These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
293 related articles for article (PubMed ID: 29427103)
1. Spinocerebellar Ataxia Type 2. Scoles DR; Pulst SM Adv Exp Med Biol; 2018; 1049():175-195. PubMed ID: 29427103 [TBL] [Abstract][Full Text] [Related]
2. Ataxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse model. Dansithong W; Paul S; Figueroa KP; Rinehart MD; Wiest S; Pflieger LT; Scoles DR; Pulst SM PLoS Genet; 2015 Apr; 11(4):e1005182. PubMed ID: 25902068 [TBL] [Abstract][Full Text] [Related]
3. ATXN2-AS, a gene antisense to ATXN2, is associated with spinocerebellar ataxia type 2 and amyotrophic lateral sclerosis. Li PP; Sun X; Xia G; Arbez N; Paul S; Zhu S; Peng HB; Ross CA; Koeppen AH; Margolis RL; Pulst SM; Ashizawa T; Rudnicki DD Ann Neurol; 2016 Oct; 80(4):600-15. PubMed ID: 27531668 [TBL] [Abstract][Full Text] [Related]
4. Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat. Scoles DR; Ho MH; Dansithong W; Pflieger LT; Petersen LW; Thai KK; Pulst SM PLoS One; 2015; 10(6):e0128769. PubMed ID: 26086378 [TBL] [Abstract][Full Text] [Related]
5. Gene co-expression network analysis for identifying modules and functionally enriched pathways in SCA2. Pflieger LT; Dansithong W; Paul S; Scoles DR; Figueroa KP; Meera P; Otis TS; Facelli JC; Pulst SM Hum Mol Genet; 2017 Aug; 26(16):3069-3080. PubMed ID: 28525545 [TBL] [Abstract][Full Text] [Related]
6. The polyglutamine protein ATXN2: from its molecular functions to its involvement in disease. Costa RG; Conceição A; Matos CA; Nóbrega C Cell Death Dis; 2024 Jun; 15(6):415. PubMed ID: 38877004 [TBL] [Abstract][Full Text] [Related]
7. In Human and Mouse Spino-Cerebellar Tissue, Ataxin-2 Expansion Affects Ceramide-Sphingomyelin Metabolism. Sen NE; Arsovic A; Meierhofer D; Brodesser S; Oberschmidt C; Canet-Pons J; Kaya ZE; Halbach MV; Gispert S; Sandhoff K; Auburger G Int J Mol Sci; 2019 Nov; 20(23):. PubMed ID: 31766565 [TBL] [Abstract][Full Text] [Related]
8. Generation of an Atxn2-CAG100 knock-in mouse reveals N-acetylaspartate production deficit due to early Nat8l dysregulation. Sen NE; Canet-Pons J; Halbach MV; Arsovic A; Pilatus U; Chae WH; Kaya ZE; Seidel K; Rollmann E; Mittelbronn M; Meierhofer D; De Zeeuw CI; Bosman LWJ; Gispert S; Auburger G Neurobiol Dis; 2019 Dec; 132():104559. PubMed ID: 31376479 [TBL] [Abstract][Full Text] [Related]
9. [Advance in research on spinocerebellar ataxia 2]. Jing F; Yang D; Chen T Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):284-287. PubMed ID: 29653012 [TBL] [Abstract][Full Text] [Related]
10. Atxn2 Knockout and CAG42-Knock-in Cerebellum Shows Similarly Dysregulated Expression in Calcium Homeostasis Pathway. Halbach MV; Gispert S; Stehning T; Damrath E; Walter M; Auburger G Cerebellum; 2017 Feb; 16(1):68-81. PubMed ID: 26868665 [TBL] [Abstract][Full Text] [Related]
11. Generation of Spinocerebellar Ataxia Type 2 induced pluripotent stem cell lines, CHOPi002-A and CHOPi003-A, from patients with abnormal CAG repeats in the coding region of the ATXN2 gene. Maguire JA; Gagne AL; Gonzalez-Alegre P; Davidson BL; Shakkottai V; Gadue P; French DL Stem Cell Res; 2019 Jan; 34():101361. PubMed ID: 30611021 [TBL] [Abstract][Full Text] [Related]
12. Simultaneous ALS and SCA2 associated with an intermediate-length Ghahremani Nezhad H; Franklin JP; Alix JJP; Moll T; Pattrick M; Cooper-Knock J; Shanmugarajah P; Beauchamp NJ; Hadjivissiliou M; Paling D; Mcdermott C; Shaw PJ; Jenkins TM Amyotroph Lateral Scler Frontotemporal Degener; 2021 Nov; 22(7-8):579-582. PubMed ID: 33284045 [TBL] [Abstract][Full Text] [Related]
14. Toxicity of pathogenic ataxin-2 in Drosophila shows dependence on a pure CAG repeat sequence. McGurk L; Rifai OM; Shcherbakova O; Perlegos AE; Byrns CN; Carranza FR; Zhou HW; Kim HJ; Zhu Y; Bonini NM Hum Mol Genet; 2021 Sep; 30(19):1797-1810. PubMed ID: 34077532 [TBL] [Abstract][Full Text] [Related]
15. Electrophysiological Studies Support Utility of Positive Modulators of SK Channels for the Treatment of Spinocerebellar Ataxia Type 2. Egorova PA; Bezprozvanny IB Cerebellum; 2022 Oct; 21(5):742-749. PubMed ID: 34978024 [TBL] [Abstract][Full Text] [Related]
16. TR-FRET-Based Immunoassay to Measure Ataxin-2 as a Target Engagement Marker in Spinocerebellar Ataxia Type 2. Bux J; Sen NE; Klink IM; Hauser S; Synofzik M; Schöls L; Auburger G; Riess O; Hübener-Schmid J Mol Neurobiol; 2023 Jun; 60(6):3553-3567. PubMed ID: 36894829 [TBL] [Abstract][Full Text] [Related]
17. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds. Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629 [TBL] [Abstract][Full Text] [Related]
18. AAV-Mediated CAG-Targeting Selectively Reduces Polyglutamine-Expanded Protein and Attenuates Disease Phenotypes in a Spinocerebellar Ataxia Mouse Model. Niewiadomska-Cimicka A; Fievet L; Surdyka M; Jesion E; Keime C; Singer E; Eisenmann A; Kalinowska-Poska Z; Nguyen HHP; Fiszer A; Figiel M; Trottier Y Int J Mol Sci; 2024 Apr; 25(8):. PubMed ID: 38673939 [TBL] [Abstract][Full Text] [Related]
20. SCA2 in the Indian population: Unified haplotype and variable phenotypic patterns in a large case series. Sonakar AK; Shamim U; Srivastava MP; Faruq M; Srivastava AK Parkinsonism Relat Disord; 2021 Aug; 89():139-145. PubMed ID: 34298214 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]