Gotowe bibliografie tematyczne / Antigen-antibody reactions

Gotowa bibliografia na temat „Antigen-antibody reactions”

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

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Artykuły w czasopismach na temat "Antigen-antibody reactions"

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Armstrong, B. "Antigen–antibody reactions". ISBT Science Series 3, nr 2 (czerwiec 2008): 21–32. http://dx.doi.org/10.1111/j.1751-2824.2008.00185.x.

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Armstrong, Beryl. "Antigen‐antibody reactions". ISBT Science Series 15, S1 (grudzień 2020): 68–80. http://dx.doi.org/10.1111/voxs.12590.

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Harada, Masataka, Masahiko Sisido, Junzo Hirose i Mamoru Nakanishi. "Photoreversible antigen-antibody reactions". FEBS Letters 286, nr 1-2 (29.07.1991): 6–8. http://dx.doi.org/10.1016/0014-5793(91)80928-v.

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Jasin, Hugo E. "Intra-Articular Antigen-Antibody Reactions". Rheumatic Disease Clinics of North America 13, nr 2 (sierpień 1987): 179–89. http://dx.doi.org/10.1016/s0889-857x(21)00841-3.

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Ouchterlony, Orjan. "Antigen - Antibody Reactions In Gels". Acta Pathologica Microbiologica Scandinavica 26, nr 4 (18.08.2009): 507–15. http://dx.doi.org/10.1111/j.1699-0463.1949.tb00751.x.

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Ouchterlony, Örjan. "ANTIGEN-ANTIBODY REACTIONS IN GELS". Acta Pathologica Microbiologica Scandinavica 32, nr 2 (18.08.2009): 231–40. http://dx.doi.org/10.1111/j.1699-0463.1953.tb00247.x.

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Littt, Mortimer. "EOSINOPHILS AND ANTIGEN-ANTIBODY REACTIONS*". Annals of the New York Academy of Sciences 116, nr 3 (16.12.2006): 964–85. http://dx.doi.org/10.1111/j.1749-6632.1964.tb52562.x.

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OEDING, PER. "STAPHYLOCOCCAL ANTIGEN-ANTIBODY REACTIONS IN AGAR". Acta Pathologica Microbiologica Scandinavica 47, nr 1 (17.08.2009): 53–64. http://dx.doi.org/10.1111/j.1699-0463.1959.tb03421.x.

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Chamritski, Irina, Mark Clarkson, Jeff Franklin i Shi Wei Li. "Real-Time Detection of Antigen–Antibody Reactions by Imaging Ellipsometry". Australian Journal of Chemistry 60, nr 9 (2007): 667. http://dx.doi.org/10.1071/ch07115.

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In the field of proteomics the quantification of the affinity of an antibody to its partners and the evaluation of its specific binding is an important issue. With an imaging ellipsometer the interaction of an antibody with immobilized antigens on a model microarray is observed in a time-resolved and label-free manner. Imaging ellipsometry was developed for real-time monitoring of the biomolecule interaction between an antigen in solution and an antibody immobilized on a silicon surface. Proteins were immobilized by the formation of carboxy-alkyl monolayers on silicon substrates, where a biotin-labelled antibody was immobilized by a biotin–streptavidin linkage. Anti-human IgG bound specifically to human antibody and protein A, similarly anti-goat IgG bound to goat antibody. No binding was observed between anti-rabbit IgG and goat antibody. All stages of the formation of the antigen–antibody complex were imaged by imaging ellipsometry. By monitoring changes in y, the mole fraction θ of the antigen–antibody binding was determined. Immunological reactions of two different antigen–antibody combinations were fitted by the Langmuir adsorption equation, and affinity constants for two reactions were calculated.
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Pfeil, Tamás, i Blanka Herbály. "A linear model for polyclonal antibody–antigen reactions". Mathematics and Computers in Simulation 198 (sierpień 2022): 20–30. http://dx.doi.org/10.1016/j.matcom.2022.02.004.

