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Artykuły w czasopismach na temat "TCR"

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Arty, Indyah Sulistyo. "SYNTHESIZE AND CITOTOXICITY TEST OF SEVERAL COMPOUNDS OF MONO PARA-HIDROXY CHALCON." Indonesian Journal of Chemistry 10, no. 1 (2010): 110–15. http://dx.doi.org/10.22146/ijc.21489.

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Five compounds of mono para-hidroxy chalcon were synthesized (TC1, TC2, TC3, TC4, and TC5) and tested their cytotoxicity against HeLa cell and Raji cell. The difference in substituent of TC1 (R4 =H), TC2 (R4 = OCH3), and TC3 (R4 = F), showed the difference of their citotoxicity against HeLa cell. The citotoxicity of TC1 (LC50 = 16.08 µg/mL) ≈ TC3 (LC50 = 13.37 µg/mL), but the substituent difference of TC2 (LC50 = 147.43 µg/mL), decreasing it citotoxicity 10 times. Like wise their citotoxicity against Raji cell of TC1 (LC50 = 36.44 µg/mL) ≈ TC3 (LC50 = 30.46 µg/mL), but the substituent differen
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Uruilal, Costanza, Abraham Talahaturuson, Wihelmina Rumahlewang, and Jogeneis Patty. "ISOLASI Trichoderma spp. DAN DAYA ANTAGONISMENYA TERHADAP SCLEROTIUM ROLFSII SACC. PENYEBAB PENYAKIT LAYU PADA TANAMAN CABAI (Capsicum anuum) SECARA IN-VITRO." JURNAL BUDIDAYA PERTANIAN 13, no. 2 (2017): 64–67. http://dx.doi.org/10.30598/jbdp.2017.13.2.64.

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The objective of this study is to isolation and agonistic test ability of Trichoderma spp. againts Sclerotium rolfsii Sacc. cause of wilting on pepper plants and has been conducted in Pathogenicity Laboratory Faculty of Agriculture Unpatti. The study use 5 treatment of isolate Trichoderma spp. (Tc3, Tc4, Tc5, Tc6 and Tc7) with 3 replications so that there are 15 experimental units. The results showed that the five isolates Trichoderma spp. has an antagonistic power to S. rolfsii with an average percentage of inhibition of S. rolfsii of 26,01%. Percentage of inhibition bolth of isolate ware not
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Bagot, Martine, Hamid Echchakir, Fathia Mami-Chouaib, et al. "Isolation of Tumor-Specific Cytotoxic CD4+ and CD4+CD8dim+ T-Cell Clones Infiltrating a Cutaneous T-Cell Lymphoma." Blood 91, no. 11 (1998): 4331–41. http://dx.doi.org/10.1182/blood.v91.11.4331.

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Abstract We have isolated several T-cell clones from lymphocytes infiltrating a human major histocompatibility class (MHC) II negative cutaneous T-cell lymphoma (CTCL). We describe here two of these clones, TC5 and TC7, with, respectively, a CD4+CD8dim+ and CD4+CD8− phenotype. Both clones mediated a specific MHC class I–restricted cytotoxic activity toward the fresh autologous tumor cells, and autologous tumor cell lines previously established with interleukin-2 (IL-2) and IL-7 from the skin and from the blood. Analysis of the T-cell receptor (TCR) Vβ gene expression showed that the tumor cell
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Bagot, Martine, Hamid Echchakir, Fathia Mami-Chouaib, et al. "Isolation of Tumor-Specific Cytotoxic CD4+ and CD4+CD8dim+ T-Cell Clones Infiltrating a Cutaneous T-Cell Lymphoma." Blood 91, no. 11 (1998): 4331–41. http://dx.doi.org/10.1182/blood.v91.11.4331.411k12_4331_4341.

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We have isolated several T-cell clones from lymphocytes infiltrating a human major histocompatibility class (MHC) II negative cutaneous T-cell lymphoma (CTCL). We describe here two of these clones, TC5 and TC7, with, respectively, a CD4+CD8dim+ and CD4+CD8− phenotype. Both clones mediated a specific MHC class I–restricted cytotoxic activity toward the fresh autologous tumor cells, and autologous tumor cell lines previously established with interleukin-2 (IL-2) and IL-7 from the skin and from the blood. Analysis of the T-cell receptor (TCR) Vβ gene expression showed that the tumor cells, which
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Goux, Delphine, Jérôme D. Coudert, Diane Maurice, et al. "Cooperating pre–T-cell receptor and TCF-1–dependent signals ensure thymocyte survival." Blood 106, no. 5 (2005): 1726–33. http://dx.doi.org/10.1182/blood-2005-01-0337.

