Loss of anti-Bax function in Gerstmann-Sträussler-Scheinker syndrome-associated prion protein mutants
about
A Drosophila model of GSS syndrome suggests defects in active zones are responsible for pathogenesis of GSS syndrome.Disease-associated mutations in the prion protein impair laminin-induced process outgrowth and survivalFamilial prion protein mutants inhibit Hrd1-mediated retrotranslocation of misfolded proteins by depleting misfolded protein sensor BiP.Presenilin 2 overexpression is associated with apoptosis in Neuro2a cells.Yeast as a tool for studying proteins of the Bcl-2 familyLuman contributes to brefeldin A-induced prion protein gene expression by interacting with the ERSE26 element
P2860
Loss of anti-Bax function in Gerstmann-Sträussler-Scheinker syndrome-associated prion protein mutants
description
2009 nî lūn-bûn
@nan
2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Loss of anti-Bax function in G ...... sociated prion protein mutants
@ast
Loss of anti-Bax function in G ...... sociated prion protein mutants
@en
type
label
Loss of anti-Bax function in G ...... sociated prion protein mutants
@ast
Loss of anti-Bax function in G ...... sociated prion protein mutants
@en
prefLabel
Loss of anti-Bax function in G ...... sociated prion protein mutants
@ast
Loss of anti-Bax function in G ...... sociated prion protein mutants
@en
P2093
P2860
P1433
P1476
Loss of anti-Bax function in G ...... sociated prion protein mutants
@en
P2093
Andréa C LeBlanc
Cynthia G Goodyer
Jennifer Hammond
Julie Jodoin
Micheal Misiewicz
Paresa N Giannopoulos
Priya Makhijani
P2860
P356
10.1371/JOURNAL.PONE.0006647
P407
P577
2009-08-14T00:00:00Z