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pro vyhledávání: '"Bryce Trotter"'
Autor:
Nathaniel Safren, Thuy P. Dao, Harihar Milaganur Mohan, Camellia Huang, Bryce Trotter, Carlos A. Castañeda, Henry Paulson, Sami Barmada, Lisa M. Sharkey
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-18 (2024)
Abstract The ubiquitin-adaptor protein UBQLN2 promotes degradation of several aggregate-prone proteins implicated in neurodegenerative diseases. Missense UBQLN2 mutations also cause X-linked amyotrophic lateral sclerosis (ALS) and frontotemporal deme
Externí odkaz:
https://doaj.org/article/081acb5bfe6a43b18e6d04ebdab2c427