Relevant bibliographies by topics / Photoactivated

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

Academic literature on the topic 'Photoactivated'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Photoactivated"

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Wei, Yaoming, Yinfa Yan, Dehua Pei, and Bing Gong. "A photoactivated prodrug." Bioorganic & Medicinal Chemistry Letters 8, no. 18 (September 1998): 2419–22. http://dx.doi.org/10.1016/s0960-894x(98)00437-5.

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Oshige, Eric S., and Paul B. Jones. "Photoactivated artificial metalloesterases." Journal of Photochemistry and Photobiology A: Chemistry 192, no. 2-3 (December 2007): 142–51. http://dx.doi.org/10.1016/j.jphotochem.2007.05.014.

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Faci, S., C. Tripon-Canseliet, A. Benlarbi-Delaï, G. Alquié, S. Formont, and J. Chazelas. "Photoactivated microwave oscillator." Electronics Letters 44, no. 15 (2008): 915. http://dx.doi.org/10.1049/el:20080990.

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Deviyanti, Sinta. "POTENSI ANTIMIKROBA PHOTO ACTIVATED DISINFECTION TERHADAP Enterococcus faecalis PADA PERAWATAN SALURAN AKAR GIGI." Cakradonya Dental Journal 11, no. 1 (May 9, 2019): 13–22. http://dx.doi.org/10.24815/cdj.v11i1.13623.

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Disinfeksi sistem saluran akar gigi sangat penting dalam perawatan saluran akar gigi. Instrumenmekanik dan agen desinfeksi atau larutan irigasi seperti NaOCL tidak efektif mengurangi jumlahbakteri di dalam saluran akar yang terinfeksi karena anatomi akar gigi yang kompleks. Kegagalanperawatan endodontik sering meninggalkan bakteri di sistem saluran akar gigi. Enterococcus faecalismerupakan salah satu mikroorganisme terpenting yang bertanggungjawab pada kegagalan perawatansaluran akar gigi. Bakteri ini kebal terhadap agen antimikroba dan mampu berkoloni membentukbiofilm di saluran akar gigi. Saat ini perangkat baru seperti photoactivated disinfection telah dicobauntuk disinfeksi saluran akar gigi. Photoactivated disinfection merupakan strategi antimikroba yangmenggunakan energi laser berkekuatan rendah untuk mengaktivasi suatu pewarna tidak toksik yangdiaktivasi sinar (photosensitizer). Energi yang dipindahkan dari photosensitizer teraktivasi ke oksigenyang tersedia, akan membentuk oksigen singlet sebagai spesies oksigen toksik. Spesies oksigen yangsangat reaktif secara kimia ini dapat merusak membran dan DNA bakteri patogen. Beberapapenelitian menunjukkan bahwa photoactivated disinfection dapat efektif mengurangi E.faecalis didalam saluran akar selama prosedur antimikroba bila digunakan bersama dengan prosedur disinfeksikonvensional untuk sterilisasi saluran akar. Photoactivated disinfection merupakan pendukung untukprotokol standar disinfeksi saluran akar gigi.Kata kunci: photoactivated disinfection, Enterococcus faecalis, perawatan saluran akar.
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Nagpal, Rajni, Shipra Singh, Payal Singh, Tushar Sharnam, and Naveen Manuja. "Photoactivated Disinfection in Endodontics." Indian Journal of Contemporary Dentistry 3, no. 1 (2015): 29. http://dx.doi.org/10.5958/2320-5962.2015.00007.8.

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de Vekki, D. A. "Hydrosilylation on photoactivated catalysts." Russian Journal of General Chemistry 81, no. 7 (July 2011): 1480–92. http://dx.doi.org/10.1134/s1070363211070139.

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Wright, Taylor, Tanja Tomkovic, Savvas G. Hatzikiriakos, and Michael O. Wolf. "Photoactivated Healable Vitrimeric Copolymers." Macromolecules 52, no. 1 (December 17, 2018): 36–42. http://dx.doi.org/10.1021/acs.macromol.8b01898.

