Jacques Derrida et l’esthétiqueRoelens, Nathalie ![]() Book published by L'Harmattan (2000) Detailed reference viewed: 94 (2 UL)![]() Jacques Derrida's religion with/out religion and the im/possibility of religious education; Biesta, Gert ![]() in Litchfield, R.G. (Ed.) Leading with hope.The Vocation of the Religious Educator. 2002 Proceedings of the Association of Professors and Researchers in Religious Education. (2002) Detailed reference viewed: 77 (1 UL)![]() Jacques Derrida’s religion with/out religion and the im/possibility of religious education.; Biesta, Gert ![]() in Murphy, M (Ed.) Social theory and educational research (2013) Detailed reference viewed: 79 (1 UL)![]() Jacques Derrida’s religion with/out religion and the im/possibility of religious education.; Biesta, Gert ![]() in Religious Education (2004), 99(1), 23-37 Detailed reference viewed: 78 (1 UL) Jacques Derrida. Deconstruction = JusticeBiesta, Gert ![]() in Peters, M.; Olssen, M.; Lankshear, C. (Eds.) Futures of critical theory: Dreams of difference (2003) Detailed reference viewed: 50 (0 UL) Jacques Fontanille, Soma et Séma, 2004Tore, Gian Maria ![]() in RSSI : Recherches Sémiotiques = RSSI: Semiotic Inquiry (2004), 24(1-3), 299-317 Detailed reference viewed: 73 (1 UL) Jacques Rancière: Education, truth, emancipation; Biesta, Gert ![]() Book published by Continuum (2010) Detailed reference viewed: 101 (0 UL) Jahn-Teller, Polarity, and Insulator-to-Metal Transition in BiMnO3 at High Pressure; ; et al in Physical Review Letters (2014), 112 The interaction of coexisting structural instabilities in multiferroic materials gives rise to intriguing coupling phenomena and extraordinarily rich phase diagrams, both in bulk materials and strained ... [more ▼] The interaction of coexisting structural instabilities in multiferroic materials gives rise to intriguing coupling phenomena and extraordinarily rich phase diagrams, both in bulk materials and strained thin films. Here we investigate the multiferroic BiMnO3 with its peculiar 6s2 electrons and four interacting mechanisms: electric polarity, octahedra tilts, magnetism, and cooperative Jahn-Teller distortion. We have probed structural transitions under high pressure by synchrotron x-ray diffraction and Raman spectroscopy up to 60 GPa. We show that BiMnO3 displays under pressure a rich sequence of five phases with a great variety of structures and properties, including a metallic phase above 53 GPa and, between 37 and 53 GPa, a strongly elongated monoclinic phase that allows ferroelectricity, which contradicts the traditional expectation that ferroelectricity vanishes under pressure. Between 7 and 37 GPa, the Pnma structure remains remarkably stable but shows a reduction of the Jahn-Teller distortion in a way that differs from the behavior observed in the archetypal orthorhombic Jahn-Teller distorted perovskite LaMnO3. [less ▲] Detailed reference viewed: 83 (5 UL) Jahrestagung des Sozialwissenschftlichen AusschussesNeugebauer, Tibor ![]() Presentation (2015) Detailed reference viewed: 22 (0 UL) Jahrmärkte in Europa im 14.-16. Jahrhundert. Regionale Untersuchungen und der Versuch einer TypologiePauly, Michel ![]() in Irsigler, Franz; Pauly, Michel (Eds.) Messen, Jahrmärkte und Stadtentwicklung in Europa (2007) Detailed reference viewed: 49 (0 UL) JAIL: a structure-based interface library for macromolecules.; ; May, Patrick et alin Nucleic Acids Research (2009), 37(Database issue), 338-41 The increasing number of solved macromolecules provides a solid number of 3D interfaces, if all types of molecular contacts are being considered. JAIL annotates three different kinds of macromolecular ... [more ▼] The increasing number of solved macromolecules provides a solid number of 3D interfaces, if all types of molecular contacts are being considered. JAIL annotates three different kinds of macromolecular interfaces, those between interacting protein domains, interfaces of different protein chains and interfaces between proteins and nucleic acids. This results in a total number of about 184,000 database entries. All the interfaces can easily be identified by a detailed search form or by a hierarchical tree that describes the protein domain architectures classified by the SCOP database. Visual inspection of the interfaces is possible via an interactive protein viewer. Furthermore, large scale analyses are supported by an implemented sequential and by a structural clustering. Similar interfaces as well as non-redundant interfaces can be easily picked out. Additionally, the sequential conservation