Academic literature on the topic 'Dextrans'

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Journal articles on the topic "Dextrans"

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Arya, J. S., D. P. Pathak, T. Gupta, and M. Madan. "Application of Enzydex During Sugar Process for Improving Sugar Yield." International Journal of Advance Research and Innovation 6, no. 3 (2018): 23–26. http://dx.doi.org/10.51976/ijari.631804.

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Dextrans are undesirable compounds, synthesized by Leuconostoc mesenteroide from sucrose, increasing the viscosity of the sugar flow and reducing industrial recovery, resulting significant losses to the sugar industries. The use of dextranase enzyme is the most efficient method for hydrolyzing the dextrans at sugar mills. A preparation of dextranase enzyme namely “Enzydex” developed by Catalysts Biotechnologies Pvt. Ltd which was shown significant reduction at very low concentration 3-5ppm during six plant trials in India and in Philippines. During plant trials, the 38-78% dextran reductions w
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Pittrof, Silke L., Larissa Kaufhold, Anja Fischer, and Daniel Wefers. "Products Released from Structurally Different Dextrans by Bacterial and Fungal Dextranases." Foods 10, no. 2 (2021): 244. http://dx.doi.org/10.3390/foods10020244.

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Dextran hydrolysis by dextranases is applied in the sugar industry and the medical sector, but it also has a high potential for use in structural analysis of dextrans. However, dextranases are produced by several organisms and thus differ in their properties. The aim of this study was to comparatively investigate the product patterns obtained from the incubation of linear as well as O3- and O4-branched dextrans with different dextranases. For this purpose, genes encoding for dextranases from Bacteroides thetaiotaomicron and Streptococcus salivarius were cloned and heterologously expressed in E
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Sanders, Jonathan R., N. Adrienne Pou, and Robert J. Roselli. "Neutral and DEAE dextrans as tracers for assessing lung microvascular barrier permeability and integrity." Journal of Applied Physiology 93, no. 1 (2002): 251–62. http://dx.doi.org/10.1152/japplphysiol.00635.2000.

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Steady-state lymph-to-plasma concentration ratios (L/Ps) of neutral dextrans, cationic DEAE dextrans, and endogenous proteins were determined under normal and increased permeability conditions in six unanesthetized yearling sheep prepared with chronic lung lymph fistulas. Fluorescent dextrans with radii ranging from 1 to 30 nm were intravenously infused, and after 24 h, perilla ketone (PK) was given to alter permeability while the dextran infusion was maintained. Plasma and lymph samples were collected before and after PK administration and analyzed for dextran and protein concentrations after
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Beck-Candanedo, Stephanie, David Viet, and Derek G. Gray. "Partitioning of charged and neutral dextran-dye derivatives in biphasic cellulose nanocrystal suspensions." Canadian Journal of Chemistry 86, no. 6 (2008): 503–11. http://dx.doi.org/10.1139/v08-005.

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The partitioning behaviour of dye-labeled dextrans of high molecular weight in aqueous suspensions of native cellulose nanocrystals was studied. Cellulose concentrations lie in the isotropic–nematic coexistence region. Blue dextrans of various molecular weights and degrees of substitution of dye molecules (anionic Cibacron blue 3G-A) were investigated. Increasing the total concentration of blue dextran and degree of dye substitution led to increasing partition coefficients. Increasing dextran molecular weight resulted in higher partition coefficients, in agreement with theory. Partition coeffi
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Whiteside, C. I., and C. J. Lumsden. "Transglomerular cationic macromolecular flux is mediated by a convection-binding mechanism." American Journal of Physiology-Renal Physiology 256, no. 5 (1989): F882—F893. http://dx.doi.org/10.1152/ajprenal.1989.256.5.f882.

