-
1
-
-
84872473797
-
Advances in veterinary research
-
Gordon WS (1946). Advances in veterinary research. Veterinary Record, 58: 518-525.
-
(1946)
Veterinary Record
, vol.58
, pp. 518-525
-
-
Gordon, W.S.1
-
2
-
-
0025910229
-
Molecular biology of prion diseases
-
Prusiner SB (1991). Molecular biology of prion diseases. Science, 252: 1515-1522.
-
(1991)
Science
, vol.252
, pp. 1515-1522
-
-
Prusiner, S.B.1
-
3
-
-
0027421540
-
Genetic and infectious prior diseases
-
Prusiner SB (1993). Genetic and infectious prior diseases. Archives of Neurology, 50: 1129-1153.
-
(1993)
Archives of Neurology
, vol.50
, pp. 1129-1153
-
-
Prusiner, S.B.1
-
4
-
-
0014190760
-
Self replication and scrapie
-
Grifft JS (1967). Self replication and scrapie. Nature, 215: 1043-1044.
-
(1967)
Nature
, vol.215
, pp. 1043-1044
-
-
Grifft, J.S.1
-
5
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
Prusiner SB (1982) Novel proteinaceous infectious particles cause scrapie. Science, 216: 136-144.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
6
-
-
0020490156
-
Identification of a protein that purifies with the scrapie prion
-
Bolton DC, McKinley MP & Prusiner SB (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
-
7
-
-
0021752457
-
Purification and structural studies of a major scrapie prion protein
-
Prusiner SB, Groth DF, Bolton DC, Kent SB & Hood LE (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
-
8
-
-
0022005315
-
A cellular gene encodes scrapie PrP 27-30 protein
-
Oesch B, Westaway D, Walchl M, McKinley MP, Kent SB, Aebersold R, Barry RA, Tempst P, Teplow DB, Hood LE, Prusiner SB & 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
Walchl, M.3
McKinley, M.P.4
Kent, S.B.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
-
9
-
-
0021884354
-
Identification of scrapie prion protein-specific mRNA in scrapie infected and uninfected brain
-
Chesebro B, Race R, Wehrly K, Nishio J, Bloom M, Lechner D, Bergstrom S, Robbins K, Mayer L, Keith JM, Garon C & Haase A (1985). Identification of scrapie prion protein-specific mRNA in scrapie infected and uninfected brain. Nature, 315: 331-333.
-
(1985)
Nature
, vol.315
, pp. 331-333
-
-
Chesebro, B.1
Race, R.2
Wehrly, K.3
Nishio, J.4
Bloom, M.5
Lechner, D.6
Bergstrom, S.7
Robbins, K.8
Mayer, L.9
Keith, J.M.10
Garon, C.11
Haase, A.12
-
10
-
-
0027332116
-
Conversion of alpha-helices into beta-sheet features in the formation of the scrapie prion proteins
-
Pan KM, Baldwin M, Nguyen J, Gasset M, Serban A, Groth D, Mehlhorn I, Huang Z, Fletterick RJ, Cohen FE & Prusiner S (1993). Conversion of alpha-helices into beta-sheet features in the formation of the scrapie prion proteins. Proceedings of the National Academy of Sciences, USA, 90: 10962-10966.
-
(1993)
Proceedings of the National Academy of Sciences, 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.11
-
11
-
-
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
-
12
-
-
0021023167
-
A protease-resistant protein is a structural component of the scrapie prion
-
McKinley MP, Bolton DC & Prusiner SB (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
-
14
-
-
0027319326
-
Mice devoid of PrP are resistant to scrapie
-
Bueler H, Aguzzi A, Sailer A, Greiner RA, 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
-
-
Bueler, H.1
Aguzzi, A.2
Sailer, A.3
Greiner, R.A.4
Autenried, P.5
Aguet, M.6
Weissmann, C.7
-
15
-
-
0030728039
-
Deadly conformations - Protein misfolding in prion disease
-
Norwich AL & Weissmann JS (1997). Deadly conformations - Protein misfolding in prion disease. Cell, 89: 499-510.
