Gotowa bibliografia na temat „CD2BP2”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Spis treści
Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „CD2BP2”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Artykuły w czasopismach na temat "CD2BP2"
Guo, Xiaobo, Gang Li, Yufeng Zhao i Bo Zhao. "TGFB Induced Factor Homeobox 2 Induces Deterioration of Bladder Carcinoma via Activating CD2 Cytoplasmic Tail Binding Protein 2". Journal of Biomedical Nanotechnology 19, nr 9 (1.09.2023): 1670–76. http://dx.doi.org/10.1166/jbn.2023.3657.
Pełny tekst źródłaKofler, Michael, Kathrin Motzny, Michael Beyermann i Christian Freund. "Novel Interaction Partners of the CD2BP2-GYF Domain". Journal of Biological Chemistry 280, nr 39 (6.07.2005): 33397–402. http://dx.doi.org/10.1074/jbc.m503989200.
Pełny tekst źródłaHeinze, M., M. Kofler i C. Freund. "Investigating the functional role of CD2BP2 in T cells". International Immunology 19, nr 11 (6.09.2007): 1313–18. http://dx.doi.org/10.1093/intimm/dxm100.
Pełny tekst źródłaAlbert, Gesa I., Christoph Schell, Karin M. Kirschner, Sebastian Schäfer, Ronald Naumann, Alexandra Müller, Oliver Kretz i in. "The GYF domain protein CD2BP2 is critical for embryogenesis and podocyte function". Journal of Molecular Cell Biology 7, nr 5 (16.06.2015): 402–14. http://dx.doi.org/10.1093/jmcb/mjv039.
Pełny tekst źródłaNielsen, Tine K., Sunbin Liu, Reinhard Lührmann i Ralf Ficner. "Structural Basis for the Bifunctionality of the U5 snRNP 52K Protein (CD2BP2)". Journal of Molecular Biology 369, nr 4 (czerwiec 2007): 902–8. http://dx.doi.org/10.1016/j.jmb.2007.03.077.
Pełny tekst źródłaKofler, Michael, Katja Heuer, Tobias Zech i Christian Freund. "Recognition Sequences for the GYF Domain Reveal a Possible Spliceosomal Function of CD2BP2". Journal of Biological Chemistry 279, nr 27 (22.04.2004): 28292–97. http://dx.doi.org/10.1074/jbc.m402008200.
Pełny tekst źródłaAndujar-Sanchez, Montserrat, Eva S. Cobos, Irene Luque i Jose C. Martinez. "Thermodynamic Impact of Embedded Water Molecules in the Unfolding of Human CD2BP2-GYF Domain". Journal of Physical Chemistry B 116, nr 24 (4.06.2012): 7168–75. http://dx.doi.org/10.1021/jp303495b.
Pełny tekst źródłaPiotukh, K., i C. Freund. "A novel hSH3 domain scaffold engineered to bind folded domains in CD2BP2 and HIV capsid protein". Protein Engineering Design and Selection 25, nr 10 (17.09.2012): 649–56. http://dx.doi.org/10.1093/protein/gzs062.
Pełny tekst źródłaGan, Zhen, Bei Wang, Yishan Lu, Shuanghu Cai, Jia Cai, JiChang Jian i Zaohe Wu. "Molecular characterization and expression of CD2BP2 in Nile tilapia (Oreochromis niloticus) in response to Streptococcus agalactiae stimulus". Gene 548, nr 1 (wrzesień 2014): 126–33. http://dx.doi.org/10.1016/j.gene.2014.07.032.
Pełny tekst źródłaKang, Yuanyuan, Bhavita Patel, Kairong Cui, Keji Zhao, Yi Qiu i Suming Huang. "A T-Cell Specific Element Activates the TAL1 Oncogene Via an Interchromosomal Interaction During Leukemogenesis". Blood 120, nr 21 (16.11.2012): 3507. http://dx.doi.org/10.1182/blood.v120.21.3507.3507.