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Abstract Intrathymic T-cell maturation critically depends on the selective expansion of thymocytes expressing a functionally rearranged T-cell receptor (TCR) β chain. In addition, TCR-independent signals also contribute to normal T-cell development. It is unclear whether and how signals from the 2 types of pathways are integrated. Here, we show that T-cell factor-1 (TCF-1), a nuclear effector of the canonical wingless/int (wnt)/catenin signaling pathway, ensures the survival of proliferating, pre-TCR+ thymocytes. The survival of pre-TCR+ thymocytes requires the presence of the N-terminal caten
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Ciurea, Stefan O., Rima M. Saliba, Ulas D. Bayraktar, et al. "Improved Early Outcomes with T-Cell Replete (TCR) Compared with T-Cell Depleted (TCD) Haploidentical Stem Cell Transplantation (HaploSCT)." Blood 118, no. 21 (2011): 320. http://dx.doi.org/10.1182/blood.v118.21.320.320.

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Abstract Abstract 320 Background: HaploSCT has been commonly performed with a TCD graft using CD34+ selection; however, this has been limited by a higher non-relapse mortality (NRM) primarily related to infectious complications. An alternative approach using a TCR bone marrow graft and high-dose post-transplant cyclophosphamide (HDPTCy) in the setting of non-myeloablative conditioning has been reported to have lower NRM and acceptable rates of GVHD. Methods: We hypothesized that TCR HaploSCT using HDPTCy is associated with improved immunologic reconstitution, less NRM and better early outcomes
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Delea, Thomas, Aaron Moynahan, Wenzhen Ge, et al. "Real-World Study of Patients with Triple-Class Exposed Relapsed/Refractory Multiple Myeloma: Analysis across a Spectrum of Advanced Disease Stage Medicare Patients in the United States." Blood 142, Supplement 1 (2023): 3773. http://dx.doi.org/10.1182/blood-2023-188591.

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Background Treatment of relapsed/refractory (RR) multiple myeloma (MM) has been transformed by novel therapies including anti-CD38 monoclonal antibodies (mAb), 2 nd and 3 rd generation immunomodulatory drugs (IMiD), and proteasome inhibitors (PI). This has resulted in increasing numbers (no.) of triple-class exposed (TCE) patients (pts), defined as pts who have received an IMiD, ≥1 PI, and ≥1 anti-CD38 mAb. Many TCE pts are exposed to ≥5 drugs in these classes (i.e. penta-exposed [PE]: ≥2 IMID, ≥2 PI, and an anti-CD38 mAb). Some are refractory to ≥1 drug in each class (triple-class refractory
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Sun, Hanli, Jiao Huang, Kai Zhan, et al. "Abstract 3598: A new strategy for T cell therapy: T cells secreting TCR anti-CD3 bispecific T-cell engager." Cancer Research 84, no. 6_Supplement (2024): 3598. http://dx.doi.org/10.1158/1538-7445.am2024-3598.

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Abstract TCR-engineered T (TCR-T) cells and TCR-anti-CD3 bispecific T-cell engagers (TCEs) are potent TCR-based therapeutic agents with distinct advantages and limitations in tumor treatment. TCR-T cells offer durable persistence within patients but necessitate personalized manufacturing and lack the capacity to harness bystander T cells. Conversely, TCEs are readily available as "off-the-shelf" products and can recruit bystander T cells, yet they exhibit a shorter lifespan. In our study, we sought to merge the merits of both approaches by engineering T cells to secrete a TCR-anti-CD3 TCE spec
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Abdulazim, Amr, Nora Prochnow, and Tara Taeihagh. "TCR or Not TCR?" Journal of Oral and Maxillofacial Surgery 69, no. 10 (2011): 2483–84. http://dx.doi.org/10.1016/j.joms.2011.05.028.

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Oros-Ortega, Iván, Alejandro Alonso-López, Jesús Pérez-Moreno, et al. "Respuesta de plántulas de Cedrela odorata a la inoculación con Rhizophagus intraradices y diferentes niveles de defoliación." Revista Mexicana de Ciencias Agrícolas 6, no. 3 (2017): 627. http://dx.doi.org/10.29312/remexca.v6i3.645.

