Готові списки джерел за темами / Domain Studies

Добірка наукової літератури з теми "Domain Studies"

Автор: Grafiati
Опубліковано: 8 вересня 2023

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Статті в журналах з теми "Domain Studies"

1

Dix, Samuel R., Ruyue Sun, Matthew J. Harris, Sarah L. Batters, Svetlana E. Sedelnikova, Patrick J. Baker, Mark S. Thomas, and David W. Rice. "TssA from Aeromonas hydrophila: expression, purification and crystallographic studies." Acta Crystallographica Section F Structural Biology Communications 74, no. 9 (September 1, 2018): 578–82. http://dx.doi.org/10.1107/s2053230x18010439.

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TssA is a core subunit of the type VI secretion system, which is a major player in interspecies competition in Gram-negative bacteria. Previous studies on enteroaggregative Escherichia coli TssA suggested that it is comprised of three putative domains: a conserved N-terminal domain, a middle domain and a ring-forming C-terminal domain. X-ray studies of the latter two domains have identified their respective structures. Here, the results of the expression and purification of full-length and domain constructs of TssA from Aeromonas hydrophila are reported, resulting in diffraction-quality crystals for the middle domain (Nt2) and a construct including the middle and C-terminal domains (Nt2-CTD).
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2

Sherman, Michael B., Alexis N. Williams, Hong Q. Smith, B. Montgomery Pettitt, Christiane E. Wobus, and Thomas J. Smith. "Structural Studies on the Shapeshifting Murine Norovirus." Viruses 13, no. 11 (October 26, 2021): 2162. http://dx.doi.org/10.3390/v13112162.

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Noroviruses are responsible for almost a fifth of all cases of gastroenteritis worldwide. The calicivirus capsid is composed of 180 copies of VP1 with a molecular weight of ~58 kDa. This coat protein is divided into the N-terminus (N), the shell (S) and C-terminal protruding (P) domains. The S domain forms a shell around the viral RNA genome, while the P domains dimerize to form protrusions on the capsid surface. The P domain is subdivided into P1 and P2 subdomains, with the latter containing the binding sites for cellular receptors and neutralizing antibodies. Reviewed here are studies on murine norovirus (MNV) showing that the capsid responds to several physiologically relevant cues; bile, pH, Mg2+, and Ca2+. In the initial site of infection, the intestinal tract, high bile and metal concentrations and low pH cause two significant conformational changes: (1) the P domain contracts onto the shell domain and (2) several conformational changes within the P domain lead to enhanced receptor binding while blocking antibody neutralization. In contrast, the pH is neutral, and the concentrations of bile and metals are low in the serum. Under these conditions, the loops at the tip of the P domain are in the open conformation with the P domain floating on a linker or tether above the shell. This conformational state favors antibody binding but reduces interactions with the receptor. In this way, MNV uses metabolites and environmental cues in the intestine to optimize cellular attachment and escape antibody binding but presents a wholly different structure to the immune system in the serum. To our knowledge, this is the first example of a virus shapeshifting in this manner to escape the immune response.
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3

Barité, Mario, and Mirtha Rauch. "Terminological studies as domain analysis." Brazilian Journal of Information Science: research trends 16 (April 5, 2022): e02140. http://dx.doi.org/10.36311/1981-1640.2022.v16.e02140.

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This paper aims to thoroughly analyze terminological studies as a particular modality of domain analysis (DA). To this end, we establish the following methodological sequence: i) a broad description of the field of terminology, with emphasis on a general characterization of the theoretical currents and the two traditional types of research: systematic research and punctual research; ii) review of the background information on the theoretical and methodological intersection between terminology and knowledge organization (KO); iii) the problematization of terminological studies seen as DA, based on the study of background information and a series of trigger questions. The answers to these questions will allow us to progress in their understanding. The results show the need to further define the profile of terminological studies to use them in KO better. They also suggest considering terminological studies as a separate DA category, specifically in relation to language for special purposes (LSP) and discourse analysis. Finally, the preliminary conclusions will guide future research in the field. In particular, we stress that terminological research methods seem not to be sufficiently recognized as suitable for application in KO.
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4

Hutchings, J. B. "Time-Domain Studies with Astrosat." Proceedings of the International Astronomical Union 14, S339 (November 2017): 117–20. http://dx.doi.org/10.1017/s1743921318002351.

