-
1
-
-
0032076463
-
Prion protein biology
-
DOI 10.1016/S0092-8674(00)81163-0
-
Prusiner SB, Scott MR, DeArmond JP, Cohen FE: Prion protein biology. Cell 1998, 93:337-348 (Pubitemid 28232079)
-
(1998)
Cell
, vol.93
, Issue.3
, pp. 337-348
-
-
Prusiner, S.B.1
Scott, M.R.2
DeArmond, S.J.3
Cohen, F.E.4
-
2
-
-
8944259890
-
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease
-
DOI 10.1002/ana.410390613
-
Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AA, Trojanowski JQ, Petersen RB, Gambetti P: Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 1996, 39:767-778 (Pubitemid 26183813)
-
(1996)
Annals of Neurology
, vol.39
, Issue.6
, 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.F.9
Trojanowski, J.Q.10
Petersen, R.B.11
Gambetti, P.12
-
3
-
-
0030953939
-
Typing prion isoforms
-
Parchi P, Capellari S, Chen SG, Petersen RB, Gambetti P, Kopp N, Brown P, Kitamoto T, Tateishi J, Giese A, Kretzschmar H: Typing prion isoforms. Nature 1997, 386:232-234
-
(1997)
Nature
, vol.386
, pp. 232-234
-
-
Parchi, P.1
Capellari, S.2
Chen, S.G.3
Petersen, R.B.4
Gambetti, P.5
Kopp, N.6
Brown, P.7
Kitamoto, T.8
Tateishi, J.9
Giese, A.10
Kretzschmar, H.11
-
4
-
-
0032816292
-
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
-
DOI 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W
-
Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar H: Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999, 46:224-233 (Pubitemid 29382879)
-
(1999)
Annals of Neurology
, vol.46
, Issue.2
, pp. 224-233
-
-
Parchi, P.1
Giese, A.2
Capellari, S.3
Brown, P.4
Schulz-Schaeffer, W.5
Windl, O.6
Zerr, I.7
Budka, H.8
Kopp, N.9
Piccardo, P.10
Poser, S.11
Rojiani, A.12
Streichemberger, N.13
Julien, J.14
Vital, C.15
Ghetti, B.16
Gambetti, P.17
Kretzschmar, H.18
-
5
-
-
12944253111
-
Genetic influence on the structural variations of the abnormal prion protein
-
Parchi P, Zou W, Wang W, Brown P, Capellari S, Ghetti B, Kopp N, Schulz-Schaeffer WJ, Kretzschmar HA, Head MW, Ironside JW, Gambetti P, Chen SG: Genetic influence on the structural variations of the abnormal prion protein. Proc Natl Acad Sci USA: 2000, 97:10168-10172
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 10168-10172
-
-
Parchi, P.1
Zou, W.2
Wang, W.3
Brown, P.4
Capellari, S.5
Ghetti, B.6
Kopp, N.7
Schulz-Schaeffer, W.J.8
Kretzschmar, H.A.9
Head, M.W.10
Ironside, J.W.11
Gambetti, P.12
Chen, S.G.13
-
8
-
-
42949128703
-
res type 1 / type 2 dichotomy in Creutzfeldt-Jakob disease
-
res type 1 / type 2 dichotomy in Creutzfeldt-Jakob disease. PLoS Pathog 2008, 4:e1000029
-
(2008)
PLoS Pathog
, vol.4
-
-
Uro-Coste, E.1
Cassard, H.2
Simon, S.3
Lugan, S.4
Bilheude, J.M.5
Perret-Liaudet, A.6
Ironside, J.W.7
Haik, S.8
Basset-Leobon, C.9
Lacroux, C.10
Peoch, K.11
Streichenberger, N.12
Langeveld, J.13
Head, M.W.14
Grassi, J.15
Hauw, J.J.16
Schelcher, F.17
Delisle, M.B.18
Andréoletti, O.19
-
9
-
-
70449524296
-
Sc types: An updated classification
-
