Academic literature on the topic 'DPPZ'
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Journal articles on the topic "DPPZ"
Choy, Tak-Kee, Chih-Yang Wang, Nam Nhut Phan, Hoang Dang Khoa Ta, Gangga Anuraga, Yen-Hsi Liu, Yung-Fu Wu, Kuen-Haur Lee, Jian-Ying Chuang, and Tzu-Jen Kao. "Identification of Dipeptidyl Peptidase (DPP) Family Genes in Clinical Breast Cancer Patients via an Integrated Bioinformatics Approach." Diagnostics 11, no. 7 (July 2, 2021): 1204. http://dx.doi.org/10.3390/diagnostics11071204.
Full textFunston, Alison M., Carleen Cullinane, Kenneth P. Ghiggino, W. David McFadyen, Stanley S. Stylli, and Peter A. Tregloan. "Dipyridophenazine Complexes of Cobalt(III): DNA Photocleavage and Photobiology." Australian Journal of Chemistry 58, no. 3 (2005): 206. http://dx.doi.org/10.1071/ch04206.
Full textQI, Shu Y., Pierre J. RIVIERE, Jerzy TROJNAR, Jean-Louis JUNIEN, and Karen O. AKINSANYA. "Cloning and characterization of dipeptidyl peptidase 10, a new member of an emerging subgroup of serine proteases." Biochemical Journal 373, no. 1 (July 1, 2003): 179–89. http://dx.doi.org/10.1042/bj20021914.
Full textAl-Samrai, Osama'a A. Y., Ahmed S. M. Al-Janabi2, and Eman A. Othman1. "Mixed Ligand Complexes of Hg-tetrazole-thiolate with phosphine, Synthesis and spectroscopic studies." Tikrit Journal of Pure Science 24, no. 5 (September 13, 2019): 10. http://dx.doi.org/10.25130/j.v24i5.860.
Full textWilson, Claire H., Hui Emma Zhang, Mark D. Gorrell, and Catherine A. Abbott. "Dipeptidyl peptidase 9 substrates and their discovery: current progress and the application of mass spectrometry-based approaches." Biological Chemistry 397, no. 9 (September 1, 2016): 837–56. http://dx.doi.org/10.1515/hsz-2016-0174.
Full textLiang, Xi-Ling, and Li-Feng Tan. "Nucleic Acid (Calf Thymus-DNA, Yeast tRNA) Binding and Cytotoxic Properties of a Dinuclear (Ru,Co) Metal Polypyridyl Complex." Australian Journal of Chemistry 63, no. 10 (2010): 1453. http://dx.doi.org/10.1071/ch10178.
Full textDi Pietro, Maria Letizia, Giuseppina La Ganga, Francesco Nastasi, and Fausto Puntoriero. "Ru(II)-Dppz Derivatives and Their Interactions with DNA: Thirty Years and Counting." Applied Sciences 11, no. 7 (March 29, 2021): 3038. http://dx.doi.org/10.3390/app11073038.
Full textShahabadi, Nahid, and Maryam Mahdavi. "DNA Interaction Studies of a Cobalt(II) Mixed-Ligand Complex Containing Two Intercalating Ligands: 4,7-Dimethyl-1, 10-Phenanthroline and Dipyrido[3,2-a:2′,3′-c]phenazine." ISRN Inorganic Chemistry 2013 (December 30, 2013): 1–7. http://dx.doi.org/10.1155/2013/604218.
Full textHe, Xiaojun, Lianhe Jin, and Lifeng Tan. "DNA-binding, topoisomerases I and II inhibition and in vitro cytotoxicity of ruthenium(II) polypyridyl complexes: [Ru(dppz)2L]2+ (L=dppz-11-CO2Me and dppz)." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 135 (January 2015): 101–9. http://dx.doi.org/10.1016/j.saa.2014.06.147.
Full textRochford, Garret, Zara Molphy, Kevin Kavanagh, Malachy McCann, Michael Devereux, Andrew Kellett, and Orla Howe. "Cu(ii) phenanthroline–phenazine complexes dysregulate mitochondrial function and stimulate apoptosis." Metallomics 12, no. 1 (2020): 65–78. http://dx.doi.org/10.1039/c9mt00187e.
Full textDissertations / Theses on the topic "DPPZ"
Derrat, Hanan S. "Organic and metal organic cationic DNA intercalators based on DPPZ analogues." Thesis, University of Sheffield, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574605.
Full textDyer, Joanne. "Designing infrared probes of DNA based on rhenium tricarbonyl DPPZ complexes." Thesis, University of Nottingham, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289455.
