Disease: Spongiform encephalopathy
- A Protein Misfolding Shaking Amplification-based method for the spontaneous generation of hundreds of bona fide prions
- A review of chronic wasting disease (CWD) spread, surveillance, and control in the United States captive cervid industry
- A53T α-synuclein mutation increases susceptibility to postoperative delayed neurocognitive recovery via hippocampal Ang-(1-7)/MasR axis
- Aberrant Enhanced NLRP3 Inflammasomes and Cell Pyroptosis in the Brains of Prion-Infected Rodent Models Are Largely Associated with the Proliferative Astrocytes
- Absence of evidence of transfusion transmission risk of Creutzfeldt-Jakob disease in the United States: Results froma 28-year lookback study
- alphanti-prion effects of anthocyanins
- Amyloid antibody therapy for early-stage Alzheimer's disease: a critical review of three recent trials
- Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease
- Antineoplastics for treating Alzheimer's disease and dementia: Evidence from preclinical and observational studies
- Assessment of the zoonotic potential of atypical scrapie prions in humanized mice reveals rare phenotypic convergence but not identity with sporadic CJD prions
- Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and <em>MAPT</em> Sub-haplotypes
- B7-H3 Expression in Breast Cancer and Brain Metastasis
- Bacterial, Viral, and Prion Infectious Diseases of the Brain
- Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophy
- Biophysical insight into anti-amyloidogenic nature of novel ionic Co(II)(phen)(H<sub>2</sub>O)<sub>4</sub>]<sup>+</sup>[glycinate]<sup>-</sup> chemotherapeutic drug candidate against human lysozyme aggregati
- Characterizing Prion-Like Protein Aggregation: Emerging Nanopore-Based Approaches
- Chronic Wasting Disease: State of the Science
- Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules
- Clinical characteristics and diagnostics of human spongiform encephalopathies: an update
- Colonoscopy and Subsequent Risk of Parkinson's Disease
- Combined approaches, including long-read sequencing, address the diagnostic challenge of HYDIN in primary ciliary dyskinesia
- Conclusive demonstration of iatrogenic Alzheimer's disease transmission in a model of stem cell transplantation
- Creutzfeldt-Jakob Disease and other prion diseases
- Cryo-EM Structures Reveal Tau Filaments from Down Syndrome Adopt Alzheimer's Disease Fold
- Curcumin as a natural potential drug candidate against important zoonotic viruses and prions: A narrative review
- Current potential pathogenic mechanisms of copper-zinc superoxide dismutase 1 (SOD1) in amyotrophic lateral sclerosis
- Detection and Characterization of Influenza A Virus Endemic Circulation in Suckling and Nursery Pigs Originating from Vaccinated Farms in the Same Production System
- Detection limitations of prion seeding activities in blood samples from patients with sporadic prion disease
- Detection of prions in matching post-mortem skin and cerebrospinal fluid samples using second-generation real-time quaking-induced conversion assay
- Development of statistical auto-segmentation method for diffusion restriction gray matter lesions in patients with newly diagnosed sporadic Creutzfeldt-Jakob disease
- Different reactive profiles of calmodulin in the CSF samples of Chinese patients of four types of genetic prion diseases
- Dysbiosis of the gut microbiota and its effect on alpha-synuclein and prion protein misfolding: consequences for neurodegeneration
- Emerging Evidence of Golgi Stress Signaling for Neuropathies
- Enhancing predictability of IDH mutation status in glioma patients at initial diagnosis: a comparative analysis of radiomics from MRI, [<sup>18</sup>F]FET PET, and TSPO PET
- Evaluation of the PrimeFlow RNA assay as a method of detection of SARS-CoV-2 single and dual Infections
- Expression of Toll-like receptors in the cerebellum during pathogenesis of prion disease
- Fatal Familial Insomnia With Significant Correlations Between Involuntary Movements and Postural Changes:Report of One Case
- Fatty acid-binding protein 5 is a functional biomarker and indicator of ferroptosis in cerebral hypoxia
- First report of a novel 108 bp deletion and five novel SNPs in PRNP gene of stray cats and in silico analysis of their possible relation with feline spongiform encephalopathy
- Foiling deadly prions
- Fractal Analysis in Neurodegenerative Diseases
- Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Sträussler-Scheinker disease
- Glymphatic inhibition exacerbates tau propagation in an Alzheimer's disease model
- Hereditary Creutzfeldt-Jakob Disease: A Case Presentation of a Rare Stroke Mimic
- Human immunodeficiency virus-associated dementia complex with positive 14-3-3 protein in cerebrospinal fluid: A case report
- Hyperacetylation mimetics within the tau filament core inhibits prion-like propagation of misfolded tau
- I<sup>123</sup>-FP-CIT (DaTSCAN) SPECT beyond the Most Common Causes of Parkinsonism: A Systematic Review
- Iatrogenic cerebral amyloid angiopathy in older adults
