Gotowe bibliografie tematyczne / Blood – Coagulation

Spis treści

  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek
  5. Streszczenia konferencji
  6. Raporty organizacyjne

Gotowa bibliografia na temat „Blood – Coagulation”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 29 lipca 2024

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Artykuły w czasopismach na temat "Blood – Coagulation"

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Maslov, Artem, i Marta Mashevska. "BLOOD COAGULATION MONITORING SYSTEM". Measuring Equipment and Metrology 81, nr 3 (2020): 24–27. http://dx.doi.org/10.23939/istcmtm2020.03.024.

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Mann, Kenneth G. "Blood Coagulation". Alcoholism: Clinical and Experimental Research 23, nr 6 (czerwiec 1999): 1111–13. http://dx.doi.org/10.1111/j.1530-0277.1999.tb04233.x.

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Norris, Lucy A. "Blood coagulation". Best Practice & Research Clinical Obstetrics & Gynaecology 17, nr 3 (czerwiec 2003): 369–83. http://dx.doi.org/10.1016/s1521-6934(03)00014-2.

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Chris Ludlam. "Blood Coagulation". Clinica Chimica Acta 186, nr 3 (styczeń 1990): 402–3. http://dx.doi.org/10.1016/0009-8981(90)90329-q.

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Dahlbäck, Björn. "Blood coagulation". Lancet 355, nr 9215 (maj 2000): 1627–32. http://dx.doi.org/10.1016/s0140-6736(00)02225-x.

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Littlewood, J., i S. Bevan. "Canine blood coagulation". Veterinary Record 125, nr 4 (22.07.1989): 97. http://dx.doi.org/10.1136/vr.125.4.97-a.

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Jamnicki, Marina, Andreas Zollinger, Burkhardt Seifert, Dragoljub Popovic, Thomas Pasch i Donat R. Spahn. "Compromised Blood Coagulation". Anesthesia & Analgesia 87, nr 5 (listopad 1998): 989–93. http://dx.doi.org/10.1097/00000539-199811000-00002.

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Jamnicki, Marina, Andreas Zollinger, Burkhardt Seifert, Dragoljub Popovic, Thomas Pasch i Donat R. Spahn. "Compromised Blood Coagulation". Anesthesia & Analgesia 87, nr 5 (listopad 1998): 989–93. http://dx.doi.org/10.1213/00000539-199811000-00002.

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Pryzdial, Edward L. G., Frank M. H. Lee, Bryan H. Lin, Rolinda L. R. Carter, Tseday Z. Tegegn i Mark J. Belletrutti. "Blood coagulation dissected". Transfusion and Apheresis Science 57, nr 4 (sierpień 2018): 449–57. http://dx.doi.org/10.1016/j.transci.2018.07.003.

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Krishnaswamy, Sriram. "Supercharged blood coagulation". Blood 113, nr 9 (26.02.2009): 1873–74. http://dx.doi.org/10.1182/blood-2008-11-188532.

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Rozprawy doktorskie na temat "Blood – Coagulation"

1

Gray, E. "Lipoproteins, blood coagulation and thrombosis". Thesis, Open University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.372834.