of binding sites was also included in the database and is retrievable via Jmol. A comprehensive download section allows the composition of representative data sets with user defined parameters. The huge data set in combination with various search options allow a comprehensive view on all interfaces between macromolecules included in the Protein Data Bank (PDB). The download of the data sets supports numerous further investigations in macromolecular recognition. JAIL is publicly available at http://bioinformatics.charite.de/jail. [less ▲] Detailed reference viewed: 500 (1 UL) Jak1 has a dominant role over Jak3 in signal transduction through γc-containing cytokine receptorsHaan, Claude ; Rolvering, Catherine ; et alin Chemistry & Biology (2011), 18(3), 314-323 Genetic deficiency of Jak3 leads to abrogation of signal transduction through the common gamma chain (γc) and thus to immunodeficiency suggesting that specific inhibition of Jak3 kinase may result in ... [more ▼] Genetic deficiency of Jak3 leads to abrogation of signal transduction through the common gamma chain (γc) and thus to immunodeficiency suggesting that specific inhibition of Jak3 kinase may result in immunosuppression. Jak1 cooperates with Jak3 in signaling through γc-containing receptors. Unexpectedly, a Jak3-selective inhibitor was less efficient in abolishing STAT5 phosphorylation than pan-Jak inhibitors. We therefore explored the roles of Jak1 and Jak3 kinase functionality in signaling using a reconstituted system. The presence of kinase-inactive Jak1 but not kinase-inactive Jak3 resulted in complete abolishment of STAT5 phosphorylation. Specific inhibition of the "analog-sensitive" mutant AS-Jak1 but not AS-Jak3 by the ATP-competitive analog 1NM-PP1 abrogated IL-2 signaling, corroborating the data with the selective Jak3 inhibitor. Jak1 thus plays a dominant role over Jak3 and these data challenge the notion that selective ATP-competitive Jak3 kinase inhibitors will be effective. © 2011 Elsevier Ltd. [less ▲] Detailed reference viewed: 88 (2 UL)![]() The Jak1 SH2 domain does not fulfill a classical SH2 function in Jak/STAT signaling but plays a structural role for receptor interaction and up-regulation of receptor surface expression; Haan, Serge ; et alin Journal of Biological Chemistry (2005), 280(27), 25760-8 The presence of a Src homology 2 (SH2) domain sequence similarity in the sequence of Janus kinases (Jaks) has been discussed since the first descriptions of these enzymes. We performed an in depth study ... [more ▼] The presence of a Src homology 2 (SH2) domain sequence similarity in the sequence of Janus kinases (Jaks) has been discussed since the first descriptions of these enzymes. We performed an in depth study to determine the function of the Jak1 SH2 domain. We investigated the functionality of the Jak1 SH2 domain by stably reconstituting Jak1-defective human fibrosarcoma cells U4C with endogenous amounts of Jak1 in which the crucial arginine residue Arg466 within the SH2 domain has been replaced by lysine. This mutant still binds to the receptor subunits gp130 and OSMR. Moreover, the SH2 R466K mutation does not affect the subcellular distribution of Jak1 as assessed by cell fractionation and confocal microscopy of cells expressing endogenous levels of non-tagged or a yellow fluorescent protein (YFP)-tagged Jak1-R466K, respectively. Likewise, the signaling capacity of Jak1 was not affected by this point mutation. However, we found that the SH2 domain is structurally important for cytokine receptor binding and surface expression of the OSMR. [less ▲] Detailed reference viewed: 109 (2 UL) JAK2 mutants (e.g., JAK2V617F) and their importance as drug targets in myeloproliferative neoplasms; Behrmann, Iris ; Haan, Claude ![]() in JAK-STAT (2013), 2(3), 25025 The Janus kinase 2 (JAK2) mutant V617F and other JAK mutants are found in patients with myeloproliferative neoplasms and leukemias. Due to their involvement in neoplasia and inflammatory disorders, Janus ... [more ▼] The Janus kinase 2 (JAK2) mutant V617F and other JAK mutants are found in patients with myeloproliferative neoplasms and leukemias. Due to their involvement in neoplasia and inflammatory disorders, Janus kinases are promising targets for kinase inhibitor therapy. Several small-molecule compounds are evaluated in clinical trials for myelofibrosis, and ruxolitinib (INCB018424, Jakafi®) was the first Janus kinase inhibitor to receive clinical approval. In this review we provide an overview of JAK2V617F signaling and its inhibition by small-molecule