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C Gilon

Showing results (31-40 of 92) with videos related to

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Journal of Molecular Biology|September 24, 1999
Miniaturized proteins: the backbone cyclic proteinomimetic approachR Kasher, D A Oren, Y Barda, et al.
Methods in Enzymology|January 1, 1991
Inhibition of protein-tyrosine kinases by tyrphostinsA Levitzki, A Gazit, N Osherov, et al.
Journal of Medicinal Chemistry|February 1, 1983
Synthesis of partially modified retro-inverso substance P analogues and their biological activityM Chorev, E Rubini, C Gilon, et al.
Biopolymers|May 1, 1991
Backbone cyclization: A new method for conferring conformational constraint on peptidesC Gilon, D Halle, M Chorev, et al.
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.
Biopolymers|December 1, 1976
Conformational studies of peptides. The crystal structures of N-acetyl-L-prolinamide and N-acetyl-(S)-thiazolidine-4-carboxamideE Benedetti, A Christensen, C Gilon, 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.
Pageof 10

Showing results (31-40 of 92) with videos related to

Sort By:
Pageof 10
Journal of Molecular Biology|September 24, 1999
Miniaturized proteins: the backbone cyclic proteinomimetic approachR Kasher, D A Oren, Y Barda, et al.
Methods in Enzymology|January 1, 1991
Inhibition of protein-tyrosine kinases by tyrphostinsA Levitzki, A Gazit, N Osherov, et al.
Journal of Medicinal Chemistry|February 1, 1983
Synthesis of partially modified retro-inverso substance P analogues and their biological activityM Chorev, E Rubini, C Gilon, et al.
Biopolymers|May 1, 1991
Backbone cyclization: A new method for conferring conformational constraint on peptidesC Gilon, D Halle, M Chorev, et al.
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.
Biopolymers|December 1, 1976
Conformational studies of peptides. The crystal structures of N-acetyl-L-prolinamide and N-acetyl-(S)-thiazolidine-4-carboxamideE Benedetti, A Christensen, C Gilon, 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.
Pageof 10