Relevant bibliographies by topics / Haemagglutination

Academic literature on the topic 'Haemagglutination'

Author: Grafiati
Published: 10 December 2022
Last updated: 29 January 2023

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Journal articles on the topic "Haemagglutination"

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Elbashir, A. M., and Sally E. Millership. "Haemagglutinating activity ofAeromonasspp. from different sources; attempted use as a typing system." Epidemiology and Infection 102, no. 2 (April 1989): 221–29. http://dx.doi.org/10.1017/s0950268800029897.

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SUMMARYThe haemagglutinating ability of 141 isolates ofAeromonasspp. for human. horse and guinea-pig erythrocytes was examined. Although the majority of isolates (136/141) agglutinated human group O erythrocytes, all the eight possible patterns of agglutination were observed. Haemagglutination of human group O erythrocytes. but not horse or guinea-pig, was associated with the ability to agglutinate yeast cells (Saccharomyces) and with aggregation in a low concentration of ammonium sulphate. Haemagglutinating ability was further characterized by reactions in the presence of mannose, galactose or fucose. All the possible patterns of inhibition with individual sugars were observed, but haemagglutination of human group O erythrocytes not inhibited by mannose, galactose or fucose was more common among isolates from patients with diarrhoea, and isolates producing a Vero cell cytotoxin than would be expected by chance. This might represent a virulence factor.
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Neethling, Diane, and Helena Nevalainen. "Mycoparasitic species of Trichoderma produce lectins." Canadian Journal of Microbiology 42, no. 2 (February 1, 1996): 141–46. http://dx.doi.org/10.1139/m96-022.

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Culture filtrates and mycelial extracts of two mycoparasitic Trichoderma species were tested for the presence of lectins, by haemagglutination with human and marsupial erythrocytes. In Trichoderma viride, haemagglutinating activity was present in both mycelial extracts and culture filtrate. While secreted lectins were only detected after 6 days of growth, the presence of mycelium-associated lectins was first noted in 3-day-old cultures. Agglutinating activity was also demonstrated in the mycelium of 6-, 9- and 13-day-old cultures of Trichoderma harzianum. In this species, however, lectins were not secreted. In all instances, haemagglutination was inhibited by N-acetylgalactosamine and related sugars. This is the first report on the occurrence of lectins in Trichoderma spp.Key words: Trichoderma, lectins, mycoparasitism.
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Marjot, T., and L. Bourantos. "Cold haemagglutination." BMJ 349, jul03 4 (July 3, 2014): g3830. http://dx.doi.org/10.1136/bmj.g3830.

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Dybkjaer, E. "Photometric Quantitation of Haemagglutination." Scandinavian Journal of Haematology 4, no. 6 (April 24, 2009): 465–72. http://dx.doi.org/10.1111/j.1600-0609.1967.tb01648.x.

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Brown, K. E., and B. J. Cohen. "Haemagglutination by parvovirus B19." Journal of General Virology 73, no. 8 (August 1, 1992): 2147–49. http://dx.doi.org/10.1099/0022-1317-73-8-2147.

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LELWALA-GURUGE, JANAKI, ÅSA LJUNGH, and TORKEL WADSTRÖM. "Haemagglutination patterns ofHelicobacter pylori." APMIS 100, no. 7-12 (July 1992): 908–13. http://dx.doi.org/10.1111/j.1699-0463.1992.tb04018.x.

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Baratov, M. O. "Problems and prospects of bovine tuberculosis serological diagnosis." Veterinary Science Today 1, no. 1 (March 29, 2021): 33–37. http://dx.doi.org/10.29326/2304-196x-2021-1-36-33-37.

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For the purposes of tuberculosis eradication on any tuberculosis-infected farm, it is necessary to identify tuberculin anergic animals, being a potential source of the infection. The purpose of this study was to analyze the role of complement fixing and haemagglutinating antibodies for the detection cattle infected with bovine tuberculosis (TB). 977 cattle of different sex and age groups on two tuberculosis-infected farms were tested thrice over time. After 35 days all tuberculin reactive cattle (132 animals; 13.5%) were subjected to complex testing using allergy and serology methods. After 40 days, (Stage 3) animals demonstrating apparent specific antibody activity and low cell immunity were tested. Allergy tests were proved to be non-informative to diagnose tuberculosis on infected farms. Complement fixing and haemagglutinating antibodies were found to be active in tuberculin anergic animals. A higher antigenicity of Ukrainian RIEVM TB antigen complex as compared to Siberian RVI one was revealed by complement fixation test as well as by indirect haemagglutination test using VIEV polysaccharide antigen; the detection rate was 68 (7.0%), 28 (2.9%) and 299 (30.6%) respectively. The correlation between seropositivity and immunoreactivity was not established. Animals, positive in complement fixation and indirect haemagglutination tests, did not react to tuberculin. Nineteen out of twenty tuberculin reactive animals showed post mortem lesions, consistent with their seropositivity during post-mortem inspection; moreover, the postmortem lesions of animals, positive in complement fixation test using Siberian RVI antigen, were consistent in all cases. The results obtained suggest a high performance of allergy test and serological test combination and a promising potential of their complex use for tuberculosis diagnosis in cattle.
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Zielonka, Anja, Alma Gedvilaite, Jochen Reetz, Uwe Rösler, Hermann Müller, and Reimar Johne. "Serological cross-reactions between four polyomaviruses of birds using virus-like particles expressed in yeast." Journal of General Virology 93, no. 12 (December 1, 2012): 2658–67. http://dx.doi.org/10.1099/vir.0.044917-0.