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Rozprawy doktorskie na temat "Antigen-antibody reactions"

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Andersson, Kerstin. "Antigen-antibody reactions a study of functional structures and non-immunological interactions /". Lund : Dept. of Biochemistry, Lund University, 1995. http://catalog.hathitrust.org/api/volumes/oclc/39264530.html.

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Thornton, Gail Marilyn. "Biolithography : selective joining using antibody-antigen reactions". Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/42816.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 1995.
Includes bibliographical references (p. 211-212).
Biolithography is a contribution to the field of Solid Free Form Fabrication. Part production is based on selective joining using antibody- antigen reactions, where the selectively is based on the thermal sensitivity of such proteins. Antibodies and antigens can be chemically immobilized to a variety of substrate materials: polymeric, ceramic and metallic. In the present investigation, antibody coated 1 [mu]m polystyrene beads and antigen coated glass surface substrates, as well as, antigen solutions were used. Both antibodies and antigens were multivalent i.e. have more that one binding site for each other; thus, two antibody coated beads could be held together by one antigen. Selective deposition was demonstrated by thermally deactivating antigen coated onto glass and precipitating antibody coated beads. Bead deposition was selective to the regions of remaining active antigens; thus, revealing the defined deactivated region. Thermal deactivation of the antigen coated substrate was first demonstrated with a 90°C water jet and improved using an argon ion laser which produced line widths on the order of tens of microns. Selective definition of geometry was an extension of the coating process precipitating not one but two bead layers and linking beads using antigen in solution. The thermal deactivation mechanism was a modified 90°C water jet that had line width resolution on the order of millimeters. Line definition was on both antigen coated bases and bound bead bases; thus, thermal deactivation was effective on both immobilized antigen (glass) and antibody (bead). The selective deposition of antibody coated substrate was demonstrated by thermally deactivating immobilized antigens and antibodies on surface substrates. Definition resolution was dependent on the thermal deactivation mechanism used.
by Gail Marilyn Thornton.
S.M.
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Tsui, Ka-kit, i 徐家傑. "Seasonal variation of serum prostate-specific antigen levels in Hong Kong". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2008. http://hub.hku.hk/bib/B40738292.

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Tsui, Ka-kit. "Seasonal variation of serum prostate-specific antigen levels in Hong Kong". Click to view the E-thesis via HKUTO, 2008. http://sunzi.lib.hku.hk/hkuto/record/B40738292.

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Luo, Cheng-Ping. "Detection of antibody antigen reactions using surface acoustic wave and electrochemical immunosensors". [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=971863121.

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Mummert, Mark E. "Stability in antigenic reactivity of the major outer surface protein, OspA, in borrelia burgdorferi, during persistent infection in Syrian hamsters". Virtual Press, 1992. http://liblink.bsu.edu/uhtbin/catkey/845968.

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The spirochete Borrelia burgdorferi is the causative agent of Lyme disease, a multisystem disorder that can cause a variety of disorders in susceptible mammalian hosts. The immune response of infected mammals, including humans, is ineffective in clearing B. burgdorferi as demonstrated by the ability to reisolate the spirochete from naturally and experimentally infected hosts after extended periods of time. Recent evidence suggests that this pathogen evades the immune response in part through changes in antigenic reactivity.The purpose of this study was to determine if outer surface protein A (OspA) of B. burqdorferi varies in the course of infection in Syrian hamsters and thus potentially plays a role in evading the host immune response. To assess the degree of change, differences in the binding of a murine monoclonal antibody (H5332) were measured using IFA and ELISA techniques over a 9-week period of time.Results of this study suggest that OspA is persistently expressed in infected Syrian hamsters for at least 9-weeks. Moreover, this protein, or at least the epitope that H5332 binds with, is stably expressed. These results indicate OspA, or at least the epitope of OspA that I probed, does not appear to contribute to the evasive mechanisms of 8. burgdorferi in Syrian hamsters.
Department of Biology
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陳磊碩 i Lui-sek Chan. "Chemical modification of immunoglobulins and the effects on antigen binding site affinity". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1993. http://hub.hku.hk/bib/B29913378.

