Biological network inferences for a protection mechanism against familial Creutzfeldt-Jakob disease with E200K pathogenic mutation

BACKGROUND: Human prion diseases are caused by abnormal accumulation of misfolded prion protein in the brain tissue. Inherited prion diseases, including familial Creutzfeldt-Jakob disease (fCJD), are associated with mutations of the prion protein gene (PRNP). The glutamate (E)-to-lysine (K) substitu...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Lee, Sol Moe, Chung, Myungguen, Hwang, Kyu Jam, Ju, Young Ran, Hyeon, Jae Wook, Park, Jun-Sun, Kim, Chi-Kyeong, Choi, Sangho, Lee, Jeongmin, Kim, Su Yeon
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4151374/
https://ncbi.nlm.nih.gov/pubmed/25149502
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8794-7-52
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados