263 related articles for article (PubMed ID: 36199580)
1. The genetic and molecular features of the intronic pentanucleotide repeat expansion in spinocerebellar ataxia type 10.
Kurosaki T; Ashizawa T
Front Genet; 2022; 13():936869. PubMed ID: 36199580
[TBL] [Abstract][Full Text] [Related]
2. Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population.
Goel D; Suroliya V; Shamim U; Mathur A; Faruq M
eNeurologicalSci; 2019 Dec; 17():100211. PubMed ID: 31737797
[TBL] [Abstract][Full Text] [Related]
3. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
Matsuura T; Yamagata T; Burgess DL; Rasmussen A; Grewal RP; Watase K; Khajavi M; McCall AE; Davis CF; Zu L; Achari M; Pulst SM; Alonso E; Noebels JL; Nelson DL; Zoghbi HY; Ashizawa T
Nat Genet; 2000 Oct; 26(2):191-4. PubMed ID: 11017075
[TBL] [Abstract][Full Text] [Related]
4. [Spinocerebellar ataxia type 10 (SCA10): a disease caused by a novel pentanucleotide repeat expansion].
Ashizawa T; Matsuura T
Rinsho Shinkeigaku; 2001 Dec; 41(12):1120-2. PubMed ID: 12235814
[TBL] [Abstract][Full Text] [Related]
5. [Molecular and genetic analysis of spinocerebellar ataxia type 10 (SCA10)].
Matsuura T
Rinsho Shinkeigaku; 2008 Jan; 48(1):1-10. PubMed ID: 18386626
[TBL] [Abstract][Full Text] [Related]
6. ATTCT and ATTCC repeat expansions in the ATXN10 gene affect disease penetrance of spinocerebellar ataxia type 10.
Morato Torres CA; Zafar F; Tsai YC; Vazquez JP; Gallagher MD; McLaughlin I; Hong K; Lai J; Lee J; Chirino-Perez A; Romero-Molina AO; Torres F; Fernandez-Ruiz J; Ashizawa T; Ziegle J; Jiménez Gil FJ; Schüle B
HGG Adv; 2022 Oct; 3(4):100137. PubMed ID: 36092952
[TBL] [Abstract][Full Text] [Related]
7. [Molecular and genetic analysis of spinocerebellar ataxia type 10 (SCA10)].
Matsuura T
Rinsho Shinkeigaku; 2008 Nov; 48(11):823-5. PubMed ID: 19198092
[TBL] [Abstract][Full Text] [Related]
8. Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: a toxic RNA gain-of-function model.
White M; Xia G; Gao R; Wakamiya M; Sarkar PS; McFarland K; Ashizawa T
J Neurosci Res; 2012 Mar; 90(3):706-14. PubMed ID: 22065565
[TBL] [Abstract][Full Text] [Related]
9. Parkinson's disease associated with pure
Schüle B; McFarland KN; Lee K; Tsai YC; Nguyen KD; Sun C; Liu M; Byrne C; Gopi R; Huang N; Langston JW; Clark T; Gil FJJ; Ashizawa T
NPJ Parkinsons Dis; 2017; 3():27. PubMed ID: 28890930
[TBL] [Abstract][Full Text] [Related]
10. Spinocerebellar Ataxia Type 10 with Atypical Clinical Manifestation in Han Chinese.
Mao C; Li X; Su Y; Luo H; Fan L; Zheng H; Fan Y; Yang Z; Zhang S; Hu Z; Hao X; Shi C; Xu Y
Cerebellum; 2023 Jun; 22(3):355-362. PubMed ID: 35441258
[TBL] [Abstract][Full Text] [Related]
11. A FEMALE CASE OF SPINOCEREBELLAR ATAXIA TYPE 10 WITH SUICIDAL BEHAVIOR AND ENDOCRINPATHIES ASSOCIATED WITH A MASSIVE EXPANSION (ATTCT) OF THE GENE ATXN10.
Ramirez-Garcia SA; Sánchez-Corona J; Volpini-Bertran V; Moran-Moguel MC; Gutiérrez-Rubio SA; Castañeda-Cisneros G; Jiménez-Gil J; Garcia-Cruz D
Actas Esp Psiquiatr; 2022 Jan; 50(1):58-62. PubMed ID: 35103298
[TBL] [Abstract][Full Text] [Related]
12. Inheritance patterns of ATCCT repeat interruptions in spinocerebellar ataxia type 10 (SCA10) expansions.
Landrian I; McFarland KN; Liu J; Mulligan CJ; Rasmussen A; Ashizawa T
PLoS One; 2017; 12(4):e0175958. PubMed ID: 28423040
[TBL] [Abstract][Full Text] [Related]
13. Recent progress in spinocerebellar ataxia type-10 (SCA10).
Lin X; Ashizawa T
Cerebellum; 2005; 4(1):37-42. PubMed ID: 15895557
[TBL] [Abstract][Full Text] [Related]
14. Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?
Matsuura T; Fang P; Pearson CE; Jayakar P; Ashizawa T; Roa BB; Nelson DL
Am J Hum Genet; 2006 Jan; 78(1):125-9. PubMed ID: 16385455
[TBL] [Abstract][Full Text] [Related]
15. Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.
Bampi GB; Bisso-Machado R; Hünemeier T; Gheno TC; Furtado GV; Veliz-Otani D; Cornejo-Olivas M; Mazzeti P; Bortolini MC; Jardim LB; Saraiva-Pereira ML;
Neuromolecular Med; 2017 Dec; 19(4):501-509. PubMed ID: 28905220
[TBL] [Abstract][Full Text] [Related]
16. Transgenic models of spinocerebellar ataxia type 10: modeling a repeat expansion disorder.
McFarland KN; Ashizawa T
Genes (Basel); 2012 Sep; 3(3):481-491. PubMed ID: 24533179
[TBL] [Abstract][Full Text] [Related]
17. Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.
McFarland KN; Liu J; Landrian I; Zeng D; Raskin S; Moscovich M; Gatto EM; Ochoa A; Teive HA; Rasmussen A; Ashizawa T
Neurogenetics; 2014 Mar; 15(1):59-64. PubMed ID: 24318420
[TBL] [Abstract][Full Text] [Related]
18. The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10.
Wakamiya M; Matsuura T; Liu Y; Schuster GC; Gao R; Xu W; Sarkar PS; Lin X; Ashizawa T
Neurology; 2006 Aug; 67(4):607-13. PubMed ID: 16924013
[TBL] [Abstract][Full Text] [Related]
19. SMRT Sequencing of Long Tandem Nucleotide Repeats in SCA10 Reveals Unique Insight of Repeat Expansion Structure.
McFarland KN; Liu J; Landrian I; Godiska R; Shanker S; Yu F; Farmerie WG; Ashizawa T
PLoS One; 2015; 10(8):e0135906. PubMed ID: 26295943
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