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Glomerular polyanion function was explored using charged and neutral [3H]dextrans in the multiple indicator-dilution experiment. Anesthetized dogs received an intrarenal bolus of 125I-labeled albumin (plasma reference), [14C]inulin (glomerular reference) and [3H]dextran (test solute), followed by rapid serial sampling of the renal venous and urine outflows. Reduced urinary recovery of cationic diethylaminoethyl dextrans (DEAE) [3H]dextrans [19.0– to 31.5–A Stokes-Einstein radius (SER)], compared with neutral [3H]dextran indicated intrarenal binding reversed by excess unlabeled cationic dextran
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Barrowcliffe, M. P., G. D. Zanelli, D. Ellison, and J. G. Jones. "Clearance of charged and uncharged dextrans from normal and injured lungs." Journal of Applied Physiology 68, no. 1 (1990): 341–47. http://dx.doi.org/10.1152/jappl.1990.68.1.341.

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To examine how molecular charge affects the transfer of molecules across the alveolar-capillary barrier, we prepared the following dextrans of equivalent molecular size (mol wt 10,000) but varying molecular charge: neutral dextran, cationic DEAE dextran, and anionic dextran sulfate. These were labeled with 99mTc. The lungs of three groups of anesthetized rabbits were insufflated with dextran aerosols, with six rabbits receiving each type, and the half-time pulmonary clearance (t1/2) was measured. Control t1/2's (95% confidence limits) were 95 (74-120), 227 (192-268), and 291 (246-345) min for
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Schmid, Jonas, Daniel Wefers, Rudi F. Vogel, and Frank Jakob. "Analysis of Structural and Functional Differences of Glucans Produced by the Natively Released Dextransucrase of Liquorilactobacillus hordei TMW 1.1822." Applied Biochemistry and Biotechnology 193, no. 1 (2020): 96–110. http://dx.doi.org/10.1007/s12010-020-03407-6.

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AbstractThe properties of the glucopolymer dextran are versatile and linked to its molecular size, structure, branching, and secondary structure. However, suited strategies to control and exploit the variable structures of dextrans are scarce. The aim of this study was to delineate structural and functional differences of dextrans, which were produced in buffers at different conditions using the native dextransucrase released by Liquorilactobacillus (L.) hordei TMW 1.1822. Rheological measurements revealed that dextran produced at pH 4.0 (MW = 1.1 * 108 Da) exhibited the properties of a viscoe
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Sarbini, Shahrul R., Sofia Kolida, Thierry Naeye та ін. "In VitroFermentation of Linear and α-1,2-Branched Dextrans by the Human Fecal Microbiota". Applied and Environmental Microbiology 77, № 15 (2011): 5307–15. http://dx.doi.org/10.1128/aem.02568-10.

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ABSTRACTThe role of structure and molecular weight in fermentation selectivity in linear α-1,6 dextrans and dextrans with α-1,2 branching was investigated. Fermentation by gut bacteria was determined in anaerobic, pH-controlled fecal batch cultures after 36 h. Inulin (1%, wt/vol), which is a known prebiotic, was used as a control. Samples were obtained at 0, 10, 24, and 36 h of fermentation for bacterial enumeration by fluorescentin situhybridization and short-chain fatty acid analyses. The gas production of the substrate fermentation was investigated in non-pH-controlled, fecal batch culture
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Hansen-Flaschen, J. H., P. N. Lanken, G. G. Pietra, P. M. Sampson, L. Johns, and A. P. Fishman. "Effect of 100% O2 on passage of uncharged dextrans from blood to lung lymph." Journal of Applied Physiology 60, no. 5 (1986): 1797–809. http://dx.doi.org/10.1152/jappl.1986.60.5.1797.

