polyglutamine

ataxin 2 ; Homo sapiens







96 Article(s)
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1 34350994 The RNA-binding protein and stress granule component ATAXIN-2 is expressed in mouse and human tissues associated with glaucoma pathogenesis. 2022 Feb 2
2 35511239 Parallel Appearance of Polyglutamine and Transactivation-Responsive DNA-Binding Protein 43 and Their Complementary Subcellular Localization in Brains of Patients With Spinocerebellar Ataxia Type 2. 2022 Jun 20 5
3 35521889 ATXN2 intermediate expansions in amyotrophic lateral sclerosis. 2022 May 6 5
4 34390268 RNA Toxicity and Perturbation of rRNA Processing in Spinocerebellar Ataxia Type 2. 2021 Nov 2
5 34565721 Effect of CAG repeats on the age at onset of patients with spinocerebellar ataxia type 2 in China. 2021 Aug 28 1
6 34845184 Autophagy in Spinocerebellar ataxia type 2, a dysregulated pathway, and a target for therapy. 2021 Nov 29 2
7 32581673 The Mechanisms of Nuclear Proteotoxicity in Polyglutamine Spinocerebellar Ataxias. 2020 1
8 32581696 Gene Deregulation and Underlying Mechanisms in Spinocerebellar Ataxias With Polyglutamine Expansion. 2020 1
9 32962458 Polyglutamine spinocerebellar ataxias: emerging therapeutic targets. 2020 Nov 2
10 30707359 EvoPPI 1.0: a Web Platform for Within- and Between-Species Multiple Interactome Comparisons and Application to Nine PolyQ Proteins Determining Neurodegenerative Diseases. 2019 Mar 2
11 30718627 Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology. 2019 Feb 4 1
12 31435879 Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2. 2019 Oct 3
13 33324888 New alternative splicing variants of the ATXN2 transcript. 2019 1
14 29080331 OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia. 2018 Jan 2
15 29427103 Spinocerebellar Ataxia Type 2. 2018 4
16 29653012 [Advance in research on spinocerebellar ataxia 2]. 2018 Apr 10 1
17 29869836 Ataxin-2: A versatile posttranscriptional regulator and its implication in neural function. 2018 Nov 1
18 30194296 Staufen1 links RNA stress granules and autophagy in a model of neurodegeneration. 2018 Sep 7 3
19 30417124 Conserved Pbp1/Ataxin-2 regulates retrotransposon activity and connects polyglutamine expansion-driven protein aggregation to lifespan-controlling rDNA repeats. 2018 1
20 30473770 Recent advances in understanding dominant spinocerebellar ataxias from clinical and genetic points of view. 2018 2
21 26861241 Effects of the enlargement of polyglutamine segments on the structure and folding of ataxin-2 and ataxin-3 proteins. 2017 Feb 2
22 27494456 C9ORF72 is a GDP/GTP exchange factor for Rab8 and Rab39 and regulates autophagy. 2017 Jul 3 2
23 28527524 C9orf72 hexanucleotide repeat expansions and Ataxin 2 intermediate length repeat expansions in Indian patients with amyotrophic lateral sclerosis. 2017 Aug 1
24 26510381 Fragment based G-QSAR and molecular dynamics based mechanistic simulations into hydroxamic-based HDAC inhibitors against spinocerebellar ataxia. 2016 Oct 3
25 26733254 ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion. 2016 Mar 1
26 27103069 Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death. 2016 Jun 15 2
27 27531668 ATXN2-AS, a gene antisense to ATXN2, is associated with spinocerebellar ataxia type 2 and amyotrophic lateral sclerosis. 2016 Oct 4
28 27597528 Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels. 2016 Dec 4
29 25457026 Intermediate-length polyglutamine in ATXN2 is a possible risk factor among Eastern Chinese patients with amyotrophic lateral sclerosis. 2015 Mar 4
30 25527265 ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 2015 Jan 20 3
31 26086378 Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat. 2015 1
32 26208502 ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry. 2015 Oct 2
33 23889603 TDP-43 pathology in polyglutamine diseases: with reference to amyotrphic lateral sclerosis. 2014 Feb 1
34 24269018 Evaluating noncoding nucleotide repeat expansions in amyotrophic lateral sclerosis. 2014 Apr 1
35 24534762 Evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease. 2014 Jul 2
36 24718895 FTLD-ALS of TDP-43 type and SCA2 in a family with a full ataxin-2 polyglutamine expansion. 2014 Oct 6
37 24954906 Direct binding of Ataxin-2 to distinct elements in 3' UTRs promotes mRNA stability and protein expression. 2014 Jul 17 1
38 25027299 Insights into the evolution and domain structure of Ataxin-2 proteins across eukaryotes. 2014 Jul 15 3
39 25098532 Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders. 2014 Sep 9 6
40 22996397 Spinocerebellar ataxia type 2: clinical presentation, molecular mechanisms, and therapeutic perspectives. 2013 Feb 2
41 23172909 Ataxin-2 interacts with FUS and intermediate-length polyglutamine expansions enhance FUS-related pathology in amyotrophic lateral sclerosis. 2013 Feb 15 1
42 23224816 Generation of human-induced pluripotent stem cells to model spinocerebellar ataxia type 2 in vitro. 2013 Oct 2
43 23735416 Quantitative profiling and identification of plasma proteins of spinocerebellar ataxia type 2 patients. 2013 1
44 21889984 The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect. 2012 Jan 5
45 22035589 Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts. 2012 May 7
46 22526021 Distinct TDP-43 pathology in ALS patients with ataxin 2 intermediate-length polyQ expansions. 2012 Aug 4
47 22684686 Brain pathology of spinocerebellar ataxias. 2012 Jul 1
48 22764223 ALS-associated ataxin 2 polyQ expansions enhance stress-induced caspase 3 activation and increase TDP-43 pathological modifications. 2012 Jul 4 8
49 22868089 ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegia. 2012 Oct 15 3
50 22916186 ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population. 2012 9