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Distribution of Misfolded Prion Protein Seeding Activity Alone Does Not Predict Regions of Neurodegeneration.
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- PLoS Biology, 2016, v. 14, n. 11, p. 1, doi. 10.1371/journal.pbio.1002579
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- Article
Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties.
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- 2014
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- Publication type:
- journal article
Constant Transmission Properties of Variant Creutzfeldt-Jakob Disease in 5 Countries.
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- Emerging Infectious Diseases, 2012, v. 18, n. 10, p. 1574, doi. 10.3201/eid1810.120792
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- Article
Candidate Cell Substrates, Vaccine Production, and Transmissible Spongiform Encephalopathies.
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- Emerging Infectious Diseases, 2011, v. 17, n. 12, p. 2262, doi. 10.3201/eid1712.110607
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- Article
Insights into Mechanisms of Chronic Neurodegeneration.
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- International Journal of Molecular Sciences, 2016, v. 17, n. 1, p. 82, doi. 10.3390/ijms17010082
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- Article
T-cell lymphoma, tropical spastic paraparesis, and malignant fibrous histiocytoma in a patient with human T-cell lymphotropic virus, type 1.
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- 1989
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- Publication type:
- journal article
CONTRIBUTION OF THE NEUROPATHOLOGY LABORATORY AT INDIANA UNIVERSITY TO THE DECIPHERING OF DOMINANTLY INHERITED DEMENTIAS: 1976-2016.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P744, doi. 10.1016/j.jalz.2016.06.1553
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- Article
Early-onset Alzheimer's disease associated with PSEN1 L166P mutation: An atypical clinical phenotype
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- 2012
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- Publication type:
- Abstract
Cognition and brain structure in Gerstmann-Straussler-Scheinker disease (PRNP F198S)
- Published in:
- 2010
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- Abstract
Transmission of Alzheimer amyloidosis to chimpanzees and monkeys: Revisited
- Published in:
- 2010
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- Publication type:
- Abstract
Human Prion Diseases and the Risk of Their Transmission During Anatomical Dissection.
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- Clinical Anatomy, 2014, v. 27, n. 6, p. 821, doi. 10.1002/ca.22403
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- Article
A Naturally Occurring Bovine Tauopathy Is Geographically Widespread in the UK.
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- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0129499
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- Article
Allelic Origin of Protease-Sensitive and Protease-Resistant Prion Protein Isoforms in Gerstmann-Sträussler-Scheinker Disease with the P102L Mutation.
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- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0032382
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- Article
Aggregated, Wild-Type Prion Protein Causes Neurological Dysfunction and Synaptic Abnormalities.
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- Journal of Neuroscience, 2008, v. 28, n. 49, p. 13258, doi. 10.1523/JNEUROSCI.3109-08.2008
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- Article
Neurodegenerative Illness in Transgenic Mice Expressing a Transmembrane Form of the Prion Protein.
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- Journal of Neuroscience, 2005, v. 25, n. 13, p. 3469, doi. 10.1523/JNEUROSCI.0105-05.2005
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- Publication type:
- Article
Post-translational changes to PrP alter transmissible spongiform encephalopathy strain properties.
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- EMBO Journal, 2013, v. 32, n. 5, p. 756, doi. 10.1038/emboj.2013.6
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- Article
Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice.
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- EMBO Journal, 2007, v. 26, n. 11, p. 2777, doi. 10.1038/sj.emboj.7601726
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- Article
A novel mutation (G217D) in the Presenilin 1 gene (PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum.
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- Acta Neuropathologica, 2002, v. 104, n. 2, p. 155, doi. 10.1007/s00401-002-0536-6
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- Article
Senile dementia associated with amyloid β protein angiopathy and tau perivascular pathology but not neuritic plaques in patients homozygous for the APOE-ε4 allele.