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Since charge as well as size may influence the passage of plasma proteins from blood to lung lymph, we used uncharged dextrans as tracers to study the effects of hyperoxic lung injury on the molecular sieving properties of the pulmonary microcirculation in unanesthetized sheep. Polydisperse [3H]dextran was infused intravenously into five sheep before and after the animals breathed 100% O2 until lymph flow increased threefold (66–84 h). Lymph-to-plasma concentration ratios (L/P) were determined for [3H]dextran fractions of graded molecular sizes (1.6–8.4 nm effective radius) from samples obtain
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Martinez-Paniagua, Melisa, Sabbir Khan, and Chirag Patel. "DDEL-18. OPTIMIZED METHOD TO QUANTIFY TTFIELDS-INDUCED PERMEABILIZATION OF CELL MEMBRANES." Neuro-Oncology 26, Supplement_8 (2024): viii125. http://dx.doi.org/10.1093/neuonc/noae165.0484.

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Abstract Tumor Treating Fields (TTFields) therapy is FDA-approved for glioblastoma. Using plate-based readouts of FITC-dextran fluorescent probes in U87 human glioblastoma cells, we previously reported increased uptake of FITC-dextrans (4-20kDa) post-TTFields exposure. However, this approach is unable to distinguish FITC-dextran uptake in live-vs-dead cells post-TTFields exposure. We demonstrate flow cytometry (FC) as a more robust and economical method to quantify the amount of FITC-dextrans entering the cells. We first identified the optimal [FITC-dextran] for the FC-based approach (titratio
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Dissertations / Theses on the topic "Dextrans"

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Nordskov, Harder FIE BARBARA. "Effect of Dextrans on Cryopreservation of Human Spermatozoa." Thesis, Malmö universitet, Fakulteten för hälsa och samhälle (HS), 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:mau:diva-24295.

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Cryopreservation is a process where a sample, e.g. cells or tissue, is preserved by cooling to sub-zero temperatures, usually -196°C. Upon freezing these materials, ice crystals form, which eventually results in cell death. In order to reduce the formation of ice crystals, cryoprotectants are added to the storage solution. Current cryoprotective agents have several weaknesses, making the development of cryoprotective agents with advanced properties of great interest. In this study, two possible non-penetrating cryoprotectants termed Dextran Sulphate Sodium Salt 80 (DSSS 80) and Dextran Sulphat
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Tournon-Aubry, Isabelle Aubry. "Intérêt de l'hémodilution normovolémique par dextrans dans le traitement des occlusions veineuses rétiniennes (étude sur 38 cas)." Montpellier 1, 1988. http://www.theses.fr/1988MON11202.

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Valdez, Michael Aaron, and Michael Aaron Valdez. "Development, Characterization, and Implementation of a System for Focused Ultrasound-Mediated Blood-Brain Barrier Opening In Mice." Diss., The University of Arizona, 2017. http://hdl.handle.net/10150/626365.

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The blood-brain barrier BBB refers to the set of specialized endothelial cells that line the vasculature in the brain and effectively control movement of molecules into and out of the brain. While necessary for proper brain function, the BBB blocks 98% of drugs from entering the brain and is the most significant barrier to developing therapies for neurodegenerative diseases. Active transport allows some specific molecules to cross the BBB, but therapeutic development using this route has had limited success. A number of techniques have been used to bypass the BBB, but are often highly invasive
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Tahir, Muhammad Nazir [Verfasser], and Petra [Akademischer Betreuer] Mischnick. "Alkynyl ethers of dextrans as Intermediates for new Functional Biopolymers / Muhammad Nazir Tahir ; Betreuer: Petra Mischnick." Braunschweig : Technische Universität Braunschweig, 2011. http://d-nb.info/1175824887/34.

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Joncquiert, Jean-Charles. "Clonage et expression chez Escherichia coli de gènes de Bacteroides impliqués dans la dégradation des dextrans." Lille 1, 1990. http://www.theses.fr/1990LIL10065.

