Статті в журналах з теми "Molecules - Biological Interests"
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Verma, Amita, Sunil Joshi, and Deepika Singh. "Imidazole: Having Versatile Biological Activities." Journal of Chemistry 2013 (2013): 1–12. http://dx.doi.org/10.1155/2013/329412.
Повний текст джерелаBilal, Muhammad, Leonardo Vieira Nunes, Marco Thúlio Saviatto Duarte, Luiz Fernando Romanholo Ferreira, Renato Nery Soriano, and Hafiz M. N. Iqbal. "Exploitation of Marine-Derived Robust Biological Molecules to Manage Inflammatory Bowel Disease." Marine Drugs 19, no. 4 (March 30, 2021): 196. http://dx.doi.org/10.3390/md19040196.
Повний текст джерелаWehbe, Rim, Jacinthe Frangieh, Mohamad Rima, Dany El Obeid, Jean-Marc Sabatier, and Ziad Fajloun. "Bee Venom: Overview of Main Compounds and Bioactivities for Therapeutic Interests." Molecules 24, no. 16 (August 19, 2019): 2997. http://dx.doi.org/10.3390/molecules24162997.
Повний текст джерелаBoss, Alan P., William M. Irvine, Karen J. Meech, Cristiano B. Cosmovici, Pascale F. Ehrenfreund, David W. Latham, David Morrison, and Stephane Udry. "COMMISSION 51: BIOASTRONOMY." Proceedings of the International Astronomical Union 4, T27A (December 2008): 179–80. http://dx.doi.org/10.1017/s1743921308025453.
Повний текст джерелаMurad, Ferid. "Discovery of Some of the Biological Effects of Nitric Oxide and its Role in Cell Signaling." Bioscience Reports 19, no. 3 (June 1, 1999): 133–54. http://dx.doi.org/10.1023/a:1020265417394.
Повний текст джерелаMurad, Ferid. "Discovery of Some of the Biological Effects of Nitric Oxide and its Role in Cell Signaling." Bioscience Reports 24, no. 4-5 (August 10, 2004): 452–74. http://dx.doi.org/10.1007/s10540-005-2741-8.
Повний текст джерелаWang, Yu-Huan, Qian-Fan Yang, Xiao Lin, Die Chen, Zhi-Yin Wang, Bin Chen, Hua-Yi Han, et al. "G4LDB 2.2: a database for discovering and studying G-quadruplex and i-Motif ligands." Nucleic Acids Research 50, no. D1 (October 29, 2021): D150—D160. http://dx.doi.org/10.1093/nar/gkab952.
Повний текст джерелаDi Costanzo, Luigi, and Barbara Panunzi. "Visual pH Sensors: From a Chemical Perspective to New Bioengineered Materials." Molecules 26, no. 10 (May 16, 2021): 2952. http://dx.doi.org/10.3390/molecules26102952.
Повний текст джерелаSheth, Tejas, C. S. Pitchumoni, and Kiron M. Das. "Management of Musculoskeletal Manifestations in Inflammatory Bowel Disease." Gastroenterology Research and Practice 2015 (2015): 1–11. http://dx.doi.org/10.1155/2015/387891.
Повний текст джерелаTarley, Cesar. "Chemical Imprinting Technology Applied to Analytical Chemistry: Current Status and Future Outlook in Brazil." Brazilian Journal of Analytical Chemistry 9, no. 35 (April 11, 2022): 7–11. http://dx.doi.org/10.30744/brjac.2179-3425.letter.crtarley.n35.
Повний текст джерелаThorogood, Adrian, and Ma'n H. Zawati. "International Guidelines for Privacy in Genomic Biobanking (or the Unexpected Virtue of Pluralism)." Journal of Law, Medicine & Ethics 43, no. 4 (2015): 690–702. http://dx.doi.org/10.1111/jlme.12312.
Повний текст джерелаLe, Thu Hac Huong, Takumi Matsushita, Ryoichi Ohta, Yuta Shimoda, Hiroaki Matsui, and Takehiko Kitamori. "Fabrication of Infrared-Compatible Nanofluidic Devices for Plasmon-Enhanced Infrared Absorption Spectroscopy." Micromachines 11, no. 12 (November 30, 2020): 1062. http://dx.doi.org/10.3390/mi11121062.
Повний текст джерелаReaves, B. J., and A. J. Wolstenholme. "The TRP channel superfamily: insights into how structure, protein–lipid interactions and localization influence function." Biochemical Society Transactions 35, no. 1 (January 22, 2007): 77–80. http://dx.doi.org/10.1042/bst0350077.
