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

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;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;
acta neuropathologica communications 2021 Vol. 9 pp. -
92
zarnescu2021actatdp-43

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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DOI:
10.1186/s40478-021-01148-z
URL:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC79928...

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