HUGO ID Detailed Result 9449

PMID	Match String	Actual String	Score	Flanking text	Edited by	Edit
16647138	PrP	PrP	1.1	accumulation of abnormal extracellular _amp_#x3b2 -helix rich prion protein (PrP PrP sc characterize CJD
16647138	PrP	PrP	1.1	isoform of a normally occurring _amp_#x3b1 -helix-rich prion protein (PrP PrP c whose function has not been clearly elucidated ( Brown
16647138	PrP	PrP	1.1	It is proposed that PrP c is associated with synaptic function circadian rhythms regulation and
16647138	PrP	PrP	1.1	The observation that PrP c regulates Cu 2 /Zn Zn 2 superoxide dismutase suggests
16647138	PrP	PrP	1.1	regulates Cu 2 /Zn Zn 2 superoxide dismutase suggests that PrP c is involved in redox balance
15210305	prion protein prp	prion protein prp	1.0	inflammatory rna profile of microglia has been recently described which contrasts with that of uninfected microglia exposed to inflammatory stimuli such as lipopolysaccharide and ifn gamma as well as prion protein prp amyloid [ 5 ].
15453089	prion protein prp	prion protein prp	1.0	the characteristic neuropathological signs of the disease are amyloid deposition of the proteinase resistant prion protein prp res or prp sc astrocytosis and spongiform degeneration.
16647138	prion protein prp	prion protein prp	1.0	neuronal loss gliosis and accumulation of abnormal extracellular _amp_#x3b2; helix rich prion protein prp sc characterize cjd.
16647138	prion protein prp	prion protein prp	1.0	this abnormal protein is an isoform of a normally occurring _amp_#x3b1; helix rich prion protein prp c whose function has not been clearly elucidated brown 1999 and prusiner 2001 .