Relevant bibliographies by topics / Time dependent fluorescence shift

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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 'Time dependent fluorescence shift'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Time dependent fluorescence shift"

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Harju, Timo O., A. Herbert Huizer, Cyril A. G. O. Varma, and Jon Songstad. "Reconstructing the Solvation Time Correlation Function from the Time-Dependent Fluorescence Stokes Shift." Acta Chemica Scandinavica 49 (1995): 829–33. http://dx.doi.org/10.3891/acta.chem.scand.49-0829.

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Gakamsky, Dmitry M., Alexander A. Goldin, Eugene P. Petrov, and Anatoly N. Rubinov. "Fluorescence decay time distribution for polar dye solutions with time-dependent fluorescent shift." Biophysical Chemistry 44, no. 1 (August 1992): 47–60. http://dx.doi.org/10.1016/0301-4622(92)85034-2.

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Li, Tanping, and Revati Kumar. "Role of excited state solvent fluctuations on time-dependent fluorescence Stokes shift." Journal of Chemical Physics 143, no. 17 (November 7, 2015): 174501. http://dx.doi.org/10.1063/1.4934661.

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Dandapat, Manika, and Debabrata Mandal. "Time-dependent fluorescence Stokes shift and molecular-scale dynamics in alginate solutions and hydrogels." Chemical Physics Letters 627 (May 2015): 67–72. http://dx.doi.org/10.1016/j.cplett.2015.03.027.

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Tröscher, Anna R., Barbara Werner, Nadia Kaouane, and Wulf Haubensak. "Spectral recording of gene expression history by fluorescent timer protein." BioTechniques 67, no. 4 (October 2019): 154–64. http://dx.doi.org/10.2144/btn-2019-0050.

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Monitoring spatio-temporal patterns of gene expression by fluorescent proteins requires longitudinal observation, which is often difficult to implement. Here, we fuse a fluorescent timer (FT) protein with an immediate early gene (IEG) promoter to track live gene expression in single cells. This results in a stimulus- and time-dependent spectral shift from blue to red for subsequent monitoring with fluorescence activated cell sorting (FACS) and live cell imaging. This spectral shift enables imputing the time point of activity post-hoc to dissociate early and late responders from a single snapshot in time. Thus, we provide a tool for tracking stimulus-driven IEG expression and demonstrate proof of concept exploiting promoter::FT fusions, adding new dimensions to experiments that require reconstructing spatio-temporal patterns of gene expression in cells, tissues or living organisms.
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Nilsson, L., and B. Halle. "Molecular origin of time-dependent fluorescence shifts in proteins." Proceedings of the National Academy of Sciences 102, no. 39 (September 14, 2005): 13867–72. http://dx.doi.org/10.1073/pnas.0504181102.

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Sakai, Hisashi, Akira Itaya, and Hiroshi Masuhara. "Time-dependent fluorescence spectral shift and unusual slow decay of exciplex in poly(N-vinylcarbazole) films." Journal of Physical Chemistry 93, no. 14 (July 1989): 5351–53. http://dx.doi.org/10.1021/j100351a010.

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Toptygin, Dmitri, Thomas B. Woolf, and Ludwig Brand. "MD Simulations of the Time-Dependent Red Shift in the Fluorescence of Trp in Protein GB1." Biophysical Journal 96, no. 3 (February 2009): 47a. http://dx.doi.org/10.1016/j.bpj.2008.12.140.

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Vazdar, Mario, Erik Wernersson, Morteza Khabiri, Lukasz Cwiklik, Piotr Jurkiewicz, Martin Hof, Ella Mann, Sofiya Kolusheva, Raz Jelinek, and Pavel Jungwirth. "Aggregation of Oligoarginines at Phospholipid Membranes: Molecular Dynamics Simulations, Time-Dependent Fluorescence Shift, and Biomimetic Colorimetric Assays." Journal of Physical Chemistry B 117, no. 39 (September 24, 2013): 11530–40. http://dx.doi.org/10.1021/jp405451e.

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Allolio, Christoph, Mohsen Sajadi, Nikolaus P. Ernsting, and Daniel Sebastiani. "An Ab Initio Microscope: Molecular Contributions to the Femtosecond Time-Dependent Fluorescence Shift of a Reichardt-Type Dye." Angewandte Chemie International Edition 52, no. 6 (January 2, 2013): 1813–16. http://dx.doi.org/10.1002/anie.201204532.

