Transcriptional changes occur presymptomatically and throughout Huntington\u27s disease (HD), motivating the study of transcriptional regulatory networks (TRNs) in HD We reconstructed a genome-scale model for the target genes of 718 transcription factors (TFs) in the mouse striatum by integrating a model of genomic binding sites with transcriptome profiling of striatal tissue from HD mouse models. We identified 48 differentially expressed TF-target gene modules associated with age- and CAG repeat length-dependent gene expression changes i
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...
In Huntington's disease (HD; MIM ID #143100), a fatal neurodegenerative disorder, transcriptional dy...
Transcriptional changes occur presymptomatically and throughout Huntington\u27s disease (HD), motiva...
Abstract Transcriptional changes occur presymptomatically and throughout Huntington's disease (HD), ...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an ab...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an a...
To gain insight into how mutant huntingtin (mHtt) CAG repeat length modifies Huntington's disease (H...
Evaluation of transcriptional changes in the striatum may be an effective approach to understanding ...
Huntington\u27s disease is a dominantly inherited neurodegenerative disease caused by the expansion ...
<div><p>In Huntington's disease (HD; MIM ID #143100), a fatal neurodegenerative disorder, transcript...
International audienceTemporal dynamics and mechanisms underlying epigenetic changes in Huntington’s...
Substantial transcriptional changes are seen in Huntington's disease (HD) brain and parallel early c...
Transcriptional dysregulation in Huntington's disease (HD) affects the expression of genes involved ...
Discriminating transcriptional changes that drive disease pathogenesis from nonpathogenic and compen...
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...
In Huntington's disease (HD; MIM ID #143100), a fatal neurodegenerative disorder, transcriptional dy...
Transcriptional changes occur presymptomatically and throughout Huntington\u27s disease (HD), motiva...
Abstract Transcriptional changes occur presymptomatically and throughout Huntington's disease (HD), ...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an ab...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an a...
To gain insight into how mutant huntingtin (mHtt) CAG repeat length modifies Huntington's disease (H...
Evaluation of transcriptional changes in the striatum may be an effective approach to understanding ...
Huntington\u27s disease is a dominantly inherited neurodegenerative disease caused by the expansion ...
<div><p>In Huntington's disease (HD; MIM ID #143100), a fatal neurodegenerative disorder, transcript...
International audienceTemporal dynamics and mechanisms underlying epigenetic changes in Huntington’s...
Substantial transcriptional changes are seen in Huntington's disease (HD) brain and parallel early c...
Transcriptional dysregulation in Huntington's disease (HD) affects the expression of genes involved ...
Discriminating transcriptional changes that drive disease pathogenesis from nonpathogenic and compen...
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...
In Huntington's disease (HD; MIM ID #143100), a fatal neurodegenerative disorder, transcriptional dy...