Sc types: an updated classification. Acta Neuropathol 2009, 118:659-671
-
(2009)
Acta Neuropathol
, vol.118
, pp. 659-671
-
-
Parchi, P.1
Strammiello, R.2
Notari, S.3
Giese, A.4
Langeveld, J.P.5
Ladogana, A.6
Zerr, I.7
Roncaroli, F.8
Cras, P.9
Ghetti, B.10
Pocchiari, M.11
Kretzschmar, H.12
Capellari, S.13
-
10
-
-
70349937836
-
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: Its effect on the phenotype and prion-type characteristics
-
Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, Langeveld JP, Parchi P, Safar JG, Zou WQ, Gambetti P: Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. Brain 2009, 132:2643-2658
-
(2009)
Brain
, vol.132
, pp. 2643-2658
-
-
Cali, I.1
Castellani, R.2
Alshekhlee, A.3
Cohen, Y.4
Blevins, J.5
Yuan, J.6
Langeveld, J.P.7
Parchi, P.8
Safar, J.G.9
Zou, W.Q.10
Gambetti, P.11
-
12
-
-
30344438495
-
Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease
-
DOI 10.2353/ajpath.2006.050766
-
Yull HM, Ritchie DL, Langeveld JPM, van Zijderveld FG, Bruce ME, Ironside JW, Head MW: Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease. Am J Pathol 2006, 168:151-157 (Pubitemid 43062568)
-
(2006)
American Journal of Pathology
, vol.168
, Issue.1
, pp. 151-157
-
-
Yull, H.M.1
Ritchie, D.L.2
Langeveld, J.P.M.3
Van Zijderveld, F.G.4
Bruce, M.E.5
Ironside, J.W.6
Head, M.W.7
-
13
-
-
77949407881
-
Experimental verification of a traceback phenomenon in prion infection
-
Kobayashi A, Sakuma N, Matsuura Y, Mohri S, Aguzzi A, Kitamoto T: Experimental verification of a traceback phenomenon in prion infection. J Virol 2010, 84:3230-3238
-
(2010)
J Virol
, vol.84
, pp. 3230-3238
-
-
Kobayashi, A.1
Sakuma, N.2
Matsuura, Y.3
Mohri, S.4
Aguzzi, A.5
Kitamoto, T.6
-
14
-
-
0026751775
-
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease
-
Kitamoto T, Shin R-W, Doh-ura K, Tomokane N, Miyazono M, Muramoto T, Tateishi J: Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am J Pathol 1992, 140:1285-1294
-
(1992)
Am J Pathol
, vol.140
, pp. 1285-1294
-
-
Kitamoto, T.1
Shin, R.-W.2
Doh-ura, K.3
Tomokane, N.4
Miyazono, M.5
Muramoto, T.6
Tateishi, J.7
-
15
-
-
0344844524
-
Humanized Knock-in Mice Expressing Chimeric Prion Protein Showed Varied Susceptibility to Different Human Prions
-
Taguchi Y, Mohri S, Ironside JW, Muramoto T, Kitamoto T: Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions. Am J Pathol 2003, 163:2585-2593 (Pubitemid 37466499)
-
(2003)
American Journal of Pathology
, vol.163
, Issue.6
, pp. 2585-2593
-
-
Taguchi, Y.1
Mohri, S.2
Ironside, J.W.3
Muramoto, T.4
Kitamoto, T.5
-
16
-
-
0027185917
-
Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Straussler syndrome
-
DOI 10.1006/bbrc.1993.1275
-
Kitamoto T, Ohta M, Doh-ura K, Hitoshi S, Terao Y, Tateishi J: Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome. Biochem Biophys Res Commun 1993, 191:709-714 (Pubitemid 23222693)
-
(1993)
Biochemical and Biophysical Research Communications
, vol.191
, Issue.2
, pp. 709-714