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Dissertations / Theses on the topic "Time dependent fluorescence shift"

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Spies, Christian [Verfasser], and Gregor [Akademischer Betreuer] Jung. "Solvent- and time-dependent fluorescence of photoacids based on pyranine / Christian Spies. Betreuer: Gregor Jung." Saarbrücken : Saarländische Universitäts- und Landesbibliothek, 2014. http://d-nb.info/1054055122/34.

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Masters, T. A. "Time-resolved fluorescence studies of enhanced green fluorescent protein and the molecular dynamics of 3-Phosphoinositide Dependent Protein Kinase 1." Thesis, University College London (University of London), 2009. http://discovery.ucl.ac.uk/19031/.

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Fluorescent proteins (FPs), particularly Enhanced Green Fluorescent Protein (EGFP), are essential tools in the study of intact biological systems. Whilst the photophysics of its progenitor, GFP, have been investigated extensively, far fewer studies of EGFP have been made. In this thesis, a full characterisation of EGFP excited state photophysics by singleand two-photon time-resolved fluorescence lifetime and anisotropy is presented. Furthermore, the two-photon transition tensor, determined by absorption and initial anisotropies, is shown to be dominated by a single element. The two-photon excited state of EGFP was subject to Stimulated Emission Depletion (STED), revealing the stimulated emission cross section, the ground state relaxation time and the time evolution of the higher order distribution moments to which anisotropy is not sensitive. The strong adherence to theoretical Debye diffusion reinforced the conclusions of the two-photon structure model, and showed EGFP to be an excellent molecule for the future development of STED. In addition, these studies provided a sound basis on which to employ single- and two-photon FRET in vivo and in vitro. Cell behaviour is governed by the transduction of molecular signals from the extracellular environment to intracellular compartments. At the centre of the PI 3-kinase signalling pathway is PDK1, a Serine/Threonine kinase, which phosphorylates numerous important downstream targets including Protein Kinase B (PKB). To date however, the regulatory mechanisms governing the behaviour of this protein remain poorly understood. Timeresolved fluorescence lifetime imaging microscopy (FLIM) was employed with FP tagged PDK1 to investigate dynamic interactions in intact cells in situ and in vivo. PDK1 was shown to dimerise in a manner dependent on PI 3-kinase activity and PDK1 PH domain lipid binding. To detail the structure of the observed intermolecular interaction, recombinant FP labelled PDK1 was produced with insect cells. Measurement of the rise in acceptor fluorescence during FRET in vitro indicated the PDK1 dimer pair exists in an antiparallel arrangement. These results provide the first insight on the structure of the dimer and demonstrate that the generation of 3-phosphorylated lipids is required for its formation.
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McGuinness, Colin Douglas. "Glucose sensing based on the intrinsic time dependent fluorescence from proteins : application of pulsed ultraviolet light emitting diodes and sol-gel derived matrices." Thesis, University of Strathclyde, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.431823.

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Jacobsson, T. Jesper. "Synthesis and characterisation of ZnO nanoparticles.An experimental investigation of some of their size dependent quantum effects." Thesis, Uppsala University, Department of Materials Chemistry, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-121715.

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ZnO nanoparticles in the size range 2.5–7 nm have been synthesised by a wet chemical method where ZnO particles were grown in basic zinc acetate solution. The optical band gap increases when the size of the particles decreases. An empirical relation between the optical band gap given from absorption measurements, and particle size given from XRD measurements has been developed and compared to other similar relations found in the literature.

   Time resolved UV-Vis spectroscopy has been used to follow the growth of particles in situ in solution. The data show that the growth mechanism not can be described by a simple Oswald ripening approach and nor by an exclusive agglomeration of smaller clusters into larger particles. The growth mechanism is more likely a combination of the proposed reaction themes. The data also reveal that particle formation do not demand a heating step for formation of the commonly assumed initial cluster Zn4O(CH3COO)6.

   Steady state fluorescence has been studied as a function of particle size during growth in solution. These measurements confirm what is found in the literature in that the visible fluorescence is shifted to longer wavelengths and loses in intensity as the particles grow. Some picosecond spectroscopy has also been done where the UV fluorescence has been investigated. From these measurements it is apparent that the lifetime of the fluorescence increases with particle size.

