Relevant bibliographies by topics / Structure Activity Relationship studies

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Structure Activity Relationship studies'

Author: Grafiati
Published: 4 June 2021
Last updated: 30 January 2023

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Journal articles on the topic "Structure Activity Relationship studies"

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Skalkos, Dimitris, James A. Hampton, Rick W. Keck, Miriam Wagoner, and Steven H. Selman. "IMINIUM SALT BENZOCHLORINS: STRUCTURE-ACTIVITY RELATIONSHIP STUDIES." Photochemistry and Photobiology 59, no. 2 (1994): 175–81. http://dx.doi.org/10.1111/j.1751-1097.1994.tb05019.x.

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German, Nadezhda A., Ann M. Decker, Brian P. Gilmour, Brian F. Thomas, and Yanan Zhang. "Truncated Orexin Peptides: Structure–Activity Relationship Studies." ACS Medicinal Chemistry Letters 4, no. 12 (2013): 1224–27. http://dx.doi.org/10.1021/ml400333a.

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Patil, Nitin A., K. Johan Rosengren, Frances Separovic, John D. Wade, Ross A. D. Bathgate, and Mohammed Akhter Hossain. "Relaxin family peptides: structure-activity relationship studies." British Journal of Pharmacology 174, no. 10 (2017): 950–61. http://dx.doi.org/10.1111/bph.13684.

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Ma, Anqi, Wenyu Yu, Yan Xiong, Kyle V. Butler, Peter J. Brown, and Jian Jin. "Structure–activity relationship studies of SETD8 inhibitors." MedChemComm 5, no. 12 (2014): 1892–98. http://dx.doi.org/10.1039/c4md00317a.

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Ko, Horng-Huey, Lo-Ti Tsao, Kun-Lung Yu, Cheng-Tsung Liu, Jih-Pyang Wang, and Chun-Nan Lin. "Structure–activity relationship studies on chalcone derivatives." Bioorganic & Medicinal Chemistry 11, no. 1 (2003): 105–11. http://dx.doi.org/10.1016/s0968-0896(02)00312-7.

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Murthi, Krishna K., Marja Dubay, Christopher McClure, et al. "Structure–activity relationship studies of flavopiridol analogues." Bioorganic & Medicinal Chemistry Letters 10, no. 10 (2000): 1037–41. http://dx.doi.org/10.1016/s0960-894x(00)00156-6.

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Tsukano, Chihiro, and Makoto Sasaki. "Structure–activity relationship studies of gymnocin-A." Tetrahedron Letters 47, no. 38 (2006): 6803–7. http://dx.doi.org/10.1016/j.tetlet.2006.07.081.

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Fuchs, James R., Bulbul Pandit, Deepak Bhasin, et al. "Structure–activity relationship studies of curcumin analogues." Bioorganic & Medicinal Chemistry Letters 19, no. 7 (2009): 2065–69. http://dx.doi.org/10.1016/j.bmcl.2009.01.104.

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Cheuka, Peter Mubanga, Diego Gonzalez Cabrera, Tanya Paquet, and Kelly Chibale. "Structure–activity relationship studies of antiplasmodial aminomethylthiazoles." Bioorganic & Medicinal Chemistry Letters 24, no. 22 (2014): 5207–11. http://dx.doi.org/10.1016/j.bmcl.2014.09.071.

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Wiker, Franziska, Nils Hauck, Stephanie Grond, and Bertolt Gust. "Caprazamycins: Biosynthesis and structure activity relationship studies." International Journal of Medical Microbiology 309, no. 5 (2019): 319–24. http://dx.doi.org/10.1016/j.ijmm.2019.05.004.

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Dissertations / Theses on the topic "Structure Activity Relationship studies"

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Just, Baringo Xavier. "Thiopeptides: Synthesis and Structure-Activity Relationship Studies." Doctoral thesis, Universitat de Barcelona, 2013. http://hdl.handle.net/10803/128268.