kinase inhibitors. In addition, myeloproliferative neoplasms are discussed regarding the role of JAK2V617F and other mutant proteins of possible relevance. We further give an overview about treatment options with special emphasis on possible combination therapies. [less ▲] Detailed reference viewed: 74 (3 UL) JAK2-V617F-induced MAPK activity is regulated by PI3K and acts synergistically with PI3K on the proliferation of JAK2-V617F-positive cells.; ; Gäbler, Karoline et alin JAK-STAT (2013), 2(3), 24574 The identification of a constitutively active JAK2 mutant, namely JAK2-V617F, was a milestone in the understanding of Philadelphia chromosome-negative myeloproliferative neoplasms. The JAK2-V617F mutation ... [more ▼] The identification of a constitutively active JAK2 mutant, namely JAK2-V617F, was a milestone in the understanding of Philadelphia chromosome-negative myeloproliferative neoplasms. The JAK2-V617F mutation confers cytokine hypersensitivity, constitutive activation of the JAK-STAT pathway, and cytokine-independent growth. In this study we investigated the mechanism of JAK2-V617F-dependent signaling with a special focus on the activation of the MAPK pathway. We observed JAK2-V617F-dependent deregulated activation of the multi-site docking protein Gab1 as indicated by constitutive, PI3K-dependent membrane localization and tyrosine phosphorylation of Gab1. Furthermore, we demonstrate that PI3K signaling regulates MAPK activation in JAK2-V617F-positve cells. This cross-regulation of the MAPK pathway by PI3K affects JAK2-V617F-specific target gene induction, erythroid colony formation, and regulates proliferation of JAK2-V617F-positive patient cells in a synergistically manner. [less ▲] Detailed reference viewed: 145 (8 UL) Jaks and cytokine receptors - an intimate relationshipHaan, Claude ; Kreis, Stephanie ; Margue, Christiane et alin Biochemical Pharmacology (2006), 72(11), 1538-46 Most cytokine receptors lack intrinsic kinase activity and many of them signal via Janus kinases (Jaks). These tyrosine kinases are associated with cytokine receptor subunits, they become activated upon ... [more ▼] Most cytokine receptors lack intrinsic kinase activity and many of them signal via Janus kinases (Jaks). These tyrosine kinases are associated with cytokine receptor subunits, they become activated upon receptor triggering and subsequently activate downstream signalling events, e.g. the phosphorylation of STAT transcription factors. The successful interplay between cytokines, their receptors and the connected Jaks not only determines signalling competence but is also vital for intracellular traffic, stability, and fate of the cognate receptors. Here, we will discuss underlying mechanisms as well as some structural features with a focus on Jak1 and two of the signal transducing receptor subunits of interleukin (IL)-6 type cytokines, gp130 and OSMR. Regions that are critically involved in Jak-binding have been identified for many cytokine receptor subunits. In most cases the membrane-proximal parts comprising the box1 and box2 regions within the receptor are involved in this association while, within Jaks, the N-terminal FERM domain, possibly together with the SH2-like domain, are pivotal for binding to the relevant receptors. The exclusive membrane localisation of Jaks depends on their ability to associate with cytokine receptors. For gp130 and Jak1, it was shown that the cytokine receptor/Jak complex can be regarded as a receptor tyrosine kinase since both molecules have the same diffusion dynamics and are virtually undissociable. Furthermore, Jaks take an active role in the regulation of the surface expression of at least some cytokine receptors, including the OSMR and this may provide a quality control mechanism ensuring that only signalling-competent receptors (i.e. those with an associated Jak) would be enriched at the cell surface. [less ▲] Detailed reference viewed: 98 (5 UL) JAM-A is a novel surface marker for NG2-Glia in the adult mouse brain.; ; Schwamborn, Jens Christian ![]() in BMC Neuroscience (2010), 11 BACKGROUND: Junctional adhesion molecule-A (JAM-A) is an adhesive protein expressed in various cell types. JAM-A localizes to the tight junctions between contacting endothelial and epithelial cells, where ... [more ▼] BACKGROUND: Junctional adhesion molecule-A (JAM-A) is an adhesive protein expressed in various cell types. JAM-A localizes to the tight junctions between contacting endothelial and epithelial cells, where it contributes to cell-cell adhesion and to the control of