BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 37735923)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Generation of a human induced pluripotent stem cell line JHUi004-A with heterozygous mutation for spinocerebellar ataxia type 12 using genome editing.
    Liu HB; Dong T; Deng L; Zhou C; Tang F; Margolis RL; Li PP
    Stem Cell Res; 2024 Jun; 77():103441. PubMed ID: 38759410
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 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. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. The spinocerebellar ataxia 12 gene product and protein phosphatase 2A regulatory subunit Bbeta2 antagonizes neuronal survival by promoting mitochondrial fission.
    Dagda RK; Merrill RA; Cribbs JT; Chen Y; Hell JW; Usachev YM; Strack S
    J Biol Chem; 2008 Dec; 283(52):36241-8. PubMed ID: 18940801
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.