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Bioorganic & Medicinal Chemistry
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May 1, 1994
Rational design of high affinity tachykinin NK1 receptor antagonists
S 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-1
P 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 brain
E 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 model
S 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 receptors
H 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 receptors
A 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 receptors
R 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 receptors
S 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 site
M 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 antagonist
V Ashwood, V Brownhill, M Higginbottom, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 113) with videos related to
Sort By:
Page
of 12
Bioorganic & Medicinal Chemistry
|
May 1, 1994
Rational design of high affinity tachykinin NK1 receptor antagonists
S 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-1
P 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 brain
E 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 model
S 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 receptors
H 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 receptors
A 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 receptors
R 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 receptors
S 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 site
M 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 antagonist
V Ashwood, V Brownhill, M Higginbottom, et al.
Page
of 12