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The present doctoral thesis has been devoted to the development of a new synthetic strategy to obtain a new member of the thiopeptide, or thiazolyl peptide, family of antibiotics. This new member, baringolin, was isolated and characterized by the Spanish pharmaceutical company Instituto Biomar S.A. Although a structure was proposed, no stereochemical information was provided. Thus, this thesis has several objectives; first, a novel modular and straightforward strategy must be developed to achieve its total synthesis, but also to facilitate the preparation of analogues. The achievement of the t
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Gabrielli, William Fullard. "Structure activity relationship studies of ochratoxin A analogues." Thesis, Stellenbosch : Stellenbosch University, 2002. http://hdl.handle.net/10019.1/53070.

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Thesis (MSc)--Stellenbosch University, 2002.<br>ENGLISH ABSTRACT: Mycotoxins have assumed worldwide importance due to the ubiquitous occurrence of toxigenic fungi, their infestation of plant-based foods and feeds and the subsequent economical and health impact it because of their contamination of commercial products. Ochratoxin A (OA) is a nephrotoxic mycotoxin produced by isolates of Aspergillus ochraceus and Penicillium verrucosum and occurs frequently in nature. The major target for toxicity of OA in mammalian species is the kidneys and it has been the major cause of Danish Porcine N
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Li, Ju-Yun. "Quantitative structure-activity relationship studies in medicinal chemistry." Case Western Reserve University School of Graduate Studies / OhioLINK, 1995. http://rave.ohiolink.edu/etdc/view?acc_num=case1062596938.

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Musa, Muftah Miloud A. "Structure activity relationship studies of new ethylene antagonists." Thesis, Curtin University, 2016. http://hdl.handle.net/20.500.11937/77805.

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Ethylene antagonists provide one of the most effective methods to reduce postharvest losses of horticulture produce. The understanding of the mode of action of 1-methylcyclopropene led to the discovery of a new class of ethylene antagonist. Cycloproparenes, benzocyclopropene and 1H-naphtho[b]cyclopropene were prepared and showed excellent inhibition of the effect of ethylene on some fruits and waxflowers.
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Dimayuga, Mario Arnulfo De Leon. "Structure-activity relationship studies of biological activities of chemicals." Case Western Reserve University School of Graduate Studies / OhioLINK, 1991. http://rave.ohiolink.edu/etdc/view?acc_num=case1055532031.

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FAN, WEIGUO. "USING MOLECULAR SIMILARITY ANALYSIS FOR STRUCTURE-ACTIVITY RELATIONSHIP STUDIES." Kent State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=kent1353964351.

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Srivastava, Sanjay. "Structure-activity relationship studies in medicinal chemistry and drug design." Case Western Reserve University School of Graduate Studies / OhioLINK, 1992. http://rave.ohiolink.edu/etdc/view?acc_num=case1056054628.

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Congdon, Molly D. "Structure Activity Relationship Studies on Isoform Selective Sphingosine Kinase Inhibitors." Diss., Virginia Tech, 2016. http://hdl.handle.net/10919/82129.

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A variety of diseases including Alzheimer's disease, asthma, cancer, fibrosis, multiple sclerosis, and sickle cell disease have been associated with elevated levels of sphingosine-1-phosphate (S1P). S1P, a pleiotropic lipid mediator involved in a broad range of cellular processes, is synthesized solely by the phosphorylation of sphingosine (Sph) and is catalyzed by the two isoforms of sphingosine kinase (SphK1 and SphK2). Therefore, SphKs are a potential therapeutic target; however, the physiological role of SphK2 is still emerging. In order to determine the role of SphK2 in vivo, more potent
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Ptchelintsev, Dmitri Stanislav. "Structure-activity relationship studies in chemoreception, toxicology and medicinal chemistry." Case Western Reserve University School of Graduate Studies / OhioLINK, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=case1060866168.

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Davies, Rachel A. "Structure-Activity Relationship Studies of Synthetic Cathinones and Related Agents." VCU Scholars Compass, 2019. https://scholarscompass.vcu.edu/etd/5953.

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Synthetic cathinones and related agents represent an international drug abuse problem, and at the same time an important class of clinically useful compounds. Structure-activity relationship studies are needed to elucidate molecular features underlying the pharmacology of these agents. Illicit methcathinone (i.e., MCAT), the prototype of the synthetic cathinone class, exists as a racemic mixture. Though the differences in potency and target selectivity between the positional and optical isomers of synthetic cathinones and related agents have been demonstrated to have important implications for
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Books on the topic "Structure Activity Relationship studies"

1

Butcher, Helen Joyce. X-ray crystallographic studies and structure-activity relationships for benzodiazepines. University of Birmingham, 1987.

