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  1. 1.   Recapitulation of cell-like KRAS4b membrane dynamics on complex biomimetic membranes
  2. Shrestha,Rebika; Chen,De; Frank,Peter; Nissley,Dwight; Turbyville,Tommy
  3. iScience. 2021, Dec 10; 25(1):
  1. 2.   Application of Post Solid-Phase Oxime Ligation to Fine-Tune Peptide-Protein Interactions
  2. Zhao,Xue Zhi; Liu, Fa; Burke,Terrence
  3. Molecules (Basel, Switzerland). 2020, JUN; 25(12):
  1. 3.   Recent Advances in Targeting the HIV-1 Tat/TAR Complex
  2. Abulwerdi, Fardokht; Legrice, Stuart
  3. Current pharmaceutical design. 2017, Jun 15; 23(28): 4112-4121.
  1. 4.   Oxime-Based Click Chemistry in the Development of 3-Isoxazolecarboxylic Acid Containing Inhibitors of Yersinia pestis Protein Tyrosine Phosphatase, YopH
  2. Bahta, M.; Burke, T. R.
  3. Chemmedchem. 2011, Aug; 6(8): 1363-1370.
  1. 5.   Self assembled bi-functional peptide hydrogels with biomineralization-directing peptides
  2. Gungormus, M.; Branco, M.; Fong, H.; Schneider, J. P.; Tamerler, C.; Sarikaya, M.
  3. Biomaterials. 2010, Oct; 31(28): 7266-7274.
  1. 6.   SAR by oxime-containing peptide libraries: Application to Tsg101 ligand optimization
  2. Liu, F.; Stephen, A. G.; Waheed, A. A.; Aman, M. J.; Freed, E. O.; Fisher, R. J.; Burke, T. R.
  3. Chembiochem. 2008 9(12): 2000-2004.
  1. 7.   Examination of acylated 4-aminopiperidine-4-carboxylic acid residues in the phosphotyrosyl+1 position of Grb2 SH2 domain-binding tripeptides
  2. Kang, S. U.; Choi, W. J.; Oishi, S.; Lee, K.; Karki, R. G.; Worthy, K. M.; Bindu, L. K.; Nicklaus, M. C.; Fisher, R. J.; Burke, T. R.
  3. Journal of Medicinal Chemistry. 2007, Apr; 50(8): 1978-1982.
  1. 8.   Utilization of achiral alkenyl amines for the preparation of high affinity Grb2 SH2 domain-binding macrocycles by ring-closing metathesis
  2. Liu, F.; Worthy, K. M.; Bindu, L.; Giubellino, A.; Bottaro, D. P.; Fisher, R. J.; Burke, T. R.
  3. Organic & Biomolecular Chemistry. 2007 5(2): 367-372.
  1. 9.   Application of azide-alkyne cycloaddition 'click chemistry' for the synthesis of Grb2 SH2 domain-binding macrocycles
  2. Choi, W. J.; Shi, Z. D.; Worthy, K. M.; Bindu, L.; Karki, R. G.; Nicklaus, M. C.; Fisher, R. J.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry Letters. 2006, Oct; 16(20): 5265-5269.
  1. 10.   Hydrazone- and hydrazide-containing N-substituted glycines as peptoid surrogates for expedited library synthesis: Application to the preparation of Tsg101-directed HIV-1 budding antagonists
  2. Liu, F.; Stephen, A. G.; Adamson, C. S.; Gousset, K.; Aman, M. J.; Freed, E. O.; Fisher, R. J.; Burke, T. R.
  3. Organic Letters. 2006, Oct; 8(22): 5165-5168.
  1. 11.   Development of Grb2 SH2 domain signaling antagonists: A potential new class of antiproliferative agents
  2. Burke, T. R.
  3. International Journal of Peptide Research and Therapeutics. 2006, Mar; 12(1): 33-48.
  1. 12.   Design and synthesis of phosphonodifluoromethyl phenylalanine (F(2)Pmp): A useful phosphotyrosyl mimetic
  2. Burke, T. R.
  3. Current Topics in Medicinal Chemistry. 2006 6(14): 1465-1471.
  1. 13.   Examination of phosphoryl-mimicking functionalities within a macrocyclic Grb2 SH2 domain-binding platform
  2. Kang, S. U.; Shi, Z. D.; Worthy, K. M.; Bindu, L. K.; Dharmawardana, P. G.; Choyke, S. J.; Bottaro, D. P.; Fisher, R. J.; Burke, T. R.
