Статті в журналах з теми "Bitopic"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Bitopic".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Wang, Huiqun, Danni Cao, James C. Gillespie, Rolando E. Mendez, Dana E. Selley, Lee-Yuan Liu-Chen, and Yan Zhang. "Exploring the putative mechanism of allosteric modulations by mixed-action kappa/mu opioid receptor bitopic modulators." Future Medicinal Chemistry 13, no. 6 (March 2021): 551–73. http://dx.doi.org/10.4155/fmc-2020-0308.
Повний текст джерелаFerrisi, Rebecca, Beatrice Polini, Caterina Ricardi, Francesca Gado, Kawthar A. Mohamed, Giovanna Baron, Salvatore Faiella, et al. "New Insights into Bitopic Orthosteric/Allosteric Ligands of Cannabinoid Receptor Type 2." International Journal of Molecular Sciences 24, no. 3 (January 21, 2023): 2135. http://dx.doi.org/10.3390/ijms24032135.
Повний текст джерелаFlores-Kim, Josué, and Andrew J. Darwin. "Phage Shock Protein C (PspC) of Yersinia enterocolitica Is a Polytopic Membrane Protein with Implications for Regulation of the Psp Stress Response." Journal of Bacteriology 194, no. 23 (September 28, 2012): 6548–59. http://dx.doi.org/10.1128/jb.01250-12.
Повний текст джерелаGao, Zhan-Guo, Kiran S. Toti, Ryan Campbell, R. Rama Suresh, Huijun Yang, and Kenneth A. Jacobson. "Allosteric Antagonism of the A2A Adenosine Receptor by a Series of Bitopic Ligands." Cells 9, no. 5 (May 12, 2020): 1200. http://dx.doi.org/10.3390/cells9051200.
Повний текст джерелаStank, Lars, Annika Frank, Stefanie Hagenow, and Holger Stark. "Talipexole variations as novel bitopic dopamine D2 and D3 receptor ligands." MedChemComm 10, no. 11 (2019): 1926–29. http://dx.doi.org/10.1039/c9md00379g.
Повний текст джерелаNewitt, John A., Nancy D. Ulbrandt, and Harris D. Bernstein. "The Structure of Multiple Polypeptide Domains Determines the Signal Recognition Particle Targeting Requirement ofEscherichia coli Inner Membrane Proteins." Journal of Bacteriology 181, no. 15 (August 1, 1999): 4561–67. http://dx.doi.org/10.1128/jb.181.15.4561-4567.1999.
Повний текст джерелаLiu, Jiquan, Yeping Xu, Pedro B. Groszewicz, Martin Brodrecht, Claudia Fasel, Kathrin Hofmann, Xijuan Tan, Torsten Gutmann, and Gerd Buntkowsky. "Novel dirhodium coordination polymers: the impact of side chains on cyclopropanation." Catalysis Science & Technology 8, no. 20 (2018): 5190–200. http://dx.doi.org/10.1039/c8cy01493k.
Повний текст джерелаAdhikari, Pramisha, Bing Xie, Ana Semeano, Alessandro Bonifazi, Francisco O. Battiti, Amy H. Newman, Hideaki Yano, and Lei Shi. "Chirality of Novel Bitopic Agonists Determines Unique Pharmacology at the Dopamine D3 Receptor." Biomolecules 11, no. 4 (April 13, 2021): 570. http://dx.doi.org/10.3390/biom11040570.
Повний текст джерелаPotapov, Andrei S., Evgenia A. Nudnova, Vladimir D. Ogorodnikov, Tatiana V. Petrenko, and Andrei I. Khlebnikov. "Synthesis of New Bitopic Tetra(pyrazolyl)-Ligands with Neopentane and O-Xylene Backbones." Scientific World Journal 2012 (2012): 1–5. http://dx.doi.org/10.1100/2012/798271.
Повний текст джерелаSchrage, Ramona, and Evi Kostenis. "Functional selectivity and dualsteric/bitopic GPCR targeting." Current Opinion in Pharmacology 32 (February 2017): 85–90. http://dx.doi.org/10.1016/j.coph.2016.12.001.
