Results for 'enzyme kinetics'

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  1.  26
    On the role of enzyme kinetic parameters in determining the effectiveness with which channelling can decrease the size of a metabolite pool.Pedro Mendes & Douglas B. Kell - 1993 - Acta Biotheoretica 41 (1-2):63-73.
    Recently, it has been argued that the phenomenon of direct transfer of intermediate metabolites between adjacent enzymes, also known as metabolic channelling, would not decrease the concentration of those intermediates in the bulk solution. However, this conclusion has been drawn by extrapolation from the results of simulations with a rather restricted set of parameters. We show that, for a number of kinetic cases, the existence of metabolic channelling can decrease the size of the soluble pool of intermediates. When the (...)(s) downstream of the channel have a catalytic capacity that is large relative to the enzymes upstream of the channel, the decrease of concentration can be substantial (3 orders of magnitude). (shrink)
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  2.  27
    Modeling the Enzyme Kinetic Reaction.Angélique Stéphanou & Nicolas Glade - 2015 - Acta Biotheoretica 63 (3):239-256.
    The Enzymatic control reactions model was presented within the scope of fractional calculus. In order to accommodate the usual initial conditions, the fractional derivative used is in Caputo sense. The methodologies of the three analytical methods were used to derive approximate solution of the fractional nonlinear system of differential equations. Two methods use integral operator and the other one uses just an integral. Numerical results obtained exhibit biological behavior of real world problem.
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  3.  8
    Modeling the Enzyme Kinetic Reaction.Abdon Atangana - 2015 - Acta Biotheoretica 63 (3):239-256.
    The Enzymatic control reactions model was presented within the scope of fractional calculus. In order to accommodate the usual initial conditions, the fractional derivative used is in Caputo sense. The methodologies of the three analytical methods were used to derive approximate solution of the fractional nonlinear system of differential equations. Two methods use integral operator and the other one uses just an integral. Numerical results obtained exhibit biological behavior of real world problem.
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  4. Kinetic Models of (M-R)-Systems.J. A. Prideaux - 2011 - Axiomathes 21 (3):373-392.
    Kinetic models using enzyme kinetics are developed for the three ways that Louie proved that Rosen’s minimal (M-R)-System can be closed to efficient cause; i.e., how the “replication” component can itself be entailed from within the system. The kinetic models are developed using the techniques of network thermodynamics. As a demonstration, each model is simulated using a SPICE circuit simulator using arbitrarily chosen rate constants. The models are built from SPICE sub-circuits representing the key terms in the chemical (...)
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  5.  38
    A fast method to estimate kinetic constants for enzyme inhibitors.S. Schnell & C. Mendoza - 2001 - Acta Biotheoretica 49 (2):109-113.
    We present a method to determine the reaction type and kinetic constants for enzyme inhibitors that decreases the number of experimental assays by at least a factor of five. It is based on a new theoretical formalism in terms of concentrations that dismisses the requirement of estimating initial velocities. Expressions for the time evolution of the concentrations of all the reactants are also given.
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  6.  8
    Kinetic proofreading by the cavity system of myoglobin: protection from poisoning.Wilson Radding & George N. Phillips - 2004 - Bioessays 26 (4):422-433.
    Throughout its matrix of atoms, myoglobin has a network of cavities that are inhabited for short lengths of time by ligands released by photolysis from the myoglobin heme. The purpose or effect of this cavity network is not clear. A recently published kinetic scheme that fits data from many native and mutant myoglobin oxygen photolysis experiments can be modified easily into a kinetic scheme that includes kinetic proofreading. Proofreading would provide protection against contaminants and, specifically, might help protect the cell (...)
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  7.  10
    Kinetic isotope effects and ‘metabolic switching’ in cytochrome P450‐catalyzed reactions.Gerald T. Miwa & Anthony Y. H. Lu - 1987 - Bioessays 7 (5):215-219.
