Tissue specific LRRK2 interactomes reveal a distinct striatal functional unit
Tissue specific LRRK2 interactomes reveal a distinct striatal functional unit
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United States: Public Library of Science
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English
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United States: Public Library of Science
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Mutations in LRRK2 are the most common genetic cause of Parkinson's disease. Despite substantial research efforts, the physiological and pathological role of this multidomain protein remains poorly defined. In this study, we used a systematic approach to construct the general protein-protein interactome around LRRK2, which was then evaluated taking...
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Full title
Tissue specific LRRK2 interactomes reveal a distinct striatal functional unit
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TN_cdi_plos_journals_2777440686
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2777440686
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ISSN
1553-7358,1553-734X
E-ISSN
1553-7358
DOI
10.1371/journal.pcbi.1010847
