The external globus pallidus: progress and perspectives

DJ Hegeman, ES Hong… - European Journal of …, 2016 - Wiley Online Library
The external globus pallidus (GP e) of the basal ganglia is in a unique and powerful position
to influence processing of motor information by virtue of its widespread projections to all …

New roles for the external globus pallidus in basal ganglia circuits and behavior

AH Gittis, JD Berke, MD Bevan, CS Chan… - Journal of …, 2014 - Soc Neuroscience
The development of methodology to identify specific cell populations and circuits within the
basal ganglia is rapidly transforming our ability to understand the function of this complex …

Mutant huntingtin impairs BDNF release from astrocytes by disrupting conversion of Rab3a-GTP into Rab3a-GDP

Y Hong, T Zhao, XJ Li, S Li - Journal of Neuroscience, 2016 - Soc Neuroscience
Brain-derived neurotrophic factor (BDNF) is essential for neuronal differentiation and
survival. We know that BDNF levels decline in the brains of patients with Huntington's …

Detection of axonal degeneration in a mouse model of Huntington's disease: comparison between diffusion tensor imaging and anomalous diffusion metrics

RG Gatto, AQ Ye, L Colon-Perez, TH Mareci… - … Resonance Materials in …, 2019 - Springer
Objective The goal of this work is to study the changes in white matter integrity in R6/2, a
well-established animal model of Huntington's disease (HD) that are captured by ex vivo …

An aptasensor for detection of potassium ions based on RecJ f exonuclease mediated signal amplification

P Miao, Y Tang, B Wang, K Han, X Chen, H Sun - Analyst, 2014 - pubs.rsc.org
An electrochemical biosensor for potassium has been developed combining specific
potassium–aptamer binding and RecJf exonuclease mediated signal amplification …

αB-Crystallin overexpression in astrocytes modulates the phenotype of the BACHD mouse model of Huntington's disease

AO Oliveira, A Osmand, TF Outeiro… - Human molecular …, 2016 - academic.oup.com
Huntington's disease (HD) is caused by an expanded polyglutamine (polyQ) tract in the
huntingtin (htt) protein. The polyQ expansion increases the propensity of htt to aggregate …

The phase coherence of the neurovascular unit is reduced in Huntington's disease

J Bjerkan, J Kobal, G Lancaster, S Šešok… - Brain …, 2024 - academic.oup.com
Huntington's disease is a neurodegenerative disorder in which neuronal death leads to
chorea and cognitive decline. Individuals with≥ 40 cytosine–adenine–guanine repeats on …

[HTML][HTML] DNA methylation leads to DNA repair gene down-regulation and trinucleotide repeat expansion in patient-derived huntington disease cells

PA Mollica, JA Reid, RC Ogle, PC Sachs… - The American journal of …, 2016 - Elsevier
Huntington disease (HD) is an autosomal dominantly inherited disease that exhibits genetic
anticipation of affected progeny due to expansions of a trinucleotide repeat (TNR) region …

Neuropathology and pathogenesis of extrapyramidal movement disorders: a critical update. II. Hyperkinetic disorders

KA Jellinger - Journal of Neural Transmission, 2019 - Springer
Extrapyramidal movement disorders comprise hypokinetic-rigid and hyperkinetic or mixed
forms, most of them originating from dysfunction of the basal ganglia (BG) and their …

Non-cell autonomous and epigenetic mechanisms of Huntington's disease

C Kim, A Yousefian-Jazi, SH Choi, I Chang… - International Journal of …, 2021 - mdpi.com
Huntington's disease (HD) is a rare neurodegenerative disorder caused by an expansion of
CAG trinucleotide repeat located in the exon 1 of Huntingtin (HTT) gene in human …