Auswahl der wissenschaftlichen Literatur zum Thema „Clot structure“
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Zeitschriftenartikel zum Thema "Clot structure"
Smith, Stephanie A., und James H. Morrissey. „Polyphosphate Enhances Fibrin Clot Structure.“ Blood 110, Nr. 11 (16.11.2007): 403. http://dx.doi.org/10.1182/blood.v110.11.403.403.
Der volle Inhalt der QuelleMihalko, Emily, und Ashley C. Brown. „Clot Structure and Implications for Bleeding and Thrombosis“. Seminars in Thrombosis and Hemostasis 46, Nr. 01 (15.10.2019): 096–104. http://dx.doi.org/10.1055/s-0039-1696944.
Der volle Inhalt der QuelleWolberg, Alisa S., Dougald M. Monroe, Harold R. Roberts und Maureane Hoffman. „Elevated prothrombin results in clots with an altered fiber structure: a possible mechanism of the increased thrombotic risk“. Blood 101, Nr. 8 (15.04.2003): 3008–13. http://dx.doi.org/10.1182/blood-2002-08-2527.
Der volle Inhalt der QuelleSmith, Stephanie A., und James H. Morrissey. „Polyphosphate enhances fibrin clot structure“. Blood 112, Nr. 7 (01.10.2008): 2810–16. http://dx.doi.org/10.1182/blood-2008-03-145755.
Der volle Inhalt der QuelleCelińska-Löwenhoff, Magdalena, Teresa Iwaniec, Agnieszka Padjas, Jacek Musiał und Anetta Undas. „Altered fibrin clot structure/function in patients with antiphospholipid syndrome: association with thrombotic manifestation“. Thrombosis and Haemostasis 112, Nr. 08 (2014): 287–96. http://dx.doi.org/10.1160/th13-11-0980.
Der volle Inhalt der QuelleCarr, M. E., und S. L. Zekert. „Abnormal clot retraction, altered fibrin structure, and normal platelet function in multiple myeloma“. American Journal of Physiology-Heart and Circulatory Physiology 266, Nr. 3 (01.03.1994): H1195—H1201. http://dx.doi.org/10.1152/ajpheart.1994.266.3.h1195.
Der volle Inhalt der QuelleGersh, Kathryn, Chandrasekaran Nagaswami und John Weisel. „Fibrin network structure and clot mechanical properties are altered by incorporation of erythrocytes“. Thrombosis and Haemostasis 102, Nr. 12 (2009): 1169–75. http://dx.doi.org/10.1160/th09-03-0199.
Der volle Inhalt der QuelleHenderson, Sara J., Jing Xia, Huayin Wu, Alan R. Stafford, Beverly A. Leslie, James C. Fredenburgh, David A. Weitz und Jeffrey I. Weitz. „Zinc promotes clot stability by accelerating clot formation and modifying fibrin structure“. Thrombosis and Haemostasis 115, Nr. 03 (2016): 533–42. http://dx.doi.org/10.1160/th15-06-0462.
Der volle Inhalt der QuelleMartinez, Marissa R., Adam Cuker, Angela M. Mills, Amanda Crichlow, Richard T. Lightfoot, Irina N. Chernysh, Chandrasekaran Nagaswami, John W. Weisel und Harry Ischiropoulos. „Enhanced lysis and accelerated establishment of viscoelastic properties of fibrin clots are associated with pulmonary embolism“. American Journal of Physiology-Lung Cellular and Molecular Physiology 306, Nr. 5 (01.03.2014): L397—L404. http://dx.doi.org/10.1152/ajplung.00265.2013.
Der volle Inhalt der QuelleJanmey, PA, JA Lamb, RM Ezzell, S. Hvidt und SE Lind. „Effects of actin filaments on fibrin clot structure and lysis“. Blood 80, Nr. 4 (15.08.1992): 928–36. http://dx.doi.org/10.1182/blood.v80.4.928.928.
