-
1
-
-
70349705441
-
Prions: Protein aggregation and infectious diseases
-
Aguzzi, A., and A. M. Calella. 2009. Prions: protein aggregation and infectious diseases. Physiol. Rev. 89:1105-1152.
-
(2009)
Physiol. Rev
, vol.89
, pp. 1105-1152
-
-
Aguzzi, A.1
Calella, A.M.2
-
2
-
-
32644461629
-
vCJD prion acquires altered virulence through trans-species infection
-
Asano, M., S. Mohri, J. W. Ironside, M. Ito, N. Tamaoki, and T. Kitamoto. 2006. vCJD prion acquires altered virulence through trans-species infection. Biochem. Biophys. Res. Commun. 342:293-299.
-
(2006)
Biochem. Biophys. Res. Commun
, vol.342
, pp. 293-299
-
-
Asano, M.1
Mohri, S.2
Ironside, J.W.3
Ito, M.4
Tamaoki, N.5
Kitamoto, T.6
-
3
-
-
36049020231
-
A general model of prion strains and their pathogenicity
-
Collinge, J., and M. R. Scott. 2007. A general model of prion strains and their pathogenicity. Science 318:930-936.
-
(2007)
Science
, vol.318
, pp. 930-936
-
-
Collinge, J.1
Scott, M.R.2
-
5
-
-
0029661942
-
Sc-detection in mouse spleen early at the preclinical stage of scrapie with collagenase-completed tissue homogenization and Sarkosyl-NaCl extraction of PrPSc
-
Sc-detection in mouse spleen early at the preclinical stage of scrapie with collagenase-completed tissue homogenization and Sarkosyl-NaCl extraction of PrPSc. Arch. Virol. 141:1863-1874.
-
(1996)
Arch. Virol
, vol.141
, pp. 1863-1874
-
-
Grathwohl, K.U.D.1
Horiuchi, M.2
Ishiguro, N.3
Shinagawa, M.4
-
6
-
-
0025794115
-
N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Sträussler syndrome
-
Kitamoto, T., T. Muramoto, C. Hilbich, K. Beyreuther, and J. Tateishi. 1991. N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Sträussler syndrome. Brain Res. 545:319-321.
-
(1991)
Brain Res
, vol.545
, pp. 319-321
-
-
Kitamoto, T.1
Muramoto, T.2
Hilbich, C.3
Beyreuther, K.4
Tateishi, J.5
-
7
-
-
0026751775
-
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease
-
Kitamoto, T., R. W. Shin, K. Doh-ura, N. Tomokane, M. Miyazono, T. Muramoto, and J. Tateishi. 1992. Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am. J. Pathol. 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
-
8
-
-
0027185917
-
Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome
-
Kitamoto, T., M. Ohta, K. Doh-ura, S. Hitoshi, Y. Terao, and J. Tateishi. 1993. Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome. Biochem. Biophys. Res. Commun. 191: 709-714.
-
(1993)
Biochem. Biophys. Res. Commun
, vol.191
, pp. 709-714
-
-
Kitamoto, T.1
Ohta, M.2
Doh-ura, K.3
Hitoshi, S.4
Terao, Y.5
Tateishi, J.6
-
9
-
-
18444371126
-
Follicular dendritic cell of the knock-in mouse provides a new bioassay for human prions
-
Kitamoto, T., S. Mohri, J. W. Ironside, I. Miyoshi, T. Tanaka, N. Kitamoto, S. Itohara, N. Kasai, M. Katsuki, J. Higuchi, T. Muramoto, and R. W. Shin. 2002. Follicular dendritic cell of the knock-in mouse provides a new bioassay for human prions. Biochem. Biophys. Res. Commun. 294:280-286.
-
(2002)
Biochem. Biophys. Res. Commun
, vol.294
, pp. 280-286
-
-
Kitamoto, T.1
Mohri, S.2
Ironside, J.W.3
Miyoshi, I.4
Tanaka, T.5
Kitamoto, N.6
Itohara, S.7
Kasai, N.8
Katsuki, M.9
Higuchi, J.10
Muramoto, T.11
Shin, R.W.12
-
10
-
-
35649016744
-
Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain
-
Kobayashi, A., M. Asano, S. Mohri, and T. Kitamoto. 2007. Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain. J. Biol. Chem. 282:30022-30028.