    The phonon spectrum of ZnO has been studied with Raman spectroscopy for a number of different particle sizes. From these measurements it is clear that there is a strong quenching of the phonons due to confinement for the small particles, and the only clearly observed vibration is one at 436 cm-1 which intensity strongly increases with particle size.   

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Aveiro, Susana Seabra. "The p22HBP heme binding protein: an NMR study of the dynamics and heme-protein interactions." Doctoral thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/14278.

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Doutoramento em Bioquímica
The work presented in this Thesis investigates the dynamics and molecular interactions of p22HBP and the p22HBP-tetrapyrrole complex. Specifically, the key residues involved when a tetrapyrrole binds to p22HBP were sought. Previous molecular modelling studies identified three possible charged residues R56, K64 and K177 as possibly being important in tetrapyrrole binding via electrostatic interactions with the propionate groups of the tetrapyrrole. A number of variants of murine p22HBP were therefore prepared and fluorescence quenching and NMR used to verify the integrity of the variants and their interaction with tetrapyrrole. The same molecular modelling studies identified a mobile loop Y171-R180 in p22HBP that decreased in mobility on tetrapyrrole binding, therefore to confirm this mobility change dynamics studies based on NMR relaxation experiments were carried out. Finally in order to obtain a non heme-binding form of human p22HBP a chimeric p22HBP was designed and constructed. This construct, and the resulting protein, will be important for future siRNA knockdown studies where rescue or recovery of function experiments are required to prove the knockdown results. Chapter one discusses the current state of the art in terms of the biological, structural and functional aspects of p22HBP. The main objectives of the Thesis are also introduced here. Chapter two presents a detailed description of the different expression vectors (pNJ2 and pet28-a) and procedures used for overexpression and purification of murine p22HBP and its variants and human p22HBP. All expression and purification systems used gave good yields and allowed isotopic labeling to be carried out. The fluorescence quenching results for tetrapyrrole binding to murine p22HBP and variants are presented in chapter three along with the dissociation constants that were found to be in the nanomolar range for wild type murine and human p22HBP. The same studies were performed for murine p22HBP variants, with hydrophobic and polar changes being introduced at R56, K64 and K177. The dissociation constants were found to double in some cases but no significant changes in the strength of hemin-protein interactions were observed. The tetrapyrrole interaction with p22HBP was also followed by NMR spectroscopy, where chemical shift mapping was used to identify binding pocket location. All the variants and wild type human p22HBP were found to bind at the same location. Chapter 4 contains the data from 2D and 3D experiments carried out on 15N/13C labelled human p22HBP that was used to obtain backbone assignments. Comparison with wild type murine p22HBP assignments, PPIX titrations and theoretical calculations based on chemical shifts (Talos+) allowed 82% of the backbone resonances to be assigned. The results from the relaxation experiments used to probe the dynamics of the mobile loop in p22HBP on binding to tetrapyrrole are presented in chapter 5. The overall protein was found to tumble isotropically in the free and bound forms however the results to probe mobility changes in the 171-180 loop on tetrapyrrole binding proved inconclusive as only residue could be assigned and this did not seem to become significantly less mobile. The final chapter describes the design and construction of a chimeric p22HBP. For these purpose, the alfa1-helix sequence of human p22HBP in the phHBP1 plasmid was replaced by its homologous sequence in hSOUL, a non heme-binding protein with identical 3D structure. The results however indicated that either the incorrect sequence was introduced into the plasmid or the purification procedure was inadequate.
O trabalho apresentado nesta Tese focou-se na dinâmica e nas interações moleculares da p22HBP e do complexo p22HBP-tetrapirrol, nomeadamente nos resíduos chave envolvidos nesta interação. Estudos prévios de modelação molecular identificaram três possíveis resíduos chave R56, K64 e K177 como sendo importantes na interação com os tetrapirróis, através de interações eletrostáticas com os grupos propionato do tetrapirrol. Foram desenhados e construídos variantes da p22HBP murina e foram desenvolvidos estudos de extinção de fluorescência e RMN para avaliar a integridade dos variantes e a sua interação com os tetrapirróis. Os mesmos estudos de modelação molecular identificaram ainda uma zona flexível (Y171-R180) na p22HBP que diminui a mobilidade com a interação do tetrapirrol. Para confirmar esta alteração de mobilidade, foram realizados estudos de dinâmica, baseados em RMN. Por fim, com o intuito de obter uma versão não funcional da p22HBP humana, foi planeada e construída uma versão quimérica da p22HBP humana. No futuro, esta nova versão da p22HBP quimérica, será importante para os estudos de knockdown envolvendo siRNA. O capítulo um introduz uma revisão dos aspetos biológicos da p22HBP nomeadamente os estudos estruturais e as possíveis funções que foram identificadas. Os principais objetivos da tese são também apresentados neste capítulo. No capítulo dois é apresentada uma descrição detalhada dos diferentes vectores de sobreexpressão (pNJ2 e pet28-a) e dos métodos de sobreexpressão e purificação da p22HBP murina e respectivos variantes, bem como da p22HBP humana. Todos os sistemas de sobreexpressão e purificação utilizados obtiveram bons rendimentos e permitiram a marcação isotópica das proteínas. No capítulo 3 são apresentados os resultados de extinção de fluorescência para a interação da p22HBP murina e humana com hemina através das constantes de dissociação determinadas na ordem dos nanomolar. Os mesmos estudos foram realizados para os variantes da p22HBP murina, com alterações hidrofóbicas e de polaridade nos resíduos R56, K64 e K177. Em alguns casos, as constantes de dissociação determinadas são mais elevadas, embora não se tenham verificado alterações significativas na força da interação proteína-hemo. As interações tetrapirrólicas com a p22HBP foram também estudadas por espectroscopia de RMN, onde foram mapeadas as diferenças nos desvios químicos para identificar a localização da zona de interação. A localização da zona de interação dos variantes da p22HBP e a p2HBP humana mantém-se igual à p22HBP murina. No capítulo 4 encontram-se os resultados das experiências 2D e 3D realizadas na p22HBP humana, isotopicamente marcada com 15N/13C, para identificar as ressonâncias da cadeia principal. 82% dos sistemas de spin da cadeia principal foram identificados através da comparação com a p22HBP murina, das titulações com PPIX e de cálculos teóricos baseados nos desvios químicos (Talos+). No capítulo 5 são apresentados os resultados das experiências de relaxação, usados para comprovarem a dinâmica do loop na p22HBP aquando da interação com o tetrapirrol. A proteína no seu todo move-se de uma forma isotrópica na forma livre e ligada. No entanto os resultados para comprovar as alterações de mobilidade no loop 171-180 na presença de hemo, foram inconclusivos uma vez que só a um resíduo foi atribuído um sistema de spin, e não foi indicativo da perda significativa de mobilidade. O último capítulo descreve o planeamento e a construção da p22HBP quimérica. Para tal, a sequência que codifica a hélix alfa 1 da p22HBP humana, no plasmídeo phHBP1, foi substituída pela sequência homóloga da SOUL humana, uma proteína com uma estrutura 3D semelhante mas não liga ao hemo. Os resultados no entanto demonstraram que ou a sequência não foi introduzida corretamente no plasmídeo ou o sistema de purificação não foi adequado.
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Gong, Yun. "Structure-property relationships of dyes as applied to dye-sensitized solar cells." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/275007.