Pełny tekst źródłaRozprawy doktorskie na temat "CD2BP2"
Mansour, Hala. "Characterization of GEXP15 as a potential regulator of protein phosphatase 1 in Plasmodium falciparum". Electronic Thesis or Diss., Université de Lille (2022-....), 2023. http://www.theses.fr/2023ULILS068.
Pełny tekst źródłaMalaria is one of the most prevalent vector-borne infectious diseases threatening 40% of the global population, causing around 300 million cases and 450,000 deaths annually, mostly affecting children under 5. With no effective vaccine and drug resistance emerging, there is an urgent need for innovative treatments. The malaria-causing Plasmodium parasite has a complex life cycle and unique cell division process. Compared to well-studied systems, limited knowledge of Plasmodium biology hampers therapeutic development. Protein phosphorylation, a key regulatory mechanism, is less understood in Plasmodium than in mammalian or yeast cells. Kinases and phosphatases involved in phosphorylation and dephosphorylation processes respectively are potential drug targets. The Protein Phosphatase type 1 catalytic subunit (PP1c) (PF3D7_1414400) operates in combination with various regulatory proteins to specifically direct and control its phosphatase activity. However, there is little information about this phosphatase and its regulators in the human malaria parasite, Plasmodium falciparum. To address this knowledge gap, we conducted a comprehensive investigation into the structural and functional characteristics of a conserved Plasmodium-specific regulator called Gametocyte EXported Protein 15, GEXP15 (PF3D7_1031600). Through in silico analysis, we identified three significant regions of interest in GEXP15: an N-terminal region hous-ing a PP1-interacting RVxF motif, a conserved domain whose function is unknown, and a GYF-like domain that potentially facilitates specific protein-protein interactions. To further elucidate the role of GEXP15, we conducted in vitro interaction studies that demonstrated a direct interaction between GEXP15 and PP1 via the RVxF-binding motif. This interaction was found to enhance the phosphatase activity of PP1. Additionally, utilizing a transgenic GEXP15-tagged line and live microscopy, we observed high expression of GEXP15 in late asexual stages of the parasite, with localization predominantly in the nucleus. Immunoprecipitation assays followed by mass spectrometry analyses revealed the interaction of GEXP15 with ribosomal- and RNA-binding proteins. Furthermore, through pull-down analyses of recombinant functional domains of His-tagged GEXP15, we confirmed its binding to PfPP1 and to the ribosomal complex via the GYF domain. Collectively, our study sheds light on the PfGEXP15-PP1-ribosome interaction, which plays a crucial role in protein translation. These findings suggest that PfGEXP15 could serve as a potential target for the development of malaria drugs
Oliveira, João Bosco Lucena de. "Determinação dos tensores polares de CH2C12/CD2C12 e os clorofluorcarbonos". [s.n.], 1991. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249373.
Pełny tekst źródłaTese (doutorado) - Universidade Estadual de Campinas, Instituto de Quimica
Made available in DSpace on 2018-07-14T01:41:45Z (GMT). No. of bitstreams: 1 Oliveira_JoaoBoscoLucenade_D.pdf: 2836729 bytes, checksum: f689a1a625f22aa90eefb1f02c9d107d (MD5) Previous issue date: 1991
Doutorado
Monzo, Pascale. "Fonctions cellulaires de CD2AP et son implication dans la cytokinese". Nice, 2004. http://www.theses.fr/2004NICE4067.
Pełny tekst źródłaWalker, Jennifer Anne. "CD22, autoimmunity and the B cell". Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612192.
Pełny tekst źródłaBarrett, Anna. "Molecular and cellular investigation of Alzheimer's disease associated risk loci : BIN1 and CD2AP". Thesis, Cardiff University, 2017. http://orca.cf.ac.uk/111373/.
Pełny tekst źródłaWöhner, Miriam [Verfasser], i Lars [Akademischer Betreuer] Nitschke. "Entwicklung einer knockin Mauslinie mit Expression von humanem CD22 zum Test therapeutischer Anwendungen künstlicher CD22-Liganden / Miriam Wöhner. Betreuer: Lars Nitschke". Erlangen : Universitätsbibliothek der Universität Erlangen-Nürnberg, 2012. http://d-nb.info/1024608700/34.