Повний текст джерелаCao, Yongkai, Ningning Sun, Jiumei Zhang, Zhiguo Liu, Yi-zhe Tang, Zhengzhi Wu, Kyeong-Man Kim, and Seung Hoon Cheon. "Correction: Design, synthesis, and evaluation of bitopic arylpiperazine-phthalimides as selective dopamine D3 receptor agonists." MedChemComm 9, no. 9 (2018): 1565. http://dx.doi.org/10.1039/c8md90042f.
Повний текст джерелаJakubik, Jan, and Esam E. El-Fakahany. "Current Advances in Allosteric Modulation of Muscarinic Receptors." Biomolecules 10, no. 2 (February 18, 2020): 325. http://dx.doi.org/10.3390/biom10020325.
Повний текст джерелаValant, C., P. M. Sexton, and A. Christopoulos. "Orthosteric/Allosteric Bitopic Ligands: Going Hybrid at GPCRs." Molecular Interventions 9, no. 3 (June 1, 2009): 125–35. http://dx.doi.org/10.1124/mi.9.3.6.
Повний текст джерелаNiklas, Beata, Bruno Lapied, and Wieslaw Nowak. "In Search of Synergistic Insect Repellents: Modeling of Muscarinic GPCR Interactions with Classical and Bitopic Photoactive Ligands." Molecules 27, no. 10 (May 20, 2022): 3280. http://dx.doi.org/10.3390/molecules27103280.
Повний текст джерелаvan der Sluis, Eli O., Erhard van der Vries, Greetje Berrelkamp, Nico Nouwen, and Arnold J. M. Driessen. "Topologically Fixed SecG Is Fully Functional." Journal of Bacteriology 188, no. 3 (February 1, 2006): 1188–90. http://dx.doi.org/10.1128/jb.188.3.1188-1190.2006.
Повний текст джерелаOzgur, Beytullah, Cory D. Dunn, and Mehmet Sayar. "Modeling Adsorption, Conformation, and Orientation of the Fis1 Tail Anchor at the Mitochondrial Outer Membrane." Membranes 12, no. 8 (July 31, 2022): 752. http://dx.doi.org/10.3390/membranes12080752.
Повний текст джерелаChen, Joseph C., David S. Weiss, Jean-Marc Ghigo, and Jon Beckwith. "Septal Localization of FtsQ, an Essential Cell Division Protein in Escherichia coli." Journal of Bacteriology 181, no. 2 (January 15, 1999): 521–30. http://dx.doi.org/10.1128/jb.181.2.521-530.1999.
Повний текст джерелаBocharov, Eduard V., Pavel E. Volynsky, Konstantin V. Pavlov, Roman G. Efremov, and Alexander S. Arseniev. "Structure elucidation of dimeric transmembrane domains of bitopic proteins." Cell Adhesion & Migration 4, no. 2 (April 2010): 284–98. http://dx.doi.org/10.4161/cam.4.2.11930.
Повний текст джерелаJo, Euijung, Barun Bhhatarai, Emanuela Repetto, Miguel Guerrero, Sean Riley, Steven J. Brown, Yasushi Kohno, Edward Roberts, Stephan C. Schürer, and Hugh Rosen. "Novel Selective Allosteric and Bitopic Ligands for the S1P3Receptor." ACS Chemical Biology 7, no. 12 (September 14, 2012): 1975–83. http://dx.doi.org/10.1021/cb300392z.
Повний текст джерелаZviling, Moti, Uzi Kochva, and Isaiah T. Arkin. "How important are transmembrane helices of bitopic membrane proteins?" Biochimica et Biophysica Acta (BBA) - Biomembranes 1768, no. 3 (March 2007): 387–92. http://dx.doi.org/10.1016/j.bbamem.2006.11.019.
Повний текст джерелаLee, Boeun, Michelle Taylor, Suzy A. Griffin, Tamara McInnis, Nathalie Sumien, Robert H. Mach, and Robert R. Luedtke. "Evaluation of Substituted N-Phenylpiperazine Analogs as D3 vs. D2 Dopamine Receptor Subtype Selective Ligands." Molecules 26, no. 11 (May 26, 2021): 3182. http://dx.doi.org/10.3390/molecules26113182.