Der volle Inhalt der QuelleDissertationen zum Thema "Clot structure"
Pan, Xiaoxi. „Fibrin clot structure alterations after particulate matter exposure“. Thesis, University of Leeds, 2016. http://etheses.whiterose.ac.uk/14310/.
Der volle Inhalt der QuelleAlzahrani, Saad Hassan S. „Cardiometabolic risk factors, clot structure and the effects of therapies in individuals with diabetes“. Thesis, University of Leeds, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540551.
Der volle Inhalt der QuelleJalal, Mohammed Mansour. „Statins exert antithrombotic action on platelet function and modulate clot formation structure and stability“. Thesis, University of Aberdeen, 2017. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=235575.
Der volle Inhalt der QuelleSauls, Derrick Lamonte. „A RABBIT MODEL OF HYPERHOMOCYSTEINEMIA: THE EFFECT OF HOMOCYSTEINE ON BLOOD CLOT STRUCTURE AND STABILITY“. NCSU, 2003. http://www.lib.ncsu.edu/theses/available/etd-03252003-183839/.
Der volle Inhalt der QuelleWang, Xin. „Manipulating fibrin structure of hematomas enhances large bone defects healing“. Thesis, Queensland University of Technology, 2016. https://eprints.qut.edu.au/100030/1/Xin_Wang_Thesis.pdf.
Der volle Inhalt der QuelleGarcia, gonzalez Xabel. „Influence de la nature du fibrinogène sur la structure et la mécanique du caillot de fibrine“. Thesis, Université Grenoble Alpes (ComUE), 2016. http://www.theses.fr/2016GREAI076/document.
Der volle Inhalt der QuelleFibrin clot formation is one of the major processes leading to blood clotting. It involves the polymerization of fibrin monomers into a network of fibrin fibres. This network controls the mechanical properties of the clot and serves as a skeleton for wound healing. Environmental factors (pH, concentration, …) have been proved to influence polymerization, however the role of fibrinogen composition on the structure of fibrin remains unexplored. This aspect might be important for the case of cardiovascular pathologies, which present abnormal fibrin structures.We have determined the relation between different sources of fibrinogen with the nano- and micro-metric structural and mechanical properties of fibrin clots. The composition in co-purified proteins of the fibrinogens has no significant importance, however the polydispersity profile controls the multiscale properties of fibrin. Indeed, x-ray scattering, multi-wavelength spectrophotometry and confocal microscopy measurements have proved that fibres from monodisperse fibrinogens are quasi-crystalline, straight and rigid. Fibres from polydisperse fibrinogens are less organised, curbed and less rigid. Finally, the mechanical properties of fibrin showed that the response of clots to deformation, as well as the scenarios of rupture are closely related to the structure, and consequently related to the profiles of polydispersity. This opens outstanding perspectives in many fields such the optimisation of fibrinogen’s use on dysfibrinogenemias or haemorrhages, tissue regeneration or the understanding between the abnormal structure of clots and cardiovascular diseases
Lim, Bernard Boon Chye. „Effects of coding polymorphisms of the coagulation factor XIII and fibrinogen genes on fibrin clot structure-function“. Thesis, University of Leeds, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.424056.
Der volle Inhalt der QuelleLau, Yee Cheng. „The prothrombotic state in atrial fibrillation : observations on fibrin clot structure and the relationship to renal dysfunction“. Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7163/.
Der volle Inhalt der QuelleDassi, Carhel. „La fibrinographie : une méthode multi-longueurs d’ondes pour la détermination de la structure du caillot en plasma“. Thesis, Université Grenoble Alpes (ComUE), 2016. http://www.theses.fr/2016GREAS028.
