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Keyword [Structure-based]
Result: 61 - 80 | Page: 4 of 7
61.
Design,Synthesis And Biological Evaluation Of Tetrazole-Containing RXR? Ligands As Anticancer Agent And Structure-Based Virtual Screening Of Novel RXR? Ligands
62.
Study On The Effect Of Colorectal Cancer Resistance To Oxaliplatin On The Genome Three-dimensionalspatial Structure Based On DLO Hi-C Technology
63.
Research On Coronary Stent Structure Based On Elastoplastic Mechanics And Fluid-solid Coupling
64.
Research On The Symmetry Of The Human Body Structure Based On The Electromyography Analysis Of The Human Body's Surface
65.
Disrupting HIV replication with structure-based design of Tat inhibitors
66.
Structure-based optimization of small molecule transcription therapy targeting the BCL6 oncoprotein
67.
Structure based design of peptide-mimetic STAT3 inhibitors
68.
Structure based design of potent inhibitors against multidrug-resistant HIV-1 protease variants
69.
Development of a structure-based drug design module for a bioengineering lab
70.
The trefoil proteins TFF1 & TFF3 in gastrointestinal cancer: A structure-based study
71.
Computational structure-based methods to anticipate HIV drug resistance evolution and accelerate inhibitor discovery
72.
Structure-based drug design for dihydrofolate reductase
73.
Incorporating protein flexibility into structure-based drug design: HIV-1 protease as a test case
74.
Hit Identification for PKCzeta Inhibitors: Structure-Based Optimization, Virtual Screening, and Biological Evaluation
75.
Structure-based design and synthesis of inhibitors of phenylethanolamine N-methyltransferase
76.
NG-nitro-L-arginine-containing peptidomimetics as selective neuronal nitric oxide synthase inhibitors. Structure-based design, synthesis, and biological evaluation and approaches toward enhanced CNS activity
77.
Structure-based drug mechanism study and inhibitor design targeting tuberculosis
78.
Refining the pharmacophore for phosphatase inhibition and structure-based design of okadaic acid analogs
79.
Structure based drug discovery of potent and specific antimicrobial agents for anthrax
80.
I. Comparison of translesion bypass of guanine-N2 monoadducts of mitomycin C and guanine -N7 monoadducts of 2,7-diaminomitosene by T7 exo-, Klenow exo-, eta and Klenow exo+ DNA polymerases. II. Structure-based design, synthesis, structure-conformation and
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