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  1. 1.   CRISPR-Cas9 Genome-Wide Knockout Screen Identifies Mechanism of Selective Activity of Dehydrofalcarinol in Mesenchymal Stem-like Triple-Negative Breast Cancer Cells
  2. Grant, Corena V; Cai, Shengxin; Risinger, April L; Liang, Huiyun; O'Keefe,Barry; Doench, John G; Cichewicz, Robert H; Mooberry, Susan L
  3. Journal of natural products. 2020, OCT 23; 83(10): 3080-3092.
  1. 2.   Multiphase Assembly of Small Molecule Microcrystalline Peptide Hydrogel Allows Immunomodulatory Combination Therapy for Long-Term Heart Transplant Survival
  2. Majumder, Poulami; Zhang, Yichuan; Iglesias, Marcos; Fan,Lixin; Kelley, James A; Andrews, Caroline; Patel,Nimit; Stagno,Jason; Oh, Byoung Chol; Furtmüller, Georg J; Lai,Christopher; Wang,Yun-Xing; Brandacher, Gerald; Raimondi, Giorgio; Schneider,Joel
  3. Small (Weinheim an der Bergstrasse, Germany). 2020, Aug 18; e2002791.
  1. 3.   An evaluation of the RNase H inhibitory effects of Vietnamese medicinal plant extracts and natural compounds
  2. Tai, B. H.; Nhut, N. D.; Nhiem, N. X.; Quang, T. H.; Nguyen, T. T. N.; Bui, T. T. L.; Huong, T. T.; Wilson, J.; Beutler, J. A.; Ban, N. K.; Cuong, N. M.; Kim, Y. H.
  3. Pharmaceutical Biology. 2011, Oct; 49(10): 1046-1051.
  1. 4.   Cytotoxic and HIF-1alpha inhibitory compounds from Crossosoma bigelovii
  2. Klausmeyer, P.; Zhou, Q.; Scudiero, D. A.; Uranchimeg, B.; Melillo, G.; Cardellina, J. H.; Shoemaker, R. H.; Chang, C. J.; McCloud, T. G.
  3. Journal of Natural Products. 2009, May 22; 72(5): 805-12.
  1. 5.   Inhibitors of the NF-kappaB activation pathway from Cryptocarya rugulosa
  2. Meragelman, T. L.; Scudiero, D. A.; Davis, R. E.; Staudt, L. M.; McCloud, T. G.; Cardellina, J. H. 2nd.; Shoemaker, R. H.
  3. Journal of Natural Products. 2009, Mar 27; 72(3): 336-9.
  1. 6.   Chemical characterization of the aqueous algistatic fraction of barley straw (Hordeum vulgare) inhibiting Microcystis aeruginosa
  2. Waybright, T. J.; Terlizzi, D. E.; Ferrier, M. D.
  3. Journal of Applied Phycology. 2009 21(3): 333-340.
  1. 7.   In vitro anticancer screening of South African plants
  2. Fouche, G.; Cragg, G. M.; Pillay, P.; Kolesnikova, N.; Maharaj, V. J.; Senabe, J.
  3. Journal of Ethnopharmacology. 2008 119(3): 455-461.
  1. 8.   A dimeric lactone from Ardisia japonica with inhibitory activity for HIV-1 and HIV-2 ribonuclease H
  2. Dat, N. T.; Bae, K.; Wamiru, A.; McMahon, J. B.; Le Grice, S. F. J.; Bona, M.; Beutler, J. A.; Kim, Y. H.
  3. Journal of Natural Products. 2007, May; 70(5): 839-841.
  1. 9.   International collaboration in drug discovery and development from natural sources