Der volle Inhalt der QuelleThe physiological role of the clot is to avoid excessive bleeding in the presence of a vascular breach. Once this function is filled, the clot must be able to be easily destroyed, so that it is not transported in the venous system and does not hamper blood circulation. The formation of a fibrin clot and its lysis are key processes of hemostasis, implying simultaneously the polymerization of the fibrinogen monomers in a fibrin fibers network, and the destruction of this constituted network.Although this network controls the physical and mechanical properties of the clot, its structure at scales smaller than the micron is poorly characterized. The main problem in the physical characterization of clot in clinical settings is the current absence of a quantitative, sensitive and reproducible measurement method.We demonstrated in this work, thanks to our method using several wavelengths, that the analysis of the visible spectra of light transmitted through a clot allows to determine simultaneously, quantitatively and in quasi-physiological conditions, several essential parameters of structure of the fibrin clot, namely the number of protofibrils per fibrin fibers, the radius and the density of fibers, and various times of clotting and lysis of the clot. This method was validated by the results with CV inferior to 6 % under all test conditions and various plasmatic profiles: normal, hypo / hyper coagulant and hypo / hyper fibrinolytic. This demonstrates the robustness and reliability of the measurement method when measuring both clotting and clot lysis.This spectrophotometric method was implemented on a modified automaton dedicated to diagnosis of patients presenting hemostatic disorders. The clinical information and the interests expected from this new test concern at the same time the quality of the fibrin network, its accelerated lysis or its resistance to fibrinolysis, and the resultant of the coagulo-lytic balance
Seyve, Landry. „Analyse de la structure du caillot en conditions physiologiques et pathologiques“. Thesis, Université Grenoble Alpes (ComUE), 2019. http://www.theses.fr/2019GREAS027.
Der volle Inhalt der QuellePhysiologically, the blood function of the clot is to stop bleeding following a vascular breach. Initially, platelets stop blood flow, quickly supported by the formation of a fibrin fibers network that strengthens and gives properties to resist the blood pressure and fibrinolysis. Fibrinogen is the basic element of the fibrin network. During a vascular breach, the release of tissue factor triggers the coagulation cascade that results in the conversion of fibrinogen to fibrin monomers by the action of thrombin. These aggregate longitudinally to form protofibrils, then laterally to form a network of fibrin fibers.To date, many stages of the clot formation have been described in detail in the literature, however the mechanisms and driving forces of the lateral aggregation of protofibrils are still poorly understood.During this work, we studied different coagulation profiles: from hypo-coagulant to hyper-coagulant, through the normal profile and using a varied range of techniques: thrombin generation, plasmin generation, Fibrinography, Fibrinography in "fibrinolysis" mode, confocal microscopy, thromboelastometry and X-ray diffraction at small angles.We have highlighted the relationship between the amount of thrombin present during clot formation and the clot structure. Indeed, the more thrombin there is, the lower the protofibrils number per fiber and the greater the number of fibers. In addition, we correlated the initiation time of lateral fibers aggregation in Fibrinography with the initiation of plasmin generation. We have thus demonstrated the production of an abnormal fibrin clot structure in the presence of dabigatran, thanks to the combined use of confocal microscopy and Fibrinography.This multimodal analysis of the clot structure under different conditions provides additional information to the scientific community to better understand the mechanisms of fibrin clot formation
Bücher zum Thema "Clot structure"
Alderman, Sharon D. Mastering weave structures: Transforming ideas into great cloth. Loveland, Colo: Interweave, 2009.
Den vollen Inhalt der Quelle findenMalouinières: Manoirs et demeures du Clos-Poulet. Brest: Editions Télégramme, 2005.
Den vollen Inhalt der Quelle findenKuryluk, Ewa. Veronica and her cloth: History, symbolism, and structure of a "true" image. Cambridge, Mass., USA: B. Blackwell, 1991.
Den vollen Inhalt der Quelle findenPetignat, André. Les moulins du Clos du Doubs: Les moulins de Soubey. Porrentruy: Soc. Jurassienne d'Émulation, 2004.
Den vollen Inhalt der Quelle finden1948-, Filler Martin, und San Francisco Museum of Modern Art., Hrsg. Art + architecture + landscape: The Clos Pegase Design Competition. San Francisco, Calif: The Museum, 1985.
