Similar articles for PMID: 19843541

Year	Number of Results
1998	1
1999	5
2000	4
2001	11
2002	9
2003	6
2004	5
2005	16
2006	11
2007	11
2008	11
2009	5
2010	16
2011	9
2012	17
2013	15
2014	14
2015	9
2016	8
2017	13
2018	9
2019	16
2020	13
2021	9
2022	8
2023	2
2024	0

1

SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7.

Janer A, Werner A, Takahashi-Fujigasaki J, Daret A, Fujigasaki H, Takada K, Duyckaerts C, Brice A, Dejean A, Sittler A. Janer A, et al. Hum Mol Genet. 2010 Jan 1;19(1):181-95. doi: 10.1093/hmg/ddp478. Hum Mol Genet. 2010. PMID: 19843541

2

SUMOylation by SUMO2 is implicated in the degradation of misfolded ataxin-7 via RNF4 in SCA7 models.

Marinello M, Werner A, Giannone M, Tahiri K, Alves S, Tesson C, den Dunnen W, Seeler JS, Brice A, Sittler A. Marinello M, et al. Dis Model Mech. 2019 Jan 11;12(1):dmm036145. doi: 10.1242/dmm.036145. Dis Model Mech. 2019. PMID: 30559154 Free PMC article.

3

Reelin is a target of polyglutamine expanded ataxin-7 in human spinocerebellar ataxia type 7 (SCA7) astrocytes.

McCullough SD, Xu X, Dent SY, Bekiranov S, Roeder RG, Grant PA. McCullough SD, et al. Proc Natl Acad Sci U S A. 2012 Dec 26;109(52):21319-24. doi: 10.1073/pnas.1218331110. Epub 2012 Dec 10. Proc Natl Acad Sci U S A. 2012. PMID: 23236151 Free PMC article.

4

A conditional pan-neuronal Drosophila model of spinocerebellar ataxia 7 with a reversible adult phenotype suitable for identifying modifier genes.

Latouche M, Lasbleiz C, Martin E, Monnier V, Debeir T, Mouatt-Prigent A, Muriel MP, Morel L, Ruberg M, Brice A, Stevanin G, Tricoire H. Latouche M, et al. J Neurosci. 2007 Mar 7;27(10):2483-92. doi: 10.1523/JNEUROSCI.5453-06.2007. J Neurosci. 2007. PMID: 17344386 Free PMC article.

5

SUMO on the road to neurodegeneration.

Dorval V, Fraser PE. Dorval V, et al. Biochim Biophys Acta. 2007 Jun;1773(6):694-706. doi: 10.1016/j.bbamcr.2007.03.017. Epub 2007 Mar 30. Biochim Biophys Acta. 2007. PMID: 17475350 Free article. Review.

6

Lentiviral vector-mediated overexpression of mutant ataxin-7 recapitulates SCA7 pathology and promotes accumulation of the FUS/TLS and MBNL1 RNA-binding proteins.

Alves S, Marais T, Biferi MG, Furling D, Marinello M, El Hachimi K, Cartier N, Ruberg M, Stevanin G, Brice A, Barkats M, Sittler A. Alves S, et al. Mol Neurodegener. 2016 Jul 28;11(1):58. doi: 10.1186/s13024-016-0123-2. Mol Neurodegener. 2016. PMID: 27465358 Free PMC article.

7

Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7.

Niewiadomska-Cimicka A, Trottier Y. Niewiadomska-Cimicka A, et al. Neurotherapeutics. 2019 Oct;16(4):1074-1096. doi: 10.1007/s13311-019-00778-5. Neurotherapeutics. 2019. PMID: 31432449 Free PMC article. Review.

8

Zander C, Takahashi J, El Hachimi KH, Fujigasaki H, Albanese V, Lebre AS, Stevanin G, Duyckaerts C, Brice A. Zander C, et al. Hum Mol Genet. 2001 Oct 15;10(22):2569-79. doi: 10.1093/hmg/10.22.2569. Hum Mol Genet. 2001. PMID: 11709544

9

Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation.

Bowman AB, Yoo SY, Dantuma NP, Zoghbi HY. Bowman AB, et al. Hum Mol Genet. 2005 Mar 1;14(5):679-91. doi: 10.1093/hmg/ddi064. Epub 2005 Jan 20. Hum Mol Genet. 2005. PMID: 15661755

10

Promyelocytic leukemia protein is redistributed during the formation of intranuclear inclusions independent of polyglutamine expansion: an immunohistochemical study on Marinesco bodies.

Kumada S, Uchihara T, Hayashi M, Nakamura A, Kikuchi E, Mizutani T, Oda M. Kumada S, et al. J Neuropathol Exp Neurol. 2002 Nov;61(11):984-91. doi: 10.1093/jnen/61.11.984. J Neuropathol Exp Neurol. 2002. PMID: 12430715

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