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K M Metters

Showing results (31-40 of 54) with videos related to

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The Journal of Pharmacology and Experimental Therapeutics|June 1, 1994
Leukotriene D4-induced increases in cytosolic calcium in THP-1 cells: dependence on extracellular calcium and inhibition with selective leukotriene D4 receptor antagonistsC C Chan, P Ecclestone, D W Nicholson, et al.
British Journal of Pharmacology|November 11, 1999
Distribution and regulation of cyclooxygenase-2 in carrageenan-induced inflammationF Nantel, D Denis, R Gordon, et al.
The Journal of Biological Chemistry|April 22, 1994
Cloning and expression of a cDNA for the human prostanoid IP receptorY Boie, T H Rushmore, A Darmon-Goodwin, et al.
FEBS Letters|January 26, 1987
Chromogranin A can act as a reversible processing enzyme inhibitor. Evidence from the inhibition of the IRCM-serine protease 1 cleavage of pro-enkephalin and ACTH at pairs of basic amino acidsN G Seidah, G N Hendy, J Hamelin, et al.
The Journal of Biological Chemistry|January 28, 1994
Cloning and expression of a cDNA for the human prostanoid FP receptorM Abramovitz, Y Boie, T Nguyen, et al.
FEBS Letters|January 31, 1994
Cloning and expression of three isoforms of the human EP3 prostanoid receptorM Adam, Y Boie, T H Rushmore, et al.
Biochemical Pharmacology|October 13, 2001
Sequestration and phosphorylation of the prostaglandin E2 EP4 receptor: dependence on the C-terminal tailD Slipetz, S Buchanan, C Mackereth, et al.
European Journal of Biochemistry|October 15, 1992
Purification of human leukotriene C4 synthase from dimethylsulfoxide-differentiated U937 cellsD W Nicholson, M W Klemba, D M Rasper, et al.
Molecular Pharmacology|August 1, 1995
Activation of the human peripheral cannabinoid receptor results in inhibition of adenylyl cyclaseD M Slipetz, G P O'Neill, L Favreau, et al.
Molecular Pharmacology|May 17, 2001
Key structural features of prostaglandin E(2) and prostanoid analogs involved in binding and activation of the human EP(1) prostanoid receptorM D Ungrin, M C Carrière, D Denis, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
The Journal of Pharmacology and Experimental Therapeutics|June 1, 1994
Leukotriene D4-induced increases in cytosolic calcium in THP-1 cells: dependence on extracellular calcium and inhibition with selective leukotriene D4 receptor antagonistsC C Chan, P Ecclestone, D W Nicholson, et al.
British Journal of Pharmacology|November 11, 1999
Distribution and regulation of cyclooxygenase-2 in carrageenan-induced inflammationF Nantel, D Denis, R Gordon, et al.
The Journal of Biological Chemistry|April 22, 1994
Cloning and expression of a cDNA for the human prostanoid IP receptorY Boie, T H Rushmore, A Darmon-Goodwin, et al.
FEBS Letters|January 26, 1987
Chromogranin A can act as a reversible processing enzyme inhibitor. Evidence from the inhibition of the IRCM-serine protease 1 cleavage of pro-enkephalin and ACTH at pairs of basic amino acidsN G Seidah, G N Hendy, J Hamelin, et al.
The Journal of Biological Chemistry|January 28, 1994
Cloning and expression of a cDNA for the human prostanoid FP receptorM Abramovitz, Y Boie, T Nguyen, et al.
FEBS Letters|January 31, 1994
Cloning and expression of three isoforms of the human EP3 prostanoid receptorM Adam, Y Boie, T H Rushmore, et al.
Biochemical Pharmacology|October 13, 2001
Sequestration and phosphorylation of the prostaglandin E2 EP4 receptor: dependence on the C-terminal tailD Slipetz, S Buchanan, C Mackereth, et al.
European Journal of Biochemistry|October 15, 1992
Purification of human leukotriene C4 synthase from dimethylsulfoxide-differentiated U937 cellsD W Nicholson, M W Klemba, D M Rasper, et al.
Molecular Pharmacology|August 1, 1995
Activation of the human peripheral cannabinoid receptor results in inhibition of adenylyl cyclaseD M Slipetz, G P O'Neill, L Favreau, et al.
Molecular Pharmacology|May 17, 2001
Key structural features of prostaglandin E(2) and prostanoid analogs involved in binding and activation of the human EP(1) prostanoid receptorM D Ungrin, M C Carrière, D Denis, et al.
Pageof 6