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Chan, Lui-sek. "Chemical modification of immunoglobulins and the effects on antigen binding site affinity /". [Hong Kong] : University of Hong Kong, 1993. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13731506.

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Johansson, Daniel X. "Expression and interaction studies of recombinant human monoclonal antibodies /". Stockholm, 2007. http://diss.kib.ki.se/2007/978-91-7357-137-1/.

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Barbar, Elisar Jamil. "Nuclear Magnetic Resonance Study of Antigen-Antibody Complexes, Including Sequence Specific Assignments and Structural Analysis of Neurophysin as an Antigen Model". PDXScholar, 1993. https://pdxscholar.library.pdx.edu/open_access_etds/1167.

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The interaction between molecules is essential in a wide range of biological processes. A detailed knowledge of these interactions is necessary for understanding these processes. Among the systems that involve important interactions is the immune system. NMR spectroscopy has a large number of spectral parameters that were used in this work to study antibody-antigen interactions. These same parameters were also used to begin a structural analysis of a medium-sized protein, neurophysin, that has important interactions with neurohormones, and served here as a model antigen. A set of ligands differing in size and charge was designed and used to probe the binding site of anti-phosphocholine antibodies. These ligands ranged from small organic species to medium sized proteins. Amino acids, peptides and proteins were homogeneously linked to phenyl phosphocholine and analyzed by NMR techniques. Transferred nuclear Overhauser effect measurements were used to determine the conformation of bound ligands. The conformational change observed in some ligands was explained as either due to the antibody selecting one conformation that already exists, or the antibody binding inducing a conformational change. Titration data and detailed NMR analysis showed a more rigid M3C65 antibody fragment upon binding. In summary, with eight examples of ligands and four examples of antibodies studied by NMR, a spectrum of effects was seen, including a lock-and-key model and limited local induced fit. The contribution of the carrier molecule to antibody binding was in restricting the conformation of the ligand. Bigger ligands that are expected to be more immunogenic, showed less binding avidity as determined by immunological assays. Fluorinated ligands were synthesized to determine the kinetics of binding using 19F NMR spectra. Higher concentration of a fragment of the antibody M3C65 was analyzed to determine assignments of some residues in the combining site of the antibody. High resolution NMR techniques were used to assign resonances in neurophysin. The physiological role of neurophysin includes hormone storage and stabilization of oxytocin and vasopressin against proteolytic degradation within the posterior pituitary. Neurophysin is a 10 KD protein that dimerizes at high concentrations needed for NMR studies. An organic cosolvent was used to lower the dimerization constant, and hence inrease the spectral resolution. This permitted sequence-specific assignments that were then used to identify residues in the neurophysin-hormone binding site. Chemical shift differences and conformational changes were observed for the residues glutamate 47 and leucine 50. The 3₁₀ helix was further stabilized towards a more ideal helix upon hormone-analog peptide binding. Some of the residues contributing to the monomer-monomer interface were also assigned. Dimerization ill1duced chemical shift differences and conformational changes were observed for phenylalanine 35, threonine 38, and alanine 69. Tyrosine: 49 and phenylalanine 22 were affected but to a lesser extent. One characteristic of neurophysin in all studied cases was dynamic equilibrium between different folding states.
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Książki na temat "Antigen-antibody reactions"

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Padlan, Eduardo. Antibody-antigen complexes. Austin: R.G. Landes, 1994.

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Herwart, Ambrosius, i Storch Wulf, red. Immunreaktionen in der Histochemie. Stuttgart: G. Fischer, 1986.

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Mayer, Gaetan. Amplification methods for the immunolocalization of rare molecules in cells and tissues. Jena, Germany: Urban & Fischer, 2001.

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Mayer, Gaétan. Amplification methods for the immunolocalization of rare molecules in cells and tissue. Jena: Urban & Fischer, 2001.

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S, Sarkisov D., i Akademii͡a︡ medit͡s︡inskikh nauk SSSR, red. Strukturnye osnovy adaptat͡s︡ii i kompensat͡s︡ii narushennykh funkt͡s︡iĭ: Rukovodstvo. Moskva: "Medit͡s︡ina", 1987.