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This work investigates the correlation of structural and photovoltaic properties of dyes used in dye-sensitized solar cells. Experimental methods, including ultraviolet-visible spectroscopy, fluorescence spectroscopy, cyclic voltammetry and electrochemical impedance spectroscopy are employed to study optical and electrochemical properties of dye molecules. Computational methods, including density functional theory and time-dependent density functional theory, are used to validate and predict the optical and electronic properties of dye molecules, in their isolated state and once embedded into a working electrode device environment that comprises a dye...TiO2 interface. The results chapters begin with the presentation of a series of quinodimethene dyes that are experimentally validated for their photovoltaic application, and associated computational studies reveal that an inner structural factor - a phenyl ring rotation occurring during the optical excitation process - leads to the competitive photovoltaic device performance of these dyes. Carbazole-based dyes are then systematically studied by computation, especially considering charge transfer paths and binding modes of these dyes on a titania surface. The theoretical models for the basic building block of this chemical family of dyes, known as MK-44, successfully support and explain structural discoveries from X-ray diffraction and reflectometry that impact of their function. A benzothiadiazole-based dye, RK-1, is then systematically studied by both experimental and computational methods, and the results show that the π-bridge composed of thiophene, benzothiadiazole and benzene rings leads to excellent charge separation; and the rotation of these rings during the optical excitation process may well be consistent with the fluorescence spectrum. Finally, the well-known ruthenium-based dyes are theoretically studied to determine the properties of different ligands connected to the metal core of the complex. Conformations with different NCS ligands are calculated in terms of energy and explain well the corresponding results from X-ray diffraction. Acid-base properties of carboxyl groups connected to pyridine ligands in N3 and N749 are theoretically calculated based on thermodynamics and density functional theory. Implicit and explicit models are both adopted to predict these acid dissociative constant values, which are generally in a good agreement with the reported experimental data. The thesis concludes with conclusions and a future outlook.
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Seidel, Marco Thomas. "Solvatationsdynamik an biologischen Grenzschichten." Doctoral thesis, [S.l.] : [s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=969974124.