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Polyomaviruses are aetiological agents of fatal acute diseases in various bird species. Genomic analysis revealed that avian polyomavirus (APyV), crow polyomavirus (CPyV), finch polyomavirus (FPyV) and goose hemorrhagic polyomavirus (GHPyV) are closely related to each other, but nevertheless form separate viral species; however, their serological relationship was previously unknown. As only APyV can be grown efficiently in tissue culture, virus-like particles (VLPs) were generated by expression of the genomic regions encoding the major structural protein VP1 of these viruses in yeast; these were used to elicit type-specific antibodies in rabbits and as antigens in serological reactions. For increased VLP assembly, a nuclear-localization signal was introduced into APyV-VP1. VLPs derived from the VP1 of the monkey polyomavirus simian virus 40 served as control. APyV-, GHPyV- and CPyV-VLPs showed haemagglutinating activity with chicken and human erythrocytes. CPyV- and GHPyV-specific sera showed slight cross-reactions in immunoblotting, haemagglutination-inhibition assay and indirect ELISA. The FPyV-specific serum inhibited the haemagglutination activity of APyV-VLPs slightly and showed a weak cross-neutralizing activity against APyV in cell-culture tests. Generally, these data indicate that the four polyomaviruses of birds are serologically distinct. However, in accordance with genetic data, a relationship between CPyV and GHPyV as well as between APyV and FPyV is evident, and grouping into two different serogroups may be suggested. The haemagglutinating activity of APyV, CPyV and GHPyV may indicate similar receptor-binding mechanisms for these viruses. Our data could be useful for the development of vaccines against the polyomavirus-induced diseases in birds and for interpretation of diagnostic test results.
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RAIDAL, SR, M. SABINE, and GM CROSS. "Laboratory diagnosis of psittacine beak and feather disease by haemagglutination and haemagglutination inhibition." Australian Veterinary Journal 70, no. 4 (April 1993): 133–37. http://dx.doi.org/10.1111/j.1751-0813.1993.tb06104.x.

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Hung, Le Dinh, and Dinh Thanh Trung. "Haemagglutination activity of lectins from extracts of some Vietnam marine sponges." Vietnam Journal of Biotechnology 17, no. 4 (November 2, 2020): 739–48. http://dx.doi.org/10.15625/1811-4989/17/4/14457.

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Aqueous extracts from 16 species of Vietnam marine sponges were examined for haemagglutination activity using native and enzyme-treated different animal and human erythrocytes. Among these, extracts from 14 species were found to have haemagglutinination activities toward at least one type of erythrocyte tested meaning that 87.5% of the surveyed marine sponge species possess haemagglutination activity. Strong activity was detected in extracts from marine sponge species Acanthella cavernosa, Axinyssa sp., Cinachyrella sp., 01NT.2.4, 3.5, 3.10, 3.11 and 3.18 with enzyme-treated various animal and human erythrocytes. In a haemagglutination–inhibition test with various monosaccharides and glycoproteins, haemagglutination activity of the extract from A. cavernosa had no affinity for any of the monosaccharides, but inhibited by porcine stomach mucin and fetuin, whereas activities of the extract from Cinachyrella sp. were strongly inhibited by monosaccharides, such as D-galactose and N-acetyl-D-galatosamine, but not with glycoproteins. The activity of Stylissa flexibilis extract was inhibited by D-galactose, porcine stomach mucin, fetuin and their asialo derivatives, suggesting the presence of lectin specific for O-glycans of this species. The activities of four sponge extracts from A. cavernosa, S. flexibilis, Axinyssa sp. and Cinachyrella sp. were stable over a wide range of pH and temperature. Haemagglutination activities of A. cavernosa, Axinyssa sp. and Cinachyrella sp. extracts were independent of the presence of divalent cations, except for the haemagglutination activity of extract from S. flexibilis, which was dependent on the presence of divalent cations. The results suggest that Vietnam marine sponges may be good sources of useful lectins for biochemical and biomedical applications.
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Book chapters on the topic "Haemagglutination"

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Wide, Leif, and Carl A. Gemzell. "Determination of Gonadotropins in Urine by a Haemagglutination Inhibition Reaction." In Ciba Foundation Symposium - Immunoassay of Hormones (Colloquia on Endocrinology, Vol. 14), 296–309. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719299.ch16.

