Thematische Bibliographien / Replicating

Inhaltsverzeichnis

  1. Zeitschriftenartikel
  2. Dissertationen
  3. Bücher
  4. Buchteile
  5. Konferenzberichte
  6. Berichte der Organisationen

Auswahl der wissenschaftlichen Literatur zum Thema „Replicating“

Autor: Grafiati
Veröffentlicht am 29. Juni 2021
Zuletzt aktualisiert am 8. Februar 2022

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Zeitschriftenartikel zum Thema "Replicating"

1

Coffman, Lucas C., Muriel Niederle und Alistair J. Wilson. „A Proposal to Organize and Promote Replications“. American Economic Review 107, Nr. 5 (01.05.2017): 41–45. http://dx.doi.org/10.1257/aer.p20171122.

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We make a two-pronged proposal to (i) strengthen the incentives for replication work and (ii) better organize and draw attention to the replications that are conducted. First we propose that top journals publish short “replication reports.” These reports could summarize novel work replicating an existing high-impact paper, or they could highlight a replication result embedded in a wider-scope published paper. Second, we suggest incentivizing replications with the currency of our profession: citations. Enforcing a norm of citing replication work alongside the original would provide incentives for replications to both authors and journals.
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Robinson, D. R., und K. Gull. „The configuration of DNA replication sites within the Trypanosoma brucei kinetoplast.“ Journal of Cell Biology 126, Nr. 3 (01.08.1994): 641–48. http://dx.doi.org/10.1083/jcb.126.3.641.

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The kinetoplast is a concatenated network of circular DNA molecules found in the mitochondrion of many trypanosomes. This mass of DNA is replicated in a discrete "S" phase in the cell cycle. We have tracked the incorporation of the thymidine analogue 5-bromodeoxyuridine into newly replicated DNA by immunofluorescence and novel immunogold labeling procedures. This has allowed the detection of particular sites of replicated DNA in the replicating and segregating kinetoplast. These studies provide a new method for observing kinetoplast DNA (kDNA) replication patterns at high resolution. The techniques reveal that initially the pattern of replicated DNA is antipodal and can be detected both on isolated complexes and in replicating kDNA in vivo. In Trypanosoma brucei the opposing edges of replicating kDNA never extend around the complete circumference of the network, as seen in other kinetoplastids. Furthermore, crescent-shaped labeling patterns are formed which give way to labeling of most of the replicating kDNA except the characteristic midzone. The configuration of these sites of replicated DNA molecules is different to previous studies on organisms such as Crithidia fasciculata, suggesting differences in the timing of replication of mini and maxicircles and/or organization of the replicative apparatus in the kinetoplast of the African trypanosome.
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Kelly, Clint D. „Rate and success of study replication in ecology and evolution“. PeerJ 7 (10.09.2019): e7654. http://dx.doi.org/10.7717/peerj.7654.

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The recent replication crisis has caused several scientific disciplines to self-reflect on the frequency with which they replicate previously published studies and to assess their success in such endeavours. The rate of replication, however, has yet to be assessed for ecology and evolution. Here, I survey the open-access ecology and evolution literature to determine how often ecologists and evolutionary biologists replicate, or at least claim to replicate, previously published studies. I found that approximately 0.023% of ecology and evolution studies are described by their authors as replications. Two of the 11 original-replication study pairs provided sufficient statistical detail for three effects so as to permit a formal analysis of replication success. Replicating authors correctly concluded that they replicated an original effect in two cases; in the third case, my analysis suggests that the finding by the replicating authors was consistent with the original finding, contrary the conclusion of “replication failure” by the authors.
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van ’t Wout, Angélique B., Hetty Blaak, Leonie J. Ran, Margreet Brouwer, Carla Kuiken und Hanneke Schuitemaker. „Evolution of Syncytium-Inducing and Non-Syncytium-Inducing Biological Virus Clones in Relation to Replication Kinetics during the Course of Human Immunodeficiency Virus Type 1 Infection“. Journal of Virology 72, Nr. 6 (01.06.1998): 5099–107. http://dx.doi.org/10.1128/jvi.72.6.5099-5107.1998.

