Huntington's disease (HD) causes widespread CNS changes and systemic abnormalities including endocrine and immune dysfunction. HD biomarkers are needed to power clinical trials of potential treatments. We used multiplatform proteomic profiling to reveal plasma changes with HD progression. Proteins of interest were evaluated using immunoblotting and ELISA in plasma from 2 populations, CSF and R6/2 mice. The identified proteins demonstrate neuroinflammation in HD and warrant further investigation as possible biomarkers
While the genetic cause of Huntington disease (HD) is known since 1993, still no cure exists. Therap...
Huntington disease (HD) is a neurodegenerative disorder caused by expansion of CAG repeats in exon 1...
Objective: Huntington’s disease (HD) is a rare neurodegenerative disease caused by the expansion of ...
Huntington's disease (HD) is an inherited neurodegenerative disorder characterized by both neurologi...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder, caused by a CAG-repea...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder, caused by a CAG-repea...
BACKGROUND: Huntington’s Disease (HD) is a hereditary, progressive neurodegenerative disorder charac...
Huntington's disease (HD) is caused by expanded CAG repeats encoding a polyglutamine tract in the hu...
Huntington's disease (HD) is caused by expanded CAG repeats encoding a polyglutamine tract in the hu...
Aggregation of polyglutamine-expanded huntingtin exon 1 (HttEx1) in Huntington's disease (HD) procee...
Huntington disease (HD) is fatal in humans within 15-20 years of symptomatic disease. Although late ...
There is an unmet need to reliably and non-invasively monitor disease progression in preclinical Hun...
a)<p>Spots numbered as shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pon...
Huntington's disease (HD) is an inherited neurodegenerative disorder characterized by both neurologi...
Molecular markers derived from cerebrospinal fluid (CSF) represent an accessible means of exploring ...
While the genetic cause of Huntington disease (HD) is known since 1993, still no cure exists. Therap...
Huntington disease (HD) is a neurodegenerative disorder caused by expansion of CAG repeats in exon 1...
Objective: Huntington’s disease (HD) is a rare neurodegenerative disease caused by the expansion of ...
Huntington's disease (HD) is an inherited neurodegenerative disorder characterized by both neurologi...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder, caused by a CAG-repea...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder, caused by a CAG-repea...
BACKGROUND: Huntington’s Disease (HD) is a hereditary, progressive neurodegenerative disorder charac...
Huntington's disease (HD) is caused by expanded CAG repeats encoding a polyglutamine tract in the hu...
Huntington's disease (HD) is caused by expanded CAG repeats encoding a polyglutamine tract in the hu...
Aggregation of polyglutamine-expanded huntingtin exon 1 (HttEx1) in Huntington's disease (HD) procee...
Huntington disease (HD) is fatal in humans within 15-20 years of symptomatic disease. Although late ...
There is an unmet need to reliably and non-invasively monitor disease progression in preclinical Hun...
a)<p>Spots numbered as shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pon...
Huntington's disease (HD) is an inherited neurodegenerative disorder characterized by both neurologi...
Molecular markers derived from cerebrospinal fluid (CSF) represent an accessible means of exploring ...
While the genetic cause of Huntington disease (HD) is known since 1993, still no cure exists. Therap...
Huntington disease (HD) is a neurodegenerative disorder caused by expansion of CAG repeats in exon 1...
Objective: Huntington’s disease (HD) is a rare neurodegenerative disease caused by the expansion of ...