Повний текст джерелаSharma, Sakshi, Goutam Brahmachari, Rajni Kant, and Vivek K. Gupta. "One-pot green synthesis of biologically relevant novel spiro[indolin-2-one-3,4′-pyrano[2,3-c]pyrazoles] and studies on their spectral and X-ray crystallographic behaviors." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 72, no. 3 (May 13, 2016): 335–43. http://dx.doi.org/10.1107/s2052520616005060.
Повний текст джерелаBédé, Lucie A., Mawa Koné, Guy R. M. Koné, Simplice C. S. Ouattara, Lamoussa Ouattara, and El Hadji S. Bamba. "Tautomeric Equilibrium Modeling: Stability and Reactivity of Benzothiazole and Derivatives." International Journal of Chemistry 11, no. 1 (April 29, 2019): 84. http://dx.doi.org/10.5539/ijc.v11n1p84.
Повний текст джерелаKowalski, Jennifer R., Geoffrey C. Hoops, and R. Jeremy Johnson. "Implementation of a Collaborative Series of Classroom-Based Undergraduate Research Experiences Spanning Chemical Biology, Biochemistry, and Neurobiology." CBE—Life Sciences Education 15, no. 4 (December 2016): ar55. http://dx.doi.org/10.1187/cbe.16-02-0089.
Повний текст джерелаSasikumar, B. "Genetic resources ofCurcuma: diversity, characterization and utilization." Plant Genetic Resources 3, no. 2 (August 2005): 230–51. http://dx.doi.org/10.1079/pgr200574.
Повний текст джерелаFaurskov Nielsen, O., K. L. Jacobsen, P. Westh, T. Radovic, B. Due Larsen, and D. H. Christensen. "Fast dynamics in molecules of biological interest." Journal of Molecular Structure 598, no. 1 (October 2001): 9–14. http://dx.doi.org/10.1016/s0022-2860(01)00799-2.
Повний текст джерелаJoram, Anju, Rashmi Sharma, and Arun Kumar Sharma. "Spectroscopic Characterization and Thermo-Gravimetric Analysis of Bioactive Copper 2-Amino 6-Methyl Benzothiazole Complexes Derived from Various Oils." Current Physical Chemistry 9, no. 1 (June 3, 2019): 58–76. http://dx.doi.org/10.2174/1877946809666190320144208.
Повний текст джерелаLisetska, I. S., and M. M. Rozhko. "Determination of endogenous intoxication in teenagers and young adults who smoke." UKRAINIAN JOURNAL OF PERINATOLOGY AND PEDIATRICS, no. 2(90) (June 30, 2022): 39–43. http://dx.doi.org/10.15574/pp.2022.90.39.
Повний текст джерелаParveen, Mehtab, Afroz Aslam, Shahab A. A. Nami, and Musheer Ahmad. "Z-Acrylonitrile Derivatives: Improved Synthesis, X-ray Structure, and Interaction with Human Serum Albumin." Current Organic Synthesis 16, no. 8 (January 20, 2020): 1149–60. http://dx.doi.org/10.2174/1570179416666191008085806.
Повний текст джерелаMarinković, B. P., A. R. Milosavljević, J. B. Maljković, D. Šević, B. A. Petruševski, D. Pavlović, D. M. Filipović, M. Terzić, and V. Pejčev. "Optical and Electron Spectrometry of Molecules of Biological Interest." Acta Physica Polonica A 112, no. 5 (November 2007): 1145–50. http://dx.doi.org/10.12693/aphyspola.112.1145.
Повний текст джерелаGutiérrez-Rodríguez, A., R. Santiago-García, S. García-Granda, J. Barluenga, M. Tomás, and K. Bieger. "Dihydrodiazaphosphinines in the synthesis of molecules of biological interest." Acta Crystallographica Section A Foundations of Crystallography 52, a1 (August 8, 1996): C455. http://dx.doi.org/10.1107/s0108767396081329.
Повний текст джерелаWinnewisser, Gisbert. "Interstellar Molecules of Prebiotic Interest." International Astronomical Union Colloquium 161 (January 1997): 5–22. http://dx.doi.org/10.1017/s0252921100014573.
Повний текст джерелаEdgecombe, Kenneth E., Donald F. Weaver, and Vedene H. Smith Jr. "Electronic structure analysis of compounds of interest in drug design: mono- and dicarboxylated pyridines." Canadian Journal of Chemistry 72, no. 5 (May 1, 1994): 1388–403. http://dx.doi.org/10.1139/v94-174.
