Relevant bibliographies by topics / Tetanus-Toxin

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Tetanus-Toxin'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Tetanus-Toxin"

1

Matsuda, Morihiro, and Nakaba Sugimoto. "Tetanus Toxin." Journal of Toxicology: Toxin Reviews 16, no. 4 (1997): 241–52. http://dx.doi.org/10.3109/15569549709016459.

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Demotz, S., A. Lanzavecchia, U. Eisel, H. Niemann, C. Widmann, and G. Corradin. "Delineation of several DR-restricted tetanus toxin T cell epitopes." Journal of Immunology 142, no. 2 (1989): 394–402. http://dx.doi.org/10.4049/jimmunol.142.2.394.

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Abstract We have characterized five human T cell clones specific for tetanus toxin. The combination of different techniques allowed us to precisely map two T cell epitopes within fragments 830-843 and 1273-1284 of tetanus toxin, as formally demonstrated by the use of corresponding synthetic peptides. The three other T cell clones were specific for regions 2-602, 604-742, and 865-1315 of tetanus toxin, respectively. The five T cell clones were shown to be restricted to HLA-DR Ag. Furthermore, the allele of HLA-DR utilized by the various epitopes has been determined. The use of HLA-DR-transfecte
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Chawla, Dr Anil Kumar, Chandrani Das, Paramdeep Singh, Mansha Tiwari, and Dr Seema Chaudhary. "Production of tetanus toxin by using media substantially free from meat and blood." Asian Journal of Pharmaceutical and Clinical Research 9, no. 6 (2016): 284. http://dx.doi.org/10.22159/ajpcr.2016.v9i6.14410.

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The present study was to redesign the conventional Mueller and Miller medium to produce tetanus toxin from Clostridium tetani. Meat based ingredients (such as Bovine Heart/ Brain/ Liver Infusion) were replaced with vegetable peptone & alternate casein hydrolysate and scaled up from 100mL to 1000mL. Modified Mueller and Miller Medium containing vegetable peptone (substitute of BHI) and alternate casein hydrolysate were used for production and scale -up of tetanus toxin. Detoxification of tetanus toxin was carried out by using formaldehyde to produce tetanus toxoid. Purification of tetanus t
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Critchley, D. R., P. G. Nelson, W. H. Habig, and P. H. Fishman. "Fate of tetanus toxin bound to the surface of primary neurons in culture: evidence for rapid internalization." Journal of Cell Biology 100, no. 5 (1985): 1499–507. http://dx.doi.org/10.1083/jcb.100.5.1499.

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We examined the nature of the tetanus toxin receptor in primary cultures of mouse spinal cord by ligand blotting techniques. Membrane components were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and transferred to nitrocellulose sheets, which were overlaid with 125I-labeled tetanus toxin. The toxin bound only to material at or near the dye front, which was lost when the cells were delipidated before electrophoresis. Gangliosides purified from the lipid extract were separated by thin-layer chromatography and the chromatogram was overlaid with 125I-toxin. The toxin boun
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Qazi, Omar, Dorothea Sesardic, Robert Tierney, et al. "Reduction of the Ganglioside Binding Activity of the Tetanus Toxin HC Fragment Destroys Immunogenicity: Implications for Development of Novel Tetanus Vaccines." Infection and Immunity 74, no. 8 (2006): 4884–91. http://dx.doi.org/10.1128/iai.00500-06.

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ABSTRACT In this study, the immunogenicities of the nontoxic HC fragment of tetanus toxin and derivatives lacking ganglioside binding activity were compared with that of tetanus toxoid after subcutaneous immunization of mice. Wild-type HC (HCWT) protein and tetanus toxoid both elicited strong antibody responses against toxoid and HC antigens and provided complete protection against toxin challenge. Mutants of HC containing deletions essential for ganglioside binding elicited lower responses than HCWT. HCM115, containing two amino acid substitutions within the ganglioside binding site, provided
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Stecher, B., G. Ahnert-Hilger, U. Weller, T. P. Kemmer та M. Gratzl. "Amylase release from streptolysin O-permeabilized pancreatic acinar cells. Effects of Ca2+, guanosine 5′-[γ-thio]triphosphate, cyclic AMP, tetanus toxin and botulinum A toxin". Biochemical Journal 283, № 3 (1992): 899–904. http://dx.doi.org/10.1042/bj2830899.