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Des gènes de la souche Bacteroides thetaiotaomicron 489 impliqués dans la dégradation du dextran ont été clonés chez E. Coli. Après criblage d'une banque génomique dans le vecteur plasmidique pBR322 et repiquage de 16000 transformants de la souche E. Coli HB101, 43 clones produisant des zones de dégradation ont été mis en évidence sur milieu riche contenant du bleu dextran t2000. Après de multiples repiquages, 10 clones se sont révélés être stables et donner des halos de dégradation reproductibles. L'étude de ces 10 plasmides a été entreprise et les cartes de restriction ont été établies. Les
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Faivre, Béatrice. "Un transporteur d'oxygène a visée transfusionnelle : l'hémoglobine-dextran 10-benzène-tetracarboxylate évaluation préclinique chez le cobaye." Vandoeuvre-les-Nancy, INPL, 1993. http://www.theses.fr/1993INPL086N.

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L'hémoglobine conjuguée au dextran-benzène-tetracarboxylate (hb-dex-btc) est un transporteur d'O2 dont les objectifs sont de se substituer, de façon temporaire, à la fonction oxyphorique des hématies et de contribuer à la restauration de la volémie. Notre travail consiste à réaliser l'évaluation pharmaco-toxicologique de cette hémoglobine. Tout d'abord, nous présentons l'historique de la recherche sur les substituts du sang, la physiologie de l'hémoglobine dans le globule rouge et dans le plasma (structure, mécanismes d'oxygénation, d'oxydation, de réduction, catabolisme) ainsi que les princip
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Foote, Jeremy B. "Polysaccharide specific B cells a study of their development and function /." Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2009. https://www.mhsl.uab.edu/dt/2009p/foote.pdf.

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Lemay, Guylaine. "Étude de la stabilité thermique des protéines de lactosérum et de leur comportement en solution, en présence de divers dextrans." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0020/MQ56761.pdf.

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Covis, Rudy. "Synthèse de polysaccharides amphiphiles à partir de dextrane et application à la stabilisation d'émulsions directes et inverses." Thesis, Vandoeuvre-les-Nancy, INPL, 2011. http://www.theses.fr/2011INPL006N/document.

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Une nouvelle famille de dérivés amphiphiles du dextrane a été obtenue par réaction du dextrane avec le 1,2-époxydodécane en milieu basique. Deux voies de synthèse ont été étudiées. La première en milieu aqueux dispersé n’a permis d’obtenir que des taux de modification faibles (< 10 %) car l’homopolymérisation de l’époxyde est prépondérante. Au contraire, la réaction en milieu organique homogène a permis la synthèse de dérivés dont le taux de modification atteint 164 %. Des émulsions huile dans eau ont été préparées par sonication en présence de plusieurs dérivés hydrosolubles (τ ≤ 25 %). La
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Van, Wyk Nathan. "Analysis of dextrin dextranase from Gluconobacter oxydans." Thesis, Stellenbosch : Stellenbosch University, 2008. http://hdl.handle.net/10019.1/2619.

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Thesis (MSc (Genetics. Institute for Plant Biotechnology (IPB)))--Stellenbosch University, 2008.<br>Dextran is a high value glucose polymer used in medicine and an array of laboratory techniques. It is synthesised by lactic-acid bacteria from sucrose but has also reportedly been produced by Gluconobacter oxydans (G. oxydans) from a range of maltooligosaccharides (MOS) via the action of dextrin dextranase (DDase). In this study the presence of DDase is investigated in two G. oxydans strains (ATCC 621H and ATCC 19357) and shown to be present in the ATCC 19357 strain, but not in the ATCC 62
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Books on the topic "Dextrans"

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Wang, Denong. The repertoire of murine antibodies to small site-filling antigenic determinant [Glc(a1-6)]3-7 in dextran. [Columbia University], 1993.

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Carter, Susan Redfield. Investigation of aqueous humor flow in the rabbit with the use of fluoresceinated dextrans. s.n.], 1989.

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International Symposium on Standardization of Albumin, Plasma Substitutes, and Plasmapheresis (1980 Geneva, Switzerland). Adland. Knopf Doubleday Publishing Group, 2009.

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Rakshit, D. End-modification reactions of Dextran. University of Birmingham, 1987.

