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Regulating Factors of PrP<sup>res</sup> Glycosylation in Creutzfeldt-Jakob Disease - Implications for the Dissemination and the Diagnosis of Human Prion Strains.
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- PLoS ONE, 2008, v. 3, n. 7, p. 1, doi. 10.1371/journal.pone.0002786
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Truncated PrP<sup>c</sup> in mammalian brain: interspecies variation and location in membrane rafts.
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- Biological Chemistry, 2006, v. 387, n. 3, p. 297, doi. 10.1515/BC.2006.039
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- Article
The N-terminal cleavage of cellular prion protein in the human brain
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- FEBS Letters, 2005, v. 579, n. 28, p. 6333, doi. 10.1016/j.febslet.2005.10.013
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The tissue-specific methylation of the human Tyrosine Hydroxylase gene reveals new regulatory elements in the first exon.
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- Journal of Neurochemistry, 2005, v. 94, n. 1, p. 129, doi. 10.1111/j.1471-4159.2005.03173.x
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- Article
Neuromelanin associated redox-active iron is increased in the substantia nigra of patients with Parkinson's disease.
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- Journal of Neurochemistry, 2003, v. 86, n. 5, p. 1142, doi. 10.1046/j.1471-4159.2003.01923.x
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The sympathetic nervous system is involved in variant Creutzfeldt-Jakob disease.
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- Nature Medicine, 2003, v. 9, n. 9, p. 1121
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Prion protein deposits match magnetic resonance imaging signal abnormalities in Creutzfeldt-Jakob disease.
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- Annals of Neurology, 2002, v. 51, n. 6, p. 797, doi. 10.1002/ana.10195
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Parkin immunoreactivity in the brain of human and non-human primates: An immunohistochemical analysis in normal conditions and in Parkinsonian syndromes.
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- Journal of Comparative Neurology, 2001, v. 432, n. 2, p. 184, doi. 10.1002/cne.1096
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Dopaminergic neurons degenerate by apoptosis in Parkinson's disease.
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- Movement Disorders, 1999, v. 14, n. 2, p. 383, doi. 10.1002/1531-8257(199903)14:2<383::AID-MDS1037>3.0.CO;2-F
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Striatal Expression of Glutamic Acid Decarboxylase Gene in Alzheimer's Disease.
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- Journal of Neurochemistry, 1998, v. 71, n. 2, p. 767, doi. 10.1046/j.1471-4159.1998.71020767.x
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Cellular prion protein localization in rodent and primate brain.
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- European Journal of Neuroscience, 1998, v. 10, n. 7, doi. 10.1046/j.1460-9568.1998.00258.x
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Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions.
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- Human Molecular Genetics, 1998, v. 7, n. 5, p. 913, doi. 10.1093/hmg/7.5.913
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Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes.
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- Human Molecular Genetics, 1997, v. 6, n. 11, p. 1771, doi. 10.1093/hmg/6.11.1771
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Expression of glutamate receptors in the human and rat basal ganglia: Effect of the dopaminergic denervation on AMPA receptor gene expression in the striatopallidal complex in parkinson's disease and rat with 6-OHDA lesion.
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- Journal of Comparative Neurology, 1996, v. 368, n. 4, p. 553, doi. 10.1002/(SICI)1096-9861(19960513)368:4<553::AID-CNE7>3.0.CO;2-3
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- Article
Dopamine transporter messenger RNA in Parkinson's disease and control substantia nigra neurons.
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- Annals of Neurology, 1994, v. 35, n. 4, p. 494, doi. 10.1002/ana.410350421
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- Article