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The molecular requirements for amylase release and the intracellular effects of botulinum A toxin and tetanus toxin on amylase release were investigated using rat pancreatic acinar cells permeabilized with streptolysin O. Micromolar concentrations of free Ca2+ evoked amylase release from these cells. Maximal release was observed in the presence of 30 microM free Ca2+. Ca(2+)-stimulated, but not basal, amylase release was enhanced by guanosine 5′-[gamma-thio]triphosphate (GTP[S]) (3-4 fold) or cyclic AMP (1.5-2 fold). Neither the two-chain forms of botulinum A toxin and tetanus toxin, under red
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Bergey, G. K., H. Bigalke, and P. G. Nelson. "Differential effects of tetanus toxin on inhibitory and excitatory synaptic transmission in mammalian spinal cord neurons in culture: a presynaptic locus of action for tetanus toxin." Journal of Neurophysiology 57, no. 1 (1987): 121–31. http://dx.doi.org/10.1152/jn.1987.57.1.121.

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Tetanus toxin reduces monosynaptic inhibitory and excitatory synaptic transmission in mouse spinal cord neurons in culture. Inhibitory transmission is preferentially reduced by the toxin; however, excitatory transmission is also ultimately reduced and blocked by the concentrations of toxin used in these studies. Recordings from monosynaptically connected cell pairs revealed a marked diminution in amplitude of evoked monosynaptic inhibitory postsynaptic potentials coincident with the onset of convulsant action at a time when evoked monosynaptic EPSPs were relatively unaffected. Increased polysy
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Galli, T., T. Chilcote, O. Mundigl, T. Binz, H. Niemann, and P. De Camilli. "Tetanus toxin-mediated cleavage of cellubrevin impairs exocytosis of transferrin receptor-containing vesicles in CHO cells." Journal of Cell Biology 125, no. 5 (1994): 1015–24. http://dx.doi.org/10.1083/jcb.125.5.1015.

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Cellubrevin is a member of the synaptobrevin/VAMP family of SNAREs, which has a broad tissue distribution. In fibroblastic cells it is concentrated in the vesicles which recycle transferrin receptors but its role in membrane trafficking and fusion remains to be demonstrated. Cellubrevin, like the synaptic vesicle proteins synaptobrevins I and II, can be cleaved by tetanus toxin, a metallo-endoprotease which blocks neurotransmitter release. However, nonneuronal cells are unaffected by the toxin due to lack of cell surface receptors for its heavy chain. To determine whether cellubrevin cleavage
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Mitchell, John. "Tetanus Toxin-enhanced GABA Immunoreactivity in Living Neurons." Journal of Histochemistry & Cytochemistry 46, no. 3 (1998): 321–26. http://dx.doi.org/10.1177/002215549804600305.

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Analysis of the connectivity between different neuronal cell types is dependent on an appreciation of their dendritic and axonal arborizations. A detailed study of the dendrites and axons of GABAergic neurons has been thwarted by the lack of a suitable technique for enhancing GABA immunoreactivity. This article describes a procedure using tetanus toxin which, when applied to organotypic hippocampal cultures, considerably enhances the immunoreactivity in the dendrites and axons of the GABA- and somatostatin-containing neurons and clearly demonstrates the co-localization of GABA and somatostatin
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Mujezinovic, Indira, Ahmed Smajlovic, and Vitomir Cupic. "The effect of haloperidol, aminooxyacetic acid and (-)-nuciferine on prolonging survival time of mice with tetanus." Veterinarski glasnik 72, no. 2 (2018): 122–28. http://dx.doi.org/10.2298/vetgl171023005m.

