-
1
-
-
0033485880
-
Prion protein expression aids cellular uptake and veratridine-induced release of copper
-
Brown D.R. Prion protein expression aids cellular uptake and veratridine-induced release of copper. Journal of Neuroscience Research 58 (1999) 717-725
-
(1999)
Journal of Neuroscience Research
, vol.58
, pp. 717-725
-
-
Brown, D.R.1
-
2
-
-
0034533064
-
Sc-like prion protein peptide inhibits the function of cellular prion protein
-
Sc-like prion protein peptide inhibits the function of cellular prion protein. Biochemical Journal 252 (2000) 511-518
-
(2000)
Biochemical Journal
, vol.252
, pp. 511-518
-
-
Brown, D.R.1
-
3
-
-
1842524044
-
Role of the prion protein in copper turnover in astrocytes
-
Brown D.R. Role of the prion protein in copper turnover in astrocytes. Neurobiology of Disease 15 (2004) 534-543
-
(2004)
Neurobiology of Disease
, vol.15
, pp. 534-543
-
-
Brown, D.R.1
-
4
-
-
0035158321
-
Anti-oxidant activity related to copper binding of native prion protein
-
Brown D.R., Clive C., and Haswell S.J. Anti-oxidant activity related to copper binding of native prion protein. Journal of Neurochemistry 76 (2001) 69-76
-
(2001)
Journal of Neurochemistry
, vol.76
, pp. 69-76
-
-
Brown, D.R.1
Clive, C.2
Haswell, S.J.3
-
5
-
-
0344255607
-
Copper(II) complexes of peptide fragments of the prion protein. Conformation changes induced by copper(II) and the binding motif in C-terminal protein region
-
Brown D.R., Guantieri V., Grasso G., Impellizzeri G., Pappalardo G., and Rizzarelli E. Copper(II) complexes of peptide fragments of the prion protein. Conformation changes induced by copper(II) and the binding motif in C-terminal protein region. Journal of Inorganic Biochemistry 98 (2004) 133-143
-
(2004)
Journal of Inorganic Biochemistry
, vol.98
, pp. 133-143
-
-
Brown, D.R.1
Guantieri, V.2
Grasso, G.3
Impellizzeri, G.4
Pappalardo, G.5
Rizzarelli, E.6
-
6
-
-
0034654304
-
Consequences of manganese replacement of copper for prion protein function and proteinase resistance
-
Brown D.R., Hafiz F., Glasssmith L.L., Wong B.-S., Jones I.M., Clive C., et al. Consequences of manganese replacement of copper for prion protein function and proteinase resistance. The EMBO Journal 19 (2000) 1180-1186
-
(2000)
The EMBO Journal
, vol.19
, pp. 1180-1186
-
-
Brown, D.R.1
Hafiz, F.2
Glasssmith, L.L.3
Wong, B.-S.4
Jones, I.M.5
Clive, C.6
-
7
-
-
0031444294
-
The cellular prion protein binds copper in vivo
-
Brown D.R., Qin K., Herms J.W., Madlung A., Manson J., Strome R., et al. The cellular prion protein binds copper in vivo. Nature 390 (1997) 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
-
8
-
-
0033571055
-
Normal prion protein has an activity like that of superoxide dismutase
-
Brown D.R., Wong B.S., Hafiz F., Clive C., Haswell S., and Jones I.M. Normal prion protein has an activity like that of superoxide dismutase. Biochemical Journal 344 (1999) 1-5
-
(1999)
Biochemical Journal
, vol.344
, pp. 1-5
-
-
Brown, D.R.1
Wong, B.S.2
Hafiz, F.3
Clive, C.4
Haswell, S.5
Jones, I.M.6
-
9
-
-
0025876226
-
N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): Implications regarding the site of conversion of PrP to the protease-resistant state
-
Caughey B., Raymond G.J., Ernst D., and Race R.E. N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): Implications regarding the site of conversion of PrP to the protease-resistant state. Journal of Virology 65 (1991) 6597-6603
-
(1991)
Journal of Virology
, vol.65
, pp. 6597-6603
-
-
Caughey, B.1
Raymond, G.J.2
Ernst, D.3
Race, R.E.4
-
10
-
-
0042477520
-
Mapping the functional domain of the prion protein
-
Cui T., Daniels M., Wong B.S., Li R., Sy M.-S., Sassoon J., et al. Mapping the functional domain of the prion protein. European Journal of Biochemistry 270 (2003) 3368-3376
-
(2003)
European Journal of Biochemistry
, vol.270
, pp. 3368-3376
-
-
Cui, T.1