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Agostini, Alessandro, Félix Sancenón, Ramón Martínez-Máñez, María D. Marcos, Juan Soto, and Pedro Amorós. "A Photoactivated Molecular Gate." Chemistry - A European Journal 18, no. 39 (August 21, 2012): 12218–21. http://dx.doi.org/10.1002/chem.201201127.

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Bonnet, Sylvestre. "Why develop photoactivated chemotherapy?" Dalton Transactions 47, no. 31 (2018): 10330–43. http://dx.doi.org/10.1039/c8dt01585f.

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Falk, Benjamin, Michael R. Zonca, and James V. Crivello. "Photoactivated Cationic Frontal Polymerization." Macromolecular Symposia 226, no. 1 (May 2005): 97–108. http://dx.doi.org/10.1002/masy.200550810.

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Dissertations / Theses on the topic "Photoactivated"

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Zibaseresht, Ramin. "Approaches to Photoactivated Cytotoxins." Thesis, University of Canterbury. Chemistry, 2006. http://hdl.handle.net/10092/1284.

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The synthesis and coordination chemistry of eleven bridging ligands, eight of which are new compounds, are described. These ligands are all based on the tridentate terpyridyl system. The other metal ion binding sites of these ligands contain pyridine/bipyridine/pyrazole rings or amine/azamacrocycles domains. In these ligands, the two metal ion binding sites are differentiated by the number of atoms in each site, the configuration of the binding site or the types of donor atom that are present. This binding site differentiation allows to use the different coordination properties of the binding sites to control the regiochemistry of the complexation, ensuring that the correct metal ion is incorporated at the correct binding site in the ligand. Many of the complexes synthesised are mono-ruthenium(II) complexes where Ru(II) ions are situated in the terpyridyl sites of the ligands. These include heteroleptic Ru(II) complexes of the type [Ru(ttp)(L)]2+, where ttp is 4'-(p-tolyl)-2,2':6',2ʺ- terpyridine, and L is the bridging ligand. Reactions of the Ru(II) complexes with a range of metal ions including Co(III) ion have been investigated. The Ru(II) complexes can be classified into three main categories depending on the type of ligands that have been employed: (1) Ru(II) complexes which can react with Co(III) ions to form heterodinuclear Ru(II)-Co(III) complexes; (2) Ru(II) complexes which react only with Ag(I) ions and no other common metal ions that we have tried; (3) Ru(II) complexes with no detectable ability to coordinate other common metal ions. Following standard cobalt chemistry, some heterodinuclear Ru(II)-Co(III) complexes of the type [(ttp)Ru(cymt)Co(X)2]3+, where X = NO2 -, Cl-, and OH-, have been successfully prepared from the corresponding Ru(II) complexes. In these heterodinuclear complexes, anions such as NO2 -, Cl-, or OH- can be readily attached to the Co(III) ions. However, attachment of a neutral species such as en ligands to the Co(III) ions in the complexes proved to be more difficult. Reactions of heterodinuclear Ru(II)-Co(III) complexes with en ligands result in removal of the cobalt ions from the complexes. This is may be a result of a significant difference in the overall charges between the complexes with anionic and the complexes with neutral ligands (3+ vs 5+). Higher overall charge of the complexes when protonable ligands such as monodentate en are present, may destabilize the complexes even more. A combination of NMR spectroscopy, ESI-MS, UV-vis spectroscopy, elemental analysis, and X-ray crystallography has been used to characterise the ligands and their complexes. The crystal structures of one new ligand and sixteen complexes are described.
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Gallagher, Theresa Bernadette. "Application of photoactivated disinfection." Thesis, University of Brighton, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.511582.

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Atherton, Jonathan Charles Christian. "Novel photoactivated chiral auxiliaries." Thesis, University of Newcastle Upon Tyne, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273482.