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Ulrich, Reineke, i Schutkowski Mike, red. Epitope mapping protocols. Wyd. 2. New York: Humana Press, 2009.

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1932-, Haber Edgar, red. Antigen binding molecules: Antibodies and T-cell receptors. San Diego: Academic Press, 1996.

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E, Morris Glenn, red. Epitope mapping protocols. Totowa, N.J: Humana Press, 1996.

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Shammala, Wesam Abu. Human plasma Kallikrein and pre-Kallikrein: Immunochemical adsorption studies using selected non-biological surfaces. Dublin: University College Dublin, 1999.

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Kolenik, Steven Andrew. The effects of interleukin-1, granulocyte macrophage colony-stimulating factor, and tumor necrosis factor-α on cultured human langerhans cells and cortical thymocytes. [New Haven: s.n.], 1990.

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Części książek na temat "Antigen-antibody reactions"

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Virella, Gabriel. "Antigen-antibody reactions". W Medical Immunology, 83–92. 7th edition. | Boca Raton : Taylor & Francis, 2020.: CRC Press, 2019. http://dx.doi.org/10.1201/9780429278990-8.

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Deshpande, S. S. "Antigen-Antibody Reactions". W Enzyme Immunoassays, 52–71. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1169-0_3.

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Mutharia, Lucy M., i Joseph S. Lam. "Antigen-Antibody Reactions". W Methods for General and Molecular Microbiology, 138–67. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555817497.ch8.

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Parija, Subhash Chandra. "Antigen–Antibody Reactions". W Textbook of Microbiology and Immunology, 189–209. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-19-3315-8_15.

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Ferenčík, Miroslav. "Antigen—antibody reactions in vitro". W Handbook of Immunochemistry, 292–308. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1552-0_11.

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Recktenwald, Diether J., Chia-Huei Chen Chen, Laura Chiu i Morgan Conrad. "Detection Schemes for Antigen-Antibody Reactions". W Lecture Notes on Coastal and Estuarine Studies, 194–206. New York, NY: Springer New York, 1988. http://dx.doi.org/10.1007/978-1-4684-7642-2_14.

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Recktenwald, Dlether J., Chia-Huei Chen Chen, Laura Chlu i Morgan Conrad. "Detection Schemes for Antigen-Antibody Reactions". W Lecture Notes on Coastal and Estuarine Studies, 194–206. New York: Springer-Verlag, 2013. http://dx.doi.org/10.1029/ln025p0194.

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Taylor, Diane Wallace. "The Inducible Defense System: Antibody Molecules and Antigen-Antibody Reactions". W Infection, Resistance, and Immunity, 105–29. Boca Raton: Routledge, 2022. http://dx.doi.org/10.1201/9780203750964-7.

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Somasegaran, Padma, i Heinz J. Hoben. "Performing Rhizobial Antigen-Antibody Reactions by Gel Immunodiffusion". W Handbook for Rhizobia, 107–11. New York, NY: Springer New York, 1994. http://dx.doi.org/10.1007/978-1-4613-8375-8_11.

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Huebner, Johannes. "Antibody-Antigen Interactions and Measurements of Immunologic Reactions". W Immunology, Infection, and Immunity, 207–32. Washington, DC, USA: ASM Press, 2015. http://dx.doi.org/10.1128/9781555816148.ch9.

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Streszczenia konferencji na temat "Antigen-antibody reactions"

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Guo, X. S., X. S. Fang, X. L. Yang, Y. Q. Chen i L. R. Wang. "Capacitive monitoring of the antigen-antibody reactions enhanced by nanogold". W 2005 IEEE Engineering in Medicine and Biology 27th Annual Conference. IEEE, 2005. http://dx.doi.org/10.1109/iembs.2005.1616654.

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Banerjee, Rupak K., Meinrad Praxmaraer, Ilhan Dilber, Peter Bungay, William van Osdol i Cynthia Sung. "Numerical Simulation of Antibody Penetration in a Solid Tumor Nodule Using Finite Element Method". W ASME 1998 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1998. http://dx.doi.org/10.1115/imece1998-0058.