-
(1997)
Cell
, vol.89
, pp. 499-510
-
-
Norwich, A.L.1
Weissmann, J.S.2
-
16
-
-
0030786717
-
Prions research: The next frontiers
-
Aguzzi A & Weissmann C (1997). Prions research: the next frontiers. Nature, 389: 795-798.
-
(1997)
Nature
, vol.389
, pp. 795-798
-
-
Aguzzi, A.1
Weissmann, C.2
-
17
-
-
0024820814
-
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
-
Scott M, Foster P, Mirenda C, Serban D, Coufal F, Walchli M, Tarchia M, Groth D, Carlson G, DeArmond SJ, Westaway D & Prusiner SB (1989). Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques. Cell, 59: 847-857.
-
(1989)
Cell
, vol.59
, pp. 847-857
-
-
Scott, M.1
Foster, P.2
Mirenda, C.3
Serban, D.4
Coufal, F.5
Walchli, M.6
Tarchia, M.7
Groth, D.8
Carlson, G.9
DeArmond, S.J.10
Westaway, D.11
Prusiner, S.B.12
-
18
-
-
0025244011
-
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
-
Prusiner SB, Scott M, Foster D, Pan KM, Groth D, Mirenda C, Torchia M, Yang SL, Serban D, Carlson GA, Hoppe PC, Westaway D & DeArmond SJ (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
-
19
-
-
0028102794
-
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein
-
Telling GC, Scott M, Hsiao KK, Foster D, Yang SL, Torchia M, Sidle KC, Collinge J, DeArmond SJ & Prusiner SB (1994). Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein. Proceedings of the National Academy of Sciences, USA, 91: 9936-9940.
-
(1994)
Proceedings of the National Academy of Sciences, USA
, 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.7
Collinge, J.8
DeArmond, S.J.9
Prusiner, S.B.10
-
20
-
-
0028882424
-
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
-
Telling GC, Scott M, Mastrianni J, Gabizon R, Torchia M, Cohen FE, DeArmond SJ & Prusiner SB (1995). Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of 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
-
21
-
-
0028782015
-
Transmission of bovine spongiform encephalopathy and scrapie to mice: Strain variation and the species barrier
-
Bruce M, Chree A, McConnell I, Foster J, Pearson G & Fraser H (1994). Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier. Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences, B343: 405-411.
-
(1994)
Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences
, vol.B343
, pp. 405-411
-
-
Bruce, M.1
Chree, A.2
McConnell, I.3
Foster, J.4
Pearson, G.5
Fraser, H.6
-
22
-
-
0029831213
-
Molecular analysis of prion strain variation and the aetiology of "new variant" CJD
-
Collinge J, Sidle KCL, Meads J, Ironside J & Hill AF (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
-
23
-
-
49749220574
-
Scrapie and Kuru
-
Hadlow WJ (1959). Scrapie and Kuru. Lancet, 2: 289-290.
-
(1959)
Lancet
, vol.2
, pp. 289-290
-
-
Hadlow, W.J.1
-
24
-
-
0030478022
-
Molecular biology and pathogenesis of prion diseases
-
Prusiner SB (1996). Molecular biology and pathogenesis of prion diseases. Trends in Biochemical Sciences, 21: 482-487.
-
(1996)
Trends in Biochemical Sciences
, vol.21
, pp. 482-487
-
-
Prusiner, S.B.1
-
25
-
-
0029132280
-
First experimental transmission of fatal familial insomnia
-
Tateishi J, Brown P, Kitamoto T, Hoque ZM, Roos R, Wollman R, Cervenakova L & Gajdusek DC (1995). First experimental transmission of fatal familial insomnia. Nature, 376: 434-435.
