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PLoS Pathogens, ISSN 1553-7366, 08/2017, Volume 13, Issue 8, p. e1006458
The function(s) of the PrP One of the most intriguing function(s) of PrPC is its involvement in cell signalling. Because of its extracellular localization, the... 
CELL-ADHESION MOLECULE | VIROLOGY | NCAM | NEURONS | RECEPTOR | MICROBIOLOGY | COPPER | MICE | PARASITOLOGY | Animals | Prion Proteins - metabolism | Humans | Prion Diseases - metabolism | Proteins | Physiological aspects | Research | Properties | Structure | Prions | Tyrosine | Thiols | Crosstalk | Nervous system | Mammals | Kinases | Cell adhesion & migration | Coupling (molecular) | Signal transduction | Signaling | Cell adhesion | Physiology | Copper | Prion protein
Journal Article
08/2017, Progress in molecular biology and translational science, ISBN 9780128112267, Volume 150, 518
Neurodegenerative diseases represent a health issue that in recent years has received increasing attention from the scientific community due to their social... 
Prions | Nervous system | Prion diseases
eBook
Progress in Molecular Biology and Translational Science, ISSN 1877-1173, 2017, Volume 150, pp. xvii - xix
Journal Article
Prion, ISSN 1933-6896, 04/2014, Volume 8, Issue sup1, pp. 1 - 1
Journal Article
Prion, ISSN 1933-6896, 2014, Volume 8, p. 1
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 2017, Volume 127, pp. 859 - 873
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of the misfolded protein PrP that represents the pathological... 
Pharmacophore modeling | 3D-QSAR | Anti-Prion agents | Theranostic tools | Prion
Journal Article
Science, ISSN 0036-8075, 7/2004, Volume 305, Issue 5684, pp. 673 - 676
Journal Article
European journal of medicinal chemistry, ISSN 0223-5234, 02/2017, Volume 127, pp. 859 - 873
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 02/2017, Volume 127, p. 859
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of the misfolded protein PrP.sup.Sc that represents the... 
Prevention | Cellular proteins | Nervous system diseases | Analysis | Prion diseases | Chemical properties | Drug discovery | Permeability | Investigations | Protein binding | Fluorescence
Journal Article
Journal of Neuroscience Research, ISSN 0360-4012, 2019
Neurodegenerative diseases are incurable debilitating disorders characterized by structural and functional neuronal loss. Approximately 30 million people are... 
Alzheimer’s disease | Parkinson’s disease | serpina3 | prion protein
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 9/2019, Volume 56, Issue 9, pp. 6121 - 6133
Journal Article
The Journal of biological chemistry, ISSN 0021-9258, 02/2019, Volume 294, Issue 14, pp. 5657 - 5665
α-Synuclein (AS) is an intrinsically disordered protein highly expressed in dopaminergic neurons. Its amyloid aggregates are the major component of Lewy... 
Index Medicus
Journal Article
Prion, ISSN 1933-6896, 01/2012, Volume 6, Issue 1, pp. 37 - 39
The conversion to a disease-associated conformer (PrP(Sc)) of the cellular prion protein (PrP(C)) is the central event in prion diseases. Wild-type PrPC... 
Mammals - metabolism | Animals | Prions - genetics | Protein Structure, Secondary | Humans | Prions - chemistry | Mutation - genetics | Molecular Dynamics Simulation | Prion Diseases - metabolism | pathogenic mutations | prions | molecular dynamics | View | human | nuclear magnetic resonance | structure | prion protein
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 10050 - 12
The precise molecular mechanism of how misfolded alpha-synuclein (alpha-Syn) accumulates and spreads in synucleinopathies is still unknown. Here, we show the... 
BETA OLIGOMERS | SCRAPIE | COEXISTENCE | TRANSMISSION | MULTIDISCIPLINARY SCIENCES | CYCLIC AMPLIFICATION | CREUTZFELDT-JAKOB-DISEASE | PATHOLOGY | ENDOCYTOSIS | PARKINSONS-DISEASE | PRP | Scrapie | Internalization | Rodents | Fibrils | Creutzfeldt-Jakob disease | Replication | Amyloid | Synuclein | Prion protein | Cell spreading | Cell migration
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 02/2017, Volume 127, pp. 859 - 873
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of the misfolded protein PrP that represents the pathological... 
3D-QSAR | Anti-Prion agents |