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The main aim of this study was to investigate the involvement of plasma lipoproteins in the blood coagulation system and the implications of this relationship in the pathogenesis of thrombosis. This study has shown that lipid peroxide-induced thrombin generation is caused by a two-fold mechanism: direct interaction of lipid peroxides with lipoprotein phospholipids and inhibition of anti-thrombin III via its heparin-binding site. Experiments using purified lipoproteins have shown that triglyceride-rich lipoproteins, i.e. chylomicra and very low density lipoproteins, are sources of procoagulant activity, whereas low density and high density lipoproteins have little effect. Further work with phospholipids extracted from chylomicra has demonstrated that lipid peroxides interact with the phospholipid component of the lipoprotein molecule and, possibly through an increase in overall negative charge, provide a suitable surface for the binding of clotting factors. Subcutaneous injection of potent lipase releasers, which are weak in vitro anticoagulants, reduce the ex vivo thrombin-generating activity of post-infusion plasma. This reduction in procoagulant activity is caused by the phospholipase action of the hepatic tri-glyceride lipase (HTGL) released. Human HTGL also enhances plasma anti-Xa activity, due to direct inhibition of Xa clotting activity, but the amidolytic activity of Xa is unaffected, thus implying that the serine site of Xa is not preferentially targeted. The phospholipid binding site of Xa appears to be involved, but this anti-Xa effect is not due to the phospholipase action of HTGL. The antithrombotic effects of heparin and heparin analogues may thus be partly due to the release of HTGL, which can reduce pro-coagulant activity via inhibition of lipid peroxide-induced thrombin generation and enhancement of plasma anti-Xa activity.
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Sowedan, Ahmed M. "Rheometrical study of blood coagulation". Thesis, Swansea University, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.678535.

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Perdomo, Joana L. "Mathematical Modeling of Blood Coagulation". Scholarship @ Claremont, 2016. https://scholarship.claremont.edu/hmc_theses/71.

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Blood coagulation is a series of biochemical reactions that take place to form a blood clot. Abnormalities in coagulation, such as under-clotting or over- clotting, can lead to significant blood loss, cardiac arrest, damage to vital organs, or even death. Thus, understanding quantitatively how blood coagulation works is important in informing clinical decisions about treating deficiencies and disorders. Quantifying blood coagulation is possible through mathematical modeling. This review presents different mathematical models that have been developed in the past 30 years to describe the biochemistry, biophysics, and clinical applications of blood coagulation research. This review includes the strengths and limitations of models, as well as suggestions for future work.
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Ramström, Sofia. "The role of platelets in whole blood coagulation /". Linköping : Univ, 2003. http://www.bibl.liu.se/liupubl/disp/disp2003/med776s.pdf.

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Tate, Geoffrey Michael. "The blood coagulation mechanism and hypercoagulability". Thesis, University of Leeds, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.281131.

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Tosenberger, Alen. "Blood flow modelling and applications to blood coagulation and atherosclerosis". Doctoral thesis, Institut Camille Jordan, CNRS UMR 5208, Université Claude Bernard Lyon 1, Université Claude Bernard Lyon 1, France, 2014. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/244806.

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Fung, Marion R. "Molecular genetics of blood coagulation factor X". Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/28783.

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Thirty thousand colonies of a bovine liver cDNA library were screened with a mixture of synthetic oligodeoxyribonucleotides coding for bovine factor X. Five positive colonies were identified, and plasmid DNA was isolated. Cleavage with restriction endonucleases showed that these plasmids (designated pBXl-5) contained inserts of 1530 bp, 770 bp, 700 bp, 1100 bp and 930 bp. DNA sequence analysis of the plasmid with the largest insert (pBXl) confirmed that bovine factor X cDNAs had been cloned. The cDNA sequence predicts that factor X is synthesized as a single chain precursor in which the light and heavy chains of plasma factor X are linked by the dipeptide Arg-Arg. The cDNA sequence also predicts that factor X is synthesized with a preproleader peptide. It is proposed that at least five specific proteolytic events occur during the conversion of preprofactor X to plasma factor Xa. A human liver cDNA library was screened by colony hybridization with a bovine factor X cDNA probe. Three of the positive plasmids contained overlapping DNA that coded for most of human factor X mRNA. A second human liver cDNA library was screened by in situ hybridization with 32P-labeled human factor X cDNA clones obtained from the first screen. Several clones were isolated that contained longer inserts. DNA sequence analysis of these clones allowed the prediction of the amino acid sequence of the precursor form of human plasma factor X. From these studies, it is predicted that human factor X is synthesized as a single polypeptide chain precursor in which the light and heavy chains of plasma factor X are linked by the tripeptide Arg-Lys-Arg. The cDNA sequence also predicts that human factor X is synthesized as a preproprotein having an aminoterminal leader peptide of 40 amino acid residues. A comparison of the amino acid sequences of human and bovine factor X shows high sequence identity around the calcium- binding regions and catalytic regions but low sequence identity around the nonfunctional regions. A human genomic phage library was screened with a human factor X cDNA as a hybridization probe. Thirty-two overlapping phage clones were isolated. Characterization of six of these clones indicates that over 32 Kbp of contiguous sequence is represented. DNA sequence and restriction map analysis shows that the factor X gene is comprised of at least 8 exons and 7 introns. No clones representing the 5' untranslated region and the prepeptide of the leader sequence were identified. Two further genomic phage libraries and two libraries specific for the 5' region of the factor X gene were screened, but no 5' end clones were obtained. Restriction enzyme mapping and Southern blot analysis indicate that thus far, the human factor X gene maps to 24 Kbp of the human genome. Comparison of the factor X gene with other vitamin K-dependent blood coagulation factor genes reveals homologous exon organization. Within the blood coagulation serine proteases factor X, factor IX, factor VII, and protein C form a closely related gene family.
Medicine, Faculty of
Biochemistry and Molecular Biology, Department of
Graduate
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Sarphie, Anna Frances. "Changes in blood coagulation associated with hyperlipidaemia". Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.319009.

