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ADAM17 substrate release in proximal tubule drives kidney fibrosis
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The Cytoplasmic Domain of A Disintegrin and Metalloproteinase 10 (ADAM10) Regulates Its Constitutive Activity but Is Dispensable for Stimulated ADAM10-dependent Shedding
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Deletion of Adam10 in endothelial cells leads to defects in organ-specific vascular structures
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NATURE MEDICINE (2007)
ACE2 inhibition worsens glomerular injury in association with increased ACE expression in streptozotocin-induced diabetic mice
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KIDNEY INTERNATIONAL (2007)
Synapse-associated protein-97 mediates α-secretase ADAM10 trafficking and promotes its activity
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Klotho converts canonical FGF receptor into a specific receptor for FGF23
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NATURE (2006)
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JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
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ADAM10 cleavage of N-cadherin and regulation of cell-cell adhesion and β-catenin nuclear signalling
K Reiss et al.
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Distinct roles for ADAM10 and ADAM17 in ectodomain shedding of six EGFR ligands
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JOURNAL OF CELL BIOLOGY (2004)
The transmembrane CXC-chemokine ligand 16 is induced by IFN-γ and TNF-α and shed by the activity of the disintegrin-like metalloproteinase ADAM10
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JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
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Cellular cholesterol depletion triggers shedding of the human interleukin-6 receptor by ADAM10 and ADAM17 (TACE)
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JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
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GENES & DEVELOPMENT (2003)
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CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION (2003)
The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for α-secretase activity in fibroblasts
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HUMAN MOLECULAR GENETICS (2002)
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KIDNEY INTERNATIONAL (2002)
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JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
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KIDNEY INTERNATIONAL (2002)
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JOURNAL OF MEMBRANE BIOLOGY (2001)
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CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION (2001)
Regulated intramembrane proteolysis: A control mechanism conserved from bacteria to humans
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CELL (2000)