Genetic Background Alters the Severity and Onset of Neuromuscular Disease Caused by the Loss of Ubiquitin-Specific Protease 14 (Usp14)

Author:

Marshall Andrea G.,Watson Jennifer A.,Hallengren Jada J.,Walters Brandon J.,Dobrunz Lynn E.,Francillon Ludwig,Wilson Julie A.,Phillips Scott E.,Wilson Scott M.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference42 articles.

1. Genetic modifiers of neurological disease;JA Kearney;Curr Opin Genet Dev,2011

2. Mechanisms underlying synaptic vulnerability and degeneration in neurodegenerative disease. Neuropathology and Applied Neurobiology: n/a-n/a;TH Gillingwater,2013

3. Ubiquitin/proteasome pathway impairment in neurodegeneration: therapeutic implications;Q Huang;Apoptosis,2010

4. Dysfunction of the ubiquitin-proteasome system in multiple disease conditions: therapeutic approaches;S Paul;Bioessays,2008

5. Redox proteomics identification of oxidatively modified brain proteins in inherited Alzheimer's disease: An initial assessment;DA Butterfield;J Alzheimers Dis,2006

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