Full textMadureira, João Paulo Lopes. "Complexos de ruténio com ligandos politioéteres e/ou polipiridílicos : síntese, caracterização estrutural e interacção com o ADN." Doctoral thesis, Universidade de Aveiro, 2005. http://hdl.handle.net/10773/15264.
Full textNesta tese são apresentados perto de quatro dezenas de novos complexos de ruténio(II), em cuja esfera de coordenação estão simultaneamente presentes um politioéter macrocíclico e um ligando polipiridílico. Os complexos sintetizados possuem as fórmulas genéricas [Ru([9]anoS3)(N-N)Cl]+ ou [Ru([12]anoS4)(N-N)]2+, em que [9]anoS3 é 1,4,7-tritiociclononano, [12]anoS4 é 1,4,7,10-tetratiociclododecano e N-N representa um ligando polipiridílico. Estes últimos foram seleccionados entre ligandos disponíveis comercialmente, de síntese conhecida da literatura, ou ainda entre novos derivados de dipirido[3,2-a:2’,3’-c]fenazina (ddpz). Os novos derivados de dppz foram concebidos com base numa das seguintes alternativas: i) expansão directa da superfície aromática; ii) acoplamento formal de pteridinas a uma unidade fenantrolina e iii) formação de ligações covalentes C-C entre dppz e grupos poliaromáticos. Foram também sintetizados duas dezenas de complexos de ruténio(II) em cuja esfera de coordenação se incluem macrociclos do tipo politioéter ou poliamina e variados ligandos monodentados, tais como halogenetos, dmso, MeCN, ou ligandos de azoto monocoordenados, como imidazol, indazol ou pirazol. Os diversos ligandos e complexos foram caracterizados por numerosas técnicas: infravermelho, Raman, RMN, absorção molecular, luminescência, espectrometria de massa (ES, FAB, EI), voltametria linear ou cíclica, espectroelectroquímica de UV/Vis/NIR ou de EPR, condutimetria, difracção de raios-X, microscopia electrónica de varrimento, ou análises elementares, para além de terem sido realizados cálculos teóricos auxiliares. Foi também estudado o comportamento em meio aquoso de alguns dos complexos sintetizados, assim como foi testada a capacidade de alguns dos complexos com ligandos polipiridílicos em interactuarem com o ADN. Para isso foram realizados ensaios de denaturação térmica, titulações de UV/Vis e estudos de luminescência em estado estacionário.
Nearly forty new ruthenium(II) complexes have been synthesised, with both polythioether macrocycles and polypyridyls present on the coordination sphere. The synthesised complexes have the general formula [Ru([9]aneS3)(N-N)Cl]+ or [Ru([12]aneS4)(N-N)]2+, where [9]aneS3, [12]aneS4, and N-N represents 1,4,7-trithiacyclononane, 1,4,7,10-tetrathiacyclododecane, and a polypyridyl ligand, respectively. N-N ligands have been selected from commercially available products, literature known compounds, and dipyridophenazine (dppz) new ligands, presented on this thesis. The new dipyridophenazine derivatives were designed with three different strategies: i) direct aromatic surface expansion; ii) pteridine formal coupling to a phenanthroline unit; and iii) C-C covalent bond formation between dppz and polyaromatic groups. Twenty ruthenium(II) complexes with a coordination sphere composed of a polythioether or polyamine macrocycle and several monodentate ligands (ex: halogens, dmso, MeCN and nitrogen heterocyles, as imidazole, indazole or pyrazole) have also been prepared. The ligands and complexes have been characterised by several techniques, namely: infrared, Raman, NMR, UV/Vis, luminescence, mass spectrometry (EI, ES, FAB), cyclic or linear voltammetry, UV/Vis/NIR and EPR spectro-electrochemistry, conductivity, X-ray diffraction, SEM, micro-analysis and theoretical calculations. Some of the complexes have been studied on aqueous or organic solutions in order to evaluate their reactivity and determine their formula on that media. Several polythioether-polypyridyl ruthenium complexes have been tested in order to evaluate theirs DNA interaction capability. The studies were conducted by UV/Vis titration, steady-state luminescence and thermal denaturation.
Ergun, Seza. "Structural And Functional Investigation Of The Interaction Of Agomelatine With Model Membranes." Master's thesis, METU, 2012. http://etd.lib.metu.edu.tr/upload/12614997/index.pdf.
Full textSouza et al., 2009). These results may indicate that agomelatine is partially buried in the hydrocarbon core of the bilayer, interacting primarily with the C2-C8 methylene region of the hydrocarbon chains. All these results highlight the fact that agomelatine interacts around the head group in such a manner that it destabilizes the membrane architecture to a large extent.
