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Investigates the surface electric field of silicon delta-doped GaAs grown by molecular beam epitaxy at a low substrate temperature using photoreflectance spectroscopy. Observations on Franz-Keldysh oscillations in the reflectance spectra; Explanation for the evolution of photoreflectance spectra; Use of photoreflectance in the study of semiconductors.

Focuses on a study which characterized the redistribution of arsenic precipitates in silicon δ-doped gallium arsenide through x-ray diffractometry and transmission electron microscopy. Experimental details; Results and discussion; Conclusion.

A technique that can reliably monitor exercise intensity plays an important role for the effectiveness and safety of an exercise prescription. A universal algorithm for the recursive estimation of exercise rate during a variety of aerobic exercises using measurements from a body-mounted triaxial accelerometer (TA) is proposed. Information about the type of exercise is not required by the algorithm and the TA can be mounted at the same location regardless of the exercise type. The algorithm involves period detection and data fusion. Experimental results demonstrate that the algorithm is effective for common aerobic exercises. [ABSTRACT FROM AUTHOR]

Little is known about the biological mechanisms underpinning the pathology of schizophrenia. We have analysed the proteome of stimulated and unstimulated peripheral blood mononuclear cells (PBMCs) from schizophrenia patients and controls as a potential model of altered cellular signaling using liquid-chromatography mass spectrometry proteomic profiling. PBMCs from patients and controls were stimulated for 72 h in vitro using staphylococcal enterotoxin B. In total, 18 differentially expressed proteins between first-onset, antipsychotic-naive patients and controls in the unstimulated and stimulated conditions were identified. Remarkably, eight of these proteins were associated with the glycolytic pathway and patient-control differences were more prominent in stimulated compared with unstimulated PBMCs. None of these proteins were altered in chronically ill antipsychotic-treated patients. Non-linear multivariate statistical analysis showed that small subsets of these proteins could be used as a signal for distinguishing first-onset patients from controls with high precision. Functional analysis of PBMCs did not reveal any difference in the glycolytic rate between patients and controls despite increased levels of lactate and the glucose transporter-1, and decreased levels of the insulin receptor in patients. In addition, subjects showed increased serum levels of insulin, consistent with the idea that some schizophrenia patients are insulin resistant. These results show that schizophrenia patients respond differently to PBMC activation and this is manifested at disease onset and may be modulated by antipsychotic treatment. The glycolytic protein signature associated with this effect could therefore be of diagnostic and prognostic value. Moreover, these results highlight the importance of using cells for functional discovery and show that it may not be sufficient to measure protein expression levels in static states. [ABSTRACT FROM AUTHOR]