    The mechanistic significance of a kinetic isotope effect on a cytochrome P‐450catalyzed reaction depends, fundamentally, on the nature of the interaction of the substrate with the active site of the enzyme as well as on the nature of the chemistry of the reaction catalyzed. Consequently, kinetic isotope effects can be used to extract information on the topology of the enzyme and the mechanism of substrate oxidation. Kinetic isotope effect studies are sometimes accompanied by ‘metabolic switching’ or a change (...)
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  8. The Structural Basis for Kinetic and Allosteric Differences between Two Bacterial Phosphofructokinases.W. Malcolm Byrnes - 1994 - Dissertation,
    The fructose 6-phosphate (Fru-6P) saturation curve for phosphofructokinase (PFK) from E. coli is sigmoidal in the presence of saturating MgATP levels, while the corresponding curve for B. stearothermophilus PFK is essentially hyperbolic. Sigmoidality can be due to apparent cooperativity arising from the kinetic mechanism of an enzyme. We have determined the kinetic mechanism of B. stearothermophilus PFK (BsPFK). BsPFK was found to obey a non rapid-equilibrium random mechanism similar to the one E. coli PFK (EcPFK) follows. Substrate inhibition by (...)
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  9.  26
    Growth factors and cell kinetics: A mathematical model applied to il-3 deprivation on leukemic cell lines.Pierre Auger, Peter Dörmer & Joachim W. Ellwart - 1992 - Acta Biotheoretica 40 (2-3):147-159.
    We assume the existence of a specific G1 protein which is an initiator of DNA replication. This initiator is supposed to be synthesized according to Michaelis-Menten kinetics. In order to start DNA replication, it is assumed that this G1 specific protein must be produced in a required amount. Intra-cellular growth inhibitors and extra-cellular growth factors control the production of the initiator. This model allows to calculate the average G1 phase time as a function of the various chemical concentrations of (...)
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  10.  20
    RubisCO Early Oxygenase Activity: A Kinetic and Evolutionary Perspective.Ireneusz Ślesak, Halina Ślesak & Jerzy Kruk - 2017 - Bioessays 39 (11):1700071.
    RubisCO is Earth's main enzyme responsible for CO2 fixation via carboxylation of ribulose-1,5-bisphosphate into organic matter. Besides the carboxylation reaction, RubisCO also catalyzes the oxygenation of RuBP by O2, which is probably as old as its carboxylation properties. Based on molecular phylogeny, the occurrence of the reactive oxygen species -removing system and kinetic properties of different RubisCO forms, we postulated that RubisCO oxygenase activity appeared in local microoxic areas, yet before the appearance of oxygenic photosynthesis. Here, in reviewing the (...)
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  11. Eschatologische Perspektiven im Hoseabuch.Dirk Kinet - 1981 - In Engelbert Neuhäusler, Rudolf Kilian, Klemens Funk & Peter Fassl (eds.), Eschatologie: bibeltheologische und philosophische Studien zum Verhältnis von Erlösungswelt und Wirklichkeitsbewältigung: Festschrift für Engelbert Neuhäusler zur Emeritierung gewidmet von Kollegen, Freunden und Schülern. St. Ottilien: EOS Verlag.
     
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  12. Commemorating the 1913 Michaelis--Menten paper Die Kinetik der Invertinwirkung: three perspectives.Ute Deichmann, Schuster Stefan, Mazat Jean-Pierre & Athel Cornish-Bowden - 2013 - FEBS 281 (2):435-463.
    Methods and equations for analysing the kinetics of enzyme-catalysed reactions were developed at the beginning of the 20th century in two centres in particular; in Paris, by Victor Henri, and, in Berlin, by Leonor Michaelis and Maud Menten. Henri made a detailed analysis of the work in this area that had preceded him, and arrived at a correct equation for the initial rate of reaction. However, his approach was open to the important objection that he took no account (...)
