Cyclooxygénase (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Cyclooxygénase" in French language version.

refsWebsite
Global rank French rank
4th place
12th place
2nd place
3rd place
234th place
147th place
18th place
118th place
149th place
80th place
2,854th place
313th place
57th place
4th place

doi.org

dx.doi.org

  • (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 (PMID 8121489, DOI 10.1038/367243a0, 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 (PMID 8967954, DOI 10.1038/384644a0, Bibcode 1996Natur.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 (ISSN 1755-3245, PMID 18952694, DOI 10.1093/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 (PMID 8967954, DOI 10.1038/384644a0, Bibcode 1996Natur.384..644K, lire en ligne)

inist.fr

jbc.org.gate2.inist.fr

issn.org

portal.issn.org

  • 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 (ISSN 1755-3245, PMID 18952694, DOI 10.1093/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 (PMID 8121489, DOI 10.1038/367243a0, 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 (PMID 8967954, DOI 10.1038/384644a0, Bibcode 1996Natur.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 (PMID 8121489, DOI 10.1038/367243a0, 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 (PMID 8967954, DOI 10.1038/384644a0, Bibcode 1996Natur.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 (ISSN 1755-3245, PMID 18952694, DOI 10.1093/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. »