Shedding of the Mer Tyrosine Kinase Receptor Is Mediated by ADAM17 Protein through a Pathway Involving Reactive Oxygen Species, Protein Kinase Cδ, and p38 Mitogen-activated Protein Kinase (MAPK)-Reference-Cited by-同舟云学术

Shedding of the Mer Tyrosine Kinase Receptor Is Mediated by ADAM17 Protein through a Pathway Involving Reactive Oxygen Species, Protein Kinase Cδ, and p38 Mitogen-activated Protein Kinase (MAPK)

Published:2011-09 Issue:38 Volume:286 Page:33335-33344
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Thorp Edward,Vaisar Tomas,Subramanian Manikandan,Mautner Lauren,Blobel Carl,Tabas Ira

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference65 articles.

1. Identification of the Product of Growth Arrest-specific Gene 6 as a Common Ligand for Axl, Sky, and Mer Receptor Tyrosine Kinases

2. Auto-Oxidation and Oligomerization of Protein S on the Apoptotic Cell Surface Is Required for Mer Tyrosine Kinase-Mediated Phagocytosis of Apoptotic Cells

3. Phagocytosis and clearance of apoptotic cells is mediated by MER

4. Mer Receptor Tyrosine Kinase Signaling Participates in Platelet Function

5. Mer tyrosine kinase (MerTK) promotes macrophage survival following exposure to oxidative stress

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