313 related articles for article (PubMed ID: 35563872)
1. Mechanistic and Therapeutic Insights into Ataxic Disorders with Pentanucleotide Expansions.
Zhang N; Ashizawa T
Cells; 2022 May; 11(9):. PubMed ID: 35563872
[TBL] [Abstract][Full Text] [Related]
2. Molecular Mechanisms and Future Therapeutics for Spinocerebellar Ataxia Type 31 (SCA31).
Ishikawa K; Nagai Y
Neurotherapeutics; 2019 Oct; 16(4):1106-1114. PubMed ID: 31755042
[TBL] [Abstract][Full Text] [Related]
3. A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia.
Seixas AI; Loureiro JR; Costa C; Ordóñez-Ugalde A; Marcelino H; Oliveira CL; Loureiro JL; Dhingra A; Brandão E; Cruz VT; Timóteo A; Quintáns B; Rouleau GA; Rizzu P; Carracedo Á; Bessa J; Heutink P; Sequeiros J; Sobrido MJ; Coutinho P; Silveira I
Am J Hum Genet; 2017 Jul; 101(1):87-103. PubMed ID: 28686858
[TBL] [Abstract][Full Text] [Related]
4. Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37.
Corral-Juan M; Serrano-Munuera C; Rábano A; Cota-González D; Segarra-Roca A; Ispierto L; Cano-Orgaz AT; Adarmes AD; Méndez-Del-Barrio C; Jesús S; Mir P; Volpini V; Alvarez-Ramo R; Sánchez I; Matilla-Dueñas A
Brain; 2018 Jul; 141(7):1981-1997. PubMed ID: 29939198
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Molecular Mechanisms in Pentanucleotide Repeat Diseases.
Loureiro JR; Castro AF; Figueiredo AS; Silveira I
Cells; 2022 Jan; 11(2):. PubMed ID: 35053321
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. [Spinocerebellar ataxia type 31].
Ishikawa K; Sato N; Niimi Y; Amino T; Mizusawa H
Rinsho Shinkeigaku; 2010 Nov; 50(11):985-7. PubMed ID: 21921537
[TBL] [Abstract][Full Text] [Related]
9. Pentanucleotide repeat-related disorders: Genetics and bioinformatic discovery and detection.
Silveira I; Bennett MF
Epilepsia; 2023 Jun; 64 Suppl 1():S22-S30. PubMed ID: 36960686
[TBL] [Abstract][Full Text] [Related]
10. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Brusco A; Gellera C; Cagnoli C; Saluto A; Castucci A; Michielotto C; Fetoni V; Mariotti C; Migone N; Di Donato S; Taroni F
Arch Neurol; 2004 May; 61(5):727-33. PubMed ID: 15148151
[TBL] [Abstract][Full Text] [Related]
11. Abnormal RNA structures (RNA foci) containing a penta-nucleotide repeat (UGGAA)n in the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis.
Niimi Y; Takahashi M; Sugawara E; Umeda S; Obayashi M; Sato N; Ishiguro T; Higashi M; Eishi Y; Mizusawa H; Ishikawa K
Neuropathology; 2013 Dec; 33(6):600-11. PubMed ID: 23607545
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. The molecular mechanisms of spinocerebellar ataxias for DNA repeat expansion in disease.
Kumar M; Tyagi N; Faruq M
Emerg Top Life Sci; 2023 Dec; 7(3):289-312. PubMed ID: 37668011
[TBL] [Abstract][Full Text] [Related]
14. Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31.
Ishiguro T; Sato N; Ueyama M; Fujikake N; Sellier C; Kanegami A; Tokuda E; Zamiri B; Gall-Duncan T; Mirceta M; Furukawa Y; Yokota T; Wada K; Taylor JP; Pearson CE; Charlet-Berguerand N; Mizusawa H; Nagai Y; Ishikawa K
Neuron; 2017 Apr; 94(1):108-124.e7. PubMed ID: 28343865
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. [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]
18. 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]
19. Solution Nuclear Magnetic Resonance Structures of ATTTT and ATTTC Pentanucleotide Repeats Associated with SCA37 and FAMEs.
Li J; Wan L; Wang Y; Chen Y; Lee HK; Lam SL; Guo P
ACS Chem Neurosci; 2023 Jan; 14(2):289-299. PubMed ID: 36580663
[TBL] [Abstract][Full Text] [Related]
20. Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.
McFarland KN; Liu J; Landrian I; Gao R; Sarkar PS; Raskin S; Moscovich M; Gatto EM; Teive HA; Ochoa A; Rasmussen A; Ashizawa T
Eur J Hum Genet; 2013 Nov; 21(11):1272-6. PubMed ID: 23443018
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
