Disruption of Protein Processing in the Endoplasmic Reticulum of DYT1 Knock-in Mice Implicates Novel Pathways in Dystonia Pathogenesis.
about
A role for cerebellum in the hereditary dystonia DYT1.Early-onset torsion dystonia: a novel high-throughput yeast genetic screen for factors modifying protein levels of torsinAΔE.TorsinA dysfunction causes persistent neuronal nuclear pore defects.Mutations in THAP1/DYT6 reveal that diverse dystonia genes disrupt similar neuronal pathways and functions.Mutant torsinA in the heterozygous DYT1 state compromises HSV propagation in infected neurons and fibroblasts.
P2860
Disruption of Protein Processing in the Endoplasmic Reticulum of DYT1 Knock-in Mice Implicates Novel Pathways in Dystonia Pathogenesis.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 2016
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Disruption of Protein Processi ...... ways in Dystonia Pathogenesis.
@en
Disruption of Protein Processi ...... ways in Dystonia Pathogenesis.
@nl
type
label
Disruption of Protein Processi ...... ways in Dystonia Pathogenesis.
@en
Disruption of Protein Processi ...... ways in Dystonia Pathogenesis.
@nl
prefLabel
Disruption of Protein Processi ...... ways in Dystonia Pathogenesis.
@en
Disruption of Protein Processi ...... ways in Dystonia Pathogenesis.
@nl
P2093
P2860
P50
P1476
Disruption of Protein Processi ...... hways in Dystonia Pathogenesis
@en
P2093
Genevieve Beauvais
Hiroyuki Kawano
Hsiang Wen
Michelle E Ehrlich
Nicole M Bode
P2860
P304
10245-10256
P356
10.1523/JNEUROSCI.0669-16.2016
P407
P577
2016-10-01T00:00:00Z