Add to ORKGstriatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington’s disease are not reflected in mutant Huntingtin inclusion prevalenc
Huntington’s disease (HD) is the most common dominantly-inherited neurodegenerative disease and affe...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an a...
Huntington disease (HD) is caused by a CAG expansion in the gene encoding the protein huntingtin and...
The 869 probesets that are differentially expressed between YAC128 and HdhQ150 striata. (XLS 137 kb
Over-representation analysis of the 2557 genes nominally significantly differentially expressed betw...
Genes altered in expression with age common to both WT and YAC128 caudate. (XLS 75 kb
TANOVA patterns of genes differentially expressed between WT and YAC128 caudate. Plots are sorted by...
Background The YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learni...
BackgroundThe YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learnin...
Analysis of the overlap of changes in gene expression in the YAC128 striatum at A. 6Â months of age ...
International audienceThe mechanisms underlying the preferential vulnerability of striatal neurons t...
o test the hypotheses that mutant huntingtin protein length and wild-type huntingtin dosage have imp...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an ab...
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder characteri...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease whose predominant neuro...
Huntington’s disease (HD) is the most common dominantly-inherited neurodegenerative disease and affe...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an a...
Huntington disease (HD) is caused by a CAG expansion in the gene encoding the protein huntingtin and...
The 869 probesets that are differentially expressed between YAC128 and HdhQ150 striata. (XLS 137 kb
Over-representation analysis of the 2557 genes nominally significantly differentially expressed betw...
Genes altered in expression with age common to both WT and YAC128 caudate. (XLS 75 kb
TANOVA patterns of genes differentially expressed between WT and YAC128 caudate. Plots are sorted by...
Background The YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learni...
BackgroundThe YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learnin...
Analysis of the overlap of changes in gene expression in the YAC128 striatum at A. 6Â months of age ...
International audienceThe mechanisms underlying the preferential vulnerability of striatal neurons t...
o test the hypotheses that mutant huntingtin protein length and wild-type huntingtin dosage have imp...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an ab...
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder characteri...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease whose predominant neuro...
Huntington’s disease (HD) is the most common dominantly-inherited neurodegenerative disease and affe...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an a...
Huntington disease (HD) is caused by a CAG expansion in the gene encoding the protein huntingtin and...