  2. Cragg, G. M.; Newman, D. J.
  3. Pure and Applied Chemistry. 2005, NOV; 77(11): 1923-1942.
  1. 10.   Evidence that HIV-1 encodes an siRNA and a suppressor of RNA silencing
  2. Bennasser, Y.; Le, S. Y.; Benkirane, M.; Jeang, K. T.
  3. Immunity. 2005, MAY; 22(5): 607-619.
  1. 11.   Molecular cytogenetics discards polyploidy in mammals
  2. Svartman, M.; Stone, G.; Stanyon, R.
  3. Genomics. 2005, APR; 85(4): 425-430.
  1. 12.   Structure of circulin B and implications for antimicrobial activity of the cyclotides
  2. Koltay, A.; Daly, N. L.; Gustafson, K. R.; Craik, D. J.
  3. International Journal of Peptide Research and Therapeutics. 2005, MAR; 11(1): 99-106.
  1. 13.   Biodiversity: A continuing source of novel drug leads
  2. Cragg, G. M.; Newman, D. J.
  3. Pure and Applied Chemistry. 2005, JAN; 77(1): 7-24.
  1. 14.   Anti-HIV cyclotides
  2. Gustafson, K. R.; McKee, T. C.; Bokesch, H. R.
  3. Current Protein & Peptide Science. 2004, OCT; 5(5): 331-340.
  1. 15.   Natural inhibitors of carcinogenesis
  2. Kinghorn, A. D.; Su, B. N.; Jang, D. S.; Chang, L. C.; Lee, D.; Gu, J. Q.; Carcache-Blanco, E. J.; Powlus, A. D.; Lee, S. K.; Park, E. J.; Cuendet, M.; Gills, J. J.; Bhat, K.; Park, H. S.; Mata-Greenwood, E.; Song, L. L.; Jong, M. H.; Pezzuto, J. M.
  3. Planta Medica. 2004, AUG; 70(8): 691-705.
  1. 16.   Solution structure of the cyclotide palicourein: Implications for the development of a pharmaceutical framework
  2. Barry, D. G.; Daly, N. L.; Bokesch, H. R.; Gustafson, K. R.; Craik, D. J.
  3. Structure. 2004 12(1): 85-94.
  1. 17.   Structure of the isoaspartyl peptidase with L-asparaginase activity from Escherichia coli
  2. Prahl, A.; Pazgier, M.; Hejazi, M.; Lockau, W.; Lubkowski, J.
  3. Acta Crystallographica Section D-Biological Crystallography. 2004 60(Part 6): 1173-1176.
  1. 18.   Unlocking the code of 14-3-3
  2. Dougherty, M. K.; Morrison, D. K.
  3. Journal of Cell Science. 2004 117(10): 1875-1884.
  1. 19.   Male mouse recombination maps for each autosome identified by chromosome painting
  2. Froenicke, L.; Anderson, L. K.; Wienberg, J.; Ashley, T.
  3. American Journal of Human Genetics. 2002 71(6): 1353-1368.
  1. 20.   Functional homologs of cyanovirin-N amenable to mass production in prokaryotic and eukaryotic hosts
  2. Mori, T.; Barrientos, L. G.; Han, Z. Z.; Gronenborn, A. M.; Turpin, J. A.; Boyd, M. R.
  3. Protein Expression and Purification. 2002 26(1): 42-49.
  1. 21.   Anti-HIV prenylated flavonoids from Monotes africanus
  2. Meragelman, K. M.; McKee, T. C.; Boyd, M. R.
  3. Journal of Natural Products. 2001 64(4): 546-548.
  1. 22.   Pharmacological evaluation of Bangladeshi medicinal plants - a review
  2. Rahman, S.; Hasnat, A.; Hasan, C. M.; Rashid, M. A.; Ilias, M.
  3. Pharmaceutical Biology. 2001 39(1): 1-6.
  1. 23.   Use of COMPARE analysis to discover functional analogues of bleomycin
  2. Deng, J. Z.; Newman, D. J.; Hecht, S. M.
  3. Journal of Natural Products. 2000 63(9): 1269-1272.
  1. 24.   Alternative transcript initiation and novel post-transcriptional processing of a leucine-rich repeat receptor-like protein kinase gene that responds to short-day photoperiodic floral induction in morning glory (Ipomoea nil)
  2. Bassett, C. L.; Nickerson, M. L.; Cohen, R. A.; Rajeevan, M. S.
  3. Plant Molecular Biology. 2000 43(1): 43-58.
  1. 25.   HIV-Inhibitory prenylated xanthones and flavones from Maclura tinctoria
  2. Groweiss, A.; Cardellina, J. H.; Boyd, M. R.
  3. Journal of Natural Products. 2000 63(11): 1537-1539.
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