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Beranová, Lenka. "Pokročilé fluorescenční metody aplikované ve výzkumu biomolekul (lipidových membrán a DNA)." Doctoral thesis, 2013. http://www.nusl.cz/ntk/nusl-327224.

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The thesis describes time dependent fluorescence shift method and fluorescence correlation spectroscopy method (FCS) with its extensions FLCS, Z-scan FCS and dual-focus FCS applied on specific problems in DNA and lipid research. Compaction mechanism of a DNA molecule smaller than a resolution of a confocal microscope was elucidated. The process was revealed to be "all or non" for a polycation spermine as a condenser in contrast with the gradual compaction caused by a cationic surfactant. Biophysical properties of a phospholipid bilayer influenced by presence of oxidized phospholipids with truncated sn-2 chain were explored. The dynamics of hydrated functional groups in the headgroup region was proved to get faster while the hydration of the headgroup region increased. These effects are in relation with the reorientation of the short sn-2 chains observed in molecular dynamics simulations. Presence of oxidized species may also influence the lateral diffusion of the lipids - a slight increase of the diffusion coefficient was observed. Decrease of hydration and mobility in the headgroup region was found as an influence of heavy water on the phospholipid membrane. These finding are in line with molecular dynamics simulations which show longer lifetimes of hydrogen bonds between water and lipid molecules in...
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WANG, YI-CHEN, and 王乙媜. "Accelerated Failure Time Model and Location Shift Model under Dependent Current Status Data." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/y5kdt2.

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碩士
國立中正大學
數學系統計科學研究所
107
This paper mainly investigates the relationship between the failure time of the dependent current status data and the covariates and apply the Copula model to specify the relationship between the observation time and the failure time. We apply two methods to estimate the regression parameter. The first method uses the redistribution algorithm to estimate the survival function of the failure time and then estimate the regression parameters by a two-stage estimation procedure under a general regression model. The second method applies the survival weighted least squares method to estimate the regression coefficient of the general regression model. Simulation studies examine the finite sample performance and compare the two methods, and finally, we analyze a tumorigenicity data for illustrations.
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Roller, Robert Stephen. "The determination of the Forster critical radius through time-dependent fluorescence decay measurements and the spectral overlap method." 2004. http://link.library.utoronto.ca/eir/EIRdetail.cfm?Resources__ID=81012&T=F.

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Books on the topic "Time dependent fluorescence shift"

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Hollenbach, David. Time-dependent photodissociation regions. [Washington, DC: National Aeronautics and Space Administration, 1995.

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Hollenbach, David. Time-dependent photodissociation regions. [Washington, DC: National Aeronautics and Space Administration, 1995.

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Hollenbach, David. Time-dependent photodissociation regions. [Washington, DC: National Aeronautics and Space Administration, 1995.

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Dipolar solvation dynamics studies by the time dependent fluorescence stokes shift. 1988.

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Antonella, Natta, and United States. National Aeronautics and Space Administration., eds. Time-dependent photodissociation regions. [Washington, DC: National Aeronautics and Space Administration, 1995.

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Strecker, Amy. Conceptualizing Landscape. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198826248.003.0002.