Повний текст джерелаBoldog, Ishtvan, Joachim Sieler, Alexander N. Chernega, and Konstantin V. Domasevitch. "4,4′-Bipyrazolyl: new bitopic connector for construction of coordination networks." Inorganica Chimica Acta 338 (October 2002): 69–77. http://dx.doi.org/10.1016/s0020-1693(02)00902-7.
Повний текст джерелаLane, J. Robert, Patrick M. Sexton, and Arthur Christopoulos. "Bridging the gap: bitopic ligands of G-protein-coupled receptors." Trends in Pharmacological Sciences 34, no. 1 (January 2013): 59–66. http://dx.doi.org/10.1016/j.tips.2012.10.003.
Повний текст джерелаReinecke, Bethany A., Huiqun Wang, and Yan Zhang. "Recent Advances in the Drug Discovery and Development of Dualsteric/ Bitopic Activators of G Protein-Coupled Receptors." Current Topics in Medicinal Chemistry 19, no. 26 (December 10, 2019): 2378–92. http://dx.doi.org/10.2174/1568026619666191009164609.
Повний текст джерелаAgnihothram, Sudhakar S., Joanne York, Meg Trahey, and Jack H. Nunberg. "Bitopic Membrane Topology of the Stable Signal Peptide in the Tripartite Junín Virus GP-C Envelope Glycoprotein Complex." Journal of Virology 81, no. 8 (January 31, 2007): 4331–37. http://dx.doi.org/10.1128/jvi.02779-06.
Повний текст джерелаCooper, Samantha Louise, Edward Wragg, Julie March, Stephen Hill, and Jeanette Woolard. "Effects of an Adenosine Receptor Bitopic Ligand on The Cardiovascular System." FASEB Journal 34, S1 (April 2020): 1. http://dx.doi.org/10.1096/fasebj.2020.34.s1.02426.
Повний текст джерелаKeov, Peter, Laura López, Shane M. Devine, Celine Valant, J. Robert Lane, Peter J. Scammells, Patrick M. Sexton, and Arthur Christopoulos. "Molecular Mechanisms of Bitopic Ligand Engagement with the M1Muscarinic Acetylcholine Receptor." Journal of Biological Chemistry 289, no. 34 (July 8, 2014): 23817–37. http://dx.doi.org/10.1074/jbc.m114.582874.
Повний текст джерелаMarie, Cécile, Manuel Miguirditchian, Denis Guillaneux, Julia Bisson, Muriel Pipelier, and Didier Dubreuil. "New Bitopic Ligands for the Group Actinide Separation by Solvent Extraction." Solvent Extraction and Ion Exchange 29, no. 2 (March 18, 2011): 292–315. http://dx.doi.org/10.1080/07366299.2011.556923.
Повний текст джерелаMorales, Paula, Gemma Navarro, Marc Gómez‐Autet, Laura Redondo, Javier Fernández‐Ruiz, Laura Pérez‐Benito, Arnau Cordomí, Leonardo Pardo, Rafael Franco, and Nadine Jagerovic. "Discovery of Homobivalent Bitopic Ligands of the Cannabinoid CB 2 Receptor**." Chemistry – A European Journal 26, no. 68 (November 9, 2020): 15839–42. http://dx.doi.org/10.1002/chem.202003389.
Повний текст джерелаBieller, Susanne, Fan Zhang, Michael Bolte, Jan W. Bats, Hans-Wolfram Lerner, and Matthias Wagner. "Bitopic Bis- and Tris(1-pyrazolyl)borate Ligands: Syntheses and Structural Characterization." Organometallics 23, no. 9 (April 2004): 2107–13. http://dx.doi.org/10.1021/om049954e.
Повний текст джерелаCaldwell, Andreia M., and Ronald L. Smith. "Membrane Topology of the ZntB Efflux System of Salmonella enterica Serovar Typhimurium." Journal of Bacteriology 185, no. 1 (January 1, 2003): 374–76. http://dx.doi.org/10.1128/jb.185.1.374-376.2003.
Повний текст джерелаQuadros, Helenita C., Aysun Çapcı, Lars Herrmann, Sarah D’Alessandro, Diana Fontinha, Raquel Azevedo, Wilmer Villarreal, et al. "Studies of Potency and Efficacy of an Optimized Artemisinin-Quinoline Hybrid against Multiple Stages of the Plasmodium Life Cycle." Pharmaceuticals 14, no. 11 (November 6, 2021): 1129. http://dx.doi.org/10.3390/ph14111129.