-
(1995)
Nature
, vol.376
, pp. 434-435
-
-
Tateishi, J.1
Brown, P.2
Kitamoto, T.3
Hoque, Z.M.4
Roos, R.5
Wollman, R.6
Cervenakova, L.7
Gajdusek, D.C.8
-
26
-
-
0030773705
-
A prion-linked psychiatric disorder
-
Samaia HB, Mari JJ, Vallada HP, Moura RP, Simpson ATG & Brentani RR (1997). A prion-linked psychiatric disorder. Nature, 390: 241.
-
(1997)
Nature
, vol.390
, pp. 241
-
-
Samaia, H.B.1
Mari, J.J.2
Vallada, H.P.3
Moura, R.P.4
Simpson, A.T.G.5
Brentani, R.R.6
-
27
-
-
0024519771
-
Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome
-
Hsiao K, Baker HF, Crow TJ, Poulter M, Owen F, Terwilliger JD, Westaway D, Ott J & Prusiner SB (1989). Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome. Nature, 338: 342-355.
-
(1989)
Nature
, vol.338
, pp. 342-355
-
-
Hsiao, K.1
Baker, H.F.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
-
28
-
-
0025869213
-
Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease
-
Hsiao K, Meiner Z, Kahana E, Cass C, Kahana I, Avrahami D, Scarlato G, Abramsky O, Prusiner SB & Gabizon R (1991). Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease. New England Journal of Medicine, 324: 1091-1097.
-
(1991)
New England Journal of Medicine
, vol.324
, pp. 1091-1097
-
-
Hsiao, K.1
Meiner, Z.2
Kahana, E.3
Cass, C.4
Kahana, I.5
Avrahami, D.6
Scarlato, G.7
Abramsky, O.8
Prusiner, S.B.9
Gabizon, R.10
-
29
-
-
0017643758
-
Unconventional viruses and the origin and disappearance of kuru
-
Gajdusek DC (1977). Unconventional viruses and the origin and disappearance of kuru. Science, 197: 943-960.
-
(1977)
Science
, vol.197
, pp. 943-960
-
-
Gajdusek, D.C.1
-
30
-
-
0028841012
-
Sporadic Creutzfeldt-Jakob disease in an 18-year-old in the UK
-
Bateman D, Hilton D, Love S, Zeidler M, Beck J & Collinge J (1995). Sporadic Creutzfeldt-Jakob disease in an 18-year-old in the UK. Lancet, 346: 1155-1156.
-
(1995)
Lancet
, vol.346
, pp. 1155-1156
-
-
Bateman, D.1
Hilton, D.2
Love, S.3
Zeidler, M.4
Beck, J.5
Collinge, J.6
-
31
-
-
0031574612
-
Predicting the CJD epidemic in humans
-
Cousens SN, Vynnycky E, Zeidler M, Will RG & Smith PG (1997). Predicting the CJD epidemic in humans. Nature, 385: 197-198.
-
(1997)
Nature
, vol.385
, pp. 197-198
-
-
Cousens, S.N.1
Vynnycky, E.2
Zeidler, M.3
Will, R.G.4
Smith, P.G.5
-
32
-
-
0026600865
-
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
-
Bueler H, Fischer M, Lang Y, Bluethmann H, Lipp HP, DeArmond SJ, Prusiner SB, Aguet M & Weissmann C (1992). Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature, 356: 577-582.
-
(1992)
Nature
, vol.356
, pp. 577-582
-
-
Bueler, H.1
Fischer, M.2
Lang, Y.3
Bluethmann, H.4
Lipp, H.P.5
DeArmond, S.J.6
Prusiner, S.B.7
Aguet, M.8
Weissmann, C.9
-
33
-
-
0027997387
-
Prion protein is necessary for normal synaptic function
-
Collinge J, Whittington MA, Sidle KC, Smith CJ, Palmer MS, Clarke AR & Jefferys JG (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
Smith, C.J.4
Palmer, M.S.5
Clarke, A.R.6
Jefferys, J.G.7
-
34
-
-
15844421385
-
Altered circadian activity rhythms and sleep in mice devoid of prion protein
-
Tobler I, Gaus SE, Deboer T, Achermann P, Fischer M, Rulicke T, Moser M, Oesch B, McBride PA & Manson JC (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
Rulicke, T.6
Moser, M.7
Oesch, B.8
McBride, P.A.9
Manson, J.C.10
-
35
-
-
13344282734
-
Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene
-
Sakaguchi S, Katamine S, Nishida N, Moriuchi R, Shigematsu K, Sugimoto T, Nakatani A, Kataoka Y, Houtani T, Shirabe S, Okada H, Hasagawa S, Miyamoto T & Noda T (1996). Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene. Nature, 380: 528-531.
