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.
Author: Chen G1,2, Li P2, Liu Z2, Zeng R2, Ma X3, Chen Y4, Xu H5, Li Z5, Lin H2.
Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia.
Author: He R1,2, Hu Y2,3, Yao L2,3, Tian Y2,3, Zhou Y2,3, Yi F2,3, Zhou L2,3, Xu H2,3, Sun Q2,3.
Rare E196A mutation in PRNP gene of three Chinese patients with Creutzfeldt-Jacob disease.
Author: Shi Q, Zhou W, Chen C, Zhang BY, Xiao K, Wang Y, Dong XP.
Polymorphism analysis of prion protein gene in eleven Pakistani goat breeds.
Author: Hassan MF, Khan SH, Babar ME, Yang L, Ali T, Khan JM, Shah SZ, Zhou X, Hussain T, Zhu T, Hussain T, Zhao D.
英文介紹
Prion雜志英文介紹
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.