Повний текст джерелаFoster, Scott, Andrew Lee, Cristina Maranto, Joshua E. Allen, Randall Lanier, Phiroze Sethna, and Varun V. Prabhu. "EXTH-104. ROLE OF CLPP AND MITOCHONDRIAL METABOLISM IN THE ANTI-CANCER EFFECTS OF IMIPRIDONE ONC201 AND ONC206 IN GLIOBLASTOMA AND DIPG." Neuro-Oncology 24, Supplement_7 (November 1, 2022): vii234. http://dx.doi.org/10.1093/neuonc/noac209.902.
Повний текст джерелаPerez, Daniel, Ana Martinez, Carmen Gil, and Nuria Campillo. "From Bitopic Inhibitors to Multitarget Drugs for the Future Treatment of Alzheimer’s Disease." Current Medicinal Chemistry 22, no. 33 (November 13, 2015): 3789–806. http://dx.doi.org/10.2174/0929867322666150812145825.
Повний текст джерелаHolzgrabe, Ulrike, and Michael Decker. "Bitopic muscarinic agonists and antagonists and uses thereof: a patent evaluation of US20160136145A1." Expert Opinion on Therapeutic Patents 27, no. 2 (December 26, 2016): 121–25. http://dx.doi.org/10.1080/13543776.2017.1272577.
Повний текст джерелаLomize, Andrei L., Jacob M. Hage, and Irina D. Pogozheva. "Membranome 2.0: database for proteome-wide profiling of bitopic proteins and their dimers." Bioinformatics 34, no. 6 (November 6, 2017): 1061–62. http://dx.doi.org/10.1093/bioinformatics/btx720.
Повний текст джерелаTahtaoui, Chouaib, Isabelle Parrot, Philippe Klotz, Fabrice Guillier, Jean-Luc Galzi, Marcel Hibert, and Brigitte Ilien. "Fluorescent Pirenzepine Derivatives as Potential Bitopic Ligands of the Human M1 Muscarinic Receptor." Journal of Medicinal Chemistry 47, no. 17 (August 2004): 4300–4315. http://dx.doi.org/10.1021/jm040800a.
Повний текст джерелаVolpato, Daniela, Michael Kauk, Regina Messerer, Marcel Bermudez, Gerhard Wolber, Andreas Bock, Carsten Hoffmann, and Ulrike Holzgrabe. "The Role of Orthosteric Building Blocks of Bitopic Ligands for Muscarinic M1 Receptors." ACS Omega 5, no. 49 (December 1, 2020): 31706–15. http://dx.doi.org/10.1021/acsomega.0c04220.
Повний текст джерелаReger, Daniel L., Russell P. Watson, and Mark D. Smith. "An Organoplatinum(II) Complex of a Bitopic, Propylene-linked Bis(pyrazolyl)methane Ligand." Journal of Chemical Crystallography 38, no. 1 (October 24, 2007): 17–20. http://dx.doi.org/10.1007/s10870-007-9264-z.
Повний текст джерелаBocharov, Eduard V., Dmitry M. Lesovoy, Olga V. Bocharova, Anatoly S. Urban, Yaroslav V. Bershacky, Pavel E. Volynsky, Roman G. Efremov, and Alexander S. Arseniev. "The Role of Protein-Lipid Interactions in the Functioning of Bitopic Membrane Proteins." Biophysical Journal 118, no. 3 (February 2020): 211a. http://dx.doi.org/10.1016/j.bpj.2019.11.1259.
Повний текст джерелаReger, Daniel L., Andrea E. Pascui, and Mark D. Smith. "Structural Variations in Copper(II) Complexes of a Bitopic Bis(pyrazolyl)methane Ligand." European Journal of Inorganic Chemistry 2012, no. 29 (May 25, 2012): 4593–604. http://dx.doi.org/10.1002/ejic.201200118.
Повний текст джерелаMeijer, Femke A., Guido J. M. Oerlemans та Luc Brunsveld. "Orthosteric and Allosteric Dual Targeting of the Nuclear Receptor RORγt with a Bitopic Ligand". ACS Chemical Biology 16, № 3 (17 лютого 2021): 510–19. http://dx.doi.org/10.1021/acschembio.0c00941.
