Literatura académica sobre el tema "Epitope library"
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Artículos de revistas sobre el tema "Epitope library"
Moriki, Takanori, Ichiro N. Maruyama, Yusuke Yamaguchi, Atsuko Igari, Yasuo Ikeda y Mitsuru Murata. "Identification of ADAMTS13 Epitopes Required for Binding to von Willebrand Factor Using Lambda Phage Surface Display." Blood 110, n.º 11 (16 de noviembre de 2007): 2707. http://dx.doi.org/10.1182/blood.v110.11.2707.2707.
Texto completoOstrowski, M., J. A. Galeota, A. M. Jar, K. B. Platt, F. A. Osorio y O. J. Lopez. "Identification of Neutralizing and Nonneutralizing Epitopes in the Porcine Reproductive and Respiratory Syndrome Virus GP5 Ectodomain". Journal of Virology 76, n.º 9 (1 de mayo de 2002): 4241–50. http://dx.doi.org/10.1128/jvi.76.9.4241-4250.2002.
Texto completoBuchli, Rico, Rodney S. VanGundy, Sonja Plompen, Aaron D. Rennels, Nicholas J. Ede y William H. Hildebrand. "Mining for Treasures: Systematic Profiling of 8-, 9-, 10-, and 11-mer HLA-B*0702-restricted CD8+ T cell epitopes from the Influenza A/Puerto Rico/8/34 (H1N1) Virus Hemagglutinin with Potential Application in Vaccine Development (B193)". Journal of Immunology 178, n.º 1_Supplement (1 de abril de 2007): LB40. http://dx.doi.org/10.4049/jimmunol.178.supp.b193.
Texto completoJette, D. C., F. T. Kreutz, B. A. Malcolm, D. S. Wishart, A. A. Noujaim y M. R. Suresh. "Epitope mapping of prostate-specific antigen with monoclonal antibodies". Clinical Chemistry 42, n.º 12 (1 de diciembre de 1996): 1961–69. http://dx.doi.org/10.1093/clinchem/42.12.1961.
Texto completoChen, Longxin, Chaoyang Zhu, Hui Guo, Runting Li, Limeng Zhang, Zhenzhen Xing, Yue Song et al. "Epitope-directed antibody selection by site-specific photocrosslinking". Science Advances 6, n.º 14 (abril de 2020): eaaz7825. http://dx.doi.org/10.1126/sciadv.aaz7825.
Texto completoSuprun, Maria, Scott H. Sicherer, Robert A. Wood, Stacie M. Jones, Donald Y. M. Leung, A. Wesley Burks, David Dunkin et al. "Mapping Sequential IgE-Binding Epitopes on Major and Minor Egg Allergens". International Archives of Allergy and Immunology 183, n.º 3 (24 de noviembre de 2021): 249–61. http://dx.doi.org/10.1159/000519618.
Texto completoHolzem, Achim, Jörg M. Nähring y Rainer Fischer. "Rapid identification of a tobacco mosaic virus epitope by using a coat protein gene-fragment–pVIII fusion library". Journal of General Virology 82, n.º 1 (1 de enero de 2001): 9–15. http://dx.doi.org/10.1099/0022-1317-82-1-9.
Texto completoYuan, Tom Z., Ana G. Lujan Hernandez, Erica Keane, Qiang Liu, Fumiko Axelrod, Shweta Kailasan, Madeleine Noonan-Shueh, Mohammad Javad Aman, Aaron K. Sato y Yasmina N. Abdiche. "Rapid exploration of the epitope coverage produced by an Ebola survivor to guide the discovery of therapeutic antibody cocktails". Antibody Therapeutics 3, n.º 3 (julio de 2020): 167–78. http://dx.doi.org/10.1093/abt/tbaa016.
Texto completoMaier, Richard H., Christina J. Maier, Raphaela Rid, Helmut Hintner, Johann W. Bauer y Kamil Önder. "Epitope Mapping of Antibodies Using a Cell Array–Based Polypeptide Library". Journal of Biomolecular Screening 15, n.º 4 (16 de marzo de 2010): 418–26. http://dx.doi.org/10.1177/1087057110363821.
Texto completoTsai, D. E. y J. D. Keene. "In vitro selection of RNA epitopes using autoimmune patient serum." Journal of Immunology 150, n.º 3 (1 de febrero de 1993): 1137–45. http://dx.doi.org/10.4049/jimmunol.150.3.1137.
