(en) Daniel Picot, Patrick J. Loll et R. Michael Garavito, « The X-ray crystal structure of the membrane protein prostaglandin H2 synthase-1 », Nature, vol. 367, no 6460, , p. 243-249 (PMID8121489, DOI10.1038/367243a0, lire en ligne)
(en) Ravi G. Kurumbail, Anna M. Stevens, James K. Gierse, Joseph J. McDonald, Roderick A. Stegeman, Jina Y. Pak, Daniel Gildehaus, Julie M. iyashiro, Thomas D. Penning, Karen Seibert, Peter C. Isakson et William C. Stallings, « Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents », Nature, vol. 384, no 6610, , p. 644-648 (PMID8967954, DOI10.1038/384644a0, Bibcode1996Natur.384..644K, lire en ligne)
Nabil Foudi, Liliane Louedec, Thierry Cachina et Charles Brink, « Selective cyclooxygenase-2 inhibition directly increases human vascular reactivity to norepinephrine during acute inflammation », Cardiovascular Research, vol. 81, no 2, , p. 269–277 (ISSN1755-3245, PMID18952694, DOI10.1093/cvr/cvn287, lire en ligne, consulté le )
harvard.edu
ui.adsabs.harvard.edu
(en) Ravi G. Kurumbail, Anna M. Stevens, James K. Gierse, Joseph J. McDonald, Roderick A. Stegeman, Jina Y. Pak, Daniel Gildehaus, Julie M. iyashiro, Thomas D. Penning, Karen Seibert, Peter C. Isakson et William C. Stallings, « Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents », Nature, vol. 384, no 6610, , p. 644-648 (PMID8967954, DOI10.1038/384644a0, Bibcode1996Natur.384..644K, lire en ligne)
Nabil Foudi, Liliane Louedec, Thierry Cachina et Charles Brink, « Selective cyclooxygenase-2 inhibition directly increases human vascular reactivity to norepinephrine during acute inflammation », Cardiovascular Research, vol. 81, no 2, , p. 269–277 (ISSN1755-3245, PMID18952694, DOI10.1093/cvr/cvn287, lire en ligne, consulté le )
nature.com
(en) Daniel Picot, Patrick J. Loll et R. Michael Garavito, « The X-ray crystal structure of the membrane protein prostaglandin H2 synthase-1 », Nature, vol. 367, no 6460, , p. 243-249 (PMID8121489, DOI10.1038/367243a0, lire en ligne)
(en) Ravi G. Kurumbail, Anna M. Stevens, James K. Gierse, Joseph J. McDonald, Roderick A. Stegeman, Jina Y. Pak, Daniel Gildehaus, Julie M. iyashiro, Thomas D. Penning, Karen Seibert, Peter C. Isakson et William C. Stallings, « Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents », Nature, vol. 384, no 6610, , p. 644-648 (PMID8967954, DOI10.1038/384644a0, Bibcode1996Natur.384..644K, lire en ligne)
nih.gov
ncbi.nlm.nih.gov
(en) Daniel Picot, Patrick J. Loll et R. Michael Garavito, « The X-ray crystal structure of the membrane protein prostaglandin H2 synthase-1 », Nature, vol. 367, no 6460, , p. 243-249 (PMID8121489, DOI10.1038/367243a0, lire en ligne)
(en) Ravi G. Kurumbail, Anna M. Stevens, James K. Gierse, Joseph J. McDonald, Roderick A. Stegeman, Jina Y. Pak, Daniel Gildehaus, Julie M. iyashiro, Thomas D. Penning, Karen Seibert, Peter C. Isakson et William C. Stallings, « Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents », Nature, vol. 384, no 6610, , p. 644-648 (PMID8967954, DOI10.1038/384644a0, Bibcode1996Natur.384..644K, lire en ligne)
Nabil Foudi, Liliane Louedec, Thierry Cachina et Charles Brink, « Selective cyclooxygenase-2 inhibition directly increases human vascular reactivity to norepinephrine during acute inflammation », Cardiovascular Research, vol. 81, no 2, , p. 269–277 (ISSN1755-3245, PMID18952694, DOI10.1093/cvr/cvn287, lire en ligne, consulté le )
sciencedirect.com
« Molecular Mechanisms of Drug Actions: From Receptors to Effectors - Pediatric Critical Care (Fourth Edition) - Chapter 117 », sur www.sciencedirect.com (consulté le ) : « Arachidonic acid is a component of membrane phospholipids released either in a one-step process, after phospholipase A2 (PLA2) action, or a two-step process, after phospholipase C and DAG lipase actions. Arachidonic acid is then metabolized by cyclooxygenase (COX) and 5-lipoxygenase, resulting in the synthesis of prostaglandins and leukotrienes, respectively. These intracellular messengers play an important role in the regulation of signal transduction implicated in pain and inflammatory responses. »