Academic literature on the topic 'Hit identification'

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Journal articles on the topic "Hit identification"

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Yi, Xiangyan, Lian Xue, Tim Thomas, and Jonathan B. Baell. "Action plan for hit identification (APHID): KAT6A as a case study." Future Medicinal Chemistry 12, no. 5 (March 2020): 423–37. http://dx.doi.org/10.4155/fmc-2019-0212.

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Here, we describe our action plan for hit identification (APHID) that guides the process of hit triage, with elimination of less tractable hits and retention of more tractable hits. We exemplify the process with reference to our high-throughput screening (HTS) campaign against the enzyme, KAT6A, that resulted in successful identification of a tractable hit. We hope that APHID could serve as a useful, concise and digestible guide for those involved in HTS and hit triage, especially those that are relatively new to this exciting and continually evolving technology.
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Volynets, Galyna P., Sergiy A. Starosyla, Mariia Yu Rybak, Volodymyr G. Bdzhola, Oksana P. Kovalenko, Vasyl S. Vdovin, Sergiy M. Yarmoluk, and Michail A. Tukalo. "Dual-targeted hit identification using pharmacophore screening." Journal of Computer-Aided Molecular Design 33, no. 11 (November 2019): 955–64. http://dx.doi.org/10.1007/s10822-019-00245-5.

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Bergeron, Charles, Michael Krein, Gregory Moore, Curt M. Breneman, and Kristin P. Bennett. "Modeling Choices for Virtual Screening Hit Identification." Molecular Informatics 30, no. 9 (August 17, 2011): 765–77. http://dx.doi.org/10.1002/minf.201100092.

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Morley, Andrew D., Angelo Pugliese, Kristian Birchall, Justin Bower, Paul Brennan, Nathan Brown, Tim Chapman, et al. "Fragment-based hit identification: thinking in 3D." Drug Discovery Today 18, no. 23-24 (December 2013): 1221–27. http://dx.doi.org/10.1016/j.drudis.2013.07.011.

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Oo, Thein H., and Cristhiam Mauricio Rojas Hernandez. "Diagnostic Performance of Heparin-Platelet Factor 4 Antibodies in the Identification of Heparin-Induced Thrombocytopenia in Cancer Population." Blood 134, Supplement_1 (November 13, 2019): 4896. http://dx.doi.org/10.1182/blood-2019-132072.

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Introduction: Cancer patients appear to have a higher risk of heparin induced thrombocytopenia (HIT) related complications than non-cancer patients; yet data on the performance of conventional diagnostic tools for HIT in cancer is limited. Our aim was to determine among cancer patients with a 4T score ≥ 4, the performance of the conventional cut-off for HIT antibody testing (IgG anti PF4) to discriminate between serotonin release assay (SRA) positive and negative cases. Methods: Retrospective and prospective analysis of cases (2002-2019) was performed of the electronic medical records of adult cancer patients at MD Anderson Cancer Center with suspected HIT. Cases were included in the analysis if the 4T score was ≥ 4 and investigated with IgG anti-PF4 optical density (HIT OD) and SRA. Logistic regression model and the receiver operating characteristic curves were conducted to identify the sensitivity and specificity of different cut-off points for the HIT OD to discriminate HIT cases based on the SRA status. Results: Among 50 cases, 18 were SRA positive. Median HIT OD was 1.03. At a cut-off point of 0.4, the HIT OD performed with a sensitivity of 0.89 and a specificity of 0.50 to discriminate the cases of SRA positive HIT. When the cut-off HIT OD was 1.0, the sensitivity was 0.78 with a specificity of 0.66. Conclusions: Our findings suggest that in cancer patients the performance of IgG anti-PF4 is similar to that of non-cancer patients for the identification of HIT cases. Disclosures Oo: Janssen and Janssen: Other: Research: site co-investigator ; Medical Education Speakers Network: Honoraria.
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E. Nichols, Sara, Robert V. Swift, and Rommie E. Amaro. "Rational Prediction with Molecular Dynamics for Hit Identification." Current Topics in Medicinal Chemistry 12, no. 18 (September 1, 2012): 2002–12. http://dx.doi.org/10.2174/156802612804910313.

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Nichols, Sara E., Robert V. Swift, and Rommie E. Amaro. "Rational Prediction with Molecular Dynamics for Hit Identification." Current Topics in Medicinal Chemistry 12, no. 18 (January 7, 2013): 2002–12. http://dx.doi.org/10.2174/1568026611212180007.