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AbstractAstrosat is a multi-instrument orbiting observatory that was launched in 2015 by the Indian Space Research Organization (ISRO). The same field of view is observed simultaneously at wavelengths ranging from gamma ray to the optical blue. This talk described the observatory’s performance, with emphasis on time-domain studies, and gave examples of results.
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5

Ponomarev, D. M., A. V. Goryachev, V. N. Zhavoronkov, and S. V. Goryunova. "Experimental time-domain antenna studies." Radiophysics and Quantum Electronics 30, no. 8 (August 1987): 763–67. http://dx.doi.org/10.1007/bf01083488.

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6

Lee, C. H. "Time-domain studies of M31." Astronomical Review 12, no. 1-4 (October 2016): 1–23. http://dx.doi.org/10.1080/21672857.2016.1270028.

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7

Patel, S. D., and C. I. Ragan. "Structural studies on mitochondrial NADH dehydrogenase using chemical cross-linking." Biochemical Journal 256, no. 2 (December 1, 1988): 521–28. http://dx.doi.org/10.1042/bj2560521.

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The structure of bovine heart mitochondrial NADH dehydrogenase was investigated by cross-linking constituent subunits with disuccinimidyl tartrate, (ethylene glycol)yl bis(succinimidyl succinate) and dimethyl suberimidate. Cross-linked products were identified by Western blotting with monospecific antisera to nine subunits of the enzyme. Cross-links between subunits within the flavoprotein, iron-protein and hydrophobic domains of the enzyme were identified. Cross-linking between the 75 kDa iron-protein-domain subunit and the 51 kDa flavoprotein-domain subunit was modulated by the substrate NADH. Cross-linking of subunits of the iron-protein and flavoprotein domains to constituents of the hydrophobic domain was also found. This was further substantiated by photolabelling subunits of the latter region, which were in contact with the membrane lipid, with 3-(trifluoromethyl)-3-(m-[125I]iodophenyl)diazirine. One such subunit of Mr 19,000 could be cross-linked to components of the iron-protein domain.
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8

Du, Jiangfeng, Kanin Wichapong, Tilman M. Hackeng, and Gerry A. F. Nicolaes. "Molecular simulation studies of human coagulation factor VIII C domain-mediated membrane binding." Thrombosis and Haemostasis 113, no. 02 (March 2015): 373–84. http://dx.doi.org/10.1160/th14-02-0180.

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SummaryThe C-terminal C domains of activated coagulation factor VIII (FVIIIa) are essential to membrane binding of this crucial coagulation cofactor protein. To provide an overall membrane binding mechanism for FVIII, we performed simulations of membrane binding through coarsegrained molecular dynamics simulations of the C1 and C2 domain, and the combined C-domains (C1+C2). We found that the C1 and C2 domain have different membrane binding properties. The C1 domain uses hydrophobic spikes 3 and 4, of its total of four spikes, as major loops to bind the membrane, whereas all four of its hydrophobic loops of the C2 domain appear essential for membrane binding. Interestingly, in the C1+C2 system, we observed cooperative binding of the C1 and C2 domains such that all four C2 domain spikes bound first, after which all four loops of the C1 domain inserted into the membrane, while the net binding energy was higher than that of the sum of the isolated C domains. Several residues, mutations of which are known to cause haemophilia A, were identified as key residues for membrane binding. In addition to these known residues, we identified residues from the C1 and C2 domains, which are involved in the membrane binding process, that have not been reported before as a cause for haemophilia A, but which contribute to overall membrane binding and which are likely candidates for novel causative missense mutations in haemophilia A.
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9

Inoue, T., and K. Goto. "Studies of Single-Domain Particles of Sm2Co17 by Domain Observation." IEEE Translation Journal on Magnetics in Japan 1, no. 8 (November 1985): 992–93. http://dx.doi.org/10.1109/tjmj.1985.4549044.

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10

Feke, Ann, Morgan Vanderwall, Wei Liu, and Joshua M. Gendron. "Functional domain studies uncover novel roles for the ZTL Kelch repeat domain in clock function." PLOS ONE 16, no. 3 (March 17, 2021): e0235938. http://dx.doi.org/10.1371/journal.pone.0235938.