Daniels, M.2
Wong, B.S.3
Li, R.4
Sy, M.-S.5
Sassoon, J.6
-
12
-
-
0028783437
-
Fragmentation of ceruloplasmin following non-enzymatic glycation reaction
-
Islam K.N., Takahashi M., Higashiyama S., Myint T., and Uozumi N. Fragmentation of ceruloplasmin following non-enzymatic glycation reaction. Journal of Biochemistry 118 (1995) 1054-1060
-
(1995)
Journal of Biochemistry
, vol.118
, pp. 1054-1060
-
-
Islam, K.N.1
Takahashi, M.2
Higashiyama, S.3
Myint, T.4
Uozumi, N.5
-
13
-
-
0035902531
-
Location and properties of metal-binding sites on the human prion protein
-
Jackson G.S., Murray I., Hosszu L.L., Gibbs N., Waltho J.P., Clarke A.R., et al. Location and properties of metal-binding sites on the human prion protein. Proceeding of the National Academy of Science USA 98 (2001) 8531-8535
-
(2001)
Proceeding of the National Academy of Science USA
, vol.98
, pp. 8531-8535
-
-
Jackson, G.S.1
Murray, I.2
Hosszu, L.L.3
Gibbs, N.4
Waltho, J.P.5
Clarke, A.R.6
-
14
-
-
3542999252
-
2+ coordination by His96 and His111 induces β-sheet formation in the unstructured amyloidogenic region of the prion protein
-
2+ coordination by His96 and His111 induces β-sheet formation in the unstructured amyloidogenic region of the prion protein. Journal of Biological Chemistry 279 (2004) 32018-32027
-
(2004)
Journal of Biological Chemistry
, vol.279
, pp. 32018-32027
-
-
Jones, C.E.1
Abdelraheim, S.R.2
Brown, D.R.3
Viles, J.H.4
-
15
-
-
3442889359
-
Synthetic mammalian prions
-
Legname G., Baskakov I.V., Nguyen H.O., Riesner D., Cohen F.E., DeArmond S.J., et al. Synthetic mammalian prions. Science 305 (2004) 673-676
-
(2004)
Science
, vol.305
, pp. 673-676
-
-
Legname, G.1
Baskakov, I.V.2
Nguyen, H.O.3
Riesner, D.4
Cohen, F.E.5
DeArmond, S.J.6
-
16
-
-
5044229685
-
BSE and vCJD cause disturbance to uric acid levels
-
Lekishvili T., Sassoon J., Thompsett A.R., Green A., Ironside J.W., and Brown D.R. BSE and vCJD cause disturbance to uric acid levels. Experimental Neurology 190 (2004) 233-244
-
(2004)
Experimental Neurology
, vol.190
, pp. 233-244
-
-
Lekishvili, T.1
Sassoon, J.2
Thompsett, A.R.3
Green, A.4
Ironside, J.W.5
Brown, D.R.6
-
17
-
-
0028820863
-
Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene
-
Krasemann S., Zerr I., Weber T., Poser S., Kretzschmar H., Hunsmann G., et al. Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene. Molecular Brain Research 34 (1995) 173-176
-
(1995)
Molecular Brain Research
, vol.34
, pp. 173-176
-
-
Krasemann, S.1
Zerr, I.2
Weber, T.3
Poser, S.4
Kretzschmar, H.5
Hunsmann, G.6
-
18
-
-
0037108168
-
Locally disordered conformer of the hamster prion protein: A crucial intermediate to PrPSc?
-
Kuwata K., Li H., Yamada H., Legname G., Prusiner S.B., Akasaka K., et al. Locally disordered conformer of the hamster prion protein: A crucial intermediate to PrPSc?. Biochemistry 41 (2002) 12277-12283
-
(2002)
Biochemistry
, vol.41
, pp. 12277-12283
-
-
Kuwata, K.1
Li, H.2
Yamada, H.3
Legname, G.4
Prusiner, S.B.5
Akasaka, K.6
-
19
-
-
1642410070
-
Alpha- and beta-cleavages of the amino terminus of the cellular prion protein
-
Mangé A., Béranger F., Peoc'h K., Onodera T., Frobert Y., and Lehmann S. Alpha- and beta-cleavages of the amino terminus of the cellular prion protein. Biology of the Cell 96 (2004) 125-132
-
(2004)
Biology of the Cell
, vol.96
, pp. 125-132
-
-
Mangé, A.1
Béranger, F.2
Peoc'h, K.3
Onodera, T.4
Frobert, Y.5
Lehmann, S.6
-
20
-
-
1842663089
-
Prions: So many fibers, so little infectivity
-
May B.C., Govaerts C., Prusiner S.B., and Cohen F.E. Prions: So many fibers, so little infectivity. Trends in Biochemical Science 29 (2004) 162-165
-
(2004)
Trends in Biochemical Science
, vol.29
, pp. 162-165
-
-
May, B.C.1
Govaerts, C.2
Prusiner, S.B.3
Cohen, F.E.4
-
21
-
-
0035910498
-
Cleavage of the amino terminus of the prion protein by reactive oxygen species
-
