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Showing results (121-130 of 271) with videos related to

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Peptides|January 1, 1997
Structural modifications of the N-terminal tetrapeptide segment of [D-Ala2]deltorphin I: effects on opioid receptor affinities and activities in vitro and on antinociceptive potencyR Schmidt, D Menard, C Mrestani-Klaus, et al.
International Journal of Peptide and Protein Research|December 1, 1996
Cyclic morphiceptin analogs: cyclization studies and opioid activities in vitroD Vogel, R Schmidt, K Hartung, et al.
Bioorganic & Medicinal Chemistry Letters|August 13, 2013
N-terminal guanidinylation of TIPP (Tyr-Tic-Phe-Phe) peptides results in major changes of the opioid activity profileGrazyna Weltrowska, Thi M-D Nguyen, Nga N Chung, et al.
Life Sciences|June 13, 2003
Conversion of delta-, kappa- and mu-receptor selective opioid peptide agonists into delta-, kappa- and mu-selective antagonistsPeter W Schiller, Grazyna Weltrowska, Thi M-D Nguyen, et al.
Clinical Cardiology|February 19, 2000
Cardiac hemangiomaJ W Ha, M H Lee, B C Chang, et al.
Peptides|November 28, 2012
Antinociceptive effects of two deltorphins analogs in the tail-immersion test in ratsJ H Kotlinska, E Gibula-Bruzda, E Witkowska, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|September 13, 2006
Synthesis and biological activity of homoarginine-containing opioid peptidesJan Izdebski, Danuta Kunce, Peter W Schiller, et al.
Clinical Microbiology Reviews|October 9, 1999
Antifungal activities of antineoplastic agents: Saccharomyces cerevisiae as a model system to study drug actionM E Cardenas, M C Cruz, M Del Poeta, et al.
Journal of Medicinal Chemistry|October 15, 1993
TIPP[psi]: a highly potent and stable pseudopeptide delta opioid receptor antagonist with extraordinary delta selectivityP W Schiller, G Weltrowska, T M Nguyen, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|April 12, 2001
Highly potent side-chain to side-chain cyclized enkephalin analogues containing a carbonyl bridge: synthesis, biology and conformationD Pawlak, M Oleszczuk, J Wójcik, et al.
Pageof 28

Showing results (121-130 of 271) with videos related to

Sort By:
Pageof 28
Peptides|January 1, 1997
Structural modifications of the N-terminal tetrapeptide segment of [D-Ala2]deltorphin I: effects on opioid receptor affinities and activities in vitro and on antinociceptive potencyR Schmidt, D Menard, C Mrestani-Klaus, et al.
International Journal of Peptide and Protein Research|December 1, 1996
Cyclic morphiceptin analogs: cyclization studies and opioid activities in vitroD Vogel, R Schmidt, K Hartung, et al.
Bioorganic & Medicinal Chemistry Letters|August 13, 2013
N-terminal guanidinylation of TIPP (Tyr-Tic-Phe-Phe) peptides results in major changes of the opioid activity profileGrazyna Weltrowska, Thi M-D Nguyen, Nga N Chung, et al.
Life Sciences|June 13, 2003
Conversion of delta-, kappa- and mu-receptor selective opioid peptide agonists into delta-, kappa- and mu-selective antagonistsPeter W Schiller, Grazyna Weltrowska, Thi M-D Nguyen, et al.
Clinical Cardiology|February 19, 2000
Cardiac hemangiomaJ W Ha, M H Lee, B C Chang, et al.
Peptides|November 28, 2012
Antinociceptive effects of two deltorphins analogs in the tail-immersion test in ratsJ H Kotlinska, E Gibula-Bruzda, E Witkowska, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|September 13, 2006
Synthesis and biological activity of homoarginine-containing opioid peptidesJan Izdebski, Danuta Kunce, Peter W Schiller, et al.
Clinical Microbiology Reviews|October 9, 1999
Antifungal activities of antineoplastic agents: Saccharomyces cerevisiae as a model system to study drug actionM E Cardenas, M C Cruz, M Del Poeta, et al.
Journal of Medicinal Chemistry|October 15, 1993
TIPP[psi]: a highly potent and stable pseudopeptide delta opioid receptor antagonist with extraordinary delta selectivityP W Schiller, G Weltrowska, T M Nguyen, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|April 12, 2001
Highly potent side-chain to side-chain cyclized enkephalin analogues containing a carbonyl bridge: synthesis, biology and conformationD Pawlak, M Oleszczuk, J Wójcik, et al.
Pageof 28