| scholarly article | Q13442814 |
| P2093 | author name string | Claudio Soto | |
| Rodrigo Morales | |||
| Baian Chen | |||
| P2860 | cites work | Generating a prion with bacterially expressed recombinant prion protein | Q24626352 |
| Prions | Q24633319 | ||
| Prion diseases of humans and animals: their causes and molecular basis | Q28209943 | ||
| Eight prion strains have PrP(Sc) molecules with different conformations | Q29617277 | ||
| Characteristics of 263K scrapie agent in multiple hamster species | Q33405664 | ||
| Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors | Q33630935 | ||
| Estimating prion concentration in fluids and tissues by quantitative PMCA. | Q33725459 | ||
| Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding | Q34084209 | ||
| Blood infectivity and the prospects for a diagnostic screening test in Creutzfeldt-Jakob disease | Q34125915 | ||
| The controversial protein-only hypothesis of prion propagation. | Q34335604 | ||
| Small protease sensitive oligomers of PrPSc in distinct human prions determine conversion rate of PrP(C). | Q34372311 | ||
| In vitro generation of infectious scrapie prions. | Q34413661 | ||
| Detection of prions in blood | Q34446509 | ||
| Generation of a new form of human PrP(Sc) in vitro by interspecies transmission from cervid prions | Q34606377 | ||
| Chronic subclinical prion disease induced by low-dose inoculum | Q34970496 | ||
| Initial fate of prions upon peripheral infection: half-life, distribution, clearance, and tissue uptake | Q35105375 | ||
| The nasal cavity is a route for prion infection in hamsters | Q35857428 | ||
| Diagnosing prion diseases: needs, challenges and hopes | Q35892062 | ||
| A quantitative, highly sensitive cell-based infectivity assay for mouse scrapie prions | Q36161465 | ||
| Pathogenesis and prevalence of variant Creutzfeldt-Jakob disease | Q36346109 | ||
| Prions and their lethal journey to the brain | Q36389302 | ||
| Protein misfolding cyclic amplification for diagnosis and prion propagation studies | Q36626077 | ||
| Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysin. | Q36976135 | ||
| Reduction of prion infectivity in packed red blood cells. | Q37022481 | ||
| Characteristics of a Short Incubation Model of Scrapie in the Golden Hamster | Q41230248 | ||
| Detection of infectious prions in urine | Q41371006 | ||
| Scrapie-Infected Spleens: Analysis of Infectivity, Scrapie-Associated Fibrils, and Protease-Resistant Proteins | Q41876639 | ||
| Transport of prion protein across the blood-brain barrier | Q41979008 | ||
| Studies on prion replication in spleen | Q43088956 | ||
| PrP(Sc) of scrapie 263K propagates efficiently in spleen and muscle tissues with protein misfolding cyclic amplification | Q43843183 | ||
| Transmission of BSE by blood transfusion in sheep | Q45186151 | ||
| Passage of murine scrapie prion protein across the mouse vascular blood-brain barrier | Q47693977 | ||
| Ultra-efficient replication of infectious prions by automated protein misfolding cyclic amplification. | Q47843274 | ||
| Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein | Q48099698 | ||
| Isolation and characterization of a proteinase K-sensitive PrPSc fraction. | Q48334584 | ||
| Pathogenesis of scrapie (strain 263K) in hamsters infected intracerebrally, intraperitoneally or intraocularly | Q48382521 | ||
| The distribution of infectivity in blood components and plasma derivatives in experimental models of transmissible spongiform encephalopathy | Q48395317 | ||
| Presymptomatic detection of prions in blood. | Q48477099 | ||
| Pre-symptomatic detection of prions by cyclic amplification of protein misfolding. | Q49113318 | ||
| Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion. | Q51037857 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | prion protein family | Q24724413 |
| P304 | page(s) | 795-800 | |
| P577 | publication date | 2014-02-01 | |
| P1433 | published in | FEBS Letters | Q1388051 |
| P1476 | title | Peripherally administrated prions reach the brain at sub-infectious quantities in experimental hamsters | |
| P478 | volume | 588 |
| Q64057223 | Combinatory FK506 and Minocycline Treatment Alleviates Prion-Induced Neurodegenerative Events via Caspase-Mediated MAPK-NRF2 Pathway |
| Q54113689 | Could Alzheimer's Disease Originate in the Periphery and If So How So? |
| Q33628006 | Downregulation of the Repressor Element 1-Silencing Transcription Factor (REST) Is Associated with Akt-mTOR and Wnt-β-Catenin Signaling in Prion Diseases Models. |
| Q40373414 | Early Minocycline and Late FK506 Treatment Improves Survival and Alleviates Neuroinflammation, Neurodegeneration, and Behavioral Deficits in Prion-Infected Hamsters |
| Q42202620 | Multiple factors contribute to the peripheral induction of cerebral β-amyloidosis. |
| Q40738433 | Pathogenic microbes, the microbiome, and Alzheimer's disease (AD). |
| Q37596801 | Prion disease: experimental models and reality |
| Q60049338 | Prion pathogenesis is unaltered in a mouse strain with a permeable blood-brain barrier |
| Q90417635 | Role of viruses, prions and miRNA in neurodegenerative disorders and dementia |
| Q39657633 | The Effects of LW-AFC on Intestinal Microbiome in Senescence-Accelerated Mouse Prone 8 Strain, a Mouse Model of Alzheimer's Disease |
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