| The first report of genetic variations in the chicken prion protein gene |
40 |
| Genetic effects of PRNP gene insertion/deletion (indel) on phenotypic traits in sheep |
13 |
| Somatostatin in Alzheimer's disease: A new Role for an Old Player |
9 |
| Chronic wasting disease management in ranched elk using rectal biopsy testing |
7 |
| Influence of the geographic distribution of prion protein gene sequence variation on patterns of chronic wasting disease spread in white-tailed deer (Odocoileus virginianus) |
7 |
| The first report of polymorphisms and genetic characteristics of the prion protein gene (PRNP) in horses |
7 |
| The prion 2018 round tables (I): the structure of PrPSc |
7 |
| Spatial heterogeneity of prion gene polymorphisms in an area recently infected by chronic wasting disease |
6 |
| Amyloid properties of the yeast cell wall protein Toh1 and its interaction with prion proteins Rnq1 and Sup35 |
6 |
| Combining autophagy stimulators and cellulose ethers for therapy against prion disease |
6 |
| The Prion 2018 round tables (II): A beta, tau, alpha-synuclein ... are they prions, prion-like proteins, or what? |
6 |
| A simple in vitro assay for assessing the efficacy, mechanisms and kinetics of anti-prion fibril compounds |
5 |
| Overexpression of a conserved HSP40 chaperone reduces toxicity of several neurodegenerative disease proteins |
5 |
| Nucleotide variants in prion-related protein (testis-specific) gene (PRNT) and effects on Chinese and Mongolian sheep phenotypes |
5 |
| Behind the potential evolution towards prion resistant species |
4 |
| Clinicopathological findings of an MM2-cortical-type sporadic Creutzfeldt-Jakob disease patient with cortical blindness during a course of glaucoma and age-related macular degeneration |
4 |
| A standard model of Alzheimer's disease? |
4 |
| The role of the prion protein in the internalization of alpha-synuclein amyloids |
4 |
| Pathological progression of genetic Creutzfeldt-Jakob disease with a PrP V180I mutation |
4 |
| Prion-based nanomaterials and their emerging applications |
3 |
| Curing of [PSI+] by Hsp104 Overexpression: Clues to solving the puzzle |
3 |
| In vitro generation of tau aggregates conformationally distinct from parent tau seeds of Alzheimer's brain |
3 |
| Enrichment of miR-126 enhances the effects of endothelial progenitor cell-derived microvesicles on modulating MC3T3-E1 cell function via Erk1/2-Bcl-2 signalling pathway |
3 |
| Role of Prion protein-EGFR multimolecular complex during neuronal differentiation of human dental pulp-derived stem cells |
3 |
| Effects of peptidyl-prolyl isomerase 1 depletion in animal models of prion diseases |
2 |
| THERPA: A small molecule database related to prion protein regulation and prion diseases progression |
2 |
| The same but different: the role of Hsp70 in heat shock response and prion propagation |
2 |
| Yeast-based screening of natural product extracts results in the identification of prion inhibitors from a marine sponge |
2 |
| A case of V180I genetic Creutzfeldt-Jakob disease presenting with conspicuous facial mimicry |
2 |
| Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia |
2 |
| Use of faecal volatile organic compound analysis for ante-mortem discrimination between CWD-positive, -negative exposed, and -known negative white-tailed deer (Odocoileus virginianus) |
2 |
| Design, implementation, and interpretation of amplification studies for prion detection |
2 |
| Impaired transport of intrinsically disordered proteins through the Sec61 and SecY translocon; implications for prion diseases |
1 |
| The associations of two SNPs in miRNA-146a and one SNP in ZBTB38-RASA2 with the disease susceptibility and the clinical features of the Chinese patients of sCJD and FFI |
1 |
| Combined findings of FDG-PET and arterial spin labeling in sporadic Creutzfeldt-Jakob disease |
1 |
| Thermodynamic characterization for the denatured state of bovine prion protein and the BSE Associated variant E211K |
1 |
| Sensitivity and specificity evaluation of multiple neurodegenerative proteins for Creutzfeldt-Jakob disease diagnosis using a deep-learning approach |
1 |
| Decrease of RyR2 in the prion infected cell line and in the brains of the scrapie infected mice models and the patients of human prion diseases |
1 |
| Unexpected prion phenotypes in experimentally transfused animals: predictive models for humans? |
1 |
| Microbial specialization by prions |
1 |
| A Chinese patient of P102L Gerstmann-Straussler-Scheinker disease contains three other disease-associated mutations in SYNE1 |
1 |
| 14-3-3 and enolase abundances in the CSF of Prion diseased rats |
1 |
| Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report |
1 |
| An autopsied case of MM1-type sporadic Creutzfeldt-Jakob disease with pathology of Wernicke encephalopathy |
1 |
| Axonal changes in experimental prion diseases recapitulate those following constriction of postganglionic branches of the superior cervical ganglion: a comparison 40 years later |
1 |
| Sodium hydroxide treatment effectively inhibits PrPCWD replication in farm soil |
1 |
| Case Report: A patient with spinocerebellar ataxia type 31 and sporadic Creutzfeldt-Jakob disease |
0 |
| The worst is yet to come: probable sporadic Creutzfeldt-Jakob disease in a well-controlled HIV patient |
0 |
| Altered gene transcription linked to astrocytes and oligodendrocytes in frontal cortex in Creutzfeldt-Jakob disease |
0 |
| Poly-L-histidine inhibits prion propagation in a prion-infected cell line |
0 |
