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International Journal of Peptide and Protein Research|December 1, 1996
Structure-activity relationship of the ring portion in backbone-cyclic C-terminal hexapeptide analogs of substance P. NMR and molecular dynamicsS Behrens, B Mathä, G Bitan, et al.Journal of Medicinal Chemistry|February 1, 1988
Dehydro keto methylene and keto methylene analogues of substance P. Synthesis and biological activityA Ewenson, R Laufer, M Chorev, et al.FEBS Letters|July 14, 1998
A peptide derived from the N-terminal region of HIV-1 Vpr promotes nuclear import in permeabilized cells: elucidation of the NLS region of the VprO Karni, A Friedler, N Zakai, et al.Journal of Medicinal Chemistry|February 1, 1986
Ketomethylene pseudopeptide analogues of substance P: synthesis and biological activityA Ewenson, R Laufer, M Chorev, et al.Bioorganic & Medicinal Chemistry|January 1, 1997
Synthesis and biological activity of semipeptoid farnesyltransferase inhibitorsH Reuveni, A Gitler, E Poradosu, et al.Journal of Chromatography|October 5, 1984
Ion-exchange chromatographic assay of peptidases acting on the C-terminal hexapeptide sequence of substance PR Laufer, U Wormser, Z Selinger, et al.Neuropeptides|May 1, 1990
Proteolytic resistance and biological activity of N-methylated analogs of [pGlu6] substance P6-11U Wormser, R Laufer, M Chorev, et al.European Journal of Biochemistry|July 1, 1985
Inhibition of substance P degradation in rat brain preparations by peptide hydroxamic acidsR Laufer, A Ewenson, C Gilon, et al.European Journal of Biochemistry|January 2, 1985
N-Bromoacetyl-amino-cyanopindolol: a highly potent beta-adrenergic affinity label blocks irreversibly a non-protein component tightly associated with the receptorM Chorev, A Feigenbaum, A K Keenan, et al.Neuropharmacology|November 1, 1990
Neurochemical mediators of the behavioural effects of receptor-selective substance P agonists administered intrathecally in the ratD Papir-Kricheli, C Gilon, M Chorev, et al.Pageof 220