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Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 1992
Identification of highest-affinity ligands by affinity selection from equimolar peptide mixtures generated by robotic synthesis
R N Zuckermann, J M Kerr, M A Siani, et al.
Science (New York, N.Y.)
|
December 16, 1998
Exploiting the basis of proline recognition by SH3 and WW domains: design of N-substituted inhibitors
J T Nguyen, C W Turck, F E Cohen, et al.
Chemistry & Biology
|
July 25, 2000
Improving SH3 domain ligand selectivity using a non-natural scaffold
J T Nguyen, M Porter, M Amoui, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 1998
A combinatorial approach to the discovery of efficient cationic peptoid reagents for gene delivery
J E Murphy, T Uno, J D Hamer, et al.
Folding & Design
|
January 1, 1997
Chiral N-substituted glycines can form stable helical conformations
P Armand, K Kirshenbaum, A Falicov, et al.
Medchemcomm
|
August 16, 2018
Exploring the links between peptoid antibacterial activity and toxicity
H L Bolt, G A Eggimann, C A B Jahoda, et al.
Biopolymers
|
January 14, 2017
Log D versus HPLC derived hydrophobicity: The development of predictive tools to aid in the rational design of bioactive peptoids
H L Bolt, C E J Williams, R V Brooks, et al.
Molecular Diversity
|
January 1, 1997
NMR structural characterization of oligo-N-substituted glycine lead compounds from a combinatorial library
E K Bradley, J M Kerr, L S Richter, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 16, 1998
Sequence-specific polypeptoids: a diverse family of heteropolymers with stable secondary structure
K Kirshenbaum, A E Barron, R A Goldsmith, et al.
Chemistry & Biology
|
July 8, 1998
Lipitoids--novel cationic lipids for cellular delivery of plasmid DNA in vitro
C Y Huang, T Uno, J E Murphy, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 1992
Identification of highest-affinity ligands by affinity selection from equimolar peptide mixtures generated by robotic synthesis
R N Zuckermann, J M Kerr, M A Siani, et al.
Science (New York, N.Y.)
|
December 16, 1998
Exploiting the basis of proline recognition by SH3 and WW domains: design of N-substituted inhibitors
J T Nguyen, C W Turck, F E Cohen, et al.
Chemistry & Biology
|
July 25, 2000
Improving SH3 domain ligand selectivity using a non-natural scaffold
J T Nguyen, M Porter, M Amoui, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 1998
A combinatorial approach to the discovery of efficient cationic peptoid reagents for gene delivery
J E Murphy, T Uno, J D Hamer, et al.
Folding & Design
|
January 1, 1997
Chiral N-substituted glycines can form stable helical conformations
P Armand, K Kirshenbaum, A Falicov, et al.
Medchemcomm
|
August 16, 2018
Exploring the links between peptoid antibacterial activity and toxicity
H L Bolt, G A Eggimann, C A B Jahoda, et al.
Biopolymers
|
January 14, 2017
Log D versus HPLC derived hydrophobicity: The development of predictive tools to aid in the rational design of bioactive peptoids
H L Bolt, C E J Williams, R V Brooks, et al.
Molecular Diversity
|
January 1, 1997
NMR structural characterization of oligo-N-substituted glycine lead compounds from a combinatorial library
E K Bradley, J M Kerr, L S Richter, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 16, 1998
Sequence-specific polypeptoids: a diverse family of heteropolymers with stable secondary structure
K Kirshenbaum, A E Barron, R A Goldsmith, et al.
Chemistry & Biology
|
July 8, 1998
Lipitoids--novel cationic lipids for cellular delivery of plasmid DNA in vitro
C Y Huang, T Uno, J E Murphy, et al.
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of 3