Cafe, Peter F. "Towards reliable contacts of molecular electronic devices to gold electrodes." Thesis, The University of Sydney, 2008. http://hdl.handle.net/2123/3870.
Full textCafe, Peter F. "Towards reliable contacts of molecular electronic devices to gold electrodes." University of Sydney, 2008. http://hdl.handle.net/2123/3870.
Full textSYNOPSIS OF THIS THESIS The aim of this thesis is to more fully understand and explain the binding mechanism of organic molecules to the Au(111) surface and to explore the conduction of such molecules. It consists of five discreet chapters connected to each other by the central theme of “The Single Molecule Device: Conductance and Binding”. There is a deliberate concentration on azine linkers, in particular those with a 1,10-phenanthroline-type bidentate configuration at each end. This linker unit is called a “molecular alligator clip” and is investigated as an alternative to the thiol linker unit more commonly used. Chapter 1 places the work in the broad context of Molecular Electronics and establishes the need for this research. In Chapter 2 the multiple break-junction technique (using a Scanning Tunnelling Microscope or similar device) was used to investigate the conductance of various molecules with azine linkers. A major finding of those experiments is that solvent interactions are a key factor in the conductance signal of particular molecules. Some solvents interfere with the molecule’s interaction with and attachment to the gold electrodes. One indicator of the degree of this interference is the extent of the enhancement or otherwise of the gold quantized conduction peak at 1.0 G0. Below 1.0 G0 a broad range for which the molecule enhances conduction indicates that solvent interactions contribute to a variety of structures which could bridge the electrodes, each with their own specific conductance value. The use of histograms with a Log10 scale for conductance proved useful for observing broad range features. vi Another factor which affects the conductance signal is the geometric alignment of the molecule (or the molecule-solvent structure) to the gold electrode, and the molecular alignment is explored in Chapters 3 for 1,10-phenanthroline (PHEN) and Chapter 4 for thiols. In Chapter 3 STM images, electrochemistry, and Density Functional Theory (DFT) are used to determine 1,10-phenanthroline (PHEN) structures on the Au(111) surface. It is established that PHEN binds in two modes, a physisorbed state and a chemisorbed state. The chemisorbed state is more stable and involves the extraction of gold from the bulk to form adatom-PHEN entities which are highly mobile on the gold surface. Surface pitting is viewed as evidential of the formation of the adatom-molecule entities. DFT calculations in this chapter were performed by Ante Bilic and Jeffery Reimers. The conclusions to Chapter 3 implicate the adatom as a binding mode of thiols to gold and this is explored in Chapter 4 by a timely review of nascent research in the field. The adatom motif is identified as the major binding structure for thiol terminated molecules to gold, using the explanation of surface pitting in Chapter 3 as major evidence and substantiated by emergent literature, both experimental and theoretical. Furthermore, the effect of this binding mode on conductance is explored and structures relevant to the break-junction experiment of Chapter 2 are identified and their conductance values compared. Finally, as a result of researching extensive reports of molecular conductance values, and having attempted the same, a simple method for predicting the conductance of single molecules is presented based upon the tunneling conductance formula.
Zbořilová, Hana. "Studium membránových vlastností liposomálních systémů pomocí fluorescenční spektroskopie." Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2021. http://www.nusl.cz/ntk/nusl-449373.
Full textChi, Danny T., and Nien-Lou Li. "DPPM Optical Communications and Reed-Solomon Codes." International Foundation for Telemetering, 1992. http://hdl.handle.net/10150/608918.
Full textPulse position modulation (PPM) has many attractions for optical communication over deep space and for intersatellite communications. This paper describes a variate of PPM, known as differential pulse position modulation (DPPM) which can double the data throughput relative to PPM. We begin this paper with a survey of various laser sources and laser modulation techniques used in modem space optical communications. We then discuss the advantages of the combination of DPPM and Reed-Solomon (RS) codes.
López-Amaya, Clara Inés. "Interaction of Candida rugosa lipase with DPPC liposomes." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/nq27441.pdf.
Full textKell, Henny. "Wechselwirkung des Lipoheptapeptides Surfactin mit Lipiddoppelschichten aus DMPC und DPPC." [S.l.] : [s.n.], 2006. http://opus.kobv.de/tuberlin/volltexte/2007/1463.
Full textBooks on the topic "DPPZ"
Pelevin, Viktor Olegovich. DPP (NN). Moskva: ĖKSMO, 2010.
