A Mutation Associated with CMT2A Neuropathy Causes Defects in Fzo1 GTP Hydrolysis, Ubiquitylation, and Protein Turnover

Por Amiott, Elizabeth A., Cohen, Mickael M., Saint-Georges, Yann, Weissman, Allan M., Shaw, Janet M.
Publicado em 2009

Sequential requirements for the GTPase domain of the mitofusin Fzo1 and the ubiquitin ligase SCF(Mdm30) in mitochondrial outer membrane fusion

Por Cohen, Mickael M., Amiott, Elizabeth A., Day, Adam R., Leboucher, Guillaume P., Pryce, Erin N., Glickman, Michael H., McCaffery, J. Michael, Shaw, Janet M., Weissman, Allan M.
Publicado em 2011

Mitochondrial Fusion and Function in Charcot-Marie-Tooth Type 2A Patient Fibroblasts with Mitofusin 2 Mutations

Por Amiott, Elizabeth A, Lott, Paul, Soto, Jamie, Kang, Peter B, McCaffery, J Michael, DiMauro, Salvatore, Abel, E Dale, Flanigan, Kevin M, Lawson, Victoria H, Shaw, Janet M
Publicado em 2008