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Sitterle, Valerie B. "Photoactivated Fixation of Cartilage Tissue." Diss., Georgia Institute of Technology, 2004. http://hdl.handle.net/1853/7609.

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Cartilage repair and/or replacement is necessary for many orthopaedic conditions including fissures from blunt trauma, autograft or allograft transplantation, and replacement of focal defects with biological or synthetic constructs. In cartilage repair, initial integration between the host tissue and repair site is desirable to allow for nutrient transport, molecular deposition to enhance fixation, and eventual stress transmission across the interface. It has been postulated that effective transport and crosslinking of newly synthesized collagen molecules across a repair site may be vital to the process of integrative repair, and recent experiments have correlated collagen deposition with the strength of such repair. Other investigations have shown that enzymatic degradation of the cartilage surface may enhance integrative repair and can increase bond strength of an adhesive to cartilage. This study explored a novel approach involving photochemical bonding of cartilage tissue samples through collagen crosslinking as a means to achieve rapid and effective initial fixation, with the goal of enhancing biological integration. Photosensitized collagen gels were first analyzed via FTIR to determine the crosslinking effects with respect to collagen type and photochemical mechanism. Using the photogellation FTIR results as a parametric guide, in vitro mechanical testing of photochemically bonded meniscal fibrocartilage and hyaline articular cartilage tissues was performed using a modified single-lap shear test. Finally, the cellular viability and bond stability of a photochemically bonded cartilage interface was evaluated over seven days of in vitro culture, where the bond strength was assessed by pushout of cores from annular defects. Results of this study have demonstrated the potential of combining enzymatic surface modification with photodynamic techniques to directly bond cartilage tissues for initial fixation.
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Woods, Stephen John. "Simulation of photoactivated bipolar devices." Thesis, University of East Anglia, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267275.

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Gao, Junping. "Pyridinium Bisretinoids: Synthesis and Photoactivated Cytotoxicity." BYU ScholarsArchive, 2007. https://scholarsarchive.byu.edu/etd/2384.

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This thesis discusses pyridinium bisretinoid compounds (PBRs), which were prepared for two purposes: 1) to use them as standards for detection of novel fluorophores in human RPE cells, which may be involved in age-related macular degeneration (AMD), and 2) to use them in the development of a targeted and triggered drug delivery system for cancer therapy. We prepared a selection of PBRs using a one-pot biomimetic method; synthesis, mechanisms for formation, and characterization of these compounds is described. We also explored the photoreactivity of three novel PBR compounds and found that these PBRs form oxidation products under blue-light irradiation. The photoinduced cytotoxity of A2P and A2EE was examined in HL-60 cells. Results from this work suggest that the PBRs presented have the potential to be involved in AMD and to be developed into a targeted and triggered drug delivery system for cancer therapy.
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Singh, Tanya N. "Ru(II) complexes as photoactivated cisplatin analogs." Columbus, Ohio : Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1150391177.

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Allen, Victoria Louise. "Photoactivated lipids as modulators of membrane protein folding." Thesis, University of Bristol, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528101.

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Tai, Hui-Chung. "Computer-aided drug design of photoactivated platinum anticancer complexes." Thesis, University of Warwick, 2011. http://wrap.warwick.ac.uk/55656/.

