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Termonology for the theory of machines and mechanisms

Mechanism and machine theory, 1983, Vol.18 (6), p.379-408

1983

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Translational imaging of the fibroblast activation protein (FAP) using the new ligand [68Ga]Ga-OncoFAP-DOTAGA

European journal of nuclear medicine and molecular imaging, 2022-05, Vol.49 (6), p.1822-1832

2022

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Distinction of microsomal prostaglandin E synthase-1 (mPGES-1) inhibition from cyclooxygenase-2 inhibition in cells using a novel, selective mPGES-1 inhibitor

Biochemical pharmacology, 2010-05, Vol.79 (10), p.1445-1454

2010

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Structural insights into the stereochemistry of the cyclooxygenase reaction

Nature (London), 2000-05, Vol.405 (6782), p.97-101

2000

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Valdecoxib: assessment of cyclooxygenase-2 potency and selectivity

The Journal of pharmacology and experimental therapeutics, 2005-03, Vol.312 (3), p.1206-1212

2005

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Development of laser-based technology for the routine first wall diagnostic on the tokamak EAST: LIBS and LIAS

Physica scripta, 2017-12, Vol.T170 (1), p.14046

2017

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Development of laser-based techniques for in situ characterization of the first wall in ITER and future fusion devices

Nuclear fusion, 2013-09, Vol.53 (9), p.93002

2013

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Time resolved imaging of laser induced ablation spectroscopy (LIAS) in TEXTOR and comparison with modeling

Physica scripta, 2016-02, Vol.T167 (1), p.14034-14038

2016

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Nitric Oxide Trapping of the Tyrosyl Radical of Prostaglandin H Synthase-2 Leads to Tyrosine Iminoxyl Radical and Nitrotyrosine Formation

The Journal of biological chemistry, 1997-07, Vol.272 (27), p.17086-17090

1997

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Characterization of Celecoxib and Valdecoxib Binding to Cyclooxygenase

Molecular pharmacology, 2003-04, Vol.63 (4), p.870-877

2003

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In situ deuterium inventory measurements of a-C:D layers on tungsten in TEXTOR by laser induced ablation spectroscopy

Physica scripta, 2014-04, Vol.T159 (1), p.14054

2014

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Laser techniques implementation for wall surface characterization and conditioning

Physica scripta, 2009-12, Vol.2009, p.014008

2009

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Inhibition of leukotriene A4 hydrolase/aminopeptidase by captopril

The Journal of biological chemistry, 1991-09, Vol.266 (25), p.16507-16511

1991

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Synthesis of potent leukotriene A(4) hydrolase inhibitors. Identification of 3-[methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic acid

Journal of medicinal chemistry, 2002-08, Vol.45 (16), p.3482-3490

2002

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Structure-activity relationship studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a potent inhibitor of leukotriene A(4) (LTA(4)) hydrolase

Journal of medicinal chemistry, 2000-02, Vol.43 (4), p.721-735

2000

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Synthesis of imidazopyridines and purines as potent inhibitors of leukotriene A4 hydrolase

Bioorganic & medicinal chemistry letters, 2003-03, Vol.13 (6), p.1137-1139

2003

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Synthesis of Potent Leukotriene A4 Hydrolase Inhibitors. Identification of 3-[Methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic Acid

Journal of medicinal chemistry, 2002-08, Vol.45 (16), p.3482-3490

2002

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Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A(4) hydrolase

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3383

2002

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Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A4 hydrolase

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3383-3386

2002

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Mechanism-based inactivation of leukotriene A4 hydrolase/aminopeptidase by leukotriene A4. Mass spectrometric and kinetic characterization

The Journal of biological chemistry, 1992-11, Vol.267 (32), p.22733-22739

1992

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Proteolytic processing of atriopeptin prohormone

Molecular pharmacology, 1986-12, Vol.30 (6), p.552-557

1986

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The bifunctional enzyme leukotriene-A4 hydrolase is an arginine aminopeptidase of high efficiency and specificity

The Journal of biological chemistry, 1994-04, Vol.269 (15), p.11269-11273

1994

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Synthesis of Imidazopyridines and Purines as Potent Inhibitors of Leukotriene A 4 Hydrolase

Bioorganic & medicinal chemistry letters, 2003, Vol.13 (6), p.1137-1139

2003

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Synthesis of Potent Leukotriene A 4 Hydrolase Inhibitors. Identification of 3-[Methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic Acid

Journal of medicinal chemistry, 2002-08, Vol.45 (16), p.3482-3490

2002

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Termonology for the theory of machines and mechanisms

Translational imaging of the fibroblast activation protein (FAP) using the new ligand [68Ga]Ga-OncoFAP-DOTAGA

Distinction of microsomal prostaglandin E synthase-1 (mPGES-1) inhibition from cyclooxygenase-2 inhibition in cells using a novel, selective mPGES-1 inhibitor

Structural insights into the stereochemistry of the cyclooxygenase reaction

Valdecoxib: assessment of cyclooxygenase-2 potency and selectivity

Development of laser-based technology for the routine first wall diagnostic on the tokamak EAST: LIBS and LIAS

Development of laser-based techniques for in situ characterization of the first wall in ITER and future fusion devices

Time resolved imaging of laser induced ablation spectroscopy (LIAS) in TEXTOR and comparison with modeling

Nitric Oxide Trapping of the Tyrosyl Radical of Prostaglandin H Synthase-2 Leads to Tyrosine Iminoxyl Radical and Nitrotyrosine Formation

Characterization of Celecoxib and Valdecoxib Binding to Cyclooxygenase

In situ deuterium inventory measurements of a-C:D layers on tungsten in TEXTOR by laser induced ablation spectroscopy

Laser techniques implementation for wall surface characterization and conditioning

Inhibition of leukotriene A4 hydrolase/aminopeptidase by captopril

Synthesis of potent leukotriene A(4) hydrolase inhibitors. Identification of 3-[methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic acid

Structure-activity relationship studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a potent inhibitor of leukotriene A(4) (LTA(4)) hydrolase

Synthesis of imidazopyridines and purines as potent inhibitors of leukotriene A4 hydrolase

Synthesis of Potent Leukotriene A4 Hydrolase Inhibitors. Identification of 3-[Methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic Acid

Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A(4) hydrolase

Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A4 hydrolase

Mechanism-based inactivation of leukotriene A4 hydrolase/aminopeptidase by leukotriene A4. Mass spectrometric and kinetic characterization

Proteolytic processing of atriopeptin prohormone

Structure−Activity Relationship Studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a Potent Inhibitor of Leukotriene A4 (LTA4) Hydrolase

The bifunctional enzyme leukotriene-A4 hydrolase is an arginine aminopeptidase of high efficiency and specificity

Synthesis of Imidazopyridines and Purines as Potent Inhibitors of Leukotriene A 4 Hydrolase

Synthesis of Potent Leukotriene A 4 Hydrolase Inhibitors. Identification of 3-[Methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic Acid

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