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 Respuesta de plántulas de Cedrela odorata a la inoculación con Rhizophagus intraradices y diferentes niveles de defoliación ; el efecto de seis tratamientos (T) sobre la tasa de crecimiento en altura (TCA) , diámetro ( TCD ) , tasa de crecimiento relativo (TCR ) y peso fresco y seco de plántulas de C. odorata se evaluaron en un vivero. Se utilizó un diseño completamente al azar con arreglo factorial (2 x 3); TS consistió en una combinación de los factores: porcentaje de defoliación (0, 50 y 90) y la inoculación de R. intraradices (con y sin inoculación). Despue
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Rozprawy doktorskie na temat "TCR"

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Groves, Tim C. "Pre-TCR and TCR-Ãß signaling during T cell development." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/NQ27657.pdf.

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Currie, James. "Stochastic modelling of TCR binding." Thesis, University of Leeds, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.590430.

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A fundamental process in the immune response to infection is the activation of T cells following contact with antigen presenting cells. This activation occurs after T cell receptors on the surface of T cells bind to immunogenic peptides expressed on the surface of antigen presenting cells. The binding of T cell receptors to ligands not only leads to the activation of T cells, it is also key to T cell selection in the thymus and the maintenance of a diverse T cell receptor repertoire. T cell receptor bindings are converted into a signal which activates a T cell but there is no universal theory
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Lacroix, France. "T cell receptor (TCR) for antigen: A comparative study between the TCR alpha/beta and TCR gamma/delta subsets in noninfected and HIV infected individuals." Thesis, University of Ottawa (Canada), 1993. http://hdl.handle.net/10393/6937.

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HIV infection is associated with characteristic quantitative changes in T-lymphocyte subsets: progressive depletion of the CD4$\sp{+}$ T-lymphocytes and an increased number of the CD8$\sp{+}$ T-lymphocyte. In this study, I report the results of a flow cytometric analysis of the expression of CD3, CD4, CD8, TCR$\alpha$/$\beta$, and TCR$\gamma$/$\delta$ antigens. I observed that CD8$\sp{+}$TCR$\alpha$/$\beta\sp{+}$ cells increased early in HIV disease (p 0.01) whereas the frequency of CD4$\sp{+}$TCR$\alpha$/$\beta\sp{+}$ cells was relatively unchanged. The frequency of TCR$\gamma$/$\delta\sp{+}
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Mariathasan, Sanjeev. "TCR-mediated signaling in thymocyte selection." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/NQ63683.pdf.

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Rivera, Reyes Brenda Mariola. "Regulation of the TCR signaling pathway." Connect to text online, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1132588714.

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Barry, A. C. "Regulation of TCR signalling by SOCS." Thesis, Queen's University Belfast, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.479241.

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Mallaun, Michel. "Proximal TCR signaling in self tolerance /." [S.l.] : [s.n.], 2008. http://edoc.unibas.ch/diss/DissB_8729.

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Huang, Elizabeth Chi-Fang. "Organisation of, and ligand-independent signalling by, the TCR, with a special emphasis on the pre-TCR." Thesis, University of Oxford, 2017. http://ora.ox.ac.uk/objects/uuid:0c01e3d4-2002-487c-a0b6-09ed20cb223b.

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Understanding how immune signalling is initiated and regulated spatiotemporally is likely to be helped by investigations of receptor stoichiometry. The pre-TCR expressed by thymocytes shares similarities in structure and signalling components with the mature TCR but, in contrast to the TCR, it has no known ligands. This thesis has therefore analysed the stoichiometry of the pre-TCR using mutagenesis- and imaging-based approaches, and explored how ligand-independent signalling might be initiated by both the TCR and pre-TCR. The mutational analysis, which required considerable optimisation becau
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Bunse, Mario. "RNAi-mediated knockdown of the endogenous TCR improves safety of immunotherapy with TCR gene-modified T cells." Doctoral thesis, Humboldt-Universität zu Berlin, Lebenswissenschaftliche Fakultät, 2015. http://dx.doi.org/10.18452/17155.

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Durch den Transfer der Gene des heterodimeren T-Zellrezeptors (TZR) mithilfe viraler Vektoren können T-Zellen programmiert werden, ein ausgewähltes Antigen spezifisch zu erkennen. In klinischen Studien wurden solche T-Zellen bereits mit Erfolg zur Immuntherapie von Krebs und viralen Infektionen eingesetzt. Genmodifizierte T-Zellen unterscheiden sich jedoch von normalen T-Zellen, weil sie neben den beiden zelleigenen auch die zwei übertragenen TZR-Gene exprimieren. Diese Situation erlaubt die Bildung vier verschiedener TZR-Heterodimere: der zelleigene TZR, der übertragene TZR und zwei gemischte
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Sommermeyer, Daniel. "Generation of dual T cell receptor (TCR) T cells by TCR gene transfer for adoptive T cell therapy." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2010. http://dx.doi.org/10.18452/16051.