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The small LOV/F-box/Kelch family of E3 ubiquitin ligases plays an essential role in the regulation of plant circadian clocks and flowering time by sensing dusk. The family consists of three members, ZEITLUPE (ZTL), LOV KELCH PROTEIN 2 (LKP2), and FLAVIN-BINDING KELCH REPEAT F-BOX PROTEIN 1 (FKF1), which share a unique protein domain architecture allowing them to act as photoreceptors that transduce light signals via altering stability of target proteins. Despite intensive study of this protein family we still lack important knowledge about the biochemical and functional roles of the protein domains that comprise these unique photoreceptors. Here, we perform comparative analyses of transgenic lines constitutively expressing the photoreceptor LOV domain or the Kelch repeat protein-protein interaction domains of ZTL, FKF1, and LKP2. Expression of each domain alone is sufficient to disrupt circadian rhythms and flowering time, but each domain differs in the magnitude of effect. Immunoprecipitation followed by mass spectrometry with the ZTL Kelch repeat domain identified a suite of potential interacting partners. Furthermore, the ZTL Kelch repeat domain can interact with the ZTL homologs, LKP2 and FKF1, and the LOV domain of ZTL itself. This suggests a hypothesis that the Kelch repeat domain of ZTL may mediate inter- and intra-molecular interactions of the three LOV/F-box/Kelch proteins and provides added insight into the composition of the protein complexes and an additional role for the Kelch repeat domain.
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Дисертації з теми "Domain Studies"

1

Batra, Sharat. "Magneto-optical studies of domain wall oscillations /." The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487265555439935.

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2

Parnas, Henrietta. "Binding studies of the SH3D domain of intersectin." Thesis, McGill University, 2010. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=87005.

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The scaffolding protein intersectin1 is involved in clathrin-mediated endocytosis, apoptosis, signal transduction and regulation of cytoskeletal rearrangements. Thus, understanding the interactions of intersectin1 with other proteins has important consequences for cell biology. It had previously been shown that Cdc42 GTPase-activating protein (CdGAP) is inhibited by intersectin1, resulting in increased actin polymerization and lamellipodia formation. The central basic-rich region of CdGAP has been shown to bind to the intersectin1 SH3D, despite not containing any previously described SH3 binding motifs. Several CdGAP peptides from its basic-rich region were found to bind to the intersectin1 SH3D in peptide array experiments, and therefore were proposed to contain novel SH3 binding motifs. Binding of a peptide causes specific chemical shift perturbations in the nuclear magnetic resonance (NMR) spectrum of a protein. In this study NMR spectroscopy was used to validate the interaction of the intersectin1 SH3D domain with peptides from several putative binding partners. The basic-rich CdGAP peptides identified in the peptide array experiments did not bind to recombinant intersectin1 SH3D in NMR titrations. Two peptides from dynamin containing typical SH3 binding motifs did not bind to intersectin1 SH3D; however, a longer proline-rich peptide from synaptojanin binds weakly. Based on homology to this synaptojanin peptide, a novel CdGAP peptide was identified that did bind to the intersectin1 SH3D. Chemical shift data was used to map the binding sites of each peptide onto the previously published structure of intersectin2 SH3D. The binding sites of the two peptides overlap, and include residues that are highly conserved amongst SH3 domains. This is the first identification of a peptide from CdGAP that binds to intersectin1 SH3D, and its homology to the synaptojanin peptide helps define the atypical binding motif of the intersectin1 SH3D domain. This study se
La protéine structurale intersectine1 est impliquée dans l'endocytose, l'apoptose, la transduction de signaux ainsi que la régulation des réarrangements du cytosquelette. La compréhension des interactions d'intersectine1 avec d'autres protéines a des conséquences importantes pour la biologie cellulaire. L'activité de la protéine activatrice de la GTPase Cdc42 (CdGAP) est empêchée par l'intersectine1 ce qui augmente la polymérisation des d'actine. La région centrale basique de CdGAP qui contrôle la liaison de la protéine avec ses substrats ne contient aucun motif qui se lie aux domaines SH3. Quelques peptides de de cette région se lient à intersectine1 SH3D en utilisant un criblage d'une banque de peptides, et ont été proposés de contenir des motifs SH3 nouveaux. La liaison avec un peptide entraîne des perturbations de déplacements chimiques dans le spectre de résonance magnétique nucléaire (RMN) d'une protéine. Dans cette recherche, la RMN fut utilisée pour étudier l'interaction du domaine SH3D de l'intersectine1 avec des peptides de quelques associés putatifs. Les peptides de CdGAP qui furent identifiés lors du criblage d'une banque de peptides ne se lient pas à l'intersectine SH3D recombinante. Deux peptides de la protéine dynamine qui contiennent des motifs SH3 typiques ne se lient pas avec l'intersectine1 SH3D, mais un plus long peptide de synaptojanine, riche en proline, se lie faiblement. Un peptide de CdGAP, identifiée par homologie avec ce peptide, s'est aussi lié. Les changements de déplacements chimiques furent utilisées pour déterminer le site de liaison sur la structure de l'intersectine2 SH3D. Les sites de liaison des deux peptides se superposent. Cette liaison se produit avec des acides aminés qui sont conservés parmi les domaines SH3. Ceci est le premier peptide de CdGAP qui se lie à l'intersectine1 SH3D. Son homologie au peptide de synaptojanine peut aider la caractérisation de ce motif de liai
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3

