<p>In cerebellar tissue, a trend in ATXN2 reduction was observed at 6 weeks and 6 months age, with significance in ATXN2 reduction being reached at 18 months of age. Also, a significant PABPC1 reduction was apparent in 6 weeks and 18 months old CAG42 mice in the cerebellum. In the cortex, a reduction of ATXN2 levels was observed in 6 weeks old animals as a trend and with significance from 6 months onwards. An elevation of PABPC1 levels became significant at 18 months of age (n = 10–12 mice/genotype/tissue).</p
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominantly inherited disorder, which is caused ...
The Ts65Dn is a popular mouse model of Down syndrome (DS). It displays DS-relevant features of learn...
The Ts65Dn is a popular mouse model of Down syndrome (DS). It displays DS-relevant features of learn...
<p>(A) In the cerebellum, a progressive insolubility of Q42-ATXN2 from 6 to 12 and 24 months was det...
<p>In the cerebellum an <i>Atxn2</i> mRNA elevation was not detectable until 6 months, whereas the <...
Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding triplet repe...
<div><p>Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding trip...
<p><b>(A)</b> No significant changes in BAC-Q22 mice compared with wild-type at 16 and 45 weeks of a...
Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding triplet repe...
<p><b>(A)</b> Representative micrographs of calbindin-28k immunostaining of PCs in the cerebellum of...
<p>(A) The protein levels of FBXW8 were significantly upregulated in the cerebellum of 18 months old...
<p>(A) Pulling either with anti-ATXN2 or anti-FBXW8 antibody, ATNX2 and FBXW8 show an interaction in...
<p><b>A)</b> BDNF protein levels (measured with ELISA) in the hippocampus, frontal cortex, parietal ...
<p>(A) Western blot analysis of soluble APPβ (sAPPβ) and actin (Actin-DEA) protein levels in DEA fra...
<p>A–D) Two animals of the indicated genotypes per age were immunoblotted and detected with an ataxi...
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominantly inherited disorder, which is caused ...
The Ts65Dn is a popular mouse model of Down syndrome (DS). It displays DS-relevant features of learn...
The Ts65Dn is a popular mouse model of Down syndrome (DS). It displays DS-relevant features of learn...
<p>(A) In the cerebellum, a progressive insolubility of Q42-ATXN2 from 6 to 12 and 24 months was det...
<p>In the cerebellum an <i>Atxn2</i> mRNA elevation was not detectable until 6 months, whereas the <...
Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding triplet repe...
<div><p>Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding trip...
<p><b>(A)</b> No significant changes in BAC-Q22 mice compared with wild-type at 16 and 45 weeks of a...
Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding triplet repe...
<p><b>(A)</b> Representative micrographs of calbindin-28k immunostaining of PCs in the cerebellum of...
<p>(A) The protein levels of FBXW8 were significantly upregulated in the cerebellum of 18 months old...
<p>(A) Pulling either with anti-ATXN2 or anti-FBXW8 antibody, ATNX2 and FBXW8 show an interaction in...
<p><b>A)</b> BDNF protein levels (measured with ELISA) in the hippocampus, frontal cortex, parietal ...
<p>(A) Western blot analysis of soluble APPβ (sAPPβ) and actin (Actin-DEA) protein levels in DEA fra...
<p>A–D) Two animals of the indicated genotypes per age were immunoblotted and detected with an ataxi...
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominantly inherited disorder, which is caused ...
The Ts65Dn is a popular mouse model of Down syndrome (DS). It displays DS-relevant features of learn...
The Ts65Dn is a popular mouse model of Down syndrome (DS). It displays DS-relevant features of learn...