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Chapter 2 traces the etymological origins of the term ‘landscape’ and discusses the theoretical and historical underpinnings of the term. In particular, it discusses how the concept of landscape has evolved from being conceptually dependent upon nature, to a much wider conception of landscape as something socially and culturally produced. This social interpretation of landscape brings it closer to its early etymological origins, to what Kenneth Olwig terms the ‘substantive nature’ of landscape. This chapter also discusses the relationship between landscape and the related concepts of property, heritage, and commons. It shows how landscape has undergone shifts in meaning over time, and argues that the most recent shift links landscape to human rights, democracy, and public space.
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Catherine A, Rogers. Part II Staking Out Theoretical Boundaries and Building the Regime, 7 Ariadne’s Thread and the Functional Thesis. Oxford University Press, 2014. http://dx.doi.org/10.1093/law/9780198713203.003.0008.

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This chapter discusses the ‘Functional Thesis’ posited as the underlying theory uniting the concepts discussed in previous chapters regarding the implementation of ethical self-regulation. The Functional Thesis labours under the presumption that acting upon ethical obligations are dependent upon the role of the agent; it assigns ‘functional roles’ to these agents that can create more flexible distinctions between identities presented in titles such as ‘lawyer’, ‘judge’, and so on. The ethical obligations presented in each role are subject to constant change as demanded by the procedural rules of international arbitration, yet a better understanding of these roles can lay the foundations for a code of conduct. And while these roles may shift to the whims of procedure, ethical expectations are, at least, constant over time.
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Book chapters on the topic "Time dependent fluorescence shift"

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Pokorna, Sarka, Agnieszka Olżyńska, Piotr Jurkiewicz, and Martin Hof. "Hydration and Mobility in Lipid Bilayers Probed by Time-Dependent Fluorescence Shift." In Springer Series on Fluorescence, 141–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/4243_2012_46.

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Toptygin, Dmitri. "Time-Dependent Spectral Shifts in Tryptophan Fluorescence: Bridging Experiments with Molecular Dynamics Simulations." In Reviews in Fluorescence 2015, 29–69. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-24609-3_2.

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Rullière, C., A. Declémy, and Ph Kottis. "Time-Dependent Fluorescence Shift in Alcoholic Solvents: A Non-Debye Behaviour Related to Hydrogen Bonds." In Springer Series in Chemical Physics, 312–14. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82918-5_84.

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Toptygin, Dmitri. "Analysis of Time-Dependent Red Shifts in Fluorescence Emission from Tryptophan Residues in Proteins." In Methods in Molecular Biology, 215–56. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-649-8_9.

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Ficek, Zbigniew, and Ryszard Tanaś. "Time-Dependent Fluorescence Spectroscopy." In Springer Series in Optical Sciences, 145–83. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3740-0_5.

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Lakowicz, Joseph R. "Time-Dependent Anisotropy Decays." In Principles of Fluorescence Spectroscopy, 321–45. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4757-3061-6_11.

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Ungar, Lowell W., and Jeffrey A. Cina. "Short-Time Fluorescence Stokes Shift Dynamics." In Advances in Chemical Physics, 171–228. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470141595.ch2.

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Wiesche, Lara. "Time-Dependent Ambulance Deployment and Shift Scheduling of Crews." In Operations Research Proceedings, 591–96. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-42902-1_80.

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Shweta, Him, Nibedita Pal, Moirangthem Kiran Singh, Sachin Dev Verma, and Sobhan Sen. "Dynamics of Water and Ions Near DNA: Perspective from Time-Resolved Fluorescence Stokes Shift Experiments and Molecular Dynamics Simulation." In Reviews in Fluorescence 2017, 231–79. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-01569-5_10.

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Huang, Dan, Hai-ping Zhu, Hui Yin, and Yu-hao Deng. "An Economic Control Chart Optimization Method for Production Process with Time-Dependent Mean Shift." In Proceedings of the 22nd International Conference on Industrial Engineering and Engineering Management 2015, 115–24. Paris: Atlantis Press, 2016. http://dx.doi.org/10.2991/978-94-6239-180-2_12.

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Conference papers on the topic "Time dependent fluorescence shift"

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Schulz, Ralf B., Martin Schweiger, Cosimo D'Andrea, Gianluca Valentini, Jörg Peter, Rinaldo Cubeddu, Simon Arridge, and Wolfhard Semmler. "Applying Time-Dependent Data for Fluorescence Tomography." In European Conference on Biomedical Optics. Washington, D.C.: OSA, 2007. http://dx.doi.org/10.1364/ecbo.2007.6626_19.

