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Academic literature on the topic 'Zelené stezky'
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Journal articles on the topic "Zelené stezky"
ALI, MUSTAPHA ALHAJI. "An Overview of the Role of Traditional Institutions in Nigeria." Asia Proceedings of Social Sciences 4, no. 3 (2019): 55–58. http://dx.doi.org/10.31580/apss.v4i3.848.
Full textDissertations / Theses on the topic "Zelené stezky"
Muth, Sabine [Verfasser]. "Regulation der Funktion dendritischer Zellen im immunologischen steady state / Sabine Muth." Mainz : Universitätsbibliothek Mainz, 2013. http://d-nb.info/1031262350/34.
Full textDöhler, Anja [Verfasser], and Manfred B. [Akademischer Betreuer] Lutz. "Regulation der Toleranzinduktion von steady-state migratorischen Dendritischen Zellen durch den Transkriptionsfaktor RelB / Anja Döhler. Betreuer: Manfred B. Lutz." Würzburg : Universitätsbibliothek der Universität Würzburg, 2013. http://d-nb.info/1042614652/34.
Full textMurárová, Lucia. "Brownfieldy v ČR v návaznosti na historické centrum." Master's thesis, Vysoké učení technické v Brně. Fakulta stavební, 2019. http://www.nusl.cz/ntk/nusl-400018.
Full textSterk, Marco Heinz [Verfasser], and Karin [Akademischer Betreuer] Schilbach. "Komparative Analyse der CDR3-Region einer alpha beta Progenitorpopulation und den daraus entstandenen alpha beta T-Zellen insbesondere resultierend durch die Stimulation mit Tumor- und Virus-spezifischen Peptiden / Marco Heinz Sterk ; Betreuer: Karin Schilbach." Tübingen : Universitätsbibliothek Tübingen, 2018. http://d-nb.info/1199945919/34.
Full textSterk, Marco H. [Verfasser], and Karin [Akademischer Betreuer] Schilbach. "Komparative Analyse der CDR3-Region einer alpha beta Progenitorpopulation und den daraus entstandenen alpha beta T-Zellen insbesondere resultierend durch die Stimulation mit Tumor- und Virus-spezifischen Peptiden / Marco Heinz Sterk ; Betreuer: Karin Schilbach." Tübingen : Universitätsbibliothek Tübingen, 2018. http://d-nb.info/1199945919/34.
Full textHEŠÍKOVÁ, Monika. "Vnímání přírodních složek krajiny aktéry cestovního ruchu na Třeboňsku." Master's thesis, 2007. http://www.nusl.cz/ntk/nusl-85758.
Full textDöhler, Anja. "Regulation der Toleranzinduktion von steady-state migratorischen Dendritischen Zellen durch den Transkriptionsfaktor RelB." Doctoral thesis, 2012. https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-72343.
Full textTolerance against self-antigens from peripheral tissues can be mediated through CD4+ CD25+ Foxp3+ regulatory T cells (Tregs). These cells develop either during thymic T cell selection (nTregs) or by conversion from naive CD4+ CD25- Foxp3- T cells in peripheral lymphoid organs (induced Tregs, iTregs). During the last years, a role for dendritic cells (DC) in the generation of iTregs has been clearly established. However, the precise DC subset and maturation stage which are required to induce iTregs against peripheral self-antigens remain unknown. Steady-state migratory DC (ssmDC) are a good candidate to carry out such function, since these cells are able to transport self-antigen from peripheral tissues to draining lymph nodes under steady-state conditions. Thus one aim of this thesis was to define the phenotype and tolerogenic capacity of ssmDC in skin-draining lymph nodes. Here, we show that ssmDC display a partially mature MHC IIint CD40hi CD80/CD86int CCR7+ phenotype and that these DC used endogenous TGF-β to convert naive T cells into iTregs in vitro. This study, together with former data generated in our laboratory, demonstrate that in transgenic K5mOVA mice, ssmDC transport and present cell-associated epidermal OVA to CD4+ OVA-specific TCR-transgenic OT-II T cells in the skin-draining lymph nodes. We also identified langerin+ dermal DC cells among the different subsets of ssmDC, as the subset which mediates the conversion of naïve OT-II T cells into CD4+ CD25+ Foxp3+ iTregs. Furthermore, we observed that CD103 was not a suitable marker for ssmDC in skin-draining lymph nodes despite that it has been correlated with tolerogenic DC in the intestine. An additional aim of this work was to investigate the impact of the transcription factor RelB on the partial maturation and migration of ssmDC. RelB is a member of the NF-κB family and has been associated with DC maturation. Initial experiments showed nuclear translocation of RelB in ssmDC and in addition, relB+/- mice as well as mice with a deficiency of the RelB-binding partner p52 had a reduced migration of ssmDC to skin-draining lymph nodes. Nevertheless, the analysis of mice with a DC-specific ablation of RelB (RelBDCko mice) revealed an increased frequency of ssmDC in skin-draining lymph nodes which was not due to an increased number or altered distribution of DC in the skin. On the one hand, these data suggest that the effects on ssmDC seen in the relB+/- mice were mediated by DC-extrinsic mechanisms. On the other hand, the increase of ssmDC in RelBDCko mice indicated that RelB might be rather a negative regulator of ssmDC migration under homeostatic conditions. Moreover, RelB also affected the maturation of ssmDC partially, since ssmDC in the skin-draining lymph nodes of RelBDCko mice expressed more CD40 on their surface, while other maturation markers as MHC II, CD80 and CD86 were not significantly altered. Finally, it was investigated how RelB deficiency in DC affects the induction and homeostasis of Tregs. To this aim we examined RelBDCko mice in which we observed an increased frequency and absolute number of Tregs in all lymphatic organs analyzed (skin-draining lymph nodes, spleen and thymus). Furthermore, Tregs showed an increased proliferation in these organs compared to control mice. In particular, Tregs in RelBDCko mice proliferated more vigorously in the skin-draining lymph nodes compared to the spleen. Thus, RelB seems to influence the tolerogenic DC capacity by regulating the expansion of Tregs generated in the thymus as well as their peripheral maintenance. By using a neutralizing anti-IL-2 antibody, we could also demonstrate that the peripheral proliferation of Tregs in the RelBDCko mice was dependent on IL-2, indicating that production of IL-2 either by conventional T cells or DC themselves is affected through RelB deficiency. In accordance with this observation, preliminary experiments showed an increased IL-2 production in the peripheral lymphoid organs of RelBDCko mice. Taken together, the data of this study strongly suggest that ssmDZ are potent inducers of iTregs in response to epidermal self-antigens in skin-draining lymph nodes. Moreover, the analysis of a novel conditional mouse model with a DC-specific deletion of RelB indicated that the migration and maturation of ssmDC is partially regulated by RelB. Since Tregs play a key role in the maintenance of peripheral tolerance, our finding that a deficiency of RelB in all DC affects the proliferation and therefore the homeostasis of Tregs provides an interesting starting-point for further investigation
Stenke, Tanja Susanne [Verfasser]. "Untersuchungen über den Einfluss der multipel hydrophoben Proteine des Equiden-Herpesvirus 1 auf die Replikation in polarisierten Zellen / von Tanja Susanne Stenke." 2006. http://d-nb.info/979204046/34.
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