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A Short Peptide Inhibitor as an Activity-Based Probe for Matriptase-2.
- Published in:
- Pharmaceuticals (14248247), 2018, v. 11, n. 2, p. 49, doi. 10.3390/ph11020049
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- Article
3,1-Benzothiazines, 1,4-Benzodioxines and 1,4-Benzoxazines as Inhibitors of Matriptase-2: Outcome of a Focused Screening Approach.
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- Pharmaceuticals (14248247), 2016, v. 9, n. 1, p. 2, doi. 10.3390/ph9010002
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- Article
Metalloprotease meprin β is activated by transmembrane serine protease matriptase-2 at the cell surface thereby enhancing APP shedding.
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- Biochemical Journal, 2015, v. 470, n. 1, p. 91, doi. 10.1042/BJ20141417
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- Article
Hepatocyte growth factor activator inhibitor type 2 (HAI-2) modulates hepcidin expression by inhibiting the cell surface protease matriptase-2.
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- Biochemical Journal, 2013, v. 450, n. 3, p. 583, doi. 10.1042/BJ20121518
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- Article
A membrane-bound FtsH protease is involved in osmoregulation in Synechocystis sp. PCC 6803: the compatible solute synthesizing enzyme GgpS is one of the targets for proteolysis.
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- Molecular Microbiology, 2007, v. 63, n. 1, p. 86, doi. 10.1111/j.1365-2958.2006.05495.x
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- Article
En Route to New Therapeutic Options for Iron Overload Diseases: Matriptase-2 as a Target for Kunitz-Type Inhibitors.
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- ChemBioChem, 2016, v. 17, n. 7, p. 595, doi. 10.1002/cbic.201500651
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- Article
Cover Picture: En Route to New Therapeutic Options for Iron Overload Diseases: Matriptase-2 as a Target for Kunitz-Type Inhibitors (ChemBioChem 7/2016).
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- ChemBioChem, 2016, v. 17, n. 7, p. 523, doi. 10.1002/cbic.201600126
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- Article
Inhibitors of Matriptase-2 Based on the Trypsin Inhibitor SFTI-1.
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- ChemBioChem, 2015, v. 16, n. 11, p. 1601, doi. 10.1002/cbic.201500200
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- Article
Ectodomain shedding of CD99 within highly conserved regions is mediated by the metalloprotease meprin β and promotes transendothelial cell migration.
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- FASEB Journal, 2017, v. 31, n. 3, p. 1226, doi. 10.1096/fj.201601113R
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- Article
A Fluorescent-Labeled Phosphono Bisbenzguanidine As an Activity-Based Probe for Matriptase.
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- Chemistry - A European Journal, 2017, v. 23, n. 22, p. 5205, doi. 10.1002/chem.201700319
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- Article
Phosphono Bisbenzguanidines as Irreversible Dipeptidomimetic Inhibitors and Activity-Based Probes of Matriptase-2.
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- Chemistry - A European Journal, 2016, v. 22, n. 25, p. 8525, doi. 10.1002/chem.201600206
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- Article
Back Cover: Phosphono Bisbenzguanidines as Irreversible Dipeptidomimetic Inhibitors and Activity-Based Probes of Matriptase-2 (Chem. Eur. J. 25/2016).
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- Chemistry - A European Journal, 2016, v. 22, n. 25, p. 8704, doi. 10.1002/chem.201601295
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- Article
A Bisbenzamidine Phosphonate as a Janus-faced Inhibitor for Trypsin-like Serine Proteases.
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- ChemMedChem, 2015, v. 10, n. 10, p. 1641, doi. 10.1002/cmdc.201500319
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- Article
Insights into Matriptase-2 Substrate Binding and Inhibition Mechanisms by Analyzing Active-Site-Mutated Variants.
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- ChemMedChem, 2012, v. 7, n. 1, p. 68, doi. 10.1002/cmdc.201100350
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- Article
Inside Cover: Insights into Matriptase-2 Substrate Binding and Inhibition Mechanisms by Analyzing Active-Site-Mutated Variants (ChemMedChem 1/2012).
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- ChemMedChem, 2012, v. 7, n. 1, p. 2, doi. 10.1002/cmdc.201190061
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- Article
The intact Kunitz domain protects the amyloid precursor protein from being processed by matriptase-2.
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- Biological Chemistry, 2016, v. 397, n. 8, p. 777, doi. 10.1515/hsz-2015-0263
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- Article
Cell surface serine protease matriptase-2 suppresses fetuin-A/AHSG-mediated induction of hepcidin.
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- Biological Chemistry, 2015, v. 396, n. 1, p. 81, doi. 10.1515/hsz-2014-0120
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- Article
Limiting the Number of Potential Binding Modes by Introducing Symmetry into Ligands: Structure-Based Design of Inhibitors for Trypsin-Like Serine Proteases.
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- Chemistry - A European Journal, 2016, v. 22, n. 2, p. 610, doi. 10.1002/chem.201503534
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- Article
Design and chemical syntheses of potent matriptase-2 inhibitors based on trypsin inhibitor SFTI-1 isolated from sunflower seeds.
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- Biopolymers, 2017, v. 108, n. 6, p. n/a, doi. 10.1002/bip.23031
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- Article
Matriptase-2 (TMPRSS6) is directly up-regulated by hypoxia inducible factor-1: identification of a hypoxia-responsive element in the TMPRSS6 promoter region.
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- Biological Chemistry, 2012, v. 393, n. 6, p. 535, doi. 10.1515/hsz-2011-0221
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- Article