Citalopram Reduces Aggregation of ATXN3 in a YAC Transgenic Mouse Model of Machado-Joseph Disease-Reference-Cited by-同舟云学术

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Citalopram Reduces Aggregation of ATXN3 in a YAC Transgenic Mouse Model of Machado-Joseph Disease

Published:2018-09-04 Issue:5 Volume:56 Page:3690-3701
ISSN:0893-7648
Container-title:Molecular Neurobiology
language:en
Short-container-title:Mol Neurobiol

Author:

Ashraf Naila S.,Duarte-Silva Sara,Shaw Emily D.,Maciel Patrícia,Paulson Henry L.,Teixeira-Castro Andreia,Costa Maria do Carmo^ORCID

Funder

Becky Babcox Research Fund, University of Michigan

National Institute of Neurological Disorders and Stroke

European Regional Development Funds (FEDER) - Competitiveness Factors Operational Programme (COMPETE); Foundation for Science and Technology

Northern Portugal Regional Operational Program

Foundation for Science and Technology (FCT); Competitiveness Factors Operational Programme

Foundation for Science and Technology

National Ataxia Foundation

Ataxia UK

Foundation for Science and Technology (FCT); POPH; QREN; Governo da República Portuguesa; EU/FSE

Publisher

Springer Science and Business Media LLC

Subject

Neuroscience (miscellaneous),Cellular and Molecular Neuroscience,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s12035-018-1331-2.pdf

Reference47 articles.

1. Costa Mdo C, Paulson HL (2012) Toward understanding Machado-Joseph disease. Prog Neurobiol 97(2):239–257. https://doi.org/10.1016/j.pneurobio.2011.11.006

2. Schols L, Bauer P, Schmidt T, Schulte T, Riess O (2004) Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol 3(5):291–304

3. Kawaguchi Y, Okamoto T, Taniwaki M, Aizawa M, Inoue M, Katayama S, Kawakami H, Nakamura S et al (1994) CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet 8(3):221–228. https://doi.org/10.1038/ng1194-221

4. Lima M, Costa MC, Montiel R, Ferro A, Santos C, Silva C, Bettencourt C, Sousa A et al (2005) Population genetics of wild-type CAG repeats in the Machado-Joseph disease gene in Portugal. Hum Hered 60(3):156–163

5. Maciel P, Costa MC, Ferro A, Rousseau M, Santos CS, Gaspar C, Barros J, Rouleau GA et al (2001) Improvement in the molecular diagnosis of Machado-Joseph disease. Arch Neurol 58(11):1821–1827

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1. CAG repeat-selective compounds reduce abundance of expanded CAG RNAs in patient cell and murine models of SCAs;2024-08-17

2. BloodDDIT4andTRIM13transcript levels mark the early stages of Machado-Joseph disease;2023-10-03

3. Blood levels of neurofilament light are associated with disease progression in a mouse model of spinocerebellar ataxia type 3;Disease Models & Mechanisms;2023-09-01

4. Tissue-Specific Vulnerability to Apoptosis in Machado-Joseph Disease;Cells;2023-05-17

5. Regional and age-dependent changes in ubiquitination in cellular and mouse models of spinocerebellar ataxia type 3;Frontiers in Molecular Neuroscience;2023-04-14

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