Texto completoTesis sobre el tema "Epitope library"
Cortini, Andrea. "Serum profiling and autoantibodies identification in Multiple Sclerosis using epitope and CSF IgG phage display libraries". Doctoral thesis, Università degli studi di Trieste, 2009. http://hdl.handle.net/10077/3073.
Texto completoMultiple sclerosis (MS) is considered the prototype of inflammatory autoimmune diseases of the central nervous system (CNS). The typical feature of the disease is the plaques of demyelination. The evolution of the plaque lesion in MS implicates an inflammatory phase followed by a recovery of functional myelin; a second step is the chronic progressive disease with axonal loss. The earlier phase of MS may be mediated by an autoimmune reaction. Whereas the role of T cells in MS pathogenesis is well established, the role of B cells and autoantibodies in demyelination and plaque formation is still unresolved. However several evidences suggest a contribute of autoantibodies in MS pathogenesis. B cells and myelin specific autoantibodies are present in the sclerosis plaques, and there is an increased production of immunoglobulin (Ig) in the cerebrospinal fluid (CSF) of more than 90% of MS patients . Typically these Ig present an oligoclonal pattern and sequencing of oligoclonal IgG showed extensive somatic mutations suggesting B cell clonal expansion and a specific antigen-driven immune response. The most extensively studied putative autoantigens are components of CNS myelin (myelin basic protein MBP, proteolipid protein PLP, myelin oligodendrocyte glycoprotein MOG). The autoantibodies in MS recognize both linear and conformational epitopes, but at present the conformational epitopes of myelin proteins have not been identified. For example, in MS, the T-cell receptors of autoreactive T lymphocytes recognize various peptides of the MBP, and, in EAE, the anti-MOG antibodies recognize only conformational epitopes. Furthermore, the progression of MS is accompanied by the decline of primary T-cell autoreactivity and by the concurrent emergence of neo-autoreactivity (epitope spreading). However recent investigation have showed that no myelin antigens, like neuron-specific enolase (NSE), retinal arrestin, beta-arrestin, may also have a role in MS pathogenesis. Autoimmunity against these antigens may be linked to neurodegeneration, defective remyelination, and predisposition to uveitis in multiple sclerosis. Several strategies, involving the phage display technology, have been employed in the attempt to discover the antigen that drives the immune response in MS. A first strategy depends on the cloning of IgG repertoire of MS patients in a phage display library screened with brain sections or known antigens. Another strategy involves large phage display libraries of random peptides screened with IgG of CSF in order to identify peptides recognized by antibodies present in CSF of MS patients. Phage display is a technique which involves the coupling of phenotype to genotype in a selectable format. It has been extensively used in molecular biology to study protein-protein interactions and to select antibodies against a wide range of different antigens. In this project we have proposed: 1. to study the autoimmune response in MS by using the phage display for the expression of antibodies involved in the disease. We wanted to make a ScFv library from B cells of CSF of different multiple sclerosis patients, to employ as tool to select a phage display Human Brain cDNA library for the identification of new antigens recognized by the immune sistem in MS patients. 2. To produce single gene mini library of putative antigens (MBP,PLP, MOG) for the generation of epitope chips to use for serotyping the immune response in different patients 3. To investigate the feasibility to use a single gene phage display mini-library as tool for epitope mapping (both linear and conformational) of novels autoantigens 4. To investigate the role of NSE(neuron specific enolase), a new possible no myelin autoantigen in multiple sclerosis, in the pathogenesis of the disease and the usefulness as possible diagnostic marker. Results: Scope 1 B-cells from liquor of two MS patients were centrifuged and the total RNA was extracted from the pellets. Total RNA was retrotranscripted and variable region of heavy and light chain of the antibodies were amplified by PCR. Heavy chain and light chain were assorted and assembled before to be cloned in the phagemid vector pDAN 5. A 2x104 independent clones library was obtained and analyzed by PCR and fingerprinting. A diversity of 30,8% for heavy chain and 72,7% for light chain was established. ScFv library was used to select a phage display Human Brain cDNA library. 