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  13.  37
    The biological significance of substrate inhibition: A mechanism with diverse functions.Michael C. Reed, Anna Lieb & H. Frederik Nijhout - 2010 - Bioessays 32 (5):422-429.
    Many enzymes are inhibited by their own substrates, leading to velocity curves that rise to a maximum and then descend as the substrate concentration increases. Substrate inhibition is often regarded as a biochemical oddity and experimental annoyance. We show, using several case studies, that substrate inhibition often has important biological functions. In each case we discuss, the biological significance is different. Substrate inhibition of tyrosine hydroxylase results in a steady synthesis of dopamine despite large fluctuations in tyrosine due to meals. (...)
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  14.  9
    Boekbesprekingen.W. Beuken, J. -M. Tison, P. Fransen, D. Kinet, P. Smulders, S. Trooster, J. Vercruysse, J. van Torre, J. Mulders, M. De Wachter & Jos Vercruysse - 1967 - Bijdragen 28 (4):448-464.
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  15.  30
    Boekbesprekingen.W. Beuken, J.-M. Tison, J. Lambrecht, D. Kinet, B. Van Dorpe, Jos Vercruysse, P. Fransen, E. De Strycker, P. Grootens, S. Trooster, J. Hansen, Jan Erkens, J. Van Torre, P. Van Doornik, C. Traets, M. De Wachter, A. Van Kol, J. Mulders, H. Robbers, A. Poncelet, H. Van Luijk, J. H. Nota, M. De Tollenaere, R. Hostie, J. Kijm, W. Heyvaert, J. De Gendt, G. Neefs, R. D'hondt, Fr Verleysen, J. Vanneste, M. Dierickx & N. Sprokel - 1968 - Bijdragen 29 (1):83-112.
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  16.  33
    Boekbesprekingen.J.-M. Tison, W. Beuken, S. Trooster, D. Kinet, J. Lambrecht, Ben Hemelsoet, E. Kerckhof, A. Cnockaert, H. Pillaert, P. Fransen, S. De Smet, P. Smulders, J. Varnneste, J. Mulders, J. Vanneste, P. Grootens, Jos Vercruysse, R. Ceusters, J. Van Torre, M. De Wachter, A. Van Kol, A. Poncelet, P. Verdeyen, M. De Tollenaere, A. Roosen, H. Van Luijk, R. Hostie, H. Somers, J. Kijm, Paul Begheyn, C. Swüste, J. De Bruyne, Bernard Van Dorpe, G. Neefs, M. Prick, L. Braeckmans & G. Verschuuren - 1968 - Bijdragen 29 (3):299-348.
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  17.  20
    Global Stability of Reversible Enzymatic Metabolic Chains.Ibrahima Ndiaye & Jean-Luc Gouzé - 2013 - Acta Biotheoretica 61 (1):41-57.
    We consider metabolic networks with reversible enzymatic reactions. The model is written as a system of ordinary differential equations, possibly with inputs and outputs. We prove the global stability of the equilibrium , using techniques of monotone systems and compartmental matrices. We show that the equilibrium does not always exist. Finally, we consider a metabolic system coupled with a genetic network, and we study the dependence of the metabolic equilibrium with respect to concentrations of enzymes. We give some conclusions concerning (...)
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  18.  11
    Revisiting Kadenbach: Electron flux rate through cytochrome c‐oxidase determines the ATP‐inhibitory effect and subsequent production of ROS.Sebastian Vogt, Annika Rhiel, Petra Weber & Rabia Ramzan - 2016 - Bioessays 38 (6):556-567.
    Mitochondrial respiration is the predominant source of ATP. Excessive rates of electron transport cause a higher production of harmful reactive oxygen species (ROS). There are two regulatory mechanisms known. The first, according to Mitchel, is dependent on the mitochondrial membrane potential that drives ATP synthase for ATP production, and the second, the Kadenbach mechanism, is focussed on the binding of ATP to Cytochrome c Oxidase (CytOx) at high ATP/ADP ratios, which results in an allosteric conformational change to CytOx, causing inhibition. (...)