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Platinum(IV) complexes are usually inert and stable compounds which can be photoactive pro-drugs to produce Pt(II) species with promising anti-cancer activity. Studies of the photochemistry of Pt(IV) complexes by time-dependent density functional theory (TDDFT) and spectroscopic methods show close agreement. Broad exploration of cis/trans geometries, trans influences, the nature of the OR− and (pseudo)halogen ligands, electron-withdrawing/donating/ delocalizing substituents on the N-ligands, and intramolecular H-bonds shows that (1) the design of platinum(IV) complexes with intense bands shifted towards longer wavelengths (~330 nm) can be achieved by introducing intramolecular Hbonds involving the OH ligands and 2-hydroxyquinoline or by iodido ligands, (2) mesomeric electron-withdrawing substituents on pyridine result in low-energy absorption with significant intensity in the visible region, and (3) the distinct makeup of the molecular orbitals in electronic transitions for cis/trans-{Pt(N3)2} isomers result in different photoproducts. In general, the comparison of the optimised geometries shows that Pt(IV) complexes with longer Pt−L bonds are more likely to undergo photoreduction with longer-wavelength light. Complex trans, trans, trans-[Pt(N3)2(OH)2(NH3)(4-nitropyridine)] was first synthesised. The experimental UV-Vis spectrum in aqueous solution correlates well with the intense band in the computed spectrum whereas the overlay in the low-energy absorption region can be improved by a solvent model. This combined computational and experimental study shows that TDDFT can be a design tool to tune the coordination environment for optimizing photoactive Pt(IV) compounds as anticancer agents without immediate need for synthesis. Additionally, molecular modeling is used to study DNA distortions induced by binding metal-containing fragments derived from cisdiamminodichloroplatinum( II) (cisplatin) and a new class of photoactive platinum anticancer drugs. Ligand field molecular mechanics (LFMM) parameters for Pt– guanine interactions are derived and validated against a range of experimental structures from the Cambridge Structural Database, published quantum mechanics/molecular mechanics (QM/MM) structures of model Pt-DNA systems and additional DFT studies. LFMM gives a good description of the local Ptguanine coordination at a fraction of the computational cost of QM/MM methods. The force field is then used to develop protocols for ligand field molecular dynamics (LFMD) simulations using experimentally characterised bifunctional DNA adducts involving both an intra- and an interstrand crosslink of cisplatin as a prelude to studying the interaction of trans-{Pt(py)2}2+ (P, py = pyridine), the major photoproduct of the novel platinum(IV) complex trans,trans,trans- [Pt(N3)2(OH)2(py)2] (17), with the DNA duplex dodecamer, d(C1C2T3C4T5C6G7T8C9T10C11C12)• d(G13G14A15G16A17C18G19A20G21A22G23G24). Based on the observed formation of a trans species when 17 is photoreduced in the presence of 5’-guanosine monophosphate plus the major-groove binding mode of the monofunctional complex cis-{Pt(NH3)2(py)}2+, P is proposed to coordinate to G7 and G19. This P-DNA adduct has a widened minor groove at one end of the platinated site and deepened minor groove at the opposite end, and exhibits a global bend of ~67° and an unwinding of ~20°. Brabec et al. subsequently demonstrated experimentally that such interstrand GG crosslinks can form as a result of the photoactivation of 17 in the presence of DNA. Such cross-links offer possibilities for specific protein–DNA interactions and suggest possible mechanisms to explain the high potency of this photoactivated complex.
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Abtahi, Seyyed Mohammad Hossein. "Synthesis and characterization of metallic nanoparticles with photoactivated surface chemistries." Thesis, Virginia Tech, 2013. http://hdl.handle.net/10919/78081.

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During recent decades metallic nanoparticles have been found very interesting due to their unique characteristics which make them suitable for different applications. In this research, for the very first time, we tried to perform selective surface photo activation chemistry on the targeted facets of nanoparticles while they are in suspension. This technique enabled us to form desired assemblies of nanoparticles. We focused on elongated shaped gold nanorod due to its unique surface plasmon resonance and probable biomedical applications. In this research we formed a dumbbell shape assembly of nanoparticles in suspension. A probable application for these assemblies can be in vivo imaging. Initially, we reproduced gold nanorods using existing techniques in prior papers and optimized them according to our research needs. A low rpm centrifugal separation technique was developed to efficiently separate synthesized gold nanorods from other shapes. Several characterization techniques were utilized to characterize nanoparticles at each step including UV-absorbance, zeta potential, and dynamic light scattering. Different generations of oligomers were synthesized to be used as gold nanorods coating, and each coating was tested and characterized using appropriate techniques. Our two-step coating replacement method using one of these photocleavable oligomers enabled us to achieve, for the very first time, selective UV photo activation of gold nanorod tips. The photo activated tips were then exposed to oppositely charged gold nanospheres to form dumbbell shape assemblies of gold nanorods and nanospheres. Furthermore, dumbbell shape assembly of nanoparticles was investigated and characterized.
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Books on the topic "Photoactivated"