-
-
Kitamoto, T.1
Ohta, M.2
Doh-ura, K.3
Hitoshi, S.4
Terao, Y.5
Tateishi, J.6
-
17
-
-
33747048121
-
The MM2-cortical form of sporadic Creutzfeldt-Jakob disease presenting with visual disturbance
-
DOI 10.1212/01.wnl.0000228224.35678.60, PII 0000611420060808000044
-
Nozaki I, Hamaguchi T, Noguchi-Shinohara M, Ono K, Shirasaki H, Komai K, Kitamoto T, Yamada M: The MM2-cortical form of sporadic Creutzfeldt-Jakob disease presenting with visual disturbance. Neurology 2006, 67:531-533 (Pubitemid 44214993)
-
(2006)
Neurology
, vol.67
, Issue.3
, pp. 531-533
-
-
Nozaki, I.1
Hamaguchi, T.2
Noguchi-Shinohara, M.3
Ono, K.4
Shirasaki, H.5
Komai, K.6
Kitamoto, T.7
Yamada, M.8
-
19
-
-
32644461629
-
VCJD prion acquires altered virulence through trans-species infection
-
DOI 10.1016/j.bbrc.2006.01.149, PII S0006291X06002312
-
Asano M, Mohri S, Ironside JW, Ito M, Tamaoki N, Kitamoto T: vCJD prion acquires altered virulence through trans-species infection. Biochem Biophys Res Commun 2006, 342:293-299 (Pubitemid 43247390)
-
(2006)
Biochemical and Biophysical Research Communications
, vol.342
, Issue.1
, pp. 293-299
-
-
Asano, M.1
Mohri, S.2
Ironside, J.W.3
Ito, M.4
Tamaoki, N.5
Kitamoto, T.6
-
20
-
-
0023499868
-
Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins
-
Kascsak RJ, Rubenstein R, Merz PA, Tonna-DeMasi M, Fersko R, Carp RI, Wisniewski HM, Diringer H: Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins. J Virol 1987, 61:3688-3693 (Pubitemid 18011463)
-
(1987)
Journal of Virology
, vol.61
, Issue.12
, 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.8
-
21
-
-
0034698505
-
Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu
-
DOI 10.1016/S0304-3940(00)01232-5, PII S0304394000012325
-
Muramoto T, Tanaka T, Kitamoto N, Sano C, Hayashi Y, Kutomi T, Yutani C, Kitamoto T: Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu. Neurosci Lett 2000, 288:179-182 (Pubitemid 30411909)
-
(2000)
Neuroscience Letters
, vol.288
, Issue.3
, pp. 179-182
-
-
Muramoto, T.1
Tanaka, T.2
Kitamoto, N.3
Sano, C.4
Hayashi, Y.5
Kutomi, T.6
Yutani, C.7
Kitamoto, T.8
-
22
-
-
0141841804
-
Association of an 11 - 12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases
-
DOI 10.1099/vir.0.19236-0
-
Satoh K, Muramoto T, Tanaka T, Kitamoto N, Ironside JW, Nagashima K, Yamada M, Sato T, Mohri S, Kitamoto T: Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases. J Gen Virol 2003, 84:2885-2893 (Pubitemid 37220268)
-
(2003)
Journal of General Virology
, vol.84
, Issue.10
, pp. 2885-2893
-
-
Satoh, K.1
Muramoto, T.2
Tanaka, T.3
Kitamoto, N.4
Ironside, J.W.5
Nagashima, K.6
Yamada, M.7
Sato, T.8
Mohri, S.9
Kitamoto, T.10
-
23
-
-
0029027854
-
Truncated forms of the human prion protein in normal brain and in prion diseases
-
Chen SG, Teplow DB, Parchi P, Teller JK, Gambetti P, Autilio-Gambetti L: Truncated forms of the human prion protein in normal brain and in prion diseases. J Biol Chem 1995, 270:19173-19180
-