Menderin, Nathan. "Studies on the Human Sp1 DNA-Binding Domain." Thesis, University of Exeter, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.507135.

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4

Hardman, C. H. "NMR studies of the A domain of HMG1." Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603702.

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This thesis describes the solution structure of the A domain of rat HMG1. First, the A domain from rat HMG1 was subcloned, over-expressed and purified from E. coli. Initial characterisation revealed a mixed population of protein species resulting from both intra- and inter-molecular disulphide bond formation. To produce a suitable sample for NMR spectroscopy the non-conserved cysteine 22 was replaced with serine by site-directed mutagenesis. This mutant protein resembles the wild-type in binding to four-way junctions and short DNA duplexes. CD and NMR spectra suggest no major structural perturbations, and the protein remains fully reduced after many weeks in solution. The structure is very similar to that of the B domain. This together with the structure of Drosophila HMG-D protein (solved during this study), confirms that different HMG-boxes from the superfamily are likely to have the same global fold. Comparison with the recent structures of two different sequence-specific HMG-box:DNA complexes reveals both some similarities and differences. Some of the differences between the A domain and the other HMG structures were confirmed by studies of backbone dynamics of the protein (studied by others). The structure provides a framework to interpret many of the mutations generated in the HMG-box, and the starting point to discover the molecular differences responsible for the different properties of A and B boxes of HMG1 and between sequence and non-sequence specific HMG-box domains. The availability of isotopically labelled protein with full 1H, 13C and 15N assignments and known three-dimensional structure will provide the means to examine directly the nature of structure-specific DNA recognition by this novel class of protein using NMR spectroscopy.
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5

Edwards, Simon David. "Structural studies of the FERM domain of moesin." Thesis, Birkbeck (University of London), 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.268755.

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6

Berthoumieu, Olivia. "Single molecule studies of seven transmembrane domain proteins." Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:ff7ae71d-5481-4523-812b-2128fe32f5fc.

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This work aimed at studying biophysical properties of two membrane proteins, one of potential nanotechnological use, bacteriorhodopsin, and one potential drug target, the NTS1 neurotensin receptor, at the single molecule scale. Bacteriorhodopsin (BR) is the only protein in the purple membrane (PM) of the halophilic organism Halobacterium salinarium. It is a light-driven proton pump converting light into a transmembrane proton gradient through isomerization of its retinal chromophore. Its stability, as well as its photoactivity remaining in dry protein layers, has made BR an attractive material for biomolecular devices. Numerous studies have been published on this topic; however, they have all used BR within the PM, on relatively large (µm-wide) surfaces. Here, conducting-probe atomic force microscopy (C-AFM) analysis was performed after removing most of the membrane lipids. For the first time, it was shown that the molecular conductance of BR can be reversibly photoswitched with predictable wavelength sensitivity. Intimate and robust coupling to gold electrodes was achieved by using a strategically engineered cysteine which, combined with partial delipidation, generated protein trimers homogenously orientated on the surface. Numerous controls using biophysical (SPR, ellipsometry, Kelvin-probe AFM) and chemical (photocurrent, cyclic voltammetry) techniques confirmed the wavelength specificity of the photoswitch, the anchoring role of the mutation and the homogenous orientation of the protein on the gold surface. Neurotensin is a brain and gastrointestinal 13 amino acid peptide acting as a neuromodulator in the central nervous system and as a hormone in the periphery. Its wide range of biological activities is primarily mediated through its binding to the neurotensin type 1 receptor (NTS1). NTS1 expressed in E.coli was purified and inserted into 100 nm brain polar lipid liposomes in a conformation which retained its ligand-binding capabilities. Initial AFM characterisation was performed as a prelude for ligand-receptor interaction studies, including high resolution imaging, force spectroscopy and solid state NMR approaches.
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7

