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Puneet Opal, MD, PhD

Affiliations: 
Northwestern University, Evanston, IL 
Area:
Neurodegeneration, Neurology
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"Puneet Opal"
Mean distance: 16.29 (cluster 11)
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Parents

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Huda Y. Zoghbi post-doc Baylor College of Medicine

Children

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Marija Cvetanovic post-doc Northwestern

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Publications

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Luttik K, Tejwani L, Ju H, et al. (2022) Differential effects of Wnt-β-catenin signaling in Purkinje cells and Bergmann glia in spinocerebellar ataxia type 1. Proceedings of the National Academy of Sciences of the United States of America. 119: e2208513119
Edamakanti CR, Opal P. (2020) Purification of Prominin-1+ Stem Cells from Postnatal Mouse Cerebellum. Journal of Visualized Experiments : Jove
Didonna A, Opal P. (2019) The role of neurofilament aggregation in neurodegeneration: lessons from rare inherited neurological disorders. Molecular Neurodegeneration. 14: 19
Hu YS, Do J, Edamakanti CR, et al. (2019) Self-assembling vascular endothelial growth factor nanoparticles improve function in spinocerebellar ataxia type 1. Brain : a Journal of Neurology
Frederick NM, Shah PV, Didonna A, et al. (2018) Loss of the dystonia gene Thap1 leads to transcriptional deficits that converge on common pathogenic pathways in dystonic syndromes. Human Molecular Genetics
Murmann AE, Yu J, Opal P, et al. (2018) Trinucleotide Repeat Expansion Diseases, RNAi, and Cancer. Trends in Cancer. 4: 684-700
Edamakanti CR, Do J, Didonna A, et al. (2018) Mutant ataxin1 disrupts cerebellar development in spinocerebellar ataxia type 1. The Journal of Clinical Investigation
Yang X, Lu B, Sun X, et al. (2018) ANP32A regulates histone H3 acetylation and promotes leukemogenesis. Leukemia
Lin NH, Huang YS, Opal P, et al. (2016) The role of gigaxonin in the degradation of the glial-specific intermediate filament protein GFAP. Molecular Biology of the Cell
Didonna A, Opal P. (2016) Advances in Sequencing Technologies for Understanding Hereditary Ataxias: A Review. Jama Neurology
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