Distinct translatome changes in specific neural populations precede electroencephalographic changes in prion-infected mice von Kaczmarczyk, Lech, Schleif, Melvin, Dittrich, Lars, Williams, Rhiannan H, Koderman, Marusa, Bansal, Vikas, Rajput, Ashish, Schulte, Theresa, Jonson, Maria, Krost, Clemens, Testaquadra, Fabio J, Bonn, Stefan, Jackson, Walker S

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Selective vulnerability to neurodegenerative disease: the curious case of Prion Protein von Jackson, Walker S

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Etiology matters: genetic and acquired prion diseases engage different mechanisms at a presymptomatic stage von Jackson, Walker

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The brain interactome of a permissive prion replication substrate von Arshad, Hamza, Eid, Shehab, Mehra, Surabhi, Williams, Declan, Kaczmarczyk, Lech, Stuart, Erica, Jackson, Walker S., Schmitt-Ulms, Gerold, Watts, Joel C.

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Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice von Xie, Kan, Ryan, Devon P., Pearson, Brandon L., Henzel, Kristin S., Neff, Frauke, Vidal, Ramon O., Hennion, Magali, Lehmann, Isabelle, Schleif, Melvin, Schröder, Susanne, Adler, Thure, Rathkolb, Birgit, Rozman, Jan, Schütz, Anna-Lena, Prehn, Cornelia, Mickael, Michel E., Weiergräber, Marco, Adamski, Jerzy, Busch, Dirk H., Ehninger, Gerhard, Matynia, Anna, Jackson, Walker S., Wolf, Eckhard, Fuchs, Helmut, Gailus-Durner, Valerie, Bonn, Stefan, de Angelis, Martin Hrabě, Ehninger, Dan

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Memory trace interference impairs recall in a mouse model of Alzheimer’s disease von Poll, Stefanie, Mittag, Manuel, Musacchio, Fabrizio, Justus, Lena C., Giovannetti, Eleonora Ambrad, Steffen, Julia, Wagner, Jens, Zohren, Lioba, Schoch, Susanne, Schmidt, Boris, Jackson, Walker S., Ehninger, Dan, Fuhrmann, Martin

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Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease von Walsh, Daniel J, Rees, Judy R, Mehra, Surabhi, Bourkas, Matthew E C, Kaczmarczyk, Lech, Stuart, Erica, Jackson, Walker S, Watts, Joel C, Supattapone, Surachai

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Manipulating the Prion Protein Gene Sequence and Expression Levels with CRISPR/Cas9 von Kaczmarczyk, Lech, Mende, Ylva, Zevnik, Branko, Jackson, Walker S

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The natural Disc1-deletion present in several inbred mouse strains does not affect sleep von Dittrich, Lars, Petese, Alessandro, Jackson, Walker S.

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Slc1a3-2A-CreERT2 mice reveal unique features of Bergmann glia and augment a growing collection of Cre drivers and effectors in the 129S4 genetic background von Kaczmarczyk, Lech, Reichenbach, Nicole, Blank, Nelli, Jonson, Maria, Dittrich, Lars, Petzold, Gabor C., Jackson, Walker S.

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Intraflagellar transport is essential for endochondral bone formation von Haycraft, Courtney J, Zhang, Qihong, Song, Buer, Jackson, Walker S, Detloff, Peter J, Serra, Rosa, Yoder, Bradley K

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Selective Vulnerability to Neurodegenerative Disease: Insights from Cell Type-Specific Translatome Studies von Jackson, Walker S, Bauer, Susanne, Kaczmarczyk, Lech, Magadi, Srivathsa S

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CalDAG-GEFI mediates striatal cholinergic modulation of dendritic excitability, synaptic plasticity and psychomotor behaviors von Crittenden, Jill R., Zhai, Shenyu, Sauvage, Magdalena, Kitsukawa, Takashi, Burguière, Eric, Thomsen, Morgane, Zhang, Hui, Costa, Cinzia, Martella, Giuseppina, Ghiglieri, Veronica, Picconi, Barbara, Pescatore, Karen A., Unterwald, Ellen M., Jackson, Walker S., Housman, David E., Caine, S. Barak, Sulzer, David, Calabresi, Paolo, Smith, Anne C., Surmeier, D. James, Graybiel, Ann M.

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Cerebellar granule neurons induce Cyclin D1 before the onset of motor symptoms in Huntington's disease mice von Bauer, Susanne, Chen, Chwen-Yu, Jonson, Maria, Kaczmarczyk, Lech, Magadi, Srivathsa Subramanya, Jackson, Walker S

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Structural and mechanistic aspects influencing the ADAM10-mediated shedding of the prion protein von Linsenmeier, Luise, Mohammadi, Behnam, Wetzel, Sebastian, Puig, Berta, Jackson, Walker S, Hartmann, Alexander, Uchiyama, Keiji, Sakaguchi, Suehiro, Endres, Kristina, Tatzelt, Jörg, Saftig, Paul, Glatzel, Markus, Altmeppen, Hermann C

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Spontaneous Generation of Prion Infectivity in Fatal Familial Insomnia Knockin Mice von Jackson, Walker S., Borkowski, Andrew W., Faas, Henryk, Steele, Andrew D., King, Oliver D., Watson, Nicki, Jasanoff, Alan, Lindquist, Susan

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power of automated high-resolution behavior analysis revealed by its application to mouse models of Huntington's and prion diseases von Steele, Andrew D, Jackson, Walker S, King, Oliver D, Lindquist, Susan

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Peculiarities of prion diseases von Jackson, Walker S, Krost, Clemens

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Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases von Jackson, Walker S., Borkowski, Andrew W., Watson, Nicki E., King, Oliver D., Faas, Henryk, Jasanoff, Alan, Lindquist, Susan

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Requirements for Mutant and Wild-Type Prion Protein Misfolding In Vitro von Noble, Geoffrey P, Walsh, Daniel J, Miller, Michael B, Jackson, Walker S, Supattapone, Surachai

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