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  19.  33
    Discrete and continuous models for heterocyst differentiation in growing filaments of blue-green bacteria.Chris G. De Koster & Aristid Lindenmayer - 1987 - Acta Biotheoretica 36 (4):249-273.
    Heterocyst spacing in blue -green bacteria is widely assumed to be due to a diffusible inhibitor. The inhibitor, a nitrogen-rich compound, probably glutamine, is produced via the N2-fixing enzymes of the heterocyst and in turn serves to suppress the induction of these enzymes and of the differentiation of vegetative cells to heterocysts. This simple morphogenetic mechanism operating in growing cellular filaments ofAnabaena species is investigated on the basis of a continuous and a discrete cellular model, as well as by cell-by-cell (...)
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  20.  33
    Using computer algebra to determine rate constants in biochemistry.M. Bayram, J. P. Bennett & M. C. Dewar - 1993 - Acta Biotheoretica 41 (1-2):53-62.
    In earlier work we have described how computer algebra may be used to derive composite rate laws for complete systems of equations, using the mathematical technique of Gröbner Bases (Bennett, Davenport and Sauro, 1988). Such composite rate laws may then be fitted to experimental data to yield estimates of kinetic parameters.Recently we have been investigating the practical application of this methodology to the estimation of kinetic parameters for the closed two enzyme system of aspartate aminotransferase (AAT) and malate dehydrogenase (...)
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  21.  29
    How Does a Helicase Unwind DNA? Insights from RecBCD Helicase.Timothy M. Lohman & Nicole T. Fazio - 2018 - Bioessays 40 (6):1800009.
    DNA helicases are a class of molecular motors that catalyze processive unwinding of double stranded DNA. In spite of much study, we know relatively little about the mechanisms by which these enzymes carry out the function for which they are named. Most current views are based on inferences from crystal structures. A prominent view is that the canonical ATPase motor exerts a force on the ssDNA resulting in “pulling” the duplex across a “pin” or “wedge” in the enzyme leading (...)
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  22.  43
    Enzyme classification and the entanglement of values and epistemic standards.Stijn Conix - 2020 - Studies in History and Philosophy of Science Part A 84:37-45.
    This paper investigates the case of enzyme classification to evaluate different ideals for regulating values in science. I show that epistemic and non-epistemic considerations are inevitably and untraceably entangled in enzyme classification, and argue that this has significant implications for the two main kinds of views on values in science, namely, Epistemic Priority Views and Joint Satisfaction Views. More precisely, I argue that the case of enzyme classification poses a problem for the usability and descriptive accuracy of (...)
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  23.  45
    The kinetic depth effect.Hans Wallach & D. N. O'Connell - 1953 - Journal of Experimental Psychology 45 (4):205.
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  24.  11
    Kinetic theory of living pattern.Lionel G. Harrison - 1993 - New York: Cambridge University Press.
    Development of the shapes of living organisms and their parts is a field of science in which there are no generally accepted theoretical principles. What form these principles are likely to take, when they emerge, is a subject in which there is a wide gulf of disagreement between physical scientists and experimental biologists. This book contains both an extensive philosophical commentary on this dichotomy in views and an exposition of the type of theory most favoured by physical scientists. In this (...)
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  25.  13
    Kinetic Beauty: The Philosophical Aesthetics of Sport.Jason Holt - 2019 - New York, NY: Routledge.
    Sport aesthetics is an important but often marginalized field in the philosophy of sport. Kinetic Beauty offers a comprehensive, principled, pluralist introduction to the philosophical aesthetics of sport. The book tackles a wide variety of issues in the philosophical aesthetics of sport, proposing a five-level analysis that coordinates extant scholarship on the same conceptual map, reveals gaps in the literature, and motivates a fresh perspective on stubborn debates and novel topics in the field. This is an excellent resource for professors (...)