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Poulin, Peter Roland. Design of a photoactivated electron gun for the ultrafast: Study of chemical reaction dynamics by electron diffraction. Dept of Chemistry, U of Toronto, 1998.

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Book chapters on the topic "Photoactivated"

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Olivi, Giovanni, and Maarten Meire. "Photoactivated Disinfection." In Lasers in Endodontics, 145–55. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-19327-4_7.

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Biteen, Julie S. "Photoactivated Localization Microscopy (PALM)." In Encyclopedia of Biophysics, 1860–62. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_481.

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Downum, Kelsey R. "Photoactivated Biocides from Higher Plants." In Natural Resistance of Plants to Pests, 197–205. Washington, DC: American Chemical Society, 1986. http://dx.doi.org/10.1021/bk-1986-0296.ch016.

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Heitz, James R. "Pesticidal Applications of Photoactivated Molecules." In ACS Symposium Series, 1–16. Washington, DC: American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0616.ch001.

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Hofmann, Klaus Peter. "Signalling States of Photoactivated Rhodopsin." In Novartis Foundation Symposium 224 - Rhodopsins and Phototransduction, 158–90. Chichester, UK: John Wiley & Sons, Ltd., 2007. http://dx.doi.org/10.1002/9780470515693.ch10.

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Achurra, Paulina, Seamus Holden, Thomas Pengo, and Suliana Manley. "Photoactivated Localization Microscopy for Cellular Imaging." In Neuromethods, 87–111. Totowa, NJ: Humana Press, 2014. http://dx.doi.org/10.1007/978-1-62703-983-3_5.

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Heitz, James R. "Development of Photoactivated Compounds as Pesticides." In ACS Symposium Series, 1–21. Washington, DC: American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0339.ch001.

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Pimprikar, G. D. "Potential Markets for the Photoactivated Pesticides." In ACS Symposium Series, 127–34. Washington, DC: American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0616.ch010.

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Krieger, Anja, Sebastian Heimann, and Giles Johnson. "Photoprotection of Non-Photoactivated Photosystem II." In Photosynthesis: from Light to Biosphere, 723–26. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_171.

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de Aguirre, Adiran, Victor M. Fernandez-Alvarez, and Feliu Maseras. "Computational Modeling of Selected Photoactivated Processes." In New Directions in the Modeling of Organometallic Reactions, 131–52. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/3418_2020_50.

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Conference papers on the topic "Photoactivated"

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Patterson, George, Eric Betzig, Jennifer Lippincott-Schwartz, and Harald Hess. "DEVELOPING PHOTOACTIVATED LOCALIZATION MICROSCOPY (PALM)." In 2007 4th IEEE International Symposium on Biomedical Imaging: From Nano to Macro. IEEE, 2007. http://dx.doi.org/10.1109/isbi.2007.357008.

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Marlor, Guy A., Robin Y. Zhang, and Robert E. McMurray, Jr. "Next generation photoactivated spatial light modulators." In IS&T/SPIE's Symposium on Electronic Imaging: Science & Technology, edited by Ming H. Wu. SPIE, 1995. http://dx.doi.org/10.1117/12.205894.

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Marlor, Guy A. "Next generation photoactivated light valve projection systems." In IS&T/SPIE's Symposium on Electronic Imaging: Science & Technology, edited by Ming H. Wu. SPIE, 1995. http://dx.doi.org/10.1117/12.205887.