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ABSTRACT To investigate the temporal relationship between human immunodeficiency virus type 1 (HIV-1) replicative capacity and syncytium-inducing (SI) phenotype, biological and genetic characteristics of longitudinally obtained virus clones from two HIV-1-infected individuals who developed SI variants were studied. In one individual, the emergence of rapidly replicating SI and non-syncytium-inducing (NSI) variants was accompanied by a loss of the slowly replicating NSI variants. In the other subject, NSI variants were always slowly replicating, while the coexisting SI variants showed an increase in the rate of replication. Irrespective their replicative capacity, the NSI variants remained present throughout the infection in both individuals. Phylogenetic analysis of the V3 region showed early branching of the SI variants from the NSI tree. Successful SI conversion seemed a unique event since no SI variants were found among later-stage NSI variants. This was also confirmed by the increasing evolutionary distance between the two subpopulations. At any time point during the course of the infection, the variation within the coexisting SI and NSI populations did not exceed 2%, indicating continuous competition within each viral subpopulation.
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Quintini, G., K. Treuner, C. Gruss und R. Knippers. „Role of amino-terminal histone domains in chromatin replication.“ Molecular and Cellular Biology 16, Nr. 6 (Juni 1996): 2888–97. http://dx.doi.org/10.1128/mcb.16.6.2888.

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Simian virus 40 minichromosomes were treated with trypsin to specifically remove the amino-terminal histone domains (tails). Trypsin treatment does not affect the spacing and the number of nucleosomes on minichromosomes but indices a more extended conformation, as shown by the reduced sedimentation coefficient of trypsinized minichromosomes compared with the untreated controls. Trypsinized minichromosomes replicate more efficiently than control minichromosomes in in vitro replication assays. The increased template efficiency appears to be due to higher rates of replicative fork movement. In vitro replication in the presence of protein-free competitor DNA shows that replicating trypsinized minichromosomes do not lose nucleosomes and replicating competitor DNA does not gain nucleosomes. This finding suggests that tailless nucleosomes are transferred from the unreplicated prefork stem to replicated DNA branches and excludes a participation of the basic histone domains in nucleosome transfer.
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Walker, Richard M., Gene A. Brewer, M. Jin Lee, Nicolai Petrovsky und Arjen van Witteloostuijn. „Best Practice Recommendations for Replicating Experiments in Public Administration“. Journal of Public Administration Research and Theory 29, Nr. 4 (14.08.2018): 609–26. http://dx.doi.org/10.1093/jopart/muy047.

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Abstract Replication is an important mechanism through which broad lessons for theory and practice can be drawn in the applied interdisciplinary social science field of public administration. We suggest a common replication framework for public administration that is illustrated by experimental work in the field. Drawing on knowledge from other disciplines, together with our experience in replicating several experiments on topics such as decision making, organizational rules, and government–citizen relationships, we provide an overview of the replication process. We then distill this knowledge into seven decision points that offer a clear set of best practices on how to design and implement replications in public administration. We conclude by arguing that replication should be part of the normal scientific process in public administration to help to build valid middle-range theories and provide valuable lessons to practice.
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Hasse, Steven B., und Michele P. Calos. „Replication control of autonomously replicating human sequence“. Nucleic Acids Research 19, Nr. 18 (1991): 5053–58. http://dx.doi.org/10.1093/nar/19.18.5053.

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8

Reggia, James A., Jason D. Lohn und Hui-Hsien Chou. „Self-Replicating Structures: Evolution, Emergence, and Computation“. Artificial Life 4, Nr. 3 (Juli 1998): 283–302. http://dx.doi.org/10.1162/106454698568594.

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Since von Neumann's seminal work around 1950, computer scientists and others have studied the algorithms needed to support self-replicating systems. Much of this work has focused on abstract logical machines (automata) embedded in two-dimensional cellular spaces. This research was motivated by the desire to understand the basic information-processing principles underlying self-replication, the potential long-term applications of programmable self-replicating machines, and the possibility of gaining insight into biological replication and the origins of life. We view past research as taking three main directions: early complex universal computer-constructors modeled after Turing machines, qualitatively simpler self-replicating loops, and efforts to view self-replication as an emergent phenomenon. We discuss our recent studies in the latter category showing that self-replicating structures can emerge from nonreplicating components, and that genetic algorithms can be applied to program automatically simple but arbitrary structures to replicate. We also describe recent work in which self-replicating structures are successfully programmed to do useful problem solving as they replicate. We conclude by identifying some implications and important research directions for the future.
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Avemann, K., R. Knippers, T. Koller und J. M. Sogo. „Camptothecin, a specific inhibitor of type I DNA topoisomerase, induces DNA breakage at replication forks.“ Molecular and Cellular Biology 8, Nr. 8 (August 1988): 3026–34. http://dx.doi.org/10.1128/mcb.8.8.3026.