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  26. Kinetic Memories. An embodied form of remembering the personal past.Marina Trakas - 2021 - Journal of Mind and Behavior 42 (2):139-174.
    Despite the popularity that the embodied cognition thesis has gained in recent years, explicit memories of events personally experienced are still conceived as disembodied mental representations. It seems that we can consciously remember our personal past through sensory imagery, through concepts, propositions and language, but not through the body. In this article, I defend the idea that the body constitutes a genuine means of representing past personal experiences. For this purpose, I focus on the analysis of bodily movements associated with (...)
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  27.  10
    Reconciling Kinetic and Quantum Theory.B. Gaveau & L. S. Schulman - 2020 - Foundations of Physics 50 (2):55-60.
    We show that in a dilute gas the wave function’s spreading is limited by scattering off other particles. This shows that quantum mechanics can be consistent with the kinetic theory of gases.
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  28.  27
    Enzyme organization and stability of metabolic pathways: A comparison of various approaches.Robert Costalat - 1996 - Acta Biotheoretica 44 (3-4):235-247.
    The aim of this paper is to compare various methods for the quantification of metabolic pathways dynamics. A Yates-Pardee metabolic pathway with enzyme organization, i.e. with spatial localization of the enzymes in a specific cellular compartment, was studied using: (i) the classical Henri-Michaelis-Menten (HMM) equations, (ii) linearization of the HMM equations in the vicinity of a steady state (linearized formalism), and (iii) Biochemical Systems Theory formalism (BST formalism). It is shown that transient solutions computed via either the linearized formalism (...)
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  29.  19
    Epicurus’ “Kinetic” and “Katastematic” Pleasures. A Reappraisal.Yosef Z. Liebersohn - 2015 - Elenchos 36 (2):271-296.
    In this paper I shall offer new definitions for what seem to be the most dominant terms in Epicurus’ theory of pleasures - “kinetic” and “katastematic”. While most of the scholarly literature treats these terms as entirely concerned with states of motion and states of stability, I shall argue that the distinction concerns whether pain is or is not removed by this or that pleasure. As the removal of pain is a necessary condition for the Epicurean goal of ataraxia and (...)
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  30.  8
    A kinetic approach to interstitial clustering in neutron irradiated metals.A. C. Damask & G. J. Dienes - 1967 - Philosophical Magazine 15 (133):199-204.
  31.  25
    Visuo-Kinetic Signs Are Inherently Metonymic: How Embodied Metonymy Motivates Forms, Functions, and Schematic Patterns in Gesture.Irene Mittelberg - 2019 - Frontiers in Psychology 10:346848.
    TThis paper aims to evidence the inherently metonymic nature of co-speech gestures. Arguing that motivation in gesture involves iconicity (similarity), indexicality (contiguity), and habit (conventionality) to varying degrees, it demonstrates how a set of metonymic principles may lend a certain systematicity to experientially grounded processes of gestural abstraction and enaction. Introducing visuo-kinetic signs as an umbrella term for co-speech gestures and signed languages, the paper shows how a frame-based approach to gesture may integrate different cognitive/functional linguistic and semiotic accounts of (...)
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  32.  10
    Methods for enzyme library creation: Which one will you choose?Lorea Alejaldre, Joelle N. Pelletier & Daniela Quaglia - 2021 - Bioessays 43 (8):2100052.
    Enzyme engineering allows to explore sequence diversity in search for new properties. The scientific literature is populated with methods to create enzyme libraries for engineering purposes, however, choosing a suitable method for the creation of mutant libraries can be daunting, in particular for the novices. Here, we address both novices and experts: how can one enter the arena of enzyme library design and what guidelines can advanced users apply to select strategies best suited to their purpose? Section (...)
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  33.  29
    Sublime Kinetic Melody: Kelly Slater and the Extreme Spectator.Carl Thomen - 2010 - Sport, Ethics and Philosophy 4 (3):319-331.
