<p>A. Schematic representation of the HD transgene expressed in R6 mice, showing location of primers used to amplify the region just downstream of the TSS in HD exon-1. B. ChIP analyses from the striatum and the cerebellum of R6/1 mice at 13- and 36-wk and from the striatum and cerebellum of R6/2 mice at 12-wk, using antibody to Me3H3K4. Error bars, sem; *, inter-tissue comparisons; §, inter-mouse line comparisons. *, p<0.05; §, p<0.05. C. Left panel. Global analysis of the level of Me3H3K4 at the HD locus. Me3H3K4 levels at the HD locus correspond to mean ChIP values at the HD promoter, HD exon-1 and HD intron-1. Error bars, sem; §, p<0.05. Right panel. Correlative analysis of CAG instability rates and Me3H3K4 levels at the HD locus. R6/1 ...
International audienceThe expansion of CAG/CTG repeats is responsible for many diseases, including H...
<p>(A) Representative GeneMapper profiles of <i>HTT</i> CAG repeat size distributions in the tail, s...
Huntington\u27s disease is a dominantly inherited neurodegenerative disease caused by the expansion ...
<p>A. Schematic representation of the human HD transgene expressed in R6 mice and of the correspondi...
<p>A. ChIP analyses from the striatum and the cerebellum of R6/1 and R6/2 mice using antibody to Me3...
<p>A. Left panel. ChIP analyses from the striatum and the cerebellum of R6/1 and R6/2 mice using ant...
<p>A. Expression of the HD transgene in the striatum and in the cerebellum of R6/1 and R6/2 mice of ...
<p>A. ChIP analyses from the striatum and the cerebellum of R6/1 and R6/2 mice at late-pathological ...
<p>A. ChIP analyses from the striatum and the cerebellum of R6/1 and R6/2 mice using antibody to pho...
<p>Graphical representation of striatal CAG instability indices from individual (A) B6, 129, (B6x129...
A) Bar graphs show the number of differential AS events in the striatum and cortex from 6 mouse KI m...
<p>(A) Representative GeneMapper profiles of <i>HTT</i> CAG repeat size distributions in the tail, s...
<p>(A) <i>Hdac3</i> mRNA expression levels in 15 week old mouse cortex, cerebellum and striatum are ...
<p>(A) Western blot analysis (<i>n</i> = 1 per lane) of microdissected brain regions from wild-type ...
<p>(A-B) Western blots of DBC1 and AMPK-α1 after AMPK-α1 immunoprecipitation from (A) the striatum o...
International audienceThe expansion of CAG/CTG repeats is responsible for many diseases, including H...
<p>(A) Representative GeneMapper profiles of <i>HTT</i> CAG repeat size distributions in the tail, s...
Huntington\u27s disease is a dominantly inherited neurodegenerative disease caused by the expansion ...
<p>A. Schematic representation of the human HD transgene expressed in R6 mice and of the correspondi...
<p>A. ChIP analyses from the striatum and the cerebellum of R6/1 and R6/2 mice using antibody to Me3...
<p>A. Left panel. ChIP analyses from the striatum and the cerebellum of R6/1 and R6/2 mice using ant...
<p>A. Expression of the HD transgene in the striatum and in the cerebellum of R6/1 and R6/2 mice of ...
<p>A. ChIP analyses from the striatum and the cerebellum of R6/1 and R6/2 mice at late-pathological ...
<p>A. ChIP analyses from the striatum and the cerebellum of R6/1 and R6/2 mice using antibody to pho...
<p>Graphical representation of striatal CAG instability indices from individual (A) B6, 129, (B6x129...
A) Bar graphs show the number of differential AS events in the striatum and cortex from 6 mouse KI m...
<p>(A) Representative GeneMapper profiles of <i>HTT</i> CAG repeat size distributions in the tail, s...
<p>(A) <i>Hdac3</i> mRNA expression levels in 15 week old mouse cortex, cerebellum and striatum are ...
<p>(A) Western blot analysis (<i>n</i> = 1 per lane) of microdissected brain regions from wild-type ...
<p>(A-B) Western blots of DBC1 and AMPK-α1 after AMPK-α1 immunoprecipitation from (A) the striatum o...
International audienceThe expansion of CAG/CTG repeats is responsible for many diseases, including H...
<p>(A) Representative GeneMapper profiles of <i>HTT</i> CAG repeat size distributions in the tail, s...
Huntington\u27s disease is a dominantly inherited neurodegenerative disease caused by the expansion ...