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- Acta Neuropathologica, 2000, v. 100, n. 1, p. 1, doi. 10.1007/s004010051186
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- Article
Experimental Bovine Spongiform Encephalopathy in Squirrel Monkeys: The Same Complex Proteinopathy Appearing after Very Different Incubation Times.
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- Pathogens, 2022, v. 11, n. 5, p. 597, doi. 10.3390/pathogens11050597
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- Article
Neuropathology of Gerstmann-Sträussler-Scheinker disease.
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- Microscopy Research & Technique, 2000, v. 50, n. 1, p. 10, doi. 10.1002/1097-0029(20000701)50:1<10::AID-JEMT3>3.0.CO;2-6
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- Article
Mechanism of PrP-Amyloid Formation in Mice Without Transmissible Spongiform Encephalopathy.
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- Brain Pathology, 2012, v. 22, n. 1, p. 58, doi. 10.1111/j.1750-3639.2011.00508.x
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- Publication type:
- Article
PET of Brain Prion Protein Amyloid in Gerstmann–Sträussler–Scheinker Disease.
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- Brain Pathology, 2010, v. 20, n. 2, p. 419, doi. 10.1111/j.1750-3639.2009.00306.x
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- Publication type:
- Article
Early-onset Dementia with Lewy Bodies.
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- Brain Pathology, 2004, v. 14, n. 2, p. 137, doi. 10.1111/j.1750-3639.2004.tb00046.x
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- Article
Prion Protein Amyloidosis.
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- Brain Pathology, 1996, v. 6, n. 2, p. 127, doi. 10.1111/j.1750-3639.1996.tb00796.x
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- Article
Ablation of Prion Protein in Wild Type Human Amyloid Precursor Protein (APP) Transgenic Mice Does Not Alter The Proteolysis of APP, Levels of Amyloid-β or Pathologic Phenotype.
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- PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0159119
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- Article
Blood reference materials from macaques infected with variant Creutzfeldt-Jakob disease agent.
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- Transfusion, 2015, v. 55, n. 2, p. 405, doi. 10.1111/trf.12841
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- Publication type:
- Article
Fukuoka-1 strain of transmissible spongiform encephalopathy agent infects murine bone marrow-derived cells with features of mesenchymal stem cells.
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- Transfusion, 2011, v. 51, n. 8, p. 1755, doi. 10.1111/j.1537-2995.2010.03041.x
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- Article
Host PrP Glycosylation: A Major Factor Determining the Outcome of Prion Infection.
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- PLoS Biology, 2008, v. 6, n. 4, p. e100, doi. 10.1371/journal.pbio.0060100
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- Publication type:
- Article
PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions.
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- Acta Neuropathologica, 2016, v. 132, n. 4, p. 611, doi. 10.1007/s00401-016-1594-5
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- Article
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.
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- Annals of Neurology, 1999, v. 46, n. 2, p. 224, doi. 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W
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- Article
Intrathecal synthesis of IgG antibodies to HTLV-I supports an etiological role for HTLV-I in tropical spastic paraparesis.
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- Annals of Neurology, 1988, v. 23, n. S1, p. S188, doi. 10.1002/ana.410230742
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- Article
Pathological and immunological observations on tropical spastic paraparesis in patients from jamaica.
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- Annals of Neurology, 1988, v. 23, n. S1, p. S156, doi. 10.1002/ana.410230735
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- Publication type:
- Article
HTLV-I-Like viral particles in spinal cord cells in jamaican tropical spastic paraparesis.
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- Annals of Neurology, 1988, v. 23, n. S1, p. S185, doi. 10.1002/ana.410230741
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- Publication type:
- Article
The role of HTLV-I in tropical spastic paraparesis in jamaica.
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- Annals of Neurology, 1988, v. 23, n. S1, p. S121, doi. 10.1002/ana.410230729
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- Publication type:
- Article
Variable Phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian Family.
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- Canadian Journal of Neurological Sciences, 2003, v. 30, n. 3, p. 233, doi. 10.1017/S0317167100002651
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- Publication type:
- Article