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Abstract The high binding specificity that monoclonal antibodies exhibit has led to great interest in using them to target tumor-associated antigens. The antibody may be coupled to a radionuclide or cytotoxic drug to create a tumor-targeted reagent that can be used to identify sites of metastatic disease and/or deliver a lethal substance to the tumor cells. However, successful application of these compounds in a clinical setting has been hindered by a poor understanding of the factors that govern antibody accumulation in a tumor. We have used a finite element method to develop a pharmacokinetic model describing the uptake of systemically-administered antibody in an early, prevascular spherical tumor nodule embedded in normal tissue. The model incorporates such processes as plasma kinetics, transcapillary transport, interstitial diffusion, binding reactions, lymphatic clearance, and antigen internalization.
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Bilyi, Olexander I., Yevgen M. Kiselyov i Volodymyr P. Novikov. "Creation of aggregate latex complexes with protein adsorbed on their surface for the study of antigen-antibody reactions with light-scattering method". W BiOS 2000 The International Symposium on Biomedical Optics, redaktorzy Tuan Vo-Dinh, Warren S. Grundfest i David A. Benaron. SPIE, 2000. http://dx.doi.org/10.1117/12.384926.

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Joseph, David. "Antigen-antibody reaction studied by laser light scattering". W 2008 International Conference on Advanced Optoelectronics and Lasers (CAOL). IEEE, 2008. http://dx.doi.org/10.1109/caol.2008.4671893.

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Tieppo, Bianca, Daniella L. Vale, Jéssica E. S. Fonsaca, Mohd Rehan, Jane Megid, Wanderson S. R. Teixeira, Daniel Grasseschi, Christiano J. S. de Matos i Lúcia A. M. Saito. "Image Processing of Antibody Detection using Machine Learning for an Optical Bio-sensing Application". W Frontiers in Optics. Washington, D.C.: Optica Publishing Group, 2023. http://dx.doi.org/10.1364/fio.2023.jw4a.60.

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We propose images processing recorded with a waveguide sensor of an immunological test based on antigen-antibody reaction. Machine Learning combining optical detection identifies bovine brucellosis antibodies and can be useful for other immunoassays.
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Lin, Jung-Yi, Da-Jen Yao i Fangang Tseng. "Functional antibody-antigen reaction on the surface of iron oxide nanoparticles". W 2006 1st IEEE International Conference on Nano/Micro Engineered and Molecular Systems. IEEE, 2006. http://dx.doi.org/10.1109/nems.2006.334714.

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David, P. J., i Deep N. Tripathi. "Cluster formation of antigen antibody reaction studied by laser light scattering". W BiOS Europe '95, redaktorzy Britton Chance, David T. Delpy i Gerhard J. Mueller. SPIE, 1995. http://dx.doi.org/10.1117/12.228666.

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Yamatogi, S., M. Fukuyama, H. Ding, M. Nishida, C. Kawamoto, Y. Amemiya, T. Ikeda i in. "Selective Detection of Antigen-Antibody Reaction using Si Ring Optical Resonators". W 2009 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2009. http://dx.doi.org/10.7567/ssdm.2009.j-8-2.

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Iida, Takuya, Shota Hamatani, Yumiko Takagi, Kana Fujiwara, Mamoru Tamura i Shiho Tokonami. "Light-induced acceleration of antigen-antibody reaction for detecting attogram-level proteins". W Optical Manipulation and Structured Materials Conference, redaktorzy Takashige Omatsu, Síle N. Chormaic i Kishan Dholakia. SPIE, 2023. http://dx.doi.org/10.1117/12.3008371.

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Nishida, M., M. Fukuyama, Y. Abe, Y. Amemiya, T. Ikeda, A. Kuroda i S. Yokoyama. "Detection of Antigen-Antibody Reaction Using Si Ring Optical Resonators Functionalized with an Immobilized Antibody-Binding Protein". W 2010 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2010. http://dx.doi.org/10.7567/ssdm.2010.p-11-1.

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