Повний текст джерелаValant, Celine, J. Robert Lane, Patrick M. Sexton, and Arthur Christopoulos. "The Best of Both Worlds? Bitopic Orthosteric/Allosteric Ligands of G Protein–Coupled Receptors." Annual Review of Pharmacology and Toxicology 52, no. 1 (February 10, 2012): 153–78. http://dx.doi.org/10.1146/annurev-pharmtox-010611-134514.
Повний текст джерелаChiu, Pei Ling, Chih Yuan Chen, Chun-Chin Lee, Meng-Hua Hsieh, Chuan-Hung Chuang, and Hon Man Lee. "Structural Variations in Novel Silver(I) Complexes with Bitopic Pyrazole/N-Heterocyclic Carbene Ligands." Inorganic Chemistry 45, no. 6 (March 2006): 2520–30. http://dx.doi.org/10.1021/ic051840n.
Повний текст джерелаCao, Yongkai, Ningning Sun, Jiumei Zhang, Zhiguo Liu, Yi-zhe Tang, Zhengzhi Wu, Kyeong-Man Kim, and Seung Hoon Cheon. "Design, synthesis, and evaluation of bitopic arylpiperazine-phthalimides as selective dopamine D3 receptor agonists." MedChemComm 9, no. 9 (2018): 1457–65. http://dx.doi.org/10.1039/c8md00237a.
Повний текст джерелаCao, Han, Marcus C. K. Ng, Siti Azma Jusoh, Hio Kuan Tai, and Shirley W. I. Siu. "TMDIM: an improved algorithm for the structure prediction of transmembrane domains of bitopic dimers." Journal of Computer-Aided Molecular Design 31, no. 9 (September 2017): 855–65. http://dx.doi.org/10.1007/s10822-017-0047-0.
Повний текст джерелаLider, Sukhikh, Smolentsev, Semitut, Filatov, and Potapov. "Synthesis, Crystal Structure, Thermal Analysis, and DFT Calculations of Molecular Copper(II) Chloride Complexes with Bitopic Ligand 1,1,2,2-tetrakis(pyrazol-1-yl)ethane." Crystals 9, no. 4 (April 24, 2019): 222. http://dx.doi.org/10.3390/cryst9040222.
Повний текст джерелаPrabhu, Varun, Caroline Cuoco, Jinkyu Jung, Abed Rahman Kawakibi, Blair Willette, Marilyn Day, Lakshmi Anantharaman, et al. "DDIS-20. IMIPRIDONE STRUCTURE ACTIVITY RELATIONSHIP UNCOVERS ONC206 AS THE NEXT BITOPIC DRD2 ANTAGONIST FOR ONCOLOGY WITH DIFFERENTIATED RECEPTOR PHARMACOLOGY." Neuro-Oncology 21, Supplement_6 (November 2019): vi67. http://dx.doi.org/10.1093/neuonc/noz175.271.
Повний текст джерелаPrabhu, Varun, Abed Rahman Kawakibi, Neel Madhukar, Mathew Garnett, Ultan McDermott, Cyril Benes, Robert Wechsler-Reya, et al. "EXTH-71. IND-ENABLING CHARACTERIZATION OF ONC206 AS THE NEXT BITOPIC DRD2 ANTAGONIST FOR NEURO-ONCOLOGY." Neuro-Oncology 21, Supplement_6 (November 2019): vi97. http://dx.doi.org/10.1093/neuonc/noz175.401.
Повний текст джерелаPrabhu, Varun, Sara Morrow, Abed Rahman Kawakibi, Yulia Jitkova, Jinkyu Jung, Neel Madhukar, Mathew Garnett, et al. "EXTH-74. IND-ENABLING CHARACTERIZATION OF DUAL DRD2- AND ClpP-TARGETING AGENT ONC206 AS THE NEXT IMIPRIDONE FOR CLINICAL NEURO-ONCOLOGY." Neuro-Oncology 22, Supplement_2 (November 2020): ii103. http://dx.doi.org/10.1093/neuonc/noaa215.428.
Повний текст джерела