DADE: a fast data anomaly detection engine for kernel integrity monitoring

The Journal of Supercomputing - In computer systems, ensuring the integrity of the kernel assumes importance as attacks against the kernel allow an adversary to obtain the highest privilege within...     

Developing a custom DSP for vision based human computer interaction applications

Multimedia Tools and Applications - As the computing power of modern devices become greater, computer vision is increasingly adopted as the means of human-computer interaction. The industry is...     

Performance characterization of a small-capacity thermoacoustic cooler for air-conditioning applications

The performance of a working prototype, operated with and without water flow through the heat exchangers, was measured and found to be in reasonably close agreement to predictions from a simulation code, DELTAE, based on linear thermoacoustic theory. Further analysis and DELTAE simulations showed that the coefficient of performance may be significantly reduced when the stack temperature profile becomes non-linear, i.e. when the system is operated for a temperature span smaller than the optimal value for a given stack length. Guidelines to avoid this condition are provided.     

Blockade of accumbens 5-HT3 receptor down-regulation by ondansetron administered during continuous cocaine administration

The present experiment examined whether ondansetron, co-administered with continuous cocaine, would block the down regulation of accumbens 5-HT3 receptors. Rats were exposed to a 14-day pretreatment regimen that involved the continuous infusion of 40 mg kg(-1) day(-1) cocaine or 0.9% saline via a subcutaneously implanted osmotic minipump. In addition to the continuous cocaine or saline administration, all subjects received daily subcutaneous (s.c.) injections of either vehicle or 0.1 mg kg(-1) ondansetron for the entire 14-day pretreatment regimen. The rats were then withdrawn from this pretreatment regimen for seven days, and slices from the nucleus accumbens obtained. The slices were perfused with 25 mM K+ in the absence and presence of 0, 12.5, 25, or 50 microM m-Chlorophenyl-biguanide HCl (mCPBG). The efflux samples were assayed for dopamine content by high pressure liquid chromatography (HPLC) with electrochemical detection. Continuous cocaine administration significantly attenuated the ability of mCPBG to facilitate K+-induce dopamine overflow compared to saline control rats. In addition, the rats that received ondansetron and cocaine during the 14-day pretreatment period, the ability of mCPBG to enhance K+ stimulated dopamine release was not significantly different from the saline control subjects. For all groups except the cocaine alone group, the effects of mCPBG on K+ stimulated dopamine release were Ca2+ dependent, suggesting that these effects are receptor mediated. These results suggest that continuous cocaine administration functionally down-regulates 5-HT3 receptors in the nucleus accumbens, and that this down-regulation can be blocked by chronic ondansetron administration. Hence, a functional down regulation of accumbens 5-HT3 receptors represents a significant contribution to the tolerance induced by continuous cocaine administration.     

Representation of change in controlled medical terminologies

Computer-based systems that support health care require large controlled terminologies to manage names and meanings of data elements. These terminologies are not static, because change in health care is inevitable. To share data and applications in health care, we need standards not only for terminologies and concept representation, but also for representing change. To develop a principled approach to managing change, we analyze the requirements of controlled medical terminologies and consider features that frame knowledge-representation systems have to offer. Based on our analysis, we present a concept model, a set of change operations, and a change-documentation model that may be appropriate for controlled terminologies in health care. We are currently implementing our modeling approach within a computational architecture.     

Nitrogen solubility in high manganese-aluminum alloyed liquid steels

The nitrogen solubility in liquid Fe-Mn and Fe-Mn-Al alloys has been measured by the gas-liquid metal equilibration technique utilizing a high frequency induction furnace under the nitrogen partial pressures of 0.1 to 0.8 atm in the temperature range of 1773 to 1873 K. The variation of the nitrogen solubility with the addition of manganese was measured by sampling and in-situ analysis of nitrogen content. Manganese significantly increased nitrogen solubility in liquid Fe-Mn and Fe-Mn-Al alloys. The nitrogen dissolution followed the Sieverts’ law for liquid Fe-Mn alloys contained manganese up to 26 mass%. Using the Wagner’s interaction parameter formalism, the experimental results were thermodynamically analyzed to determine the first- and second-order interaction parameters of manganese and aluminum on nitrogen in high Mn-Al alloyed liquid steels. No temperature dependence of these values was observed in the temperature range of 1773 to 1873 K. e _N ^Mn = ?0.023, r _N ^MN = 0 r _N ^Mn,Al = 0 (Mn≤26 mass%, Al≤0.4 mass%, 1773–1873 K).     

An in vitro tissue culture bilayer model to examine early events in Mycobacterium tuberculosis infection

A tissue culture bilayer system that mimics some aspects of early alveolar infection by Mycobacterium tuberculosis was developed. This model incorporates human lung epithelial type II pneumocyte (A549) (upper chamber) and endothelial cell (lower chamber) layers separated by a microporous membrane. This construction makes it possible to observe and quantify the passage of bacteria through the two layers, to observe the interaction of the bacteria with the various cell types, and to examine the basic mechanisms of immune cell recruitment to the site of infection. After 10(7) organisms were added to the upper chamber we microscopically observed large numbers of bacteria attached to and within the pneumocytes and we determined by viable-cell counting that a small percentage of the inoculum (0.02 to 0.43%) passed through the bilayer into the lower chamber. When peripheral blood mononuclear cells were added to the lower chamber, microscopic examination indicated a migration of the mononuclear cells through the bilayer to the apical surface, where they were seen associated with the mycobacteria on the pneumocytes. The added complexity of the bilayer system offers an opportunity to define more precisely the roles of the various lung cell types in the pathogenesis of early tuberculosis.     

Specific recognition of HLA-E, but not classical, HLA class I molecules by soluble CD94/NKG2A and NK cells

The CD94/NKG2 receptors expressed by subpopulations of NK cells and T cells have been implicated as receptors for a broad range of both classical and nonclassical HLA class I molecules. To examine the ligand specificity of CD94/NKG2 proteins, a soluble heterodimeric form of the receptor was produced and used in direct binding studies with cells expressing defined HLA class I/peptide complexes. We confirm that CD94/NKG2A specifically interacts with HLA-E and demonstrate that this interaction is dependent on the association of HLA-E with peptide. Moreover, no interaction between CD94/NKG2A and classical HLA class I molecules was observed, as assayed by direct binding of the soluble receptor or by functional assays using CD94/NKG2A+ NK cells. The role of the peptide associated with HLA-E in the interaction between HLA-E and CD94/NKG2A was also assessed. All class I leader sequence peptides tested bound to HLA-E and were recognized by CD94/NKG2A. However, amino acid variations in class I leader sequences affected the stability of HLA-E. Additionally, not all HLA-E/peptide complexes examined were recognized by CD94/NKG2A. Thus CD94/NKG2A recognition of HLA-E is controlled by peptide at two levels; first, peptide must stabilize HLA-E and promote cell surface expression, and second, the HLA-E/peptide complex must form the ligand for CD94/NKG2A.