Zobrazeno 1 - 6 of 6 pro vyhledávání: '"J Y, Crider"'
2
Affinities, selectivities, potencies, and intrinsic activities of natural and synthetic prostanoids using endogenous receptors: focus on DP class prostanoids
Autor: N A, Sharif, J Y, Crider, S X, Xu, G W, Williams
Publikováno v: The Journal of pharmacology and experimental therapeutics. 293(2)
The prostanoid receptor-subtype binding affinities, selectivities, potencies, and intrinsic activities of four natural prostanoids and six synthetic DP class prostanoids were determined using binding and functional assays with endogenous receptors. S
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4ef10fb5595c6caebf080f46c8d87050
https://pubmed.ncbi.nlm.nih.gov/10772998
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3
AL-8810: a novel prostaglandin F2 alpha analog with selective antagonist effects at the prostaglandin F2 alpha (FP) receptor
Autor: B W, Griffin, P, Klimko, J Y, Crider, N A, Sharif
Publikováno v: The Journal of pharmacology and experimental therapeutics. 290(3)
A novel analog of prostaglandin F(2alpha) [AL-8810; (5Z, 13E)-(9S, 11S,15R)-9,15-dihydroxy-11-fluoro-15-(2-indanyl)-16,17,18,19, 20-pentanor-5,13-prostadienoic acid] has been discovered with uniquely low efficacy (E(max)) at the endogenous prostaglan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3c2159b643a857707acc689d31cd36f9
https://pubmed.ncbi.nlm.nih.gov/10454504
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4
Prostaglandin DP receptors positively coupled to adenylyl cyclase in embryonic bovine tracheal (EBTr) cells: pharmacological characterization using agonists and antagonists
Autor: J Y, Crider, B W, Griffin, N A, Sharif
Publikováno v: British journal of pharmacology. 127(1)
Various prostaglandin agonists representing various classes of receptor subtypes were evaluated for their ability to stimulate adenylyl cyclase via the endogenous DP receptor in embryonic bovine tracheal (EBTr) cells. Two antagonists were used to blo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cd361bbbda5e45464988fb79e622e7be
https://pubmed.ncbi.nlm.nih.gov/10369474
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5
Pharmacology of [3H]prostaglandin E1/[3H]prostaglandin E2 and [3H]prostaglandin F2alpha binding to EP3 and FP prostaglandin receptor binding sites in bovine corpus luteum: characterization and correlation with functional data
Autor: N A, Sharif, S X, Xu, G W, Williams, J Y, Crider, B W, Griffin, T L, Davis
Publikováno v: The Journal of pharmacology and experimental therapeutics. 286(2)
Specific binding of [3H]prostaglandin (PG) E1, [3H]PGE2 and [3H]PGF2alpha to washed total particulate homogenates of bovine corpus luteum comprised 60 to 82% of total binding. Scatchard analysis of competition data revealed the presence of an apparen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::edb6e510350db3c41dde41fbbb579326
https://pubmed.ncbi.nlm.nih.gov/9694973
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6
FP prostaglandin receptors mediating inositol phosphates generation and calcium mobilization in Swiss 3T3 cells: a pharmacological study
Autor: B W, Griffin, G W, Williams, J Y, Crider, N A, Sharif
Publikováno v: The Journal of pharmacology and experimental therapeutics. 281(2)
A detailed pharmacological characterization of the prostaglandin (PG) receptor coupled to phosphoinositide (PI) turnover and intracellular calcium mobilization in Swiss 3T3 mouse fibroblast cells was undertaken. The pharmacological profile of this fu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::59009c0b9646a2df4403661755dcb95f
https://pubmed.ncbi.nlm.nih.gov/9152393
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