McMahon H.E.M., Mangé A., Nishida N., Créminon C., Casanova D., and Lehmann S. Cleavage of the amino terminus of the prion protein by reactive oxygen species. Journal of Biological Chemistry 276 (2001) 2286-2291
-
(2001)
Journal of Biological Chemistry
, vol.276
, pp. 2286-2291
-
-
McMahon, H.E.M.1
Mangé, A.2
Nishida, N.3
Créminon, C.4
Casanova, D.5
Lehmann, S.6
-
22
-
-
0028874320
-
A 60-kDa prion protein (PrP) with properties of both the normal and scrapie-associated forms of PrP
-
Priola S.A., Caughey B., Wehrly K., and Chesebro B. A 60-kDa prion protein (PrP) with properties of both the normal and scrapie-associated forms of PrP. Journal of Biological Chemistry 270 (1995) 3299-3305
-
(1995)
Journal of Biological Chemistry
, vol.270
, pp. 3299-3305
-
-
Priola, S.A.1
Caughey, B.2
Wehrly, K.3
Chesebro, B.4
-
24
-
-
0031866162
-
Cellular prion protein localization in rodent and primate brain
-
Salès N., Rodolfo K., Hässig R., Faucheux B., Di Giamberdino L., and Moya K.L. Cellular prion protein localization in rodent and primate brain. European Journal of Neuroscience 10 (1998) 2464-2471
-
(1998)
European Journal of Neuroscience
, vol.10
, pp. 2464-2471
-
-
Salès, N.1
Rodolfo, K.2
Hässig, R.3
Faucheux, B.4
Di Giamberdino, L.5
Moya, K.L.6
-
25
-
-
0034598968
-
cDNA cloning of turtle prion protein
-
Simonic T., Duga S., Strumbo B., Asselta R., Ceciliani F., and Ronchi S. cDNA cloning of turtle prion protein. FEBS Letters 469 (2000) 33-38
-
(2000)
FEBS Letters
, vol.469
, pp. 33-38
-
-
Simonic, T.1
Duga, S.2
Strumbo, B.3
Asselta, R.4
Ceciliani, F.5
Ronchi, S.6
-
26
-
-
0035900494
-
Molecular cloning of the cDNA coding for Xenopus laevis prion protein
-
Strumbo B., Ronchi S., Bolis L.C., and Simonic T. Molecular cloning of the cDNA coding for Xenopus laevis prion protein. FEBS Letters 508 (2001) 170-174
-
(2001)
FEBS Letters
, vol.508
, pp. 170-174
-
-
Strumbo, B.1
Ronchi, S.2
Bolis, L.C.3
Simonic, T.4
-
27
-
-
0028322017
-
An increased percentage of long amyloid beta protein secreted by familial amyloid beta protein precursor (beta APP717) mutants
-
Suzuki N., Cheung T.T., Cai X.D., Odaka A., Otvos Jr. L., Eckman C., et al. An increased percentage of long amyloid beta protein secreted by familial amyloid beta protein precursor (beta APP717) mutants. Science 264 (1994) 1336-1340
-
(1994)
Science
, vol.264
, pp. 1336-1340
-
-
Suzuki, N.1
Cheung, T.T.2
Cai, X.D.3
Odaka, A.4
Otvos Jr., L.5
Eckman, C.6
-
28
-
-
0038001458
-
Generation of hydrogen peroxide from mutant forms of the prion protein fragment PrP121-231
-
Turnbull S., Tabner B.J., Brown D.R., and Allsop D. Generation of hydrogen peroxide from mutant forms of the prion protein fragment PrP121-231. Biochemistry 42 (2003) 7675-7681
-
(2003)
Biochemistry
, vol.42
, pp. 7675-7681
-
-
Turnbull, S.1
Tabner, B.J.2
Brown, D.R.3
Allsop, D.4
-
29
-
-
0037159185
-
Protease-sensitive scrapie prion protein in aggregates of heterogeneous sizes
-
Tzaban S., Friedlander G., Schonberger O., Horonchik L., Yedidia Y., Shaked G., et al. Protease-sensitive scrapie prion protein in aggregates of heterogeneous sizes. Biochemistry 41 (2002) 12868-12875
-
(2002)
Biochemistry
, vol.41
, pp. 12868-12875
-
-
Tzaban, S.1
Friedlander, G.2
Schonberger, O.3
Horonchik, L.4
Yedidia, Y.5
Shaked, G.6
-
30
-
-
27744547982
-
Reactive oxygen species-mediated beta-cleavage of the prion protein in the cellular response to oxidative stress
-
Watt N.T., Taylor D.R., Gillott A., Thomas D.A., Perera W.S., and Hooper N.M. Reactive oxygen species-mediated beta-cleavage of the prion protein in the cellular response to oxidative stress. Journal of Biological Chemistry 280 (2005) 35914-35921
-
(2005)
Journal of Biological Chemistry
, vol.280
, pp. 35914-35921
-
-
Watt, N.T.1
Taylor, D.R.2
Gillott, A.3
Thomas, D.A.4
Perera, W.S.5
Hooper, N.M.6
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