- Impairment of the glial phagolysosomal system drives prion-like propagation in a Drosophila model of Huntington's disease
- Industrialization possibilities of purified pig sperm hyaluronidase
- Infectious Diseases of the Brain and Spine: Parasitic and Other Atypical Transmissible Diseases
- Liquid-liquid phase separation of the prion protein is regulated by the octarepeat domain independently of histidines and copper
- MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study
- Measuring Antibody-Mediated Tau Fibril Uptake in Microglia by Flow Cytometry
- miR-519a-3p, found to regulate cellular prion protein during Alzheimer's disease pathogenesis, as a biomarker of asymptomatic stages
- Mutations in human prion-like domains: pathogenic but not always amyloidogenic
- N-Glycosylation as a Modulator of Protein Conformation and Assembly in Disease
- Neurodegenerative disease pathways are perturbed in patients with cancer who self-report cognitive changes and anxiety: A pathway impact analysis
- New implications for prion diseases therapy and prophylaxis
- New Light on Prions: Putative Role of PrP<sup>c</sup> in Pathophysiology of Mood Disorders
- Novel method for classification of prion diseases by detecting PrP(res) signal patterns from formalin-fixed paraffin-embedded samples
- Population structure and migration in the Eastern Highlands of Papua New Guinea, a region impacted by the kuru epidemic
- Precision proteoform design for 4R tau isoform selective templated aggregation
- Prion agents (1st section)
- Prion forensics: a multidisciplinary approach to investigate CWD at an illegal deer carcass disposal site
- Prion meeting 2023: implications of a growing field
- Prodromal Parkinson disease signs are predicted by a whole-blood inflammatory transcriptional signature in young Pink1<sup>-/-</sup> rats
- Progressive multifocal leukoencephalopathy associated with systemic lupus erythematosus: longitudinal observation of lymphocytes, JC virus in cerebrospinal fluid, and brain magnetic resonance imaging
- Progressive supranuclear palsy phenotype as an atypical clinical presentation of Creutzfeldt-Jakob disease: A case report and review of the literature
- Q&A with Zhentao Zhang
- Referral of a Patient With Ocular Symptoms to the Stroke Clinic: Not Always the Usual Suspect!
- RNA as a component of scrapie fibrils
- Robert Hertz, Anthropophagic Practices and Traditional South Fore Mortuary Rites in Papua New Guinea
- Roving Eye and Head in a Patient With Genetic Creutzfeldt-Jakob Disease
- RT-QuIC detection of chronic wasting disease prion in platelet samples of white-tailed deer
- Seeding Activity of Skin Misfolded Tau as a Biomarker for Tauopathies
- Seeding competent TDP-43 persists in human patient and mouse muscle
- Selective Vulnerability to Neurodegenerative Disease: Insights from Cell Type-Specific Translatome Studies
- Sensitive detection of pathological seeds of alpha-synuclein, tau and prion protein on solid surfaces
- Sleep disturbance in clinical and preclinical scrapie-infected sheep measured by polysomnography
- Slow to Respond: A Rapidly Progressive Case of Sporadic Creutzfeldt-Jakob Disease
- Spectral Fluorescence Pathology of Protein Misfolding Disorders
- Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10-year review of United Kingdom surveillance
- Synthesis of bioengineered heparin chemically and biologically similar to porcine-derived products and convertible to low MW heparin
- Targeting Neuroinflammation by Pharmacologic Downregulation of Inflammatory Pathways Is Neuroprotective in Protein Misfolding Disorders
- Temporal serum neurofilament light chain concentrations in sheep inoculated with the agent of classical scrapie
- Tetrahydrofolate levels influence 2-aminoacrylate stress in <em>Salmonella enterica</em>
- The 23rd Annual Meeting of the Rocky Mountain Virology Association
- The PINK1/Parkin pathway of mitophagy exerts a protective effect during prion disease
- The rapid progression of Creutzfeldt-Jakob disease with concomitant COVID-19 infection: a case report
- The structural line between prion and "prion-like": Insights from prion protein and tau
- Tryptophan residues in TDP-43 and SOD1 modulate the cross-seeding and toxicity of SOD1
- Two Waves of Specific B Cell Memory Immunoreconstruction Observed in Anti-HHV1-3 IgG Kinetics after Hematopoietic Stem Cell Transplantation
- Vaccination with structurally adapted fungal protein fibrils induces immunity to Parkinson's disease
- Variably protease-sensitive prionopathy with methionine homozygosity at codon 129 in the prion protein gene
- VCP/p97 mediates nuclear targeting of non-ER-imported prion protein to maintain proteostasis
- Viroids, Satellite RNAs and Prions: Folding of Nucleic Acids and Misfolding of Proteins
- What Are the Roles of Cellular Prion Protein in Normal and Pathologic Conditions?
- When prion disease Isn't suspected: prion disease as the cause of terminal decline in chronic mixed dementia
- α-Synuclein seed amplification technology for Parkinson's disease and related synucleinopathies