Academic literature on the topic 'Proteine hic'

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Journal articles on the topic "Proteine hic"

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Jørgensen, Mikkel G., Deo P. Pandey, Milena Jaskolska, and Kenn Gerdes. "HicA of Escherichia coli Defines a Novel Family of Translation-Independent mRNA Interferases in Bacteria and Archaea." Journal of Bacteriology 191, no. 4 (2008): 1191–99. http://dx.doi.org/10.1128/jb.01013-08.

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ABSTRACT Toxin-antitoxin (TA) loci are common in free-living bacteria and archaea. TA loci encode a stable toxin that is neutralized by a metabolically unstable antitoxin. The antitoxin can be either a protein or an antisense RNA. So far, six different TA gene families, in which the antitoxins are proteins, have been identified. Recently, Makarova et al. (K. S. Makarova, N. V. Grishin, and E. V. Koonin, Bioinformatics 22:2581-2584, 2006) suggested that the hicAB loci constitute a novel TA gene family. Using the hicAB locus of Escherichia coli K-12 as a model system, we present evidence that su
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Avraamides, C., M. E. Bromberg, J. P. Gaughan, S. M. Thomas, A. Y. Tsygankov, and T. S. Panetti. "Hic-5 promotes endothelial cell migration to lysophosphatidic acid." American Journal of Physiology-Heart and Circulatory Physiology 293, no. 1 (2007): H193—H203. http://dx.doi.org/10.1152/ajpheart.00728.2006.

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Endothelial cell migration is critical for proper blood vessel development. Signals from growth factors and matrix proteins are integrated through focal adhesion proteins to alter cell migration. Hydrogen peroxide-inducible clone 5 (Hic-5), a paxillin family member, is enriched in the focal adhesions in bovine pulmonary artery endothelial (BPAE) cells, which migrate to lysophosphatidic acid (LPA) on denatured collagen. In this study, we investigate the role of Hic-5 in LPA-stimulated endothelial cell migration. LPA recruits Hic-5 to the focal adhesions and to the pseudopodia in BPAE cells plat
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Heitzer, Marjet D., and Donald B. DeFranco. "Hic-5, an adaptor-like nuclear receptor coactivator." Nuclear Receptor Signaling 4, no. 1 (2006): nrs.04019. http://dx.doi.org/10.1621/nrs.04019.

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In recent years, numerous nuclear receptor-interacting proteins have been identified that influence nuclear transcription through their direct modification of chromatin. Along with coactivators that possess histone acetyltransferase (HAT) or methyltransferase activity, other coactivators that lack recognizable chromatin-modifying activity have been discovered whose mechanism of action is largely unknown. The presence of multiple protein-protein interaction motifs within mechanistically undefined coactivators suggests that they function as adaptor molecules, either recruiting or stabilizing pro
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Kusano, Shuichi, and Nancy Raab-Traub. "I-mfa Domain Proteins Interact with Axin and Affect Its Regulation of the Wnt and c-Jun N-Terminal Kinase Signaling Pathways." Molecular and Cellular Biology 22, no. 18 (2002): 6393–405. http://dx.doi.org/10.1128/mcb.22.18.6393-6405.2002.

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ABSTRACT I-mfa has been identified as an inhibitor of myogenic basic helix-loop-helix transcription factors, and a related human I-mfa domain-containing protein (HIC) also has been identified as a protein that regulates Tat- and Tax-mediated expression of viral promoters. HIC and I-mfa represent a family of proteins that share a highly conserved cysteine-rich domain, termed the I-mfa domain. We show here that both I-mfa domain proteins, HIC and I-mfa, interacted in vivo with the Axin complex through their C-terminal I-mfa domains. This interaction inhibited Axin-mediated downregulation of free
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Konini, Angjelina, Mingsong Kang, and Seyed M. Moghadas. "Simulating Immune Interference on the Effect of a Bivalent Glycoconjugate Vaccine againstHaemophilus influenzaeSerotypes “a” and “b”." Canadian Journal of Infectious Diseases and Medical Microbiology 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/5486869.

