<p>(A) The protein levels of FBXW8 were significantly upregulated in the cerebellum of 18 months old CAG42 mice compared to wild-type (n = 9–11 mice/genotype). (B) Soluble levels of Q22-ATXN2 were unchanged after FBXW8 overexpression, while for Q74-ATXN2 a slight reduction was apparent. With respect to insoluble levels, Q22-ATXN2 was again not influenced by FBXW8 overexpression, while the Q74-ATXN2 reduction became significant. FBXW8 levels were significantly increased by its overexpression both in the soluble and insoluble fraction (n = 7).</p
Die Ursache der neurodegenerativen Erkrankung Spinozerebelläre Ataxie Typ 2 (SCA2) ist eine expandie...
<p>A) Western blot analysis of cerebellar lysates stained with 1C2 antibody (for the polyglutamine e...
Die Ursache der neurodegenerativen Erkrankung Spinozerebelläre Ataxie Typ 2 (SCA2) ist eine expandie...
<p>(A) Pulling either with anti-ATXN2 or anti-FBXW8 antibody, ATNX2 and FBXW8 show an interaction in...
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>In cerebellar tissue, a trend in ATXN2 reduction was observed at 6 weeks and 6 months age, with s...
Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding triplet repe...
<div><p>The involvement of the ubiquitin-proteasome system (UPS) in the course of various age-associ...
The involvement of the ubiquitin-proteasome system (UPS) in the course of various age-associated neu...
The involvement of the ubiquitin-proteasome system (UPS) in the course of various age-associated neu...
<p>(A) In the cerebellum, a progressive insolubility of Q42-ATXN2 from 6 to 12 and 24 months was det...
The involvement of the ubiquitin-proteasome system (UPS) in the course of various age-associated neu...
<p>(A) Overexpression of CAG22-ATXN2 and CAG74-ATXN2 led to significantly decreased <i>PABPC1</i> tr...
<p><b>(A)</b> qRT-PCR analyses of cerebellar RNAs from wild-type and BAC-Q22 mice show unchanged <i>...
Die Ursache der neurodegenerativen Erkrankung Spinozerebelläre Ataxie Typ 2 (SCA2) ist eine expandie...
<p>A) Western blot analysis of cerebellar lysates stained with 1C2 antibody (for the polyglutamine e...
Die Ursache der neurodegenerativen Erkrankung Spinozerebelläre Ataxie Typ 2 (SCA2) ist eine expandie...
<p>(A) Pulling either with anti-ATXN2 or anti-FBXW8 antibody, ATNX2 and FBXW8 show an interaction in...
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>In cerebellar tissue, a trend in ATXN2 reduction was observed at 6 weeks and 6 months age, with s...
Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding triplet repe...
<div><p>The involvement of the ubiquitin-proteasome system (UPS) in the course of various age-associ...
The involvement of the ubiquitin-proteasome system (UPS) in the course of various age-associated neu...
The involvement of the ubiquitin-proteasome system (UPS) in the course of various age-associated neu...
<p>(A) In the cerebellum, a progressive insolubility of Q42-ATXN2 from 6 to 12 and 24 months was det...
The involvement of the ubiquitin-proteasome system (UPS) in the course of various age-associated neu...
<p>(A) Overexpression of CAG22-ATXN2 and CAG74-ATXN2 led to significantly decreased <i>PABPC1</i> tr...
<p><b>(A)</b> qRT-PCR analyses of cerebellar RNAs from wild-type and BAC-Q22 mice show unchanged <i>...
Die Ursache der neurodegenerativen Erkrankung Spinozerebelläre Ataxie Typ 2 (SCA2) ist eine expandie...
<p>A) Western blot analysis of cerebellar lysates stained with 1C2 antibody (for the polyglutamine e...
Die Ursache der neurodegenerativen Erkrankung Spinozerebelläre Ataxie Typ 2 (SCA2) ist eine expandie...