polyglutamine

ataxin 2 ; Homo sapiens







96 Article(s)
Download
PMID
Title
Pub. Year
#Total Relationships
51 22956915 ATXN2-CAG42 sequesters PABPC1 into insolubility and induces FBXW8 in cerebellum of old ataxic knock-in mice. 2012 3
52 23196570 [Conjoint pathological cascades mediated by RNA-binding proteins, TDP-43, FUS and ataxin-2]. 2012 2
53 23197749 Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis. 2012 Dec 11 8
54 21292779 Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients. 2011 May 1 5
55 21399888 A comprehensive review of spinocerebellar ataxia type 2 in Cuba. 2011 Jun 3
56 21479228 PolyQ repeat expansions in ATXN2 associated with ALS are CAA interrupted repeats. 2011 Mar 29 10
57 21562248 Evaluating the prevalence of polyglutamine repeat expansions in amyotrophic lateral sclerosis. 2011 Jun 14 3
58 21660502 Model organisms reveal insight into human neurodegenerative disease: ataxin-2 intermediate-length polyglutamine expansions are a risk factor for ALS. 2011 Nov 6
59 21741123 Ataxin-2 intermediate-length polyglutamine: a possible risk factor for Chinese patients with amyotrophic lateral sclerosis. 2011 Oct 7
60 20740007 Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS. 2010 Aug 26 3
61 21105231 Motor neuron disease: polyQ expansions in ataxin-2—a risk factor for amyotrophic lateral sclerosis? 2010 Nov 1
62 19201647 Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2. 2009 Mar 1
63 20030245 [Molecular genetic approach to spinocerebellar ataxias]. 2009 Nov 1
64 26023252 Therapeutic prospects for spinocerebellar ataxia type 2 and 3. 2009 Dec 3
65 18236424 Birth after pre-implantation genetic diagnosis (PGD) of spinocerebellar ataxia 2 (Sca2). 2008 Feb 3
66 18418684 Spinocerebellar ataxia 2 (SCA2). 2008 1
67 18499737 Spinocerebellar ataxia type 2 (SCA2): clinical features and genetic analysis. 2008 Oct 2
68 19043961 [Molecular analysis of the CAG repeat among patients with Type-2 spinocerebellar ataxia in the Mexican population]. 2008 Sep-Oct 3
69 17097639 Parkin is an E3 ubiquitin-ligase for normal and mutant ataxin-2 and prevents ataxin-2-induced cell death. 2007 Feb 3
70 17392519 Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules. 2007 Apr 2
71 15663938 An integrative approach to gain insights into the cellular function of human ataxin-2. 2005 Feb 11 5
72 15747371 Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort. 2005 Apr 1
73 15827014 Saccade velocity as a surrogate disease marker in spinocerebellar ataxia type 2. 2005 Apr 1
74 15895563 The pathogenesis of spinocerebellar ataxia. 2005 1
75 16023918 Partial resistance of ataxin-2-containing olivary and pontine neurons to axotomy-induced degeneration. 2005 Aug 15 4
76 16115810 Ataxin-2 and huntingtin interact with endophilin-A complexes to function in plastin-associated pathways. 2005 Oct 1 1
77 16128876 Positron emission tomography and magnetic resonance imaging in spinocerebellar ataxia type 2: a study of symptomatic and asymptomatic individuals. 2005 Sep 3
78 17132942 Molecular genetics of spinocerebellar ataxia type 8 (SCA8). 2005 Apr 1
79 12490063 Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats. 2002 Fall 5
80 11305872 Recruitment of nonexpanded polyglutamine proteins to intranuclear aggregates in neuronal intranuclear hyaline inclusion disease. 2001 Apr 1
81 11471052 Identification and expression of a mouse ortholog of A2BP1. 2001 Aug 3
82 11563629 Non-expanded polyglutamine proteins in intranuclear inclusions of hereditary ataxias--triple-labeling immunofluorescence study. 2001 Aug 1
83 11719247 Transglutaminase-dependent formation of protein aggregates as possible biochemical mechanism for polyglutamine diseases. 2001 Oct-Nov 1 1
84 10712199 High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles. 2000 Mar 1
85 10915763 CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2). 2000 Jul 22 1
86 10928570 The molecular biology of the autosomal-dominant cerebellar ataxias. 2000 Jul 1
87 10970064 Recent advances in degenerative ataxias. 2000 Aug 1
88 10210910 Clinical and molecular analysis of 11 Sicilian SCA2 families: influence of gender on age at onset. 1999 May 1
89 10222770 [Correlation of clinichopathological features and CAG repeats in SCA2]. 1999 Apr 1
90 10353790 Linkage disequilibrium at the SCA2 locus. 1999 May 2
91 10478584 Identification of five spinocerebellar ataxia type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan. 1999 Sep 2
92 10505630 Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study. 1999 Oct 1 4
93 9112595 Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus. 1997 Apr 1
94 9158145 Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families. 1997 May 2
95 8896556 Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT. 1996 Nov 1
96 7477379 Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias. 1995 Nov 23 1