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Subcellular distribution of the prion protein in sickness and in health
Susan F. Godsave
*
,
Peter Peters
, Holger Wille
*
Corresponding author for this work
M4I - Nanoscopy
Institute of Nanoscopy
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Keyphrases
Sickness
100%
Prion Protein
100%
PrPC
100%
Subcellular Distribution
100%
PrPSc
71%
Central Nervous System
28%
Prion
28%
Disease Stage
14%
Alzheimer's Disease
14%
Cellular Processes
14%
Cell Behavior
14%
Neuroprotection
14%
Plasma Membrane
14%
Cell Surface
14%
Hippocampus
14%
Glycoprotein
14%
Beta Sheet
14%
Transmembrane
14%
Cellular Prion Protein
14%
Creutzfeldt-Jakob Disease
14%
Protein Misfolding
14%
Bovine Spongiform Encephalopathy
14%
Clinical Disease
14%
C-terminus
14%
Prion Disease
14%
Scrapie
14%
Prion Types
14%
Aggregation State
14%
GPI-anchored Protein (GPI-AP)
14%
Long Incubation Period
14%
Scrapie Prions
14%
INIS
diseases
100%
proteins
100%
subcellular distribution
100%
central nervous system
50%
cancer
25%
sheets
25%
pathology
25%
death
25%
populations
25%
membranes
25%
molecules
25%
genetics
25%
aggregation
25%
nervous system diseases
25%
anchors
25%
surfaces
25%
plasma
25%
conversion
25%
hippocampus
25%
glycoproteins
25%
incubation
25%
bovine
25%
Biochemistry, Genetics and Molecular Biology
Subcellular Localization
100%
Prion Protein
100%
Scrapie
33%
Genetics
16%
Isoform
16%
Cell Membrane
16%
C-Terminus
16%
Conformation
16%
Glycoprotein
16%
Incubation Time
16%
Glycosyl
16%
Protein Misfolding
16%
Creutzfeldt-Jakob Disease
16%
Beta Sheet
16%
Bovine Spongiform Encephalopathy
16%
Phosphatidylinositol
16%
Neuroscience
Prion Disease
20%