COX-2 expression and function in the hyperalgesic response to paw inflammation in mice. - Wikidata - awgldk - TriplyDB

COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

http://www.wikidata.org/entity/Q37042403

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Pharmacokinetic-pharmacodynamic modelling of the analgesic effects of lumiracoxib, a selective inhibitor of cyclooxygenase-2, in rats.Reversible suppression of cyclooxygenase 2 (COX-2) expression in vivo by inducible RNA interference.Anti-inflammatory activity of Ocimum americanum L. essential oil in experimental model of zymosan-induced arthritis.IL10 released by a new inflammation-regulated lentiviral system efficiently attenuates zymosan-induced arthritis Feedback regulation of cyclooxygenase-2 transcription ex vivo and in vivo.Co-induction of cyclooxygenase-2 [correction of cyclooxyenase-2] and early growth response gene (Egr-1) in spinal cord in a clinical model of persistent inflammation and hyperalgesia Hypoxia promotes tumor growth in linking angiogenesis to immune escape.

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COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

http://www.wikidata.org/entity/Q37042403

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on October 2008

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

@en

COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

@nl

type

label

COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

@en

COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

@nl

prefLabel

COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

@en

COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

@nl

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J.PLEFA.2008.08.001

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Prostaglandins, Leukotrienes and Essential Fatty Acids

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COX-2 expression and function in the hyperalgesic response to paw inflammation in mice.

@en

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Harvey R Herschman

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Igor Spigelman

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Naveen K Jain

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Tomo-o Ishikawa

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Cytokine-mediated inflammatory hyperalgesia limited by interleukin-10

Carrageenan-induced paw edema in rat elicits a predominant prostaglandin E2 (PGE2) response in the central nervous system associated with the induction of microsomal PGE2 synthase-1

Cyclooxygenases: structural, cellular, and molecular biology

A new and sensitive method for measuring thermal nociception in cutaneous hyperalgesia

Suppressed injury-induced rise in spinal prostaglandin E2 production and reduced early thermal hyperalgesia in iNOS-deficient mice.

Interleukin-1beta-mediated induction of Cox-2 in the CNS contributes to inflammatory pain hypersensitivity.

Cyclooxygenase 2 (COX-2) as a target for therapy and noninvasive imaging.

Constitutive cyclooxygenase-2 is involved in central nociceptive processes in humans.

Pharmacological profile of parecoxib: a novel, potent injectable selective cyclooxygenase-2 inhibitor.

Rofecoxib [Vioxx, MK-0966; 4-(4'-methylsulfonylphenyl)-3-phenyl-2-(5H)-furanone]: a potent and orally active cyclooxygenase-2 inhibitor. Pharmacological and biochemical profiles.

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183-190

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scholarly article

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10.1016/J.PLEFA.2008.08.001

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6

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79

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2008-10-01T00:00:00Z

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23293942

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18829279

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