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Schulz, Ralf B., Martin Schweiger, Cosimo D'Andrea, Gianluca Valentini, Jörg Peter, Rinaldo Cubeddu, Simon Arridge, and Wolfhard Semmler. "Applying time-dependent data for fluorescence tomography." In European Conference on Biomedical Optics, edited by Kai Licha and Vasilis Ntziachristos. SPIE, 2007. http://dx.doi.org/10.1117/12.728357.

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Simon, John D., and Shyh-Gang Su. "Solvation Dynamics and the Time-Dependent Stoke Shift." In OE LASE'87 and EO Imaging Symp (January 1987, Los Angeles), edited by Mostafa A. El-Sayed. SPIE, 1987. http://dx.doi.org/10.1117/12.966910.

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ROERICH, VL C., A. N. STAROSTIN, and A. A. PANTELEEV. "MANY-BODY APPROACHES TO TIME-DEPENDENT RESONANCE FLUORESCENCE." In Proceedings of the Conference. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812705129_0009.

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Vincent, Michel, Jacques Gallay, and Alexander P. Demchenko. "Photophysics of indole in polar solvent: Analysis of fluorescence lifetime distributions and time-dependence spectral shifts." In The 54th international meeting of physical chemistry: Fast elementary processes in chemical and biological systems. AIP, 1996. http://dx.doi.org/10.1063/1.50165.

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Pu, Yang, Guichen Tang, B. B. Das, C. H. Liu, Asima Pradhan, and Robert R. Alfano. "Ultrafast time-dependent fluorescence spectroscopy for human breast cancer detection." In SPIE BiOS, edited by Robert R. Alfano and Stavros G. Demos. SPIE, 2012. http://dx.doi.org/10.1117/12.906254.

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Cheng, Wayne. "Real-time Compensation for Angular-dependent Color Shift in TN LCDs." In 2006 IEEE LEOS Annual Meeting. IEEE, 2006. http://dx.doi.org/10.1109/leos.2006.278930.

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Ceffa, Nicolo' G., Paolo Pozzi, Margaux Bouzin, Cassia A. Marquezin, Laura Sironi, Laura D'Alfonso, Maddalena Collini, and Giuseppe Chirico. "Fluorescence cross-correlation spectroscopy for time dependent flows: a numerical investigation." In SPIE BiOS, edited by Bonnie L. Gray and Holger Becker. SPIE, 2015. http://dx.doi.org/10.1117/12.2077088.

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Yamamoto, Yoshiki, Hideki Makiyama, Takumi Hasegawa, Shinobu Okanishi, Keiichi Maekawa, Hiroki Shinkawata, and Yasuo Yamaguchi. "Time-dependent Vth shift of silicon on thin BOX under large back bias." In 2017 IEEE SOI-3D-Subthreshold Microelectronics Technology Unified Conference (S3S). IEEE, 2017. http://dx.doi.org/10.1109/s3s.2017.8308738.

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Lakowicz, Joseph R., Ignacy Gryczynski, Henryk Szmacinski, Kazimierz Nowaczyk, and Michael L. Johnson. "Advances in frequency-domain fluorometry, gigahertz instrumentation, time-dependent photomigration, and fluorescence lifetime imaging." In New York - DL tentative, edited by Daniel L. Akins and Robert R. Alfano. SPIE, 1992. http://dx.doi.org/10.1117/12.56701.

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Reports on the topic "Time dependent fluorescence shift"

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Frost, Bruce. Time- and Irradiance-Dependent Behavior of the Quantum Yield of Chlorophyll alpha Fluorescence. Fort Belvoir, VA: Defense Technical Information Center, September 2001. http://dx.doi.org/10.21236/ada627704.

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Perry, Mary J. Time- and Irradiance-Dependent Behavior of the Quantum Yield of Chlorophyll alpha Fluorescence. Fort Belvoir, VA: Defense Technical Information Center, August 2001. http://dx.doi.org/10.21236/ada628016.

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You might also be interested in the extended bibliographies on the topic 'Time dependent fluorescence shift' for particular source types:
Journal articles
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