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The structure of replicating simian virus 40 minichromosomes, extracted from camptothecin-treated infected cells, was investigated by biochemical and electron microscopic methods. We found that camptothecin frequently induced breaks at replication forks close to the replicative growth points. Replication branches were disrupted at about equal frequencies at the leading and the lagging strand sides of the fork. Since camptothecin is known to be a specific inhibitor of type I DNA topoisomerase, we suggest that this enzyme is acting very near the replication forks. This conclusion was supported by experiments with aphidicolin, a drug that blocks replicative fork movement, but did not prevent the camptothecin-induced breakage of replication forks. The drug teniposide, an inhibitor of type II DNA topoisomerase, had only minor effects on the structure of these replicative intermediates.
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Avemann, K., R. Knippers, T. Koller und J. M. Sogo. „Camptothecin, a specific inhibitor of type I DNA topoisomerase, induces DNA breakage at replication forks“. Molecular and Cellular Biology 8, Nr. 8 (August 1988): 3026–34. http://dx.doi.org/10.1128/mcb.8.8.3026-3034.1988.

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The structure of replicating simian virus 40 minichromosomes, extracted from camptothecin-treated infected cells, was investigated by biochemical and electron microscopic methods. We found that camptothecin frequently induced breaks at replication forks close to the replicative growth points. Replication branches were disrupted at about equal frequencies at the leading and the lagging strand sides of the fork. Since camptothecin is known to be a specific inhibitor of type I DNA topoisomerase, we suggest that this enzyme is acting very near the replication forks. This conclusion was supported by experiments with aphidicolin, a drug that blocks replicative fork movement, but did not prevent the camptothecin-induced breakage of replication forks. The drug teniposide, an inhibitor of type II DNA topoisomerase, had only minor effects on the structure of these replicative intermediates.
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Dissertationen zum Thema "Replicating"

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Wood, Evan Alexander. „Designing hypercyclic replicating networks /“. St Andrews, 2007. http://hdl.handle.net/10023/360.

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Wood, Evan A. „Designing hypercyclic replicating networks“. Thesis, University of St Andrews, 2007. http://hdl.handle.net/10023/360.

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In the last 20 years there has been a number of synthetic and natural product based molecular replicators published in the literature. The majority of these systems have focused on the minimal model with only a few examples of cross-catalytic or reciprocal replication. Of the cross-catalytic systems investigated the majority focus around the use of natural products, oligonucleotides, peptides etc. This thesis will investigate the design, synthesis and kinetic analysis of both synthetic minimal and reciprocal replicating systems, and how these two forms of replication interact in a complex hypercyclic network. Chapter 1 introduces key concepts such as molecular recognition, intramolecularity/ enzyme kinetic, bisubstrate systems and the work conducted into replication systems to date. Chapter 2 describes the design, synthesis and kinetic analysis of a reciprocal replicating system, based on Diels-Alder and 1,3-dipolar cycloadditions, before going on to discuss what we have learned and how this system can be improved. Chapter 3 focuses on the design, synthesis and kinetic analysis of a replicating network (minimal and reciprocal replication), based on 1,3-dipolar cycloadditions. Initial individual systems are examined in isolation to determine their behavior and nature. After which the systems are combined to observe how each species interacts in a potential complex hypercyclic network. Chapter 4 investigates the redesign of the replicating network in Chapter 3 in order to overcome the problems identified from its kinetic analysis. Chapter 5 introduces the shift in direction away from kinetically controlled replicating networks towards systems in thermodynamic equilibrium.
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Bengtsson, Marie. „The art of replicating /“. Linköping : Department of Management and Engineering, Linköping University, 2008. http://www.bibl.liu.se/liupubl/disp/disp2008/arts462s.pdf.

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Uhlig, Tobias [Verfasser]. „Self-Replicating Individuals / Tobias Uhlig“. München : Verlag Dr. Hut, 2015. http://d-nb.info/1077404018/34.

