1) Hereditary prion diseases
遗传性朊病毒病
2) Prions and Epigemtic Inheritance
朊病毒和后基因遗传
3) prion diseases
朊病毒病
1.
The fundamental patho-genic mechanism of prion diseases involves the post-translational conversion of PrPC into its infectious isoformPrPSc, but it remains still unclear that how prion propagation leads to apoptosis of neuronal cells.
朊病毒病,即传染性海绵状脑病(transmissiblespongiformencephalopathies,TSEs),是一类致死性的神经退行性疾病,存在散发性、感染性和遗传性3种形式。
2.
On the basis of a brief account of human prion diseases, this paper elucidates the differences between vCJD and bovine spongiform encephalopathy (BSE) and presents the evidence conforming that vCJD is caused by the BSE agent.
本文在概述人朊病毒的基础上 ,重点阐述新型克 -雅氏病与早先已知的各种人朊病毒病的区别和它是由牛海绵状脑病朊病毒引起的证据 ,并对牛海绵状脑病并非源于痒病而是原于牛散发性朊病毒病、影响新型克-雅氏病流行规模的主要因素和该病的主要预防措施等问题进行了讨
3.
Since the emerging of bovine spongiform encephalopathy and variant Creutzfeldt-Jacob disease (vCJD), the threat of prion diseases on public health became increasingly remarkable.
朊病毒病(Prion disease)是一组累及人和动物的传染性神经退行性疾病，随着疯牛病和人类变异性克雅氏病(variant Creutzfeldt-Jacob disease，vCJD)的出现，该类疾病对公共卫生和人类健康的威胁日益显著。
4) Prions
朊病毒
1.
Prions, generally called Proteinaceous Infectious Particales (PrP), are manifest as one kind of subacutely spongiform encephalopathies in human and animals, whose pathogens are infective protein without nucleic acids.
朊病毒(Proteinaceous Infectious Particales简称Prions)病是一种人和动物共患的亚急性海绵状脑病,其病原是一种具有传染性的不含核酸的病原体,故称为感染性朊病毒蛋白(PrP)。
5) prion
[英]['pri:ɔn] [美]['pri'ɑn]
朊病毒
1.
Solvent Accessibility and Computer Modeling Analysis on the Native and the Mutants of Human Prion Protein;
人朊病毒蛋白及其突变体的溶剂可及性和模拟分析
2.
Research advance in prion pathogenesis;
朊病毒致病机理的研究进展
6) Prion(PrPSC)
朊病毒(PrPSC)
补充资料：显性遗传性营养不良型大疱性皮肤松解病
显性遗传性营养不良型大疱性皮肤松解病
dominant dystrophic epidermolysis bullosa
又名“增生性大疱性表皮松解症”。婴儿早期或儿童发病、四肢较多，因创伤最多之故。损害常为血疱，缓慢痊愈，愈后留下萎缩性的薄疤或肥厚性的瘢痕疙瘩，手部偶有毁损性的瘢痕发生。在所有部位表皮囊肿和粟丘疹是常见的。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条