-
(2007)
J. Biol. Chem
, vol.282
, pp. 30022-30028
-
-
Kobayashi, A.1
Asano, M.2
Mohri, S.3
Kitamoto, T.4
-
11
-
-
70349308578
-
A traceback phenomenon can reveal the origin of prion infection
-
Kobayashi, A., M. Asano, S. Mohri, and T. Kitamoto. 2009. A traceback phenomenon can reveal the origin of prion infection. Neuropathology 29: 619-624.
-
(2009)
Neuropathology
, vol.29
, pp. 619-624
-
-
Kobayashi, A.1
Asano, M.2
Mohri, S.3
Kitamoto, T.4
-
12
-
-
0037447071
-
Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene
-
Korth, C., K. Kaneko, D. Groth, N. Heye, G. Telling, J. Mastrianni, P. Parchi, P. Gambetti, R. Will, J. Ironside, C. Heinrich, P. Tremblay, S. J. DeArmond, and S. B. Prusiner. 2003. Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene. Proc. Natl. Acad. Sci. U. S. A. 100:4784-4789.
-
(2003)
Proc. Natl. Acad. Sci. U. S. A
, vol.100
, pp. 4784-4789
-
-
Korth, C.1
Kaneko, K.2
Groth, D.3
Heye, N.4
Telling, G.5
Mastrianni, J.6
Parchi, P.7
Gambetti, P.8
Will, R.9
Ironside, J.10
Heinrich, C.11
Tremblay, P.12
DeArmond, S.J.13
Prusiner, S.B.14
-
13
-
-
0043128815
-
Iatrogenic Creutzfeldt-Jakob disease with florid plaques
-
Kretzschmar, H. A., S. Sethi, Z. Földvári, O. Windl, V. Querner, I. Zerr, and S. Poser. 2003. Iatrogenic Creutzfeldt-Jakob disease with florid plaques. Brain Pathol. 13:245-249.
-
(2003)
Brain Pathol
, vol.13
, pp. 245-249
-
-
Kretzschmar, H.A.1
Sethi, S.2
Földvári, Z.3
Windl, O.4
Querner, V.5
Zerr, I.6
Poser, S.7
-
14
-
-
35348941241
-
Sc types in Creutzfeldt-Jakob disease is not the rule
-
Sc types in Creutzfeldt-Jakob disease is not the rule. Lab. Invest. 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
-
15
-
-
8944259890
-
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease
-
Parchi, P., R. Castellani, S. Capellari, B. Ghetti, K. Young, S. G. Chen, M. Farlow, D. W. Dickson, A. A. F. Sima, J. Q. Trojanowski, R. B. Petersen, and P. Gambetti. 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.F.9
Trojanowski, J.Q.10
Petersen, R.B.11
Gambetti, P.12
-
16
-
-
0030953939
-
Typing prion isoforms
-
Parchi, P., S. Capellari, S. G. Chen, R. B. Petersen, P. Gambetti, N. Kopp, P. Brown, T. Kitamoto, J. Tateishi, A. Giese, and H. Kretzschmar. 1997. Typing prion isoforms. Nature 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
-
17
-
-
0032816292
-
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
-
Parchi, P., A. Giese, S. Capellari, P. Brown, W. Schulz-Schaeffer, O. Windl, I. Zerr, H. Budka, N. Kopp, P. Piccardo, S. Poser, A. Rojiani, N. Streichemberger, J. Julien, C. Vital, B. Ghetti, P. Gambetti, and H. Kretzschmar. 1999. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann. Neurol. 46:224-233.
-
(1999)
Ann. Neurol
, vol.46
, 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
-
18
-
-
12944253111
-
Genetic influence on the structural variations of the abnormal prion protein
-
Parchi, P., W. Zou, W. Wang, P. Brown, S. Capellari, B. Ghetti, N. Kopp, W. J. Schulz-Schaeffer, H. A. Kretzschmar, M. W. Head, J. W. Ironside, P. Gambetti, and S. G. Chen. 2000. Genetic influence on the structural variations of the abnormal prion protein. Proc. Natl. Acad. Sci. U. S. A. 97:10168-10172.
-
(2000)
Proc. Natl. Acad. Sci. U. S. A
, 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
-
19
-
-
70449524296
-
Sc types: An updated classification
-
29 August, doi:10.1007/s00401-009-0585-1
-
Sc types: an updated classification. Acta Neuropathol. doi:10.1007/s00401-009-0585-1.
-
(2009)
Acta Neuropathol
-
-
Parchi, P.1
Strammiello, R.2
Notari, S.3
Giese, A.4
Langeveld, J.P.M.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
-
20
-
-
0037071874
-
A change in the conformation of prions accompanies the emergence of a new prion strain
-
Peretz, D., R. A. Williamson, G. Legname, Y. Matsunaga, J. Vergara, D. R. Burton, S. J. DeArmond, S. B. Prusiner, and M. R. Scott. 2002. A change in the conformation of prions accompanies the emergence of a new prion strain. Neuron 34:921-932.