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Although the motions of proteins are fundamental for their function, for pragmatic reasons, the consideration of protein elasticity has traditionally been neglected in drug discovery and design. This review details protein motion, its relevance to biomolecular interactions and how it can be sampled using molecular dynamics simulations. Within this context, two major areas of research in structure-based prediction that can benefit from considering protein flexibility, binding site detection and molecular docking, are discussed. Basic classification metrics and statistical analysis techniques, which can facilitate performance analysis, are also reviewed. With hardware and software advances, molecular dynamics in combination with traditional structure-based prediction methods can potentially reduce the time and costs involved in the hit identification pipeline.
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Protopopov, M. V., S. A. Starosyla, O. V. Borovykov, V. N. Sapelkin, Y. V. Bilokin, V. G. Bdzhola, and S. M. Yarmoluk. "Hit identification of CK2 inhibitors by virtual screening." Biopolymers and Cell 33, no. 4 (August 31, 2017): 291–301. http://dx.doi.org/10.7124/bc.00095b.

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Park, Jun-Kyu, Suwoong Lee, Aaron Park, and Sung-June Baek. "Adaptive Hit-Quality Index for Raman Spectrum Identification." Analytical Chemistry 92, no. 15 (June 4, 2020): 10291–99. http://dx.doi.org/10.1021/acs.analchem.0c00209.

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Goodnow, Robert A. "Hit and lead identification: Integrated technology-based approaches." Drug Discovery Today: Technologies 3, no. 4 (December 2006): 367–75. http://dx.doi.org/10.1016/j.ddtec.2006.12.009.

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Dissertations / Theses on the topic "Hit identification"

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Nordqvist, Anneli. "Hit Identification and Hit Expansion in Antituberculosis Drug Discovery : Design and Synthesis of Glutamine Synthetase and 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase Inhibitors." Doctoral thesis, Uppsala universitet, Avdelningen för organisk farmaceutisk kemi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-155428.

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Since the discovery of Mycobacterium tuberculosis (Mtb) as the bacterial agent causing tuberculosis, the permanent eradication of this disease has proven challenging. Although a number of drugs exist for the treatment of tuberculosis, 1.7 million people still die every year from this infection. The current treatment regimen involves lengthy combination therapy with four different drugs in an effort to combat the development of resistance. However, multidrug-resistant and extensively drug-resistant strains are emerging in all parts of the world. Therefore, new drugs effective in the treatment of tuberculosis are much-needed. The work presented in this thesis was focused on the early stages of drug discovery by applying different hit identification and hit expansion strategies in the exploration of two new potential drug targets, glutamine synthetase (GS) and 1-deoxy-D-xylulose-5-phosphate reductoisomerase (DXR). A literature survey was first carried out to identify new Mtb GS inhibitors from compounds known to inhibit GS in other species. Three compounds, structurally unrelated to the typical amino acid derivatives of previously known GS inhibitors, were then discovered by virtual screening and found to be Mtb GS inhibitors, exhibiting activities in the millimolar range. Imidazo[1,2-a]pyridine analogues were also investigated as Mtb GS inhibitors. The chemical functionality, size requirements and position of the substituents in the imidazo[1,2-a]pyridine hit were investigated, and a chemical library was designed based on a focused hierarchical design of experiments approach. The X-ray structure of one of the inhibitors in complex with Mtb GS provided additional insight into the structure–activity relationships of this class of compounds. Finally, new α-arylated fosmidomycin analogues were synthesized as inhibitors of Mtb DXR, exhibiting IC50 values down to 0.8 µM. This work shows that a wide variety of aryl groups are tolerated by the enzyme. Cinnamaldehydes are important synthetic intermediates in the synthesis of fosmidomycin analogues. These were prepared by an oxidative Heck reaction from acrolein and various arylboronic acids. Electron-rich, electron-poor, heterocyclic and sterically hindered boronic acids could be employed, furnishing cinnamaldehydes in 43–92% yield.
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Li, Hui. "Algorithms for the selection of optimal spaced seed sets for transposable element identification." Miami University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=miami1283178156.

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Nobili, Alberto [Verfasser]. "Improving biocatalysts via semi-rational protein design : use of a multiple sequence alignment platform to reduce screening efforts and facilitate hit identification / Alberto Nobili." Greifswald : Universitätsbibliothek Greifswald, 2016. http://d-nb.info/1113294191/34.