17 clones with an high reactivity were obtained and after sequencing 6 clones on 17 have shown to be the same antigen(antigen A ); the reactivity on other two antigens obtained with the selection (antigen B and C) of CSF from 18 MS patients and 16 patients with other neurological disease (OND) was tested by ELISA to evaluate diagnostic value of this protein. The results shown that SM response was statistically different from OND response; the ELISA test gave a specificity of 94,12% and a significance of 53,85 %. The reactivity for the antigen B was also evaluated on sera of MS patients and controls. The MS response was statistically different from OND response and shown a specificity of 97,44% and a significance of 58,62 %. Scope 2&3 We have generated three single gene mini libraries of the major antigens in MS (MBP, MOG and PLP); cDNA of each gene was obtained by RT-PCR and after fragmentation cloned in a phagemid vector (pEP1) to obtain a mini-library for each gene. We have obtained a 2x105 for MBP, 2.4x104 for MOG and 1.6x106 for PLP independent clones library. MBP and MOG libraries were characterized by PCR and fingerprinting. Sequencing analysis shown that the entire MBP transcript variant 7 mRNA (664-1177 nt) and MOG isoform alpha 1 mRNA (262-918 nt) were represented in the respective library. To testing the capacity of selecting a single epitope from our libraries, we have performed a selection test with a commercial monoclonal antibody that recognize MBP 82-98 epitope; after three selection panning all selected clones contain the nucleotidic sequence 906- 956 nt (MBP transcript variant 7 mRNA) which encodes the immunogenic epitope recognized by the monoclonal antibody. Scope 4 The reactivity of sera from 31 MS patients and 14 healthy controls was tested by ELISA on NSE ; statistical analysis of the results shown that the two populations were significantly different.
XXI Ciclo
1981
Marson, Lorena. "Phage-display epitope library development for biomarkers identification in autoimmune diseases of the Central Nervous System". Doctoral thesis, Università degli studi di Trieste, 2012. http://hdl.handle.net/10077/7405.
Texto completoThe principal aim of my PhD was the setting of a protocol for the creation of phage libraries to display cDNA fragments encoding real ORF sequences, that could correspond to potential epitopes. A similar phage display library contains all the potential ORF repertoire of a cell or tissue. This tool can be specially used in the study of autoimmune diseases to perform different kind of analysis, such as the identification of epitopes involved in pathological reaction, the comparison between healthy and pathological conditions, or between different pathological conditions. A complex protocol was developed. It provides for: cDNA normalization, cDNA fragmentation to obtain peptides with useful size, and ORF enrichment to obtain really coding fragments. With this system we have created a epitopes library from Human brain mRNA.
Il principale obiettivo del mio lavoro di ricerca è la messa a punto di un protocollo per la costruzione di librerie fagiche di frammenti di cDNA codificanti per frammenti ORF, e che quindi potrebbero corrispondere a potenziali epitopi. Questo tipo di librerie contengono, potenzialmente, tutto il repertorio ORF di una cellula o di un tessuto e possono quindi essere utilizzate nello studio di malattie autoimmuni al fine di identificare nuovi epitopi coinvolti nella risposta immunitaria, di fare un confronto tra lo stato patologico e quello sano o tra diverse condizioni patologiche. Abbiamo quindi messo a punto un complesso protocollo che prevede: la normalizzazione del cDNA, la sua frammentazione per ottenere peptidi di dimensioni opportune, e l'arricchimento in frammenti realmente codificanti. Con questo sistema abbiamo realizzato una libreria di epitopi a partire da mRNA di cervello umano.
XXIV Ciclo
1984
Löfblom, John. "Staphylococcal surface display for protein engineering and characterization". Doctoral thesis, KTH, Skolan för bioteknologi (BIO), 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4584.
Texto completoQC 20100809
Sharav, Tumenjargal. "Tumor-spezifische T-Zellen und T-Zellepitope bei kutanen Lymphomen". Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2005. http://dx.doi.org/10.18452/15220.
