PrP(Sc )accumulation in neuronal plasma membranes links Notch-1 activation to dendritic degeneration in prion diseases

por DeArmond, Stephen J, Bajsarowicz, Krystyna
Publicado 2010

Convection-Enhanced Delivery of AAV2-PrPshRNA in Prion-Infected Mice

por Ahn, Misol, Bajsarowicz, Krystyna, Oehler, Abby, Lemus, Azucena, Bankiewicz, Krystof, DeArmond, Stephen J.
Publicado 2014

Evidence That Bank Vole PrP Is a Universal Acceptor for Prions

por Watts, Joel C., Giles, Kurt, Patel, Smita, Oehler, Abby, DeArmond, Stephen J., Prusiner, Stanley B.
Publicado 2014

Continuous Quinacrine Treatment Results in the Formation of Drug-Resistant Prions

por Ghaemmaghami, Sina, Ahn, Misol, Lessard, Pierre, Giles, Kurt, Legname, Giuseppe, DeArmond, Stephen J., Prusiner, Stanley B.
Publicado 2009

Resistance of Bovine Spongiform Encephalopathy (BSE) Prions to Inactivation

por Giles, Kurt, Glidden, David V., Beckwith, Robyn, Seoanes, Rose, Peretz, David, DeArmond, Stephen J., Prusiner, Stanley B.
Publicado 2008

Conserved properties of human and bovine prion strains on transmission to guinea pigs

por Safar, Jiri G., Giles, Kurt, Lessard, Pierre, Letessier, Frederic, Patel, Smita, Serban, Ana, DeArmond, Stephen J., Prusiner, Stanley B.
Publicado 2011

Protease-Resistant Prions Selectively Decrease Shadoo Protein

por Watts, Joel C., Stöhr, Jan, Bhardwaj, Sumita, Wille, Holger, Oehler, Abby, DeArmond, Stephen J., Giles, Kurt, Prusiner, Stanley B.
Publicado 2011

Pharmacokinetics of Quinacrine Efflux from Mouse Brain via the P-glycoprotein Efflux Transporter

por Ahn, Misol, Ghaemmaghami, Sina, Huang, Yong, Phuan, Puay-Wah, May, Barnaby C. H., Giles, Kurt, DeArmond, Stephen J., Prusiner, Stanley B.
Publicado 2012

Levels of the Mahogunin Ring Finger 1 E3 Ubiquitin Ligase Do Not Influence Prion Disease

por Silvius, Derek, Pitstick, Rose, Ahn, Misol, Meishery, Delisha, Oehler, Abby, Barsh, Gregory S., DeArmond, Stephen J., Carlson, George A., Gunn, Teresa M.
Publicado 2013

Asymptomatic deer excrete infectious prions in feces

por Tamgüney, Gültekin, Miller, Michael W., Wolfe, Lisa L., Sirochman, Tracey M., Glidden, David V., Palmer, Christina, Lemus, Azucena, DeArmond, Stephen J., Prusiner, Stanley B.
Publicado 2009

The Prion Disease Database: a comprehensive transcriptome resource for systems biology research in prion diseases

por Gehlenborg, Nils, Hwang, Daehee, Lee, Inyoul Y., Yoo, Hyuntae, Baxter, David, Petritis, Brianne, Pitstick, Rose, Marzolf, Bruz, DeArmond, Stephen J., Carlson, George A., Hood, Leroy
Publicado 2009

Intracerebral Infusion of Antisense Oligonucleotides Into Prion-infected Mice

por Nazor Friberg, Karah, Hung, Gene, Wancewicz, Ed, Giles, Kurt, Black, Chris, Freier, Sue, Bennett, Frank, DeArmond, Stephen J, Freyman, Yevgeniy, Lessard, Pierre, Ghaemmaghami, Sina, Prusiner, Stanley B
Publicado 2012

Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases

por Kim, Mee-Ohk, Cali, Ignazio, Oehler, Abby, Fong, Jamie C, Wong, Katherine, See, Tricia, Katz, Jonathan S, Gambetti, Pierluigi, Bettcher, Brianne M, DeArmond, Stephen J, Geschwind, Michael D
Publicado 2013

Trafficking of prion proteins through a caveolae-mediated endosomal pathway

por Peters, Peter J., Mironov, Alexander, Peretz, David, van Donselaar, Elly, Leclerc, Estelle, Erpel, Susanne, DeArmond, Stephen J., Burton, Dennis R., Williamson, R. Anthony, Vey, Martin, Prusiner, Stanley B.
Publicado 2003

Protease-Sensitive Synthetic Prions

por Colby, David W., Wain, Rachel, Baskakov, Ilia V., Legname, Giuseppe, Palmer, Christina G., Nguyen, Hoang-Oanh B., Lemus, Azucena, Cohen, Fred E., DeArmond, Stephen J., Prusiner, Stanley B.
Publicado 2010

Default Mode Network quantitative diffusion and resting‐state functional magnetic resonance imaging correlates in sporadic Creutzfeldt‐Jakob disease

por Paoletti, Matteo, Caverzasi, Eduardo, Mandelli, Maria Luisa, Brown, Jesse A., Henry, Roland G., Miller, Bruce L., Rosen, Howard J., DeArmond, Stephen J., Bastianello, Stefano, Seeley, William W., Geschwind, Michael D.
Publicado 2022

White matter involvement in sporadic Creutzfeldt-Jakob disease

por Caverzasi, Eduardo, Mandelli, Maria Luisa, DeArmond, Stephen J., Hess, Christopher P., Vitali, Paolo, Papinutto, Nico, Oehler, Abby, Miller, Bruce L., Lobach, Irina V., Bastianello, Stefano, Geschwind, Michael D., Henry, Roland G.
Publicado 2014

A systems approach to prion disease

por Hwang, Daehee, Lee, Inyoul Y, Yoo, Hyuntae, Gehlenborg, Nils, Cho, Ji-Hoon, Petritis, Brianne, Baxter, David, Pitstick, Rose, Young, Rebecca, Spicer, Doug, Price, Nathan D, Hohmann, John G, DeArmond, Stephen J, Carlson, George A, Hood, Leroy E
Publicado 2009

Down-Regulation of Shadoo in Prion Infections Traces a Pre-Clinical Event Inversely Related to PrP(Sc) Accumulation

por Westaway, David, Genovesi, Sacha, Daude, Nathalie, Brown, Rebecca, Lau, Agnes, Lee, Inyoul, Mays, Charles E., Coomaraswamy, Janaky, Canine, Brenda, Pitstick, Rose, Herbst, Allen, Yang, Jing, Ko, Kerry W. S., Schmitt-Ulms, Gerold, DeArmond, Stephen J., McKenzie, Debbie, Hood, Leroy, Carlson, George A.
Publicado 2011