Den vollen Inhalt der Quelle findenL, Raina J. Structural and functional changes in the joint family system: A study based on D.C.M. workers. New Delhi: Concept Pub. Co., 1989.
Den vollen Inhalt der Quelle findenTemir, Şebnem Ruhsar. Şile ve Şile bezi: Geçmişten günümüze = Şile and Şile cloth : from past to present. Ankara: T.C. Kültür ve Turizm Bakanlığı Kütüphaneler ve Yayımlar Genel Müdürlüğü, 2010.
Den vollen Inhalt der Quelle findenDictionnaire du Paris disparu: Sites & monuments : buttes, casernes, cimetières, clos, collèges, couvents, églises, folies, gares, gibets, hôpitaux, hôtels particuliers, îles, jardins, lieux-dits, ponts, portes, ports, prisons. Paris: Parigramme, 1998.
Den vollen Inhalt der Quelle findenCurry, Nicola, und Raza Alikhan. Normal platelet function. Herausgegeben von Patrick Davey und David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0281.
Der volle Inhalt der QuelleMastering Weave Structures: Transforming Ideas into Great Cloth. Interweave Press, 2004.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Clot structure"
Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk und I. Savysyuk. „(ClO2)2Sn(ClO4)6“. In Structure Types. Part 9: Space Groups (148) R-3 - (141) I41/amd, 598–99. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02702-4_410.
Der volle Inhalt der QuelleÖchsner, Andreas. „Composite Laminate Analysis Tool—CLAT“. In Advanced Structured Materials, 199–202. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-32390-4_7.
Der volle Inhalt der QuelleVillars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk und I. Savysyuk. „Co(ClO4)2“. In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 617. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_382.
Der volle Inhalt der QuelleVillars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, N. Melnichenko-Koblyuk et al. „Co[ClO4]2“. In Structure Types. Part 5: Space Groups (173) P63 - (166) R-3m, 705. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-46933-9_577.
Der volle Inhalt der QuelleVillars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, I. Savysyuk und R. Zaremba. „Mg(ClO2)2∙6H2O“. In Structure Types. Part 10: Space Groups (140) I4/mcm – (136) P42/mnm, 736. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-19662-1_615.
Der volle Inhalt der QuelleVillars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, N. Melnichenko-Koblyuk et al. „Ba[ClO4]2[H2O]3“. In Structure Types. Part 5: Space Groups (173) P63 - (166) R-3m, 75. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-46933-9_30.
Der volle Inhalt der QuelleVillars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, N. Melnichenko-Koblyuk et al. „Ti[ClO4]3[CON2H4]6“. In Structure Types. Part 5: Space Groups (173) P63 - (166) R-3m, 400. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-46933-9_304.
Der volle Inhalt der QuelleMorgan, Lynette. „Greenhouses and protected cropping structures.“ In Hydroponics and protected cultivation: a practical guide, 11–29. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789244830.0002.
Der volle Inhalt der QuelleMorgan, Lynette. „Greenhouses and protected cropping structures.“ In Hydroponics and protected cultivation: a practical guide, 11–29. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789244830.0011.
Der volle Inhalt der QuelleVillars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, N. Melnichenko-Koblyuk et al. „[NH4]Co[ClO4]2Cl2[NH3]6“. In Structure Types. Part 5: Space Groups (173) P63 - (166) R-3m, 735. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-46933-9_604.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Clot structure"
Berthomier, Thibaud, Ali Mansour, Luc Bressollette, Frederic Le Roy und Dominique Mottier. „Venous blood clot structure characterization using scattering operator“. In 2016 2nd International Conference on Frontiers of Signal Processing (ICFSP). IEEE, 2016. http://dx.doi.org/10.1109/icfsp.2016.7802960.