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Introduction. Tetanus, also known as lockjaw, is a very dangerous, infectious, acute, usually afebrile disease characterised by muscle spasms. The causative agent of the disease is the bacterium Clostridium tetani. This pathogen produces a specific neurotoxin, termed tetanus toxin, with two components: tetanospasmin and tetanolysin. Light chains of tetanospasmin cleavage synaptobrevin, which in turn prevent release of the inhibitory neurotransmitter GABA into the synaptic cleft. The ?-motor neurons are, therefore, under no inhibitory control, as a result of which they undergo sustained excitat
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Dissertations / Theses on the topic "Tetanus-Toxin"

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Michaelides, Alecos. "Chemical and enzymatic fragmentation of tetanus toxin and immunological studies on anti-tetanus toxin and toxoid sera." Thesis, University of Ottawa (Canada), 1996. http://hdl.handle.net/10393/9661.

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This thesis describes the immunization protocols for the production of antibodies against tetanus toxin and toxoid in guinea pigs and mice. Antibodies were successfully raised against the toxin without mortalities in either species. The murine sera obtained, were isotyped by ELISA and the toxin was proven to be a superior antigen in eliciting production of IgG$\rm\sb{2a}$ and IgG$\sb3$. The two isotypes which have demonstrated antitumor activity. The anti-toxoid sera exhibited a lower reactivity towards the toxin and toxoid when compared with anti-toxin sera. The reactivity of recombinant teta
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Johnston, Louise. "Transcutaneous immunisation with antigens derived from tetanus toxin." Thesis, Imperial College London, 2008. http://hdl.handle.net/10044/1/4657.

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Transcutaneous immunisation (TCI) is a novel needle-free method of vaccine delivery, which involves the application of soluble antigens onto the surface of intact skin. In this thesis, the immunogenicity and neutralising potency of tetanus neurotoxin (TeNT) fragments were compared to that of tetanus toxoid (TTxd) following TCI. In addition, to understand the mechanisms of induction of immune response by TCI, in vitro and in vivo interaction of tetanus proteins with skin immune cells was also investigated. The 50kDa recombinant carboxyl-terminal fragment of tetanus toxin (HCWT) and a 50kDa HC m
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Sheppard, A. J. "Studies on production and characterisation of monoclonal antibodies to tetanus toxin, and their use for developing immunopurified tetanus toxoid and toxin." Thesis, Open University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235280.

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Sundstrom, Lars Eric. "An electrophysiological study of tetanus toxin-induced hippocampal epilepsy." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.256376.

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Colville, Caroline Anne. "The interaction of tetanus toxin with adrenal chromaffin cells." Thesis, University of Edinburgh, 1992. http://hdl.handle.net/1842/19641.

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Tetanus toxin exerts its primary biological effect by impairing the release of inhibitory neurotransmitters in the central nervous system; the mechanism of this blockade, however, remains unknown. Studies using adrenal medullary chromaffin cells, which are closely related to the toxin's target neurones but much more accessible to biochemical investigation, have the potential to provide information on various aspects of the intoxication process of tetanus. Nicotine-evoked (but not basal) secretion of catecholamines from intact chromaffin cells was inhibited by tetanus toxin in a dose-dependent
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Scott, Nathan. "Anti-tetanus toxin chelating recombinant antibodies by phage display." Thesis, Imperial College London, 2008. http://hdl.handle.net/10044/1/4638.

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Chelating Recombinant Antibodies (CRAbs) are a form of high affinity tandem single chain antibody (scFv) with two component scFvs which target non‐overlapping epitopes on the same antigen molecule. The optimised inter‐scFv linker allows simultaneous engagement of the scFvs resulting in a synergistic improvement in affinity. High affinity is a desirable characteristic in therapeutic antibodies since it strongly correlates with improved potency. Building upon previous work, this thesis describes the development of a phage‐display based approach toward isolating CRAbs with both the optimal scFv p
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Parton, Robert Glenn. "The binding and internalisation of tetanus toxin by neuronal tissue." Thesis, University of Leicester, 1987. http://hdl.handle.net/2381/35122.

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Sweeney, Sean Thomas. "Targetted expression of tetanus toxin light chain in Drosophilia melanogaster." Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627065.