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Shastri, S. V. Dextrous Robot Hands. Springer New York, 1990.

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Venkataraman, Subramanian T., and Thea Iberall, eds. Dextrous Robot Hands. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4613-8974-3.

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V, Shastri S., Iberall Thea, IEEE Computer Society, United States. Office of Naval Research., Workshop on Dextrous Robot Hands (1988 : Philadelphia, Pa.), and IEEE International Conference on Robotics and Automation (1988 : Philadelphia, Pa.), eds. Dextrous robot hands. Springer-Verlag, 1990.

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Bhambra, Kalwant Singh. The fractionation of dextran using ethanol. Aston University. Department of Chemical Engineering, 1985.

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Asghar, M. A. Alkaline degradations of carbohydrates, particularly Dextran. University of Birmingham, 1990.

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D, Klemm, and Heinze Thomas 1958-, eds. Polysaccharides II. Springer, 2006.

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Book chapters on the topic "Dextrans"

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Litvan, H., J. I. Casas, and J. M. Villar-Landeira. "Volume Replacement Therapy with Dextrans: Are Dextrans Still Useful in Volume Replacement?" In Volume Replacement. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-72170-0_4.

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Sandoval, Ruben M., and Bruce A. Molitoris. "Fluorescent Dextrans in Intravital Multi-Photon Microscopy." In Advances in Intravital Microscopy. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9361-2_10.

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Schomburg, Dietmar, and Dörte Stephan. "Dextrin dextranase." In Enzyme Handbook 12. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61117-9_17.

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Kabat, Elvin A. "Molecular Biology of Anti-α-(1→6)dextrans." In ACS Symposium Series. American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1993-0519.ch011.

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Hansen-Flaschen, John H., and Alfred P. Fishman. "Studies of Pulmonary Endothelial Permeability Using Tritiated Dextrans." In Endothelial Cell Biology in Health and Disease. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-0937-6_5.

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Gosselet, N. M., A. M. Layre, V. Wintgens, and C. Amiel. "Physicochemical study of modified dextrans with a β-cyclodextrin polymer." In Trends in Colloid and Interface Science XVII. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b93966.

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Vansteenkiste, S., E. Schacht, L. Seymour, and R. Duncan. "Blood Clearance and Body Distributions of Glycosylated Dextrans in Rats." In ACS Symposium Series. American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1993-0520.ch026.

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Ijima, N., and N. Murase. "Glass Transition Observed with Cross-Linked Dextrans Containing a Small Amount of Water." In Food Engineering Series. Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2578-0_9.

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Bahary, William S., Michael P. Hogan, Mahmood Jilani, and Michael P. Aronson. "Size-Exclusion Chromatography of Dextrans and Pullulans with Light-Scattering, Viscosity, and Refractive Index Detection." In Advances in Chemistry. American Chemical Society, 1995. http://dx.doi.org/10.1021/ba-1995-0247.ch012.

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Raices, Marcela, and Maximiliano A. D’Angelo. "Analysis of Nuclear Pore Complex Permeability in Mammalian Cells and Isolated Nuclei Using Fluorescent Dextrans." In Methods in Molecular Biology. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2337-4_4.

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Conference papers on the topic "Dextrans"

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Jonna, Prashanth, and Madhav Rao. "HADAR Hand: 13-DoF Hybrid Actuation-Based Dextrous Anthropomorphic Robotic Hand." In 2025 International Conference On Rehabilitation Robotics (ICORR). IEEE, 2025. https://doi.org/10.1109/icorr66766.2025.11062954.

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Xu, Xiangqun, Liu Wu, Ruikang K. Wang, James B. Elder, and Valery V. Tuchin. "Optical clearing of blood by dextrans." In International Conference on Lasers, Applications, and Technologies 2002 Laser Applications in Medicine, Biology, and Environmental Science, edited by Gerhard Mueller, Valery V. Tuchin, Gennadii G. Matvienko, Christian Werner, and Vladislav Y. Panchenko. SPIE, 2003. http://dx.doi.org/10.1117/12.518630.

