Active Transport of the Ubiquitin Ligase MID1 along the Microtubules Is Regulated by Protein Phosphatase 2A
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference35 articles.
1. Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations.;J So;Am J Med Genet A,2005
2. The MID1/PP2A complex: a key to the pathogenesis of Opitz BBB/G syndrome.;S Schweiger;Bioessays,2003
3. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.;NA Quaderi;Nat Genet,1997
4. FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules.;J Perry;Genomics,1999
5. Subclassification of the RBCC/TRIM superfamily reveals a novel motif necessary for microtubule binding.;KM Short;J Biol Chem,2006
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