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Die Herstellung von T-Zellen mit definierten Spezifitäten durch den Transfer von T-Zellrezeptor (TCR) Genen ist eine effiziente Methode, um Zellen für eine Immuntherapie bereitzustellen. Eine besondere Herausforderung ist dabei, ein ausreichend hohes Expressionsniveau des therapeutischen TCR zu erreichen. Da T-Zellen mit einem zusätzlichen TCR ausgestattet werden, entsteht eine Konkurrenzsituation zwischen dem therapeutischen und dem endogenen TCR. Bevor diese Arbeit begonnen wurde war nicht bekannt, welche TCR nach einem Gen-Transfer exprimiert werden. Daher haben wir Modelle etabliert, in de
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Książki na temat "TCR"

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T, Petrie Howard, ed. Non-TCR-mediated mechanisms of thymocyte differentiation. Academic Press, 2000.

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T, Petrie Howard, ed. Non-TCR-mediated mechanisms of thymocyte differentiation. Academic Press, 2000.

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Ruffi, Lapo. Lapo Ruffi, Edificio TCR: Pistoia, Italy, 2008-2009. Forma, 2011.

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Groves, Tim C. Pre-TCR and TCRab signaling during T cell development. National Library of Canada = Bibliothèque nationale du Canada, 1997.

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Hammad, Nazik. A transgenic TCR model for studying the veto phenomenon. National Library of Canada, 1994.

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Bi, Yunchen. Study of the Calcium Regulation Mechanism of TCR Activation Using Nanodisc and NMR Technologies. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54618-5.

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Cheng, Gordon W. Functions of CD45 in TCR signaling in CD4p+sCD8p+s double-positive thymocytes. National Library of Canada = Bibliothèque nationale du Canada, 1999.

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Ford, Megan. The role and mechanism of B6/1pr TCR[alpha beta]+CD4-CD8- T cells in immune response regulation. National Library of Canada, 2001.

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Galley, Kevin Andrew. Analysis of junctional region diversity of TCR[beta] cDNA from pancreatic islet-infiltrating T cells of young prediabetic nonobese diabetic mice. National Library of Canada, 1994.

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Korpela, Mikko. Organizational Information Systems in the Context of Globalization: IFIP TC8 & TC9. Springer US, 2003.

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Części książek na temat "TCR"

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Maeurer, Markus J. "TCR Analyses." In Analyzing T Cell Responses. Springer Netherlands, 2005. http://dx.doi.org/10.1007/1-4020-3623-x_14.

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Jameson, Stephen C., and Kristin A. Hogquist. "Options for TCR Interactions: TCR Agonists, Antagonists and Partial Agonists." In MHC Molecules: Expression, Assembly and Function. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4684-6462-7_11.

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Vandenbark, Arthur A., George Hashim, and Halina Offner. "TCR Peptide Therapy in Autoimmunity." In Progress in Immunology Vol. VIII. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-51479-1_82.

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Rhein, Simone, and Neşe Çakmak-Görür. "TCR Gene Therapy for Cancer." In Methods in Molecular Biology. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2441-8_6.

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Peruzzi, Benedetta, Sara Bencini, and Roberto Caporale. "TCR Vβ Evaluation by Flow Cytometry." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1311-5_8.

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Venu, Y., T. Nireekshana, B. Phanisaikrishna, Ramavath Gnanendar, and S. Ravikumar. "Reducing TCR Harmonics Using Sequential Switching." In Advances in Automation, Signal Processing, Instrumentation, and Control. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-8221-9_233.

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Porcelli, S., P. A. Bleicher, J. L. Greenstein, S. P. Balk, C. Terhorst, and M. B. Brenner. "Lymphocytes Bearing Either γδ-TCR or αβ-TCR Can Recognize Non-MHC Encoded CD1 Molecules." In Progress in Immunology. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83755-5_5.

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Yamaguchi, Rui, Seiya Imoto, and Satoru Miyano. "A TCR Sequence Data Analysis Pipeline: Tcrip." In Immunopharmacogenomics. Springer Japan, 2015. http://dx.doi.org/10.1007/978-4-431-55726-5_2.