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Prakash, Gupta Satya, and Bahal R, eds. QSAR and molecular modeling studies in heterocyclic drugs. Springer-Verlag, 2006.

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Eric, Fanchon, ed. Structure and dynamics of biomolecules: Neutron and synchrotron radiation for condensed matter studies. Oxford University Press, 2000.

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Dastmalchi, Siavoush, Maryam Hamzeh-Mivehroud, and Babak Sokouti. Quantitative Structure–Activity Relationship. CRC Press, 2018. http://dx.doi.org/10.1201/9781351113076.

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Horspool, Keith Ronald. Structure-activity studies on antitumour imidazotetrazionones. Aston University. Departmentof Pharmaceutical Sciences, 1988.

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Boutla, E. Structure and activity relationship in low temperature shift catalysis. UMIST, 1993.

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Horisberger, Jean-Daniel. The Na,K-ATPase: Structure-function relationship. R.G. Landes, 1994.

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name, No. Quantitative structure-activity relationship (QSAR) models of mutagens and carcinogens. CRC Press, 2002.

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Isaac, J. Structure/activity relationship of Cu/ZnO/Al203 methanol synthesis catalysts. UMIST, 1997.

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Zemicael, F. W. Structure/activity relationship of cu/zno/al2o3 methanol synthesis catalysis. UMIST, 1993.

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Book chapters on the topic "Structure Activity Relationship studies"

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Oishi, Tohru. "Structure-Activity Relationship Studies of Maitotoxin Based on Chemical Synthesis." In Cutting-Edge Organic Synthesis and Chemical Biology of Bioactive Molecules. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6244-6_6.

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Sharma, Brij K., Prithvi Singh, and Yenamandra S. Prabhakar. "Advances in Structure–Activity Relationship Studies on Potassium Channel Modulators." In Ion Channels and Their Inhibitors. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-19922-6_8.

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Gombar, Vijay K. "Quantitative Structure-Activity Relationship Studies: Acute Toxicity of Environmental Contaminants." In QSAR in Environmental Toxicology - II. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3937-0_11.

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Patil, Vaishali M., and Satya P. Gupta. "Quantitative Structure–Activity Relationship Studies on Sulfonamide-Based MMP Inhibitors." In Matrix Metalloproteinase Inhibitors. Springer Basel, 2012. http://dx.doi.org/10.1007/978-3-0348-0364-9_6.

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Wang, Peng-liang, Ke-yin Ma, Yu-cang Du, Lu-hua Lai, and Xiao-jie Xu. "Structure—activity relationship studies of memory enhancing peptide ZNC(C)PR." In Peptides. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-010-9066-7_69.

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Patil, Vaishali M., and Satya P. Gupta. "Structure–Activity Relationship Studies of Hydroxamic Acids as Matrix Metalloproteinase Inhibitors." In Hydroxamic Acids. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-38111-9_4.

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Tjoeng, F. S., P. R. Bovy, R. B. Garland, et al. "Structure-activity relationship studies of RGD analogs containing β-amino acids." In Peptides. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_101.

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Van Rietschoten, J., R. Romi, M. Crest, et al. "Structure activity relationship studies on kaliotoxin, a peptidic K+ channel blocker." In Peptides. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_175.

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Maloy, W. L., D. L. MacDonald, C. J. Messler, and M. M. Brasseur. "Antibacterial activity of caerulien precursor factors (CPF) and structure-activity relationship studies to improve activity and selectivity." In Peptides 1992. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1470-7_355.

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Baltz, Richard H. "Daptomycin and A54145: Structure-Activity Relationship (SAR) Studies Enabled by Combinatorial Biosynthesis." In Natural Products. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118794623.ch23.

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Conference papers on the topic "Structure Activity Relationship studies"

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Wang, Kevin, Spencer Hahn, Hari Santhapuram, et al. "Abstract 4462: Structure-activity relationship studies for PSMA-targeted tubulysin conjugates." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-4462.

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Agharkar, Priyanka A., Manivannan Ethirajan, Jianqun Liao, et al. "Abstract 3756: Structure activity relationship studies of novel FAK inhibitor C4." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-3756.