Williams, Samantha Catherine. "Studies of the domain structure of complement factor B." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358907.

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8

Ali, M. "Structural studies of Xenopus laevis Quaking protein QUA1 domain." Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595447.

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A recent report showed that a specific point mutation of glutamate to glycine (E48G) in the QUA1 domain affects both the oligomerisation and the RNA-binding properties of the murine Quaking homologue (QkI). The mutation has also been shown to be embryonic lethal in mice at around day 10 of gestation. The aims of this thesis were to investigate the structural features of QUA1 domain and explain why E48G mutants fail to dimerize. The first objective was pursued by expression and purification of the Xenopus laevis Quaking homologue (pXqua) QUA1 motif, followed by biophysical characterization and structural studies using solution-state nuclear magnetic resonance (NMR) spectroscopy. The second objective was addressed by biophysical characterization of an E48G mutant of the QUA1 domain, prepared using site directed mutagenesis. The QUA1 dimer was shown to comprise two α-helical hairpins assembling via an unusually small and polar protein-protein interface. Based on this structure, we proposed that the properties of the E48G mutant could be explained by disruption of salt-bridge interactions, either between E43 and R46 of the same protomer or R38 of the other protomer. This hypothesis was tested by generating a series of QUA1 mutants by site directed mutagenesis and analyzing them using analytical SEC, both as cleaved proteins and as MBP fusion proteins. Moreover, a separate mutational analysis was performed to compare the pXqua QUA1 domain with the corresponding regions in other STAR/GSG proteins. Sequence alignment of the QUA1 region showed proline residue in the predicted helix α1 of SAM68 and SF1. Corresponding mutations were made in pXqua QUA1 domain and the effect was investigated by studying their oligomerisation.
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9

Pommer, Ansgar J. "Mechanistic studies on the DNase domain of colicin E9." Thesis, University of East Anglia, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361425.

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10

Scott, Nerida Robyn. "Folding studies of the glucocorticoid receptor DNA-binding domain." Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627279.

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Книги з теми "Domain Studies"

1

Tückmantel, Philippe. Scanning Probe Studies of Structural and Functional Properties of Ferroelectric Domains and Domain Walls. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-72389-7.

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2

Kozarova, Anna. Structure-function studies between the regulatory domain of human PKCa [alpha] and the PKCa [alpha] catalytic domain. Sudbury, Ont: Laurentian University, School of Graduate Studies, 2004.

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3

Zhang, Xuejun. Studies in domain decomposition: multilevel methods and the biharmonic Dirichlet problem. New York: Courant Institute of Mathematical Sciences, New York University, 1991.

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4

Jun-Young, Kim, Svensson Per-Gunnar, Foundation of International Studies on Social Security., and International Research Seminar on Issues in Social Security (6th : 1999 : Sigtuna, Sweden), eds. Domain linkages and privatization in social security. Aldershot, Hampshire, England: Ashgate, 2000.

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5

Per-Gunnar, Svensson, ed. Domain Linkages and Privatization in Social Security. London: Taylor and Francis, 2017.

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6

Ghubāshī, Ṭulbah ʻAbd al-ʻĀl. Aḥkām nazʻ al-milkīyah wa-taqyīdihā li-maṣlaḥat al-ghayr fī al-sharīʻah al-Islāmīyah: Dirāsah fiqhīyah muqāranah. [al-Zaqāzīq]: Jāmiʻat al-Azhar, Kullīyat al-Dirāsāt al-Islāmīyah wa-al-ʻArabīyah, al-Banāt bi-al-Zaqāzīq, 2001.

