Dysregulation of corticostriatal connectivity in Huntington's disease: a role for dopamine modulation
C Rangel-Barajas, GV Rebec - Journal of Huntington's …, 2016 - content.iospress.com
Aberrant communication between striatum, the main information processing unit of the basal
ganglia, and cerebral cortex plays a critical role in the emergence of Huntington's disease …
ganglia, and cerebral cortex plays a critical role in the emergence of Huntington's disease …
Subcellular clearance and accumulation of Huntington disease protein: a mini-review
Huntington's disease (HD) is an autosomal dominant, progressive neurodegenerative
disease caused by an expanded polyglutamine (polyQ) tract in the N-terminal region of …
disease caused by an expanded polyglutamine (polyQ) tract in the N-terminal region of …
Cellular and molecular mechanisms of neuronal dysfunction in Huntington's disease
J Caboche, P Vanhoutte, L Boussicault, E Roze… - Handbook of Behavioral …, 2016 - Elsevier
Huntington's disease (HD) is the most frequent neurodegenerative disease caused by an
expansion of polyglutamines (CAG). The main clinical manifestations of HD are chorea …
expansion of polyglutamines (CAG). The main clinical manifestations of HD are chorea …
Directed differentiation of human pluripotent stem cells to telencephalic lateral ganglionic eminence progenitors using small molecules
S Joy - 2016 - orca.cardiff.ac.uk
This thesis focused on directing the differentiation of pluripotent stem cells towards
telencephalic lateral ganglionic eminence-like fate. The study aimed at developing …
telencephalic lateral ganglionic eminence-like fate. The study aimed at developing …
[引用][C] Saccades, eye-hand movement and cognition in Huntington's disease: a 12 month study
EA Toh - 2016 - University of Otago