Der volle Inhalt der QuelleChueh, Juyu, Christine F. Silva, Ajay K. Wakhloo und Matthew J. Gounis. „In-Vitro Clot Modeling for the Preclinical Assessment of Mechanical Thrombectomy in Acute Ischemic Stroke“. In ASME 2010 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2010. http://dx.doi.org/10.1115/sbc2010-19230.
Der volle Inhalt der QuelleMarsh, James J., Peter G. Chiles, Ni-Cheng Liang und Timothy A. Morris. „Disorganized Fibrin Clot Structure In Patients With Chronic Thromboembolic Pulmonary Hypertension“. In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a4098.
Der volle Inhalt der QuelleKhan, Ahsan, Eduard Shantsila, Y. C. Lau, Lewis Hardy, Helen Philippou und Gregory Lip. „BS20 Comparison of various anticoagulants on clot structure in atrial fibrillation“. In British Cardiovascular Society Annual Conference ‘Digital Health Revolution’ 3–5 June 2019. BMJ Publishing Group Ltd and British Cardiovascular Society, 2019. http://dx.doi.org/10.1136/heartjnl-2019-bcs.183.
Der volle Inhalt der QuelleKhan, Ahsan, Eduard Shantsila, Y. C. Lau, Lewis Hardy, Helen Philippou und Gregory Lip. „BS42 How warfarin and antiplatelets affect clot structure in atrial fibrillation“. In British Cardiovascular Society Annual Conference ‘Digital Health Revolution’ 3–5 June 2019. BMJ Publishing Group Ltd and British Cardiovascular Society, 2019. http://dx.doi.org/10.1136/heartjnl-2019-bcs.204.
Der volle Inhalt der QuelleTORBET, J. „MAGNETIC ORIENTATION IN BIOLOGY: VIRUS STRUCTURE - BLOOD CLOT ASSEMBLY - CELL GUIDANCE“. In Proceedings of the International Workshop on Materials Analysis and Processing in Magnetic Fields. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812701800_0026.
Der volle Inhalt der QuelleRajshekhar, Gannavarpu, Basanta Bhaduri, Krishnarao Tangella und Gabriel Popescu. „Three-dimensional fractal structure of a blood clot using quantitative phase imaging“. In Digital Holography and Three-Dimensional Imaging. Washington, D.C.: OSA, 2014. http://dx.doi.org/10.1364/dh.2014.dm4b.4.
Der volle Inhalt der QuelleLiang, Xin M., Dayong Gao und Nathan J. Sniadecki. „The Role of Thrombin, Fibrinogen, and Fibronectin on Platelet Clot Retraction Forces Analyzed Using Microposts“. In ASME 2010 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2010. http://dx.doi.org/10.1115/sbc2010-19614.
Der volle Inhalt der QuelleSiebenlist, K. R., J. T. Prchal und M. W. Masesson. „FIBRINOGEN BIRMINGHAM; A NEW CONGENITAL HETERODIMERIC DYSFIBRINOGENEMIA WITH DEFECTIVE FIBRINOPEPTIDE A RELEASE (Aα 16 Arg→His)“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643338.
Der volle Inhalt der QuelleHoser, M., und G. F. Savidge. „DIFFERENCES IN PEPTIDE MAPS OF a POLYMERS FROM FIBRIN PRODUCED IN THE PRESENCE AND ABSENCE OF ERYTHROCYTES“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643320.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Clot structure"
Wang, T. The crystal and molecular structure of azatranes: Azavanadatran (Z=t-Bu), monoazasilatrane (Z=H), azalithatrane (Z=Clo*4*), azaphosphatrane (Z=Me), azagermatrane (Z=t-Bu) and Azaalumatran (Z=nothing). Office of Scientific and Technical Information (OSTI), April 1996. http://dx.doi.org/10.2172/251132.
Der volle Inhalt der QuelleDufour, Quentin, David Pontille und Didier Torny. Contracter à l’heure de la publication en accès ouvert. Une analyse systématique des accords transformants. Ministère de l'enseignement supérieur et de la recherche, April 2021. http://dx.doi.org/10.52949/2.
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