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Objective.We sought to evaluate the immune responses to a bivalentHaemophilus influenzaeglycoconjugate vaccine against serotypes “a” (Hia) and “b” (Hib) in the presence of the preexisting immunity to Hib.Methods.We developed a stochastic simulation model of humoral immune response to investigate the antigenic challenge of a bivalent combined glycoconjugate vaccine and a bivalent unimolecular glycoconjugate vaccine. We compared simulation outcomes in the absence of any preexisting immunity with an already primed immune response having specific memory B cells and/or anti-Hib antibodies.Results.T
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Ryu, Jaewook, Ukjin Lee, Jiye Park, Do-Hyun Yoo, and Jung Hoon Ahn. "A Vector System for ABC Transporter-Mediated Secretion and Purification of Recombinant Proteins in Pseudomonas Species." Applied and Environmental Microbiology 81, no. 5 (2014): 1744–53. http://dx.doi.org/10.1128/aem.03514-14.

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ABSTRACTPseudomonas fluorescensis an efficient platform for recombinant protein production.P. fluorescenshas an ABC transporter secreting endogenous thermostable lipase (TliA) and protease, which can be exploited to transport recombinant proteins across the cell membrane. In this study, the expression vector pDART was constructed by insertingtliDEF, genes encoding the ABC transporter, along with the construct of the lipase ABC transporter recognition domain (LARD), into pDSK519, a widely used shuttle vector. When the gene for the target protein was inserted into the vector, the C-terminally fu
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Thomas, S. M., M. Hagel, and C. E. Turner. "Characterization of a focal adhesion protein, Hic-5, that shares extensive homology with paxillin." Journal of Cell Science 112, no. 2 (1999): 181–90. http://dx.doi.org/10.1242/jcs.112.2.181.

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Paxillin is a focal adhesion scaffolding protein which was originally identified as a substrate of the oncogenic tyrosine kinase, v-src. Paxillin has been proposed to be involved in regulation of focal adhesion dynamics. Two alternatively spliced mouse paxillin cDNAs were cloned and in the process, a paxillin-related protein, Hic-5, was also identified. Cloning and characterization of Hic-5 indicates that this protein shares extensive homology with paxillin. Although Hic-5 was originally characterized as a TGF-beta-inducible gene and proposed to be a transcription factor involved in senescence
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Yang, Yan-ping, Wayne R. Thomas, Pele Chong, Sheena M. Loosmore, and Michel H. Klein. "A 20-Kilodalton N-Terminal Fragment of the D15 Protein Contains a Protective Epitope(s) against Haemophilus influenzae Type a and Type b." Infection and Immunity 66, no. 7 (1998): 3349–54. http://dx.doi.org/10.1128/iai.66.7.3349-3354.1998.

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ABSTRACT A conserved 80-kDa minor outer membrane protein, D15, ofHaemophilus influenzae has been shown to be a protective antigen in laboratory animals against H. influenzae type a (Hia) or type b (Hib) infection. To localize the protective B-cell epitope(s) within the D15 protein and to further explore the possibility of using synthetic peptides as vaccine antigens, a 20-kDa N-terminal fragment of D15 protein (truncated D15 [tD15]) was expressed as a fusion protein with glutathioneS-transferase in Escherichia coli. The tD15 moiety was cleaved from glutathione S-transferase by using thrombin a
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Rathore, Vipul B., Masato Okada, Peter J. Newman, and Debra K. Newman. "Paxillin family members function as Csk-binding proteins that regulate Lyn activity in human and murine platelets." Biochemical Journal 403, no. 2 (2007): 275–81. http://dx.doi.org/10.1042/bj20061618.

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SFKs (Src family kinases) contribute importantly to platelet function in haemostasis. SFK activity is controlled by Csk (C-terminal Src kinase), which phosphorylates a C-terminal tyrosine residue on SFKs, resulting in inhibition of SFK activity. Csk is recruited to sites of SFK activity by tyrosine-phosphorylated Csk-binding proteins. Paxillin, a multidomain adaptor protein, has been shown to act as a Csk-binding protein and to inhibit Src activity during growth factor signalling. Human platelets express Hic-5, a member of the paxillin family; however, its ability to act as a Csk-binding prote
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Tanaka, Takuro, Koichiro Ikeda, Shuichi Yamamoto, and Noriko Yoshimoto. "Elution Profiles of Antibody-Drug Conjugates in Preparative Chromatography." MATEC Web of Conferences 333 (2021): 14001. http://dx.doi.org/10.1051/matecconf/202133314001.