(1995)
J Biol Chem
, vol.270
, pp. 19173-19180
-
-
Chen, S.G.1
Teplow, D.B.2
Parchi, P.3
Teller, J.K.4
Gambetti, P.5
Autilio-Gambetti, L.6
-
24
-
-
0031765769
-
Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues
-
Jiménez-Huete A, Lievens PM, Vidal R, Piccardo P, Ghetti B, Tagliavini F, Frangione B, Prelli F: Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues. Am J Pathol 1998, 153:1561-1572 (Pubitemid 28509913)
-
(1998)
American Journal of Pathology
, vol.153
, Issue.5
, pp. 1561-1572
-
-
Jimenez-Huete, A.1
Lievens, P.M.J.2
Vidal, R.3
Piccardo, P.4
Ghetti, B.5
Tagliavini, F.6
Frangione, B.7
Prelli, F.8
-
25
-
-
0027520888
-
-
Rogers M, Yehiely F, Scott M, Prusiner SB: Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells. 1993, 90:3182-3186
-
(1993)
Conversion of Truncated and Elongated Prion Proteins into the Scrapie Isoform in Cultured Cells
, vol.90
, pp. 3182-3186
-
-
Rogers, M.1
Yehiely, F.2
Scott, M.3
Prusiner, S.B.4
-
26
-
-
30144437736
-
GFP-tagged PrP supports compromised prion replication in transgenic mice
-
DOI 10.1016/j.bbrc.2005.12.085, PII S0006291X05027956
-
Bian J, Nazor KE, Angers R, Jernigan M, Seward T, Centers A, Green M, Telling GC: GFP-tagged PrP supports compromised prion replication in transgenic mice. Biochem Biophys Res Commun 2006, 340:894-900 (Pubitemid 43053913)
-
(2006)
Biochemical and Biophysical Research Communications
, vol.340
, Issue.3
, pp. 894-900
-
-
Bian, J.1
Nazor, K.E.2
Angers, R.3
Jernigan, M.4
Seward, T.5
Centers, A.6
Green, M.7
Telling, G.C.8
-
27
-
-
1942533390
-
Effects of different experimental conditions on the PrPSc core generated by protease digestion
-
Notari S, Capellari S, Giese A, Westner I, Baruzzi A, Ghetti B, Gambetti P, Kretzschmar HA, Parchi P: Effects of different experimental conditions on the PrPSc core generated by protease digestion. J Biol Chem 2004, 279:16797-16804
-
(2004)
J Biol Chem
, vol.279
, pp. 16797-16804
-
-
Notari, S.1
Capellari, S.2
Giese, A.3
Westner, I.4
Baruzzi, A.5
Ghetti, B.6
Gambetti, P.7
Kretzschmar, H.A.8
Parchi, P.9
-
28
-
-
33749254251
-
Classification of sporadic Creutzfeldt-Jakob disease revisited
-
DOI 10.1093/brain/awl224
-
Cali I, Castellani R, Yuan J, Al-Shekhlee A, Cohen ML, Xiao X, Moleres FJ, Parchi P, Zou WQ, Gambetti P: Classification of sporadic Creutzfeldt-Jakob disease revisited. Brain 2006, 129:2266-2277 (Pubitemid 44522113)
-
(2006)
Brain
, vol.129
, Issue.9
, pp. 2266-2277
-
-
Cali, I.1
Castellani, R.2
Yuan, J.3
Al-Shekhlee, A.4
Cohen, M.L.5
Xiao, X.6
Moleres, F.J.7
Parchi, P.8
Zou, W.-Q.9
Gambetti, P.10
-
29
-
-
35348941241
-
Sc types in Creutzfeldt-Jakob disease is not the rule
-
Sc types in Creutzfeldt-Jakob disease is not the rule. Lab Invest 2007, 87:1103-1112
-
(2007)
Lab Invest
, vol.87
, pp. 1103-1112
-
-
Notari, S.1
Capellari, S.2
Langeveld, J.3
Giese, A.4
Strammiello, R.5
Gambetti, P.6
Kretzschmar, H.A.7
Parchi, P.8
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