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Smith, Brian. "Protein models in blood coagulation and fibrinolysis". Thesis, University of Oxford, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239327.

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Head, Denise Marie. "Pharmacological modulation of the blood coagulation cascade". Thesis, King's College London (University of London), 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298832.

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Książki na temat "Blood – Coagulation"

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A, Zwaal R. F., i Hemker H. C, red. Blood coagulation. Amsterdam: Elsevier, 1986.

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Matthias, Fritz Reinhard. Blood Coagulation Disorders. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-83098-3.

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University of Sheffield. Biomedical Information Service., red. Blood coagulation factors. Sheffield: Universi y of Sheffield Biomedical Information Service, 1985.

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Altieri, Dario C. The coagulation-inflammation interface: Coagulation assembly on leukocytes. New York: Springer, 1997.

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Sibinga, C. Th Smit, P. C. Das i P. M. Mannucci, red. Coagulation and Blood Transfusion. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3900-1.

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1951-, High Katherine A., i Roberts H. R, red. Molecular basis of thrombosis and hemostasis. New York: M. Dekker, 1995.

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Davie, E. W., i E. Kakishita. Blood coagulation, fibrinolysis, and platelets. Tokyo: Springer, 1996.

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A, Zwaal R. F., red. Coagulation and lipids. Boca Raton, Fla: CRC Press, 1989.

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P, Antovic Jovan, i Blombäck Margareta, red. Essential guide to blood coagulation. Chichester, West Sussex, UK: Wiley-Blackwell, 2010.

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Theodore S. Zimmerman Memorial Conference: Progress in Vascular Biology, Hemostasis, and Thrombosis (1990 La Jolla, San Diego, Calif.). Progress in vascular biology, hemostasis, and thrombosis. New York, N.Y: New York Academy of Sciences, 1991.

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Części książek na temat "Blood – Coagulation"

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Baldo, Brian A. "Blood Coagulation". W Safety of Biologics Therapy, 479–513. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30472-4_10.

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Levine, Martin. "Blood Coagulation". W Topics in Dental Biochemistry, 175–201. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-88116-2_11.

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Preissner, Klaus T. "Blood Coagulation". W Encyclopedia of Immunotoxicology, 116–21. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-54596-2_182.

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Innocente, Salvatore. "Blood Coagulation". W Textbook of Angiology, 501–7. New York, NY: Springer New York, 2000. http://dx.doi.org/10.1007/978-1-4612-1190-7_41.

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Preissner, Klaus T. "Blood Coagulation". W Encyclopedia of Immunotoxicology, 1–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27786-3_182-2.

