BackgroundThe YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learning and memory tasks and alterations in its transcriptional profile. We examined the changes in the transcriptional profile in the YAC128 mouse model of HD at 6, 12 and 18 months and compared these with those seen in other models and human HD caudate.ResultsDifferential gene expression by genotype showed that genes related to neuronal function, projection outgrowth and cell adhesion were altered in expression. A Time-course ANOVA revealed that genes downregulated with increased age in wild-type striata were likely to be downregulated in the YAC128 striata. There was a substantial overlap of concordant gene expression changes in the YAC128 stria...
striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntingt...
Huntington disease (HD) is caused by a CAG expansion in the gene encoding the protein huntingtin and...
Huntington's disease (HD), caused by a CAG repeat expansion in the huntingtin (HTT) gene, is charact...
BackgroundThe YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learnin...
Background The YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learni...
Evaluation of transcriptional changes in the striatum may be an effective approach to understanding ...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an a...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an ab...
To test the hypotheses that mutant huntingtin protein length and wild-type huntingtin dosage have im...
Abstract Transcriptional changes occur presymptomatically and throughout Huntington's disease (HD), ...
Substantial transcriptional changes are seen in Huntington's disease (HD) brain and parallel early c...
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder characteri...
Transcriptional changes occur presymptomatically and throughout Huntington\u27s disease (HD), motiva...
Selective neuronal degeneration of caudate and putamen, collectively known as the striatum, is a dis...
Analysis of the overlap of changes in gene expression in the YAC128 striatum at A. 6Â months of age ...
striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntingt...
Huntington disease (HD) is caused by a CAG expansion in the gene encoding the protein huntingtin and...
Huntington's disease (HD), caused by a CAG repeat expansion in the huntingtin (HTT) gene, is charact...
BackgroundThe YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learnin...
Background The YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learni...
Evaluation of transcriptional changes in the striatum may be an effective approach to understanding ...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an a...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an ab...
To test the hypotheses that mutant huntingtin protein length and wild-type huntingtin dosage have im...
Abstract Transcriptional changes occur presymptomatically and throughout Huntington's disease (HD), ...
Substantial transcriptional changes are seen in Huntington's disease (HD) brain and parallel early c...
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder characteri...
Transcriptional changes occur presymptomatically and throughout Huntington\u27s disease (HD), motiva...
Selective neuronal degeneration of caudate and putamen, collectively known as the striatum, is a dis...
Analysis of the overlap of changes in gene expression in the YAC128 striatum at A. 6Â months of age ...
striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntingt...
Huntington disease (HD) is caused by a CAG expansion in the gene encoding the protein huntingtin and...
Huntington's disease (HD), caused by a CAG repeat expansion in the huntingtin (HTT) gene, is charact...