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International Journal of Peptide and Protein Research
|
September 1, 1987
Analogs of oxytocin containing a modified peptide bond
M Lebl, E E Sugg, G van Binst, et al.
Journal of Medicinal Chemistry
|
February 3, 2006
Novel benzodiazepine photoaffinity probe stereoselectively labels a site deep within the membrane-spanning domain of the cholecystokinin receptor
Elizabeth M Hadac, Eric S Dawson, James W Darrow, et al.
International Journal of Peptide and Protein Research
|
June 1, 1988
Cholecystokinic activity of N alpha-hydroxysulfonyl-[Nle28,31]CCK26-33 analogues modified at the C-terminal residue
E E Sugg, M Serra, J E Shook, et al.
The Journal of Biological Chemistry
|
January 5, 1991
Allele-specific activation of genetically engineered receptors
C D Strader, T Gaffney, E E Sugg, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 1, 1994
A further analysis of the contraction induced by activation of cholecystokinin A receptors in guinea pig isolated ileum longitudinal muscle-myenteric plexus
M Corsi, S Palea, C Pietra, et al.
Life Sciences
|
November 3, 1986
Synthesis and biological evaluation of N alpha-hydroxysulfonyl-[Nle28,31]-CCK26-33
E E Sugg, J E Shook, M Serra, et al.
Journal of Medicinal Chemistry
|
January 6, 1995
CCK-A receptor selective antagonists derived from the CCK-A receptor selective tetrapeptide agonist Boc-Trp-Lys(Tac)-Asp-MePhe-NH2 (A-71623)
E E Sugg, M J Kimery, J M Ding, et al.
Biochemistry
|
March 9, 1993
Synthetic charybdotoxin-iberiotoxin chimeric peptides define toxin binding sites on calcium-activated and voltage-dependent potassium channels
K M Giangiacomo, E E Sugg, M Garcia-Calvo, et al.
Proceedings of the Western Pharmacology Society
|
January 1, 1987
N-terminal cyclization of a nonsulfated CCK analogue exhibits opioid antagonist activity in vitro
P K Lemcke, E Sugg, M Malarchik, et al.
The Biochemical Journal
|
January 15, 1992
Purification and characterization by fast-atom-bombardment mass spectrometry of the polymorphonuclear-leucocyte-elastase-generated A alpha (1-21) fragment of fibrinogen from human blood after incubation with calcium ionophore A23187
R S Dewey, J M Liesch, H R Williams, et al.
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of 6
Search research articles
Search
Showing results (31-40 of 52) with videos related to
Sort By:
Page
of 6
International Journal of Peptide and Protein Research
|
September 1, 1987
Analogs of oxytocin containing a modified peptide bond
M Lebl, E E Sugg, G van Binst, et al.
Journal of Medicinal Chemistry
|
February 3, 2006
Novel benzodiazepine photoaffinity probe stereoselectively labels a site deep within the membrane-spanning domain of the cholecystokinin receptor
Elizabeth M Hadac, Eric S Dawson, James W Darrow, et al.
International Journal of Peptide and Protein Research
|
June 1, 1988
Cholecystokinic activity of N alpha-hydroxysulfonyl-[Nle28,31]CCK26-33 analogues modified at the C-terminal residue
E E Sugg, M Serra, J E Shook, et al.
The Journal of Biological Chemistry
|
January 5, 1991
Allele-specific activation of genetically engineered receptors
C D Strader, T Gaffney, E E Sugg, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 1, 1994
A further analysis of the contraction induced by activation of cholecystokinin A receptors in guinea pig isolated ileum longitudinal muscle-myenteric plexus
M Corsi, S Palea, C Pietra, et al.
Life Sciences
|
November 3, 1986
Synthesis and biological evaluation of N alpha-hydroxysulfonyl-[Nle28,31]-CCK26-33
E E Sugg, J E Shook, M Serra, et al.
Journal of Medicinal Chemistry
|
January 6, 1995
CCK-A receptor selective antagonists derived from the CCK-A receptor selective tetrapeptide agonist Boc-Trp-Lys(Tac)-Asp-MePhe-NH2 (A-71623)
E E Sugg, M J Kimery, J M Ding, et al.
Biochemistry
|
March 9, 1993
Synthetic charybdotoxin-iberiotoxin chimeric peptides define toxin binding sites on calcium-activated and voltage-dependent potassium channels
K M Giangiacomo, E E Sugg, M Garcia-Calvo, et al.
Proceedings of the Western Pharmacology Society
|
January 1, 1987
N-terminal cyclization of a nonsulfated CCK analogue exhibits opioid antagonist activity in vitro
P K Lemcke, E Sugg, M Malarchik, et al.
The Biochemical Journal
|
January 15, 1992
Purification and characterization by fast-atom-bombardment mass spectrometry of the polymorphonuclear-leucocyte-elastase-generated A alpha (1-21) fragment of fibrinogen from human blood after incubation with calcium ionophore A23187
R S Dewey, J M Liesch, H R Williams, et al.
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of 6