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Andreu, Alice. "Tetanus toxin fragment C as a targeting moiety for gene delivery." Thesis, Imperial College London, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419230.

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Box, Michael Andrew. "Characterisation of the binding properties and gene delivery potential of tetanus toxin." Thesis, Imperial College London, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248341.

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Books on the topic "Tetanus-Toxin"

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L, Simpson Lance, ed. Botulinum neurotoxin and tetanus toxin. Academic Press, 1989.

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R, DasGupta Bibhuti, and International Conference on Botulinum, Tetanus Neurotoxins: Neurotransmission and Biomedical Aspects (1992 : Madison, Wis.), eds. Botulinum and tetanus neurotoxins: Neurotransmission and biomedical aspects. Plenum Press, 1993.

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F, Brin Mitchell, Jankovic Joseph, and Hallett Mark, eds. Scientific and therapeutic aspects of botulinum toxic. Lippincott William & Wilkins, 2002.

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Stafstrom, Carl E. Disorders Caused by Botulinum Toxin and Tetanus Toxin. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0156.

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Anaerobic organisms of the genus Clostridia (C) can cause significant human disease. Exotoxins secreted by C botulinum and C tetani cause botulism and tetanus, respectively (summarized in Table 156.1). Botulinum neurotoxin causes neuromuscular blockade by interfering with vesicular acetylcholine release, leading to cholinergic blockade at the neuromuscular junctions of skeletal muscle, and consequently, symmetric flaccid paralysis. Tetanus toxin prevents release of inhibitory neurotransmitters at central synapses, leading to overactivity of motor neurons and muscle rigidity and spasms. This ch
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Botulinum Neurotoxin and Tetanus Toxin. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-12-644445-2.x5001-6.

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Simpson, Lance. Botulinum Neurotoxin and Tetanus Toxin. Elsevier Science & Technology Books, 2012.

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Lipman, Jeffrey, and Robert J. Boots. Diagnosis, assessment, and management of tetanus, rabies, and botulism. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0245.

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Tetanus, rabies and botulism are all infections characterized by the production of a neurotoxin, and generally do not give rise to a systemic inflammatory response. Typically tetanus result from the infection of wounds by the ubiquitious soil-borne bacteria Clostridium tetanii, botulism is most commonly due to toxin produced in food contaminated with Clostridium botulinum. Rabies usually results from an animal bite infected with the rabies virus of the Lyssavirus group. Neurological involvement by all three infections is characterized by paralysis and autonomic instability with tetanus also be
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Löhr, Achim. Etablierung eines nichtviralen Transportersystems, basierend auf der schweren Kette des Tetanus Toxin, zum zelltypspezifischen Transfer von Nukleinsäuren in neuronale Zellen als Grundlage für eine gentherapeutische Behandlung des Neuroblastoms. 1999.

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Dasgupta, B. R. Botulinum and Tetanus Neurotoxins: Neurotransmission And Biomedical Aspects. Springer, 2013.

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Book chapters on the topic "Tetanus-Toxin"

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Dunkley, Peter R., Peter P. Presek, Florian Dreyer, and Paula E. Jarvie. "Tetanus Toxin." In Toxins and Targets. Routledge, 2022. http://dx.doi.org/10.4324/9781315076911-13.

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Considine, Robert V., Lance L. Simpson, and Joseph R. Sherwin. "Tetanus Toxin and Protein Kinase C." In Botulinum and Tetanus Neurotoxins. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-9542-4_26.

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Rappuoli, R., and M. Pizza. "Toxin-Based Vaccines (Diphtheria, Tetanus, Pertussis)." In Vaccines. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-59955-2_8.

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Benke, Timothy A., and John Swann. "The Tetanus Toxin Model of Chronic Epilepsy." In Advances in Experimental Medicine and Biology. Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-6376-8_16.

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Bigalke, H., F. Bartels, T. Binscheck, et al. "Activation and Inactivation of Tetanus Toxin in Chromaffin Cells." In Botulinum and Tetanus Neurotoxins. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-9542-4_25.