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Monoclonal antibody drug conjugate (ADCs) have received much attention as pharmaceutical agents for treating serious diseases such as cancer. However, it is difficult to separate them on the basis of the drug to antibody ratio, DAR. Hydrophobic chromatography (HIC) is commonly used for the analysis of the drug to antibody ratio, DAR. The retention of ADCs on HIC can be controlled by the hydrophobic nature of ADCs, depending on the mobile phase conditions. They are sometimes performed at the restricted conditions where the solubility is too low. Ion exchange chromatography (IEC) using electrost
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Dissertations / Theses on the topic "Proteine hic"

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Thebault, Sabine. "Caractérisation d'une nouvelle protéine humaine contenant un domaine homologue à l'I-mfa : implication dans la régulation de l'expression de deux rétrovirus humains, HTLV-I et HIV-1." Montpellier 1, 2000. http://www.theses.fr/2000MON1T013.

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Hetti, Arachchilage Madara Dilhani. "Coevolution of epitopes in HIV-1 pre-integration complex proteins: protein-protein interaction insights." Kent State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=kent1530646538935895.

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Li, Chun-bong. "Mechanisms of HIV-1 Tat induced immune response." Click to view the E-thesis via HKUTO, 2005. http://sunzi.lib.hku.hk/hkuto/record/B31537169.

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Li, Chun-bong, and 李振邦. "Mechanisms of HIV-1 Tat induced immune response." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2005. http://hub.hku.hk/bib/B31537169.

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Treptow, Till. "Identifizierung und Charakterisierung zweier neuer Proteine, die mit dem HIV-Rev-Protein interagieren." Diss., lmu, 2009. http://nbn-resolving.de/urn:nbn:de:bvb:19-109373.

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Tsui, Brian. "Insulin Metabolism and Protein Degradation by HEPG2 Hepatocytes Treated with HIV-Protease Inhibitors." The University of Arizona, 2007. http://hdl.handle.net/10150/624329.

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Class of 2007 Abstract<br>Objectives: To explore the effects of human immunodeficiency virus protease inhibitors (HPI) on insulin metabolism and protein degradation in HepG2 hepatocytes in vitro. Methods: To see if HIV-protease inhibitors affect insulin degradation in a dose-dependent manner, HepG2 cells were incubated with various concentrations of tipranavir, indinavir, or atazanavir. After 125I-insulin was added, its degradation was measured by precipitation with trichloroacetic acid (TCA). To see the effect of HPIs on protein degradation, HepG2 cells labeled overnight with 3H-leucine were
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Cherry, Elana. "Trans-dominant negative inhibition of human immunodeficiency virus type 1 replication by expression of protease-reverse transcriptase fusion proteins." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0019/NQ50069.pdf.

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Mishra, Subrata H. "Structure and Energetics of RNA - Protein Interactions for HIV RREIIB Targeting Zinc Finger Proteins." unrestricted, 2008. http://etd.gsu.edu/theses/available/etd-06302008-144759/.

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Thesis (Ph. D.)--Georgia State University, 2008.<br>Title from file title page. Markus W. Germann, committee chair; Kathryn B. Grant , W. David Wilson, committee members. Electronic text (147 p. : ill. (some col.)) : digital, PDF file. Description based on contents viewed Oct. 6, 2008. Includes bibliographical references.
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Murzycki, Jennifer E. "Probing Protein Dynamics Through Mutational and Computational Studies of HIV-1 Protease: A Dissertation." eScholarship@UMMS, 2006. https://escholarship.umassmed.edu/gsbs_diss/166.

