-
1
-
-
0033562770
-
Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease
-
Alperovitch A., Zerr I., Pocchiari M., Mitrova E., dePedro-Cuesta J., Hegyi I., Collins S., Kretzschmar H., vanDuijn C., Will R.G. Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease. Lancet. 353:1999;1673-1674.
-
(1999)
Lancet
, vol.353
, pp. 1673-1674
-
-
Alperovitch, A.1
Zerr, I.2
Pocchiari, M.3
Mitrova, E.4
DePedro-Cuesta, J.5
Hegyi, I.6
Collins, S.7
Kretzschmar, H.8
VanDuijn, C.9
Will, R.G.10
-
3
-
-
0034913977
-
Prion protein gene polymorphism and Alzheimer's disease: One modulatory trait of cognitive decline?
-
Casadei V.M., Ferri C., Calabrese E., Franceschi M., Veglia F., Licastro F., Mariani C., Grimaldi L.M.E. Prion protein gene polymorphism and Alzheimer's disease: one modulatory trait of cognitive decline? J. Neurol. Neurosurg. Psychiatry. 71:2001;279-280.
-
(2001)
J. Neurol. Neurosurg. Psychiatry
, vol.71
, pp. 279-280
-
-
Casadei, V.M.1
Ferri, C.2
Calabrese, E.3
Franceschi, M.4
Veglia, F.5
Licastro, F.6
Mariani, C.7
Grimaldi, L.M.E.8
-
4
-
-
0033845154
-
Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD
-
Combarros O., Sánchez-Guerra M., Llorca J., Alvarez-Arcaya A., Berciano J., Peña N., Fernández-Viadero C. Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD. Neurology. 55:2000;593-595.
-
(2000)
Neurology
, vol.55
, pp. 593-595
-
-
Combarros, O.1
Sánchez-Guerra, M.2
Llorca, J.3
Alvarez-Arcaya, A.4
Berciano, J.5
Peña, N.6
Fernández-Viadero, C.7
-
5
-
-
0037041441
-
Danger - misfolding proteins
-
Ellis R.J., Pinheiro T.J.T. Danger - misfolding proteins. Nature. 416:2002;483-484.
-
(2002)
Nature
, vol.416
, pp. 483-484
-
-
Ellis, R.J.1
Pinheiro, T.J.T.2
-
6
-
-
0035812297
-
c and Doppel: Insights from mutational analysis
-
c and Doppel: insights from mutational analysis. Gene. 275:2001;1-18.
-
(2001)
Gene
, vol.275
, pp. 1-18
-
-
Mastrangelo, P.1
Westaway, D.2
-
7
-
-
0021271971
-
Clinical diagnosis of Alzheimer's disease: Report of the NINCDA-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease
-
McKhaan G., Drachman D., Folstein M., Katzman R., Price D., Stadlan E.M. Clinical diagnosis of Alzheimer's disease: report of the NINCDA-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology. 34:1984;934-944.
-
(1984)
Neurology
, vol.34
, pp. 934-944
-
-
McKhaan, G.1
Drachman, D.2
Folstein, M.3
Katzman, R.4
Price, D.5
Stadlan, E.M.6
-
8
-
-
0034714488
-
Examination of the human prion protein-like gene Doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease
-
Mead S., Beck J., Dickinson A., Fisher E.M.C., Collinge J. Examination of the human prion protein-like gene Doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease. Neurosci. Lett. 290:2000;117-120.
-
(2000)
Neurosci. Lett.
, vol.290
, pp. 117-120
-
-
Mead, S.1
Beck, J.2
Dickinson, A.3
Fisher, E.M.C.4
Collinge, J.5
-
9
-
-
0035957003
-
Two different neurodegenerative diseases caused by proteins with similar structures
-
Mo H., Moore R.C., Cohen F.E., Westaway D., Prusiner S.B., Wright P.E., Dyson H.J. Two different neurodegenerative diseases caused by proteins with similar structures. Proc. Natl. Acad. Sci. USA. 98:2001;2352-2357.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 2352-2357
-
-
Mo, H.1
Moore, R.C.2
Cohen, F.E.3
Westaway, D.4
Prusiner, S.B.5
Wright, P.E.6
Dyson, H.J.7
-
10
-
-
0025820942
-
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease
-
Palmer M.S., Dryden A.J., Hughes J.T., Collinge J. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature. 352:1991;340-342.
-
(1991)
Nature
, vol.352
, pp. 340-342
-
-
Palmer, M.S.1
Dryden, A.J.2
Hughes, J.T.3
Collinge, J.4
-
11
-
-
0342858819
-
First report of polymorphisms in the prion-like protein gene (PRND): Implications for human prion diseases
-
Peoch K., Guérin C., Brandel J.P., Launay J.M., Laplanche J.L. First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases. Neurosci. Lett. 286:2000;144-148.
-
(2000)
Neurosci. Lett.
, vol.286
, pp. 144-148
-
-
Peoch, K.1
Guérin, C.2
Brandel, J.P.3
Launay, J.M.4
Laplanche, J.L.5
-
13
-
-
0035865398
-
Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain
-
Rossi D., Cozzio A., Flechsig E., Klein M.A., Rülicke T., Aguzzi A., Weissmann C. Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain. EMBO J. 20:2001;694-702.
-
(2001)
EMBO J.
, vol.20
, pp. 694-702
-
-
Rossi, D.1
Cozzio, A.2
Flechsig, E.3
Klein, M.A.4
Rülicke, T.5
Aguzzi, A.6
Weissmann, C.7
-
14
-
-
0034804089
-
Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases: Alzheimer's disease and other neurological disorders
-
Schröder B., Franz B., Hempfling P., Selbert M., Jürgens T., Kretzschmar H.A., Bodemer M., Poser S., Zerr I. Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases: Alzheimer's disease and other neurological disorders. Hum. Genet. 109:2001;319-325.
-
(2001)
Hum. Genet.
, vol.109
, pp. 319-325
-
-
Schröder, B.1
Franz, B.2
Hempfling, P.3
Selbert, M.4
Jürgens, T.5
Kretzschmar, H.A.6
Bodemer, M.7
Poser, S.8
Zerr, I.9
-
15
-
-
0032485258
-
Chaperoning brain diseases
-
Welch W.J., Gambetti P. Chaperoning brain diseases. Nature. 392:1998;23-24.
-
(1998)
Nature
, vol.392
, pp. 23-24
-
-
Welch, W.J.1
Gambetti, P.2
-
16
-
-
0036607438
-
Mammalian prion proteins: Enigma, variation and vaccination
-
Westaway D., Carlson G.A. Mammalian prion proteins: enigma, variation and vaccination. Trends Biochem. Sci. 27:2002;301-307.
-
(2002)
Trends Biochem. Sci.
, vol.27
, pp. 301-307
-
-
Westaway, D.1
Carlson, G.A.2
-
17
-
-
2442735162
-
Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: A systematic analysis of predisposing mutations and allelic variation in the PRNP gene
-
Windl O., Dempster M., Estibeiro J.P., Lathe R., de Silva R., Esmonde T., Will R., Springbett A., Campbell T.A., Sidle K.C.L., Palmer M.S., Collinge J. Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene. Hum. Genet. 98:1996;259-264.
-
(1996)
Hum. Genet.
, vol.98
, pp. 259-264
-
-
Windl, O.1
Dempster, M.2
Estibeiro, J.P.3
Lathe, R.4
De Silva, R.5
Esmonde, T.6
Will, R.7
Springbett, A.8
Campbell, T.A.9
Sidle, K.C.L.10
Palmer, M.S.11
Collinge, J.12
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