Pełny tekst źródłaBraae, Anne. "Exploring potential functional variants in the Alzheimer's disease associated genes, CD2AP, EPHA1 and CD33". Thesis, University of Nottingham, 2016. http://eprints.nottingham.ac.uk/33083/.
Pełny tekst źródłaBhatt, Arshiya [Verfasser]. "Unraveling details of CIN85/CD2AP assistance to SLP65-mediated B cell activation / Arshiya Bhatt". Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020. http://d-nb.info/1217842810/34.
Pełny tekst źródłaKlein, Jörg. "Verwendung von Gene-Targeting-Techniken zur Etablierung neuer Mauslinien mit Mutationen in B-Zell-Signalwegen". [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=976107953.
Pełny tekst źródłaMari, Muriel. "Caractérisation structurale et fonctionnelle de RABIP4 et CD2AP/CMS, deux effecteurs de la petite GTPase RAB4". Nice, 2002. http://www.theses.fr/2002NICE5727.
Pełny tekst źródłaKsiążki na temat "CD2BP2"
Books, Bchimak. Buchhaltung: Einfaches Einnahmen- und Ausgaben Kassenbuch Für Kleinunternehmen, Einfaches Buchhaltungsbuch Für Selbstständige, Freiberufler und Als Haushaltsbuch Für Die Buchhaltung, über 3300 Einträge Auf 120 Seiten). Cd22. Independently Published, 2021.
Znajdź pełny tekst źródłaCzęści książek na temat "CD2BP2"
Medway, Christopher, i Kevin Morgan. "CD2-Associated Protein (CD2AP)". W Genetic Variants in Alzheimer's Disease, 201–8. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7309-1_11.
Pełny tekst źródłaNewton, Dianne L., Luke H. Stockwin i Susanna M. Rybak. "Anti-CD22 Onconase: Preparation and Characterization". W Therapeutic Antibodies, 425–43. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-554-1_22.
Pełny tekst źródłaKreitman, Robert J., David J. P. FitzGerald i Ira Pastan. "BL22: A Milestone in Targeting CD22". W Next Generation Antibody Drug Conjugates (ADCs) and Immunotoxins, 151–76. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-46877-8_8.
Pełny tekst źródłaTopp, Max, i Tobias Feuchtinger. "Management of Hypogammaglobulinaemia and B-Cell Aplasia". W The EBMT/EHA CAR-T Cell Handbook, 147–49. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-94353-0_28.
Pełny tekst źródłaSmith, K. G. C., i D. T. Fearon. "Receptor Modulators of B-Cell Receptor Signalling — CD19/CD22". W Current Topics in Microbiology and Immunology, 195–212. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57066-7_6.
Pełny tekst źródłaDrgona, Lubos, i Lucia Masarova. "CD22, CD30, CD33, CD38, CD40, SLAMF-7 and CCR4". W Infectious Complications in Biologic and Targeted Therapies, 89–112. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-11363-5_6.
Pełny tekst źródłaBlasioli, J., i C. C. Goodnow. "Lyn/CD22/SHP-1 and Their Importance in Autoimmunity". W Current Directions in Autoimmunity, 151–60. Basel: KARGER, 2001. http://dx.doi.org/10.1159/000060551.
Pełny tekst źródłaCornall, R. J., C. C. Goodnow i J. G. Cyster. "Regulation of B Cell Antigen Receptor Signaling by the Lyn/CD22/SHP1 Pathway". W Current Topics in Microbiology and Immunology, 57–68. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-58537-1_5.
Pełny tekst źródłaFearon, Douglas T. "Non-Structural Determinants of Immunogenicity and the B Cell Co-Receptors, CD19, CD21, and CD22". W Advances in Experimental Medicine and Biology, 181–86. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5355-7_20.