Texto completoThe major goals of this work was the identification of tumour-associated T cell epitopes (TATE) in cutaneous T cell lymphoma (CTCL) and the characterisation of the tumour-specific cytolytic immune response. Two tumour-specific cytolytic T cell clones were established from the tumour-infiltrating lymphocytes (TIL) of one CTCL-patient. The potential natural T cell epitopes and mimotopes (epitopes without natural correlates but with more T cell stimulating capacity) for these T cell clones were identified using a combinatorial peptide library. The quantity and quality of the T cell response was different. The functional avidity of the peptides differed more than 3 orders of magnitude. The cytolysis and cytokine release did not correlate for each peptide. Some of the mimotopes were injected into CTCL-patients for therapeutic purpose. The frequency of the mimotope-specific T cell increased during the first vaccination cycles and a tumouricidal capacity could be observed. This first clinical application of the mimotopes showed the capacity of the mimotopes for the modulation of weak anti-tumour immune response. The identification of the new TATE allowed further characterisation of the tumour-specific T cells in the periphery and in the tumour of the patient. High frequency of the tumour-specific T cells could be detected in the tumour but they failed to show effector functions in comparison to the tumour-specific T cells in the peripheral blood. The tumour-specific T cells had the effector memory phenotype but expressed none or less amount of the cytolytic effector molecules. The reason for the suboptimal anti-tumour response in CTCL could be the immunesuppressive cytokine TGF-beta.
McMahan, Rachel H. "Relating TCR-peptide-MHC affinity to immunogenicity for the design of tumor vaccines /". Connect to full text via ProQuest. Limited to UCD Anschutz Medical Campus, 2007.
Buscar texto completoTypescript. Includes bibliographical references (leaves 133-156). Free to UCD affiliates. Online version available via ProQuest Digital Dissertations;
Ahsendorf, Henrike Verfasser], Bertram [Akademischer Betreuer] [Brenig, Bertram [Gutachter] Brenig, Christiane [Gutachter] Stahl-Hennig y El Wahed Ahmed [Gutachter] Abd. "Selection and characterization of human recombinant antibodies against Orthopoxviruses from an immunoglobulin library and mapping of functional epitopes of Vaccinia virus surface proteins / Henrike Ahsendorf ; Gutachter: Bertram Brenig, Christiane Stahl-Hennig, Ahmed Abd El Wahed ; Betreuer: Bertram Brenig". Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020. http://d-nb.info/1208221833/34.
Texto completoAhsendorf, Henrike [Verfasser], Bertram [Akademischer Betreuer] Brenig, Bertram [Gutachter] Brenig, Christiane [Gutachter] Stahl-Hennig y El Wahed Ahmed [Gutachter] Abd. "Selection and characterization of human recombinant antibodies against Orthopoxviruses from an immunoglobulin library and mapping of functional epitopes of Vaccinia virus surface proteins / Henrike Ahsendorf ; Gutachter: Bertram Brenig, Christiane Stahl-Hennig, Ahmed Abd El Wahed ; Betreuer: Bertram Brenig". Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020. http://d-nb.info/1208221833/34.
Texto completoTseng, Sy-Woei y 曾斯偉. "Construction of phage-display peptide library for the screening of antibody epitope". Thesis, 2000. http://ndltd.ncl.edu.tw/handle/04418277385769813527.
Texto completo國立中興大學
分子生物學研究所
88
Abstract Phage display technology, consisting of the expression of target sequence in the surface of phage particles and the affinity selection, is a biological system that facilitates the cloning and rapid selection of peptides or proteins from large combinatorial libraries. Libraries are generated by cloning of a batch of DNA encoding millions of variants of certain ligands into the phage genome or phagemid as a fusion to the gene encoding one of the phage coat proteins. Upon expression, the fusion coat protein is incorporated into new phage particles that are assembled in the bacterium and consequently presented on the phage surface, with its genetic material residing within the phage particles. The purpose of this study is to construct a random peptide library containing both linear and conformational epitopes to serve as an “all purpose” peptide source for searching of disease-related peptides. To achieve this goal, EcoRI-HindIII DNA fragments encoding 45 amino acid residues, of which 36 have random sequences, were cloned into the corresponding sites of the modified pCANTAB5E plasmid and the resulted plasmids were transformed into E. coli TG1. The percentage of insert-containing colonies in the transformants was evaluated by PCR using primers flanking the insert DNAs. Approximately, 83% of the clones contained inserts. The expression of the insert gene was determined by colony immunoblot analysis of a portion of the original clones using the antibody specific for E-Tag which is located downstream of the insert. The number of clone capable of expression coincided with the percentage of the insert-containing clones. Finally, the diversity of the library was evaluated by sequencing of 10 randomly picked clones. The results indicated that all exhibited difference sequences. The diversity of the library was estimated to be 4.4 x 106 according to the above information,. To establish a system for identification of disease-related peptides, affinity selection was performed using sera from system lupus erythematosus patients.