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7

Ray, Pampa. DNA binding studies of the transcriptional activator NifA and its C-terminal domain. Birmingham: University of Birmingham, 2000.

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8

Gardin, Jean Claude. Artificial intelligence and expert systems: Case studies in the knowledge domain of archaeology. Chichester [England]: E. Horwood, 1988.

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9

Ji ti chan quan xia de Zhongguo nong di zheng shou wen ti yan jiu: Studies on Chinese farmland expropriation under. Shanghai: Shanghai ren min chu ban she, 2009.

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10

Behrle, Charles D. Computer simulation studies of multiple broadband target localization via frequency domain beamforming for planar arrays. Monterey, California: Naval Postgraduate School, 1988.

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Частини книг з теми "Domain Studies"

1

Denecke, Kerstin. "Case Studies." In Sentiment Analysis in the Medical Domain, 83–92. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-30187-2_13.

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2

Bartecki, Krzysztof. "Time-Domain Representation." In Studies in Systems, Decision and Control, 89–106. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-27501-7_6.

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3

Bacciotti, Andrea. "Frequency Domain Approach." In Studies in Systems, Decision and Control, 139–64. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-02405-5_8.

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4

Smith, Carlota S. "The Domain of Tense." In Studies in Linguistics and Philosophy, 161–82. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2617-0_6.

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5

Block, Walter E. "Debate on Eminent Domain." In Palgrave Studies in Classical Liberalism, 335–63. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-28353-7_19.

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6

Davidsson, Per. "Entrepreneurship as a Research Domain." In International Studies in Entrepreneurship, 21–40. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-26692-3_2.

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7

Salamon, Justyn. "Temperature domain in West Greenlandic." In Typological Studies in Language, 703–20. Amsterdam: John Benjamins Publishing Company, 2015. http://dx.doi.org/10.1075/tsl.107.22sal.

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8

Wu, Keng C. "Time-Domain Studies and Filter Design." In Pulse Width Modulated DC-DC Converters, 97–115. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-6021-0_8.

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9

Goodman, James. "Global Studies: Contested Fields, One Domain?" In Revisiting the Global Imaginary, 49–64. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-14911-6_4.

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10

Erez, Eden Shalom, and Inon Zuckerman. "DoNA—A Domain-Based Negotiation Agent." In Studies in Computational Intelligence, 261–71. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30307-9_18.

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Тези доповідей конференцій з теми "Domain Studies"

1

Ćiprijanović, Aleksandra, Diana Kafkes, Sydney Jenkins, K. Downey, Gabriel Perdue, S. Madireddy, T. Johnston, and Brian Nord. "Domain Adaptation for Cross-Domain Studies of Merging Galaxies." In Domain Adaptation for Cross-Domain Studies of Merging Galaxies. US DOE, 2021. http://dx.doi.org/10.2172/1825309.

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2

Ćiprijanović, Aleksandra. "Domain Adaptation for Cross-Domain Studies in Astronomy: Merging Galaxies Identification." In Domain Adaptation for Cross-Domain Studies in Astronomy: Merging Galaxies Identification. US DOE, 2021. http://dx.doi.org/10.2172/1827857.

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3

Lovrencic, Sandra, and Mirko Cubrilo. "University Studies Ontology-Domain Modeling." In 2007 11th International Conference on Intelligent Engineering Systems. IEEE, 2007. http://dx.doi.org/10.1109/ines.2007.4283672.

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4

Ganguly, Debarati, Sanghamitro Das, Ashish Rojatkar, and Debatosh Guha. "Ultrawideband pawn DRA: Time domain studies." In 2011 IEEE Indian Antenna Week (IAW). IEEE, 2011. http://dx.doi.org/10.1109/indianaw.2011.6264921.

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5

Kumar, Jitender, S. Bhardwaj, A. M. Awasthi, Alka B. Garg, R. Mittal, and R. Mukhopadhyay. "Novel Studies of Ferroelectric Domain-Wall Dynamics." In SOLID STATE PHYSICS, PROCEEDINGS OF THE 55TH DAE SOLID STATE PHYSICS SYMPOSIUM 2010. AIP, 2011. http://dx.doi.org/10.1063/1.3606312.