Повний текст джерелаFlores-Parra, Angelina, and Rosalinda Contreras. "Boron coordination compounds derived from organic molecules of biological interest." Coordination Chemistry Reviews 196, no. 1 (January 2000): 85–124. http://dx.doi.org/10.1016/s0010-8545(99)00053-3.
Повний текст джерелаQuinto, M. A., P. R. Montenegro, J. M. Monti, O. A. Fojón, and R. D. Rivarola. "Electron capture by swift ions from molecules of biological interest." Journal of Physics B: Atomic, Molecular and Optical Physics 51, no. 16 (July 19, 2018): 165201. http://dx.doi.org/10.1088/1361-6455/aad152.
Повний текст джерелаVillani, P., S. Orlando, A. Santagata, A. De Bonis, S. Veronesi, and A. Giardini. "Nanosecond and femtosecond laser spectroscopy of molecules of biological interest." Applied Surface Science 253, no. 19 (July 2007): 7783–86. http://dx.doi.org/10.1016/j.apsusc.2007.02.089.
Повний текст джерелаPrince, K. C., P. Bolognesi, V. Feyer, O. Plekan, and L. Avaldi. "Study of complex molecules of biological interest with synchrotron radiation." Journal of Electron Spectroscopy and Related Phenomena 204 (October 2015): 335–44. http://dx.doi.org/10.1016/j.elspec.2015.08.010.
Повний текст джерелаLuger, P., A. Bach, B. Dittrich, M. Messerschmidt, and A. Wagner. "Charge density and topological properties of larger molecules of biological interest." Acta Crystallographica Section A Foundations of Crystallography 58, s1 (August 6, 2002): c351. http://dx.doi.org/10.1107/s0108767302099026.
Повний текст джерелаHegedus, L. S. "Chromium carbene complexes in the synthesis of molecules of biological interest." Pure and Applied Chemistry 62, no. 4 (January 1, 1990): 691–98. http://dx.doi.org/10.1351/pac199062040691.
Повний текст джерелаBotek, Edith, Claudia Giribet, Martín Ruiz de Azúa, Ricardo Martín Negri, and Delia Bernik. "Evaluation of the Molecular Polarizability Using the IPPP−CLOPPA−INDO/S Method. Application to Molecules of Biological Interest." Journal of Physical Chemistry A 112, no. 30 (July 2008): 6992–98. http://dx.doi.org/10.1021/jp711620m.
Повний текст джерелаScuderi, D., A. Paladini, M. Satta, D. Catone, F. Rondino, A. Filippi, S. Piccirillo, M. Speranza, and A. Giardini Guidoni. "Solvent free interactions in contact pairs of molecules of biological interest: Laser spectroscopic and electrospray mass spectrometric studies." International Journal of Photoenergy 6, no. 1 (2004): 17–21. http://dx.doi.org/10.1155/s1110662x04000030.
Повний текст джерелаArsenou, E., M. Fousteris, A. Koutsourea, and S. Nikolaropoulos. "7-Keto-Δ5-Steroids: Key-Molecules Owning Particular Biological and Chemical Interest." Mini-Reviews in Medicinal Chemistry 3, no. 6 (September 1, 2003): 557–67. http://dx.doi.org/10.2174/1389557033487953.
Повний текст джерелаHolstein, J. J., P. Luger, C. Paulmann, and B. Dittrich. "Validation of charge-density refinements and application to molecules of biological interest." Acta Crystallographica Section A Foundations of Crystallography 64, a1 (August 23, 2008): C380. http://dx.doi.org/10.1107/s0108767308087862.
Повний текст джерелаŚmiałek, M. A., K. Tanzer, M. Neustetter, S. Huber, R. Schürmann, I. Bald, and S. Denifl. "Electron ionization and low energy electron attachment to molecules of biological interest." Journal of Physics: Conference Series 635, no. 7 (September 7, 2015): 072025. http://dx.doi.org/10.1088/1742-6596/635/7/072025.
Повний текст джерелаFlores-Parra, Angelina, and Rosalinda Contreras. "ChemInform Abstract: Boron Coordination Compounds Derived from Organic Molecules of Biological Interest." ChemInform 31, no. 13 (June 9, 2010): no. http://dx.doi.org/10.1002/chin.200013258.
Повний текст джерелаSanto, Marisa, and Marye Anne Fox. "Hydrogen bonding interactions between Starburst dendrimers and several molecules of biological interest." Journal of Physical Organic Chemistry 12, no. 4 (April 1999): 293–307. http://dx.doi.org/10.1002/(sici)1099-1395(199904)12:4<293::aid-poc88>3.0.co;2-q.
