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A Golgi localization signal identified in the Menkes recombinant protein.
Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
Actin and microtubule regulation of trans-Golgi network architecture, and copper-dependent protein transport to the cell surface.
The Menkes disease ATPase (ATP7A) is internalized via a Rac1-regulated, clathrin- and caveolae-independent pathway.
Activation of ADP-ribosylation factor regulates biogenesis of the ATP7A-containing trans-Golgi network compartment and its Cu-induced trafficking.
Novel membrane traffic steps regulate the exocytosis of the Menkes disease ATPase.
Identification of a di-leucine motif within the C terminus domain of the Menkes disease protein that mediates endocytosis from the plasma membrane.
Menkes and Wilson diseases.
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein.
Characterization of the exon structure of the Menkes disease gene using vectorette PCR.
Cloning the Wilson disease gene.
Genomic studies of gene expression: regulation of the Wilson disease gene.
Trafficking of the Menkes copper transporter ATP7A is regulated by clathrin-, AP-2-, AP-1-, and Rab22-dependent steps.