Abstract
In this paper, we envision an approach for the automatic generation of a user interface (W) prototype from a system domain model (or core model), that captures the main domain entities and transactions, and a system use case model, which captures. the intended user tasks. This prototype allows the early validation of executable core system models, and can be used as a basis for subsequent developments. The envisioned solution uses OCL to add preciseness and semantic richness both to the domain and use case UML models. The generated UI provides some usability enhancements that are derived from the model's pre-conditions.

Abstract
This paper proposes a new real-time communication scheme for IEEE 802.11e HCCA networks. The proposed communication scheme is called Group Sequential Communication (GSC) and it aims the reduction of the polling overhead associated to the real-time message transmission when using the HCCA function. The GSC scheme partially eliminates the polling inefficiency, by means of a virtual token passing procedure among polled stations. Thus, it reduces the number of exchanged messages between the HCCA controller and the polled stations. The GSC uses a real-time group concept, where the real-time members of the group are granted a sequential access to the communication medium.

Abstract
Recent advances in the application of semiconductor nanocrystals, or quantum dots, as biochemical sensors are reviewed. Quantum dots have unique optical properties that make them promising alternatives to traditional dyes in many luminescence based bioanalytical techniques. An overview of the more relevant progresses in the application of quantum dots as biochemical probes is addressed. Special focus will be given to configurations where the sensing dots are incorporated in solid membranes and immobilized in optical fibers or planar waveguide platforms.

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Abstract
Williams-Beuren syndrome (WBS), a neurodevelopmental genetic disorder whose manifestations include visuospatial impairment, provides a unique model to link genetically determined loss of neural cell populations at different levels of the nervous system with neural circuits and visual behavior. Given that several of the genes deleted in WBS are also involved in eye development and the differentiation of retinal layers, we examined the retinal phenotype in WBS patients and its functional relation to global motion perception. We discovered a low-level visual phenotype characterized by decreased retinal thickness, abnormal optic disk concavity, and impaired visual responses in WBS patients compared with age-matched controls by using electrophysiology, confocal and coherence in vivo imaging with cellular resolution, and psychophysics. These mechanisms of impairment are related to the magnocellular pathway, which is involved in the detection of temporal changes in the visual scene. Low-level magnocellular performance did not predict high-level deficits in the integration of motion and 3D information at higher levels, thereby demonstrating independent mechanisms of dysfunction in WBS that will require remediation strategies different from those used in other visuospatial disorders. These findings challenge neurodevelopmental theories that explain cortical deficits based on low-level magnocellular impairment, such as regarding dyslexia.