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How proteins undergo conformational changes to bind a ligand is one of the most fundamental questions of protein biology. MD simulations provide a useful computational tool for studying the theoretical movements of protein in solution on nanosecond timescales. The results of these simulations can be used to guide experimental design. By correlating the theoretical models with the results of experimental studies, we can obtain a significant amount of information about protein dynamics. This study represents the application of both computational and traditional experimental techniques to study p
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Douglas, Chanel Catherine. "A study into the protein/protein interactions involved in HIV-1 capsid assembly." Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2007. https://www.mhsl.uab.edu/dt/2008r/douglas.pdf.

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Books on the topic "Proteine hic"

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O, Freed Eric, and SpringerLink (Online service), eds. HIV Interactions with Host Cell Proteins. Springer-Verlag Berlin Heidelberg, 2010.

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Närvänen, Ale. Synthetic peptides as probes for protein interactions and as antigenic epitopes. University of Jyväskylä, 1990.

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March, Darren. Designing new antiviral drugs for AIDS: HIV-1 protease and its inhibitors. R.G. Landes, 1996.

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International, Symposium on the Immunobiology of Proteins and Peptides (6th 1990 Scottsdale Ariz ). Immunobiology of proteins and peptides VI: Human immunodeficiency virus, antibody immunoconjugates, bacterial vaccines, and immunomodulators. Plenum Press, 1991.

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Workshop on Mechanisms and Specificity of HIV Entry into Host Cells (1989 San Francisco, Calif.). Mechanisms and specificity of HIV entry into host cells. Plenum Press, 1991.

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Mansfield, Richard G. The protean player: The concept and practice pf doubling in the plays of Shakespeare and his contemporaries c. 1576-1631. University of East Anglia, 1989.

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Edwin J. Cohn and the development of protein chemistry: With a detalied account of his work on the fractionation of blood during and after World War II. Published by Center for Blood Research, Inc., 2002.

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Dessauer, Herbert C. Patterns of snake evolution suggested by their proteins: A contribution in celebration of the distinguished scholarship of Robert F. Inger on the occasion of his sixty-fifth birthday. Field Museum of Natural History, 1987.

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International Washington Spring Symposium (10th 1990 George Washington University). Advances in molecular biology and targeted treatment for AIDS. Plenum Press, 1991.

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Livingston, Schuyler, Benjamin Young, Martin Markowitz, Poonam Mathur, and Bruce L. Gilliam. HIV Virology. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190493097.003.0017.

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HIV is a member of the lentivirus subfamily of retroviruses. Two distinct groups of viruses are pathogenic in humans: HIV-1 and HIV-2. Both are transmitted sexually and known to cause immunodeficiency disease. HIV enters the cell through use of the CD4 receptor and chemokine co-receptors, primarily CCR5 and CXCR4. The viral genome is transcribed from RNA to DNA by reverse transcriptase and integrated into the host genome by integrase. The HIV genome encodes 15 proteins, comprising three categories: structural, regulatory, and accessory. After budding from the host cell, the virus matures into
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Book chapters on the topic "Proteine hic"

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Schöndorf, Theodor H., and Irene Witt. "Protein C Concentration after Elective Hip Surgery." In Protein C, edited by Irene Witt. De Gruyter, 1985. http://dx.doi.org/10.1515/9783110852707-019.

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Ott, David E. "HIV-1 Biology at the Protein Level." In HIV-1 Proteomics. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6542-7_2.

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Wagner, Todd. "Protease Inhibitors." In Mental Health Practitioner's Guide to HIV/AIDS. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-5283-6_69.

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Hirono, Shuichi, Kenji Nagata, Akihiro Ivioriuchi, et al. "HGF-Related Proteins in Hepatocellular Carcinoma (HCC)." In Liver Cirrhosis. Springer Japan, 2001. http://dx.doi.org/10.1007/978-4-431-68343-8_11.

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Petry, H., O. Ast, E. De Rosny, et al. "Inhibition of HIV-1 Replication by Peptidic Protease Inhibitors." In HIV-Infekt. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-59683-4_11.

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Breitkreutz, R., A. Babylon, M. Beichert, et al. "Protein- und Aminosäurenstoffwechsel bei HIV-Infektion. Therapeutische Optionen und Ergebnisse klinischer Prüfungen." In HIV-Infekt. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-59683-4_68.