paracellular permeability. RESULTS: So far, the expression pattern of JAM-A has not been described in detail for the different cell types of the adult brain. Here we show that a subset of proliferating cells in the adult mouse brain express JAM-A. We further clarify that these cells belong to the lineage of NG2-glia cells. Although these mitotic NG2-glia cells express JAM-A, the protein never shows a polarized subcellular distribution. Also non-mitotic NG2-glia cells express JAM-A in a non-polarized pattern on their surface. CONCLUSIONS: Our data show that JAM-A is a novel surface marker for NG2-glia cells of the adult brain. [less ▲] Detailed reference viewed: 142 (0 UL) JAM-C is an apical surface marker for neural stem cells.; ; et al in Stem Cells & Development (2012), 21(5), 757-66 Junctional adhesion molecule-C (JAM-C) is an adhesive cell surface protein expressed in various cell types. JAM-C localizes to the apically localized tight junctions (TJs) between contacting endothelial ... [more ▼] Junctional adhesion molecule-C (JAM-C) is an adhesive cell surface protein expressed in various cell types. JAM-C localizes to the apically localized tight junctions (TJs) between contacting endothelial and epithelial cells, where it contributes to cell-cell adhesions. Just as those epithelial cells, also neural stem cells are highly polarized along their apical-basal axis. The defining feature of all stem cells, including neural stem cells (NSCs) is their ability to self renew. This self-renewal depends on the tight control of symmetric and asymmetric cell divisions. In NSCs, the decision whether a division is symmetric or asymmetric largely depends on the distribution of the apical membrane and cell fate determinants on the basal pole of the cell. In this study we demonstrate that JAM-C is expressed on neural progenitor cells and neural stem cells in the embryonic as well as the adult mouse brain. Furthermore, we demonstrate that in vivo JAM-C shows enrichment at the apical surface and therefore is asymmetrically distributed during cell divisions. These results define JAM-C as a novel surface marker for neural stem cells. [less ▲] Detailed reference viewed: 141 (2 UL) James Bond's Most Secret WeaponLeprévost, Franck ![]() in Proceedings of the 3rd International Conference on Applications in Information Technology (2018) This conference presents in a non-conventional way secret-key and public-key cryptology from its origins to the present days. Detailed reference viewed: 104 (4 UL) JANE - The Java Ad Hoc Network Development Environment; ; Hiedels, Christian ![]() in 40th Annual Simulation Symposium, 2007. ANSS '07. (2007) This work describes a Java based development platform which is intended to support ad hoc network researchers in application and protocol design. Software development within this environment is expected ... [more ▼] This work describes a Java based development platform which is intended to support ad hoc network researchers in application and protocol design. Software development within this environment is expected to follow a bottom up approach. Basic functionality is implemented in elementary components which can be combined to more complex ones by using well defined interfaces. With dynamically changing network links being rather the common case than a failure situation, asynchronous communication has been selected as the main communication paradigm within this platform. Reusability of components in different execution contexts by providing an appropriate machine abstraction is a further important design decision which drove the platform development. Code written once can be executed in a pure simulation mode, in a hybrid setting with real devices being attached to a running simulation and, finally, in a setting using real devices only. Software development following this three-tier development process paired with the platform's rich visualization features emerged to significantly ease the burden of debugging and parameterizing in such highly dynamic and inherently distributed environments. In conjunction with a core middleware platform a rich set of generic services has been implemented with the most important ones being described in this work. Several application programs have already been implemented on top of these services. These applications which are described in this work as well serve as a proof of concept for both the platform itself and the utilized set of generic services [less ▲] Detailed reference viewed: 91 (1 UL) |
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