Enfermidades por Prións
Heinrich Heine University Düsseldorf
Düsseldorf, AlemaniaPublicacións en colaboración con investigadores/as de Heinrich Heine University Düsseldorf (8)
2019
-
Development of a new largely scalable in vitro prion propagation method for the production of infectious recombinant prions for high resolution structural studies
PLoS Pathogens, Vol. 15, Núm. 10
-
Proteomic studies reveal disrupted in schizophrenia 1 as a player in both neurodevelopment and synaptic function
International Journal of Molecular Sciences, Vol. 20, Núm. 1
2014
-
Loss of Prion Protein Leads to Age-Dependent Behavioral Abnormalities and Changes in Cytoskeletal Protein Expression
Molecular Neurobiology, Vol. 50, Núm. 3, pp. 923-936
2012
-
Human and rat brain lipofuscin proteome
Proteomics, Vol. 12, Núm. 15-16, pp. 2445-2454
-
Proteomic, genomic and translational approaches identify CRMP1 for a role in schizophrenia and its underlying traits
Human Molecular Genetics, Vol. 21, Núm. 20, pp. 4406-4418
2009
-
Oligomer assembly of the C-terminal DISC1 domain (640-854) is controlled by self-association motifs and disease-associated polymorphism S704C
Biochemistry, Vol. 48, Núm. 32, pp. 7746-7755
2008
-
Insolubility of disrupted-in-schizophrenia 1 disrupts oligomer-dependent interactions with nuclear distribution element 1 and is associated with sporadic mental disease
Journal of Neuroscience, Vol. 28, Núm. 15, pp. 3839-3845