Cargando…
In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP(V180I) Mutation
Both sporadic variably protease-sensitive prionopathy (VPSPr) and familial Creutzfeldt-Jakob disease linked to the prion protein (PrP) V180I mutation (fCJD(V180I)) have been found to share a unique pathological prion protein (PrP(Sc)) that lacks the protease-resistant PrP(Sc) glycosylated at residue...
Autores principales: | Wang, Zerui, Yuan, Jue, Shen, Pingping, Abskharon, Romany, Lang, Yue, Dang, Johnny, Adornato, Alise, Xu, Ling, Chen, Jiafeng, Feng, Jiachun, Moudjou, Mohammed, Kitamoto, Tetsuyuki, Lee, Hyoung-gon, Kim, Yong-Sun, Langeveld, Jan, Appleby, Brian, Ma, Jiyan, Kong, Qingzhong, Petersen, Robert B., Zou, Wen-Quan, Cui, Li |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614145/ https://www.ncbi.nlm.nih.gov/pubmed/30612334 http://dx.doi.org/10.1007/s12035-018-1459-0 |
Ejemplares similares
-
Further Characterization of Glycoform-Selective Prions of Variably Protease-Sensitive Prionopathy
por: Zhang, Weiguanliu, et al.
Publicado: (2021) -
PrP(res) deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD)
por: Takao, Masaki, et al.
Publicado: (2018) -
Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease
por: Xiao, Xiangzhu, et al.
Publicado: (2013) -
Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease
por: Xiao, Xiangzhu, et al.
Publicado: (2013) -
Prion infectivity is encoded exclusively within the structure of proteinase K-resistant fragments of synthetically generated recombinant PrP(Sc)
por: Wang, Fei, et al.
Publicado: (2018)