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Human Molecular Genetics|November 17, 2010
Comparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxiaJuliette J Kahle, Natali Gulbahce, Chad A Shaw, et al.
Neuron|September 28, 2010
SCA1-like disease in mice expressing wild-type ataxin-1 with a serine to aspartic acid replacement at residue 776Lisa Duvick, Justin Barnes, Blake Ebner, et al.
Human Molecular Genetics|October 6, 2023
Dysregulation of alternative splicing in spinocerebellar ataxia type 1Victor Olmos, Evrett N Thompson, Neha Gogia, et al.
The Journal of Clinical Investigation|May 11, 2026
Oligodendrocyte dysfunction contributes to motor deficits and Purkinje cell axonopathy in spinocerebellar ataxia type 1Changwoo Lee, Rosalie M Grijalva, Leon Tejwani, et al.
The Journal of Clinical Investigation|August 28, 2025
Peripherally administered androgen receptor-targeted antisense oligonucleotide rescues spinal pathology in a murine SBMA modelChangwoo Lee, Zhigang Yu, Curtis J Kuo, et al.
Nature|March 14, 2008
Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1Janghoo Lim, Juan Crespo-Barreto, Paymaan Jafar-Nejad, et al.
Genes|October 20, 2020
Genetic Risk of Autism Spectrum Disorder in a Pakistani PopulationMadiha Khalid, Hashim Raza, Terri M Driessen, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 31, 2013
Polyglutamine disease toxicity is regulated by Nemo-like kinase in spinocerebellar ataxia type 1Hyoungseok Ju, Hiroshi Kokubu, Tiffany W Todd, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2022
Differential effects of Wnt-β-catenin signaling in Purkinje cells and Bergmann glia in spinocerebellar ataxia type 1Kimberly Luttik, Leon Tejwani, Hyoungseok Ju, et al.
Plos Genetics|January 2, 2008
dAtaxin-2 mediates expanded Ataxin-1-induced neurodegeneration in a Drosophila model of SCA1Ismael Al-Ramahi, Alma M Pérez, Janghoo Lim, et al.
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