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Ehrt, Christiane [Verfasser], Daniel [Akademischer Betreuer] Rauh, and Stefan M. [Gutachter] Kast. "Protein binding site comparison : The impact of binding site similarity on hit identification in early drug discovery / Christiane Ehrt ; Gutachter: Stefan M. Kast ; Betreuer: Daniel Rauh." Dortmund : Universitätsbibliothek Dortmund, 2019. http://d-nb.info/1197903011/34.

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Spadaro, Alessandro [Verfasser], and Rolf W. [Akademischer Betreuer] Hartmann. "Pharmacophore aided hit identification, structural optimization and biological evaluation of benzothiazole derivatives as new potent and selective non-steroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 / Alessandro Spadaro. Betreuer: Rolf W. Hartmann." Saarbrücken : Saarländische Universitäts- und Landesbibliothek, 2012. http://d-nb.info/1052338666/34.

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Chen, Zhiqiang. "Identification of HIF-1 inhibitors." Thesis, University of Manchester, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.503047.

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Seddon, Deborah Ann. "Impossible identifications : Shakespeare and his readers (1830-1930)." Thesis, University of Cambridge, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.616135.

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Benson, Claire Elizabeth. "Genetics of familial hip osteoarthritis :identification of genetic susceptibility factors." Thesis, Queen's University Belfast, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491996.

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Osteoarthritis is already a major cause of disability worldwide and with an ageing population the associated socio-economic burden is expected to soar. Complex interactions between genetic and environmental factors are responsible for the initiation of osteoarthritis. There is a clear genetic contribution to hip' osteoarthritis but to date no major susceptibility gene has been identified. A large collection of affected sib pairs with hip osteoarthritis had already been recruited from Northern Ireland (416 participants) and Nottingham (115 participants) . Additional unaffected (n=42) family members were recruited. As part of a genome wide screen 160 microsatellite markers from chromosomes 9, 10, 11, 14, 19, 20, 21 and 22 were typed in each family member (n=531)and controls (n=49). Candidate genes were identified in areas suggesting positive linkage. Single nucleotide polymorphism (SNP) typing or sequencing were used to investigate these genes further. The three regions most suggestive of linkage were found in chromosomes 9 (at 74.4mB), 11 (at 11.7mB) and 19 (at 8mB). Ten of the candidate genes identified were typed with SNPs in one member of each family (n=206) and controls (n=49). The ten exons of the other gene, osteoclast stimulating factor 1 (OSTFl), were sequenced in both cases (n=40) and controls (n= 8). The only candidate gene with significantly positive results was the collagen type V, alpha 3 gene (COL5A3) on chromosome 19. One haplotype block was significantly more common in the control population (p=O.Ol). Further analyses of the COL5A3 gene and its neighbouring genes are currently underway. Identification of a major susceptibility gene will improve our understanding of the underlying pathogenesis and potentially identify new targets for drug therapy. The global impact of finding a major susceptibility gene for hip osteoarthritis should encourage us to continue with our search to elucidate the genetics of familial hip osteoarthritis
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Crozier, J. R. "Enjoying Jesus Christ and the riches of his grace do you know how rich you are in Christ? a seven-week adventure /." Online full text .pdf document, available to Fuller patrons only, 2003. http://www.tren.com.

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Ledwaba, Neria Hunadi. "Identification of employees needs to be addressed in the HIV/AIDS programme at Aventis Pharmaceutical Company." Diss., Pretoria : [s.n.], 2003. http://upetd.up.ac.za/thesis/available/etd-11182003-132232.

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Books on the topic "Hit identification"

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Hit and lead profiling: Identification and optimization of drug-like molecules. Weinheim: Wiley-VCH, 2009.

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Identitás és hit: A kárpátaljai magyar görög katolikusok identifikációs útjai. Budapest: Intermix, 2007.

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Dort, H. M. Vletter-van. Meldingsplicht voor beursvennootschappen: Een analyse van het Engelse, Belgische en Nederlandse recht. Deventer: Kluwer, 1994.

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Hip hop underground: The integrity and ethics of racial identification. Philadelphia: Temple University Press, 2009.

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Clark, Jack. Hot Wheels, the ultimate redline guide: Identification and values. Paducah, Ky: Collector's Books, 2003.

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Bos, Rein. Identificatie-mogelijkheden in preken uit het Oude Testament. Kampen: J.H. Kok, 1992.