Find full textPrinting, London College of. Ladybird: DPPS project, 1986. London: LCP, 1986.
Find full textPrinting, London College of. Virago: DPPS poblishing project 1986. London: LCP, 1986.
Find full textPrinting, London College of. Souvenir Press: DPPS publishing project 1986. London: LCP, 1986.
Find full textPrinting, London College of. Virago Press: DPPS publishing project 1986. London: LCP, 1986.
Find full textPrinting, London College of. Academic Press: DPPS publishing project 1986. London: LCP, 1986.
Find full textPrinting, London College of. Michael Joseph: DPPS publishing project 1986. London: LCP, 1986.
Find full textPrinting, London College of. Michael Joseph: DPPS publishing project 1986. London: LCP, 1986.
Find full textPrinting, London College of. Pergamon Press: DPPS publishing project 1986. London: LCP, 1986.
Find full textPrinting, London College of. B & H: DPPS publishing project 1986. London: LCP, 1986.
Find full textBook chapters on the topic "DPPZ"
Zhang, Hui Emma, and Mark D. Gorrell. "DPP9." In Encyclopedia of Signaling Molecules, 1418–22. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101597.
Full textGorrell, Mark D., and Hui Emma Zhang. "DPP8." In Encyclopedia of Signaling Molecules, 1414–17. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101654.
Full textZhang, Hui Emma, and Mark D. Gorrell. "DPP9." In Encyclopedia of Signaling Molecules, 1–5. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4614-6438-9_101597-1.
Full textGorrell, Mark D., and Hui Emma Zhang. "DPP8." In Encyclopedia of Signaling Molecules, 1–5. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4614-6438-9_101654-1.
Full textGooch, Jan W. "DPP." In Encyclopedic Dictionary of Polymers, 242. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3983.
Full textPerron, R. "The Dipalmitoylphosphatidylcholine (DPPC) — Water System." In Properties of Water in Foods, 37–47. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5103-7_3.
Full textPham, Ngoc-Yen T., Christos Argyropoulos, and Nhan Dinh. "Dipeptidyl Peptidase-4 (DPP4) Inhibitors." In Diabetes and Kidney Disease, 583–99. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-86020-2_27.
Full textMundici, Daniele. "Classi fulminee per DPP." In UNITEXT, 27–31. Milano: Springer Milan, 2011. http://dx.doi.org/10.1007/978-88-470-1884-6_5.
Full textMundici, Daniele. "Fast Classes for DPP." In UNITEXT, 27–30. Milano: Springer Milan, 2012. http://dx.doi.org/10.1007/978-88-470-2361-1_5.
Full textChiou, C. L. "Institutionalizing the Tangwai: The DPP." In Democratizing Oriental Despotism, 90–104. London: Palgrave Macmillan UK, 1995. http://dx.doi.org/10.1057/9780230389687_6.
Full textConference papers on the topic "DPPZ"
Zheng, Jiping, and Ganfeng Lu. "k-SDPP: Fixed-Size Video Summarization via Sequential Determinantal Point Processes." In Twenty-Ninth International Joint Conference on Artificial Intelligence and Seventeenth Pacific Rim International Conference on Artificial Intelligence {IJCAI-PRICAI-20}. California: International Joint Conferences on Artificial Intelligence Organization, 2020. http://dx.doi.org/10.24963/ijcai.2020/108.
Full textImranpasha, Bharat Kumar, and S. L. N. Rao. "Interaction of β – N – oxalyl – L – α, β – diaminopropionic acid (ODAP) with Langmuir monolayers of DPPC, DPPG and cholesterol." In DAE SOLID STATE PHYSICS SYMPOSIUM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0016881.
Full textYu, Xiaochun, Yen-Tzu Lin, Wing-Chiu Tam, Osei Poku, and R. D. Blanton. "Controlling DPPM through Volume Diagnosis." In 2009 27th IEEE VLSI Test Symposium (VTS). IEEE, 2009. http://dx.doi.org/10.1109/vts.2009.49.
Full textKalinowski, Marcos, and Guilherme Horta Travassos. "Uma Abordagem Probabilística para Análise Causal de Defeitos de Software." In Simpósio Brasileiro de Qualidade de Software. Sociedade Brasileira de Computação - SBC, 2012. http://dx.doi.org/10.5753/sbqs.2012.15335.
Full textMahmoud, Yousef. "Toward Reconfigurable DPP Converters." In 2022 13th International Renewable Energy Congress (IREC). IEEE, 2022. http://dx.doi.org/10.1109/irec56325.2022.10001949.