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Fedinec, Alexander A., Teresa Duda, Bernard Bizzini, Nigel G. F. Cooper, and Rameshwar K. Sharma. "Tetanus Toxin Inhibits a Membrane Guanylate Cyclase Transduction System." In Botulinum and Tetanus Neurotoxins. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-9542-4_28.

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Ambrose, Elizabeth A. "Botulinum Neurotoxin, Tetanus Toxin, and Anthrax Lethal Factor Countermeasures." In Topics in Medicinal Chemistry. Springer International Publishing, 2016. http://dx.doi.org/10.1007/7355_2016_8.

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Bizzini, Bernard, Mohamed Khiri, and Martine Carlotti. "Tetanus Toxin as a Tool for Investigating the Structural Bases of Neurotropism." In Botulinum and Tetanus Neurotoxins. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-9542-4_5.

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Lazarovici, Philip, Alexander Fedinec, and Bernard Bizzini. "Tetanus Toxin Biotinylation and Localization of Binding Sites in Catecholaminergic Cultures and Granules." In Botulinum and Tetanus Neurotoxins. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-9542-4_27.

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Mellanby, Jane. "Tetanus Toxin as a Tool for Investigating the Consequences of Excessive Neuronal Excitation." In Botulinum and Tetanus Neurotoxins. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-9542-4_31.

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Conference papers on the topic "Tetanus-Toxin"

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Eskikand, Parvin Zarei, Mark J. Cook, Anthony N. Burkitt, and David B. Grayden. "Reduced Synaptic Heterogeneity in a Tetanus Toxin Model of Epilepsy: Insights from Computational Modeling." In 2024 46th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2024. https://doi.org/10.1109/embc53108.2024.10782071.

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Park, Sang-Eon, Mark J. Connolly, and Robert E. Gross. "A characterization of epileptogenesis presented in hippocampal neural activity in a rat tetanus toxin model." In 2019 41st Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC). IEEE, 2019. http://dx.doi.org/10.1109/embc.2019.8857262.

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Okada, Tomoko, and Norihiko Minoura. "Fluorescence emission and polarization analyses for evaluating binding of ruthenium metalloglycocluster to lectin and tetanus toxin c-fragment." In BiOS, edited by Samuel Achilefu and Ramesh Raghavachari. SPIE, 2010. http://dx.doi.org/10.1117/12.841792.

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Reports on the topic "Tetanus-Toxin"

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Henderson, Terry J., and Rossitza K. Gitti. Conformational Changes in Small Ligands Upon Tetanus Toxin Binding. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada485632.

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Rogers, Terry B. Mechanism of Action of the Presynaptic Neurotoxin, Tetanus Toxin. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada246780.

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Rogers, Terry B. Mechanism of Action of the Presynaptic Neurotoxins Tetanus Toxin. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada246495.

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Cosman, M., L. Zeller, F. C. Lightstone, V. V. Krishnan, and R. Balhorn. Screening Mixtures of Small Molecules for Binding to Multiple Sites on the Surface Tetanus Toxin C Fragment by Bioaffinity NMR. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/15005029.

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วรรณลภากร, ณศมน. ผลระยะยาวของการให้วัคซีนไอกรนชนิดเต็มเซลล์ หรือไร้เซลล์ในเด็กทารกที่คลอดจากมารดาที่ได้รับวัคซีนไอกรนขณะตั้งครรภ์. คณะแพทยศาสตร์ จุฬาลงกรณ์มหาวิทยาลัย, 2018. https://doi.org/10.58837/chula.res.2018.26.

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Background: Pertussis vaccination in pregnant women is a strategy currently recommended to foster passive maternal immunity and minimize severe complications from pertussis in not yet completely vaccinated infants. However, the potential interference of maternal antibodies on the development of infant antibody responses induced by childhood whole cell pertussis (wP) and acellular pertussis (aP) vaccination is not well-defined. Methods: This randomized controlled trial (NCT02408926) followed healthy term infants born to tetanus diphtheria acellular pertussis (Tdap)-vaccinated mothers at a terti
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