  3. Journal of Medicinal Chemistry. 2005, JUN 16; 48(12): 3945-3948.
  1. 14.   Cutting edge: Expression of IL-1 receptor-associated kinase-4 (IRAK-4) proteins with mutations identified in a patient with recurrent bacterial infections alters normal IRAK-4 interaction with components of the IL-1 receptor complex
  2. Medvedev, A. E.; Thomas, K.; Awomoyi, A.; Kuhns, D. B.; Gallin, J. I.; Li, X. X.; Vogel, S. N.
  3. Journal of Immunology. 2005, JUN 1; 174(11): 6587-6591.
  1. 15.   Design and synthesis of conformationally constrained Grb2 SH2 domain binding peptides employing alpha-methylphenylalanyl based phosphotyrosyl mimetics
  2. Oishi, S.; Karki, R. G.; Kang, S. U.; Wang, X. Z.; Worthy, K. M.; Bindu, L. K.; Nicklaus, M. C.; Fisher, R. J.; Burke, T. R.
  3. Journal of Medicinal Chemistry. 2005, FEB 10; 48(3): 764-772.
  1. 16.   Structure-based design, synthesis and biochemical testing of novel and potent Smac peptido-mimetics
  2. Sun, H. Y.; Nikolovska-Coleska, Z.; Chen, J. Y.; Yang, C. Y.; Tomita, Y.; Pan, H. G.; Yoshioka, Y.; Krajewski, K.; Roller, P. P.; Wang, S. M.
  3. Bioorganic & Medicinal Chemistry Letters. 2005, FEB 1; 15(3): 793-797.
  1. 17.   Evaluation of macrocyclic Grb2 SH2 domain-binding peptide mimetics prepared by ring-closing metathesis of C-terminal allylglycines with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic
  2. Oishi, S.; Karki, R. G.; Shi, Z. D.; Worthy, K. M.; Bindu, L.; Chertov, O.; Esposito, D.; Frank, P.; Gillette, W. K.; Maderia, M.; Hartley, J.; Nicklaus, M. C.; Barchi, J. J.; Fisher, R. J.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry. 2005 13(7): 2431-2438.
  1. 18.   Utilization of a common pathway for the synthesis of high affinity macrocyclic Grh2 SH2 domain-binding peptide mimetics that differ in the configuration at one ring junction
  2. Shi, Z. D.; Karki, R. G.; Worthy, K. M.; Bindu, L. K.; Nicklaus, M. C.; Fisher, R. J.; Burke, T. R.
  3. Chemistry & Biodiversity. 2005 2(4): 447-456.
  1. 19.   Structure-based design of potent, conformationally constrained Smac mimetics
  2. Sun, H. Y.; Nikolovska-Coleska, Z.; Yang, C. Y.; Xu, L.; Liu, M. L.; Tomita, Y.; Pan, H. G.; Yoshioka, Y.; Krajewski, K.; Roller, P. P.; Wang, S. M.
  3. Journal of the American Chemical Society. 2004, DEC 29; 126(51): 16686-16687.
  1. 20.   A one-step synthesis of N-alpha-Fmoc-4-O-[O ',O ''-di-tert-butyl-2-(2-fluoromalonyl)]-L-tyrosine from commercially available starting material
  2. Kang, S. U.; Burke, T. R.
  3. Tetrahedron Letters. 2004, NOV 15; 45(47): 8611-8613.
  1. 21.   (Salen)Mn(III) compound as a nonpeptidyl mimic of catalase: DFT study of the metal oxidation by a peroxide molecule
  2. Abashkin, Y. G.; Burt, S. K.
  3. Journal of Physical Chemistry B. 2004 108(8): 2708-2711.
  1. 22.   Synthesis of alpha,alpha-disubstituted 4-phosphonophenylalanine analogues as conformationally-constrained phosphotyrosyl mimetics
  2. Oishi, S.; Kang, S. U.; Liu, H. P.; Zhang, M. C.; Yang, D. J.; Deschamps, J. R.; Burke, T. R.
  3. Tetrahedron. 2004 60(13): 2971-2977.
  1. 23.   Enantioselective synthesis of (S)-3-carboxy-4-((carboxy)difluoromethyl)phenylalanine in protected form and its incorporation into a PTP-1B-directed tripeptide
  2. Kang, S. U.; Yang, G.; Li, W.; Zhang, Z. Y.; Burke, T. R.
  3. Chemistry & Biodiversity. 2004 1(4): 626-633.
  1. 24.   A new addition to the structural bioinformatics toolbox: 3D models of short bioactive peptides from multiple sequences using feedback restrained molecular dynamics (FRMD)
  2. Cachau, R. E.; Gonzalez-Sapienza, G.; Burt, S. K.; Ventura, O. N.
  3. Cellular and Molecular Biology. 2003 49(6): 973-983.
  1. 25.   Tripeptide inhibitors of Yersinia protein-tyrosine phosphatase
  2. Lee, K.; Gao, Y.; Yao, Z. J.; Phan, J.; Wu, L.; Liang, J.; Waugh, D. S.; Zhang, Z. Y.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry Letters. 2003 13(15): 2577-2581.
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