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Sneha, Patil, Balaji Seetharaman, and Paul Shapshak. "Amyloidogenic Pattern Prediction of HIV-1 Proteins." In Global Virology II - HIV and NeuroAIDS. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7290-6_33.

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Jöbstl, B., M. Barcova, C. Speth, L. Kacani, and M. P. Dierich. "Role of Adenylate Cyclase and p70S6-Kinase in the Regulation of gp41 Envelope Protein-Induced IL-10 Expression in Human Monocytes." In HIV-Infekt. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-59683-4_7.

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Dicker, Ira B., Michael A. Walker, Zeyu Lin, et al. "Simple and Accurate In Vitro Method for Predicting Serum Protein Binding of HIV Integrase Strand Transfer Inhibitors." In HIV-1 Integrase. John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118015377.ch19.

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Zhao, Xue Zhi, and Terrence R. Burke. "Application of Protein Covalent Modification to Studying Structure and Function of HIV-1 Integrase and Its Inhibitors." In HIV-1 Integrase. John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118015377.ch27.

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Conference papers on the topic "Proteine hic"

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Church, W., T. Messier, P. Howard, J. Amiral, D. Meyer, and K. Mam. "A SHARED EPITOPE ON HUMAN PROTEIN C, FACTOR X, FACTOR VII, AND PROTTOBIN DEFINED BY A MONOCLONAL ANTIBODY." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643937.

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A monoclonal antibody prepared against hunan protein C (HPC) was found to react with several other vitamin K-dependent blood proteins. Using a competitive inhibition solid-phase radioinminoassay with HPC, binding of 125I-HPC to the antibody was inhibited by purified prothrombin, Factor X, and Factor VII in addition to protein C. Other vitamin K-dependent proteins including Factor IX, protein S, and bone-GLA protein did not compete for binding of 125I-HPC to the antibody. The effect of calciun ion on the binding of antibody to 125I-HPC was examined in a solid-phase imnunoassay system with the a
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Sugo, T., S. Tanabe, K. Shinoda, and M. Matsuda. "MONOCLONAL ANTIBODIES THAT RECOGNIZE Ca2+-INDUCED CONFORMER OF PROTEIN C, INDEPENDENT OF GLA RESIDUES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643644.

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Monoclonal antibodies (MCA’s) were prepared against human protein C (PC) according to Köhler &amp; Milstein, and those that recognize the Ca2+-dependent PC conformers were screened by direct ELISA in the presence of 2 mM either CaCl2 or EDTA. Out of nine MCAߣs thus screened, five MCA's designated as HPC-1˜5, respectively, were found to react with PC in the presence of Ca2+ but not EDTA. By SDS-PAGE coupled with Western Blotting performed in the presence of 2 mM CaCl2, we found that two MCA’s HPC-1 and 2, recognized the light chain, and two others, HPC-3 and 4, recognized the heavy chain of PC.
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Freeman, L., V. Hornsey, D. S. Pepper, P. R. Foster, L. Winkelman, and J. Dawes. "PROTEIN AGGREGATES IN HEATED BLOOD PRODUCTS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644019.

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Heating of blood products to reduce viral infectivity is now a standard practice. Such treatment may also modify the constituent proteins, reducing their activity or altering their structure with potentially harmful consequences for the recipient. Partially denatured proteins frequently form aggregates, which are often immunogenic and could precipitate immune complex formation, allergic reactions and kidney damage. In addition they may contribute to the development of AIDS after HIV infection by inducing a persistent state of T-cell activation.Protein aggregate formation in factor VIII and fac
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Schleuning, W. D. "THE BIOCHEMISTRY AND CELL BIOLOGY OF SINGLE CHAIN UROKINASE TYPE PLASMINOGEN ACTIVATOR." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642956.

