Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Amodeo

Showing results (31-40 of 43) with videos related to

Pageof 5
Sort By:
FEBS Letters|December 12, 1997
Design of mu selective opioid dipeptide antagonistsA Capasso, P Amodeo, G Balboni, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|September 1, 1996
Delta-selective opioid peptides containing a single aromatic residue in the message domain: an NMR conformational analysisO Crescenzi, P Amodeo, G Cavicchioni, et al.
Peptide Research|January 1, 1992
Solution structure of deltorphin I at 265 K: a quantitative NMR studyP Amodeo, A Motta, T Tancredi, et al.
FEBS Letters|December 27, 1995
Conformational analysis of potent and very selective delta opioid dipeptide antagonistsP Amodeo, G Balboni, O Crescenzi, et al.
Biopolymers|April 1, 1992
Conformational analysis of an opioid peptide in solvent media that mimic cytoplasm viscosityP A Temussi, D Picone, G Saviano, et al.
Biopolymers|May 1, 1991
New insights on mu/delta selectivity of opioid peptides: conformational analysis of deltorphin analoguesT Tancredi, P A Temussi, D Picone, et al.
Biopolymers|June 1, 1993
Synthesis, biological activity, and conformational analysis of [pGlu6,N-MePhe8,Aib9] substance P (6-11): a selective agonist for the NK-3 receptorM Tallon, D Ron, D Halle, et al.
Biochemical and Biophysical Research Communications|February 15, 1994
Selective opioid dipeptidesP A Temussi, S Salvadori, P Amodeo, et al.
European Journal of Biochemistry|August 15, 1994
Conversion of enkephalin and dermorphin into delta-selective opioid antagonists by single-residue substitutionT Tancredi, S Salvadori, P Amodeo, et al.
Biochemistry|October 3, 2001
Thiol/disulfide interconversion in bovine lens aldose reductase induced by intermediates of glutathione turnoverP G Vilardo, A Scaloni, P Amodeo, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
FEBS Letters|December 12, 1997
Design of mu selective opioid dipeptide antagonistsA Capasso, P Amodeo, G Balboni, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|September 1, 1996
Delta-selective opioid peptides containing a single aromatic residue in the message domain: an NMR conformational analysisO Crescenzi, P Amodeo, G Cavicchioni, et al.
Peptide Research|January 1, 1992
Solution structure of deltorphin I at 265 K: a quantitative NMR studyP Amodeo, A Motta, T Tancredi, et al.
FEBS Letters|December 27, 1995
Conformational analysis of potent and very selective delta opioid dipeptide antagonistsP Amodeo, G Balboni, O Crescenzi, et al.
Biopolymers|April 1, 1992
Conformational analysis of an opioid peptide in solvent media that mimic cytoplasm viscosityP A Temussi, D Picone, G Saviano, et al.
Biopolymers|May 1, 1991
New insights on mu/delta selectivity of opioid peptides: conformational analysis of deltorphin analoguesT Tancredi, P A Temussi, D Picone, et al.
Biopolymers|June 1, 1993
Synthesis, biological activity, and conformational analysis of [pGlu6,N-MePhe8,Aib9] substance P (6-11): a selective agonist for the NK-3 receptorM Tallon, D Ron, D Halle, et al.
Biochemical and Biophysical Research Communications|February 15, 1994
Selective opioid dipeptidesP A Temussi, S Salvadori, P Amodeo, et al.
European Journal of Biochemistry|August 15, 1994
Conversion of enkephalin and dermorphin into delta-selective opioid antagonists by single-residue substitutionT Tancredi, S Salvadori, P Amodeo, et al.
Biochemistry|October 3, 2001
Thiol/disulfide interconversion in bovine lens aldose reductase induced by intermediates of glutathione turnoverP G Vilardo, A Scaloni, P Amodeo, et al.
Pageof 5