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Gervois, Nadine, Bing-Yuan Wei, Paolo Dellabona, Jean Peccoud, Christophe Benoist, and Diane Mathis. "Structure of the TCR-Ag-MHC Complex." In T Lymphocytes. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3054-1_2.

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Neagu, Monica, and Carolina Constantin. "Signal Transduction in Immune Cells and Protein Kinases." In Advances in Experimental Medicine and Biology. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-49844-3_5.

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AbstractImmune response relies upon several intracellular signaling events. Among the protein kinases involved in these pathways, members of the protein kinase C (PKC) family are prominent molecules because they have the capacity to acutely and reversibly modulate effector protein functions, controlling both spatial distribution and dynamic properties of the signals. Different PKC isoforms are involved in distinct signaling pathways, with selective functions in a cell-specific manner.In innate system, Toll-like receptor signaling is the main molecular event triggering effector functions. Vario
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Streszczenia konferencji na temat "TCR"

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Myrick, Wilbur, Nobuyasu Shiga, Julian St James, and Ahmad Byagowi. "Timing, Communications, and Ranging SDR (TCR-SDR) for IoT Wireless Synchronization." In 2024 IEEE International Symposium on Precision Clock Synchronization for Measurement, Control, and Communication (ISPCS). IEEE, 2024. http://dx.doi.org/10.1109/ispcs63021.2024.10747731.

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Wang, Haoyan, Yuhang Yang, Yifei Huang, Tianyi Zang, and Yadong Liu. "TDLM: A Diffusion Language Model for TCR Sequence Exploration and Generation." In 2024 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2024. https://doi.org/10.1109/bibm62325.2024.10821797.

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Andrews, Sean. "Staring at the sun: advanced TCR materials for robust thermal imaging." In Infrared Technology and Applications LI, edited by David Z. Ting, Gabor F. Fulop, Masafumi Kimata, and Michael H. MacDougal. SPIE, 2025. https://doi.org/10.1117/12.3056866.

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Mao, Yelu, Xiaoyu Shi, Ming-Sheng Shang, and Ying Zhang. "TCR." In the 2018 2nd International Conference. ACM Press, 2018. http://dx.doi.org/10.1145/3234804.3234819.

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Alrhmoun, S., M. S. Fisher, J. A. Lopatnikova, et al. "ADVANCED CANCER IMMUNOTHERAPY: HARNESSING SINGLE-CELL SEQUENCING TO DISCOVER NATURALLY-OCCURRING ANTIGEN-SPECIFIC TCRS." In XI МЕЖДУНАРОДНАЯ КОНФЕРЕНЦИЯ МОЛОДЫХ УЧЕНЫХ: БИОИНФОРМАТИКОВ, БИОТЕХНОЛОГОВ, БИОФИЗИКОВ, ВИРУСОЛОГОВ, МОЛЕКУЛЯРНЫХ БИОЛОГОВ И СПЕЦИАЛИСТОВ ФУНДАМЕНТАЛЬНОЙ МЕДИЦИНЫ. IPC NSU, 2024. https://doi.org/10.25205/978-5-4437-1691-6-217.

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Adoptive cell therapy, particularly T cell receptor–engineered T (TCR-T) cell therapy, represents a cutting-edge and promising strategy for treating solid tumors [1]. Current methods for developing TCR-T cell therapies yield a limited number of candidate TCRs [2], missing the comprehensive view of the repertoire, which may impede the identification of the most effective TCRs. This limitation highlights the need for new techniques in TCR-T cell therapy development.
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Zhou, Jun, Zhenzhou Wu, Mengren Man, et al. "Llama-TCR: Generate De Novo TCR with Large Language Model." In 2024 IEEE Conference on Artificial Intelligence (CAI). IEEE, 2024. http://dx.doi.org/10.1109/cai59869.2024.00158.

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Tomimura, Toshio, Yasushi Koito, Taewan Do, Masaru Ishizuka, and Tomoyuki Hatakeyama. "On Simple Prediction Method for Thermal Contact Resistance Between Wavy Surfaces With Thermal Interface Material Under Low Mean Nominal Contact Pressure (Fundamental Study Based on 1-D Model)." In ASME 2015 International Technical Conference and Exhibition on Packaging and Integration of Electronic and Photonic Microsystems collocated with the ASME 2015 13th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/ipack2015-48302.