Full textYin, Jun, and Yong Huang. "Investigation of Process-Induced Cell Membrane Stability Using Molecular Dynamics Simulation." In ASME 2009 International Manufacturing Science and Engineering Conference. ASMEDC, 2009. http://dx.doi.org/10.1115/msec2009-84374.
Full textAruk, Natasha, Cathrine V. Jansson-Boyd, and Nathan Crilly. "What users know about the design process." In DPPI '11: Designing Pleasurable Products and Interfaces. New York, NY, USA: ACM, 2011. http://dx.doi.org/10.1145/2347504.2543533.
Full textWang, Jingyuan, Zhiyong Xu, and Weisheng Hu. "Improved DPPM modulation for optical wireless communications." In Asia-Pacific Optical and Wireless Communications, edited by Cedric F. Lam, Chongcheng Fan, Norbert Hanik, and Kimio Oguchi. SPIE, 2004. http://dx.doi.org/10.1117/12.522349.
Full textIles, Harrison, and Yousef Mahmoud. "DPP Converters with Reduced Sensors." In IECON 2022 – 48th Annual Conference of the IEEE Industrial Electronics Society. IEEE, 2022. http://dx.doi.org/10.1109/iecon49645.2022.9969018.
Full textMohd, Hur Munawar Kabir, Ainee Fatimah Ahmad, Shahidan Radiman, Faizal Mohamed, Nur Ratasha Alia Md Rosli, Muhammad Taqiyuddin Mawardi Ayob, and Irman Abdul Rahman. "Interaction between silicon dioxide and dipalmitoylphosphatidylcholine (DPPC) vesicles." In THE 2014 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2014 Postgraduate Colloquium. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4895172.
Full textReports on the topic "DPPZ"
Miller, Paul Matthew. Plasma Sciences Exposition at APS-DPP. Office of Scientific and Technical Information (OSTI), September 2017. http://dx.doi.org/10.2172/1391881.
Full textSmine, Georges E., and Vason P. Srini. Area Efficient Cells for LagerIV's DPP Library. Fort Belvoir, VA: Defense Technical Information Center, August 1989. http://dx.doi.org/10.21236/ada632157.
Full textNogradi Jr, Paul, Oscar Martinez, Abiodun Adeniyi, and Blake Van Hoy. Test Report for DPP-1 Regulatory Compliance Testing. Office of Scientific and Technical Information (OSTI), April 2022. http://dx.doi.org/10.2172/1869080.
Full textDEPARTMENT OF DEFENSE WASHINGTON DC. Defense Planning and Programming Category (DPPC) Definitions and Program Element Code Assignments. Fort Belvoir, VA: Defense Technical Information Center, January 1993. http://dx.doi.org/10.21236/ada259820.
Full textFriedman, Alex. Comments on initiatives submitted for APS-DPP-CPP meeting, Madison WI, July 22-26, 2019. Office of Scientific and Technical Information (OSTI), July 2019. http://dx.doi.org/10.2172/1544478.
Full textHutzler, Patricia I. Defense Planning and Programming Categories: A Special Tool for Special Needs. Volume 3. Appendix E. Proposed Expanded DPPC Structure. Fort Belvoir, VA: Defense Technical Information Center, April 1990. http://dx.doi.org/10.21236/ada230860.
Full textShiyu, LIU, DENG Huan, and CHEN Qiu. Effect of DPP-4 inhibitor on Cognitive Dysfunction in Diabetes :A systematic review and meta-analysis protocol. INPLASY - International Platform of Registered Systematic Review Protocols, April 2020. http://dx.doi.org/10.37766/inplasy2020.4.0185.
Full textHegland, Troels Jacob, and Søren Qvist Eliasen. Rekruttering til og fastholdelse i dansk fiskeri - med særlig fokus på Fiskeriskolens uddannelse. Centre for Blue Governance, Aalborg University, 2022. http://dx.doi.org/10.54337/aau460210943.
Full textWilke, et al. Vergleich der Gesundheitskosten von Typ-2 Diabetikern bei der Anwendung von Empagliflozin, DPP-4-Hemmern und GLP-1-Agonisten. Monitor Versorgungsforschung, 2022. http://dx.doi.org/10.24945/mvf.06.22.1866-0533.2448.
Full textYang, Fan, Quanlin Zhao, Youzi Dong, Baohua Li, and Bobiao Ning. Pancreatic safety of DPP-4 Inhibitors in type 2 diabetes millitus A protocol for systematic review and network meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, March 2022. http://dx.doi.org/10.37766/inplasy2022.3.0014.
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