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Ramos Colon, Cyf N., Yeon Sun Lee, Sara M. Hall, Josephine Lai, Frank Porreca, and Victor J. Hruby. "Structure-Activity Relationship Studies of Dynorphin A Analogs at the Kappa Opioid Receptor." In The 24th American Peptide Symposium. Prompt Scientific Publishing, 2015. http://dx.doi.org/10.17952/24aps.2015.096.

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Ketron, Adam, David E. Graves, and Neil Osheroff. "Abstract 2529: Structure-activity relationship studies of the type II topoisomerase poison amsacrine." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-2529.

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Du, Zhenjiao, and Yonghui Li. "Quantitative Structure-activity Relationship Study on Antioxidant Dipeptides." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/cpyc1755.

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Antioxidative peptides have attracted increasing interest of researchers and consumers. Compared to wet chemistry methods, quantitative structure-activity relationship (QSAR) analysis as a in silicon method can be more efficient and cost effective and has been successfully applied to activity prediction of angiotensin I-converting enzyme inhibitory activity and bitterness of peptides. However, there are only few QSAR studies on antioxidative activity, particularly for dipeptides which have demonstrated ideal absorption ability in intestinal compared to larger peptides. This study aimed to cond
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Lu, Rong, Hai-xia Ma, Wei-ping Liu, and Wen-xin Li. "Studies on quantitative structure-activity-relationship inhibitory effects of benzoic acid derivatives on tyrosinase." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE 2010). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5516550.

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Angelo, Rafaela M., Andreia K. Io, Matheus P. Almeida, et al. "OntoQSAR: an Ontology for Interpreting Chemical and Biological Data in Quantitative Structure-Activity Relationship Studies." In 2020 IEEE 14th International Conference on Semantic Computing (ICSC). IEEE, 2020. http://dx.doi.org/10.1109/icsc.2020.00042.

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Johnson, Jeremy J., Deeba N. Syed, Vaqar M. Adhami, et al. "Abstract A67: Dietary xanthones for prostate cancer chemoprevention: From fruit extract to structure activity relationship studies." In Abstracts: AACR International Conference on Frontiers in Cancer Prevention Research‐‐ Dec 6–9, 2009; Houston, TX. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1940-6207.prev-09-a67.

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Sun, Cuixiang, Peng Zhao, Diana Hunt, et al. "Abstract 3857: Discovery and structure-activity relationship studies of TP-2846: a novel tetracycline antileukemia agent." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-3857.

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Sun, Cuixiang, Peng Zhao, Diana Hunt, et al. "Abstract 3857: Discovery and structure-activity relationship studies of TP-2846: a novel tetracycline antileukemia agent." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-3857.

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Reports on the topic "Structure Activity Relationship studies"

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Avery, Mitchell A. Drug Development of the Antimalarial Agent Artemisinin: Total Synthesis, Analog Synthesis, and Structure-Activity Relationship Studies. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/adb152141.

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Spiers, Donald, Arieh Gertler, Harold Johnson, and James Spain. An In Vitro and In Vivo Investigation of the Diverse Biological Activities of Bovine Placental Lactogen. United States Department of Agriculture, 1993. http://dx.doi.org/10.32747/1993.7568087.bard.

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In order to understand the structure-function relationship of bovine placental lactogen (bPL) and initiate production of material for in vivo testing, 28 different bPL analogues were prepared by either truncation or site-directed mutagenesis. The effect of these mutations was determined by measuring binding capacity, ability to homodimerize extracellular domains (ECDs) of several lactogenic and somatogenic receptors, and by in vitro bioassays. Two analogues were prepared in large amounts for in vivo studies. These studies (a) identified the residues responsible for the somatogenic activity of
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Kim, Yun-mi, Samuel Farrah, and Ronald H. Baney. Structure--Antimicrobial Activity Relationship Comparing a New Class of Antimicrobials, Silanols, to Alcohols and Phenols. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada447843.

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Nolan, David S., Ann S. Almgren, and John B. Bell. Studies of the relationship between environmental forcing and the structure and dynamics of tornado-like vortices. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/782526.

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Idakwo, Gabriel, Sundar Thangapandian, Joseph Luttrell, Zhaoxian Zhou, Chaoyang Zhang, and Ping Gong. Deep learning-based structure-activity relationship modeling for multi-category toxicity classification : a case study of 10K Tox21 chemicals with high-throughput cell-based androgen receptor bioassay data. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/41302.