-
(1996)
Nature
, vol.380
, pp. 528-531
-
-
Sakaguchi, S.1
Katamine, S.2
Nishida, N.3
Moriuchi, R.4
Shigematsu, K.5
Sugimoto, T.6
Nakatani, A.7
Kataoka, Y.8
Houtani, T.9
Shirabe, S.10
Okada, H.11
Hasagawa, S.12
Miyamoto, T.13
Noda, T.14
-
36
-
-
0025212147
-
Cellular isoform of the scrapie agent protein participates in lymphocyte activation
-
Cashman NR, Loertsche R, Nalbantoglu J, Shaw I, Kascsak RJ, Bolton DC & Bendheim PE (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
Loertsche, R.2
Nalbantoglu, J.3
Shaw, I.4
Kascsak, R.J.5
Bolton, D.C.6
Bendheim, P.E.7
-
37
-
-
0029557978
-
Regulation of intracellular free calcium levels by the cellular prion protein
-
Whatley SA, Powell JF, Politopoulou G, Campbell IC, Brammer MJ & Percy NS (1995). Regulation of intracellular free calcium levels by the cellular prion protein. NeuroReport, 6: 2333-2337.
-
(1995)
NeuroReport
, vol.6
, pp. 2333-2337
-
-
Whatley, S.A.1
Powell, J.F.2
Politopoulou, G.3
Campbell, I.C.4
Brammer, M.J.5
Percy, N.S.6
-
38
-
-
0030569412
-
Metal-dependent alpha-helix formation promoted by the glycine-rich octapeptide region of prion protein
-
Miura T, Hori-i A & Takeuchi H (1996). Metal-dependent alpha-helix formation promoted by the glycine-rich octapeptide region of prion protein. FEBS Letters, 396: 248-252.
-
(1996)
FEBS Letters
, vol.396
, pp. 248-252
-
-
Miura, T.1
Hori-i, A.2
Takeuchi, H.3
-
39
-
-
0031444294
-
The cellular prion protein binds copper in vivo
-
Brown DR, Qin K, Herms JW, Madlung A, Manson J, Strome R, Fraser PE, Kruck T, von Bohlen A, Schulz-Schaeffer W, Giese A, Westaway D & Kretzschmar H (1997). 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
-
41
-
-
0031194455
-
Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity
-
Brown DR, Schulz-Schaeffer WJ, Schmidt B & Kretzschmar HA (1997). Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity. Experimental Neurology, 146: 104-112.
-
(1997)
Experimental Neurology
, vol.146
, pp. 104-112
-
-
Brown, D.R.1
Schulz-Schaeffer, W.J.2
Schmidt, B.3
Kretzschmar, H.A.4
-
42
-
-
0023663071
-
Scrapie prion protein contains a phosphatidylinositol glycolipid
-
Stahl N, Borchelt DR, Hsiao K & Prusiner SB (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
-
43
-
-
0025304678
-
Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells
-
Borchelt DR, Scott M, Taraboulos A, Stahl N & Prusiner SB (1990). Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells. Journal of Cell Biology, 110: 743-752.
-
(1990)
Journal of Cell Biology
, vol.110
, pp. 743-752
-
-
Borchelt, D.R.1
Scott, M.2
Taraboulos, A.3
Stahl, N.4
Prusiner, S.B.5
-
44
-
-
0027204276
-
A prion protein cycles between the cell surface and an endocytic compartment in cultured neuroblastoma cells
-
Shyng SL, Huber MT & Harris DA (1993). A prion protein cycles between the cell surface and an endocytic compartment in cultured neuroblastoma cells. Journal of Biological Chemistry, 268: 15922-15928.