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Prywes, Noam. „Towards Self-Replicating Informational Polymers“. Thesis, Harvard University, 2016. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493609.

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The capability to transmit information from generation to generation is an essential feature of life. In all terrestrial life, DNA and RNA contain information in the form of a sequence of monomers and are copied in every generation. The RNA world hypothesis posits that there was a time in the history of life when all cellular functions were accomplished by RNA catalysts. However, the initial emergence of those RNA catalysts is not yet fully understood. Nonenzymatic RNA polymerization has been proposed as a potential stepping- stone from prebiotic chemistry to the RNA world. In searching for alternatives to the chemically trapped triphosphate nucleotides found in modern biology, chemical modifications of RNA have been discovered that allow for the copying of RNA. However, the copying of sequences rich in adenine and uracil residues remains a significant challenge. In chapter 2 we use chemically activated oligonucleotides as catalysts to copy all four monomers sequentially, potentially creating a route for the copying of any sequence without a polymerase and contributing to a model for the emergence of evolution. Replacing uracil with 2-thiouracil and 2-thiothymine, modified forms of uracil found in modern life, has proven to improve the reactivity and fidelity of nonenzymatic RNA polymerization. In chapter 3, we tested these alternatives to uracil as substrates and components of an RNA polymerase ribozyme. We discovered that they were superior in the context of ribozyme mediated RNA polymerization both in terms of faster rate and higher fidelity. We then synthesized ribozymes in which every instance of uracil was replaced by either 2-thiouracil or 2-thiothymine and found them to retain some activity. We hypothesize that these alternative nucleobases could have conferred significant benefits to early life forms. To explore alternative genetic systems to DNA and RNA, in chapter 4 of this thesis we synthesized an organic-soluble copolymer with two different monomers capable of reversible covalent bond formation with one another. We show that information copying is possible with this polymer by synthesizing a polymer with a sequence complementary to a template while it is still covalently bound to that template, demonstrating that nucleic acids are not the only molecules capable of information storage and replication. Together, these results assist in the construction of artificial life and expand the possibilities for the emergence of life.
Chemistry and Chemical Biology
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Najmabadi, Hossein. „Characterization of the Self-Replicating Kirsten Murine Leukemia Viral DNA: Replication and Tetracycline Resistance“. Thesis, University of North Texas, 1989. https://digital.library.unt.edu/ark:/67531/metadc798479/.

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This research project deals with the characterization of self-replicating Kirsten murine viral DNA. The replication of this viral DNA and tetracycline resistance conferred to bacteria by this viral DNA will be studied. The restriction endonuclease and Southern blot analysis revealed a fragment of pBR322 from the Hind III and Pst I site that is located in the 3' end of the MLV-K:E molecule. Single stranded sequencing of the two terminal ends of this fragment verified that the 3' end of MLV-K:E contains identical sequence homology to pBR322. The presence of this pBR322 fragment explains the unusual properties of the MLV-K:E molecule. However, tetracycline resistance is less in E. Coli containing MLV-K:E than E. coli containing pBR322 as determined by zone of inhibition assay. This may be due to alteration in the promoter region of the tetracycline gene.
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Wu, Cunle. „cDNA clones contain autonomously replicating sequences“. Thesis, McGill University, 1992. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=41041.