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The thermal contact resistance (TCR) is the crucial issue in the field of heat removal from systems like electronic equipment, satellite thermal control systems, and so on. To cope with the problem, a lot of studies have been done mainly for flat rough surfaces. However, as pointed out so far, there are still wide discrepancies among measured and predicted TCRs, even for similar materials. To investigate the key factors for the abovementioned discrepancies, a fundamental analysis was conducted in our previous study [1] using a simple contact surface model, which was composed of the unit cell m
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Wołczyn´ski, Waldemar S., Edward Guzik, Wojciech Wajda, and Bogusz Kania. "Columnar → Equiaxed Structure Transition in Solidifying Rolls." In 2010 14th International Heat Transfer Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/ihtc14-23048.

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As the first step of simulation, a temperature field for solidifying cast steel and cast iron roll was created. The convection in the liquid is not comprised since in the first approximation, the convection does not influence the analysed occurrence of the C → E (columnar to equiaxed grains) transition in the roll. The obtained temperature field allows to study the dynamics of its behavior observed in the middle of the mould thickness. This midpoint of the mould thickness was treated as an operating point for the C → E transition. A full accumulation of the heat in the mould was postulated for
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Newby, Richard A., Wen-Ching Yang, and Ronald L. Bannister. "Use of Thermochemical Recuperation in Combustion Turbine Power Systems." In ASME 1997 International Gas Turbine and Aeroengine Congress and Exhibition. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/97-gt-044.

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The performance and practicality of heavy duty combustion turbine power systems incorporating thermochemical recuperation (TCR) of natural gas has been estimated to assess the potential merits of this technology. Process models of TCR combustion turbine power systems based on the Westinghouse 501F combustion turbine were developed to conduct the performance evaluation. Two TCR schemes were assessed — Steam-TCR and Flue Gas-TCR. Compared to conventional combustion turbine power cycles, the TCR power cycles show the potential for significant plant heat rate improvements, but their practicality i
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Dretvik, Svein-Egil, Stian Svardal, and Steinar Kristoffersen. "Kristin Titanium Catenary Risers (TCR)." In ASME 2003 22nd International Conference on Offshore Mechanics and Arctic Engineering. ASMEDC, 2003. http://dx.doi.org/10.1115/omae2003-37352.

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The gas export from A˚sgard B has experienced vortex induced vibrations (VIV) internally in the flow caused by the irregularities in the carcass of the flexible risers. The VIV is amplified through resonance in the topside piping causing vibrations and fatigue resulting in gas leakage. So far extensive work have been carried out without succeeding in establishing predictable model for description of the VIV phenomena. For the Kristin project Titanium Catenary Risers (TCR) have been developed as an alternative to gas export through flexible risers. This paper will present the work performed to
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Raporty organizacyjne na temat "TCR"

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Russell, Michael, Vincent Paquit, Luke Scime, and Alka Singh. TCR Data Management Plan. Office of Scientific and Technical Information (OSTI), 2021. http://dx.doi.org/10.2172/1814318.

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Huning, Alex, and Randall Fair. TCR Postulated Accident and MHA Dose Assessment. Office of Scientific and Technical Information (OSTI), 2021. http://dx.doi.org/10.2172/1778087.

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Shirvan, Koroush. Validation of Robustness in TCR Design Strategies. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/1964002.

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Dehoff, Ryan, and Michael Russell. Quality Procedures for TCR Metal Core Structure Advanced Manufacturing Process. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1814370.

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Schappel, Danny, and Kurt Terrani. Key Material Properties for Thermo-Structural Analysis of TCR Core Components. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1558508.

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Scime, Luke, Michael Sprayberry, David Collins, et al. Report on diagnostic and predictive capabilities of the TCR digital platform. Office of Scientific and Technical Information (OSTI), 2021. http://dx.doi.org/10.2172/1831630.

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Li, Meimei, Xuan Zhang, Wei-Ying Chen, and Florent Heidet. Progress Report on the Assessment of the Material Performance for TCR Applications. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1608042.

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Li, Meimei, Xuan Zhang, Wei-Ying Chen, and Florent Heidet. Progress Report on the Assessment of the Material Performance for TCR Applications. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1701716.

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Field, Kevin, Joseph Simpson, Maxim Gussev, et al. Handbook of advanced manufactured material properties from TCR structure builds at ORNL – FY19. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1817605.

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Huning, Alex, Randall Fair, Alyson Coates, and Bruce Lin. TCR Input to NUREG-1537 Process for Advanced Nuclear Technologies Derived from Additive Manufacturing. Office of Scientific and Technical Information (OSTI), 2021. http://dx.doi.org/10.2172/1805005.

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