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Deep learning (DL) has attracted the attention of computational toxicologists as it offers a potentially greater power for in silico predictive toxicology than existing shallow learning algorithms. However, contradicting reports have been documented. To further explore the advantages of DL over shallow learning, we conducted this case study using two cell-based androgen receptor (AR) activity datasets with 10K chemicals generated from the Tox21 program. A nested double-loop cross-validation approach was adopted along with a stratified sampling strategy for partitioning chemicals of multiple AR
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Chornodon, Myroslava. FEAUTURES OF GENDER IN MODERN MASS MEDIA. Ivan Franko National University of Lviv, 2021. http://dx.doi.org/10.30970/vjo.2021.49.11064.

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The article clarifies of gender identity stereotypes in modern media. The main gender stereotypes covered in modern mass media are analyzed and refuted. The model of gender relations in the media is reflected mainly in the stereotypical images of men and woman. The features of the use of gender concepts in modern periodicals for women and men were determined. The most frequently used derivatives of these macroconcepts were identified and analyzed in detail. It has been found that publications for women and men are full of various gender concepts that are used in different contexts. Ingeneral,
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Altstein, Miriam, and Ronald Nachman. Rationally designed insect neuropeptide agonists and antagonists: application for the characterization of the pyrokinin/Pban mechanisms of action in insects. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7587235.bard.

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The general objective of this BARD project focused on rationally designed insect neuropeptide (NP) agonists and antagonists, their application for the characterization of the mechanisms of action of the pyrokinin/PBAN (PK-PBAN) family and the development of biostable, bioavailable versions that can provide the basis for development of novel, environmentally-friendly pest insect control agents. The specific objectives of the study, as originally proposed, were to: (i) Test stimulatory potencies of rationally designed backbone cyclic (BBC) peptides on pheromonotropic, melanotropic, myotropic and
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Barg, Rivka, Kendal D. Hirschi, Avner Silber, Gozal Ben-Hayyim, Yechiam Salts, and Marla Binzel. Combining Elevated Levels of Membrane Fatty Acid Desaturation and Vacuolar H+ -pyrophosphatase Activity for Improved Drought Tolerance. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7613877.bard.

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Background to the topic: In previous works we have shown that Arabidopsis and tomato over-expressing H+-pyrophosphatase show increased tolerance to drought imposed by withholding irrigation of young plants in pots (Park et al. 2005). In addition, young tobacco plants over-expressing fatty acid desaturase 3 (OEX-FAD3) also showed increasing tolerance to drought stress (Zhang et al 2005), and similarly OEX-FAD3 young tomato plants (unpublished data from ARO), hence raising the possibility that pyramiding the two could further improve drought tolerance in tomato. Based on these findings the speci
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Popel, Maiia V., and Mariya P. Shyshkina. The areas of educational studies of the cloud-based learning systems. [б. в.], 2019. http://dx.doi.org/10.31812/123456789/3245.

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The article analyzes the current stage of educational studies of the cloud-based learning systems. The relationship between the notions of the cloud-based learning system and the cloud-based learning environment are investigated. It was found that the researchers paid most attention to the design of a cloud-based learning environment. However, in the process of a cloud-based environment design, the researchers consider a cloud-based system as a component within the cloud-based learning environment of as a stage in the process of design. It is shown that in the research literature there is no s
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BARKHATOV, NIKOLAY, and SERGEY REVUNOV. A software-computational neural network tool for predicting the electromagnetic state of the polar magnetosphere, taking into account the process that simulates its slow loading by the kinetic energy of the solar wind. SIB-Expertise, 2021. http://dx.doi.org/10.12731/er0519.07122021.

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The auroral activity indices AU, AL, AE, introduced into geophysics at the beginning of the space era, although they have certain drawbacks, are still widely used to monitor geomagnetic activity at high latitudes. The AU index reflects the intensity of the eastern electric jet, while the AL index is determined by the intensity of the western electric jet. There are many regression relationships linking the indices of magnetic activity with a wide range of phenomena observed in the Earth's magnetosphere and atmosphere. These relationships determine the importance of monitoring and predicting ge
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