-
(1993)
Journal of Biological Chemistry
, vol.268
, pp. 15922-15928
-
-
Shyng, S.L.1
Huber, M.T.2
Harris, D.A.3
-
45
-
-
0028305135
-
A glycolipid-anchored prion protein is endocytosed via clathrin-coated pits
-
Shyng S-L, Heuser JE & Harris DA (1994). A glycolipid-anchored prion protein is endocytosed via clathrin-coated pits. Journal of Cell Biology, 125: 1239-1250.
-
(1994)
Journal of Cell Biology
, vol.125
, pp. 1239-1250
-
-
Shyng, S.-L.1
Heuser, J.E.2
Harris, D.A.3
-
46
-
-
0029962468
-
Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains
-
Vey M, Pilkuhn S, Wille H, Nixon R, DeArmond SJ, Smart EJ, Andersen RG, Taraboulos A & Prusiner SB (1996). Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains. Proceedings of the National Academy of Sciences, USA, 93: 14945-14949.
-
(1996)
Proceedings of the National Academy of Sciences, 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
Andersen, R.G.7
Taraboulos, A.8
Prusiner, S.B.9
-
47
-
-
0030940607
-
Identification of candidate proteins binding to prion protein
-
Yehiely F, Bamborough P, Da Costa M, Perry BJ, Thinakaran G, Cohen FE, Carlson GA & Prusiner SB (1997). Identification of candidate proteins binding to prion protein. Neurobiology of Disease, 3: 339-355.
-
(1997)
Neurobiology of Disease
, vol.3
, pp. 339-355
-
-
Yehiely, F.1
Bamborough, P.2
Da Costa, M.3
Perry, B.J.4
Thinakaran, G.5
Cohen, F.E.6
Carlson, G.A.7
Prusiner, S.B.8
-
48
-
-
0031466157
-
Complementary hydropathy identifies a cellular prion protein receptor
-
Martins VR, Graner E, Garcia-Abreu J, Souza SJ, Mercadante AF, Veiga SS, Zanata SM, Neto VM & Brentani RR (1997). Complementary hydropathy identifies a cellular prion protein receptor. Nature Medicine, 3 1376-1382.
-
(1997)
Nature Medicine
, vol.3
, pp. 1376-1382
-
-
Martins, V.R.1
Graner, E.2
Garcia-Abreu, J.3
Souza, S.J.4
Mercadante, A.F.5
Veiga, S.S.6
Zanata, S.M.7
Neto, V.M.8
Brentani, R.R.9
-
49
-
-
0024292045
-
Biological implications of complementary hydropathy of amino acids
-
Brentani RR (1988). Biological implications of complementary hydropathy of amino acids. Journal of Theoretical Biology, 135: 495-499.
-
(1988)
Journal of Theoretical Biology
, vol.135
, pp. 495-499
-
-
Brentani, R.R.1
-
50
-
-
0025034361
-
Complementary hydropathy and the evolution of interacting polypeptides
-
Brentani RR (1990). Complementary hydropathy and the evolution of interacting polypeptides. Journal of Molecular Evolution, 31: 239-243.
-
(1990)
Journal of Molecular Evolution
, vol.31
, pp. 239-243
-
-
Brentani, R.R.1
-
51
-
-
0029029804
-
The antisense homology box: A new motif within proteins that encodes biological active peptides
-
Baranyi L, Campbell W, Ohshima K, Fujimoto S, Boros M & Okada H (1995). The antisense homology box: A new motif within proteins that encodes biological active peptides. Nature Medicine, 1: 894-901.