    This paper aims to examine the awesome, almost spiritual feeling I experience as an?extreme spectator? while watching Kelly Slater ride the monstrous waves of Pipeline. Drawing on the aesthetics of Kant and Schopenhauer, I examine the experience of the sublime and how it, in conjunction with the perceived kinetic melody of Slater's movements and his karmic connection to the environment in which he thrives, gives rise to the deeply felt awe of the extreme spectator. My intention is to use Slater's (...)
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  34.  14
    Deubiquitinating Enzymes in Model Systems and Therapy: Redundancy and Compensation Have Implications.Sarah Zachariah & Douglas A. Gray - 2019 - Bioessays 41 (11):1900112.
    The multiplicity of deubiquitinating enzymes (DUBs) encoded by vertebrate genomes is partly attributable to whole genome duplication events that occurred early in chordate evolution. By surveying the literature for the largest family of DUBs (the ubiquitin-specific proteases), extensive functional redundancy for duplicated genes has been confirmed as opposed to singletons. Dramatically conflicting results have been reported for loss of function studies conducted through RNA interference as opposed to inactivating mutations, but the contradictory findings can be reconciled by a recently proposed (...)
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  35.  28
    Kinetics of pleuridial growth in antithamnion plumula (rhodophyceae).Cécile Lambert, Roger Buis & Marie-Thérèse L'Hardy-Halos - 1992 - Acta Biotheoretica 40 (2-3):169-175.
    The filamentous and branched thallus of Antithamnion plumula is constitued of two different kinds of branches with apical growth: the cladomial axes with a continuous or indefinite growth, and the pleuridia with a limited growth. The size of the pleuridia depends on their position with respect to the lateral cladomial axes.The growth kinetics of 35 pleuridia were analysed using Nelder's generalized logistics. Each sigmoidal curve, which was divided into four growth stages from the instantaneous acceleration variations, was thus characterized (...)
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  36.  26
    Kinetic epidemiological model for elucidating sexual difference of hypertension (KCIS no.20).Amy M.-F. Yen & Tony H.-H. Chen - 2011 - Journal of Evaluation in Clinical Practice 17 (1):130-135.
  37.  11
    Kinetic Synaesthesia: Experiencing Dance in Multimedia Scenographies.Marc Boucher - 2004 - Contemporary Aesthetics 2.
  38.  53
    Digestive enzyme secretion, intuition, and the history of science: Part II. [REVIEW]Lois Isenman - 2009 - Foundations of Science 14 (4):331-349.
    A companion paper explored the role of intuition in the genesis of an alternative theory for the secretion of pancreatic digestive enzymes, looking through the lens of three philosophers/historians of science. Gerald Holton, the last scholar, proposed that scientific imagination is shaped by a number of thematic presuppositions, which function largely below awareness. They come in pairs of opposites that alternately gain cultural preeminence. The current paper examines three thematic presuppositions inherent to both the generally accepted model for digestive (...) secretion and most consciousness-centered views of higher-level cognition—discreteness, reduction, and simplicity. Since they often build on each other, together they are referred to as the simplicity worldview . Also considered are the three opposite thematic assumptions inherent to both the alternative model for digestive enzyme secretion and intuition-friendly views of higher-level cognition—the continuum, holism, and complexity—together referred to as the complexity worldview . The article highlights the potential importance to scientific knowledge of this currently less favored worldview. (shrink)
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  39.  6
    Chemical kinetics and diffusion approach: the history of the Klein–Kramers equation.Stefano Zambelli - 2010 - Archive for History of Exact Sciences 64 (4):395-428.
    In this essay, the first statistical and stochastic treatments of chemical dynamics are analyzed and discussed, in particular the diffusive description of chemical reactions. The first part of the paper introduces the historical and methodological basis of the theories about stochastic processes and diffusion as well as their lesser-known applications in chemical kinetics, which were advanced by Jens Anton Christiansen (1888–1969). In the second, part we will focus our attention on the early works of Oskar Benjamin Klein (1894–1977) and (...)
