Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce

The early-onset torsion dystonia-associated protein, torsinA, displays molecular chaperone activity in vitro

(2010) Alexander J. Burdette et al.   CELL STRESS & CHAPERONES

Chemical enhancement of torsinA function in cell and animal models of torsion dystonia

(2010) S. Cao et al.   Disease Models & Mechanisms

ΔFY mutation in human torsina induces locomotor disability and abberant synaptic structures in Drosophila

(2009) Dae-Weon Lee et al.   MOLECULES AND CELLS

Abnormal structure-function relationships in hereditary dystonia

(2009) M. Carbon et al.   NEUROSCIENCE

Increased c-fos expression in the central nucleus of the amygdala and enhancement of cued fear memory in Dyt1 ΔGAG knock-in mice

(2009) Fumiaki Yokoi et al.   NEUROSCIENCE RESEARCH

Dystonia-associated mutations cause premature degradation of torsinA protein and cell-type-specific mislocalization to the nuclear envelope

(2008) L. M. Giles et al.   HUMAN MOLECULAR GENETICS

Novel TOR1A mutation p.Arg288Gln in early-onset dystonia (DYT1)

(2008) B Zirn et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Consequences of the DYT1 mutation on torsinA oligomerization and degradation

(2008) K.L. Gordon et al.   NEUROSCIENCE