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Lambrou, Evan C. AIDS: Scare or scam? New York: Vantage Press, 1994.

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De natuurlijke historie van aids: Naar een nieuw paradigma? Utrecht: Gopher Publishers, 2006.

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A. S. J. van Proosdij. Arnoldo's Zakflora: Wat in het wild groeit en bloeit op Aruba, Bonaire en Curaçao. 3rd ed. Amsterdam: Natuurwetenschappelijke Studiekring voor het Caraïbisch Gebied, 2001.

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The ultimate guide to Hot Wheels variations: Identification & price guide to more than 2,000 collector number packs! Iola, WI: Krause Publications, 2002.

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Book chapters on the topic "Hit identification"

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Zhang, Yixin. "Hit Identification and Hit Follow-Up." In A Handbook for DNA-Encoded Chemistry, 357–76. Hoboken, NJ: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118832738.ch16.

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Harner, Mary J., Guille Metzler, Caroline A. Fanslau, Luciano Mueller, and William J. Metzler. "1D NMR Methods for Hit Identification." In Applied Biophysics for Drug Discovery, 131–52. Chichester, UK: John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781119099512.ch8.

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Mazanetz, Michael, Richard Law, and Mark Whittaker. "Hit and Lead Identification from Fragments." In De novo Molecular Design, 143–200. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527677016.ch6.

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Dunlap, Norma, and Donna M. Huryn. "Drug discovery: hit and lead identification." In Medicinal Chemistry, 19–50. New York, NY : Garland Science, Taylor & Francis Group, LLC, [2018]: Garland Science, 2018. http://dx.doi.org/10.1201/9781315100470-2.

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Hyman, Daniel, and Lynn Voss. "Patient Identification Errors and HIT: Friend or Foe?" In Safety of Health IT, 143–52. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31123-4_11.

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Stumpfe, Dagmar, and Jürgen Bajorath. "CRITICAL ASSESSMENT OF VIRTUAL SCREENING FOR HIT IDENTIFICATION." In Chemoinformatics for Drug Discovery, 113–30. Hoboken, NJ: John Wiley & Sons, Inc, 2013. http://dx.doi.org/10.1002/9781118742785.ch6.

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Walse, Björn, Andrew P. Turnbull, and Susan M. Boyd. "Tailoring Hit Identification and Qualification Methods for Targeting Protein-Protein Interactions." In Applied Biophysics for Drug Discovery, 29–59. Chichester, UK: John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781119099512.ch3.

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Brough, Stephen J., and Parita Shah. "Use of Aequorin for G protein-Coupled Receptor Hit Identification and Compound Profiling." In Methods in Molecular Biology, 181–98. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-317-6_13.

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Walsh, Terence A. "Early Stage Hit Triage for Plant Chemical Genetic Screens and Target Site Identification." In Methods in Molecular Biology, 191–99. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-592-7_18.

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Cutinho, Pretisha Flora, C. H. S. Venkataramana, and B. V. Suma. "In Silico Hit Identification, Drug Repurposing, Pharmacokinetic and Toxicity Prediction of c-Met Kinase Inhibitors for Cancer Therapy." In Special Publications, 54–59. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781839160783-00054.

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Conference papers on the topic "Hit identification"

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Pei-Pei Chen, Tzu-Chun Yeh, Jyh-Shing Roger Jang, and Wenshan Liou. "AutoRhythm: A music game with automatic hit-time generation and percussion identification." In 2015 IEEE International Conference on Multimedia and Expo (ICME). IEEE, 2015. http://dx.doi.org/10.1109/icme.2015.7177487.

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Wu, Xiongjun, Guoxiang Liu, and Vyacheslav Romanov. "Machine learning applications for frac-hit identification: A field data use case." In Second International Meeting for Applied Geoscience & Energy. Society of Exploration Geophysicists and American Association of Petroleum Geologists, 2022. http://dx.doi.org/10.1190/image2022-3742713.1.

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Sheng, Khoo Boon, Abdullah Aziz Saad, and Mohamad Khairi Ishak. "Development of a Virtual Vehicle Identification for Tracking Hit-and-Run Vehicle." In 2022 IEEE International Conference on Artificial Intelligence in Engineering and Technology (IICAIET). IEEE, 2022. http://dx.doi.org/10.1109/iicaiet55139.2022.9936747.