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  40.  9
    Geochemical Kinetics.Youxue Zhang - 2008 - Princeton University Press.
    This book offers a comprehensive exploration of geochemical kinetics--the application of chemical kinetics to geological problems, both theoretical and practical.
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  41.  25
    Diffusion kinetics in dilute binary alloys with the h.c.p. crystal structure.A. R. Allnatt, I. V. Belova & G. E. Murch - 2014 - Philosophical Magazine 94 (22):2487-2504.
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  42.  16
    Climb kinetics of dislocation loops in aluminium.P. S. Dobson, P. J. Goodhew & R. E. Smallman - 1967 - Philosophical Magazine 16 (139):9-22.
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  43.  25
    Kinetics of circular DNA molecule digestion by restriction endonuclease computation of kinetic constants from time dependence of fragment concentrations.Petr Karlovský - 1986 - Acta Biotheoretica 35 (4):279-292.
    A model for kinetics of circular substrate cleavage by restriction endonuclease was formulated. The aim of the analysis of the model was to extract kinetic constants for all target sites from time- dependence of fragment concentration in reaction products. That was proved to be possible for molecules with an odd number of fragments only. A symmetry of the molecules with an even number of fragment is the cause. A solution for molecules with an odd number of fragments was found (...)
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  44. Further Kinetics of Gravitational Motion.Peter G. Bass - 2004 - Apeiron 11 (1).
     
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  45.  95
    Philosophy and the kinetic theory of gases.Henk W. de Regt - 1996 - British Journal for the Philosophy of Science 47 (1):31-62.
    This article examines the role of philosophy in the development of the kinetic theory of gases. Two opposing accounts of this role, by Peter Clark and John Nyhof, are discussed and criticized. Contrary to both accounts, it is argued that philosophical views of scientists can fundamentally influence the results of their scientific work. This claim is supported by a detailed analysis of the philosophical views of Maxwell and Boltzmann, and of their work on the kinetic theory, especially concerning the so-called (...)
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  46.  3
    Kinetics of the crystallization of icosahedral phase in ultra thin deposits of Al62Cu25.5Fe12.5alloy.N. Bonasso & P. Pigeat - 2006 - Philosophical Magazine 86 (3-5):275-280.
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  47.  15
    Kinetic Values, Mobility (in)equalities, and Ageing in Smart Urban Environments.Jaana Parviainen - 2021 - Ethical Theory and Moral Practice 24 (5):1139-1153.
    The idea of the right to mobility has been fundamental to modern Western citizenship and is expressed in many legal and government documents. Although there is widespread acceptance regarding the importance of mobility in older adults, there have been few attempts to develop ethical and theoretical tools to portray mobility equalities in old age. This paper develops a novel conceptualisation of kinetic values focusing on older adults whose ability to move has been restricted for internal and external reasons. Informed by (...)
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  48.  12
    Reaction kinetics of non-localised particle–trap complexes.A. V. Barashev, S. I. Golubov, YuN Osetsky & R. E. Stoller - 2010 - Philosophical Magazine 90 (7-8):897-906.
  49.  27
    Kinetics of the allotropic hcp–fcc phase transformation in cobalt.Rico Bauer, Eric A. Jägle, Wolfgang Baumann & Eric Jan Mittemeijer - 2011 - Philosophical Magazine 91 (3):437-457.
  50.  14
    The kinetics of mammalian gene expression.James L. Hargrove, Martin G. Hulsey & Elmus G. Beale - 1991 - Bioessays 13 (12):667-674.
    When rates of transcription from specific genes change, delays of variable length intervene before the corresponding mRNAs and proteins attain new levels. For most mammalian genes, the time required to complete transcription, processing, and transport of mRNA is much shorter than the period needed to achieve a new, steady‐state level of protein. Studies of inducible genes have shown that the period required to attain new levels of individual mRNAs and proteins is related to their unique half‐lives. The basis for this (...)
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