Results 261 to 270 of about 186,613 (302)
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Expression of Cyclooxygenase-1 and Cyclooxygenase-2 in the human prostate
Urology, 2000To determine the cell-specific expression of the two major isoforms of cyclooxygenase (COX-1 and COX-2) in human noncancerous and cancerous prostatic tissues.Thirty-one specimens of prostate carcinoma (CaP) and 10 specimens of benign prostatic hyperplasia (BPH) were stained with mouse antihuman COX-1 and COX-2 monoclonal antibodies.
A, Kirschenbaum +6 more
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Cyclooxygenase-1 and Cyclooxygenase-2 in the Human Optic Nerve Head
Experimental Eye Research, 1997To investigate the hypothesis that eicosanoids act as cellular mediators in the optic nerve head of normals and of patients with glaucoma, we have determined the presence of the two cyclooxygenase (COX) isoforms in human tissue. Histological sections of optic nerve heads were studied by immunohistochemistry. Age matched normal donors were compared with
A H, Neufeld +3 more
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Cloning and Expression of Cyclooxygenase-1 and Cyclooxygenase-2
2010Cyclooxygenase (COX) enzymes play important roles in normal physiology and during inflammation of various cells and tissues. In order to help understand the functions of these enzymes, their genes can be cloned to facilitate the production of the proteins in recombinant form.
Nicholas R, Staten, Beverly A, Reitz
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Perspectives on the Cyclooxygenase-2/ Cyclooxygenase-1 Hypothesis
JCR: Journal of Clinical Rheumatology, 1998The introduction of the cyclooxygenase (COX) hypothesis to explain both the therapeutic effects and the toxicity of nonsteroidal anti-inflammatory drugs (NSAIDs) has provided direction for the development of preferential and highly selective COX-2 inhibitors, which retain efficacy against inflammation with reduced risk of toxicity. However, the complex
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Different Methods for Testing Potential Cyclooxygenase-1 and Cyclooxygenase-2 Inhibitors
2010The need for the development of selective agents, which only inhibit the mainly "harmful" cyclooxygenase-2 (COX-2) while leaving physiological COX-1 mostly unaffected, still remains, especially after the recent issues related to cardiovascular toxicity caused by some COX-2 selective agents.
Stefan, Laufer, Sabine, Luik
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Characteristics of cyclooxygenase-1 and cyclooxygenase-2-deficient mice
1996The prostaglandins (PGs) are a diverse group of autocrine and paracrine hormones that mediate many cellular and physiological processes. Prostaglandin H2 (PGH2) is an obligate intermediate in formation of prostaglandins1, the formation of which from arachidonic acid (AA) is catalysed by prostaglandin H synthase, an enzyme with two known isoforms ...
S. G. Morham, R. Langenbach
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Ontogeny of cyclooxygenase-1 and cyclooxygenase-2 gene expression in ovine lung
American Journal of Physiology-Lung Cellular and Molecular Physiology, 1998Prostacyclin is a key mediator of pulmonary vascular and parenchymal function during late fetal and early postnatal life, and its synthesis in whole lung increases during that period. The rate-limiting enzyme in prostacyclin synthesis in the developing lung is cyclooxygenase (COX).
T S, Brannon +6 more
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Caveolin‐1 facilitates cyclooxygenase‐2 protein degradation
Journal of Cellular Biochemistry, 2009AbstractCyclooxygenase‐2 (COX‐2) plays major roles in diverse physiological and pathological processes such as inflammation and tumorigenesis. Transcriptional control of COX‐2 has been extensively investigated and characterized, but its post‐translational control is less clear. Here, we report a novel mechanism by which COX‐2 is degraded.
Shu-Fen, Chen +8 more
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Cyclooxygenase 1 and cyclooxygenase 2 expression is abnormally regulated in human nasal polyps
Journal of Allergy and Clinical Immunology, 2002There is evidence that impairment of prostanoid metabolism might be involved in the pathogenesis of nasal polyps (NPs). Prostanoids are synthesized by 2 cyclooxygenase (Cox) enzymes, one constitutive (Cox-1) and another inducible (Cox-2).The aim of these studies was to investigate Cox-1 and Cox-2 regulation in NPs of aspirin-tolerant human patients ...
Joaquim, Mullol +6 more
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The American Journal of Medicine, 1998
Both isoforms of cyclo-oxygenase, COX-1 and COX-2, are inhibited to varying degrees by all of the available nonsteroidal anti-inflammatory drugs (NSAIDs). Because inhibition of COX-1 by NSAIDs is linked to gastrointestinal ulcer formation, those drugs that selectively inhibit COX-2 may have less gastrointestinal toxicity.
B, Cryer, M, Feldman
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Both isoforms of cyclo-oxygenase, COX-1 and COX-2, are inhibited to varying degrees by all of the available nonsteroidal anti-inflammatory drugs (NSAIDs). Because inhibition of COX-1 by NSAIDs is linked to gastrointestinal ulcer formation, those drugs that selectively inhibit COX-2 may have less gastrointestinal toxicity.
B, Cryer, M, Feldman
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