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Fasano, Antonio, i Adélia Sequeira. "Blood Coagulation". W Hemomath, 79–158. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-60513-5_2.

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Kim, Cheorl-Ho. "Blood Coagulation as Coagulation Dysregulation". W Glycoimmunology in Xenotransplantation, 221–25. Singapore: Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-7691-1_16.

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Matthias, Fritz Reinhard. "Physiology of Blood Coagulation and Hemostasis". W Blood Coagulation Disorders, 1–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-83098-3_1.

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Matthias, Fritz Reinhard. "Fibrinolytic and Long-Term — Therapy in the Arterial Vessel System". W Blood Coagulation Disorders, 246–67. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-83098-3_10.

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Matthias, Fritz Reinhard. "Cerebrovascular Diseases". W Blood Coagulation Disorders, 268–74. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-83098-3_11.

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Streszczenia konferencji na temat "Blood – Coagulation"

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Razavi, Jahan, i Amin Arbabian. "Chromatic Properties of Blood During Coagulation". W 2019 41st Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC). IEEE, 2019. http://dx.doi.org/10.1109/embc.2019.8856365.

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Minkyung Lee, Hyunchul Kim, Yunjung Kim, Won Young Lee, Ku Youn Baik, N. K. Kaushik i Guangsup Cho. "Blood coagulation with atmospheric-plasma jets". W 2012 IEEE 39th International Conference on Plasma Sciences (ICOPS). IEEE, 2012. http://dx.doi.org/10.1109/plasma.2012.6383715.

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Vinogradova, O. N., i V. G. Chelnov. "Blood coagulation by atmospheric pressure plazma". W 2008 International Conference Modern Technique and Technologies - (MTT 2008). IEEE, 2008. http://dx.doi.org/10.1109/spcmtt.2008.4897514.

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Miura, T., M. Inagaki, M. Taki, N. Saito, T. Meguro i K. Yamada. "GRANULOCYTE ELASTASE RELEASE DURING BLOOD COAGULATION". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643166.

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Granulocyte elastase (ELP) has a high-potency fibrinolytic activity. Hence, there is a possibility that ELP acts as a thrombolytic enzyme like plasmin in thrombolysis. We investigated the release of ELP from granulocytes, especially during blood coagulation.The biological activity of ELP was measured using a synthetic substrate, Suc-Ala-Tyr-Leu-Val-pNA. The immunological activity assayed as an alpha-l-antitrypsin-ELP complex was measured using an anti-ELP antibody (Merck), because more than 90% of ELP in blood forms alpha-l-antitrypsin-ELP complexes.The ELP activity in granulocytes extracted by 2 mol/1 KSCN was 10 mU/106 cells. This fibrinolytic activity corresponds to 1-2 U of plasmin in the fibrin plate method.The ELP release from separated granulocytes was observed by adding Ca2+, and the release was increased by Ca ionophore A 23187. The release was dose-dependent as far as 10 mM Ca2+ (final concentration) and the maximum release was obtained within 15 minutes. However, the ELP release was not produced by thrombin.The level of alpha-l-antitrypsin-ELP complex in serum was twice higher and that in heparinized plasma was 1.5 times higher than that in sodium citrated plasma. ELP was not released from granulocytes incubated in both prekallikrein deficient plasma and Factor XII deficient plasma containing 10 mM Ca2+. But addition of normal plasma (about 10%) resulted in ELP releaseThese results suggest that the ELP release from granulocytes is dependent on Ca2+ and the release is relevant to the blood coagulation system, especially to contact factors.
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Cheng, Zhigang, Hongli Liu i Zhengqing Zhao. "Design of embedded blood coagulation detecting system". W 2017 32nd Youth Academic Annual Conference of Chinese Association of Automation (YAC). IEEE, 2017. http://dx.doi.org/10.1109/yac.2017.7967449.

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Aida, Y., i K. Shimano. "Modelling of blood coagulation in cerebral aneurysms". W BIOMED 2013. Southampton, UK: WIT Press, 2013. http://dx.doi.org/10.2495/bio130051.

