Zobrazeno 1 - 10
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pro vyhledávání: '"G. Bechis"'
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Akademický článek
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Akademický článek
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Autor:
Hervé Rochat, Yvon Berland, Régis Guieu, J. Sampol, G. Halimi, G. Bechis, F. Sampieri, B. Dussol
Publikováno v:
Journal of Liquid Chromatography & Related Technologies. 22:1829-1841
Assays of adenosine and its derivatives in biological fluids involve fluorimetric, radioimmunological or chromatographic analyses. Techniques currently used are tedious because they involve either an extraction using immunological methods or one or t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3e3f4df8e8e1037f146ddb50cf0ef2f
https://doi.org/10.1081/jlc-100101769
https://doi.org/10.1081/jlc-100101769
Autor:
G. Halimi, F. Sampieri, F. Couraud, Hervé Rochat, Y. Berland, G. Bechis, Régis Guieu, J. Sampol, B. Dussol
Publikováno v:
General Pharmacology: The Vascular System. 31:553-561
1. Adenosine acts on a family of G-protein-coupled receptors called purinoreceptors. 2. Four subtypes have been cloned and pharmacologically characterized. 3. The principal pharmacological data and structure-function relations for agonist interaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b0aa9ae549f06d30ab67224e7a8b381
https://doi.org/10.1016/s0306-3623(98)00071-8
https://doi.org/10.1016/s0306-3623(98)00071-8
Publikováno v:
Clinica Chimica Acta. 230:63-68
Although it is well established that adenosine is released during acute ischemia, little is known of the behaviour of adenosine levels following treatment of coronary lesion by percutaneous transluminal coronary angioplasty (PTCA). Using high perform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebf076f9c6eb6d78e9e630154a873b8d
https://doi.org/10.1016/0009-8981(94)90089-2
https://doi.org/10.1016/0009-8981(94)90089-2
Autor:
R, Guieu, B, Dussol, G, Halimi, G, Bechis, F, Sampieri, Y, Berland, J, Sampol, F, Couraud, H, Rochat
Publikováno v:
General pharmacology. 31(4)
1. Adenosine acts on a family of G-protein-coupled receptors called purinoreceptors. 2. Four subtypes have been cloned and pharmacologically characterized. 3. The principal pharmacological data and structure-function relations for agonist interaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2e9f93ce28fbfa0cfa430d0c82c91721
https://pubmed.ncbi.nlm.nih.gov/9792214
https://pubmed.ncbi.nlm.nih.gov/9792214
Autor:
Marianick Juin, H. Henry, Régis Guieu, R. Gola, Jean Pouget, F. Sampieri, D. Mallet, Hervé Rochat, Christiane Devaux, G. Bechis
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 25(1)
Background:Adenosine is a powerful natural vasodilator that participates in the control of cerebral and meningeal blood flow. In this context, it could be involved in the pathophysiology of migraine, since it was previously reported that intravenous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40227c53d5c063e24200e081f4ded795
https://pubmed.ncbi.nlm.nih.gov/9532282
https://pubmed.ncbi.nlm.nih.gov/9532282
Publikováno v:
Clinical neuropharmacology. 19(6)
After a review of the metabolism and pharmacology of adenosine, this work will examine the various therapeutic possibilities involving the use of agonists or antagonists of adenosine A1 or A2 receptors in neurological disorders. Promising preclinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e5b27fd59e2460e29365dc244dfaa7
https://pubmed.ncbi.nlm.nih.gov/8937786
https://pubmed.ncbi.nlm.nih.gov/8937786
Publikováno v:
Pain. 68(2-3)
Recent studies have reported the possibilities of relieving neuropathic pain by administering adenosine or its analogs. In order to determine if there exists a metabolic anomaly of this nucleoside in patients with neuropathic pain, circulating adenos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b059bf6994c7966e1a60e97dbb12d796
https://pubmed.ncbi.nlm.nih.gov/9121814
https://pubmed.ncbi.nlm.nih.gov/9121814