000 01327 a2200361 4500
005 20250516062005.0
264 0 _c20120221
008 201202s 0 0 eng d
022 _a1083-351X
024 7 _a10.1074/jbc.M111.286195
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWestergard, Laura
245 0 0 _aA naturally occurring C-terminal fragment of the prion protein (PrP) delays disease and acts as a dominant-negative inhibitor of PrPSc formation.
_h[electronic resource]
260 _bThe Journal of biological chemistry
_cDec 2011
300 _a44234-44242 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural
650 0 4 _aAnimals
650 0 4 _aBrain
_xmetabolism
650 0 4 _aGenes, Dominant
650 0 4 _aGenotype
650 0 4 _aMice
650 0 4 _aMice, Transgenic
650 0 4 _aModels, Genetic
650 0 4 _aNeurodegenerative Diseases
_xgenetics
650 0 4 _aPrPSc Proteins
_xchemistry
650 0 4 _aProtein Structure, Tertiary
650 0 4 _aScrapie
_xgenetics
650 0 4 _aTime Factors
700 1 _aTurnbaugh, Jessie A
700 1 _aHarris, David A
773 0 _tThe Journal of biological chemistry
_gvol. 286
_gno. 51
_gp. 44234-44242
856 4 0 _uhttps://doi.org/10.1074/jbc.M111.286195
_zAvailable from publisher's website
999 _c21257032
_d21257032