Search Results - "O'NEILL, G. P"
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The discovery of rofecoxib, [MK 966, VIOXX ®, 4-(4′-methylsulfonylphenyl)-3-phenyl-2(5 H)-furanone], an orally active cyclooxygenase-2 inhibitor
Published in Bioorganic & medicinal chemistry letters (05-07-1999)“…The development of a COX-2 inhibitor rofecoxib (MK 966, Vioxx®) is described. It is essentially equipotent to indomethacin both in vitro and in vivo but…”
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Rofecoxib [Vioxx, MK-0966; 4-(4'-methylsulfonylphenyl)-3-phenyl-2-(5H)-furanone]: a potent and orally active cyclooxygenase-2 inhibitor. Pharmacological and biochemical profiles
Published in The Journal of pharmacology and experimental therapeutics (01-08-1999)“…The discoveries that cyclooxygenase (COX)-2 is an inducible form of COX involved in inflammation and that COX-1 is the major isoform responsible for the…”
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Expression of the cysteinyl leukotriene 1 receptor in normal human lung and peripheral blood leukocytes
Published in American journal of respiratory and critical care medicine (2001)“…The cysteinyl leukotrienes (CysLTs) are important mediators of human asthma. Pharmacologic and clinical studies show that the CysLTs exert most of their…”
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Molecular Characterization and Expression of Cloned Human Galanin Receptors GALR2 and GALR3
Published in Journal of neurochemistry (01-12-1998)“…: Galanin is a 29‐ or 30‐amino acid peptide with wide‐ranging effects on hormone release, feeding behavior, smooth muscle contractility, and somatosensory…”
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Overexpression of human prostaglandin G/H synthase-1 and -2 by recombinant vaccinia virus: inhibition by nonsteroidal anti-inflammatory drugs and biosynthesis of 15-hydroxyeicosatetraenoic acid
Published in Molecular pharmacology (01-02-1994)“…Human prostaglandin G/H synthase (hPGHS)-1 and hPGHS-2, key enzymes in the formation of prostanoids from arachidonic acid, were expressed at high levels in…”
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Activation of the human peripheral cannabinoid receptor results in inhibition of adenylyl cyclase
Published in Molecular pharmacology (01-08-1995)“…The human peripheral cannabinoid (CB2) receptor has been cloned by reverse transcription-polymerase chain reaction from human spleen RNA and expressed, to…”
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Characterization of the human cysteinyl leukotriene CysLT1 receptor
Published in Nature (London) (24-06-1999)“…The cysteinyl leukotrienes-leukotriene C4(LTC4), leukotriene D4(LTD4) and leukotriene E4(LTE4)-are important mediators of human bronchial asthma…”
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Selective modulation of chemokinesis, degranulation, and apoptosis in eosinophils through the PGD2 receptors CRTH2 and DP
Published in Journal of allergy and clinical immunology (01-12-2001)“…Background: PGD2 is the major prostanoid released by mast cells during an allergic response. Its role in the allergic response, however, remains unclear…”
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Expression of prostaglandin G/H synthase-1 and -2 protein in human colon cancer
Published in Cancer research (Chicago, Ill.) (15-06-1995)“…Prostaglandin G/H synthase (PGHS), a key enzyme leading to the formation of prostaglandins, is the target of nonsteroidal antiinflammatory drugs. Two forms of…”
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Mechanism of selective inhibition of human prostaglandin G/H synthase-1 and -2 in intact cells
Published in Biochemical pharmacology (11-10-1996)“…Selective inhibitors of prostaglandin synthase-2 (PGHS-2) possess potent anti-inflammatory, antipyretic, and analgesic properties but demonstrate reduced…”
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The iron chelator desferrioxamine attenuates postischemic ventricular dysfunction
Published in The American journal of physiology (01-12-1987)“…Recent evidence suggests that postischemic myocardial dysfunction ("stunning") may be mediated by oxygen free radicals, but the mechanism by which they produce…”
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Characterization of the Human Cysteinyl Leukotriene 2 Receptor
Published in The Journal of biological chemistry (29-09-2000)“…The contractile and inflammatory actions of the cysteinyl leukotrienes (CysLTs), LTC4, LTD4, and LTE4, are thought to be mediated through at least two distinct…”
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Mutation of serine-516 in human prostaglandin G/H synthase-2 to methionine or aspirin acetylation of this residue stimulates 15- R-HETE synthesis
Published in FEBS letters (28-03-1994)“…Prostaglandin G/H synthase (PGHS) is a key enzyme in cellular prostaglandin (PG) synthesis and is the target of non-steroidal anti-inflammatory agents. PGHS…”
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Authorship patterns in theory based versus research based journals
Published in Scientometrics (01-03-1998)Get full text
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Discovery of a receptor related to the galanin receptors
Published in FEBS letters (05-03-1999)“…We report the isolation of a cDNA clone named GPR54, which encodes a novel G protein-coupled receptor (GPCR). A PCR search of rat brain cDNA retrieved a clone…”
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Evidence for a pathogenetic role of xanthine oxidase in the "stunned" myocardium
Published in The American journal of physiology (01-03-1987)“…Recent evidence suggests that postischemic myocardial dysfunction (or myocardial "stunning") may be mediated by oxygen free radicals, but the mechanism for…”
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Characterization of autocrine inducible prostaglandin H synthase-2 (PGHS-2) in human osteosarcoma cells
Published in Inflammation research (01-02-1997)“…The human osteosarcoma 143.98.2 cell line was found to express high levels of prostaglandin synthase-2 (PGHS-2) without detectable levels of prostaglandin…”
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The C3a receptor antagonist SB 290157 has agonist activity
Published in Immunology Letters (15-09-2005)“…The anaphylatoxin C3a is an important immune regulator with a number of distinct functions in both innate and adaptive immunity. Many of these roles have been…”
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Expression of the Synechocystis sp. strain PCC 6803 tRNA(Glu) gene provides tRNA for protein and chlorophyll biosynthesis
Published in Journal of Bacteriology (01-11-1990)“…In the cyanobacterium Synechocystis sp. strain PCC 6803 (Synechocystis 6803) delta-aminolevulinic acid (ALA), the sole precursor for the synthesis of the…”
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Cross-species comparison of 5-lipoxygenase-activating protein
Published in Molecular pharmacology (01-12-1992)“…To identify regions of 5-lipoxygenase-activating protein (FLAP) important for the function of the protein and the binding of leukotriene biosynthesis…”
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