Prion is the first international peer-reviewed open access journal to focus exclusively on protein folding and misfolding, protein assembly disorders, protein-based and structural inheritance. The goal is to foster communication and rapid exchange of information through timely publication of important results using traditional as well as electronic formats. The overriding criteria for publication in Prion are originality, scientific merit and general interest.
朊病毒是第一个国际同行评审的开放获取期刊,专门关注蛋白质折叠和错误折叠,蛋白质组装障碍,蛋白质为基础的和结构遗传。目标是通过使用传统和电子格式及时公布重要结果,促进沟通和信息的快速交流。在朊病毒中发表的首要标准是原创性、科学价值和普遍兴趣。
The prion 2018 round tables (I): the structure of PrPSc
来源期刊:PrionDOI:10.1080/19336896.2019.1569450
The Prion 2018 round tables (II): Aβ, tau, α-synuclein… are they prions, prion-like proteins, or what?
来源期刊:PrionDOI:10.1080/19336896.2019.1569451
Spatial heterogeneity of prion gene polymorphisms in an area recently infected by chronic wasting disease
来源期刊:PrionDOI:10.1080/19336896.2019.1583042
Combining autophagy stimulators and cellulose ethers for therapy against prion disease
来源期刊:PrionDOI:10.1080/19336896.2019.1670928
In vitro generation of tau aggregates conformationally distinct from parent tau seeds of Alzheimer’s brain
来源期刊:PrionDOI:10.1080/19336896.2018.1545524
Amyloid properties of the yeast cell wall protein Toh1 and its interaction with prion proteins Rnq1 and Sup35
来源期刊:PrionDOI:10.1080/19336896.2018.1558763
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
来源期刊:PrionDOI:10.1080/19336896.2019.1631680
Use of faecal volatile organic compound analysis for ante-mortem discrimination between CWD-positive, -negative exposed, and -known negative white-tailed deer (Odocoileus virginianus)
来源期刊:PrionDOI:10.1080/19336896.2019.1607462
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
来源期刊:PrionDOI:10.1080/19336896.2019.1607464
Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia
来源期刊:PrionDOI:10.1080/19336896.2019.1617027
Deciphering the BSE-type specific cell and tissue tropisms of atypical (H and L) and classical BSE
来源期刊:PrionDOI:10.1080/19336896.2019.1651180
Axonal changes in experimental prion diseases recapitulate those following constriction of postganglionic branches of the superior cervical ganglion: a comparison 40 years later
来源期刊:PrionDOI:10.1080/19336896.2019.1595315
A case of V180I genetic Creutzfeldt-Jakob disease presenting with conspicuous facial mimicry
来源期刊:PrionDOI:10.1080/19336896.2019.1651181
Rodent models allow BSE discrimination of goat prions and reveal geographical differences in the biological properties of scrapie
来源期刊:NoneDOI:10.1080/19336896.2019.1615197
Sensitivity and specificity evaluation of multiple neurodegenerative proteins for Creutzfeldt-Jakob disease diagnosis using a deep-learning approach
来源期刊:PrionDOI:10.1080/19336896.2019.1639482
Sodium hydroxide treatment effectively inhibits PrPCWD replication in farm soil
来源期刊:PrionDOI:10.1080/19336896.2019.1617623
Michael Ter-Avanesyan (1949-2018) – Advent of the scientist
来源期刊:PrionDOI:10.1080/19336896.2018.1563427
Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report
来源期刊:PrionDOI:10.1080/19336896.2019.1631679
Significant enhanced expressions of aquaporin-1, -4 and -9 in the brains of various prion diseases
来源期刊:PrionDOI:10.1080/19336896.2019.1660487
Michael Ter-Avanesyan (1949-2018) - life in science
来源期刊:PrionDOI:10.1080/19336896.2019.1567201
An autopsied case of MM1-type sporadic Creutzfeldt-Jakob disease with pathology of Wernicke encephalopathy
来源期刊:PrionDOI:10.1080/19336896.2018.1545525
THERPA v2: an update of a small molecule database related to prion protein regulation and prion disease progression
来源期刊:PrionDOI:10.1080/19336896.2019.1689789
The worst is yet to come: probable sporadic Creutzfeldt–Jakob disease in a well-controlled HIV patient
来源期刊:PrionDOI:10.1080/19336896.2019.1648985
Prion-dependent proteome remodeling in response to environmental stress is modulated by prion variant and genetic background
来源期刊:PrionDOI:10.1080/19336896.2019.1583041
The insomnia phenotype in genetic Creutzfeldt–Jakob disease based on the E200K mutation
来源期刊:PrionDOI:10.1080/19336896.2019.1590938