-
(2002)
Neuron
, vol.34
, pp. 921-932
-
-
Peretz, D.1
Williamson, R.A.2
Legname, G.3
Matsunaga, Y.4
Vergara, J.5
Burton, D.R.6
DeArmond, S.J.7
Prusiner, S.B.8
Scott, M.R.9
-
21
-
-
27744459883
-
Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease
-
Polymenidou, M., K. Stoeck, M. Glatzel, M. Vey, A. Bellon, and A. Aguzzi. 2005. Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease. Lancet Neurol. 4:805-814.
-
(2005)
Lancet Neurol
, vol.4
, pp. 805-814
-
-
Polymenidou, M.1
Stoeck, K.2
Glatzel, M.3
Vey, M.4
Bellon, A.5
Aguzzi, A.6
-
22
-
-
57549096688
-
The POM monoclonals: A comprehensive set of antibodies to non-overlapping prion protein epitopes
-
Polymenidou, M., R. Moos, M. Scott, C. Sigurdson, Y. Z. Shi, B. Yajima, I. Hafner-Bratkovic, R. Jerala, S. Hornemann, K. Wuthrich, A. Bellon, M. Vey, G. Garen, M. N. James, N. Kav, and A. Aguzzi. 2008. The POM monoclonals: a comprehensive set of antibodies to non-overlapping prion protein epitopes. PLoS One 3:e3872.
-
(2008)
PLoS One
, vol.3
-
-
Polymenidou, M.1
Moos, R.2
Scott, M.3
Sigurdson, C.4
Shi, Y.Z.5
Yajima, B.6
Hafner-Bratkovic, I.7
Jerala, R.8
Hornemann, S.9
Wuthrich, K.10
Bellon, A.11
Vey, M.12
Garen, G.13
James, M.N.14
Kav, N.15
Aguzzi, A.16
-
23
-
-
0032076463
-
Prion protein biology
-
Prusiner, S. B., M. R. Scott, J. P. DeArmond, and F. E. Cohen. 1998. Prion protein biology. Cell 93:337-348.
-
(1998)
Cell
, vol.93
, pp. 337-348
-
-
Prusiner, S.B.1
Scott, M.R.2
DeArmond, J.P.3
Cohen, F.E.4
-
25
-
-
0026542341
-
Autolytic transition of μ-calpain upon activation as resolved by antibodies distinguishing between the pre- and post-autolysis forms
-
Saido, T. C., S. Nagao, M. Shiramine, M. Tsukaguchi, H. Sorimachi, H. Murofushi, T. Tsuchiya, H. Ito, and K. Suzuki. 1992. Autolytic transition of μ-calpain upon activation as resolved by antibodies distinguishing between the pre- and post-autolysis forms. J. Biochem. 111:81-86.
-
(1992)
J. Biochem
, vol.111
, pp. 81-86
-
-
Saido, T.C.1
Nagao, S.2
Shiramine, M.3
Tsukaguchi, M.4
Sorimachi, H.5
Murofushi, H.6
Tsuchiya, T.7
Ito, H.8
Suzuki, K.9
-
26
-
-
0028855851
-
N3(pE), in senile plaques
-
N3(pE), in senile plaques. Neuron 14:457-466.
-
(1995)
Neuron
, vol.14
, pp. 457-466
-
-
Saido, T.C.1
Iwatsubo, T.2
Mann, D.M.A.3
Shimada, H.4
Ihara, Y.5
Kawashima, S.6
-
27
-
-
0344844524
-
Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions
-
Taguchi, Y., S. Mohri, J. W. Ironside, T. Muramoto, and T. Kitamoto. 2003. Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions. Am. J. Pathol. 163:2585-2593.
-
(2003)
Am. J. Pathol
, vol.163
, pp. 2585-2593
-
-
Taguchi, Y.1
Mohri, S.2
Ironside, J.W.3
Muramoto, T.4
Kitamoto, T.5
-
28
-
-
30344438495
-
Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease
-
Yull, H. M., D. L. Ritchie, J. P. M. Langeveld, F. G. van Zijderveld, M. E. Bruce, J. W. Ironside, and M. W. Head. 2006. Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease. Am. J. Pathol. 168:151-157.
-
(2006)
Am. J. Pathol
, vol.168
, 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
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