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Bonnet, Sylvestre. "Photoactivated chemotherapy in hypoxic cancer cells (Conference Presentation)." In 17th International Photodynamic Association World Congress, edited by Tayyaba Hasan. SPIE, 2019. http://dx.doi.org/10.1117/12.2528324.

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Amaro, Francisco, Miguel Gómez-Mendoza, Ana B. Descalzo, Luis Rivas, and Guillermo Orellana. "Self-sterilizing photoactivated catheters to prevent nosocomial infections." In 17th International Photodynamic Association World Congress, edited by Tayyaba Hasan. SPIE, 2019. http://dx.doi.org/10.1117/12.2525896.

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Cheng, Pan, and Hao He. "Photoactivated Endogenous Molecules to Stimulate Cellular Ca2+ Increase." In Asia Communications and Photonics Conference. Washington, D.C.: OSA, 2016. http://dx.doi.org/10.1364/acpc.2016.as4a.2.

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Mobarry, Clark, and Aaron Lewis. "Implementations Of Neural Networks Using Photoactivated Conducting Biological Materials." In 1986 Int'l Computing Conference, edited by Asher A. Friesem, Emanuel Marom, and Joseph Shamir. SPIE, 1987. http://dx.doi.org/10.1117/12.936995.

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Sitterle, Valerie B., and David W. Roberts. "Photoactivated methods for enabling cartilage-to-cartilage tissue fixation." In Biomedical Optics 2003, edited by Lawrence S. Bass, Nikiforos Kollias, Reza S. Malek, Abraham Katzir, Udayan K. Shah, Brian J. F. Wong, Eugene A. Trowers, et al. SPIE, 2003. http://dx.doi.org/10.1117/12.476397.

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Yee Hoh, Tjun. "Correction of multiple-blinking artefacts in photoactivated localisation microscopy." In Microscience Microscopy Congress 2021 incorporating EMAG 2021. Royal Microscopical Society, 2021. http://dx.doi.org/10.22443/rms.mmc2021.162.

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Lee, Seunghyun, Hyemin Kim, Seungjun Shin, Junsang Doh, and Chulhong Kim. "Super-resolution atomic force photoactivated microscopy of biological samples (Conference Presentation)." In Photons Plus Ultrasound: Imaging and Sensing 2017, edited by Alexander A. Oraevsky and Lihong V. Wang. SPIE, 2017. http://dx.doi.org/10.1117/12.2251288.

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Reports on the topic "Photoactivated"

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Kochevar, Irene E. Sealing Penetrating Eye Injuries With Photoactivated Bonding. Fort Belvoir, VA: Defense Technical Information Center, September 2010. http://dx.doi.org/10.21236/ada540409.

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Kochevar, Irene E. Sealing Penetrating Eye Injuries with Photoactivated Bonding. Fort Belvoir, VA: Defense Technical Information Center, September 2012. http://dx.doi.org/10.21236/ada568974.

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Kochevar, Irene E. Sealing Penetrating Eye Injuries With Photoactivated Bonding. Fort Belvoir, VA: Defense Technical Information Center, September 2013. http://dx.doi.org/10.21236/ada591047.

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Johnson, Anthony, and Sheri DeMartelaere. Sealing Penetrating Eye Injuries Using Photoactivated Bonding. Fort Belvoir, VA: Defense Technical Information Center, September 2012. http://dx.doi.org/10.21236/ada573365.

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Johnson, Anthony, and Irene Kochevar. Sealing Penetrating Eye Injuries Using Photoactivated Bonding. Fort Belvoir, VA: Defense Technical Information Center, October 2014. http://dx.doi.org/10.21236/ada618512.

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Cramer, Christopher J. Scientific Computation Application Partnerships in Materials and Chemical Sciences, Charge Transfer and Charge Transport in Photoactivated Systems, Developing Electron-Correlated Methods for Excited State Structure and Dynamics in the NWChem Software Suite. Office of Scientific and Technical Information (OSTI), November 2017. http://dx.doi.org/10.2172/1408275.

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