Glutamine

ataxin 1 ; Mus musculus







11 Article(s)
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Title
Pub. Year
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1 33436887 Mood alterations in mouse models of Spinocerebellar Ataxia type 1. 2021 Jan 12 4
2 34479994 Sphingolipid metabolism governs Purkinje cell patterned degeneration in Atxn1[82Q]/+ mice. 2021 Sep 7 1
3 32878998 Ataxin-1 regulates B cell function and the severity of autoimmune experimental encephalomyelitis. 2020 Sep 22 2
4 29427101 Spinocerebellar Ataxia Type 1: Molecular Mechanisms of Neurodegeneration and Preclinical Studies. 2018 1
5 24594842 The histone deacetylase HDAC3 is essential for Purkinje cell function, potentially complicating the use of HDAC inhibitors in SCA1. 2014 Jul 15 4
6 24930030 Focused cerebellar laser light induced hyperthermia improves symptoms and pathology of polyglutamine disease SCA1 in a mouse model. 2014 Oct 2
7 22884877 LANP mediates neuritic pathology in Spinocerebellar ataxia type 1. 2012 Dec 4
8 22001907 Vascular endothelial growth factor ameliorates the ataxic phenotype in a mouse model of spinocerebellar ataxia type 1. 2011 Oct 16 4
9 20869591 SCA1-like disease in mice expressing wild-type ataxin-1 with a serine to aspartic acid replacement at residue 776. 2010 Sep 23 1
10 17322884 Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes. 2007 Mar 6
11 8789437 Cloning and developmental expression analysis of the murine homolog of the spinocerebellar ataxia type 1 gene (Sca1). 1996 Jan 3