Rai, Chung-I. y 雷仲益. "Identification of the epitope recognized by enhancing monoclonal antibody against dengue virus using phage-displayed library". Thesis, 2006. http://ndltd.ncl.edu.tw/handle/59300346968131685111.
Texto completo國立成功大學
醫學檢驗生物技術學系
94
Dengue virus (DV), consists of four serotypes (DEN1-4), is the causative agent of mild dengue fever and lift-threatening dengue hemorrhagic fever and dengue shock syndrome (DHF/DSS). The antibody dependent enhancement (ADE) hypothesis has been proposed to explain why more severe manifestations of DHF/DSS occur predominantly during secondary infection with different serotypes. However, the epitopes recognized by these enhancing antibodies are unclear. Recently, anti-prM monoclonal antibody (mAb 70-21) which recognized all DV serotypes without neutralizing activity were generated and demonstrated as an enhancing antibody for DV infection. In this study, the epitope recognized by mAb 70-21 was identified using a phage-displayed random peptide library. After three rounds of biopanning, immunopositive phage clones showed specific binding to mAb 70-21 but not to normal mouse serum or purified normal mouse IgG by ELISA. DNA sequencing and GCG analysis of these phage clones showed a consensus sequence, QNNLGPR, which shared sequence homology to the amino acid 58-61 of dengue prM protein and N-terminus of heat shock protein 60. Moreover, phage clones induced-antisera recognized not only these clones but also synthetic peptide of the consensus sequence. In addition, phage-induced antisera also bound to normal Vero or RD cells as demonstrated by indirect fluorescent assay. Western blot analysis and immunoprecipitation showed heat shock protein 60 in BHK-21 cell lysate was recognized by phage clones induced-antisera. Like mAb70-21, these phage-induced antisera also could enhance dengue virus infection of BHK-21 cells. Moreover, antibodies against QNNLGPR synthetic peptide were significantly increased in dengue patients with severe syndrome. Taken together, our results suggest that antibodies which recognized the epitope shared by prM of DV and heat shock protein 60 may enhance DV infection of host cells, which may play a role in the development of DHF or DSS.
Ahsendorf, Henrike. "Selection and characterization of human recombinant antibodies against Orthopoxviruses from an immunoglobulin library and mapping of functional epitopes of Vaccinia virus surface proteins". Doctoral thesis, 2019. http://hdl.handle.net/21.11130/00-1735-0000-0005-137B-C.
Texto completoLibros sobre el tema "Epitope library"
Renatus, Flavius Vegetius. Epitoma rei militaris. Stutgardiae: B.G. Teubner, 1995.
Buscar texto completoP, Milner N., ed. Vegetius, epitome of military science. Liverpool: Liverpool University Press, 1993.
Buscar texto completoRenatus, Flavius Vegetius. Vegetius : epitome of military science. Liverpool, [Eng.]: Liverpool University Press, 1993.
Buscar texto completo1925-, Stelten Leo F., ed. Epitoma rei militaris. New York: P. Lang, 1990.
Buscar texto completoRenatus, Flavius Vegetius. Epitoma rei militaris. Oxford: Clarendon Press, 2004.
Buscar texto completoRenatus, Flavius Vegetius. Epitoma rei militaris =: Das gesamte Kriegswesen. Aarau: Sauerlander, 1986.
Buscar texto completoRenatus, Flavius Vegetius. The earliest English translation of Vegetius' De re militari. Heidelberg: C. Winter Universitätsverlag, 1988.
Buscar texto completo1892-, Phillips Thomas Raphael, ed. The military institutions of the Romans. Westport, CT: Greenwood Press, 1985.
Buscar texto completoRenatus, Flavius Vegetius. Le livre de l'art de chevalerie de Vegesce: Traduction anonyme de 1380. Helsinki: Suomalainen Tiedeakatemia, 1989.
Buscar texto completoRenatus, Flavius Vegetius. Compendio delle istituzioni militari. 2a ed. Catania: Edizioni del Prisma, 1997.
Buscar texto completoCapítulos de libros sobre el tema "Epitope library"
Midoro-Horiuti, Terumi y Randall M. Goldblum. "Epitope Mapping with Random Phage Display Library". En Methods in Molecular Biology, 477–84. Totowa, NJ: Humana Press, 2014. http://dx.doi.org/10.1007/978-1-62703-992-5_28.
