TDP-43 proteinopathy alters the ribosome association of multiple mRNAs including the glypican Dally-like protein (Dlp)/GPC6

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ID: 273868
2021
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Abstract
Amyotrophic lateral sclerosis (ALS) is a genetically heterogeneous neurodegenerative disease in which 97% of patients exhibit cytoplasmic aggregates containing the RNA binding protein TDP-43. Using tagged ribosome affinity purifications in Drosophila ...
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zarnescu2021actatdp-43 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Erik M. Lehmkuhl, Suvithanandhini Loganathan, Eric Alsop, Alexander D. Blythe, Tina Kovalik, Nicholas P. Mortimore, Dianne Barrameda, Chuol Kueth, Randall J. Eck, Bhavani B. Siddegowda, Archi Joardar, Hannah Ball, Maria E. Macias, Robert Bowser, Kendall Van Keuren-Jensen, Daniela C. Zarnescu
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Journal acta neuropathologica communications
Year 2021
DOI
10.1186/s40478-021-01148-z
URL
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992842/?report=reader
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