Global proteomics of Ubqln2-based murine models of ALS
Global proteomics of Ubqln2-based murine models of ALS
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Cold Spring Harbor: Cold Spring Harbor Laboratory Press
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English
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Cold Spring Harbor: Cold Spring Harbor Laboratory Press
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Contents
Familial forms of neurodegenerative diseases commonly involve mutation of aggregation-prone proteins or components of the protein degradation machinery that act on aberrant proteins. Ubqln2 encodes a member of the UBL/UBA family of proteasome shuttle factors that is thought to facilitate proteasomal degradation of substrates, and mutation of this g...
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Full title
Global proteomics of Ubqln2-based murine models of ALS
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TN_cdi_proquest_journals_2360502704
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2360502704
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E-ISSN
2692-8205
DOI
10.1101/2020.02.22.956524
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https://www.proquest.com/docview/2360502704?pq-origsite=primo&accountid=13902