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Tomlinson, Chris, Rachel Lawrence, Stuart Best, Grace Boden, Thomas Alanine, James Wasp, Bethany Smith, et al. "Abstract 1757: Developing sensitive assays to facilitate hit identification of RNA modifying enzymes." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-1757.

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Zhong, Xin, Yoke San Wong, Wen Feng Lu, Kelvin W. C. Foong, and Alan Ho-lun Cheng. "A Dental Matching Approach Using Partial Surface Features for Human Identification." In ASME 2012 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/detc2012-70890.

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A novel 3D dental identification framework is presented. The objective is to develop a methodology to enable computer-automated matching of complex dental surfaces with possible missing regions for human identification. Thus far, there is no reported attempt at 3D dental identification given partially available dental casts or impressions. This approach overcomes a number of key hurdles in traditional 2D methods. Given the 3D digital form of a dental cast surface, the developed method will facilitate the search for the closest match in the database of digitized dental casts. A salient curvature matching algorithm (SCM) is proposed for pose estimation which includes algorithms for feature extraction, feature description and correspondence. The feature point extraction algorithm could extract more salient features and the correspondence algorithm is more robust for pose estimation compared to known works. Experimental results show 85.7% hit rate at rank-1 accuracy based on matching of 7 partial sets to a database of 100 full sets in significantly reduced retrieval time. The hit rate increases to 100% with parameter adjustment. This work aims to enable computer-aided 3D dental identification and the proposed method could be adjunctively used with the traditional 2D dental identification method, as the available dental source for identification is still primarily 2D radiographs. Limitations of the methodology and future directions in matching highly fragmented and partial dental surfaces are discussed.
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Vanden Eynde, Jean Jacques, Térence Honoré, Annie Mayence, and Tien Huang. "Identification of a Hit in a Small Library of Potential Antiplasmodial Imidazo[4,5-b]pyridines." In 1st International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecmc-1-a034.

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Fromond, Claudia, Xavier Espanel, Laurent Chene, Philippe Masson, Benaïssa Boubia, Christian Montalbetti, and Pierre Broqua. "Abstract 99: Identification of G9a inhibitors by AlphaLisa™ technology and hit confirmation using MT-Glo™." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-99.

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Kulik, A., K. Esser, D. Niederacher, H. Neubauer, and T. Fehm. "First-Hit™ – a novel, phenotypic screening approach for the identification of differentiation inducing compounds in TNBC." In 39. Jahrestagung der Deutschen Gesellschaft für Senologie. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1688016.

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Zhang, Yaojie, Bing Xu, and Tiejun Zhao. "CN-HIT-MI.T at SemEval-2019 Task 6: Offensive Language Identification Based on BiLSTM with Double Attention." In Proceedings of the 13th International Workshop on Semantic Evaluation. Stroudsburg, PA, USA: Association for Computational Linguistics, 2019. http://dx.doi.org/10.18653/v1/s19-2101.

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Richards, Edward, Gu Zhang, Jennifer Permuth-Wey, Zhu-Peng Li, Sridevi Challa, William Kong, Dan Su, et al. "Abstract 154: Identification of TGFβ-regulated long noncoding RNAs in mammary epithelia: lncRNA-HIT mediated TGFβ-induced EMT and breast cancer metastasis." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-154.

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Reports on the topic "Hit identification"

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Liu, Guoxiang, Xiongjun Wu, and Vyacheslav Romanov. Machine Learning Application for Frac-Hit Identification: Field Data Use Case. Office of Scientific and Technical Information (OSTI), October 2022. http://dx.doi.org/10.2172/1893843.

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Banerjee, Onil, Martin Cicowiez, Ana Rios, and Cicero De Lima. Climate Change Impacts on Agriculture in Latin America and the Caribbean: An Application of the Integrated Economic-Environmental Modeling (IEEM) Platform. Inter-American Development Bank, November 2021. http://dx.doi.org/10.18235/0003794.

