Mutational suppression of transferrin receptor shedding can be compensated by distinct metalloproteases acting on alternative sites
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/S0014-5793(03)00004-8/fullpdf
Reference32 articles.
1. Diverse Cell Surface Protein Ectodomains Are Shed by a System Sensitive to Metalloprotease Inhibitors
2. Membrane protein secretases
3. A metalloproteinase disintegrin that releases tumour-necrosis factor-α from cells
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5. An Essential Role for Ectodomain Shedding in Mammalian Development
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1. Intracellular Signaling and Desmoglein 2 Shedding Triggered by Human Adenoviruses Ad3, Ad14, and Ad14P1;Journal of Virology;2015-11
2. Implication of the proprotein convertases in iron homeostasis: Proprotein convertase 7 sheds human transferrin receptor 1 and furin activates hepcidin;Hepatology;2013-05-15
3. Substantial changes of cellular iron homeostasis during megakaryocytic differentiation of K562 cells;Development, Growth & Differentiation;2009-07-06
4. Proteomic Identification of Desmoglein 2 and Activated Leukocyte Cell Adhesion Molecule as Substrates of ADAM17 and ADAM10 by Difference Gel Electrophoresis;Molecular and Cellular Biology;2006-07
5. Release of the Soluble Transferrin Receptor Is Directly Regulated by Binding of Its Ligand Ferritransferrin;Journal of Biological Chemistry;2006-02
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