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Ren, Tingting, Yang Xu, Xuemei Yang, Jing Zhang i Xianhong Li. "Studies on Calibration of Blood Coagulation Analyzer". W 2021 3rd International Academic Exchange Conference on Science and Technology Innovation (IAECST). IEEE, 2021. http://dx.doi.org/10.1109/iaecst54258.2021.9695761.

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Kim, Y. H., H. S. Rhim, H. S. Uhm i E. H. Choi. "Atmospheric pressure air plasma jet assisted blood coagulation". W 2011 IEEE 38th International Conference on Plasma Sciences (ICOPS). IEEE, 2011. http://dx.doi.org/10.1109/plasma.2011.5993283.

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Vikinge, Trine P., Kenny M. Hansson, Johan Benesch, Knut Johansen, Mats Ranby, Tomas L. Lindahl, Ingemar Lundstroem i Pentti Tengvall. "Blood plasma coagulation studied by surface plasmon resonance". W BiOS Europe '98, redaktorzy Francesco Baldini, Nathan I. Croitoru, Martin Frenz, Ingemar Lundstroem, Mitsunobu Miyagi, Riccardo Pratesi i Otto S. Wolfbeis. SPIE, 1999. http://dx.doi.org/10.1117/12.336920.

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Nguyen, Phuc V., Junghwan Oh i Hyun Wook Kang. "Blood coagulation using High Intensity Focused Ultrasound (HIFU)". W SPIE BiOS, redaktorzy Bernard Choi, Nikiforos Kollias, Haishan Zeng, Hyun Wook Kang, Brian J. F. Wong, Justus F. Ilgner, Guillermo J. Tearney i in. SPIE, 2014. http://dx.doi.org/10.1117/12.2037171.

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Raporty organizacyjne na temat "Blood – Coagulation"

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Crandall, Craig G., Victor Convertino i Andre Cap. Effects of Thermal Status on Markers of Blood Coagulation During Simulated Hemorrhage. Fort Belvoir, VA: Defense Technical Information Center, kwiecień 2013. http://dx.doi.org/10.21236/ada577217.

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Crandall, Craig G., Victor Convertino i Andre Cap. Effects of Thermal Status on Markers of Blood Coagulation During Simulated Hemorrhage. Fort Belvoir, VA: Defense Technical Information Center, kwiecień 2014. http://dx.doi.org/10.21236/ada600964.

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Crandall, Craig G., Victor Convertino i Andre Cap. Effects of Thermal Status on Markers of Blood Coagulation During Simulated Hemorrhage. Fort Belvoir, VA: Defense Technical Information Center, kwiecień 2015. http://dx.doi.org/10.21236/ada616416.

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Viksna, Ludmila, Oksana Kolesova, Aleksandrs Kolesovs, Ieva Vanaga i Seda Arutjunana. Clinical characteristics of COVID-19 patients (Latvia, Spring 2020). Rīga Stradiņš University, grudzień 2020. http://dx.doi.org/10.25143/fk2/hnmlhh.

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Data include following variables: Demographics, epidemiological history, comorbidities, diagnosis, complications, and symptoms on admission to the hospital. Also, body’s temperature and SpO2. Blood cells: white cells count (WBC), neutrophils (Neu), lymphocytes (Ly), eosinophils (Eo) and monocytes (Mo), percentages of segmented and banded neutrophils, erythrocytes (RBC), platelet count (PLT), hemoglobin (Hb), and hematocrit (HCT); Inflammatory indicators: erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP); Tissue damage indicators: alanine aminotransferase (ALT), lactate dehydrogenase (LDH), and troponin T (TnT); Electrolytes: potassium and sodium concentration; Renal function indicators: creatinine and glomerular filtration rate (GFR); Coagulation tests: D-dimer, prothrombin time, and prothrombin index on admission to the hospital.
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