178 related articles for article (PubMed ID: 18940801)
1. 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]
2. N-terminal phosphorylation of protein phosphatase 2A/Bβ2 regulates translocation to mitochondria, dynamin-related protein 1 dephosphorylation, and neuronal survival.
Merrill RA; Slupe AM; Strack S
FEBS J; 2013 Jan; 280(2):662-73. PubMed ID: 22583914
[TBL] [Abstract][Full Text] [Related]
3. Deletion of a Neuronal Drp1 Activator Protects against Cerebral Ischemia.
Flippo KH; Lin Z; Dickey AS; Zhou X; Dhanesha NA; Walters GC; Liu Y; Merrill RA; Meller R; Simon RP; Chauhan AK; Usachev YM; Strack S
J Neurosci; 2020 Apr; 40(15):3119-3129. PubMed ID: 32144179
[TBL] [Abstract][Full Text] [Related]
4. A developmentally regulated, neuron-specific splice variant of the variable subunit Bbeta targets protein phosphatase 2A to mitochondria and modulates apoptosis.
Dagda RK; Zaucha JA; Wadzinski BE; Strack S
J Biol Chem; 2003 Jul; 278(27):24976-85. PubMed ID: 12716901
[TBL] [Abstract][Full Text] [Related]
5. Unfolding-resistant translocase targeting: a novel mechanism for outer mitochondrial membrane localization exemplified by the Bbeta2 regulatory subunit of protein phosphatase 2A.
Dagda RK; Barwacz CA; Cribbs JT; Strack S
J Biol Chem; 2005 Jul; 280(29):27375-82. PubMed ID: 15923182
[TBL] [Abstract][Full Text] [Related]
6. Oxidative stress promotes autophagic cell death in human neuroblastoma cells with ectopic transfer of mitochondrial PPP2R2B (Bbeta2).
Cheng WT; Guo ZX; Lin CA; Lin MY; Tung LC; Fang K
BMC Cell Biol; 2009 Dec; 10():91. PubMed ID: 20017961
[TBL] [Abstract][Full Text] [Related]
7. Differential autophagic cell death under stress with ectopic cytoplasmic and mitochondrial-specific PPP2R2B in human neuroblastoma cells.
Fang K; Li HF; Hsieh CH; Li DY; Song DC; Cheng WT; Guo ZX
Apoptosis; 2013 May; 18(5):627-38. PubMed ID: 23381641
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. PKA/AKAP1 and PP2A/Bβ2 regulate neuronal morphogenesis via Drp1 phosphorylation and mitochondrial bioenergetics.
Dickey AS; Strack S
J Neurosci; 2011 Nov; 31(44):15716-26. PubMed ID: 22049414
[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. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. Tongue Protrusion and Feeding Dystonia Can Develop in PPP2R2B-Related Spinocerebellar Ataxia.
Neo S; Magrinelli F; Cordivari C; Bhatia KP
Mov Disord Clin Pract; 2024 May; 11(5):578-579. PubMed ID: 38419473
[No Abstract] [Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]