Texto completoVanniasinkam, Thiru, Mary D. Barton, Tongted Phumoonna Das y Michael W. Heuzenroeder. "B-Cell Epitope Mapping Using a Library of Overlapping Synthetic Peptides in an Enzyme-Linked Immunosorbent Assay". En Epitope Mapping Protocols, 121–28. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7841-0_8.
Texto completoSmith, George P. y Jamie K. Scott. "Using an epitope library to identify peptide ligands for antibodies against folded epitopes". En Peptides, 485–88. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_186.
Texto completoVolkmer-Engert, R., J. Hellwig, B. Ehrhard, W. Höhne y J. Schneider-Mergener. "Characterization of the interaction between the monoclonal antibody CB 4-1 and its peptide epitope GATPQDLNTM using a soluble and a cellulose-bound peptide epitope library". En Peptides 1994, 473–74. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_213.
Texto completoWen, Fei, Mason R. Smith y Huimin Zhao. "Construction and Screening of an Antigen-Derived Peptide Library Displayed on Yeast Cell Surface for CD4+ T Cell Epitope Identification". En Methods in Molecular Biology, 213–34. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9597-4_13.
Texto completoWen, Fei y Huimin Zhao. "Construction and Screening of an Antigen-Derived Peptide Library Displayed on Yeast Cell Surface for CD4+ T Cell Epitope Identification". En Methods in Molecular Biology, 245–64. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-589-7_15.
Texto completoBent, Margaret. "25.Washington, Library of Congress, M2.1 .C6 1400 Case: A Neglected English Fragment". En Epitome musical, 529–52. Turnhout, Belgium: Brepols Publishers, 2022. http://dx.doi.org/10.1484/m.em-eb.5.132718.
Texto completoGembero-Ustárroz, María. "4. Music Books for Lima Cathedral and their Social Context in the Early Seventeenth Century: Black Slaves as a Guarantee for Producing a New Plainchant Library". En Epitome musical, 105–26. Turnhout, Belgium: Brepols Publishers, 2021. http://dx.doi.org/10.1484/m.em-eb.5.129719.
Texto completoBrahma, Sandipan y Steven Henikoff. "CUT&RUN Profiling of the Budding Yeast Epigenome". En Methods in Molecular Biology, 129–47. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2257-5_9.
Texto completoMoret, E. E., R. M. J. Liskamp y J. P. Tollenaere. "Structure-based design of epitope mimetics". En Pharmacochemistry Library, 371–81. Elsevier, 1997. http://dx.doi.org/10.1016/s0165-7208(97)80079-7.
Texto completoActas de conferencias sobre el tema "Epitope library"
LOFTUS, J. C., E. F. Plow, A. L. Frelinger III, M. A. Smith, S. D’ouza y M. H. Ginsberg. "LOCALIZATION AND CHEMICAL SYNTHESIS OF A DIVALENT CATION REGULATED EPITOPE IN PLATELET MEMBRANE GPIIb". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643959.
Texto completoLu, Yang, Yongpeng Xiao, Qiao Li y Man Liu. "An introduction to main B-cell epitope prediction methods and software based on phase display library". En 2011 23rd Chinese Control and Decision Conference (CCDC). IEEE, 2011. http://dx.doi.org/10.1109/ccdc.2011.5968954.
Texto completoMorrissey, J. H., D. S. Fair y T. S. Edgington. "STRUCTURE AND PROPERTIES OF THE HUMAN TISSUE FACTOR APOPROTEIN". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643738.
Texto completoMurata, Kenji, Kayoko Saso, Linh T. Nguyen, Douglas Millar, Marcus O. Butler, Pamela S. Ohashi y Naoto Hirano. "Abstract 568: Decoding shared antigenic epitopes and their cognate TCR genes in melanoma TILs using a library of paired human cell-based pHLA multimers and artificial APCs". En Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-568.
Texto completoMurata, Kenji, Kayoko Saso, Linh T. Nguyen, Douglas Millar, Marcus O. Butler, Pamela S. Ohashi y Naoto Hirano. "Abstract 568: Decoding shared antigenic epitopes and their cognate TCR genes in melanoma TILs using a library of paired human cell-based pHLA multimers and artificial APCs". En Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-568.
Texto completoMarquerie, G., A. Duperray, G. Uzan y R. Berthier. "BIOSYNTHETIC PATHWAYS OF THE PLATELET FIBRINOGEN RECEPTOR IN HUMAN MEGAKARYOCYTES". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642954.
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