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We have shown that nine cDNA clones, which were derived from an oligo (dT) primed cDNA library of human embryonic lung fibroblast (IMR90), are capable of supporting autonomous replication of bacterial plasmid in mammalian (HeLa) cells. Two of these cDNA clones contain a region homologous to "O"-family middle repetitive sequences; the other seven clone hybridize with neither "O"-family nor Alu family sequences and are called NOA clones. Oligo (dT) primed cDNA of IMR90 has been demonstrated to be an enriched source for autonomously replicating sequences. Two out of three "O"-family homologous cDNA clones and seven out of ten NOA clones were capable of autonomous replication. In contrast, none of the five clones, which contained Alu repetitive sequences, demonstrated replicative potential. The two autonomously replicating, "O"-family homologous cDNA, 343 and 363, were characterized in the greatest detail. In particular, sequence and structural features of a 448 bp fragment of cDNA 343, which was capable of supporting autonomous replication activity, were: extensive asymmetrical A/T-rich regions; 10/11 match to yeast ARS consensus; scaffold attachment region consensus of Drosophila; bent DNA; a DNA unwinding element and an in vitro matrix binding activity. We have used a PCR-based mapping strategy to identify an in vivo initiation zone located in a region of approximately 1.6 kb which is inclusive of cDNA 343. The 343 sequence has been localized to the long arm (6q22-6qter) of human chromosome 6 by both Southern analysis of hamster-human cell hybrids and in situ hybridization. Transcripts homologous to 343 have been detected in both poly(A$ sp+$) and non-poly(A$ sp+$) RNA fractions to be 1.3 kb and 5 kb, respectively; the 1.3 kb transcript is greatly enriched in poly(A$ sp+$) RNA fraction, and the 5 kb transcript is present predominantly in non-poly(A$ sp+$) RNA fraction. The detailed characterization of 343 genomic locus demonstrated that the 343 sequence is conserv
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Penzes, Zoltan. „Defective replicating RNAs of coronavirus infectious bronchitis virus : investigation of replication and genome packaging signals“. Thesis, University of Hertfordshire, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283879.

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Nguyen, Rémi. „Dynamic combinatorial mesophases and self-replicating systems“. Strasbourg, 2010. http://www.theses.fr/2010STRA6285.

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Mon travail de thèse a consisté à développer des systèmes de blocs amphiphiles combinatoires dynamiques pour étudier de possibles phénomènes d’auto-organisation hiérarchique dans l’espace et dans le temps. Pour cela, j’ai combiné des associations réversibles de blocs hydrophiles et hydrophobes en étudiant deux types possibles de contrôle : a) un contrôle moléculaire externe sur les liaisons entre blocs de manière à forcer l’expression d’une mésophase particulière ; et b) un contrôle supramoléculaire interne dicté par la formation préférentielle d’une mésophase, avec sélection spontanée des blocs qui la composent. Lors de ce travail, j’ai pu démontrer pour la première fois la possibilité d’étendre la chimie combinatoire dynamique aux systèmes à micro-séparation de phase. Pour y parvenir, j’ai développé un nouveau type d’objets dynamiques (Dynablocks) et j’ai pu mettre en évidence des comportements très originaux de ces derniers qu’ils soient d’ordre cinétique (auto-réplication) ou thermodynamique (sélection au sein de mélange) ; j’ai également montré que ces deux aspects pouvaient être réunis au sein de processus d’auto-organisation. Pour caractériser les mélanges, de nouvelles méthodes de combinaisons linéaires pour l’analyse des diffusions du rayonnement ont été développées. Cette étude fondamentale constitue une nouvelle ouverture de la chimie combinatoire dynamique aux frontières avec deux domaines d’importance : a) la science des matériaux et b) la chimie des systèmes – en particulier des systèmes autonomes minimaux (i. E. Autopoiétiques)
My PhD work consisted in developing combinatorial dynamic systems of amphiphilic block copolymers to study their hierarchical self-organization processes in space and time. For this I combined reversible associations between hydrophobic and hydrophilic blocks, focusing on two possible kinds of control of these responsive systems: a) an external molecular control on the reversible covalent bonds between the blocks in order to favour the expression of a particular mesophase; and b) an internal supramolecular control driven by the preferential formation of a mesophase leading to spontaneous selection of its own composing blocks. During this work, I demonstrated for the first time the possibility to extend dynamic combinatorial chemistry to systems with phase micro-separation. For this, I developed a new type of dynamic molecules (Dynablocks) and I discovered some interesting behaviours from the mesophases I obtained, such as self-replication on a kinetic point of view, or selection/adaptation process within a mixture on a thermodynamic point of view. I also demonstrated that these to aspects could be coupled together in an auto-organization process. To characterize those complex mixtures, new analytical methods were developed for scattering techniques, based on linear combinations. This fundamental study opens a new field of investigation for dynamic combinatorial chemistry in relations with two important domains: a) material science and b) system chemistry – particularly minimal autonomous systems (i. E. Autopoietics systems)
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Myers, Shere Lynne. „Cellular Effects of Replicating a Polypurine-Polypyrimidine Sequence and the Interactions of DUE-B with Replication Proteins“. Wright State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=wright1292507800.

