<p>Some of these genes were also differentially expressed in other models like Huntington’s disease (HD; [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0118120#pone.0118120.ref017" target="_blank">17</a>]), AR knock out (ARKO; [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0118120#pone.0118120.ref018" target="_blank">18</a>]), and Atrophy [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0118120#pone.0118120.ref019" target="_blank">19</a>,<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0118120#pone.0118120.ref020" target="_blank">20</a>].</p><p>The list and fold change of differentially expressed genes found in three KD/SBMA mouse models (as compared ...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an ab...
Background The YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learni...
To test the hypotheses that mutant huntingtin protein length and wild-type huntingtin dosage have im...
) gene. Although KD/SBMA has been traditionally considered a motor neuron disease, emerging evidence...
BACKGROUND: Kennedy's disease/Spinobulbar muscular atrophy (KD/SBMA) is a degenerative neuromuscula...
Kennedy's disease/Spinobulbar muscular atrophy (KD/SBMA) is a degenerative neuromuscular disease aff...
<p>Cluster output represents colorimetrically indicated log2 ratio change. Female HSA-AR Tg and WT m...
<p>Diagram representing the number of genes whose expression differed from controls. Gene numbers we...
TANOVA patterns of genes differentially expressed between WT and YAC128 caudate. Plots are sorted by...
<p>Cluster output represents colorimetrically indicated log2 ratio change. Male Tg mice and female T...
<p>*Expanded gene names, listed in alphabetical order: ACTC1 = actin, alpha, cardiac muscle 1; CDH4 ...
Huntington’s disease (HD) is an inherited neurodegeneration that causes a severe progressive illness...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease, resulting in expansion...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an a...
Huntington's disease (HD) is an autosomal dominant neurodegeneration, characterised by a movement di...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an ab...
Background The YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learni...
To test the hypotheses that mutant huntingtin protein length and wild-type huntingtin dosage have im...
) gene. Although KD/SBMA has been traditionally considered a motor neuron disease, emerging evidence...
BACKGROUND: Kennedy's disease/Spinobulbar muscular atrophy (KD/SBMA) is a degenerative neuromuscula...
Kennedy's disease/Spinobulbar muscular atrophy (KD/SBMA) is a degenerative neuromuscular disease aff...
<p>Cluster output represents colorimetrically indicated log2 ratio change. Female HSA-AR Tg and WT m...
<p>Diagram representing the number of genes whose expression differed from controls. Gene numbers we...
TANOVA patterns of genes differentially expressed between WT and YAC128 caudate. Plots are sorted by...
<p>Cluster output represents colorimetrically indicated log2 ratio change. Male Tg mice and female T...
<p>*Expanded gene names, listed in alphabetical order: ACTC1 = actin, alpha, cardiac muscle 1; CDH4 ...
Huntington’s disease (HD) is an inherited neurodegeneration that causes a severe progressive illness...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease, resulting in expansion...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an a...
Huntington's disease (HD) is an autosomal dominant neurodegeneration, characterised by a movement di...
Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an ab...
Background The YAC128 model of Huntington’s disease (HD) shows substantial deficits in motor, learni...
To test the hypotheses that mutant huntingtin protein length and wild-type huntingtin dosage have im...