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Read, Charles H., Sandra A. Eash, and Samir Najjar. "Experiences with the Haemagglutination Method of Human Growth Hormone Assay." In Ciba Foundation Symposium - Immunoassay of Hormones (Colloquia on Endocrinology, Vol. 14), 45–62. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719299.ch4.

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Nisha, P., Manuel Thomas, and T. K. Neelima. "Role of Lectin in Biofilm Inhibition, Haemagglutination, Endocytosis and Phagocytosis." In Aquatic Lectins, 287–304. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0432-5_13.

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de Lange, Gerda G., Fred M. van Leeuwen, Peter H. van Eede, Patrick J. Lincoln, and C. Paul Engelfriet. "Monoclonal Antibodies to Immunoglobulin Allotypes: Specificity and Reactivity in Haemagglutination and ELISA Techniques." In Advances in Forensic Haemogenetics, 157–61. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71150-3_33.

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Serrano, R., F. Carrapiço, and R. Vidal. "Haemagglutination Activity by Extracts of Symbiotic Bacteria Present in the System Azolla-Anabaena." In Biological Nitrogen Fixation for the 21st Century, 175. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5159-7_79.

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Ciznar, Ivan, Firdausi Qadri, Shafiqul Haq, and Shaik Abu Hossain. "Haemagglutinating Shigellae." In Molecular Pathogenesis of Gastrointestinal Infections, 231–36. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-5982-1_30.

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Davenporat, F. M., A. V. Hennessy, J. Drescher, and R. G. Webster. "Analytical, Serological and Clinical Experiences with the Haemagglutinating Subunits of Influenza A Virus." In Ciba Foundation Symposium - Cellular Biology of Myxovirus Infections, 272–98. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719367.ch12.

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Schultze, Beate, Luis Enjuanes, Dave Cavanagh, and Georg Herrler. "N-Acetylneuraminic Acid Plays a Critical Role for the Haemagglutinating Activity of Avian Infectious Bronchitis Virus and Porcine Transmissible Gastroenteritis Virus." In Coronaviruses, 305–10. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2996-5_47.

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"Haemagglutination test." In BSAVA Guide to Procedures in Small Animal Practice, 156–59. British Small Animal Veterinary Association, 2014. http://dx.doi.org/10.22233/9781905319831.2.47.

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Prince, CP. "Treponema Pallidum Haemagglutination Assay (Tpha)." In Practical Manual of Medical Microbiology, 159. Jaypee Brothers Medical Publishers (P) Ltd., 2009. http://dx.doi.org/10.5005/jp/books/10654_42.

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Conference papers on the topic "Haemagglutination"

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Oehler, G., H. Klaus, E. Spanuth, and K. E. Stötzer. "DETECTION OF SOLUBLE FIBRIN MONOMER COMPLEXES - COMPARISON OF A HAEMAGGLUTINATION ASSAY WITH THE ETHANOL GELATION TEST." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644886.

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Hypercoagulability and disseminated intravascularcoagulation (DIC) are characterized by the presenceof circulating fibrin monomer complexes in plasma.In342 patients with possible DIC fibrin monomers, fibrinogen, reptilase time, antithrombin III and othercoagulation parameters were determined at frequent intervals.Testing of soluble fibrin monomer complexeswas performed using a sensitive and reliable haemagglut- ination assay, with red cells sensitized by fibrin monomers (FM-Test) and the ethanol gelation test(EGT). Method comparison regarding the influence offibrinogen levels and fibrin degradation products shows that high fibrinogen levels lead to false positive results with EGT. The same effect is observed forfibrin degradation products and EGT whereas no influence of fibrinogen level and fibrin degradation products on the FM-Test occurs.It could be shown that with normal fibrinogen concentrations (200-400 mg/dl) the positive test results by FMT and EGT are comparable, whereas with fibrinogen concentrations below 200 mg/dl the number of positive results obtained with the EGT amounted to half the number given by FMT. In the case of fibrinogen concentrations above 400 mg/dl, positive results obtained with EGT were 3.3 times higher than FMT. Nearlyidentical results were obtained by comparing the influence of degradation products. In case of high degradation product concentrations, EGT gives 4.5 timesmore positive results than FMT.Further we compared the number of positive test results obtained by the FMT with the level of AT III because it is wellknown that the AT IIIHevel decreases caused by proteolytic activity generated in DIC.In this study it could be shown that fibrin monomer increases in parallel with the decrease of AT III. Thiseffect does not occur with fibrin degradation products.
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