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Bücher zum Thema "Replicating"

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Dormitzer, Philip R., Christian W. Mandl und Rino Rappuoli, Hrsg. Replicating Vaccines. Basel: Springer Basel, 2011. http://dx.doi.org/10.1007/978-3-0346-0277-8.

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Gabowitsch, Mischa, Hrsg. Replicating Atonement. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2.

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Kaplan, Marilyn E. Replicating historic elevator enclosures. Washington, D.C: National Park Service, U.S. Dept. of the Interior, 1989.

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Hartnell, Tim. Replicating reality: Exploring computer simulations. London: Interface, 1985.

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W, Mandl Christian, Rappuoli Rino und SpringerLink (Online service), Hrsg. Replicating Vaccines: A New Generation. Basel: Springer Basel, 2011.

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Replicating dreams: A comparative study of Grameen bank and its replication, Kashf Foundation, Pakistan. Karachi: Oxford University Press, 2009.

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O'Brien, Thomas J. How option replicating portfolio insurance works: Expanded details. New York: SalomonBrothers Center for the Study of Financial Institutions, 1988.

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O'Brien, Thomas J. How option replicating portfolio insurance works: Expanded details. New York: Salomon Brothers Center for the Study of Financial Institutions, Leonard N. Stern School of Business, New York University, 1989.

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Akihiko, Takahashi. Replicating exemplary practices in mathematics education among APEC economies. Singapore: APEC Human Resource Development Working Group, 2010.

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Bolt, Nancy. Building careers--reflecting culture and communities: Replicating the Urban Library Program. St. Paul, MN: St. Catherine University, 2009.

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Buchteile zum Thema "Replicating"

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Gabowitsch, Mischa. „Replicating Atonement: The German Model and Beyond“. In Replicating Atonement, 1–21. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_1.

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von Bieberstein, Alice. „Memorial Miracle: Inspiring Vergangenheitsbewältigung Between Berlin and Istanbul“. In Replicating Atonement, 237–65. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_10.

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Gabowitsch, Mischa. „Foils and Mirrors: The Soviet Intelligentsia and German Atonement“. In Replicating Atonement, 267–302. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_11.

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Mihr, Anja. „From Guilty Generation to Expert Generation? Personal Reflections on Second Post-war Generation West German Atonement“. In Replicating Atonement, 305–23. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_12.

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Neiman, Susan. „Notes After Mississippi“. In Replicating Atonement, 325–39. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_13.

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Seraphim, Franziska. „A Japan that Cannot Say Sorry?“ In Replicating Atonement, 25–46. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_2.

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Haugbolle, Sune. „“Best Practices” of Global Memory and the Politics of Atonement in Lebanon“. In Replicating Atonement, 47–70. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_3.

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David, Lea. „Lost in Transaction in Serbia and Croatia: Memory Content as a Trade Currency“. In Replicating Atonement, 73–97. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_4.

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Kaya, Ayhan. „Turkish Vergangenheitsbewältigung: The Unbearable Burden of the Past“. In Replicating Atonement, 99–127. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_5.

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Nießer, Jacqueline. „Which Commemorative Models Help? A Case Study from Post-Yugoslavia“. In Replicating Atonement, 131–61. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65027-2_6.

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Konferenzberichte zum Thema "Replicating"

1

Heighton, M. „Replicating Historic Vessels“. In Historic Ships 2012. RINA, 2012. http://dx.doi.org/10.3940/rina.hist.2012.08.

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2

Luu, Devin K., Cedric Dumas, Timothy R. Coles, Jinling Wang und Caroline G. L. Cao. „Replicating Contralateral Haptic Feedback“. In 2015 IEEE International Conference on Systems, Man, and Cybernetics (SMC). IEEE, 2015. http://dx.doi.org/10.1109/smc.2015.84.

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3

Gong, L. „Securely replicating authentication services“. In Proceedings. The 9th International Conference on Distributed Computing Systems. IEEE, 1989. http://dx.doi.org/10.1109/icdcs.1989.37934.

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O'Toole, James, und Scott Nettles. „Concurrent replicating garbage collection“. In the 1994 ACM conference. New York, New York, USA: ACM Press, 1994. http://dx.doi.org/10.1145/182409.182425.