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Bizios, R., F. A. Blumenstock, P. J. Del Vecchio, and A. B. Malik. "PERMSELECTIVITY OF CULTURED ENDOTHELIAL MONOLAYERS: EFFECT OF SIZE AND CHARGE OF THE TRANSPORTED MOLECULES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643351.

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Known molecular size neutral dextrans (molecular weight (MW) range ∼6,000-∼500,000), anionic (dextran sulfate, ∼500,000 MW), and cationic (DEAE-dextran, ∼500,000 MW) were used to determine the permselectivity characteristics of bovine pulmonary arterial endothelial monolayers. The experimental system consisted of two compartments separated by a gelatinized polycarbonate membrane (0.8 μm pore size) on one side of which endothelial monolayers were grown to confluence. Dextran solutions (1 gram %) were prepared in phosphate buffered saline buffer (containing 0.5 gram % serum albumin) and placed o
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Wang, Ruikang K., Xiangqun Xu, James B. Elder, and Valery V. Tuchin. "Possible mechanisms for optical clearing of whole blood by dextrans." In Biomedical Optics 2003, edited by Alexander V. Priezzhev and Gerard L. Cote. SPIE, 2003. http://dx.doi.org/10.1117/12.479191.

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Charron, Luc, Andrea Harmer, and Lothar Lilge. "Development of poly-l-lysine-coated calcium-alginate microspheres encapsulating fluorescein-labeled dextrans." In Photonics North 2005, edited by Warren C. W. Chan, Kui Yu, Ulrich J. Krull, Richard I. Hornsey, Brian C. Wilson, and Robert A. Weersink. SPIE, 2005. http://dx.doi.org/10.1117/12.628831.

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Wang, Shougang, Babak Baseri, James J. Choi, Yao-Sheng Tung, Barclay Morrison, and Elisa E. Konofagou. "Delivery of fluorescent dextrans through the ultrasound-induced blood-brain barrier opening in mice." In 2008 IEEE Ultrasonics Symposium (IUS). IEEE, 2008. http://dx.doi.org/10.1109/ultsym.2008.0416.

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Yemane, Petros Tesfamichael, Andreas Aslund, Kristin Grendstad Saterbo, et al. "The Effect of Sonication on Extravasation and Distribution of Nanoparticles and Dextrans in Tumor Tissue Imaged by Multiphoton Microscopy." In 2018 IEEE International Ultrasonics Symposium (IUS). IEEE, 2018. http://dx.doi.org/10.1109/ultsym.2018.8580082.

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Masedunskas, Andrius, and Roberto Weigert. "Internalization of fluorescent dextrans in the submandibular salivary glands of live animals: a study combining intravital two-photon microscopy and second harmonic generation." In Biomedical Optics (BiOS) 2008, edited by Ammasi Periasamy and Peter T. C. So. SPIE, 2008. http://dx.doi.org/10.1117/12.768051.

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Hinchet, Ronan, Velko Vechev, Herbert Shea, and Otmar Hilliges. "DextrES." In The 31st Annual ACM Symposium. ACM Press, 2018. http://dx.doi.org/10.1145/3242587.3242657.

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Saldeen, T., R. Moalli, F. M. Hasan, A. Carvalho, and M. Eriksson. "EFFECT OF DEXTRAN ON PLASMINOGEN ACTIVATOR INHIBITOR (PAI)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644445.

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Adult respiratory distress syndrome (ARDS) is often associated with impaired fibrinolysis and appearance of microemboli in the lung. Increased production of PAI, associated with acute lung injury, may contribute to this process. In patients at risk of developing microembolic complications, aeteinistration of dextran reduced the incidence of ARDS. Accordingly, we studied the effect of dextran adninistration on plasma PAI levels in a rabbit model of endotoxin-induced lung injury and in patients. E coli endotoxin (500 μg/kg bw, infused over 5 min) was administrered to three groups of anesthetized
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Reports on the topic "Dextrans"

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Norris, D. K. Tectonic Developments and Major Dextral Faults. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1987. http://dx.doi.org/10.4095/126942.