-
(1995)
Nature Medicine
, vol.1
, pp. 894-901
-
-
Baranyi, L.1
Campbell, W.2
Ohshima, K.3
Fujimoto, S.4
Boros, M.5
Okada, H.6
-
52
-
-
0027483615
-
Neurotoxicity of a prion protein fragment
-
Forloni G, Angeretti N, Chiesa R, Monzani E, Salmona M, Bugiani 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
Bugiani, O.6
Tagliavini, F.7
-
53
-
-
0029054937
-
The N-terminal domain of a glycolipid-anchored prion protein is essential for its endocytosis via clathrin-coated pits
-
Shyng S-L, Moulder KJ, Laesko A & Harris DA (1995). The N-terminal domain of a glycolipid-anchored prion protein is essential for its endocytosis via clathrin-coated pits. Journal of Biological Chemistry, 270: 14793-14800.
-
(1995)
Journal of Biological Chemistry
, vol.270
, pp. 14793-14800
-
-
Shyng, S.-L.1
Moulder, K.J.2
Laesko, A.3
Harris, D.A.4
-
54
-
-
0026442278
-
Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid
-
Gasset M, Baldwin MA, Lloyd DH, Gabriel JM, Holtzman DM, Cohen F, Fletterick R & Prusiner SB (1992). Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid. Proceedings of the National Academy of Sciences, USA, 89: 10940-10944.
-
(1992)
Proceedings of the National Academy of Sciences, 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
-
55
-
-
0027283062
-
Prion protein is strongly immunolocalized at the postsynaptic domain of the human neuromuscular junctions
-
Askanas V, Bilak M, Engel WK, Leclec A & Tome F (1993). Prion protein is strongly immunolocalized at the postsynaptic domain of the human neuromuscular junctions. Neuroscience Letters, 159: 111-114.
-
(1993)
Neuroscience Letters
, vol.159
, pp. 111-114
-
-
Askanas, V.1
Bilak, M.2
Engel, W.K.3
Leclec, A.4
Tome, F.5
-
56
-
-
0031015906
-
Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy
-
Hill AF, Zeidler M, Ironside J & Collinge J (1997). Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy. Lancet, 349: 99-100.
-
(1997)
Lancet
, vol.349
, pp. 99-100
-
-
Hill, A.F.1
Zeidler, M.2
Ironside, J.3
Collinge, J.4
-
57
-
-
0024580902
-
Pathogenesis of scrapie in mice after intragastric infection
-
Kimberlin RH & Walker CA (1989). Pathogenesis of scrapie in mice after intragastric infection. Virus Research, 12: 213-220.
-
(1989)
Virus Research
, vol.12
, pp. 213-220
-
-
Kimberlin, R.H.1
Walker, C.A.2
-
58
-
-
0031444295
-
A crucial role for B cells in neuroinvasive scrapie
-
Klein MA, Frigg R, Flechsig E, Raeber AJ, Kalinke U, Bluethmann H, Bootz F, Suter M, Zinkernagel RM & Aguzzi A (1997). A crucial role for B cells in neuroinvasive scrapie. Nature, 390: 687-690.
-
(1997)
Nature
, vol.390
, pp. 687-690
-
-
Klein, M.A.1
Frigg, R.2
Flechsig, E.3
Raeber, A.J.4
Kalinke, U.5
Bluethmann, H.6
Bootz, F.7
Suter, M.8
Zinkernagel, R.M.9
Aguzzi, A.10
-
59
-
-
0029825830
-
A normal host prion protein (PrPC) is required for scrapie spread within the central nervous system
-
Brandner S, Raeber A, Sailer A, Blattler T, Fischer M, Weissmann C & Aguzzi A (1996). A normal host prion protein (PrPC) is required for scrapie spread within the central nervous system. Proceedings of the National Academy of Sciences, USA, 93: 13148-13151.
-
(1996)
Proceedings of the National Academy of Sciences, USA
, vol.93
, pp. 13148-13151
-
-
Brandner, S.1
Raeber, A.2
Sailer, A.3
Blattler, T.4
Fischer, M.5
Weissmann, C.6
Aguzzi, A.7
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