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Guess, Trent M., und Lorin P. Maletsky. „Computational Modeling of a Dynamic Knee Simulator for Reproduction of Joint Loading“. In ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-43069.

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A three-dimensional dynamic computational model was developed for the dual purposes of predicting and replicating joint loading generated by a five-axis dynamic knee simulator. The model was verified through an analog knee that was constrained for accurate modeling and instrumented to directly measure joint forces. The verified model was then used to generate control profiles to the five axes of the simulator for replication of desired joint loading. Reproduction of a walking profile is demonstrated.
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Reed, Kyle B., James Patton und Michael Peshkin. „Replicating Human-Human Physical Interaction“. In 2007 IEEE International Conference on Robotics and Automation. IEEE, 2007. http://dx.doi.org/10.1109/robot.2007.364032.

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Ellery, Alex A. „Are Self-Replicating Machines Feasible?“ In AIAA SPACE 2015 Conference and Exposition. Reston, Virginia: American Institute of Aeronautics and Astronautics, 2015. http://dx.doi.org/10.2514/6.2015-4653.

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8

Williams, Lance. „Self-Replicating Distributed Virtual Machines“. In Artificial Life 14: International Conference on the Synthesis and Simulation of Living Systems. The MIT Press, 2014. http://dx.doi.org/10.7551/978-0-262-32621-6-ch114.

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Karamchandani, Sunil, Satyajit Sinari, Amrita Aurora und Dharmesh Ruparel. „The Gesture Replicating Robotic Arm“. In 2013 International Symposium on Computational and Business Intelligence (ISCBI). IEEE, 2013. http://dx.doi.org/10.1109/iscbi.2013.11.

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Ghezzi, Giacomo, und Harald C. Gall. „Replicating mining studies with SOFAS“. In 2013 10th IEEE Working Conference on Mining Software Repositories (MSR 2013). IEEE, 2013. http://dx.doi.org/10.1109/msr.2013.6624050.

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Berichte der Organisationen zum Thema "Replicating"

1

Hou, Kewei, Chen Xue und Lu Zhang. Replicating Anomalies. Cambridge, MA: National Bureau of Economic Research, Mai 2017. http://dx.doi.org/10.3386/w23394.

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Lin, Jacky, Genevieve Selden, John Shoven und Clemens Sialm. Replicating the Dow Jones Industrial Average. Cambridge, MA: National Bureau of Economic Research, März 2021. http://dx.doi.org/10.3386/w28528.

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FINFROCK SH. MCNP5 CALCULATIONS REPLICATING ARH-600 NITRATE DATA. Office of Scientific and Technical Information (OSTI), Oktober 2011. http://dx.doi.org/10.2172/1047869.

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Buijvoets, Martinus, Bob Walrave, Jukka-Matti Turtiainen und Gregory Watson. Replicating Lean Six Sigma Green Belt Education. Purdue University, 2021. http://dx.doi.org/10.5703/1288284317328.

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5

Kaliberov, Sergey A. Therapy of Breast Cancers Using Conditionally Replicating Adenovirus. Fort Belvoir, VA: Defense Technical Information Center, August 2005. http://dx.doi.org/10.21236/ada447528.

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Dewhurst, Stephen. New Conditionally Replicating Adenovirus Vectors for Breast Cancer Therapy. Fort Belvoir, VA: Defense Technical Information Center, September 2008. http://dx.doi.org/10.21236/ada502798.

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Brumbach, Michael T., Alex James Mirabal, Michael Kalan, Ana B. Trujillo und Kevin Hale. Materials Chemistry and Performance of Silicone-Based Replicating Compounds. Office of Scientific and Technical Information (OSTI), November 2014. http://dx.doi.org/10.2172/1164595.

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Matt Nurse, Matt Nurse. Fighting fake news by replicating the motivated numeracy effect. Experiment, September 2017. http://dx.doi.org/10.18258/10022.

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Robert Bratton. Progress in Developing Finite Element Models Replicating Flexural Graphite Testing. Office of Scientific and Technical Information (OSTI), Juni 2010. http://dx.doi.org/10.2172/989881.

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Roberts, Scott Alan, und Peter Randall Schunk. A non-linear elastic constitutive framework for replicating plastic deformation in solids. Office of Scientific and Technical Information (OSTI), Februar 2014. http://dx.doi.org/10.2172/1148928.

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