The following pages link to Molecular neurology of prion disease (Q35488760):
Displaying 50 items.
- Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey (Q24606150) (← links)
- Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice (Q24651920) (← links)
- Rapid folding of the prion protein captured by pressure-jump (Q28236967) (← links)
- Neuroserpin binds Abeta and is a neuroprotective component of amyloid plaques in Alzheimer disease (Q28252760) (← links)
- Isolation of proteinase K-sensitive prions using pronase E and phosphotungstic acid (Q28744075) (← links)
- Physical, chemical and kinetic factors affecting prion infectivity (Q28830528) (← links)
- Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP (Q28943533) (← links)
- Identification of a gene regulatory network associated with prion replication (Q30458186) (← links)
- Nosocomial transmission of sporadic Creutzfeldt-Jakob disease: results from a risk-based assessment of surgical interventions (Q30477510) (← links)
- Aptamers against prion proteins and prions. (Q30860694) (← links)
- From high-throughput cell culture screening to mouse model: identification of new inhibitor classes against prion disease (Q31023317) (← links)
- Scrapie infectivity is quickly cleared in tissues of orally-infected farmed fish (Q33246844) (← links)
- Directed evolution of an anti-prion protein scFv fragment to an affinity of 1 pM and its structural interpretation (Q33256919) (← links)
- Repetitive immunization enhances the susceptibility of mice to peripherally administered prions (Q33506629) (← links)
- The Retinoic Acid Receptor Beta (Rarb) Region of Mmu14 Is Associated with Prion Disease Incubation Time in Mouse (Q33769410) (← links)
- Manganese upregulates cellular prion protein and contributes to altered stabilization and proteolysis: relevance to role of metals in pathogenesis of prion disease (Q33856313) (← links)
- Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins (Q33910752) (← links)
- Kuru in the 21st century--an acquired human prion disease with very long incubation periods (Q33997105) (← links)
- Variant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion protein (Q34153667) (← links)
- Population screening for variant Creutzfeldt-Jakob disease using a novel blood test: diagnostic accuracy and feasibility study (Q34153674) (← links)
- Pharmacological chaperone for the structured domain of human prion protein. (Q34199756) (← links)
- Searching for reliable premortem protein biomarkers for prion diseases: progress and challenges to date (Q34342895) (← links)
- Molecular pathology of human prion disease (Q34462913) (← links)
- Review: contribution of transgenic models to understanding human prion disease. (Q34474868) (← links)
- A naturally occurring variant of the human prion protein completely prevents prion disease. (Q34480161) (← links)
- Sod1 deficiency reduces incubation time in mouse models of prion disease (Q34563121) (← links)
- Immunomodulation for prion and prion-related diseases (Q34565644) (← links)
- Assessing proteinase K resistance of fish prion proteins in a scrapie-infected mouse neuroblastoma cell line (Q34580839) (← links)
- Solid-State NMR Studies of Amyloid Fibril Structure (Q35327629) (← links)
- MRI detection of prion protein plaques in variant Creutzfeldt-Jakob disease. (Q35400644) (← links)
- Infectious prion protein alters manganese transport and neurotoxicity in a cell culture model of prion disease (Q35499246) (← links)
- Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS. (Q35681248) (← links)
- Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice (Q36187263) (← links)
- Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene (Q36226900) (← links)
- Prion Type-Dependent Deposition of PRNP Allelic Products in Heterozygous Sheep (Q36434304) (← links)
- Protective V127 prion variant prevents prion disease by interrupting the formation of dimer and fibril from molecular dynamics simulations (Q36610875) (← links)
- Mad fly disease. (Q36726496) (← links)
- Insights into prion strains and neurotoxicity (Q36856446) (← links)
- Low activity of complement in the cerebrospinal fluid of the patients with various prion diseases (Q36860739) (← links)
- Cerebrospinal fluid markers in Creutzfeldt-Jakob disease (Q36865663) (← links)
- Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series (Q36944491) (← links)
- Review. The origin of the prion agent of kuru: molecular and biological strain typing. (Q36968647) (← links)
- Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease. (Q36968659) (← links)
- Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysin. (Q36976135) (← links)
- Discovery and Preliminary SAR of Arylpiperazines as Novel, Brainpenetrant Antiprion Compounds (Q36991608) (← links)
- Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study (Q37097991) (← links)
- Detection of proteinase K resistant proteins in the urine of patients with Creutzfeldt-Jakob and other neurodegenerative diseases (Q37135774) (← links)
- Spontaneous generation of infectious prion disease in transgenic mice (Q37343768) (← links)
- Molecular pathology of human prion diseases (Q37462236) (← links)
- Surgery and risk of sporadic Creutzfeldt-Jakob disease in Denmark and Sweden: registry-based case-control studies. (Q37466846) (← links)