Pełny tekst źródłaHan, Shoufa, Brian E. Collins i James C. Paulson. "Synthesis of 9-Substituted Sialic Acids as Probes for CD22-Ligand Interactions on B Cells". W ACS Symposium Series, 2–14. Washington, DC: American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0960.ch001.
Pełny tekst źródłaStreszczenia konferencji na temat "CD2BP2"
Vasconcelos, D. N., A. C. F. Santos, M. A. MacDonald, M. M. Sant’Anna, B. N. C. Tenório, A. B. Rocha, V. Morcelle, N. Appathurai i L. Zuin. "Ultrafast dissociation of CD2Cl2 and CH2Cl2". W 25TH INTERNATIONAL CONFERENCE ON THE APPLICATION OF ACCELERATORS IN RESEARCH AND INDUSTRY. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5127724.
Pełny tekst źródłaLe, Thuc Duy, Lin Liu, Emre Kiciman, Sofia Triantafyllou i Huan Liu. "The KDD 2022 Workshop on Causal Discovery (CD2022)". W KDD '22: The 28th ACM SIGKDD Conference on Knowledge Discovery and Data Mining. New York, NY, USA: ACM, 2022. http://dx.doi.org/10.1145/3534678.3542890.
Pełny tekst źródłaEggers, David F., W. Lewis-Bevan i M. C. L. Gerry. "Vibration-rotation infrared spectra of CHDF2". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1986. http://dx.doi.org/10.1364/oam.1986.wj3.
Pełny tekst źródłaShah, Nirali N., Haneen Shalabi, Bonnie Yates, Constance Yuan, Haiying Qin, Amanda Ombrello, Hao-Wei Wang i in. "Abstract LB-146: Phase I CD22 CAR T-cell trial updates". W 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-lb-146.
Pełny tekst źródłaShah, Nirali N., Haneen Shalabi, Bonnie Yates, Constance Yuan, Haiying Qin, Amanda Ombrello, Hao-Wei Wang i in. "Abstract LB-146: Phase I CD22 CAR T-cell trial updates". W 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-lb-146.
Pełny tekst źródłaZanetti, SR, T. Velazco-Hernandez, F. Gutierrez-Agüera, H. Roca-Ho, D. Sánchez-Martínez, P. Petazzi, R. Torres i in. "CD19 and CD22-directed biespecific CAR for B-cell Acute Lymphoblastic Leukemia". W 32. Jahrestagung der Kind-Philipp-Stiftung für pädiatrisch onkologische Forschung. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1687121.
Pełny tekst źródłaVitkina, Tatyana, Karolina Sidletskaya i Yulia Denisenko. "Expression of CD282+/CD284+ on blood granulocytes and its relationship to cytokine status in patients with stable chronic obstructive pulmonary disease". W ERS International Congress 2021 abstracts. European Respiratory Society, 2021. http://dx.doi.org/10.1183/13993003.congress-2021.pa3423.
Pełny tekst źródłaYao, Xin, Patricia Burke, Joyce O. Obidi, Xiaoru Chen, Haifeng Bao, Yihong Yao i Jiaqi Huang. "Abstract 4420: Factors potentially contributing to sensitivities of CD22-targeting agents in B-cell malignancies". W Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-4420.
Pełny tekst źródłaGouble, Agnès, Cécile Schiffer-Mannioui, Severine Thomas, Anne-Sophie Gautron, Laurent Poirot i Julianne Smith. "Abstract 3763: UCART22: allogenic adoptive immunotherapy of leukemia by targeting CD22 with CAR T-cells". W Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-3763.
Pełny tekst źródłaMussai, Francis J., Dario Campana, Deepa Bhojwani, Maryalice Stetler-Stevenson, Seth M. Steinberg, Sebastien Morisot, Curt I. Civin, Alan S. Wayne i Ira Pastan. "Abstract 4356: Cytotoxicity of the anti-CD22 immunotoxin HA22 against pediatric acute lymphoblastic leukemia (ALL)". W Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-4356.
Pełny tekst źródła