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Journal of Neurochemistry|April 24, 2008
ATP-binding cassette transporter A7 regulates processing of amyloid precursor protein in vitroSharon L Chan, Woojin Scott Kim, John B Kwok, et al.Journal of Inorganic Biochemistry|April 1, 2006
Gender and genetic background effects on brain metal levels in APP transgenic and normal mice: implications for Alzheimer beta-amyloid pathologyChrista J Maynard, Roberto Cappai, Irene Volitakis, et al.Journal of Neuropathology and Experimental Neurology|October 18, 2011
Gene knockout of tau expression does not contribute to the pathogenesis of prion diseaseVictoria A Lawson, Helen M Klemm, Jeremy M Welton, et al.Advances in Neurobiology|July 5, 2017
Prion DiseasesBenjamin C Whitechurch, Jeremy M Welton, Steven J Collins, et al.Therapeutic Delivery|May 8, 2013
Immunotherapeutic approaches in prion disease: progress, challenges and potential directionsMarcus W Brazier, Alexandra I Mot, Anthony R White, et al.Journal of Neurochemistry|April 29, 2005
Prion protein glycosylationVictoria A Lawson, Steven J Collins, Colin L Masters, et al.Free Radical Biology & Medicine|May 6, 2008
A manganese-superoxide dismutase/catalase mimetic extends survival in a mouse model of human prion diseaseMarcus W Brazier, Susan R Doctrow, Colin L Masters, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 4, 2004
Retinoid-modulated MAT1 ubiquitination and CAK activityQiaojun He, Hui Peng, Steven J Collins, et al.Biochemistry|January 9, 2008
Formation of a high affinity lipid-binding intermediate during the early aggregation phase of alpha-synucleinDavid P Smith, Deborah J Tew, Andrew F Hill, et al.Brain Research|January 11, 2011
The neuroprotective domains of the amyloid precursor protein, in traumatic brain injury, are located in the two growth factor domainsFrances Corrigan, Chi L L Pham, Robert Vink, et al.Pageof 27