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T McKnight

Showing results (101-110 of 113) with videos related to

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Bioorganic & Medicinal Chemistry|May 1, 1994
Rational design of high affinity tachykinin NK1 receptor antagonistsS Boyle, S Guard, M Higginbottom, et al.
Journal of Investigative Surgery : the Official Journal of the Academy of Surgical Research|March 1, 1996
Characterization of a murine model of acute lung injury (ALI): a prominent role for interleukin-1P S Choban, T Mcknight, L Flancbaum, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1983
Metorphamide: isolation, structure, and biologic activity of an amidated opioid octapeptide from bovine brainE Weber, F S Esch, P Böhlen, et al.
Journal of Cataract and Refractive Surgery|November 1, 1988
Posterior capsular opacification and intraocular lens decentration. Part I: Comparison of various posterior chamber lens designs implanted in the rabbit modelS O Hansen, K D Solomon, G T McKnight, et al.
British Journal of Pharmacology|June 16, 1999
Comparison of the effects of [Phe1psi(CH2-NH)Gly2]nociceptin(1-13)NH2 in rat brain, rat vas deferens and CHO cells expressing recombinant human nociceptin receptorsH Okawa, B Nicol, R Bigoni, et al.
British Journal of Pharmacology|October 1, 1991
Pharmacological specificity of novel, synthetic, cyclic peptides as antagonists at tachykinin receptorsA T McKnight, J J Maguire, N J Elliott, et al.
British Journal of Pharmacology|October 1, 1992
L-689,660, a novel cholinomimetic with functional selectivity for M1 and M3 muscarinic receptorsR J Hargreaves, A T McKnight, K Scholey, et al.
British Journal of Pharmacology|November 1, 1990
A novel series of non-quaternary oxadiazoles acting as full agonists at muscarinic receptorsS B Freedman, E A Harley, S Patel, et al.
Molecular Pharmacology|January 1, 1986
Conformationally constrained tachykinin analogs which are selective ligands for the eledoisin binding siteM A Cascieri, G G Chicchi, R M Freidinger, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
PD 176252--the first high affinity non-peptide gastrin-releasing peptide (BB2) receptor antagonistV Ashwood, V Brownhill, M Higginbottom, et al.
Pageof 12

Showing results (101-110 of 113) with videos related to

Sort By:
Pageof 12
Bioorganic & Medicinal Chemistry|May 1, 1994
Rational design of high affinity tachykinin NK1 receptor antagonistsS Boyle, S Guard, M Higginbottom, et al.
Journal of Investigative Surgery : the Official Journal of the Academy of Surgical Research|March 1, 1996
Characterization of a murine model of acute lung injury (ALI): a prominent role for interleukin-1P S Choban, T Mcknight, L Flancbaum, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1983
Metorphamide: isolation, structure, and biologic activity of an amidated opioid octapeptide from bovine brainE Weber, F S Esch, P Böhlen, et al.
Journal of Cataract and Refractive Surgery|November 1, 1988
Posterior capsular opacification and intraocular lens decentration. Part I: Comparison of various posterior chamber lens designs implanted in the rabbit modelS O Hansen, K D Solomon, G T McKnight, et al.
British Journal of Pharmacology|June 16, 1999
Comparison of the effects of [Phe1psi(CH2-NH)Gly2]nociceptin(1-13)NH2 in rat brain, rat vas deferens and CHO cells expressing recombinant human nociceptin receptorsH Okawa, B Nicol, R Bigoni, et al.
British Journal of Pharmacology|October 1, 1991
Pharmacological specificity of novel, synthetic, cyclic peptides as antagonists at tachykinin receptorsA T McKnight, J J Maguire, N J Elliott, et al.
British Journal of Pharmacology|October 1, 1992
L-689,660, a novel cholinomimetic with functional selectivity for M1 and M3 muscarinic receptorsR J Hargreaves, A T McKnight, K Scholey, et al.
British Journal of Pharmacology|November 1, 1990
A novel series of non-quaternary oxadiazoles acting as full agonists at muscarinic receptorsS B Freedman, E A Harley, S Patel, et al.
Molecular Pharmacology|January 1, 1986
Conformationally constrained tachykinin analogs which are selective ligands for the eledoisin binding siteM A Cascieri, G G Chicchi, R M Freidinger, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
PD 176252--the first high affinity non-peptide gastrin-releasing peptide (BB2) receptor antagonistV Ashwood, V Brownhill, M Higginbottom, et al.
Pageof 12