXMANN, S. E. & PLÜCKTHUN, A. (1996b). Effect of single point mutations in citrate synthase on binding to GroEL. FEBS Lett. 380, 152-156.
-
(1996)
FEBS Lett.
, vol.380
, pp. 152-156
-
-
Zahn, R.1
Lindner, P.2
Axmann, S.E.3
Plückthun, A.4
-
320
-
-
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. natn. Acad. Sci. USA 97, 145-150.
-
(2000)
Proc. Natn. Acad. Sci. USA
, 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
-
321
-
-
0030576536
-
Conformational states bound by the molecular chaperones GroEL and SecB: A hidden unfolding (annealing) activity
-
ZAHN, R., PERRETT, S. & FERSHT, A. R. (1996c). Conformational states bound by the molecular chaperones GroEL and SecB: a hidden unfolding (annealing) activity. J. molec. Biol. 261, 43-61.
-
(1996)
J. Molec. Biol.
, vol.261
, pp. 43-61
-
-
Zahn, R.1
Perrett, S.2
Fersht, A.R.3
-
322
-
-
0030061845
-
Catalysis of amide proton exchange by the molecular chaperones GroEL and SecB
-
ZAHN, R., PERRETT, S., STENBERG, G. & FERSHT, A. R. (1996d). Catalysis of amide proton exchange by the molecular chaperones GroEL and SecB. Science 271, 642-645.
-
(1996)
Science
, vol.271
, pp. 642-645
-
-
Zahn, R.1
Perrett, S.2
Stenberg, G.3
Fersht, A.R.4
-
323
-
-
0028260023
-
Destabilization of the complete protein secondary structure on binding to the chaperone GroEL
-
ZAHN, R., SPITZFADEN, C., OTTIGER, M., WÜTHRICH, K. & PLÜCKTHUN, A. (1994b). Destabilization of the complete protein secondary structure on binding to the chaperone GroEL. Nature 368, 261-265.
-
(1994)
Nature
, vol.368
, pp. 261-265
-
-
Zahn, R.1
Spitzfaden, C.2
Ottiger, M.3
Wüthrich, K.4
Plückthun, A.5
-
324
-
-
0030810150
-
Human prion proteins expressed in Escherichia coli and purified by high-affinity column refolding
-
ZAHN, R., VON SCHROETTER, C. & WÜTHRICH, K. (1997). Human prion proteins expressed in Escherichia coli and purified by high-affinity column refolding. FEBS Lett. 417, 400-404.
-
(1997)
FEBS Lett.
, vol.417
, pp. 400-404
-
-
Zahn, R.1
Von Schroetter, C.2
Wüthrich, K.3
-
325
-
-
0033551776
-
Proteasomal degradation and N-terminal protease resistance of the codon 145 mutant prion protein
-
ZANUSSO, G., PETERSEN, R. B., JIN, T., JING, Y, KANOUSH, R., FERRARI, S., GAMBETTI, P. & SINGH, N. (1999). Proteasomal degradation and N-terminal protease resistance of the codon 145 mutant prion protein. J. biol. Chem. 274, 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
-
326
-
-
0029116625
-
Conformational transitions in peptides containing two putative α-helices of the prion protein
-
ZHANG, H., KANEKO, K., NGUYEN, J. T., LIVSHITS, T. L., BALDWIN, M. A., COHEN, F. E., JAMES, T. L. & PRUSINER, S. B. (1995). Conformational transitions in peptides containing two putative α-helices of the prion protein. J. molec. Biol. 250, 514-526.
-
(1995)
J. Molec. Biol.
, vol.250
, pp. 514-526
-
-
Zhang, H.1
Kaneko, K.2
Nguyen, J.T.3
Livshits, T.L.4
Baldwin, M.A.5
Cohen, F.E.6
James, T.L.7
Prusiner, S.B.8
-
327
-
-
0343683408
-
Physical studies of conformational plasticity in a recombinant prion protein
-
ZHANG, H., STÖCKL, J., MEHLHORN, I., GROTH, D., BALDWIN, M. A., PRUSINER, S. B., JAMES, T. L. & COHEN, F. E. (1997). Physical studies of conformational plasticity in a recombinant prion protein. Biochemistry 36, 3543-3553.
-
(1997)
Biochemistry
, vol.36
, pp. 3543-3553
-
-
Zhang, H.1
Stöckl, J.2
Mehlhorn, I.3
Groth, D.4
Baldwin, M.A.5
Prusiner, S.B.6
James, T.L.7
Cohen, F.E.8
|