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6

Gratton, Enrico, and Beniamino Barbieri. "Molecular Dynamics Studies Using Frequency-Domain Fluorometry." In OE LASE'87 and EO Imaging Symp (January 1987, Los Angeles), edited by E. R. Menzel. SPIE, 1987. http://dx.doi.org/10.1117/12.966933.

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7

Ciprijanoivc, Aleksandra. "Towards flexible domain adaptation methods for cross-datasets studies of galaxies." In Towards flexible domain adaptation methods for cross-datasets studies of galaxies. US DOE, 2023. http://dx.doi.org/10.2172/1971798.

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8

Kida, N. "THz time-domain spectroscopic studies on magnetoresistive manganites." In Physics in local lattice distortions. AIP, 2001. http://dx.doi.org/10.1063/1.1363098.

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9

McVitie, S., C. Brownlie, J. N. Chapman, and C. D. W. Wilkinson. "Lorentz microscopy studies of domain wall trap structures." In INTERMAG Asia 2005: Digest of the IEEE International Magnetics Conference. IEEE, 2005. http://dx.doi.org/10.1109/intmag.2005.1463526.

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10

Melo, Bianca, Rossana Andrade, and Ticianne Darin. "Longitudinal user experience studies in the IoT domain." In IHC '22: XXI Brazilian Symposium on Human Factors in Computing Systems. New York, NY, USA: ACM, 2022. http://dx.doi.org/10.1145/3554364.3559135.

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Звіти організацій з теми "Domain Studies"

1

Cross, L. E. Ferroelectric Domain Studies. Fort Belvoir, VA: Defense Technical Information Center, December 2001. http://dx.doi.org/10.21236/ada413114.

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2

Messick, Troy E. Structural and Biochemical Studies of the Ovarian Tumor Domain. Fort Belvoir, VA: Defense Technical Information Center, May 2007. http://dx.doi.org/10.21236/ada587186.

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3

Wu, Weida. In situ scanning probe microscopy studies of cross-coupled domains and domain walls. Final technical report. Office of Scientific and Technical Information (OSTI), October 2019. http://dx.doi.org/10.2172/1568814.

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4

Smith, Steven O. Rotational Resonance NMR Structural Studies of the Neu Receptor Transmembrane Domain. Fort Belvoir, VA: Defense Technical Information Center, May 1995. http://dx.doi.org/10.21236/ada295872.

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5

Durocher, K. E., T. K. Kyser, and G. D. Delaney. Pressure-temperature-time-fluid studies in the Glennie Domain, Trans-Hudson Orogen: a progress report. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1995. http://dx.doi.org/10.4095/205409.

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6

Nohaile, Michael James. Structural studies of the activation of the two component receiver domain NTRC by multidimensional heteronuclear NMR. Office of Scientific and Technical Information (OSTI), May 1996. http://dx.doi.org/10.2172/373862.

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7

VILLA-ALEMAN, ELIEL. TIME DOMAIN THERMOREFLECTANCE (TDTR) STUDIES OF MICROSTRUCTURAL CHARACTERIZATION OF AS-FABRICATED AND/OR IRRADIATED TPBAR COMPONENTS. Office of Scientific and Technical Information (OSTI), August 2021. http://dx.doi.org/10.2172/1817898.

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8

Bleeker, W., and C. Beaumont-Smith. Thematic structural studies in the Slave Province: preliminary results and implications for the Yellowknife Domain, Northwest Territories. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1995. http://dx.doi.org/10.4095/202908.

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9

Luck, Linda A. Substrate Induced Conformational Studies of the Hormone Binding Domain of the Human Estrogen Receptor by Fluorine NMR. Fort Belvoir, VA: Defense Technical Information Center, January 2000. http://dx.doi.org/10.21236/ada378790.

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Stern, R. A., S. B. Lucas, E. C. Syme, A. H. Bailes, D J Thomas, A. D. Leclair, and L. Hulbert. Geochronological studies in the Flin Flon Domain, Manitoba-Saskatchewan, NATMAP Shield Margin Project area: results for 1992-1993. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1993. http://dx.doi.org/10.4095/193335.

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