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In this paper, we assess the economy-wide impact of Climate Change (CC) on agriculture and food security in 20 Latin American and the Caribbean (LAC) countries. Specifically, we focus on the following three channels through which CC may affect agricultural and non-agricultural production: (i) agricultural yields; (ii) labor productivity in agriculture, and; (iii) economy-wide labor productivity. We implement the analysis using the Integrated Economic-Environmental Model (IEEM) and databases for 20 LAC available through the OPEN IEEM Platform. Our analysis identifies those countries most affected according to key indicators including Gross Domestic Product (GDP), international commerce, sectoral output, poverty, and emissions. Most countries experience negative impacts on GDP, with the exception of the major soybean producing countries, namely, Brazil, Argentina and Uruguay. We find that CC-induced crop productivity and labor productivity changes affect countries differently. The combined impact, however, indicates that Belize, Nicaragua, Guatemala and Paraguay would fare the worst. Early identification of these hardest hit countries can enable policy makers pre-empting these effects and beginning the design of adaptation strategies early on. In terms of greenhouse gas emissions, only Argentina, Chile and Uruguay would experience small increases in emissions.
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Chhoeung, Norinmony, Sesokunthideth Chrea, and Nghia Nguyen. Cambodia’s Cash Transfer Program during COVID-19. Asian Development Bank Institute, December 2022. http://dx.doi.org/10.56506/rrmz8095.

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In 2019, Cambodia had been enjoying its steady economic growth until the coronavirus disease (COVID-19) pandemic hit the country from February 2020 in the form of severe infectious diseases, causing both economic and social problems for people from all walks of life, especially poor and vulnerable families. The IDPoor Equity Card, a poverty identification and registration system, was introduced in Cambodia to provide cash to poor pregnant women and children since 2016. Given its continued success, Cambodian Prime Minister Samdech Hun Sen announced the implementation of the Cash Transfer Program (CTP) using the IDPoor Card system. The CTP provided cash to poor and vulnerable households across the country affected by the pandemic. Executing the first large-scale cash transfer program in history presented significant challenges for the Government of Cambodia. In addition to implementing the program, which had to adhere to the three principles of equity–equality–efficiency, the government had other challenges to overcome, such as the limited number of tablets and facilities to accommodate the many people waiting in line to withdraw cash. Under the guidance of the central government, particularly the Economic and Finance Policy Committee, a technical working group was established to lead the implementation process; coordination among local governments, local councils, agencies, and the poor and needy; review of the IDPoor database; establishment of the digital payment system; and training of local government staff. This enabled the CTP to effectively distribute cash to poor and vulnerable households during the pandemic.
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Porter, Dale A., and Kornelia Polyak. Identification of a Receptor for Tumor Suppressor HIN-1. Fort Belvoir, VA: Defense Technical Information Center, May 2003. http://dx.doi.org/10.21236/ada416631.

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van Os, J., M. G. T. M. Bartholomeus, L. J. J. Jeurissen, and C. G. van Reenen. Rekenregels rundvee voor de Landbouwtelling : verantwoording van het gebruik van het Identificatie & Registratiesysteem. Wageningen: Wettelijke Onderzoekstaken Natuur & Milieu, 2017. http://dx.doi.org/10.18174/413579.

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van Os, J., L. J. J. Jeurissen, and H. H. Ellen. Rekenregels pluimvee voor de Landbouwtelling: verantwoording van het gebruik van het Identificatie- & Registratiesysteem. Wageningen: Wettelijke Onderzoekstaken Natuur & Milieu, 2019. http://dx.doi.org/10.18174/479211.

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van Os, J., J. L. L. Jeurissen, and J. C. Verkaik. Rekenregels schapen en geitenvoor de Landbouwtelling : verantwoording van het gebruik van het Identificatie & Registratiesysteem. Wageningen: Wettelijke Onderzoekstaken Natuur & Milieu, 2020. http://dx.doi.org/10.18174/525138.

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Sawatzky, C., and G. Pe-Piper. Provenance identification of detrital quartz using hot-cathode cathodoluminescence: an atlas of source rocks. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2012. http://dx.doi.org/10.4095/291336.

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Kozachenko, Nadiia. Artificial relevance as a way to strengthen an argument. The Institute for Logic, Language and Computation, Universiteit van Amsterdam, April 2022. http://dx.doi.org/10.31812/123456789/6685.

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Abstract:
Some of the subjective reactions of an argumentation agent are determined not so much by his emotional or personal characteristics, but by the presence of implicit components of the agent's epistemic state, which can be explicated and formalized. The identification of these components makes it possible to use them to refine the argumentation strategy.
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Gardland, Frank C., Edward D. Gorham, Steve O. Cunnion, Milan R. Miller, and Louis L. Balazs. Trends and Methods in Identification of Human Immunodeficiency Virus (HIV) Seropositivity in Active-Duty U.S. Navy Enlisted Personnel: 1986-1989. Fort Belvoir, VA: Defense Technical Information Center, September 1991. http://dx.doi.org/10.21236/ada249770.

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