1. Aberrance of GAP43/p-GAP43 Closely Associates with the Pathology of Neuron Loss in Prion-Infected Rodent Models
    Xiao-Xi Jia et al, 2024, Molecular Neurobiology CrossRef
  2. Comparative Analysis of Gene Expression Profiles Between Cortex and Thalamus in Chinese Fatal Familial Insomnia Patients
    Chan Tian et al, 2013, Molecular Neurobiology CrossRef
  3. The effect of PrP Sc accumulation on inflammatory gene expression within sheep peripheral lymphoid tissue
    Anton G. Gossner et al, 2015, Veterinary Microbiology CrossRef
  4. Genotype by environment interactions for chronic wasting disease in farmed US white-tailed deer
    Christopher M Seabury et al, 2022, G3 Genes|Genomes|Genetics CrossRef
  5. Global Protein Differential Expression Profiling of Cerebrospinal Fluid Samples Pooled from Chinese Sporadic CJD and non-CJD Patients
    Cao Chen et al, 2014, Molecular Neurobiology CrossRef
  6. Transcriptome analysis of CNS immediately before and after the detection of PrPSc in SSBP/1 sheep scrapie
    Anton G. Gossner et al, 2014, Veterinary Microbiology CrossRef
  7. Activation of the AMPK-ULK1 pathway plays an important role in autophagy during prion infection
    Xue-Yu Fan et al, 2015, Scientific Reports CrossRef
  8. MicroRNA Alterations in a Tg501 Mouse Model of Prion Disease
    Janne M. Toivonen et al, 2020, Biomolecules CrossRef
  9. Proteomics Analyses for the Global Proteins in the Brain Tissues of Different Human Prion Diseases*
    Qi Shi et al, 2015, Molecular & Cellular Proteomics CrossRef
  10. Proteomic Analyses for the Global S-Nitrosylated Proteins in the Brain Tissues of Different Human Prion Diseases
    Li-Na Chen et al, 2016, Molecular Neurobiology CrossRef
  11. Apparent Reduction of ADAM10 in Scrapie-Infected Cultured Cells and in the Brains of Scrapie-Infected Rodents
    Cao Chen et al, 2014, Molecular Neurobiology CrossRef
  12. Analyses of the Similarity and Difference of Global Gene Expression Profiles in Cortex Regions of Three Neurodegenerative Diseases: Sporadic Creutzfeldt-Jakob Disease (sCJD), Fatal Familial Insomnia (FFI), and Alzheimer’s Disease (AD)
    Chan Tian et al, 2014, Molecular Neurobiology CrossRef
  13. Case Report: Genetic Creutzfeldt–Jakob Disease With a G114V Mutation and One Octapeptide Repeat Deletion as a Mimic of Frontotemporal Dementia
    Xue Lin et al, 2022, Frontiers in Neurology CrossRef