Повний текст джерелаBruni, Renato, Davide Barreca, Michele Protti, Virginia Brighenti, Laura Righetti, Lisa Anceschi, Laura Mercolini, Stefania Benvenuti, Giuseppe Gattuso, and Federica Pellati. "Botanical Sources, Chemistry, Analysis, and Biological Activity of Furanocoumarins of Pharmaceutical Interest." Molecules 24, no. 11 (June 8, 2019): 2163. http://dx.doi.org/10.3390/molecules24112163.
Повний текст джерелаNahon-Esteve, Sacha, Arnaud Martel, Célia Maschi, Jean-Pierre Caujolle, Stéphanie Baillif, Sandra Lassalle, and Paul Hofman. "The Molecular Pathology of Eye Tumors: A 2019 Update Main Interests for Routine Clinical Practice." Current Molecular Medicine 19, no. 9 (October 11, 2019): 632–64. http://dx.doi.org/10.2174/1566524019666190726161044.
Повний текст джерелаBolognesi, P., M. C. Castrovilli, P. O’Keeffe, A. R. Casavola, D. Catone, S. Turchini, and L. Avaldi. "Photofragmentation of organic molecules of biological interest: The pyrimidine and 2Br–pyrimidine cases." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 279 (May 2012): 118–23. http://dx.doi.org/10.1016/j.nimb.2011.10.063.
Повний текст джерелаDiaz, C., and A. Pesce. "S-H bond cleavage in molecules of biological interest with CpFe(dppe)I." Applied Organometallic Chemistry 14, no. 10 (2000): 557–60. http://dx.doi.org/10.1002/1099-0739(200010)14:10<557::aid-aoc38>3.0.co;2-f.
Повний текст джерелаSimons, John P. "Getting into shape? The interaction of molecules of biological interest with molecules of water: from simplicity to complexity." Comptes Rendus Chimie 6, no. 1 (January 2003): 17–31. http://dx.doi.org/10.1016/s1631-0748(03)00008-0.
Повний текст джерелаBurgos-Solórzano, G. I., J. F. Brennecke, and M. A. Stadtherr. "Solubility measurements and modeling of molecules of biological and pharmaceutical interest with supercritical CO2." Fluid Phase Equilibria 220, no. 1 (June 2004): 57–69. http://dx.doi.org/10.1016/j.fluid.2004.01.036.
Повний текст джерелаWeinkauf, Rainer, Charles Desfrançois, and John Simons. "Molecules of Biological Interest in the Gas Phase EuroConference on Fundamental Studies and Applications." Molecular Physics 100, no. 12 (June 20, 2002): 2001. http://dx.doi.org/10.1080/00268970210149308.
Повний текст джерелаWeinkauf, Rainer, Charles DesfranGois, and John Simons. "Molecules of Biological Interest in the Gas Phase EuroConference on Fundamental Studies and Applications." Molecular Physics 100, no. 10 (May 20, 2002): 1645. http://dx.doi.org/10.1080/00268970210149308a.
Повний текст джерелаOrtega, Paula, Rafael Gómez, and F. Javier de la Mata. "Thiol ended carbosilane dendrimers. A multivalent platform for the binding of molecules of biological interest." Tetrahedron Letters 56, no. 38 (September 2015): 5299–302. http://dx.doi.org/10.1016/j.tetlet.2015.07.085.
Повний текст джерелаRemijan, A., Y. ‐S Shiao, D. N. Friedel, D. S. Meier, and L. E. Snyder. "A Survey of Large Molecules of Biological Interest toward Selected High‐Mass Star‐forming Regions." Astrophysical Journal 617, no. 1 (December 10, 2004): 384–98. http://dx.doi.org/10.1086/425266.
Повний текст джерелаGoel, R. K., and Km C. Gupta. "Electronic and vibrational spectra of N-heterocyclic molecules of biological interest and effect of solvents." Journal of Raman Spectroscopy 16, no. 1 (February 1985): 1–6. http://dx.doi.org/10.1002/jrs.1250160102.
Повний текст джерелаKnighten, Jennifer M., Takreem Aziz, Donald J. Pleshinger, Naga Annamdevula, Thomas C. Rich, Mark S. Taylor, Joel F. Andrews, Christian T. Macarilla, and C. Michael Francis. "Algorithm for biological second messenger analysis with dynamic regions of interest." PLOS ONE 18, no. 5 (May 11, 2023): e0284394. http://dx.doi.org/10.1371/journal.pone.0284394.
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