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Items: 1 to 20 of 25


Motor and Cerebellar Architectural Abnormalities during the Early Progression of Ataxia in a Mouse Model of SCA1 and How Early Prevention Leads to a Better Outcome Later in Life.

Ibrahim MF, Power EM, Potapov K, Empson RM.

Front Cell Neurosci. 2017 Sep 20;11:292. doi: 10.3389/fncel.2017.00292. eCollection 2017.


The Multiple Faces of Spinocerebellar Ataxia type 2.

Antenora A, Rinaldi C, Roca A, Pane C, Lieto M, Saccà F, Peluso S, De Michele G, Filla A.

Ann Clin Transl Neurol. 2017 Aug 10;4(9):687-695. doi: 10.1002/acn3.437. eCollection 2017 Sep. Review.


Ataxin-2: From RNA Control to Human Health and Disease.

Ostrowski LA, Hall AC, Mekhail K.

Genes (Basel). 2017 Jun 5;8(6). pii: E157. doi: 10.3390/genes8060157. Review.


Gene co-expression network analysis for identifying modules and functionally enriched pathways in SCA2.

Pflieger LT, Dansithong W, Paul S, Scoles DR, Figueroa KP, Meera P, Otis TS, Facelli JC, Pulst SM.

Hum Mol Genet. 2017 Aug 15;26(16):3069-3080. doi: 10.1093/hmg/ddx191.


Loss of the golgin GM130 causes Golgi disruption, Purkinje neuron loss, and ataxia in mice.

Liu C, Mei M, Li Q, Roboti P, Pang Q, Ying Z, Gao F, Lowe M, Bao S.

Proc Natl Acad Sci U S A. 2017 Jan 10;114(2):346-351. doi: 10.1073/pnas.1608576114. Epub 2016 Dec 27.


Motor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive Review.

Alves-Cruzeiro JM, Mendonça L, Pereira de Almeida L, Nóbrega C.

Front Neurosci. 2016 Dec 15;10:572. doi: 10.3389/fnins.2016.00572. eCollection 2016. Review.


Epithelial-to-mesenchymal transition drives a pro-metastatic Golgi compaction process through scaffolding protein PAQR11.

Tan X, Banerjee P, Guo HF, Ireland S, Pankova D, Ahn YH, Nikolaidis IM, Liu X, Zhao Y, Xue Y, Burns AR, Roybal J, Gibbons DL, Zal T, Creighton CJ, Ungar D, Wang Y, Kurie JM.

J Clin Invest. 2017 Jan 3;127(1):117-131. doi: 10.1172/JCI88736. Epub 2016 Nov 21.


Drosophila ataxin-2 gene encodes two differentially expressed isoforms and its function in larval fat body is crucial for development of peripheral tissues.

Vianna MC, Poleto DC, Gomes PF, Valente V, Paçó-Larson ML.

FEBS Open Bio. 2016 Oct 7;6(11):1040-1053. eCollection 2016 Nov.


The RNA-binding protein ATX-2 regulates cytokinesis through PAR-5 and ZEN-4.

Gnazzo MM, Uhlemann EE, Villarreal AR, Shirayama M, Dominguez EG, Skop AR.

Mol Biol Cell. 2016 Oct 15;27(20):3052-3064. Epub 2016 Aug 24.


Nuclear retention of full-length HTT RNA is mediated by splicing factors MBNL1 and U2AF65.

Sun X, Li PP, Zhu S, Cohen R, Marque LO, Ross CA, Pulst SM, Chan HY, Margolis RL, Rudnicki DD.

Sci Rep. 2015 Jul 28;5:12521. doi: 10.1038/srep12521.


Genetic ablation of ataxin-2 increases several global translation factors in their transcript abundance but decreases translation rate.

Fittschen M, Lastres-Becker I, Halbach MV, Damrath E, Gispert S, Azizov M, Walter M, Müller S, Auburger G.

Neurogenetics. 2015 Jul;16(3):181-92. doi: 10.1007/s10048-015-0441-5. Epub 2015 Feb 27.


Insights into the evolution and domain structure of Ataxin-2 proteins across eukaryotes.

Jiménez-López D, Guzmán P.

BMC Res Notes. 2014 Jul 15;7:453. doi: 10.1186/1756-0500-7-453.


A CREB3-ARF4 signalling pathway mediates the response to Golgi stress and susceptibility to pathogens.

Reiling JH, Olive AJ, Sanyal S, Carette JE, Brummelkamp TR, Ploegh HL, Starnbach MN, Sabatini DM.

Nat Cell Biol. 2013 Dec;15(12):1473-85. doi: 10.1038/ncb2865. Epub 2013 Nov 3.


Increased neuronal activity fragments the Golgi complex.

Thayer DA, Jan YN, Jan LY.

Proc Natl Acad Sci U S A. 2013 Jan 22;110(4):1482-7. doi: 10.1073/pnas.1220978110. Epub 2013 Jan 7.


ETS1 regulates the expression of ATXN2.

Scoles DR, Pflieger LT, Thai KK, Hansen ST, Dansithong W, Pulst SM.

Hum Mol Genet. 2012 Dec 1;21(23):5048-65. doi: 10.1093/hmg/dds349. Epub 2012 Aug 21.


ALS-associated ataxin 2 polyQ expansions enhance stress-induced caspase 3 activation and increase TDP-43 pathological modifications.

Hart MP, Gitler AD.

J Neurosci. 2012 Jul 4;32(27):9133-42. doi: 10.1523/JNEUROSCI.0996-12.2012.


Cell biology of spinocerebellar ataxia.

Orr HT.

J Cell Biol. 2012 Apr 16;197(2):167-77. doi: 10.1083/jcb.201105092. Review.


Massive expansion of SCA2 with autonomic dysfunction, retinitis pigmentosa, and infantile spasms.

Paciorkowski AR, Shafrir Y, Hrivnak J, Patterson MC, Tennison MB, Clark HB, Gomez CM.

Neurology. 2011 Sep 13;77(11):1055-60. doi: 10.1212/WNL.0b013e31822e5627. Epub 2011 Aug 31.


Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS.

Elden AC, Kim HJ, Hart MP, Chen-Plotkin AS, Johnson BS, Fang X, Armakola M, Geser F, Greene R, Lu MM, Padmanabhan A, Clay-Falcone D, McCluskey L, Elman L, Juhr D, Gruber PJ, Rüb U, Auburger G, Trojanowski JQ, Lee VM, Van Deerlin VM, Bonini NM, Gitler AD.

Nature. 2010 Aug 26;466(7310):1069-75. doi: 10.1038/nature09320.


Genetic variance in the spinocerebellar ataxia type 2 (ATXN2) gene in children with severe early onset obesity.

Figueroa KP, Farooqi S, Harrup K, Frank J, O'Rahilly S, Pulst SM.

PLoS One. 2009 Dec 14;4(12):e8280. doi: 10.1371/journal.pone.0008280.

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