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Urokinase was discovered in the late nineteenth century, as an enzymatic principle in urine, that initiates the dissolution of blood clots. The basis of this phenomenon was recognized more than fifty years ago as the activation of plasminogen, the precursor of a tryptic protease, then known as profibrinolysin. Despite this long history, detailed data on the biochemistry of plasminogen activation have only become available recently. Urokinase (now designated urokinase-type plasminogen activator : u-PA) is synthesized and secreted as a single chain polypeptide (Mr-: 53,000) by many cell types. S
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Kawai, Y., R. R. Montgomery, K. Furihata, and T. J. Kunicki. "EXPRESSION OF PLATELET ALLOANTIGENS ON HUMAN ENDOTHELIAL CELLS AND HEL CELLS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642813.

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Analogs of platelet membrane glycoproteins IIb and IIIa (GPIIb-IIIa) have been shown to be synthesized and expressed by human endothelial cells (HEC), a human erythroleukemia cell line (HEL) and various other cells. Previous studies from our laboratory demonstrated that the platelet alloantigen P1A1, is expressed on HEC GPIIIa. Other alloantigen systems, namely, Pen and Bak, are known to be localized on platelet GPIIIa and GPIIb, respectively. Utilizing additional antibodies from patients with PTP specific for Pena, Baka, and Bakb allo-antigens, and isoantibodies (iso-ab) from a patient with G
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Karges, H. E., P. Fuhge, and N. Heimburger. "PROPERTIES AND VIRUS SAFETY OF A PASTEURIZED ANTITHROMBINIII-CONCENTRATE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644154.

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The possible occurance of up to now unknown human pathogenic viruses makes it necessary to reconsider thestrategies for the preparation of each plasma protein concentrate used for substitution therapy. Even up to now safe products may be contaminated by infectious particles in the near future. Hence, each procedure for the preparation of such proteins should critically be checked for the elimination of contaminating proteins and should contain an inactivation step for pathogenic agents.Since about 4 decades the pasteurization of albumin in presence of stabilizers has been found to be a safe an
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Futamura, N., S. Aluru, D. Ranjan, and K. Mehrotra. "Efficient algorithms for protein solvent accessible surface area." In Proceedings Fourth International Conference/Exhibition on High Performance Computing in the Asia-Pacific Region. IEEE, 2000. http://dx.doi.org/10.1109/hpc.2000.843502.

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Atilgan, Emrah, and Jianjun Hu. "Efficient protein-ligand docking using sustainable evolutionary algorithms." In 2010 10th International Conference on Hybrid Intelligent Systems (HIS 2010). IEEE, 2010. http://dx.doi.org/10.1109/his.2010.5600082.

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Nakamura, K., K. Iijima, N. Inoue, J. Nishioka, and K. Suzuki. "INHERITED DEFICIENCY OF FUNCTIONAL PROTEIN S IN A JAPANESE FAMILY." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644297.

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A family with a history of severe recurrent venous thromboembolic disease in some of the members was studied over three generations. In the propositus, a 36-year-old Japanese man, assays for the coagulation, anticoagulation and fibrinolytic factors including fibrinogen, plasminogen, antithrombin III and protein C associated with inherited venous thrombotic disease were normal. While markedly decreased protein S, a cofactor of activated protein C, was revealed. The functional protein S activity in plasma was lower than 5% of normal. The same laboratory data were shown in his paternal uncle and
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Junior, Francisco Nascimento, Ing Ren Tsang, and George D. C. Cavalcanti. "A SVM for GPCR Protein Prediction Using Pattern Discovery." In 2008 8th International Conference on Hybrid Intelligent Systems (HIS). IEEE, 2008. http://dx.doi.org/10.1109/his.2008.51.

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Reports on the topic "Proteine hic"

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Pinter, Abraham. HIV Vaccines Based on Novel MULV-HIV Fusion Proteins. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada373677.

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Wong-Staal, Flossie. Transdominant Rev and Protease Mutant Proteins of HIV/SIV as Potential Antiviral Agents In vitro and In vivo. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada251525.

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Wong-Staal, Flossie. Transdominant Rev and Protease Mutant Proteins of HIV/SIV as Potential Antiviral Agents In vitro and In vivo (AIDS). Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada269541.

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Block, Michelle L. The Role of Protein Radicals in Chronic Neuroimmune Dysfunction and Neuropathology in Response to a Multiple-Hit Model of Gulf War Exposure. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada613307.

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