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Prion|June 16, 2015
Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein geneLin Sun, Xia Li, Xiang Lin, et al.Prion|February 3, 2018
Genetic effects of PRNP gene insertion/deletion (indel) on phenotypic traits in sheepJie Li, Sarantsetseg Erdenee, Shaoli Zhang, et al.Prion|January 9, 2018
Overexpression of a conserved HSP40 chaperone reduces toxicity of several neurodegenerative disease proteinsSei-Kyoung Park, Fatih Arslan, Vydehi Kanneganti, et al.Prion|December 12, 2017
Curing of [PSI+] by Hsp104 Overexpression: Clues to solving the puzzleLois E Greene, Xiaohong Zhao, Evan EisenbergPrion|November 7, 2017
Electron microscopic and confocal laser microscopy analysis of amyloid plaques in chronic wasting disease transmitted to transgenic miceBeata Sikorska, Agata Gajos, Andrzej Bogucki, et al.Prion|September 29, 2017
More stressed out with age? Check your RNA granule aggregationMarie C Lechler, Della C DavidPrion|September 30, 2017
An inter-domain regulatory mechanism controls toxic activities of PrPCAlex J McDonald, Bei Wu, David A HarrisPrion|May 25, 2016
A transfectant RK13 cell line permissive to classical caprine scrapie prion propagationRohana P Dassanayake, Dongyue Zhuang, Thomas C Truscott, et al.Prion|May 22, 2015
Characteristics of Korean patients with suspected Creutzfeldt-Jakob disease with 14-3-3 protein in cerebrospinal fluid: Preliminary study of the Korean Creutzfeldt-Jakob disease active surveillance programJae-Sung Lim, Hyung-Min Kwon, Jae-Won Jang, et al.Prion|May 7, 2015
Regulating extracellular proteostasis capacity through the unfolded protein responseJoseph C Genereux, R Luke WisemanPageof 69