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Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
January 24, 2016
Phosphoproteomics in translational research: a sarcoma perspective
J Noujaim, L S Payne, I Judson, et al.
Molecular and Cellular Biology
|
August 1, 1988
Structure-function analysis of synthetic and recombinant derivatives of transforming growth factor alpha
D Defeo-Jones, J Y Tai, R J Wegrzyn, et al.
The Biochemical Journal
|
February 1, 1990
The selectivity of statine-based inhibitors against various human aspartic proteinases
R A Jupp, B M Dunn, J W Jacobs, et al.
Journal of Medicinal Chemistry
|
December 1, 1985
Renin inhibitors. Syntheses of subnanomolar, competitive, transition-state analogue inhibitors containing a novel analogue of statine
J Boger, L S Payne, D S Perlow, et al.
Journal of Medicinal Chemistry
|
May 15, 1992
HIV-1 protease inhibitors based on hydroxyethylene dipeptide isosteres: an investigation into the role of the P1' side chain on structure-activity
S D Young, L S Payne, W J Thompson, et al.
Journal of Medicinal Chemistry
|
October 1, 1988
Renin inhibitors containing hydrophilic groups. Tetrapeptides with enhanced aqueous solubility and nanomolar potency
M G Bock, R M DiPardo, B E Evans, et al.
Journal of Medicinal Chemistry
|
March 1, 1991
Renin inhibitors containing conformationally restricted P1-P1' dipeptide mimetics
P D Williams, D S Perlow, L S Payne, et al.
Antimicrobial Agents and Chemotherapy
|
December 1, 1995
L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase
S D Young, S F Britcher, L O Tran, et al.
Journal of Medicinal Chemistry
|
July 20, 1992
A series of potent HIV-1 protease inhibitors containing a hydroxyethyl secondary amine transition state isostere: synthesis, enzyme inhibition, and antiviral activity
T J Tucker, W C Lumma, L S Payne, et al.
Nature
|
May 5, 1983
Novel renin inhibitors containing the amino acid statine
J Boger, N S Lohr, E H Ulm, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
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Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
January 24, 2016
Phosphoproteomics in translational research: a sarcoma perspective
J Noujaim, L S Payne, I Judson, et al.
Molecular and Cellular Biology
|
August 1, 1988
Structure-function analysis of synthetic and recombinant derivatives of transforming growth factor alpha
D Defeo-Jones, J Y Tai, R J Wegrzyn, et al.
The Biochemical Journal
|
February 1, 1990
The selectivity of statine-based inhibitors against various human aspartic proteinases
R A Jupp, B M Dunn, J W Jacobs, et al.
Journal of Medicinal Chemistry
|
December 1, 1985
Renin inhibitors. Syntheses of subnanomolar, competitive, transition-state analogue inhibitors containing a novel analogue of statine
J Boger, L S Payne, D S Perlow, et al.
Journal of Medicinal Chemistry
|
May 15, 1992
HIV-1 protease inhibitors based on hydroxyethylene dipeptide isosteres: an investigation into the role of the P1' side chain on structure-activity
S D Young, L S Payne, W J Thompson, et al.
Journal of Medicinal Chemistry
|
October 1, 1988
Renin inhibitors containing hydrophilic groups. Tetrapeptides with enhanced aqueous solubility and nanomolar potency
M G Bock, R M DiPardo, B E Evans, et al.
Journal of Medicinal Chemistry
|
March 1, 1991
Renin inhibitors containing conformationally restricted P1-P1' dipeptide mimetics
P D Williams, D S Perlow, L S Payne, et al.
Antimicrobial Agents and Chemotherapy
|
December 1, 1995
L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase
S D Young, S F Britcher, L O Tran, et al.
Journal of Medicinal Chemistry
|
July 20, 1992
A series of potent HIV-1 protease inhibitors containing a hydroxyethyl secondary amine transition state isostere: synthesis, enzyme inhibition, and antiviral activity
T J Tucker, W C Lumma, L S Payne, et al.
Nature
|
May 5, 1983
Novel renin inhibitors containing the amino acid statine
J Boger, N S Lohr, E H Ulm, et al.
Page
of 1