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Dubick, Michael A., Gary M. Zaucha, Don W. Korte, Wade Jr., and Charles E. Acute and Subacute Toxicity of 7.5% Hypertonic Saline/6% Dextran-70 (HSD) in Dogs. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada244808.

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Dubick, M. A., J. J. Summary, J. Y. Greene, J. W. Holcroft, and C. E. Wade. Assessment of 7.5% NaCl /6% Dextran-70 (HSD) Effects on Serum or Plasma Protein Determinations. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada232833.

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Struik, L. C. Dextral strike-slip through Wells Gray Provincial Park, British Columbia. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1985. http://dx.doi.org/10.4095/120056.

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Lin, Yi-En, and Mei-Chun Chen. Dextran-40 administration may reduce partial flap failure rates: A systematic review and meta-analysis protocol. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2023. http://dx.doi.org/10.37766/inplasy2023.12.0013.

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Grasby, S. E., and E. W. Mountjoy. Compressional and Dextral Motion Along the Chatter Creek Fault, Main Ranges, British Columbia. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1991. http://dx.doi.org/10.4095/132622.

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Dubick, Michael A., and Charles E. Wade. Prekallikrein and Protease Inhibitor Levels in Plasma from Conscious, Hemorrhaged and Euvolemic Swine Infused with 7.5% NaCl/6% Dextran-70. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada211966.

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Yeo, G. M. Late Carboniferous Dextral Movement On the CobequidHollow Fault System, Nova Scotia : Evidence and Implications. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1986. http://dx.doi.org/10.4095/120392.

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ตัณฑะพานิชกุล, วิวัฒน์, วิจิตรา จงวิศาล, ธวัชชัย ชรินพาณิชกุล та วรัญ แต้ไพสิฐพงษ์. เครื่องทดสอบขอบเขตการระเบิดของฝุ่นผง : รายงาน. จุฬาลงกรณ์มหาวิทยาลัย, 1996. https://doi.org/10.58837/chula.res.1996.29.

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Abstract:
วัตถุประสงค์หลักของโครงการสิ่งประดิษฐ์นี้คือ การพัฒนาปรับปรุงเครื่องต้นแบบชุดที่สองสำหรับทดสอบคุณสมบัติการระเบิดของวัสดุฝุ่นผง ทำการศึกษาวัดค่าความเข้มข้นต่ำสุดที่ระเบิดได้ (Lower Explosion Limit, LEL) ของตัวอย่างฝุ่นผงประเภทต่างๆ ภายในประเทศ และทำการศึกษาอิทธิพลของขนาดอนุภาคเฉลี่ย และปริมาณความชื้นที่มีต่อค่า LEL ตลอดจนเสนอแนวทางป้องกันและแนวทางควบคุมความเสียหายจากการระเบิดของฝุ่นผงในโรงงานอุตสาหกรรม ตัวอย่างฝุ่นผงส่วนใหญ่จะผ่านการเตรียมตัวอย่างตามขั้นตอนที่ระบุไว้ก่อนทดสอบการระเบิด จากการศึกษาเบื้องต้นพบว่า ตัวอย่างฝุ่นผง 4 ชนิด (lycopodium, HDPE, dextrin และ sulfur) ให้ค่า LEL ใกล้เคียงกับค
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Dubick, M. A., A. F. Kilani, J. J. Summary, J. Y. Greene, and C. E. Wade. Further Evaluation of the Effects of 7.5% NaCl/6% Dextran-70 (HSD) administration on Coagulation and Platelet Aggregation in Hemorrhaged and Euvolemic Swine. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ada266477.

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