131 related articles for article (PubMed ID: 37066173)
1. Bidirectional transcription at the
Zhou C; Liu HB; Bakhsh FJ; Wu B; Ying M; Margolis RL; Li PP
bioRxiv; 2023 Apr; ():. PubMed ID: 37066173
[TBL] [Abstract][Full Text] [Related]
2. Bidirectional Transcription at the PPP2R2B Gene Locus in Spinocerebellar Ataxia Type 12.
Zhou C; Liu HB; Jahanbakhsh F; Deng L; Wu B; Ying M; Margolis RL; Li PP
Mov Disord; 2023 Dec; 38(12):2230-2240. PubMed ID: 37735923
[TBL] [Abstract][Full Text] [Related]
3. Role of Bβ1 overexpression in the pathogenesis of SCA12.
Zhou C; Tang F; Dong T; Liu HB; Deng L; Margolis RL; Li PP
Mov Disord; 2024 May; ():. PubMed ID: 38798069
[TBL] [Abstract][Full Text] [Related]
4. Molecular clues unveiling spinocerebellar ataxia type-12 pathogenesis.
Kumar M; Sahni S; A V; Kumar D; Kushwah N; Goel D; Kapoor H; Srivastava AK; Faruq M
iScience; 2024 May; 27(5):109768. PubMed ID: 38711441
[TBL] [Abstract][Full Text] [Related]
5. Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12.
O'Hearn EE; Hwang HS; Holmes SE; Rudnicki DD; Chung DW; Seixas AI; Cohen RL; Ross CA; Trojanowski JQ; Pletnikova O; Troncoso JC; Margolis RL
Mov Disord; 2015 Nov; 30(13):1813-1824. PubMed ID: 26340331
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. The CAG repeat in SCA12 functions as a cis element to up-regulate PPP2R2B expression.
Lin CH; Chen CM; Hou YT; Wu YR; Hsieh-Li HM; Su MT; Lee-Chen GJ
Hum Genet; 2010 Aug; 128(2):205-12. PubMed ID: 20533062
[TBL] [Abstract][Full Text] [Related]
8. Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats in PPP2R2B.
Srivastava AK; Takkar A; Garg A; Faruq M
Brain; 2017 Jan; 140(1):27-36. PubMed ID: 27864267
[TBL] [Abstract][Full Text] [Related]
9. Spinocerebellar ataxia type 12: clues to pathogenesis.
Cohen RL; Margolis RL
Curr Opin Neurol; 2016 Dec; 29(6):735-742. PubMed ID: 27748686
[TBL] [Abstract][Full Text] [Related]
10. SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia.
Holmes SE; Hearn EO; Ross CA; Margolis RL
Brain Res Bull; 2001 Oct-Nov 1; 56(3-4):397-403. PubMed ID: 11719278
[TBL] [Abstract][Full Text] [Related]
11. Spinocerebellar ataxia type 12.
O'Hearn E; Holmes SE; Margolis RL
Handb Clin Neurol; 2012; 103():535-47. PubMed ID: 21827912
[TBL] [Abstract][Full Text] [Related]
12. Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.
Sato K; Yabe I; Fukuda Y; Soma H; Nakahara Y; Tsuji S; Sasaki H
Arch Neurol; 2010 Oct; 67(10):1257-62. PubMed ID: 20937954
[TBL] [Abstract][Full Text] [Related]
13. Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12.
Dong Y; Wu JJ; Wu ZY
Parkinsonism Relat Disord; 2015 Apr; 21(4):398-401. PubMed ID: 25634432
[TBL] [Abstract][Full Text] [Related]
14. Generation of an Induced pluripotent stem cell (iPSC) line (IGIBi011-A) from a Spinocerebellar ataxia type 12 gait dominant patient.
Zahra S; Kapoor H; Ahmad I; Kamai A; Srivastava AK; Faruq M
Stem Cell Res; 2024 Apr; 76():103319. PubMed ID: 38340452
[TBL] [Abstract][Full Text] [Related]
15. SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.
Fujigasaki H; Verma IC; Camuzat A; Margolis RL; Zander C; Lebre AS; Jamot L; Saxena R; Anand I; Holmes SE; Ross CA; Dürr A; Brice A
Ann Neurol; 2001 Jan; 49(1):117-21. PubMed ID: 11198281
[TBL] [Abstract][Full Text] [Related]
16. Generation of a human induced pluripotent stem cell line JHUi003-A with homozygous mutation for spinocerebellar ataxia type 12 using genome editing.
Feng H; Li Q; Margolis RL; Li PP
Stem Cell Res; 2021 May; 53():102346. PubMed ID: 34087983
[TBL] [Abstract][Full Text] [Related]
17. Generation of three spinocerebellar ataxia type-12 patients derived induced pluripotent stem cell lines (IGIBi002-A, IGIBi003-A and IGIBi004-A).
Kumar D; Hussain A; Srivastava AK; Mukerji M; Mukherjee O; Faruq M
Stem Cell Res; 2018 Aug; 31():216-221. PubMed ID: 30130680
[TBL] [Abstract][Full Text] [Related]
18. Evidence of a common founder for SCA12 in the Indian population.
Bahl S; Virdi K; Mittal U; Sachdeva MP; Kalla AK; Holmes SE; O'Hearn E; Margolis RL; Jain S; Srivastava AK; Mukerji M
Ann Hum Genet; 2005 Sep; 69(Pt 5):528-34. PubMed ID: 16138911
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial dysfunction and oxidative stress contribute to the pathogenesis of spinocerebellar ataxia type 12 (SCA12).
Wang YC; Lee CM; Lee LC; Tung LC; Hsieh-Li HM; Lee-Chen GJ; Su MT
J Biol Chem; 2011 Jun; 286(24):21742-54. PubMed ID: 21471219
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]