Transmission studies of chronic wasting disease to transgenic mice overexpressing human prion protein using the RT-QuIC assay by Brent Race, Katie Williams, Bruce Chesebro

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Prion-associated cerebral amyloid angiopathy is not exacerbated by human phosphorylated tau aggregates in scrapie-infected mice expressing anchorless prion protein by Brent Race, Katie Williams, James F. Striebel, Bruce Chesebro

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Inactivation of chronic wasting disease prions using sodium hypochlorite. by Katie Williams, Andrew G Hughson, Bruce Chesebro, Brent Race

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Toll-like receptor 2 confers partial neuroprotection during prion disease. by James A Carroll, Brent Race, Katie Williams, Bruce Chesebro

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RNA-seq and network analysis reveal unique glial gene expression signatures during prion infection by James A. Carroll, Brent Race, Katie Williams, James Striebel, Bruce Chesebro

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Innate immune responses after stimulation with Toll-like receptor agonists in ex vivo microglial cultures and an in vivo model using mice with reduced microglia by James A. Carroll, Brent Race, Katie Williams, James F. Striebel, Bruce Chesebro

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CD11c is not required by microglia to convey neuroprotection after prion infection. by James A Carroll, James F Striebel, Chase Baune, Bruce Chesebro, Brent Race

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CD11c is not required by microglia to convey neuroprotection after prion infection by James A. Carroll, James F. Striebel, Chase Baune, Bruce Chesebro, Brent Race

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Detection of prion infectivity in fat tissues of scrapie-infected mice. by Brent Race, Kimberly Meade-White, Michael B A Oldstone, Richard Race, Bruce Chesebro

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Microglia are not required for prion-induced retinal photoreceptor degeneration by James F. Striebel, Brent Race, Katie Williams, James A. Carroll, Mikael Klingeborn, Bruce Chesebro

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Strain specific resistance to murine scrapie associated with a naturally occurring human prion protein polymorphism at residue 171. by James F Striebel, Brent Race, Kimberly D Meade-White, Rachel LaCasse, Bruce Chesebro

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Second passage experiments of chronic wasting disease in transgenic mice overexpressing human prion protein by Brent Race, Chase Baune, Katie Williams, James F. Striebel, Andrew G. Hughson, Bruce Chesebro

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Early Generation of New PrPSc on Blood Vessels after Brain Microinjection of Scrapie in Mice by Bruce Chesebro, James Striebel, Alejandra Rangel, Katie Phillips, Andrew Hughson, Byron Caughey, Brent Race

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Reduced SOD2 expression does not influence prion disease course or pathology in mice by Simote T. Foliaki, Brent Race, Katie Williams, Chase Baune, Bradley R. Groveman, Cathryn L. Haigh

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Chronic Wasting Disease Agents in Nonhuman Primates by Brent Race, Kimberly D. Meade-White, Katie Phillips, James Striebel, Richard Race, Bruce Chesebro

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Neural cell engraftment therapy for sporadic Creutzfeldt-Jakob disease restores neuroelectrophysiological parameters in a cerebral organoid model by Katie Williams, Simote T. Foliaki, Brent Race, Anna Smith, Tina Thomas, Bradley R. Groveman, Cathryn L. Haigh

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Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein by Brent Race, Katie Williams, Andrew G. Hughson, Casper Jansen, Piero Parchi, Annemieke J. M. Rozemuller, Bruce Chesebro

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Efficacy of Wex-cide 128 disinfectant against multiple prion strains. by Chase Baune, Bradley R Groveman, Andrew G Hughson, Tina Thomas, Barry Twardoski, Suzette Priola, Bruce Chesebro, Brent Race

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The PINK1/Parkin pathway of mitophagy exerts a protective effect during prion disease. by Anne Ward, Forrest Jessop, Robert Faris, Jason Hollister, Daniel Shoup, Brent Race, Catharine M Bosio, Suzette A Priola

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Efficacy of Wex-cide 128 disinfectant against multiple prion strains by Chase Baune, Bradley R. Groveman, Andrew G. Hughson, Tina Thomas, Barry Twardoski, Suzette Priola, Bruce Chesebro, Brent Race

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